CA2302806A1 - Macrophage derived chemokine (mdc), mdc analogs, mdc inhibitor substances, and uses thereof - Google Patents

Abstract

The present invention provides purified and isolated polynucleotide sequences encoding a novel macrophage-derived C-C chemokine designated "Macrophage Derived Chemokine" (MDC), and polypeptide fragments and analogs thereof. Also provided are materials and methods for the recombinant or synthetic production of the chemokine, fragments, and analogs; and purified and isolated chemokine protein, and polypeptide fragments and analogs thereof. Also provided are antibodies reactive with the chemokine and methods of making and using all of the foregoing. Also provided are assays for identifying modulators of MDC chemokine activity.

Description

MACROPHAGE DERIVED CHEMOIaNE (MDC), MDC ANALOGS, MDC ll~IHIBITOR SUBSTANCES. AND USES THEREOF
This application is a continuation-in-part of U.S. Patent Application Serial No.
09/067,447, filed April 28, 1998, and a continuation-in-part of U. S. Patent Application Serial No.
08/939,107, fill September 26, 1997, (Attorney docket No. 27866/34188), and a continuation-in-part of U. S. Patent Application Serial No. 08/660, 542, filed June 7, 1996, and a continuation-in-part of U.S. Patent Application Serial No. 08/558,658, filed November 16, 1995, and a continuation-in part ofU.S. Patent Application Serial No. 08/479,620, filed June 7, 1995. These applications are hereby incorporated by reference in their entirety.
The present invention relates generally to chemokines and more particularly to purified and isolated polynucleotides encoding a novel human C-C chemokine, to purified and isolated chemokine protein encoded by the polynucleotides, to chemokine analogs, to materials and methods for the recombinant production of the novel chemokine protein and analogs, to antibodies reactive with the novel chemokine, to chemokine inhibitors, and to uses of all of the foregoing materials. Of particular interest is the use of chemokine inhibitor substances to treat allergic conditions such as asthma.
Chemokines, also known as "intercrines" and "SIS cytokines", comprise a family of small secreted proteins (e.g., 70-100 amino acids and about 8-10 kiloDaitons) which attract and activate leukocytes and thereby aid in the stimulation and regulation of the immune system.

2 5 The name "chemokine" is derived from chemotactic cytokine, and refers to the ability of these proteins to stimulate chemotaxis of leukocytes. Indeed, chemokines may comprise the main attractants for inflammatory cells into pathological tissues. See generally, Baggiolini et al., Armu.
Rev Immunol, I5: 675-705 (1997); and Baggiolini et al., Advances in Immunolog)r, 55:97-179 (1994), both of which are incorporated by reference herein. While leukocytes comprise a rich 3 0 source of chemokines, several chemokines are expressed in a multitude of tissues. Baggiolini et al. (1994), Table II.

Preciously identified chemokines generally exhibit 20-70% amino acid identity to each other and contain four highly-conserved cysteine residues. Based on the relative position of the first two of these cysteine residues, chemokines have been further classified into two subfamilies. In the "C-X C" or "a" subfamily, encoded by genes localized to human chromosome 4, the first two cysteines are separated by one amino acid. In the "C-C" or "~i" subfamily, encoded by genes on human chromosome 17, the first two cysteines are adjacent. X-ray crystallography and NMR studies of several chemokines have indicated that, in each family, the first and third cysteines form a first disulfide bridge, and the second and fourth cysteines form a second disulfide bridge, strongly influencing the native conformation of the proteins. In humans alone, more than ten distinct sequences have been described for each chemokine subfiunily.
Chemokines of both subfi~cnities have characteristic leader sequences of twenty to twenty-five amino acids.
The C-X-C chemokines, which include IL-8, GROaJ~i/y, platelet basic protein, Platelet Factor 4 (PF4), IP-10, NAP2, and others, share approximately 25% to 60% identity when airy two amino acid sequences are compared (except for the GROal~3/y members, which are 84-88% idemical with each other). Most of the C-X-C chemokines (excluding IP-10 and Platelet Factor 4) share a common E-I,-R tri-peptide motif upstream of the first two cysteine residues, and are potent stimulants of neutrophils, causing rapid shape change, chemotaxis, respiratory bursts, and degranulation. These effects are mediated by seven-transmembrane-domain rhodopsin-like G protein-coupled rexeptors; a receptor specific for IIr8 has been cloned by Holmes et al., 2 0 Science, 253:1278-80 ( 1991 ), while a similar receptor (77% identity) which recognizes IL-8, GRO and NAP2 has been cloned by Murphy and Tiffany, Science, 253:1280-83 (1991).
Progressive truncation of the N-terminal amino acid sequence of certain C-X-C
chemokines, including IG8, is associated with marked increases in activity.
The C-C cheanokines, which include Macrophage Inflammatory Proteins MIP-la and MIP-1(3, Monocyte cheanoattractant profane 1, 2, 3, and 4 (MCP-1/2/3/4), RANTES, I-309, eotaxin, TARC, and others, share 25% to 70% amino acid identity with each other. Previously-identified C-C chemokines activate monoc5rtes, causing calcium flux and chemotaxis. More selective effects are seen on lymphocytes, for example, T lymphocytes, which respond best to RANTES. Several seven-transmembrane-domain G protein-coupled receptors for C-C
3 0 chemokines have been cloned to date, including a C-C chemokine receptor-1 (CCRl) which recognizes, e.g., MIP-la andRANTES (Neoteetal., Cell, 72:415-425 (1993)); a CCR2 receptor which has two splice variants and which recognizes, e.g., MCP-1 (Charo et al., Proc. Nat. Acad.
Sci., 91:2752-56 (1994)); CCR3, which recognizes, e.g., eotaxin, RANTES, and (Combadiere, J. Bio~ Chem., 270:16491 (1995)); CCR4, which recognizes MIP-1 a, P;ANTES, and MCP-1 (Power et a1, J. Bio~ Chem., 270:19495 (1995)); and CCRS, which recognizes MIP-la, MIP-lei, and RANTES (Samson ~t aL, Biochemstry, 35:3362 (1996)). Several CC
chemokines have been shown to act as attractants for activated T lymphocytes.
See Baggiolini et al. (1997).
Truncation of the N-terminal amino acid sequ~ce of certain C-C chemokines also has been associated with alterations in activity. For example, mature RANTES
(1-68) is processed by CD26 (a dipeptidyl aminopeptidase specific for the sequence NIi2-X-Pro- . . .) to generate a RANTES (3-68) form that is capable of interacting with and transducing a signal through CCRS (like the RANTES (1-68) form), but is one hundred-fold reduced in its capacity to stimulate through the receptor CCRl. See Proost et al., J. Biol. Chem., 273(13): 7222-7227 (1998); and Oravecz et al., J. Fxp. Med, 186: 1865-1872 (1997). United States Patent Nos.

5;459,128, 5,705,360, and 5,739,103 to Rollins and Zhang purport to describe N-terminal deletions of chemokine MCP-1 that inhibit receptor binding to the corresponding endogenous chemokine.
The roles of a number of chemokines, particularly IL-8, have been well documented in various pathological conditions. See generally Baggiolini et al.(1994), supra, 2 0 Table VII. Psoriasis, for example, has been linked to over-production of IL,-8, and several studies have observed high levels of I>i8 in the synovial fluid of inflamed joints of patients suffering from rheumatic diseases, osteoarthritis, and gout.
The role of C-C chemokines in pathological conditions also has been documented, albeit less comprehensively than the role of IL-8. For example, the concentration of MCP-1 is 2 5 higher in the synovial fluid of patients suffering from rheumatoid arthritis than that of patients suffering from other arthritic diseases. The MCP-1 dependent influx of mononuclear phagocytes may be an important event in the development of idiopathic pulmonary fibrosis.
The role of C-C
chemokines in the recruitment of monocytes into atherosclerotic areas is currently of intense interest, with enhanced MCP-1 expression having been detected in macrophage-rich arterial wall 3 0 areas but not in normal arterial tissue. Expression of MCP-1 in malignant cells has been shown to suppress the ability of such cells to form tumors in vivo. (See U.S. Patent No. 5,179,078, incorporated herein by reference.) A need therefore exists for the identification and characterization of additional C-C chemokines, to further elucidate the role of this important family of molecules in pathological conditions, and to develop improved treatments for such conditions utilizing chemokine-derived products.
With respect to the involvement of chemolcines in allergic diseases, interest has focused on chemokines belonging to the CC family, such as RATTTES, eotaxin, eotaxin-2, MCP-3 and MCP-4, because of their ability to cause migration of human eosinophils in vitro and in vivo.
The ability ofthese chemokines to selectively activate human eosinophil migration appears to be due primarily to their activation of chemokine receptor CCR3. A need exists to elucidate the involvement of these and other chemokines in eosinophil stimulation and activation, to facilitate better treatments for late-phase allergic reactions, such as asthma [see Aalbers et a~, Eur.Respir.J., 6:840(1993); and Frigas et al., J. Allergy Clip. Immunol., 77:527(1986)], in which eosinophil activation and migration have been implicated.
Chemokines of the C-C subfamily have been shown to possess utility in medical imaging, e.g., for imaging sites of infection, inflammation, and other sites having C-C chemokine receptor molecules. See, e.g., Kunkel et al., U.S. Patent No. 5,413,778, incorporated herein by reference. Such methods involve chemical attachment of a labeling agent (eg., a radioactive isotope) to the C-C chemokine using art recognized techniques (see, e.g., U.S.
Patent Nos.
4,965,392 and 5,037,630, incorporated herein by reference), administration of the labeled 2 0 chemokine to a subject in a pharmaceutically acceptable carrier, allowing the labeled chemokine to accumulate at a target site, and imaging the labeled chemolcine in vivo at the target site. A
need in the art exists for additional new C-C chemokines to increase the available arsenal of medical imaging tools.
The C-C che<nokines RANTES, M~-a, and MIP-1(3 also have been shown to be 2 5 the primary mediators of the suppressive effect of human T cells on the human immunodeficiency virus (HIV), the agent responsible for causing human Acquired Immune Deficiency Syndrome (AIDS). These chemokines show a dose-dependent ability to inhibit specific strains of HIV from infecting cultured T cell lines [Cocchi et a~, Science, 270:1811 (1995)]. In addition, International patent publication number WO 97/44462, filed by Institut Pasteur, describes the use of fragments 3 0 and analogs of the chemokine RANTES as antagonists, to block RANTES
interaction with its receptors, for the purpose of suppressing HIV. The C-X-C chemokine stromal derived factor-1 6 . PCT/US98/20270 _$-(SDF-1) also is capable of blocking infection by T-tropic HIV-1 strains. See Winkler et al., Science, 279:389-393 (1998). However, the processes through which chemokines exert their protective effects have not been fully elucidated, and these chemokines in fact may stimulate HIV
replication in cells exposed to the chemokines before HIV infection. See Kelly et a~, J. Irrtmunol., 160:3091-3095 (1998). Moreover, not all~ested strains of the virus are equally susceptible to the inlu'bitory effects of chemokines; therefore, a need exists for additional C-C
chemokines for use as inhibitors of strains of HIV.
Similarly, it has been established that certain chemokine receptors such as CCRS
[International Patent Publication No. WO 97/44055, published 27 November 1997], CCR8, CCR2, and CXCR4) are essential co-receptors (with the CD4 receptor) for HIV-1 entry into susceptible cells, and that progression to AI17S is delayed in patients having certain variant alleles of these receptors. A need exists for additional therapeutics to inhibit HIV-1 infection and/or proliferation by interfering with HIV-1 entry and/or proliferation in susceptible cells.
More generally, due to the importance of chemokines as mediators of chemotaxis and inflammation, a need exists for the identification and isolation of new members of the chemokine family to facilitate modulation of inflammatory and immune responses.
For example, substances that promote inflamtnation may promote the healing of wounds or the speed of recovery from conditions such as pneumonia, where inflammation is important to eradication of infection. Modulation of inflammation is similarly important in 2 0 pathological conditions manifested by inflanunation. Crohn's disease, manifested by chronic inflammation of all layers of the bowel, pain, and diarrhea, is one such pathological condition.
The failure rate of drug therapy for Crohn's disease is relatively high, and the disease is often recurrent even in patients receiving surgical intervention. The identification, isolation, and characterizaxion of novel chemokines facilitates modulation of inflammation.
2 5 Similarly, substances that induce an immune response may promote palliation or healing of arty number of pathological conditions. Due to the important rote of leukocytes (e.g., neutrophils and monocytes) in cell-mediated immune responses, and due to the established role of chemokines in leukocyte chemotaxis, a need exists for the identification and isolation of new chemokines to facilitate modulation of imriiune responses.
3 0 Additionally, the established correlation between chemokine expression and inflammatory conditions and disease states provides diagnostic and prognostic indications for the use of chemokines, as well as for antibody substances that are specifically immunoreactive with chemokines; a need exists for the identification and isolation of new chemokines to facilitate such diagnostic and prognostic indications.
In addition to their ability to attract and activate leukocytes, some chemokines, such as IIr-8, have been shown to be capable of affecting the proliferation of non-leukocytic cells.
See Tuschil, J. Invest. Dermatol., 99:294-298 (1992). A need exists for the identification and isolation of new chemokines to facilitate modulation of such cell proliferation.
It will also be apparent from the foregoing discussion of chemokine activities that a need exists for modulators of chemokine activities, to inhibit the effects of endogenously-produced chemokines and/or to promote the activities of endogenously-produced or exogenously administered chemokines. Such modulators typically include small molecules, peptides, chemokine fi-agments and analogs, andJor antibody substances. Chemokine inhibitors interfere with chemokine signal transduction, i.e., by binding chemokine molecules, by competitively or non-competitively binding chemokine receptors, andlor by interfering with signal transduction downstream finm the chemokine n~eptors. A need exists in the art for egective assays to rapidly screen putative chemokine modulators for modulating activity.
For all of the aforementioned reasons, a need exists for recombinant methods of production of newly discovered chemokines, which methods facilitate clinical applications involving the chemokines and chemokine inhibitors.
2a The present invention provides novel purified and isolated polynucleotides and polypeptides, antibodies, and methods and assays that fulfill one or more of the needs outlined above.
For example, the invention provides purified and isolated polynucleotides (i.e., DNA and RNA, both sense and antisense strands) encoding a~novel human chemokine of the C-C
subfamily, herein designated "Macrophage Derived Chemokine" or "MDC".
Preferred DNA
sequences of the invention include genomic and cDNA sequences and chemically synthesized DNA sequences. The cDNA and deduced amino acid sequence of human MDC has been 3 0 published. See, e.g., International Patent Publication No. WO 96/40923, published 19 December 1996; and Godiska et al., J. F..,xp. Med, 185(9): 1595-1604 (199'x. Compare International -7_ Publication No. WO 96/39521 (12 December 1996); and Chang et al., J. Biol.
Chem., 272(40):
25229-25237 (1997).
Polynucleotides encoding non-human vertebrate forms of MDC, especially mammalian and avian forms of N1DC, also are intended as aspects of the invention.
The nucleotide sequence of a cDNA, designated MDC cDNA, encoding this chemokine, is set forth in SEQ D7 NO: 1, which sequence includes 5' and 3' non-coding sequences. A preferred DNA of the present invention comprises nucleotides 20 to 298 of SEQ
ff~ NO. 1, which nucleotides comprise the MDC coding sequence.
The human MDC protein comprises a putative twenty-four amino acid signal sequence at its amino terminus. Another preferred DNA of the present invention comprises nucleotides 92 to 298 of SEQ 1D NO. 1, which nucleotides comprise the putative coding sequence of the mature (secreted) 1V1DC protein, without the signal sequence.
The amino acid sequence of human chemokine 1V1DC is set forth in SEQ >D NO:
2. Pry polynucleotides of the present invention include, in addition to those polynucleotides described above, polynucleotides that encode the amino acid sequence set forth in SEQ m NO:
2, and that differ from the polynucleotides described in the preceding paragraphs only due to the well-known degeneracy of the genetic code.
Similarly, since twenty-four amino acids (positions -24 to -1) of SEQ D7 NO: 2 comprise a putative signal peptide that is cleaved to yield the mature MDC
chemokine, preferred 2 0 polynucleotides include those which encode amino acids 1 to 69 of SEQ m NO: 2. Thus, a preferred polynucleotide is a purified polynucleotide encoding a polypeptide having an amino acid sequence comprising amino acids 1-69 of SEQ m NO: 2.
Among the uses for the polynucleotides of the present invention is the use as a hybridization probe, to identify and isolate genomic DNA encoding human MDC, which gene is 2 5 likely to have a three exon/two intron structure characteristic of C-C
chemokines genes. (See Baggiolini et al. (1994), supra); to identify and isolate DNAs having sequences encoding non-human proteins homologous to MDC; to identify human and non-human chemokine genes having similarity to the MDC gene; and to identify those cells which express lVmC and the conditions under which this protein is expressed. Polynucleotides encoding human MDC have been 3 0 employed to successfi~lly isolate polynucleotides encoding at least three exemplary non-human embodiments ofMDC (rat, mouse, macaque). (See SEQ 1D NOs: 35-38 & 45-46.) -8_ Hybridization probes of the invention also have diagnostic utility, e.g., for screening for inflanunation in human tissue, such as colon tissue. More particularly, hybridization studies using an MDC polynucleotide hybridization probe distinguished colon tissue of patients with Crohn's disease (MDC hybridization detected in epithelium, lamina propria, Payer's patches, and smooth muscle) from normal human colon tissue (no hybridization above background).
Generally speaking, a continuous portion of the MDC cDNA of the invention that is at least about 14 nucleotides, and preferably about 18 nucleotides, is useful as a hybridization probe of the invention. Thus, in one embodiment, the invention includes a DNA
comprising a continuous portion of the nucleotide sequence of SEQ D7 NO: 1 or of the non-coding strand complementary thereto, the continuous portion comprising at least 18 nucleotides, the DNA being capable of hybridizing under stringent conditions to a coding or non-coding strand of a human MDC gene. For diagnostic utilities, hybridization probes of the invention preferably show hybridization specificity for MDC gene sequences. Thus, in a preferred embodiment, hybridization probe DNAs of the invention fail to hybridize under the stringent conditions to other human chemokine genes (e.g., MCP-1 genes, MCP-2 genes, MCP-3 genes, RANTES
genes, M1P-la genes, NEP-1[i genes, and I-309 genes, etc.).
In another aspect, the invention provides a purified polynucleotide which hybridizes under stringent conditions to the non-coding strand of the DNA of SEQ ID NO: 1.
Similarly, the invention provides a purified polynucleotide which, but for the redundancy of the 2 0 genetic code, would hybridize under stringent conditions to the non-coding strand of the DNA
of SEQ ID NO: 1. Exemplary stringent hybridization conditions are as follows:
hybridization at 42°C in SX SSC, 20 rnM NaP04, pH 6.8, 50% formamide; and washing at 42°C in 0.2X SSC.
Those skilled in the art understand that it is desirable to vary these conditions empirically based on the length and the GC nucleotide base content of the sequences to by hybridized, and that formulas for determining such variation exist. [See, e.g., Sambrook et al., Molecular Cloning:
a Laboratory Manual. Second Edition, Cold Spring Harbor, New York: Cold Spring Harbor Laboratory (1989).]
In another aspect, the invention includes plasmid and viral DNA vectors incorporating DNAs of the invention, including any of the DNAs described above or elsewhere 3 0 herein. Preferred vectors include expression vectors in which the incorporated MDC-encoding cDNA is operatively linked to an endogenous or heterologous expression control sequence. Such expression vectors may further include polypeptide-encoding DNA sequences operably linked to the MDC-encoding DNA sequences, which vectors may be expressed to yield a fusion protein comprising the NIDC polypeptide of interest.
In another aspect, the invention includes a prokaryotic or eukaryotic host cell stably transfected or transformed with a~NA or vector of the present invention. In preferred host cells, the mature lViDC polypeptide encoded by the DNA or vector of the imrention is expressed. The DNAs, vectors, and host cells of the present invention are useful, e.g., in methods for the re<:ombinant production of large quantities of MDC polypeptides of the present invention.
Such methods are themselves aspects of the invention. For example, the invention includes a method for producing MDC wherein a host cell of the invention is grown in a suitable nutrient medium and ivmC protein is isolated from the cell or the medium.
Knowledge of DNA sequences encoding 1VI,DC makes possible determination of the chromosomal location of Ivl,DC coding sequences, as well as identification and isolation by DNA/DNA hybridization of genomic DNA sequences encoding the MDC expression control regulatory sequences such as promoters, operators, and the like.
According to another aspect of the invention, host cells may be modified by activating an endogenous 1VI,DC gene that is not normally expressed in the host cells or that is expressed at a lower level than is desired. Such host cells are modified (e.g., by homologous recombination) to express lvIDC by replacing, in whole or in part, the naturally-occurring lvIDC
2 0 promoter with part or all of a heterologous promoter so that the host cells express MDC. In such host cells, the heterologous promoter DNA is operatively linked to the lVmC
coding sequences, i. e., controls transcription of the 1VIDC coding sequences. See, for example, PCT International Publication No. WO 94/12650; PCT International Publication No. WO 92120808;
and PCT
International Publication No. WO 91/09955. The invention also contemplates that, in addition to heterologous promoter DNA, amplifiable marker DNA (e.g., ado, dhfr, and the multi-functional CAD gene which encodes carbamyl phosphate synthase, aspartate transcarbamylase, and dihydro-orotase) and/or iron DNA may be recombined along with the heterologous promoter DNA into the host cells. If linked to the lvIDC coding sequences, amplification of the marker DNA by standard selection methods results in co-amplification of the NiDC coding sequences in such host 3 o cells.

- lp -The DNA sequence information provided by the present invention also makes possible the development, by homologous recombination or "knockout" strategies [see, Capecchi, Science, 244: 1288-1292 (1989)], of rodents that fail to express functional MDC or that express a variant of MDC. Such rodents are useful as models for studying the activities of MDC, MDC
variants, and MDC modulators in vivo. Rodents having a humanized immune system are useful as models for studying the activities of MDC and MDC modulators toward HIV
infection and proliferation.
In yet another aspect, the invention includes purified and isolated MDC
polypeptides. Mammalian and avian MDC polypeptides are specifically contemplated. A
prefer peptide is a purified chemolcine polypeptide having an amino acid sequence comprising amino acids 1 to 69 of SEQ ID NO: 2 (human mature MDC). Throughout the application, human mature MDC usually will be referred to simply as "MDC" or as "mature MDC". In instances where context warrants, such as certain descriptions of experiments that involve both human and non-lmrnan mature MDCs and/or that involve MDC fragments and analogs, human mature MDC
will sometimes be specifically referred to as "human" and will sometimes be referred to as "MDC(1-69)."
Mouse and Rat MDC polypeptides of the invention are taught in SEQ ID NOs:
36 and 38. The sequence in SEQ ff~ NO: 36 depicts a complete murine MDC, consisting of a 24 residue leader peptide (residues -24 to -1 of SEQ ID NO: 36) and a 68 residue murine mature MDC. The sequence in SEQ ID NO: 38 depicts a partial rat MDC, consisting of 13 residues of the leader peptide (residues -13 to -1) and the complete 68 residue rat mature MDC.
The polypeptides of the present invention may be purified from natural sources, but are preferably produced by recombinant procedures, using the DNAs, vectors, and/or host cells of the present invention, or are chemically synthesized. Purified polypeptides of the 2 5 invention may be glycosylated or non-glyclosylated, water soluble or insoluble, oxidized, reduced, etc., depending on the host cell selected, recombinant production method, isolation method, processing, storage buffer, and the like.
Moreover, an aspect of the invention includes MDC polypeptide analogs wherein one or more amino acid residues is added, deleted, or replaced from the MDC
polypeptides of the 3 0 present invention, which analogs retain one or more of the biological activities characteristic of the C-C chemokines, especially of MDC. The small size of MDC facilitates chemical synthesis of such polyp~tide analogs, which may be scxeened for MDC biological activities (e. g., the ability to induce macrophage chemotaxis, or inhibit monocyte chemotaxis) using the many activity assays described herein. Alternatively, such polypeptide analogs may be produced recombinantly using well-known procedures, such as site-directed mutagenesis of MDC-encoding DNAs of the invention, followed by recombinant expression of the resultant DNAs.
In a related aspect, the invention includes polypeptide analogs wherein one or more amino acid residues is added, deleted, or replaced from the 1V>DC polypepddes of the present invention, which analogs lank the biological activities of C-C chemokines or MDC, but which are capable of competitively or non-competitively inhibiting the binding of MDC
polypeptides with a C-C chemokine receptor. Such polypeptides are useful, e.g., for modulating the biological activity of endogenous IVjDC in a host, as well as useful for medical imaging methods described above.
Certain specific analogs of MDC are contemplated to modulate the structure, intermolecular binding characteristics, and biological activities of MDC. For example, amino-terminal (N-terminal) and carboxy-terminal (C-terminal) deletion analogs (truncations) are specifically contemplated to change MDC structure and function. Among the amino terminal deletion analogs that are specifically contemplated are analogs wherein 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 amino tenxdnal residues have been deleted (i.e., deletions up to the conserved cysteine pair at positions 12 and 13 of human, marine, and rat mature 1W7C). As set forth in detail below, 2 0 a~perimental data indicates that most or all of these analogs will possess reduced 11~C biological activities and, in fact, will act as inhibitors of one or more biological activities of mature MDC.
Additionally, the following single-amino acid alterations (alone or in combination) are specifically contemplated: (1) substitution of a non-basic amino acid for the basic arginine and/or lysine amino acids at positions 24 and 27, respectively, of SEQ ID NO:
2; (2) substitution of a charged or polar amino acid (e.g., serine, lysine, arginine, histidine, aspartate, glutamate, asparagine, glutamine or cysteine) for the tyrosine amino acid at position 30 of SEQ 1D NO: 2, the tryptophan amino acid at position 59 of SEQ 1D NO: 2, and/or the valine amino acid at position 60 of SEQ m NO: 2; and (3) substitution of a basic or small, non-charged amino acid (e.g., lysine, arginine, histidine, glycine, alanine) for the glutamic acid amino acid at position 50 of SEQ m NO: 2. Specific analogs having these amino acid alterations are encompassed by the following formula (SEQ m NO: 25):
Met Ala Arg Leu Gln Thr Ala Leu Leu Val Val Leu Val Leu Leu Ala -24 -20 -_ -15 -10 Val Ala Leu Gln Ala Thr Glu Ala Gly Pro Tyr Gly Ala Asn Met Glu Asp Ser Val Cys G~rs Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Xaa Val Val Xaa His Phe Xaa Trp Thr Ser Asp Ser G~rs Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Xaa Ile CSrs Ala Asp Pro Arg Val Pro Xaa Xaa Lys Met Ile Leu Asn Lys Leu Ser Gln wherein the amino acid at position 24 is selected from the group consisting of arginine, glycine, alanine, valine, leucine, isolauxne, proline, serine, threonine, phenylalanine, tyrosine, tryptophan, aspartate, glutamate, asparagine, glutamine, cysteine, and methionine; wherein the amino acid at 2 5 position 27 is independently selected from the group consisting of lysine, glycine, alanine, valine, leucine, isoleucine, proline, serine, threonine, phenylalanine, tyrosine, tryptophan, aspartate, glutamate, asparagine, glutamine, cysteine, and methionine; wherein the amino acid at position 30 is independently selected from the group consisting of tyrosine, serine, lysine, arginine, histidine, aspartate, glutamate, asparagine, glutamine, and cysteine; wherein the amino acid at 3 0 position 50 is independently selected from the group consisting of glutamic acid, lysine, arginine, histidine, glycine, and alanine; wherein the amino acid at position 59 is independently selected from the group consisting of tryptophan, serine, lysine, argirune, histidine, aspartate, glutamate, asparagine, glutamine, and cysteine; and wherein the amino acid at position 60 is independently selected from the group consisting of valine, serine, lysine, argmine, histidine, aspartate, glutamate, aspaiagine, glutamine, and cysteine. Such MDC polypeptide analogs are specifically contemplated to modulate the binding characteristics of MDC to chemokine receptors and/or other molecules (e.g., heparin, glycosaminoglycans, erythrocyte chemokine receptors) that are considered to be important in presenting lVmC to its receptor. In one preferred embodiment, 1VIDC polypeptide analogs of the invention comprise amino acids 1 to 69 of SEQ
ID NO: 25.
The following additional analogs have been synthesized and also are intended as aspects of the invention: (a) a polypeptide comprising a sequence of amino acids identified by positions 1 to 70 of SEQ ID NO: 30; (b) a polypeptide comprising a sequence of amino acids identified by positions 9 to 69 of SEQ )D NO: 2; (c) a polypeptide comprising a sequence of amino aads identified by positions 1 to 69 of SEQ ID NO: 31; and (d) a polypeptide comprising a sequence of amino acids identified by positions 1 to 69 of SEQ ID NO: 32.
As set forth in detail below, experimental data indicates that the addition of as few as one additional amino aad at the amino terminus of human mature lvmC is sufficient to confer useful MDC inhibitory properties to the resultant analog. Thus, all amino terminal addition analogs are contemplated as an aspect of the invention. Such addition analogs include the addition of one or a few randomly selected amino acids; the addition of common tag sequences (e.g., polyhistidine sequences, hemagglutinin sequences, or other sequences commonly used to facilitate purification); and chemical additions to the amino terminus (e.g., the addition of an amino terminal aminooxypentane moiety). See Proudfoot et al., J. Biol. Chem., 271:2599-2603 2 0 (1996); Simmons et al., Science, 276 (5310): 276-279 (1997).
Also as set forth in detail below, evidence exists that mature NiDC is cleaved in vii by a dipeptidyl amino peptidase, resulting in an lViDC(3-69) forn that exhibits at least some activities antagonistic to MDC. An additional aspect of the invention includes analogs wherein the proline at position 2 of a mature NJDC (e.g., human, marine, and rat NJDC) is deleted or 2 5 changed to an amino acid other than proline. Such analogs are collectively referred to as "MDC~Pro2 polypeptides." Those IvmCAPro2 polypeptides that retain 11~C
biological activities are contemplated as useful in all indications wherein mature 11~C
is useful; and are expected to be less susceptible to activity-destroying depeptidyl amino peptidases that recognize and cleave the sequence NH2-Xaa Pro- (e.g., CD26). Those MDCOProZ polypeptides that lack 3 0 MDC biological activities are contemplated as being used as lvmC
inhibitors.

It will be appreciated that, while the foregoing analogs were often described with reference to human mature MDC, similar analogs of other vertebrate MDC's, especially mammalian MDC's, also are contemplated as aspects of the invention.
It also will be appreciated that it may be advantageous to express MDC or MDC
analogs as fusions with immunoglobuliri sequences, human serum albumin sequences, yr other sequences, or to perform other standard chemical modifications, for the purpose of extending the serum half life of the MDC or 1VIDC analog. See, e.g., Yeh et al., Proc.
Nat'l. Acad Sci. U.S.A., 89(5): 1904-1908 (1992); Sambrook et al., supra. The definition of polypeptides of the invention is intended to encompass such modifications.
In related aspects, the invention provides purified and isolated polynucleotides encoding such MDC polypeptide analogs, which polynucleotides are useful for, e.g., recombinantly producing the IVIDC polypeptide analogs; plasmid and viral vectors incorporating such polynucleotides, and prokaryotic and eukaryotic host cells stably transformed with such DNAs or vectors.
In another aspect, the imrention includes antibody substances (eg., monoclonal and polyclonal antibodies, single chain antibodies, chimeric or humanized antibodies, antigen-binding fragments of antibodies, and the like) which are immunoreactive with MDC
polypeptides and polypeptide analogs of the invention. Such antibodies are useful, e.g., for purifying polypeptides of the present invention, for quantitative measurement of endogenous MDC in a host, e.g., using 2 0 well-known ELISA techniques, and for modulating binding of MDC to its receptor(s). The invention fixrrl~r includes hybridoma cell lines that produce antibody substances of the invention.
Exemplary antt'bodies of the invention include monoclonal antibodies 252Y and 2522, which are produced by hybridoma cell line 252Y and hybridoma cdt line 2522, respectively. The hybridoma cell lines are themselves aspects of the invention, and have been deposited with the American Type Culture Collection (ATCC Accession Nos. HB-12433 and HB-12434, respectively).
Another exemplary antibody of the invention is monoclonal antibody 272D, which is produced by hybridoma cell line 272D (itself an aspect of the invention and deposited with the American Type Culture Collection (ATCC Accession No. HB-12498).
Recombinant MDC polypeptides and polypeptide analogs of the invention may be 3 0 utilized in a like manner to antibodies in binding reactions, to identify cells expressing receptors) of NIDC and in standard expression cloning techniques to isolate poiynucleotides encoding the receptor(s). Such NN1DC polypeptides, MDC polypeptide analogs, and MDC
receptor polypeptides are useful for modulation of MDC chemokine activity, and for identification of polypeptide and chemical (e.g., small molecule) MDC agorusts and antagonists.
Additional aspects of the invention relate to pharmaceutical utilities of NiDC
polypeptides and polypeptide analogs of the invention. For example, MDC has been shown to modulate leukocyte chemotaxis. In particular, MDC has been shown to induce macrophage chemotaxis and to inhibit monocyte chemotaxis. Thus, in one aspect, the invention includes a method for modulating (e.g., up-regulating or down-regulating) leukocyte chemotaxis in a mammalian host comprising the step of administering to the mammalian host an IviDC polypeptide or polypeptide analog of the imrention, wherein the IvIDC polypeptide or IVIDC
polypeptide analog modulates leukocyte chemotaxis in the host. In preferred methods, the leukocytes are monocytes and/or macrophages. For example, empirically determined quantities of IvIDC are administered (e.g., in a pharmaceutically acceptable carrier) to induce macrophage chemotaxis or to inhibit monocyte chemotaxis, whereas inhibitory NIDC polypeptide analogs are employed to achieve the opposite effect.
In another aspect, the invention provides a method for palliating an inflammatory or other pathological condition in a patient, the condition characterized by at least one of (i) monocyte chemotaxis toward a site of inflammation in said patient or (ii}
fibroblast cell proliferation, the method comprising the step of administering to the patient a therapeutically 2 0 eive amount of MDC. In one embodiment, a therapeutically effective amount of MDC is an amount capable of inhibiting monocyte chemotaxis. In another embodiment, a therapeutically effective amount of 1VIDC is an amount capable of inhibiting fibroblast cell proliferation. Such therapeutically effective amounts are empirically determined using art-recognized dose-response assays.
As an additional aspect, the invention provides a pharmaceutical composition comprising an 1VIDC polypeptide or polypeptide analog of the invention in a pharmaceutically acceptable carries. Similarly, the invention relates to the use of a composition according to the invention for the treatment of disease states, e.g., inflammatory disease states. In one embodiment, the inflammatory disease state is characterized by monocyte chemotaxis toward a 3 0 site of inflaimrnation in a patiem having the disease state. In another embodiment, the disease state is characterized by fibroblast cell proliferation in a patient having the disease state.

NB7C induced chemotaxis of natural killer cells (NK) can lead to enhanced cytotoxieity of targeted NK cells against carious forms of cancers. These forms of cancers include all solid tumor and cancerous cells found in various organs and skin (e.g., breast, ovarian, prostate, kidney, lung, pancreas, liver and bone cancers}. NK cells also play an important role in antibody-dependent cell-mediated cytotoxicity. Stimulation of this process with N)DC or MDC
agonists would lead to improved immune response to tumors. [See generally ~nunolo~r (Ed.
Kuby, J.} pp 304-6, W.H. Freeman and Co., New York, New York (1992)].
Similarly, NK cells lead to viral immunity. MDC may be used to potentiate resistance to common viral diseases (e.g., influenza and rhinoviruses) by stimulating NK conferred viral immunity by stimulating antigen-specific TH memory cells. Ed. Kuby J. pp 420-425, W.H. Freeman and Co. New York, New York (1992}]. "Treatmeraa' as used herein includes both prophylactic and therapeutic treatment.
The apparent optimal concentration of mature MDC in receptor binding and chemotaxis eacp~imems is about 10 ng/ml. Thus, for therapeutic methods involving the systemic administration of MDC (or MDC analogs retain;ng a desired NiDC biological activity), doses and dosing schedules are preferably selected to maintain circulating concentrations in blood of about 0.1-10 nglml. Preferred approaches for preparing a dose and maintaining such levels in the bloods include administration oflVmC in a bolus fashion, so as to administer approximately 0.1-10 mg of ~. This administration is repeated in order to maintain the stated blood concentration. For example, MDC is stable at 1 mg/ml in phosphate-buffered saline (PBS) and is administered to experimental animals using this formulation. This formulation, either liquid or lyophilized and reconstituted, is suitable for human parenteral use, e.g., via intravenous injection. Other formulations can be devised to concentrate the protein drug and stabilize it for use years after its preparation. [See, e.g., Stability and Characterization of Protein and Peptide Drugs; Case Histories, Wang YJ and Pearhnan R. (Eds.), Plenum Press, New York (1993) (describing methods for the preparation of cytokines and other similar protein drug formulations by the inclusion of a variety of excipients to maintain solubility and stability and minimize aggregation )]. Exemplary excipients include citrate, EDTA, detergents of the Tween fiimily, zwittergent family, or pluronic fi~mily, and amino acids such as cysteine to maintain the proper oxido-3 0 reductant state.

'In a second preferred approach, MDC is administered using any of a number of drug delivery methods that are known in the art to facilitate slow-release of the bioactive product.
This can be accomplished as easily as employing intramusculature administration [see for example M. Groves in Parental Technology Manual, Second edition" M.J. Groves (Ed.), Interpharm Press, Inc., Prairie View, IL, pp. 6-7 (1988)] to cause the MDC to be adsorbed into the blood stream over a delayed period of time. Alternatively, the MDC product can be delivered using a number of drug delivery methods [see for a general review LM Sanders, in Peptide and Protein Drug Delivery, V.H.L. Lee (Ed.), Marvel Dekker, Inc., New York, pp. 785-806 {1991)]. For example, MDC is incorporated into biodegradable microspheres, such as poly(laetic-co-glycolic acid of PLGA) microspheres as shown using Human Growth Hormone, [Tracy, Biotechnol.
Progress, 14: 108-115 (1988)], or leuprolide acetate microspheres [Okada et al., Pharm. Res, 8:
787-791 (1991)] which can permit administrations as infrequently as once monthly. A variety of other drug delivery approaches will be apparent to those in the art, including dry powder formulations suitable for inhalation made available by Inhale Corporation, Palo Alto, Calif., and transderma! delivery made available by Atza Corporation, Palo Alto, Calif.
It will also be apparent from the teachings herein relating to the various activities of MDC that modulators of MDC activities, to inhibit the effects of endogenously produced MDC
andlor to promote the activities of endogenously produced or exogenously administered MDC, have therap~tic utility. Such modulators typically include small molecules, peptides, chemokine 2 0 fragments and analogs, and/or antibody substances. MDC inhibitors interfere with MDC signal transduction, e.g., by binding MDC molecules, by competitively or non-competitively binding MDC receptors on target cells, and/or by interfering with signal transduction in the target cells downstream from the chemokine receptors. Thus, in another aspect, the invention provides assays to screen putative chemokine modulators for modulating activity. Modulators identified by 2 5 methods of the invention also are considered aspects of the invention.
In one embodiment, the imrention provides a method for identifying a chemical compound having MDC modulating activity comprising the steps of (a) providing first and second receptor compositions comprising MDC receptors; (b) providing a control composition comprising delectably-labeled MDC; (c) providing a test composition comprising detectably-3 0 labeled MDC and further comprising the chemical compound; (d) contacting the first receptor composition with the control composition under conditions wherein MDC is capable of binding to MDC receptors; (e) contacting the second receptor composition with the test composition under conditions wherein MDC is capable of binding to 1V>DC receptors; (f) washing the first and second receptor compositions to remove detestably-labeled MDC that is unbound to MDC
receptors; (g) measuring detestably-labeled IViDC in the first and second receptor compositions;
and (h) identifying a chemical compound having MDC modulating activity, wherein MDC
modulating activity is correlated with a difference in detestably-labeled MDC
between the first second receptor compositions.
As reported herein, the chemokine receptor CCR4 has been demonstrated to be a high affinity receptor for NiDC. Thus, in a preferred embodiment of the foregoing method, the first and second receptor compositions comprise the MDC receptor that is CCR4.
Since CCR4 is a membrane protein, a preferred embodiment for practicing the method is one wherein the first and second receptor compositions comprise CCR4-containing cell membranes derived from cells that express CCR4 on their surface. The cell membranes may be on intact cells, or may constitute an isolated fiaction of cells that express CCR4. Cells that naturally express CCR4 and cells that have been transformed or transfected to express CCR4 recombinantly are contemplated. In an alternative embodiment, cells (e.g., eosinophils) that express an lVmC
receptor other than CCR4 are used to provide the composition comprising IvIDC receptors.
In a related aspect, the invention provides a method for identifying a modulator of binding between NII')C and CCR4, comprising the steps of (a) contacting IV~C and CCR4 2 0 both in the presence of, and in the absence of, a putative modulator compound; (b) detecting binding between MDC and CCR4; and (c) identifying a putative modulator compound in view of decreased or increased binding between NB'~C and CCR4 in the presence of the putative modulator, as compared to binding in the absence of the putative modulator.
The contacting is performed, for example, by combining MDC with cell membranes that contain CCR4, in a 2 5 buffered aqueous suspension.
In one embodiment, the method is performed with labeled MDC. In step (b), binding between MDC and CCR4 is detected by detecting labeled 11~C bound to CCR4. In a preferred embodiment, the comacting step comprises contacting a suspension of cell membranes comprising CCR4 with a solution containing MDC. In a highly preferred embodiment, the 3 0 method fiuther comprises the steps of recovering the cell membranes from the suspension after WO 99/15666 .. PCTlUS98120270 the contacting step (e.g., via filtration of the suspension); and washing the cell membranes prior to the detecting step to remove unbound 1VIDC.
In an alternative embodiment, the method is performed with a host cell expressing CCR4 on its stuface. In step (b), binding between MDC and CCR4 is detected by measuring the conversion of GTP to GDP in the host ce-71.
In yet another alternative embodiment, the method is performed with a host cell that expresses CCR4 on its surface, and binding between MDC and CCR4 expressed in the host cell is detected by measuring cAIVIP levels in the host cell.
It will be appreciated that assays for modulators such as those described above are often performed by itnmobilizmg (e.g., on a solid support) one of the binding partners (e.g.,1V)DC
or a fragment thereof that is capable of binding CCR4, or CCR4 or a fragment thereof that is capable of binding MDC). In a preferred variation, the non-immobilized binding partner is labeled with a detectable agent. The immobilized binding partner is contacted with the labeled binding partner in the presence and in the absence of a putative modulator compound capable of specifically reacting with MDC or CCR4; binding between the immobilized binding partner and the labeled binding partner is detected; and modulating compounds are identified as those compounds that affect binding between the immobilized binding partner and the labeled binding partner.
In yet another embodiment, the invention provides a method for identifying a chemical compound having IVjDC modulating activity, comprising the steps of (a) providing first and second receptor compositions comprising MDC receptors; (b) contacting the first receptor compo~tion with a control composition comprising detectably-labeled Iv>DC; (c) contacting the second receptor composition with a test composition comprising delectably-labeled IvmC and further comprising the chemical compound; (d) washing the first and second receptor 2 5 compositions to remove delectably-labeled IVmC that is unbound to IvmC
receptors; (e) measuring delectably-labeled 11~C in the first and second receptor compositions after the washing; and (f) identifsring a chemical compound having MDC modulating activity, wherein N117C modulating activity is correlated with a difference in delectably-labeled NIDC between the first and the second receptor compositions.
3 0 In yet another embodiment, N>DC binding to its receptor is measured by measurement of the activation of a reporter gene that has been coupled to the receptor using procedures that have been reported in the art for other receptors. See, e.g., Himmler et al., Journal of Receptor Research, 13:79-94 (1993).
MDC-binding fragments of high affinity receptors of MDC are specifically contemplated as inhibitor compounds of the invention; antibodies to such receptors also are contemplated as inhibitor compounds of the invention.
As taught herein in detail, 11~C stimulates eosinophil chemotaxis through a pathway that apparently does not involve the chanokine receptor CCR4. This discovery provides for the design of assays to identify modulators of MDC activity that have specificity for CCR4-mediated activities without affecting lvmC-induced stimulation of eosinophils, and vice versa.
~ For example, in one anbodiment, the invention provides a method for identifying a modulator of binding between lVmC and eosinophils, comprising the steps of (a) contacting MDC and a composition comprising an MDC receptor that is expressed on eosinophil cell membranes in the presence and in the absence of a putative modulator compound;
(b) detecting binding between MDC and the composition; and (c) identifying a putative modulator compound in view of decreased or increased binding between MDC and the composition in the presence of the putative modulator, as compared to binding in the absence of the putative modulator.
To identify modulators with eosinophil-specificity, the method, in a preferred embodiment, fiuther comprising the steps of (d) contacting lVmC and a composition comprising CCR4 in the presence and in the absence of the putative modulator compound;
(e) detecting 2 0 binding between IvmC and CCR4; (f) identifying a putative modulator compound in view of decreased or increased binding between MDC and CCR4 in the presence of the putative modulator, as compared to binding in the absence of the putative modulator;
and (g) selecting a modulator identified in step (c) as causing increased or decreased binding and identified in step (f) as failing to cause increased or decreased binding. To identify modulators with specificity 2 5 towards CCR4, in step (g) one selects a modulator identified in step (f) as causing increased or decreased binding and identified in step (c) as failing to cause increased or decreased binding.
MDC's involvement in various aspects of immune responses is described in detail below. Based on the involvement of Nll~C in immune response, the administration of IV1DC
antagonists is indicated, for example, in the treatment anaphylaxis [Brown, A.F., .l. Accic~ Emerg.
30 Med, 12(2):89-100 (1995)], shock [Brown (1995) supra], ischemia, reperfixsion injury and cerrxral ischemia [Lindsberg et al., Ann. Neurol., 30(2):117-129 (1991)], atherogenesis [Handley et al., Drug Dev Res., 7:361-375 (1986)], Crohn's disease [Denizot et al., Digestive Diseases a»d Sciences, 37(3):432-437 (1992)], ischemic bowel necrosis/necrotizing enterocolitis [Denizot et al. (1992), suprcx and Caplan et al., Acta Pediat. Suppl., 396:11-17 (1994)], ulcerative colitis (Denziot et al. (1992), supra), ischemic stroke [Satoh et al., Stroke, 23:1090-1092 (1992)], ischemic brain injury [Lindsberg et al., StroJre, 21:1452-1457 (1990) and Lindsberg et al. (1991), supra], systemic lupus erythematosus {Matsuzaki et al., Clinica Chimica Acts, 210:139-144 (1992)], acute pancreatitis [Kald et al., Pancreas, 8(4):440-442 (I993)], septicemia (Kald et al.
(1993), supra), acute post-streptococcal glomerulonephritis [Mezzano et al., J. Am. Soc.
Nephro~, 4:235-242 (1993)], pulmonary edema resulting from IL-2 therapy [Rabinovichi et al., J. Clin. Irrvest., 89:1669-1673 (1992)], ischemic renal failure [Grino et aL, Annals of Internal Medicine, 121(5):345-347 (1994)]; pre-term labor [Hoffrnan et al., Am. J.
Obstet. Gynecol., 162(2):525-528 (1990) and Maki et al., Proc. Natl. Acad Sci. USA, 85:728-?32 (1988)], adult respiratory distress syndrome [Rabinovichi et al., J. Appl. Phsiol., 74(4):1791-1802 (1993);
Matsumoto etal., Clip. Exp. Pharmocol. Physiol., 19:509-515 (1992); and Rodriguez Roisin et arl, J. Clir~ Irrv~es~, 93:188-194 (1994)]. "Treatment" as used herein includes both prophylactic and therapeutic treatment.
MDC acts as a chemoattractant for TH2 differerniated memory cells, which produce the cytokines ILr4, IL-5, IL-10 and others. It is expected that, in some instances, MDC
leads to an immune state in which THl cytokine driven responses are reduced.
In such instances, 2 0 antagonism of MDC would lead to a state in which THl cytokine driven responses are enhanced.
Modulation of the THl-TH2 balance may lead to enhanced "immune surveillance,"
and improved eradication of viral and parasitic infections. Administration of MDC
antagonists of the invention to mammalian subjects, especially humans, for the purposes of ameliorating pathological conditions assoaated with undesirable or excessive TH2 responses and/or less-than-desirable THl responses are contemplated as additional aspects of the invemion.
Administration of sui~cient MDC antagonists to substa~ially reduce ex~dogenous IL-10, a THl immune suppressing cytokine, would lead to enhanced cytotoxic T-lymphocyte mediated immunity and immune surveillance [see Muller et al., J. Infect. Dis , 177: 586-94 (1998); Kenney et al., J. Infect.
Dis , 177: 815-9 (1998)]. In these situations an effective dose and dosing schedule can be determined by monitoring circulating IL-10 levels and increasing the dose and frequency of administration to reduce IL,-10 levels to near normal levels. Treatment of chronic or persistent viral infections and wo ~nst~s Prrms9snoz~o parasitic infections is specifically contemplated, especially in combination with other antiviral or anti-parasitic infection therapeutics. Similarly, treatment or prevention of graft failure or graft rejection with MDC antagonists is contemplated. The administration of MDC
antagonists is indicated, for example, in Leishmaniasis [Li et al., Infect. Immunol., 64:5248-5254 {1996);
Krishnan et al., J. Immunol., 156(2):653-62 (1996)], opportunistic lung infections in cystic fibrosis patients [Mosey et al., APMIS, 105(11):838-42 (1997)], to delay HIV-1 induced immunodefic~ency [Bergen et al., Rer. Yiro~, 147(2-3) :103-108 ( 1996); Barker et al., Proc. Natl.
Acad Sci. USA, 92(24):11135-9 (1995); Jason et al., J. Acquir. Immune. Defic.
Syndrome Retrovirol., 10(4): 471-6 (1995); Maggi et al., J. Biol. Regal. Homeost.
Agents, 9(3): 78-81 (1995)], chronic interstitial lung disease [Kunkel et al., Sarcoidosis Yasc.
Dose Lung Dis , 13:
120-128 (1996)], in neurological disorders associated with a TH2 response [Windhagen et al., Chem. Immunol., 63: 171-86 (1996); Bai et al., Clin. Immureol. Immunopathol., 83(2): 117-26 (1997)], colorectal cancer [Pellegrini et al., Cancer Immunol. Immunother., 42(1): 1-8 (1996)], viral infection, for example various speaes of herpes and hepatitis [Spruance et al., Aretiviral Res , 28(1): 39-55 (1995); Pope et al., J. Immunol., 156(9): 3342-9 (1996);
Bartoletti et al., Gastroenterol., 112(1): 193-199 (1997)], candidiasis and other fungal infections [Spaccapelo et al., J. Immunol., 155(3): 1349-60 (1995); Fidel etat., J. Infect. Dis, 176(3):
728-39 (1995);
Cenci etal., J. IrfectDi~, 171(5): 1279-88 (1995)j, chronic pneumonia [Johansen et al., Behring Inst. Mitt., 98: 269-73 (199'1)], solid tumor cancer [Khan eta~, CytoldnesMol.
They., 2(1): 39-46 (1996)], Bordella pertussis respiratory infection [Ryan et al., J. Infect Dis., 175(5): 1246-50 (1997)], systemic lupus erythrematosus [Segal et al., J. Immunol., 158(6):
2648-53 (1997)], Bullous pemphigoidd pathog~esis (Deptia et a1, Arch. Dermatol Res , 289(12):
667-70 (1997)], glomerulonephritis [Kitching et al., Kidney Inf., 53(1): 112-8 (1998); Huang et al., J. Am Soc.
Nepro~, 8(7): 1101-8 (1997); Tipping et al., Eur. J. Immunol., 27(2): 515-21 (1997)], pulmonary respiratory syncytial virus infection [Russell et al., Eur. J. Immunol., 27(12): 3341-9 (1997)], complications of trauma associated with surgical stress [Decker et a~, Surgery, 119(3): 316-25 (1996)], celiac disease [Karban et al., Isr. J. Med Sci., 33(3): 209-14 (1997)], Gulf War syndrome [Rook et al., Lancet, 349(9068): 1831-3 (1997)], ameoboc3rte infection, for example Plasmodium falciparum [Elghazali et al., Clin. Exp. Immunol., 109(1): 84-9 (1997)] and schistosomamansoni[Wolowczuketa~, Immunol., 91(1): 35-44 (1997)], and B-cell lymphoma, especially mucosa-assoaated lymphoid tissue type [Greiner et al., Am .I.
Pathol., 150(5): 1583-93 (1997)]. "Treatment" as used herein includes both prophylactic and therapeutic treatment.
In fad, the expression pattern of MDC (or TARC) and its receptor CCR4 provide a unique indication for IVmC in viva in inducing a cellular complex (e.g., dendritic and/or macrophage cells; TH2 antigen-specific memory cells, and antigen-specific B
cells} geared to producing a strong humoral immune r~eesponse. The induced complex is contemplated to produce antigen-specific antibodies and TH2-specific cytokines (ILr2, IL,-4, IL,-5, and/or IL-10) and additional chemokines, including additional lvmC, with local concentrations of the chemokines and cytokines that potentiate the activity of the complex possibly being quite high. The cellular complex is specifically contemplated to be involved in the establishment of a humoral response to "recall antigens," since another chemokine/receptor pair (M>P3aJCCR6) appears to be specific for "naive" responses to new antigens. Thus, administration of MDC or IVmC
agonists for the purpose of inducing or augmenting a response to "recall antigens" is specifically contemplated as an aspect of the intention. Similarly, administration of MDC antagonists is indicated when suppression of such an immune response is desired. Administration of Ivfi3C
antagonists to treat conditions and disorders mediated (directly or indirectly) by TH2 cell migration, including but not limited to autoimmune conditions, lupus erythematosus, multiple sclerosis, scleroderma, asthma, and atopic allergy, is specifically contemplated.
With respect to any of the conditions, disorders, and disease states identified in the 2 0 preceding paragraphs, an exemplary method of treatment comprises the steps of identifying a human subject in need of therapeutic or prophylactic treatment for one of the above-identified conditions, disorders, or disease states; and administering~to the human subject a therapeutically or prophylactically effective amount of an 1V87C antagonist compound. By "therapeutically effective amount" is meant a dose and dosing schedule that is sufficient to cure the disease state, 2 5 or to reduce the symptoms or severity of the disease state. By "prophylactically effective amount"
is meant a dose and dosing schedule that is sufficient to reduce the likelihood of occurrence of a disease states or delay its onset, relative to human subjects that are considered to have equivalent risk of developing the disease state but whom are not treated with an lVmC
antagonist.
Therapeutically effective amounts are readily determined by dose-response studies that are 3 0 conventionally performed in the art.

WO 99/15666 PCT/US98I°20270 In one highly preferred embodiment, the invention includes a method of inhibiting proliferation of a mammalian immunodeficiency virus comprising the step of contacting marrnnalian cells that are infected with a mammalian immunodeficiency virus with a composition comprising an MDC-IV antagonist compound or TARC-IV antagonist compound, in an amount effective to inhibit proliferation of said virus in said cells. The family of mammalian immunodeficiency viruses is intended to include human immunodeficiency viruses, such as strains of HIV-1 and HIV-2, and analogous viruses known to infect other mammalian species, including but not limited to simian and feline immunodeficiency viruses. The method can be performed in vitro (e.g., in cell culture), but preferably is performed in vivo by administering the antagonist to s 0 an infecxed subject, e.g., an HIV infected human subject. (In yet another embodiment, the method is performed prophylacticly on a subject at risk of developing an HIV
infection, e.g., due to the subject's likelihood of exposure to contaminated blood samples, contaminated needles, or intimate exposure to an HIV-infected person.) The term "MDC-IV antagonist compound" refers to compounds thax antagonize the apparent Immunodeficiency Virus-proliferative effects of MDC in infected cells. Thus, the term "MDGIV antagonist compound" is meant to include any compound that is capable of inhibiting proliferation of the immunodeficiency virus in a manner analogous to either the inhibition reported herein for 1VIDC neutralizing antibodies or the inhibition reported herein for certain 1VIDC analogs (e.g., analogs having amino terminal additions or truncations). For example, 2 0 anti-MDC antibodies are highly preferred MDC-IV antagonist compounds. For treatment of humans infected with an HIV virus, humanized antibodies are highly preferred.
Similarly, polypeptides that comprise an antigen binding fragment of an anti-1VIDC
antibody and that are capable of binding to 11~C are preferred 1VIDGIV antagonist compounds.
As described elsewhere herein in greater detail, amino-terminal truncations of mat<we human 1~C(1-69) possess antiproliferative activity against HIV-1. Thus, another set of preferred lVmC-IV antagonist compounds are polypeptides whose amino acid sequence consists of a portion of the amino acid sequence set forth in SEQ ID NO: 2 su~cient to bind to the chemokine receptor CCR4, said portion having an amino-terminus between residues 3 and 12 of SEQ ID NO: 2 (i.e., analogs lacking at least three amino acids from the amino terminus of 3 0 lViDC(1-69). Amino tenrucsal deletion analogs that have been further modified, e.g., by including an oligopeptide tag to facilitate purification, or by including an initiator methionine for bacterial expression, are also contemplated.
Amino-terminal additions to mature MDC also result in analogs possessing antiproliferative activity against HIV-1. Thus, another set of preferred 1VIDC-IV antagonist compounds are polypeptides that comprise a mature MDC sequence (e.g., amino acids 1-69 of SEQ ID N0: 1), and that further comprise a chemical addition to the amino terminus of the mottos NL<~C sequence to rider said polypeptide antagonistic to IvmC.
Additions of additional amino acids and other chemical moieties are contemplated.
It will fiirther be appreciated that substitution of amino acids in a mature MDC
sequence (especially substitutions in the amino terminus of mature 1VIDC) may be expected, in some instances, to result in analogs possessing antiproliferative activity against HIV-1. Such analogs also are intended IVLDC-IV antagonist compounds, and are identifiable using HIV
proliferation assays described herein.
It is postulated that MDC's HIV-prolife~rative effects are mediated, at least in part, through the chemokine receptor CCR4. Thus, the family of MDC-IV antagonist compounds includes polypeptides that comprise the C-C chemokine receptor 4 (CCR4) amino acid sequence set forth in SEQ ID NO: 34 or that comprise a continuous fi~agment thereof that is capable of binding to MDC or TARC. Such polypeptides are expected to bind endogenous MDC
and thereby inhibit HIV proliferation in a manner analogous to anti-MDC
antibodies. Also 2 0 contemplated are anti-CCR4 antibodies, which are expected to block MDC-CCR4 interactions, thereby inhibiting IVmC-induced HIV proliferation.
As descn'bed herein in detail, the chemokine TARC possesses sequence similarity to MDC, possesses various overlapping biological activities, and, like IvIDC, binds to the chemokine receptor CCR4. These similarities suggest that compounds that inhibit TARC-CCR4 interactions will also be useful for inhibiting proliferation of immunodeficiency viruses.
Compounds that inhibit TARC-induced proliferation of such viruses are collectively referred to as "TARC-IV antagonist compounds." Such compounds include anti-CCR4 antibodies, anti-TARC antibodies (especially humanized versions); and polypeptides that are capable of binding to TARC and that comprise an antigen-binding fragment of an anti-TARC
antibody.
3 0 It is also contemplated that modifications to the amino terminus of mature TARC
polypeptides will result in TARC-IV antagonist compounds, in a manner analogous to what has been reported herein for MDC analogs. Thus, TARC-IV antagonist compounds for use in methods of the invention include polypeptides that have an amino acid sequence consisting of a portion of the amino acid sequence set forth in SEQ 1D NO: 43 that is sufficient to bind to the chemokine receptor CCR4, said portion having an-amino-terminus between residues 1 and 10 of SEQ ID NO: 43. Polypeptide comprising mature TARC sequences, and further comprising chemical additions to the amino terminus to render the polypeptide antagonistic to TARC also are contemplated. Polypeptides comprising the mature TARC amino acid sequence, into which substitutions have been introduced to confer HIV antiproliferative activity, also are contemplated as TARC-IV antagonist compounds.
In another highly preferred embodiment, the invention includes a method of inhibiting platelet aggregation in a mammalian subject (especially a human subject) comprising the step of administering to a mammalian subject a composition comprising an MDC-PA antagonist compound or TARC-PA antagonist compound, in an amount effective to inhibit platelet aggregation in the subject. Such methods may be performed for therapeutic purposes, e.g., in patients suffering from undesirable blood clotting, or for prophylactic purposes on a subject at risk of developing undesirable blood clotting or coagulation. Such patients would include, e.g., patients who have previously suffered myocardial infarction or stroke or other clotting disorders, or who are deemed to be at high risk for developing such conditions.
The term "IVmGPA antagonist compound" refers to compounds that antagonize 2 0 the apparent Platelet Aggregating effects of MDC. Thus, the term "MDC-PA
antagonist compound" is meant to include any compound that is capable of inhibiting platelet aggregation that is observable after administration of 1VIDC to a mammalian subject (e.g., to a mouse or rat).
Those compounds described above as MDC-IV antagonist compounds are specifically contemplated as lVmC PA antagonist compounds as well. For example, anti-MDC
antibodies are 2 5 highly preferred lVmGPA antagonist compounds. For treatment of humans, humanized antibodies are highly pref~Ted. Similarly, polypeptides that comprise an antigen-binding fragment of an anti-NmC antibody and that are capable of binding to Nn7C are preferred IvmC-PA
antagonist compounds. All 1VlDC analogs that inlu'b'rt the platelet aggregating effects of lVmC also are preferred. Analogs having additions, deletions, and/or substitutions in the amino terminus are 3 0 specifically contemplated.

The structural and functional similarities between M'DC and TARC reported herein indicate that compounds that intu'bit TARC-CCR4 interactions will be useful for inhibiting platelet aggegation. Compounds that inhibit TARC-induced platelet aggregation are collectively referred to as "TARC PA antagonist compounds." Such compounds include anti-CCR4 antibodies, anti-s TARC antibodies (especially humanized versions); various TARC analogs described elsewhere herein, and polypeptides that are capable of binding to TARC and that comprise an antigen-binding fragment of an anti-TARC antibody.
As described herein in detail, the expression patterns of 1V1DC and its receptor, CCR4, provide an indication for the use of MDC as an adjuvant in a vaccine.
Thus, in another aspect, the invention includes a vaccine composition comprising an antigen of interest in a suitable pharmaceutical earner, improved by the inclusion of MDC in the vaccine composition. The antigen of interest may be any composition intended to generate a desirable immune response in a human or other animal. Such compositions would include, for example, killed or attenuated pathogens or antigenic portions thereof. In a related aspect, the invention includes a method of immunizing a human or animal, wherein the improvement comprises administering MDC to the human or animal, either concurrently or before or after administering an antigen of interest. As explained above, MDC is contemplated to preferentially augment an immune response to "recall antigens." Accordingly, in a preferred embodiment, IvIDC is included in a booster vaccine composition.
2 0 For any of the therapeutic indications and methods descn'bed above, another aspect of the invention relates to the use of indicated compounds (e.g., MDC, MDC
fragments or analogs,1VR7C agonists, or MDC antagonists) for preparation of a medicament for the therapeutic indication. For example, the invention includes the use of an MDC antagonist for preparation of a medicament for suppressing a humoral response to recall arnigens.
2 5 The foregoing aspects and numerous additional aspects will be apparent from the drawing and detailed description which follow.
BRIEF DESC'RIp'fION OF THE DRAWING
FIGURE I is a comparison of the amino acid sequence of human M'DC (SEQ ID
3 0 NO: 2) with the amino acid sequences of other, previously characterized human C-C chemokines:
MCP-3 [Van Damme et al., .I. Exp. Med, 176:59 (1992)] (SEQ ID N0: I8); MCP-1 WO 99/15666 . PCT/US98/20270 [Matsushima et al., J. Exp. Med, 169:1485 (1989)] (SEQ ID NO: 19); MCP-2 (mature form) [Van Damme et al., supra; Chang et al., Int. Immunol., 1:388 (1989)] (SEQ ID
NO: 20);
RAN'TES [Schall et al., J. Immunol., 141:1018 (1988)] (SEQ ID NO: 21); MIP-lei [Brown et al., J. Immunol., 142:679 (1989)] (SEQ ID NO: 22); MIP-la [Nakao et al., Mol.
Cell Biol., 10:3646 (1990)] (SEQ ff~ NO: 23); ana I-309 [Miller et al., J. Immunol., 143:2907 {1989)]
(SEQ ID NO: 24). A slash "/" marks the site at which putative signal peptides are cleaved.
Dashes are inserted to optimize alignment of the sequences.
Figure 2 is a graph depicting the chemotactic effect (measured in fluorescence units) of increasing concentrations of MDC on human mononuclear cell migration in a chemotaxis assay. . Closed circles show the response of human mononuclear cells derived from the cell line THIS-1. The op~ diamond shows the response to the positive control, zymosan activated serum (ZAS).
Figure 3 is a graph depicting the chemotactic effect (measured in fluorescence units) of increasing concentrations of MDC on human polymorphonuclear (pmn) leukocyte migration. Closed circles show response to MDC, and an open diamond shows the response to the positive control, IL-8.
Figure 4 is a graph depicting the chemotactic effect (measured in fluorescence units) of increasing concentrations of MDC on macrophage and monocyte migration. Closed circles show the response to MDC of macrophages derived from the cell line THP-1. Open circles 2 0 show the response to MDC of monocytes derived from the cell line THP-1.
Figure 5 is a graph depicting the chemotactic effect (measured in fluorescence units) of increasing concentrations of MDC on guinea pig peritoneal macrophage migration.
Closed arcles show the response of macxophages to MDC. An open triangle shows the response to the positive control, zymosan activated serum (ZAS).
2 5 Figure 6 is a graph depicting the chemotactic-inhibitory effect (measured in fluorescence units) of increasing concentrations of MDC on THP-1 monocyte migration induced by MCP-1. Closed circles depict the chemotactio-inhibitory effects of MDC
where chemotaxis has been induced by MCP-1. Open circles depict the chemotactio-inhibitory effects of MDC in a control experiment wherein only the basal medium (RPMI with 0.2% BSA (RBSA), no MCP-1) 3 0 was employed. The zero point on the x axis corresponds to the response of cells to MCP-1 and RBSA in the absence of any MDC.

Figure 7 is a graph depicting the effect (measured in counts per minute (cpm)) of increasing concentrations of MDC on fibroblast proliferation. Closed circles depict the proliferative response with purified MDC that was recombinantly produced in CHO cells (Example lOF). Open circles depict the response with chemically synthesized MDC (Example 11).
Figure 8 schematically depicts the construction of mammalian expression vector pDC 1.
Figure 9 depicts the nucleotide and deduced amino acid sequence (SEQ m NOs:
39 and 40) of a S. cerevisiae alpha factor pre-pro/human MDC cDNA chimeric construct used to express human MDC in yeast.
Figure 10 depicts the structure of plasmid pYGL/preproMDC, used to express human MDC in yeast.
Figure 11 depicts the inlu'bitory effects of the anti-MDC a~'bodies 252Y and on the binding of the fusion protein MDC-SEAP to the RFC receptor designated CCR4. Binding (depicted as percent of maximal binding) is plotted as a function of increased concentrations of antibody Figure 12 depicts the inhibitory effects of the anti-MDC antibodies 252Y and on the NIDC-induced chemotaxis of CCR4-transfected L1.2 cells. The number of cells observed migrating toward MDC in a standard chemotaxis assay are plotted as a function of increased 2 0 concentrations of antibody.
The preset invention is illustrated by the following examples related to a human cDNA, designated MDC cDNA, encoding a novel C-C chemokine designated MDC (for "macrophage-derived chemolcine"). More particularly, Example 1 describes the isolation of a partial MDC cDNA from a human macrophage cDNA library. Example 2 describes the isolation of additional cDNAs from the cDNA library using the cDNA from Example 1 as a probe, one of these additional cDNAs containing the entire MDC coding sequence.
Additionally, Example Z
presents a composite MDC cDNA nucleotide sequence and presents a characterization of the 3 0 deduced amino acid sequence of the chemohine (1VIDC) encoded thereby. In Example 3, experiments are described which reveal the level of MDC gene expression in various human tissues. The geatest MDC gene expression was observed in the thymus, with much weaker expression detectable in spleen and lung tissues. Example 4 describes more particularly the expression of the MDC gene during monocyte maturation into macrophages and during inducement of HL60 cell differentiation to a macrophage-like cell type.
Since MDC gene expression was detected in thymus and spleen in Example 3, in situ hybridization studies were conducted to locaiize further the MDC gene expression in these tissues. Moreover, in situ hybridization revealed a correlation between elevated MDC gene expression in inflamed tissues, as exemplified using intestinal tissue from Crohn's diseased patients. These in situ hybridization experiments are described in Example 5.
Example 6 descxibes the recombinant production of MDC as a GST fusion protein in prokaryotic cells, as well as the cleavage of the fusion protein and purification of the recombinant MDC. Example 7 describes alternative DNA constructs useful for expression of recombinant MDC protein, and describes the production of MDC by a bacterial host transformed with such a construct.
Example 8 provides experimental protocols for purification of recombinant MDC
produced, e.g., as descn'bed in Example 7. Examples 9 and 10 provide protocols for the recombinant production ofMDC in yeast and mammalian cells, respectively. In addition, Example 10 provides additional protocols for purification of recombinant MDC, and describes the determination of the amino terminus of MDC recombinantly produced in mammalian cells.
2 0 Example 11 describes production of MDC and MDC polypeptide analogs by peptide synthesis.
Certain preferred analogs are specifically described in Example 11.
Examples 12-17 provide protocols for the determination of MDC biological activities. For instance, Example 12 provides an assay of IvlI3C effects upon basophils, mast cells, and eosinophils. NmC-induced chemotaxis of eosinophils is specifically demonstrated. Example 2 5 13 describes assays of chemoattractant and cell-activation properties of MDC on monocyteslmacrophages, n~trophils, and ganulocytes. MDC induced macrophage ehemotaxis, but inhibited monocyte chemotaxis.
Examples 14-17 provide protocols for the determination of MDC biological activities in vivo. Example 14 provides an MDC tumor growth- inhibition assay.
Examples 15 3 0 and 16 provide protocols for assaying MDC activity via intraperitoneal and subcutaneous injection, respectively. Example 17 provides protocols for determining the myelosuppressive activity of MDC.
Example 18 provides protocols for generating antibodies that are specifically immunoreactive with NmC, including polyclonal, monoclonal, and humanized antibodies. Uses of the antibodies also are described.
Example 19 provides a calcium flux assay for determining the ability of MDC to induce cellular activation.
Example 20 provides assays and experimental results relating to the HIV
proliferative and anti-proliferative effects of human mature MDC and NmC
antagonists.
Example 21 demonstrates the anti-proliferative effects of lVmC on fibroblasts.
Example 22 provides in vitro assays for the effects of MDC upon the proliferation of additional cell types. Example 23 provides an in viva assay for determining the anti-proliferative effects of lVmC on fibroblasts.
Example 24 describes the chromosomal localization of the human MDC gene.
Example 25 describes procedures which identified the CC chemokine receptor "CCR4" as a high affinity binding partner of MDC. Examples 26 and 27 provide assays for identifying MDC modulators.
Example 28 describes the isolation of cDNAs encoding rat, mouse, and macaque MDC, and characterizes the MDC proteins encoded thereby. Example 29 further characterizes 2 0 selected MDC analogs.
Example 30 describes experiments that demonstrate that anti-IVmC monoclonal antibodies are effective for neutralizing biological activities of MDC that were elucidated in other examples.
Example 31 describes experiments that demonstrate that 11~C induces chemotaxis of TH2 helper cells, a discovery with therapeutic implications as discussed in Example 31 and elsewhere herein.
Example 32 describes platelet-aggregating activities of MDC, and describes the use of MDC and MDC antagonists to modulate platelet aggregation.
Example 33 provides exemplary assays to demonstrate the therapeutic efficacy of 3 0 an MDC antagonist to modulate immune responses in a mammalian host.

A partial cDNA for a new C-C chemokine, designated pMP390, was isolated from a ma~xophage cDNA library as described in U.S. Patent Application Serial No.
08/939,107, filed September 26, 1997, and in related international publication number WO
96140923, both of which are incorporated herein by reference. Sequence comparisons were performed on December 14, 1994, by the BLAST Network Service of the National Center for Biotechnology Information (e-mail: "blast@ncbi.nlm.nih.gov"), using the alignment algorithm of Altschul et al., J. Mol. Biol., 215: 403-410 (1990). The sequence analysis revealed that a portion of the isolated macrophage cDNA. clone designated pMP390 contained a gene sequence having approximately 60-70~/0 identity with previously-identified chemokine genes, including the human MCP-3 gene and rat MIP-lei gene.
The 2.85 kb cDNA insert of pMP390 was subcloned into the vector pBluescript SK (Stratagene, La Jolla CA) to facilitate complete sequencing. The complete sequence of this pMP390 cDNA corresponds to nucleotides 73 to 2923 of SEQ B? NO: 1 (and to deduced amino acids -6 to 69 of SEQ ID NO 2). The sequence that was originally compared to database sequences corresponds to nucleotides 73 to 610 of SEQ ID NO: 1.
Isolation of additional cDNA clones having 2 0 the c;omRlete MDC codin$~~e_~auence Using the pMP390 cDNA clone isolated in Example 1, additional cDNA clones were isolated from the same human macrophage cDNA library, these additional cDNAs containing additional 5' sequence and encoding the complete amino acid sequence of a macrophage derived chemokine. The additional cloning and sequencing is described in detail in U.S.S.N. 08/939,107 and WO 96/40923, incorporated herein by reference.
Ofthe additional clones, clones designated pMP390-12 and pMP390B contained the largest additional 5' coding sequence, each extending an additional 72 nucleotides upstream of the sequence previously obtained from the cDNA clone pMP390. A composite DNA
sequence, herein designated MDC cDNA, was generated by alignment of the pMP390 and 3 0 pMP390-12 cDNA sequences. This 2923 base pair composite cDNA sequence, and the deduced amino aad sequence of the chemokine MDC, are set forth in SEQ TL7 NOs: 1 and 2, respectively.

Manual comparison of the deduced MDC amino acid sequence with sequences of known chemokines indicates that the MDC cDNA sequence encodes a novel C-C
chemokine ninety-three amino acids in length, sharing 28-34% amino acid identity with other C-C
chemokines (Figure 1). As aligned in Figure 1, MDC shares 29% amino acid identity with MCP-I
and MIP-la, 28% identity with MCP-2, 32% identity with I-309, 33% identity with MCP-3 and MIP-lei, and 34% identity with RANTES. Importantly, the four cysteine residues characteristic of the chemokines are conserved in MDC. Five additional residues also are completely conserved in the eight sequences presented in Fig. 1.
The first 24 amino acids of the 93 amino acid MDC sequence are predominantly hydrophobic and are consistent with von Heijne's rules [Nucleic Acids Res , 14: 4683-90 ( 1986)]
governing signal cleavage. These features and the polypeptide comparison in Fig. 1 collectively suggest that the MDC cDNA encodes a twenty-four amino acid signal peptide that is cleaved to produce a mature form ofMDC beginning with the glycine residue at position 1 of SEQ m NO:
2. This prediction was confirmed by direct sequencing of MDC protein produced recombinantly I5 in mammalian cells, as described below in Example 10. The MDC composite cDNA sequence shown in SEQ ID NO: I extends nineteen nucleotides upstream of the predicted initiating methionine codon, and 2.6 kb downstream of the termination codon.
T~eternination ofMDC CTe_n_e Expression in Human Tissues Northern blot analysis were conducted to determine the tissues in which the MDC
gene is expressed.
A radiolabeled pMP390 5' fragment which corresponds to the region of the MDC
cDNA encoding the putative mature form of MDC plus 163 bases of the adjacent 3' noncoding region was used to probe Multiple Tissue Northern blots (Clontech, Palo Alto, CA) containing RNA from various normal human tissues. The probe was denatured by boiling prior to use, and the hybridizations were conducted according to the manufacturer's specifications.
Autoradiographs were exposed 5 days at -80°C with 2 intensifying screens.
The greatest MDC gene expression was observed in the thymus, with much weaker 3 0 expression detectable in spleen and lung tissues. Expression of MDC in tissue from the small intestine was at even lower levels, and no expression was detected in brain, colon, heart, kidney, liver, ovary, pancreas, placenta, prostate, skeletal muscle, testis, or peripheral blood leukocytes.
As discussed in detail below in Example 25, MDC is a ligand for the CC
chemokine receptor CCR4, which receptor also has been reported to be a ligand far the chemokine TARC. See Imai et al., J. Biol.'Chem., 272: 15036-15042 (I997). Like MDC, TARC
is abundantly expressed in the thymus, with little expression observed in other tissues. More particularly, CCR4 is expressed on T cells, especially CD4'" T cells [See Imai et al. (1997), and Power et al., J. Biol Chem., 270: 19495-19500 (1995)], while MDC and TARC are expressed by cells of the dendritic lineage which form a major component of the thymic architecture. See Godiska et al., J. F.xp. Med, 185: 1595-1604 (1997), incorporated herein by reference; and Imai et al., J. Biol. Chem., 271: 21514-21521 (1996). These expression patterns suggest a biological activity of MDC, CCR4, and TARC in T cell development, since immature progenitor cells undergo differentiation and expansion (leading to the establishment of the major T cell lineages and the elimination of potentially autoreactive T cells) ' within the highly specialized microenvironment of the thymus. See von Boehmer, Current Biology, 7: 308-310 (1997). The fact that MDC also is expressed at high levels in cultured macrophages suggests an MDC activity in the initiation and/or triggering of the immune response, by facilitating the interaction of T cells with antigen-presenting cells at sites of inflammation.
These expression pattern data suggest therapeutic utilities of MDC (or MDC
2 0 mimetics or agonists) to stimulate beneficial immune responses. For example, MDC, MDC
agonists, or MDC mimetics may be administered to augment/enhance T cell activation where T
cell activation may be beneficial. The use of MDC as an adjuvant in vaccine development or in tumor immunotherapy is specifically contemplated.
Conversely, the expression pattern data also indicates a therapeutic utility for 2 5 modulators of MDC's interaction with CCR4 in T cell-mediated autoimmune diseases, including but not limited to psoriasis, graft versus host disease, and allograft rejection, and in T cell and/or B cell mediated allergic responses.

Because the cDNAs encoding MDC were isolated from a human macrophage cDNA library, MDC gene expression during differentiation of monocytes into macrophages was examined.
A.
Human monocytes from a single donor were cultured on a series of tissue culture plates, and cells from one plate were harvested after 0, 2, 4 or 6 days. See generally Elstad et al., J. Immunol. 140:1618-1624; Tjoelker et al., Nature, 374:549-552 (1995). Under these conditions, the monocytes differentiated into macrophages by days 4-6 [Stafforini et al., J. Bio~
Chem., 265: 9682-9687 (1990)J.
A Northern blot of RNA (10 pg per lane) isolated from the cells harvested at each time point was prepared and probed, using a radiaolabeled pMP390 fragment. No signal was detectable in RNA from freshly isolated monocytes, whereas a very strong signal was generated from cells that had differentiated into macrophages after six days of culture.
Cells cultured for four days produced a much weaker signal, whereas the signal generated from cells cultured for two days could be seen only after prolonged exposure of the filter.
B.
To confirm the expression of MDC in differentiated human macrophages, culture 2 0 supernatants were analyzed by western blotting with anti-MDC monoclonal antibodies produced as described below in Example I8. Several plates of human macrophages were differentiated by growth on plastic for eight days in the presence of macrophage colony stimulating factor (0.5 ng/ml, R&D Systems, Minneapolis, Nhnnesota).
The medium from the differentiated macrophage cell cultures was removed and 2 5 replaced with similar medium or with medium containing low density lipoprotein (LDL, Sigma), oxidized LDL (oxidized by incubation in SpM CuS04~SHZO according to the method of Maiden et al., J. Biol. Chem., 266:13901 (1991)), or dexamethazone (6 nM, Sigma Chemical Co.).
Following 3 days of each treatment, the culture medium was removed, brought to pH 6.8 by the addition of HCI, and passed over a Heparin-Sepharose CL-6B column (Phannacia, Piscataway, 3 0 Nn. The column was washed with 0.2 M NaCI in 20 mM Tris, pH 8, and eluted with 0.6 M NaCI
in 20 mM Tris, pH 8. The eluted material was fractionated on an 18% acrylamide SDS-PAGE

WO 99/15666 PCT/US98r10270 gel (NOVE3~ and electroblotted to PVDF membrane (Millipore, Bedford MA). The filter was blocked, washed, and reacted with monoclonal antibodies against MDC using standard techniques (Sacnbrook et al.). In each of the culture media analyzed, MDC protein was detected at a concentration of approximately 0.5 pg/ml, thus confirming expression of MDC in differentiated human macrophages.
Expression of MDC also was analyzed in human epithelial cell lines. The colon epithelial cell line T84 (ATCC #CCL-248) was grown in DMEM/F12 medium (GIBCO, Gaithersburg MD), and the lung epithelial cell line A549 (ATCC #CCL-185) was grown in F12 medium. Screening for the presence of MDC mRNA in the cells and MDC protein in the culture medium was performed as described above for macrophages. No evidence of MDC
expression was detectable by either method in these cell lines.
In addition, samples of the T84 cell line were treated for 1 day with TNFa (5 ng/ml, PeproTech, Rocky Hill, New Jersey), TGF-~i (1 ng/ml, R&D Systems), or interferon-'y (200 U/ml, PeproTech), each with or without addition of recombinant MDC at 100 ng/ml (derived from CHO cell transfectants; see Ex. 10). Samples of the A549 cell line were treated with 50 ng/ml PMA (Sigma Ch~nical Co.) for 0, 1, 3, 5, or 7 days. None of these treatments resulted in detectable expression of MDC mRNA in the T84 or A549 cells when screened by Northern blotting as described above.
2 0 C.
Further examination of MDC gene expression in macrophages was conducted by treating the human cel! line HI.60 with either 1% DMSO (Sigma Chemical Co.) or 50 ng/ml PMA
(Sigma). Treatment with DMSO induces differentiation of HL60 cells into a granulocytic cell type, whereas PMA induces their differentiation into a macrophage lineage [Perussia et al., Blooa;
S8: 836-843 (1981)]. RNA was isolated from untreated cells and from cells treated for one or three days with DMSO or PMA, electrophoresed (lOpg/Iane), and blotted. The Northern blot of the RNA was probed with the radiolabeled pMP390 5' fragment described in Example 3.
After three days of PMA treatment, the HL.-60 cells clearly expressed MDC
mRNA, although the level of expression was apparently less than that of macrophages after six 3 0 days of culture (see above). No expression was seen after one day of treatment or in untreated cells. Fucth~, no detectable expression of MDC was induced by treatment with DMSO for one or three days.
Because MDC gene expression was detected in the thymus and spleen, in situ hybridization was carried out to localize the source of the message in these tissues. Further, in situ hybridization was used to correlate MDC gene expression with tissue inflammation, using intestinal tissue from Crohn's diseased patients as an example. The procedures used for these experiments are described in detail in U.S.S.N. 08/939,107 and WO 96/40923, both of which are incorporated by reference.
Observed hybridization of the anti-sense strand indicated that the MDC gene was expressed in cells throughout the cortex of normal human thymus, with weak signal in the follicles. Expression of MDC in the thymus may indicate a T lymphocyte developmental role of MDC. Expression in normal human spleen was localized to cells of the red pulp, whereas little signal was din the white pulp. A high level of expression in inflamed tonsil was localized to the epithelial region, although inflammatory cells appeared to have infiltrated the entire tissue sample.
Colon samples from patients with Crohn's disease exhibited hybridization in cells of the epithelium, lamina propria, Payees patches, and smooth muscle. In contrast, normal human 2 0 colon showed no hybridization above background. The observed pattern of 1V1DC expression in the colons of Crohn's disease patients closely correlates with the expression of a maerophage-specific gene, Platelet Activating Factor Acetylhydrolase (PAF-AITj [Tjoelker et al., supra]. This result, together with the data presented in Example 4, suggest that macrophages express MDC
cDNA in viva during pathogenic inflammation. Moreover, the identification of MDC in Crohn's 2 5 disease colon tissue samples suggest diagnostic relevance of MDC levels (e.g., in a patient's blood, stool sample, and/or intestinal lesions} to a patient's disease state or clinical prognosis.
3 0 To produce recombinant MDC protein, the sequence encoding the putative mature form of the protein was amplified by PCR and cloned into the vector pGEX-3X
(Pharmacia, Piscataway, NJ). The pGEX vector is designed to produce a fusion protein comprising glutathione-S-transferase (GST), encoded by the vector, and a protein encoded by a DNA
fragment inserted into the vector's cloning site.
An MDC cDNA fragment was amplified by PCR using the primers 390-2R (SEQ
ID NO: 8) and 390-FX2 (SEQ lI? NO: 1 I~. Primer 390-FX2 contains a BamH I
restriction site, followed by a sequence encoding a thrombin cleavage site [Chang et al., Eur.
J. Biochem., 151:217 (1985)] followed by bases 92-115 of SEQ ID NO: 1. The thrombin cleavage site is as follows: leucine-valine-proline-arginine-glycine-proline, in which glycine and proline are the first two residues of the mature form of MDC. Treatment of the recombinant fusion protein with thrombin is expected to cleave the arginine-glycine bond of the fission protein, releasing the mature chemolcine from the GST fusion.
The PCR product was purified by agarose gel electrophoresis, digested with BamH
I endonuclease, and cloned into the BamH I site of pGEX-3X. This pGEX-3X/MDC
construct was transformed into E. coli XL-1 Blue cells (Stratagerie, La Jolla CA), and individual transformants were isolated and grown. Plasmid DNA fibm individual transformants was purified and partially sequenced using an automated sequencer and primer GEXS (SEQ ID
NO: 12), which hybridizes to the pGEX-3X vector near the BamHI cloning site. The sequence obtained with this primer confirmed the presence of the desired N1DC insert in the proper orientation.
Induction of the GST-MDC fusion protein was achieved by growing the transformed XL-1 Blue culture at 37°C in LB medium (supplemented with carbenicillin) to an optical density at wavelength 600 nm of 0.4, followed by further incubation for 4 hours in the presence of 0.25 to 1.0 mM Isopropyl ~i-D-Thiogalactopyranoside (Sigma Chemical Co., St.
Louis MO).
The fusion protein, produced as an insoluble inclusion body in the bacteria, was 2 5 purified as follows. Cells were harvested by centrifugation; washed in 0.15 M NaCI, 10 mM Tris, pH 8, 1 mM EDTA; and treated with 0.1 mg/ml lysozyme (Sigma Chemical Co.) for 15 minutes at room temperature. The lysate was cleared by sonication, and cell debris was pelleted by centrifugation for 10 minutes at 12,000 X g. The fusion protein-containing pellet was resuspended in 50 mM Tris, pH 8, and 10 mM EDTA, layered over 50% glycerol, and centrifuged for 30 min. at 6000 X g. The pellet was resuspended in standard phosphate buffered saline solution (PBS) free of Mg~ and Ca~. The fusion protein, which remained insoluble, was approximately 80-90'/n of the protein mass and migrated in denaturing SDS-polyacrylamide gels with a relative molecular weight of 33 kD. The protein yield, as judged by Coomassie staining, was approximately 100 mg/1 of E. coli culture.
The fusion protein was subjected to thrombin digestion to cleave the GST from the mature MDC protein. The digestion~eaction (20-40 ug fusion protein, 20-30 units human thrombin (4000 U/ mg (Sigma) in 0.5 ml PBS) was incubated 16-48 hrs. at room temperature and loaded on a denaturing SDS PAGE gel to fractionate the reaction products. The gel was soaked in 0.4 M KCl to visualize the GST and MDC protein bands, which migrated as fragments of approximately 26 kD and 7 kD, respectively.
The identity of the 7 kD SDS PAGE fragtnent was conf rmed by partial amino acid sequence analysis. First, the protein was excised from the gel, electroeluted in 25 mM Tris base and 20 mM glycine, and collected onto a PVDF membrane in a ProSpin column (Applied Biosystems, Foster City, CA). Subjecting the sample to automated sequencing (Applied Biosystems Model 473A, Foster City, CA) yielded 15 residues of sequence information, which corresponded exactly to the expected N terminus of the predicted mature form of MDC (SEQ ID
NO: 2, amino acid residues 1 to 15).
2 0 MDC peptides and analogs can be expressed using a variety of bacterial expression systems including E. coli, Bacillus subtilis, streptomyces lividans, and many others. [For a general review see "Gene Expression Technology" in Vol. 185: pp. 1-283, Ed. D.V. Goeddel, Academic Press, San Diego, CA (1990).] In general, an expression cassette comprised of a transcription el~nent (a promoter), a translation element, a coding region to be expressed (for example MDC), and a transcription ternnination element is developed and optimized to effect significant gene expression. This cassette is incorporated into either episomal plasmids, which confer stable propagation, or into integration vectors to mediate the insertion or creation (via homologous recombination) of an expression cassette within the host genome. The gene can be expressed directly or can be fused to signal sequences (e.g., peXB, ompA, esl2) to 3 0 direct secretion of the gene product out of the cytoplasm into either the periplasmic space or media, or to other leader sequ~ces (e.g., ubiquitin) to enhance the folding or otherwise stabilize WO 99/15666 PCTIUS9$/202'IO
the recombinantly expressed coding region. The gene product, either properly folded or not, can be recovered in a crude state or as inclusion bodies from the cells following a fermentation phase and either directly purified or refolded prior to purification.
A. Conctn~ction and testing o~Bacterial_ MI~C Expression Vector P2-390 The portion of the MDC cDNA encoding the predicted mature MDC protein was cloned into a plasmid containing the arabinose promoter (araB) and the pelB
leader sequence [see Better et al., Science, 240:1041-43 (1988)].
More pardcx~larly, an MDC cDNA was amplified by PCR using approximately 0.1 pg of pMP390-12 as template and synthetic oligonucleotide primers 390-2R (SEQ
ID N0:8) and 390-Pel (SEQ D7 NO: 13). Primer 390-Pel contains an Nco I restriction site, followed by two cytosine residues, followed by bases 92 to 1 I S of SEQ ID NO: 1.
The expected PCR product of 232 by was purified by agarose gel electrophoresis, digested with Nco I and BamH I, and cloned along with a portion of the arabinose operon and peIB leader sequence (Better et al., supra) into the vector pUCl9 (New England Biolabs, Beverly, MA). The resultant construct, designated P2-390, encodes a fusion of the pelB
leader (encoded by the vector) to the mature MDC protein. The sequence of this construct was confirmed by automated sequencing using the primers Aral (SEQ ID N0:28) and Ara2 (SEQ ID
NO:29), which annul to the vector adjacent to the cloning site. The plasmid P2-390 was transformed into the E. coli strain MC1061 using standard procedures, and an ampicillin resistant clone was selected for MDC production. The clone was grown in a 3 liter fermenter (Applikon, Foster City, CA) and MDC production was induced by the addition of 50% arabinose to a final concentration of O.I%. After one day of cultivation in the presence of arabinose, the cells were harvested.
Western blotting revealed that MDC was present within the cells at a level of approximately 4 2 5 pg/g of cell paste and was secreted into the culture medium to a level of approximately 1 pg/ml.
B. Protocol for bacterial expression of MDC using pl a id 2-390 The plasmid P2-390 was transformed into E. coli strain SB7219 (Sheppard and Englesbexg, J. Molec. Biol., 25:443-454 (1967) and Wilcox et al., J. Biol.
Chem., 249:2946-2952 3 0 (I974)). SB7219 is a prototrophic strain incapable of degrading arabinose, the inducer of the araB promoter used to transcribe the pelB-MDC coding region. The genotype of SB7219 is E.

WO 99/ISfi66 PCT/US98/20270 coliKl2 F' del(cealb-lac)3 del(ara735) rpsL150(strR) ~,'. The production strain SB7219:P2-390 was grown in the fermenter (run FC563) in a fed batch format. A frozen aliquot of the seed is inoculated into 250 ml of fermentation basal medium in the shake flask. The composition of the basal medium is as follows:
Basal Medium Component Quantity per L

Na3citrate lg 5.4% FeCl3 6Hz0 2 ml glucose 2 g NaHzPO,; H20 3 g KzHP04 6 g (NH,~SO~ 5 g 20% yeast extract solution5 ml 1 M CaCIZ 0.5 ml 1 M MgCl2 2.0 ml trace elements 4 ml trace vitamins 2 ml 1% thiamine 1 ml tetracycline 5 mg 2 0 pH is set to 7.0 Trace Elements Solution Component Quantity per L

Boric Acid 5.0 g Copper Sulfate SHiO 2.0 g Potassium Iodide 1.0 g Manganese sulfate 10 g Molybdic acid o.s g ZnCl2 {Anhydrous) 5.2 g Cobalt chloride 0.5 g Tr$ce Vitamin Solution Component Quantity per L

Sodium Hydroxide, 50% 1.3 ml Riboflavin 0.42 g Folic Acid 0.04 g D-Pantothenic Acid (hemicalcium5.4 g salt) Ncotiinic Acid (niacin) 6.1 g Pyridoxine HCl 1.4 g Biotin 0.06 g The shake flask culture is grown at 3TC and 220 RPM to an optical density corresponding to mid-exponential growth (approximately ODD ~ 0.7). The inocuium is added to the fermentor containing 1.5 L of basal media and grown at 30'C for 5 hours. A feed is then initiated at 3.6 ml/hr and exponentially increased to effect a doubling time of 5 hr until a maximum of 18 ml/hr 2 5 of feed is achieved.

Feed Medium Component Quantity per L

Na3citrate Sg 5.4%FeCl3 . 6H20 10 ml glycerol 500 g ~4)2SO4 5 g 1 M CaCl2 4 ml 1 M MgCiz 100 ml 1 M MnClz 0.4 ml trace elements 10 ml When the wet cell mass is approximately 100gIL, 20 ml of 50% arabinose solution is added to induce expression of MDC. The temperature is raised to 37°C and the feed rate is decreased to 12 ml/hr. The fermentation is allowed to continue for approximately 20 more hours, at which time the cell paste is harvested from the tank and stored frozen at -70°C. The MDC contained in the cell paste is suitable for recovery by mechanical lysis, re-folding, and purification as described below in Example 8.
C. Direct Exrrcession ~f MDC in E. coli 2 0 In a similar way, MDC that is directly expressed (i. e., without a fused in-fr ame leader sequence) is engineered into the same vector. The plasmid pBARS/MDC/RC
is a plasmid id~tical to P2-390 except for the elimination of the pelB leader sequence. In addition, the first fourteen perc~t of the MDC(1-69) coding sequence (amino acid codons 1-6 and 8-10) have been modified to change cytosine residues at codon position three to either an adenosine or thymidine 2 5 nucleotide (while preserving the encoded amino acid). Additionally, a translation initiation codon was added. Thus, the coding sequence in pBARS/MDC/RC begins:
5' ATG GGA CCA TAT GGA GCA AAT ATG GAA GAT AGT ...... (SEQ ID NO: 44 ) E. coli strain SB7219 harboring this plasmid is gown in a fermentor essentially as described above and the MDC that is produced is similarly recovered.

_ 4,4, _ D. P2-390 Slariant e~ , ression vector In addition, a derivative of P2-390 pBARS/PeIB/MDCIRC in which the amino acid codons described above in part C were substituted for the wild-type sequence was created. E.
coli SB7219 harboring this plasmid is grown in a fermentor in a comparable fashion and the MDC
produced is similarly recovered.
Purification of Recombinant MDC from Bacteria and Culture Medium The following are experim~tal protocols for purification of the recombinant MDC
l0 produced as described in Example 7.
A. Recovery and Purification of secreted recombinant MDC.
The secxeted recombinant MDC protein is purified from the bacterial culture media by, e.g., adapting methods previously described for the purification of recombinantly produced RAN'TES chemokine [Kuna et al., J. Immunol., 149:636-642 (1992)], MGSA
chemokine [Horuk et a~, J. Bio~ Chem. 268: 541-46 (1993)], and IP-10 chemokine (expressed in insect cells) [Sarris et al., J. Exp. Med, 178:1127-1132 (1993)].
B. Recover;t and Re-folding of~~,~ Bound in Inclusion Bodies 2 0 Methods for recovery of inclusion bodies from E. coli paste has been weU
d[see Lin et a~, Biotechniques, Il (6): 748-52 (1991); Myers et al., Prot.
Express. Purl, f., 2: 136-143 (1991); Krueger et al., BioPharm., pp. 40-45 (March, 1989); Marston et a~, "Solubilization ofProtein Aggregates," Methods in Enzymology, MP Deutcher (Ed.), Academic Press, New York, 182: 264-276 (1990)]. Briefly, MDC is released from intact cells using a mechanical lysis device (e.g., Mauton-Gaulin). The cell paste is resuspended (20-30% wlv) in buffer [for example, containing 50 mM Tris HCI, pH 8.0, 1 mM EDTA, 50 mM NaCI, 0.2 mglml lysozymey and 0.5% (v/v) Triton X-100] and passed through the machine at a constant pressure of 8-12,000 PSI for one to two passes at 4-15°C. The soluble components of the cell are separated from MDC and the other cellular-derived insoluble components by applying a 3 0 centrifugal force of approximately 12,000 X g for a period of about 5-10 minutes. The insoluble pelleted material is then re-suspended and re-centrifixged using dilute solutions of detergent [for WO 99/156bb PCT/US98I20270 example, 0.5% (v/v) Triton X-100 and 10 mM EDTA, pH 8.0]. Other wash steps can be used, including 0.5% (v/v) Zwittergent 3-14 (Calbiochem, Inc.), as well as treatments to minimize viscosity including lysozyme, DNase, Nonidet and EDTA [see Bartholome-DeBelder et al., Mol.
Microbiol., 2:519 (1988)].
To achieve proper folding of MDC contained in exclusion bodies, inclusion body preparations are reduced at a protein concentration of 5-10 mg/ml in 6 M
guanidine~HCl containing O.1M TrisHCl, pH 8.6, 20% (3-mercaptoethanol, for 1 hour at 37°C. Complete reduction results in a completely clear solution. Confirmation of complete reduction is obtained using an analytical reverse phase (rp) HPLC procedure. For example, a Vydac C4 analytical column (e.g., 214 nm) is equilibrated in 5% acetonitrile/water/0.1%
trifluoroacetic acid. The sample is injected and a linear gradient with increasing acetylnitrile content is run at a rate of 2%
increase per minute. A single peak indicates that complete reduction of the MDC protein has been achieved.
The pH of the solution containing the fully reduced MDC is gradually lowered to 4.0 with 10% HCI. The MDC is then recovered from the reduction solution using preparative rpHPLC [e.g., a Vydak C4 preparative column with the gradient as described above] to remove HCl salts and denaturant. The recovered MDC is then diluted into 2 M
guanidine~HCl, 0.1 M
TiisHCl, pH 8.6, 8 mM cysteine, 1 mM cystine to a protein concentration of 2 g/L. The solution is stirred slowly at room temperature for 4-8 hours and shielded from light.
The concentration 2 0 of properly refolded MDC is monitored using the analytical rpHPLC method described above and is distinguished from reduced MDC by a 2-4 minute reduction in retention time on the HPLC
column, relative to the reduced MDC. Confirmation of disulfide bond formation in refolded MDC
is confirmed using mass spectrometry [i.e., MALDI MS].
2 5 C. Purification of refolded MDC
MDC is purified using a two column procedure as follows: SP-Sepharose-fast flow (Pharmacia) resin is packed for column purification and equilibrated in loading buffer (0.2 M
NaCI, 20 mM Tris base, pH 7.5). The recovered, refolded MDC solution is diluted with buffer until the conductivity of the supernatant equals 18-19 mS, and the pH is adjusted to 7.5. The 3 0 solution is filtered to remove insoluble materials and applied to the column to a capacity of 0.5 Feed mg MDC/ml of resin. Loading buffer is then used until the OD2,o returns to baseline. MDC is eluted using a higher salt buffer (0.6 M NaCI, 20 mM Tris, pH 7.5).
The SP-Sephadex elution peak is then chromatographed on an WP I~-Propyl (C3) hydrophobic interaction column (JT Baker #7585-02). The column is equilibrated with 2.4 M
NaCI, 20 mM Tris, pH 7.5. The 0.6 MlVaCI containing S-P eluate is then adjusted with the appropriate amount of 5 M NaCI to bring the salt concentration of the eluate to 2.4M NaCI. The adjusted eluate is loaded onto the propyl column at 2 mg of MDC/ml and washed with 2.4 M
NaCI, 20 mM Tris, pH 7.5, until the OD28o returns to baseline. The column is then washed with two column volumes of 2.0 M NaCI, 20 mM NaCI. The purified MDC is eluted from the column with 0.8 MNaCI, 20 mM Tris, pH 7.5. Purified MDC is then filter sterilized and stored at -70°C.
Following are protocols for the recombinant expression of MDC in yeast and for the purification of the recombinant MDC. Heterologous expression of human genes using microbial hosts can be an effective method to produce therapeutic proteins both for research and commercial manufacture. Secretion from yeast hosts (see recent review by Romanos, Yeast, 8:
423-488 (1992)) such as Saccharomyces cerevisiae (Price et al., Gene, 55:287 (1987)) Kluy~eromyces lactis (Fleer et al., BiolTeclmology, 9: 968-975 (1991)), Pichia pastoris, (Cregg et al., BiolTechnology, ll: 905-910 (1993)), Schizosaccharomyces pombe (Broker et al., FEES
Lett., 248: 105-110 (1989)), and related organisms provide a particularly useful approach to obtain both high titer production of crude bulk product and rapid recovery and purification.
These expression systems typically are comprised of an expression cassette containing a strong transcriptional segment of DNA or promoter to effect high levels of mRNA
expression in the host.
2 5 The mRNA typically encodes a coding region of interest preceded by an in fi-ame leader sequence, e.g., S. cerevisiae pre-pro alpha factor (Brake et al., Proc. Nat. Acac~ Sci., 81: 4642-4646 ( 1984)) or equivalent signal, which directs the mature gene product to the culture medium. As taught below, MDC can be expressed in such a manner.
In one exemplary protocol, the coding region of the MDC cDNA is amplified from pMP390-12 by PCR, using as primers synthetic oligonucleotides containing the MDC cDNA
sequences present in primers 390-1F (SEQ m NO: 7) and 390-2R (SEQ B7 NO: 8). A
DNA

WO 99/15666 PC1'IUS98I20270 encoding the yeast pre-pro-alpha leader sequence is amplified from yeast genomic DNA in a PCR
reaction using one primer containing bases 1-20 of the alpha mating factor gene and another primer complimentary to bases 255-235 of this gene [Kurjan and Herskowitz, Cell, 30: 933-943 (1982)]. The pre-pro-alpha leader coding sequence and MDC coding sequence fragments are ligated into a plasmid containing the yeast alcohol dehydrogenase (ADH2) promoter, such that the promoter directs expression of a fusion protein consisting of the pre-pro-alpha factor fused to the mature MDC polypeptide. A's taught by Rose and Broach, Meth. Enz , 185:
234-279, D.
Goeddel, ed., Academic Press, Inc., San Diego, CA (1990), the vector fiuther includes an ADH2 transcription terminator downstream of the cloning site, the yeast "2-nucron"
replication origin, the yeast leu-2d gene, the yeast REP 1 and REP2 genes, the ~ coli beta-lactamase gene, and an E coli origin of replication. The beta-lactamase and l~-2d genes provide for selection in bacteria and yeast, respectively. The leu-2d gene also facilitates increased copy number of the plasmid in yeast to induce higher levels of expression. The REP 1 and REP2 genes encode proteins involved in regulation of the plasmid copy number.
The DNA construct described in the preceding paragraph is transformed into yeast cells using a known method, e.g., lithium acetate treatment [Steams et al., Meth. Enz , supra, pp.
280-297]. The ADH2 promoter is induced upon exhaustion of glucose in the growth media [Price et a~, Gene, 55:287 (1987)]. The pre-pro-alpha s~uence effects secretion of the fusion protein from the cells. Concomitantly, the yeast KEX2 protein cleaves the pre-pro sequence from the mature MDC chemokine [Bitter et. al., Proc. Nato Acad Sci. USA, 81:5330-5334 (1984)].
Alternatively, IvmC is recombinantly expressed in yeast using a commercially available expression system, e.g., the Pichia Expression System (Invitrogen, San Diego, CA), following the manufacturer's instructions. This system also relies on the pre-pro-alpha sequence to direct secretion, but transcription of the insert is driven by the alcohol oxidase (AOXl) 2 5 promoter upon induction by methanol.
The secreted IVmC is purified from the yeast growth medium by, e.g., the methods used to purify IVmC from bacterial and mammalian cell supernatants (see Examples 8 and 10).
N~7C was expressed in yeast as follows. Using standard molecular biological methods (Sambrook et al., Molecular Cloning: a Laboratory Manual, Second Edition, Cold 3 0 Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989)) such as those described above, the S. cerevisiae alpha factor pre-pro sequence (codons 1-85 in Figure 9) was fused to the presumptive mature form of MDC (SEQ m NO: 1, positions 1-69; codons 86-155 in Fig. 9).
Expression of the resultant coding region is under control of the K. lactis LAC4 promoter present in the plasmid pYGL/preproMDC (see Figure 10). This plasmid is a derivative of the K. lactis expression plasmid developed by Fleer et al., (supra) and used to secrete high titers of human serum albumin. This vector class is deriv~l from the plasmid pKDl, a 21t like plasmid from in K.
drosophilarium (Chen et al., Nucleic Acids Research, 14: 447-81 (1986)). These vectors are autonomously replicated and mauitained at high copy number and have been shown to confer high levels of protein production when K. lactis strains containing these plasmids are grown in either galactose or lactose as "inducing" agents and as the sole carbon source. The construct pYGL/preproMDC confers to the host both resistance to 6418 (200 mglL) and the giycolytic enzyme phosphoglucokinase (PGK). E~cient selection for transformed cells containing the plasmid is effected by providing a sole carbon source that requires processing via the glycolytic pathway of intermediary metabolism.
Plasmid pYGLIpreproMDC was transformed into the pgko deficient host strain FBOS (Delta Biotechnology Limited) by selecting for 6418 resistance in YEPPglycerol/ethanol medium (0.5% yeast extract, 1% peptone, 1 M KPO,, pH 7.0, containing 3%
glycerol and 2%
ethanol). Following clonal isolation, the transformed seed was grown in shake flask production medium YEPPgaI (0.5% yeast extract, 1% peptone, 1 M KP04, pH 7.0, containing 2% galactose as sole carbon source). SDS-PAGE analysis of the culture medium indicated that a protein 2 0 species of the molecular weight expected of that for mature MDC was present. This protein migrated comparably to synthetic MDC (Gryphon Sciences Corporation). Titration data using dilutions of purified synthetic MDC and culture supernatants in Coomassie blue stained SDS-PAGE gels suggested that MDC was present in the range of 4-10 mg/L.
Western analyses using an anti MDC monoclonal antibody did not reveal the 2 5 presence of MDC-related degrad~ion products, even after further culturing of the seed 24 hours past the completion of growth. This observation suggested that the seed is capable of producing and stably accumulating MDC, indicating that high cell fermentation methods would be effective to increase titer.
The MDC production seed was used to inoculate a fermentor maintained at 26°C
3 0 contairring a batch medium. The composition of the batch medium ( 1200 ml) was as follows: 7.5 g Yeast extract; 0.6 g MgSO,; 6.0 g NH4S04; 9.6 g KHiF'O,; 26.4 g KzHP04; 11 mg CaCl2; 5.0 WO 99/15b66 PCT/US98/20270 ml 1000X vitamins [Bitter et al., J.Mec~ Yirol., 25(2):123-140 (1988)]; 2.5 ml 1000X trace elements [Bitter et al. (1988)]; and 1.2 g 30% galactose.
One hour following inoculation, a feed was initiated at a rate of 12 ml/hour and maintained for four days. The feed medium composition (1500 ml) was as follows: Galactose, 600 g; yeast extract, 50 g; MgS04, 4 g; NH4SO4, 40 g; ICHzP04, 60 g; KZHPO4, 165 g; 1000X
trace elements, i 5 ml; 1 OOOX vitamins, 30 ml; 4% CaClz solution, 20 ml.
Samples were collected and analyzed throughout the run. MDC accumulated during the first three days of the fermentation to a final titer of approximately 50 mg/L as determined from purification recovery experiments. The primary protein species present is MDC.
Significant levels of degradation were not observed by SDS-PAGE analysis. A
sample of the harvest supernatant was partially purified using ion exchange chromatography.
Following dialysis into phosphate buffered saline, the yeast-produced MDC exhibited a single molecular mass of 8088 daltons, as compared with the theoretical value of 8086, well within the expected error of the measurement.
Yeast-produced MDC was fiuther analyzed for biological activity by calcium flux assay and found to exhibit activity comparable to the activity of synthetic MDC and CHO-produced MDC. Using the assay described below in Example 25, yeast-produced MDC was also successful in competing with synthetic MDC-SEAP for binding to CCR4 recombinantly expressed on a mammalian cell surface.
Recombinant Production of MDC in Mammalian Cells MDC was recombinantly producxd in mammalian cells according to the following procedures.
A. Synthesis of Expression Vector 390HXE
A truncated version of the MDC cDNA was synthesized by PCR using pMP390-12 as template and the synthetic oligonucleotides 390RcH (SEQ ID NO: 14) and 394RcX (SEQ
D7 NO: 15) as primers. Primer 390RcH contains a Hind III restriction site followed by bases 1 to 20 of SEQ ID NO: 1; primer 390RcX contains an Xba I restriction site followed by the sequence complimentary to bases 403 to 385 of SEQ ID NO: 1.

-$0-The expected 423 by PCR product was purified by agarose gel electrophoresis and cloned into Hind 1TIlXba I-digested pRc/CMV ((InVitrogen, San Diego CA) a vector which allows for direct expression in mammalian cells). The resulting plasmid, designated 390I-1~, contained bases 1 to 403 of SEQ ID NO: 1. The sequence of the insert was confirmed by automated sequencing using the primers DC03 (SEQ D7 NO: 16) and JHSP6 (SEQ 1D
NO: 3).
Primer DC03 anneals to the pRcICMV vector sequence adjacent to the cloning site.
B. g3mthesis of~F pression Vector 390 mX
Another MDC cDNA construct was generated by PCR, using pMP390-12 as template and the primers 390RcH (SEQ 1D NO: 14) and 390mycRX (SEQ 1D NO: 17).
Primer 390mycRX contains an Xba I restriction site, a sequence complementary to the sequence encoding a "myc" epitope [Fowlkes et al., BioTechniques, 13:422-427 (1992)], and a sequence complementary to bases 298 to 278 of SEQ B7 NO: 1. This reaction amplified the expected 354 by fragment containing bases 1 to 298 of SEQ 1D NO: 1 fused to a "myc" epitope at the lVmC
carboxy ten:ninus. This epitope can be used to facilitate immunoprecipitation, affinity purification, and detection ofthe N~7C-myc fusion protein by Western blotting. The fragment was cloned into pRc/CMV to generate the plasmid 390IdrnX. The sequence of the insert was confirmed by automated sequencing using the primer DC03 (SEQ ID NO: 16).
2 0 C. Expression ofMDC in 293T and N 0 Ce lc Two transfection protocols were used to express the two MDC cDNA constructs described above in subparts A. and B.: transient transfection into the human embryonic kidney cell line 293T and stable transfection into the mouse myeloma cell line NSO
(ECAGC 85110503).
Transient transfection of 293T cells was carried out by the calcium phosphate precipitation protocol of Chen and Okayama, BioTechniques, 6:632-638 (1988) andMol. Cel.
Bio~, 87:2745-2752 (1987). Cells and supernatants were harvested four days after transfection.
A Northern blot was prepared from 4 p,g of total RNA from each cell lysate and probed with a radiolabeled lViDC fi~ag~ment prepared by PCR The template for the labeling reaction was a PCR
3 0 fi~agnent previously g~erated by amplifying pMP390 with the primers 390-1F
(SEQ 117 NO: 17) and 390-4R (SEQ TD NO: 9). Approximately 30 ng of this fragment was employed in a PCR

reaction containing the following: 1.5 mM MgCl2, 50 mM KC1, 10 mM Tris, pH
8.4, 0.2 mM
dATP, 0.2 mM dTTP, 0.2 mM dGTP, 1 pM dCTP, 50 pCi a32P-dCTP (DuPont/New England Nuclear, Boston MA), 2.5 U Taq polymerise, and 10 pg/ml each of primers 390-1F
and 390-2R.
The reaction was denatured by heating for 4 minutes at 94°C, followed by 15 cycles of amplification (denaturation for 15 seconds at 94°C, annealing for 15 seconds at 60°C, and extension for 3 0 seconds at 72°C). The probe was purified by passage over a G-25 Quick Spin column (BMB). Conditions for hybridization were as follows: The filters were incubated at 42°C
for 16 hours with 5 x 10' counts per minute {cpm) of the probe, in 40-50 ml of a solution containing 50% formamide, SX Denhardt's solution, SX SSC (1X SSC is 0.15 M
NaCI, 15 mM
sodium citrate), SO mM sodium phosphate, pH 6.5, and 0.1 mg/ml sheared salmon sperm DNA
(Sigma, St. Louis MO).
Filters were subsequently washed in 0.5 X SSC and 0.2% SDS at 42°C
for 30 minutes. Autoradiography was carried out at -80°C with one intensif5ring screen for sixteen hours.
The MDC DNA constructs were vezy highly expressed in the transfected cells and not detectable in the non-transfected cells.
For stable transfections, NSO cells were grown to 80% confluency in D-MEM
(Gibco), collected by centrifugation, and washed with PBS. Twenty pg of plasmid DNA was iinearized with Sca I restriction endonuclease (BMB), added to the cells, and incubated on ice for 15 minutes in a 0.4 cm gap cuvette (BioRad, Hercules CA). The cells were eleetroporated with 2 0 two pulses of 3 microfarad at 1.5 kilovolts. Cells were diluted into 20 ml D-MEM, incubated at 37°C in 5% COZ for 24 hours, and selected by plating into 96-well plates at various dilutions in D-MEM containing 800 pg/ml geneticin. Wells containing single drug-resistant colonies were expanded in selective media. Total RNA was analyzed by Northern blotting as described in the preceding paragraph. Message for MDC was seen only in transfected cell lines.
2 5 MDC is purified from mammalian culture supernatants by, e.g., adapting methods described for the purification of recombinant TCA3 chemokine [Wilson et al., J. Immu»ol., 145:2745-2750 (1990], or as described below in subpart F.
D. F~xpression of MDC in C O Cellc 3 0 PCR was used to amplify bases 1 to 403 of the MDC cDNA clone (SEQ >D NO:
1) using primers 390RcH and 390RcX (SEQ. ll7 NOs: 14 and 15), as described above in subpart A. The fragment was cloned into the I~ndIII and XbaI sites of the expression vector pDCI, a pUC 19 derivative that contains the cytomegalovirus (CMV) promoter to drive expression of the insert. More specifically, vector pDC 1, depicted in Figure 8, was derived from pRc/CMV and pSV2-dhfr {ATCC vector #37146). Vector pDCI is similar to the mammalian expression vector pRdCMV (Invitrogen, San Diego) except that pDCl carries the mouse dihydrofolate reductase (dhfr) gene as a selectable marker, in place of the neomycin phosphotransferase gene.
Transcription of the target gene in pDC 1 is under the control of the strong CMV promoter. See St~berg eta~, J. Virology, 49:190-199 (1984). Additionally, a polyadenylation sequence from the bovine growth hormone gene [Goodwin and Rottman, J. Biol. Chem., 267:16330-(1992)] is provided on the 3' side of the target gene. The dhfr expression cassette [Subramani et a~, Mol. CeIX Biol. l: 854-864 (1981)] allows selection for pDCl in cells lacking a functional dhfr gene.
XI~l Blue bacteria (Stratagene) were transformed with the.pDCl/MDC plasmid using standard techniques of CaCl2 incubation and heat shock (Sambrook et al.
). Transformants were grown in LB medium containing 100 lrg/ml carbenicillin. Plasmid DNA from individual transformed clones was isolated using the Promega Wizard Maxiprep system (Madison, WI) and its sequence was confirmed by automated sequencing using the primers 390-IF
and 390-2R (SEQ
B7 NOs: 7 & 8). The plasmid was linearized by restriction digestion with Pvu I
endonuclease (Boehringer Mannheim), which cuts once within the vector sequence.
2 0 The Chinese hamster ovary (CHO) cell line used for production of MDC was DG-44, which was derived by deleting the dhfr gene. See Urlaub et al., Cell, 33:405 (1983). For electroporation, 10' of these CHO cells were washed in PBS, resuspended in 1 ml PBS, mixed with 25 ug of linearized plasmid, and transferred to a 0.4 cm cuvette. The suspension was electroporated with a Biorad Gene Pulser {Richmond, CA) at 290 volts, 960 pFarad.
2 5 Transfectants were selected by growth in a medium (Cat. No. 12000, Gibco, Gaithersburg, MD) containing 10~~o dialyzed fetal bovine serum (FBS) (Hyclone, Logan, UT) and lacking hypoxanthine and thymidine. Cells from several hundred transfected colonies were pooled and re-plated in a' medium containing 20 nM methotrexate {Sigma, St. Louis, MO).
Colonies surviving this round of selection were isolated and expanded in a medium containing 20 nM
3 0 methotrexate.

WO 99!15666 PCT/US98/20270 E. ' Purification of MDC for pro in q, ~en,~cing Transfected CHO clones were grown on plastic tissue culture dishes to approximately 90% confluence in a' medium, at which time the medium was replaced with PS
medium containing 0.2% to 1.0% FBS. PS medium consists of the components listed in Table 2, below (purchased as a premixed powder form Hycione, Logan UT), supplemented with the following additional components: (1) 3 g/1 sodium bicarbonate (Sigma, St.
Louis, MO); (2) 2 ~tg/l sodium selenite (Sigma); (3) 1% soy bean hydrolysate (Quest International, Naarden, The Netherlands); (4) lx ferrous sulfate/EDTA solution (Sigma); (5) 1.45 ml/1 EX-CYTE VLE
solution (Bayer, Kankakee, IL); (6) 10 pg/ml recombinant insulin (Nucellin, EIi Lily, Indianapolis, IN); (7) 0.1% pluronic F-68 (Sigma); (8) 30 gg/ml glycine (Sigma); (9) 50 pM
ethanolamine (Sigma); and (10) 1 mM sodium pyruvate (Sigma}.

Com onent Powder #5 m/L

Sodium Chloride 4.0 Potassium Chloride 0.4 Sodium Phos hate Dibasic, 0.07102 Anhydrous Sodium Phos hate Monobasic 0.0625 Ma esium Sulfate, Anh drous 0.1 U
Cupric sulfate 5 Hz0 0.00000125 o Ferrous Sulfate 7 0 0.000417 z Zinc Sulfate 7 H20 0.0004315 Ferric Mtrate 9 H 0 0.00005 Calcium Chloride, Anhydrous 0.11661 Masznesium Chloride. Anhydrous0 I
I

L-Alanine 0 L-Ar ' 'ne HCl 0.15 L-As ara ' a 0 0.075 L-As antic Acid 0.04 L-C teine HCl 0 0.03 d O L-C stine 2 HCl 0.12 L-Glutamic Acid 0.02 L-Glutamine 0.5 Gl cine 0.02 L-Histidine HCl 0 0.04 L-Isoleucine 0.15 L-Leucine 0.15 L-L sine HCl 0.1 L-Methionine 0.05 L-Proline I 0.05 WO 99/15666 PCTlUS98IZ0270 -$$-L-Phenylainine 0.05 L-Serine 0.075 L-Threonine 0.075 L-T to han 0.02 L- osine 2 Na 2 0 0.075 L-Valine 0.12$

Biotin 0.001 D-Calcium Pantothenate 0.0025 Choline Chloride 0.015 Folic Acid 0.005 i-Inositol 0.175 Ncotinamide 0.005 Pyridoxal HCl 0.005 Pyrdoxine HCl 0.005 Riboflavin 0.001 Thiamine HCl 0.005 Cyanocobalamine 0.001 OTHER D-Glucose 1.0 H oxanthine Na 0.005 Th 'dine 0.005 Putrescine 2HC1 0.000081 Sodium vate 0.11004 Linoleic Acid 0.0001 DL-A1 ha Li oic Acid 0.0002 Phenol Red Na Salt 0.0086022 After two additional days in culture, an aliquot of each supernatant was mixed with an equal volume of acetone. The precipitated proteins were pelleted by centrifugation, fractionated on an 18% Tris Glycine gel (NOVEL, and blotted to a PVDF membrane (Mllipore, Bedford, MA).

WO 99/15(66 PCT/US98/20270 MDC bound to the membrane was detected by a crude preparation of monoclonal antibody to MDC (prepared as described in Example 18). Cells from the clone secreting the highest level of MDC protein (approx. 1 Itg/ml) were removed from the plate by treatment with a solution of 0.5% trypsin and 5.3 mM EDTA (GIBCO) and used to start a suspension culture in a' medium plus 10% fetal bovine serum (FBS). Over the course of 8 days, 5 volumes ofPS
medium were added to the culture. Proteins were precipitated from the culture supernatant by addition of polyethylene glycol (MW 8000, Union Carbide, Danbury, CT) to 20 (weight/volume), fractionated on an 18% Tris glycine gel, and electroblotted to a PVDF
membrane (lVfillipore, Bedford, MA) in CAPS buffer (3-[Cyclohexylamino]-1-propanesulfonic acid, pH 10.4) (Sigma, St. Louis, MO). A strip of the filter was removed for detection of MDC
by western blotting with the supernatant from a hybridoma cell line producing anti-MDC
monoclonal antibodies (See Example 18). The reactive band, which migrated with an apparent molecular weight of 6.4 kD, was excised from the remaining portion of the filter.
Using an automated sequencer (Applied Biosystems, Model 473A, Foster City, CA), the sequence of the N-terminus of the protein was determined to be:
GPYGANMEDS. This sequence is identical to that of residues 1 to 10 of SEQ m NO. 2, corresponding to the N-terminus of the predicted mature form of MDC.
F. p~cation of MDC for biologica~i~s_ 2 0 For gowth of larger cultures, MDC-expressing CHO cells were grown to 80%
confluence on tissue culture plates in a' medium. The cells were removed from the plates by treatment with trypsin and EDTA and resuspended at a density of 3 x 105 cellslml in PS medium plus 1% FBS in a spinner flask at 37 °C. Additional P5/1% FBS medium was added as needed to keep the cell density in the range of 1 x 106 to 3 x 106.
After 11 days in culture, the cells were removed from the medium by filtration.
The pH of the culture medium was adjusted to 6.8, and it was passed over a heparin-Sepaharose CL-6B column (Phannacia, Piscataway, Nn. After washing with 0.2 M NaCI in potassium phosphate buffer, pH 7, the column was eluted with a linear gradient of 0.2 to 0.7 M NaCI.
Fractions were analyzed by SDS-PAGE and Coomassie stained to determine which of them 3 0 contained MDC. MDC eluted from the column at approximately 0.6 M NaCI.

The fractions cornaining MDC were pooled and concentrated by ultrafiltration in stirred-cell chamber (Amicon, Beverly, MA) using a filter with a MW cutoff of 3 kD.
Octylglucoside (10 mM final concentration, Boehringer Mannheim Biochemicals) was added to the concentrated MDC, which subsequently was passed through a Sephacryl HR100 column (Pharmacia, Piscataway, Nn. Fractions were analyzed by SDS-PAGE for the presence of MDC.
The final yield of MDC protein was approximately 0.1 mg/liter of culture supernatant, and the purity was estimated to be greater than 95%, as judged by Coomassie staining.
Production of MDC a_n_d MDC nalogc by Pelt it de S, h is MDC and MDC polypeptide analogs are prepared by chemical peptide synthesis using techniques that have been used successfully for the production of other chemokines such as II,-8 [Clark-Lewis et al., J. Biol Chem., 266:23128-34 (1991)] and MCP-1.
Such methods are advantageous because they are rapid, reliable for short sequences such as chemokines, and enable the selective introduction of novel, unnatural amino acids and other chemical modifications.
For example, MDC and MDC analogs were chemically synthesized using optimized stepwise solid-phase methods [Schnolzer et al., Int. J. Pept.
Protein Res , 40:180 ( 1992)] based on t-butyloxycarbonyl (Boc) chemistries of Merrifield [J. Am.
Chem. Soc., 85:2149-2154 (1963)] on an Applied Biosystems 430A Peptide Synthesizer (Foster City, CA).
The proteins were purified by reverse-phase HPLC and characterized by standard methods, including electrospray mass spectrometry and nuclear magnetic resonance.
The chemically synthesized MDC corresponded to the mature form of recombinant MDC, consisting of residues 1 to 69 of SEQ ll~ NO. 2. Several methods were used to compare the chemically synthesized MDC to the recombinant MDC produced by CHO cell transfectants as described in Example 10. The migration of chemically synthesized MDC was identical to that of the recombinant MDC in denaturing SDS-PAGE (18% Tris glycine gel, NOVEL. In addition, the proteins reacted similarly in western blot analysis using monoclonal and polyclonal antibodies raised against bacterially produced MDC as described below in Example 18. The chemically synthesized MDC also appeared to behave in the same manner as the recombinant MDC in 3 0 immunoprecipitation assays with the anti-MDC monoclonal antibodies. These studies indicate -$$-that the denatured and the non-denatured structures of chemically synthesized IVmC are similar to those of recombinant MDC.
The following MDC analogs also have been chemically synthesized:
1. "MDC (n+1)" (SEQ m NO: 30) consists of Ixucine followed by residues 1 to 69 of SEQ
m NO. 2. This analog has alternatively been referred to herein as "IVmC(0-69)."
2. "MDC (9-69)" consists of residues 9 to 69 of SEQ m NO. 2.
3. "MDC-yl" (SEQ m NO: 31) consists of residues 1 to 69 of SEQ ID NO. 2, with the following substitution: Residues 59-60 (Trp-Val) were replaced with the sequence Tyr-Leu. A related analog "NlDC-wvas" consists of residues 1 to 69 of SEQ m NO. 2, with the following substitution: Residues 59-60 (Trp-Val) were replaced with the sequence Ala-Ser.
4. "1VB7C-eyfy" (SEQ m NO: 32) consists of residues 1 to 69 of SEQ ID NO. 2, with the following substitution: Residues 28-31 (T~s-Phe-Tyr-Trp) were replaced with the sequence Glu-Tyr-Phe-Tyr, derived from the amino acid sequence of the chemokine RArTTES (residues 26-29 of SEQ m NO: 21).
The analogs "MDC (n+1)", "MDC (9-69)", and "lVmC-yl" are expected to be antagonists of MDC activity, inhibiting MDC activity by competitively binding to the same receptor that recognizes IVlI7C. Alternatively, they may effect inhibition by forming inactive heterodimers with the native IvmC. Possible activities of the analog "IVmC-eyfy" include inhibition of MDC as 2 0 described for the previous analogs. Alternatively, "MDC-eyfy" may confer some of the activities typical of the chemolcine RAN'fES, such as chemotaxis of T lymphocytes, monocytes, or eosinophils.
Additionally, the following single-amino acid alterations (alone or in combination) are specifically contemplated: (1) substitution of a non-basic amino acid for the basic arginine 2 5 and/or lysine amino acids at positions 24 and 27, respectively, of SEQ m NO: 2; (2) substitution of a charged or polar amino acid (e.g., serine, lysine, arginine, histidine, aspastatc, glutamate, asparagine, glutamine or cysteine) for the tyrosine amino acid at position 30 of SEQ m NO: 2, the tryptophan amino acid at position 59 of SEQ m NO: 2, and/or the valine amino acid at position 60 of SEQ m NO: 2; and (3) substitution of a basic or small,~non-charged amino acid 3 0 (e.g., lysine, arginine, histidine, glycine, alanine) for the glutamic acid amino acid at position 50 of SEQ m NO: 2. Specific analogs having these amino acid alterations are encompassed by the following formula (SEQ m NO: 25):
Met Ala Arg Leu Gln Thr Ala Leu Leu Val Val Leu Val Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Pro err Gly Ala Aan Met Glu Asp Ser Val Cars Cars Arg Aep T~rr Val Arg err Arg Leu Pro Leu Xaa Val Val Xaa His Phe Xaa Trp Thr Ser Asp Ser G'ye Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Xaa Ile Gars Ala Asp Pro Arg Val Pro Xaa Xaa Lys Met Ile Leu Rsn Lys Leu Ser Gln wherein the amino acid at position 24 is selected from the group consisting of arginine, glycine, alanine, valine, leucine, isol~cine, proline, serine, threonine, phenylalanine, tyrosine, tryptophan, aspartate, glutamate, asparagine, glutamine, cysteine, and methionine; wherein the amino acid at position 27 is independently selected from the group consisting of lysine, glycine, alanine, valine, 2 5 leucine, isoleucine, proline, serine, threonine, phenylalanine, tyrosine, tryptophan, aspartate, glutamate, asparagine, glutamine, cysteine, and methionine; wherein the amino acid at position is independently selected from the group consisting of tyrosine, serine, lysine, arginine, histidine, aspartate, glutamate, asparagine, giutamine, and cysteine; wherein the amino acid at position 50 is independently selected from the group consisting of glutamic acid, lysine, arginine, 3 0 histidine, glycine, and alanine; wherein the amino acid at position 59 is independently selected from the group consisting of tryptophan, serine, lysine, arginine, histidine, aspartate, glutamate, asparagine, glutamine, and cysteine; and wherein the amino acid at position 60 is independently selected from the group consisting of valine, serine, lysine, arginine, histidine, aspartate, glutamate, asparagine, glutamine, and cysteine. Such MDC polypeptide analogs are specifically _(~_ contemplated to modulate the binding characteristics of MDC to chemokine receptors and/or other molecules (e.g., heparin, glycosaminoglycans, erythrocyte chemokine receptors) that are considered to be important in presenting MDC to its receptor.
Additionally, analogs wherein the proline at position 2 of SEQ iD NO: 1 is deleted or substituted for by another amino acid are specifically contemplated. Such mutants will collectively be referred to as "MDC~Pro2 polypeptides." As described below in Example 20, MDC (3-69) derived from an H1V-infected T cell line displays properties that are, at least in some respects, opposite or antagonistic from properties observed for mature MDC (1-69). It is hypothesized that a dipeptidyl amino peptidase such as CD26 [Oravecz et al., J. F.xper. Med, 186:1865 (1997)] possesses a specificity for the sequence NHZ-X-Pro (wherein X
is any amino acid), and that the dipeptidase therefore is capable of converting mature MDC
(1-69) (having the amino terminus NH2-Gly-Pro-Tyr) to the MDC (3-69) form in vivo. It is expected that the dipeptidase CD26 will not cleave the amino terminus from lldDC~Pro2 polypeptides, rendering such mutants more stable than MDC(1-69) in vivo. MDCAPro2 polypeptides that retain the biological activities of mature MDC (1-69) are useful in all therapeutic indications wherein MDC
(1-69) is useful as a therapeutic, whereas MDC~Pro2 polypeptides that antagonize the activity of mature MDC (1-69) (e.g., by competitively binding but failing to signal through CCR4) are useful as MDC antagonists. In preferred embodiments, substitution of the proline with a glycine, alanine, valine, leucine, isoleucine, serine, threonine, phenylalanine, tyrosine, or tryptophan is 2 0 contemplated. Introducing the MDCOPro2 mutation into any of the analogs described above is also specifically contemplated.
After synthesis, synthetic MDC or MDC analogs may be reduced and refolded substanbaily as described in Example 8 for bacterially-produced MDC bound in inclusion bodies, or using procedures that are well-known in the art. See, e.g., Protein Folding, T.E. Creighton (Ed.), W.H. Freeman & Co., New York, NY (1992): van Kimmenade et al., Eur. J.
Biochem., 173: 109-114 (1988); and PCT publication no. WO 89/01046.
Recombinant techniques such as those described in the preceding examples also are contemplated for preparing MDC polypeptide analogs. More particularly, polynucleotides encoding MDC are modified to encode polypeptide analogs of interest using well-known 3 0 techniques, e.g., site-directed mutagenesis and the polymerase chain reaction. See generally Sambrook et al., supra, Chapter 15. The modified polynucleotides are expressed recvmbinantly, and the recombinant MDC polypeptide analogs are purified, as described in the preceding examples.
The chemoattractant and/or cell-activation properties of MDC or MDC
polypeptide analogs on one or more types of cells involved in the inflammatory process (e.g., T
lymphocytes, monocytes, macrophages, bas~phils, eosinophds, neutrophils, mast cells, and natural killer cells), on endothelial cells, epithelial cells, fibroblasts, or others are assayed by art-recognized t~hniques that have been used for numerous other chemokines. Native MDC, recombinant MDC or MDC polypeptide analogs, or synthetic MDC or MDC
polypeptide analogs purified and isolated as described in one or more of the preceding examples are assayed for activity as described in the following examples with respect to MDC.
~lnaL L
Assay of MDC Effects upon ~soyhils, Mast Cells~and Eosinoyhils The effect of MDC upon basophils, mast cells, and eosinophils is assayed, e.g., by methods described by Weber et al., J. Immunol., 154: 4166-4172 (1995) for the assay of MCP-1/213 activities. In these methods, changes in free cytosolic calcium and release of proinflammatory mediators (such as histamine and leukotriene) are measured.
Blocking chemokine-mediated activation of these cell types has implications in the treatment of late-phase 2 0 allergic reactions, in which secretion of proin$amznatory mediators plays a significant role [Weber et al., supra].
In one signaling assay, synthetic MDC (0.01 - 10 nM) caused dose-dependent chemotaxis of purified human eosinophils (maximum chemotaxis approximately four-fold greater than in controls). The relative chemotactic activity of MDC, in relation to other known 2 5 chemotactic factors of eosinophils, was as follows: MDC # eotaxin <
RANZ'ES < MCP-4 s eotaxin-2. Eotaxin-2 and MCP-4 were especially potent, whereas RArTTES effects were intermediate, about one log less potent than MCP-4 or eotaxin 2. MDC induced eosinophil migration and shape change even though it did not elicit measurable cytosolic calcium elevations in the eosinophils during these responses. In contrast, the MDC analog MDC(9-69) displayed no 3 0 chemotactic activity in the same assay. This data demonstrates a biological activity and utility for MDC in stimulating the chemotaxis of eosinophils, and further demonstrates a utility of MDC
modulators for modulating this chemotactic activity.

In reported studies with human eosinophils, CCR3 was identified as a critical receptor for a variety of CC chemokines that exert effects on eosinophils, including eotaxin, RA1VTES, MCP-4 and eotaxin-2. See, e.g., Garcia Zepeda, et al., J. Immunol.
157:5613 (1996);
Forssman et al.; J. Exp. Med, 185:2171 (1997); Stellato et al., J. Clin.
Invest , 99:926 (1997);
and White et al., J. Leukoc. Biol. 62:667 (1997). Also, as reported elsewhere herein, the chemokine MDC binds and signals through the chemokine receptor CCR4. However, it was determined that the eosinophil-chemotactic activity of MDC appears to operate in a manner independent ofthe chemokine receptors CCR3 and CCR4. CCR3-transfected HEK
cells labeled with Fura-2 demonstrated a rapid rise in intracellular free calcium following stimulation with 10-50 nM eotaxin, eotaxin-2, or MCP-4, but not with 10-100 nM MDC. Similarly, purified eosinophils cultured for 72 hours in 10 ng/mI IL-5 and labeled with Fura-2 demonstrated a rapid rise in intracellular free calcium following stimulation with 10-50 nM
eotaxin, eotaxin-2, or MCP-4, whereas no such rise was observed following stimulation with MDC (up to 100 nM). In addition, a CCR3 blocking monoclonal antibody was found to inhibit eotaxin-and eotaxin-2-induced chemotaxis of eosinophils, but not chemotaxis induced by MDC.
Two lines of evidence suggest that NIDC-induced chemotaxis of eosinophils operates independently of CCR4. F'ust, ~sinophil cDNA (generated from eosinophil RNA using oligo-dT or random primers) was screened via PCR. CCR4 could not be detected in either the oligo-dT or random primed cDNA, even though the same PCR primers amplif ed CCR4 fram 2 0 genomic DNA, and even though CCR3 mRNA was readily amplifyable. Thus, it appears that eosinophils do not express CCR4. S~;ond, chemotaxis experiments with TARC, a chemokine known to signal through CCR4, have failed (at concentrations up to 100 nlVl) to induce chemotaxis of eosinophils.
The fact that IvlDC apparently exerts its effects on eosinophils in a CCR4-2 5 independent manna indicates that, when selecting 1VIDC modulators to treat allergic reactions in which eosinophils play a role, modulators that will have fewer side-effects are those that modulate MDC-induced chemotaxis of eosinophils without modulating MDC's signaling through CCR4.
Assays are provided herein to select such modulators.

Assay of Chemoattractant and Cell-Activation Properties of MDC upon Human The effects of MDC upon human monocytes/macrophages or human neutrophils is evaluated, e.g., by methods described by Devi et al., J. Immunol., 153:
5376-5383 (1995) for evaluating murine TCA3-induced activation of neutrophils and macrophages.
Indices of activation measured in such studies include increased adhesion to fibrinogen due to integrin activation, ch~notaxis, induction of reactive nitrogen intermediates, respiratory burst (superoxide 1o and hydrogen peroxide production), and exocytosis of lysozyme and elastase in the presence of cytochalasin B. As discussed by Devi et al., these activities correlate to several stages of the leukocyte response to inflammation. This leukocyte response, reviewed by Springer, Cell, 76:301-3I4 (1994), involves adherence of leukocytes to endothelial cells of blood vessels, migration through the endothelial layer, chemotaxis toward a source of chemokines, and site-specific release of inflammatory mediators. The involvement of MDC at any one of these stages provides an important target for clinical intervention, for modulating the inflammatory response.
In one art-recognized chemotaxis assay, a modified Boyden chamber assay, leukocytes to be tested are fluorescemly labeled with calcein by incubating for 20 minutes at room temperature. The labeled cells are washed twice with serum-fi-ee RPMI, resuspended in RPMI
containing 2 mg/mI of BSA, and then added quantitatively to the upper wells of the chambers, which are separated finm the lower wells by a polycarbonate filter (Neuroprobe Inc. Cabin John, IVm). IBC diluted in the same medium as the leukocytes is added to the lower wells at various concentrations. Chambers are incubated for 2 hours at 37 °C. At the end of the assay, cells that have not migrated through the membrane are removed by rinsing the filter with PBS and scraping 2 5 with a rubber policeman. Cells that have migrated through the filter are quantitated by reading fluorescence per well in a fluorescent plate reader (Cytoffuor, Nflllipore Inc., Boston, MA).
A series of experiments were performed using art-recognized procedures to determine the chemotactic properties ofMDC. Initially, the response of human mononuclear cells to MDC was determined. The effect of 1~C on the chemotactic response of polymorphonuclear 3 0 leukocytes (granulocytes) also was examined.
It has been established that MCP-1, which is a C-C chemokine, causes both recruitment and activation of monocytes but appears to have limited ability to induce the migration of macrophages. The failure of MCP-1 to attract macrophages appears to be correlated to the differentiation process: as monocytic cells differentiate, there is a progressive decrease in cell response to MCP-1 [Denholm and Stankus, Cytokine, 7: 436-440 (1995)]. The biological activities of MCP-1 appear to correlate with the expression of this chemokine, with MCP-1 mRNA being found in monocytes but dece~easing as these cells differentiate.
The pattern of expression of MDC appears to be the reverse of that described for MCP-1, with the amount of mRNA for MDC increasing as monocytes differentiate to macrophages. To determine whether this e~cpression pattern correlates to the biological response to MDC, the effects of MDC on the migration of monocytes and macrophages were compared.
1o A number of different leukocyte cells types were analyzed in chemotaxis and chemotaxis inhibition assays. Human mononuclear and polymorphonuclear leukocytes were isolated from peripheral blood using methods known in the art [Denholm et al., Amer. J. Pathol., 135:571-580 (1989)]. Second, the human monocytic cell line,'THP-1 (obtained from the ATCC, Rockville, MD, and maintained in culture in RPMI with 10% FBS and with pennicillin/steptomycin) was employed. THP-1 cells can be cultured as monocytes or can be induced to differentiate to macrophages by treatment with phorbol myristate acetate (PMA) [Denholm and Stankus, Cytokine, 7:436-440 (1995)]. In some experiments monocytic TI3P-1 cells were employed, and in others monocytic THP-1 cells were differentiated to macrophages by 2 0 incubation with phorbol myristate acetate (PMA). Third, guinea pig peritoneal macrophages were obtained essentially as described in Yoshimura, J. Immunol., 150:5025-5032 (1993). Briefly, animals were given an intraperitoneal injection of 3% sterile thioglycollate (DIFCO) two days prior to cell harvest: Macrophages were obtained from the peritoneal cavity by lavage with phosphate buffered saline (PBS) with 1 mM EDTA and 0.1% glucose. Cells were washed once 2 5 by centrifugation and then utilized in chemotaxis assays as described below.
Assays of chemotactic activity were carried out, using the cell preparations described above, essentially as described by Denholm and Stankus, Cytometry, 19:366-369 (1995), using 96-well chambers (Neuroprobe Inc., Cabin John, MD) and cells labeled with the fluorescent dye, calcein (Molecular Probes, Eugene, OR). Polycarbonate filters used in this assay 3 0 were PVP-free (Neuroprobe Inc.); filter pore sizes used for different cell types were: 5 pm for monocytes and THP-1 cells, 3 pm for polymorphonuclear leukocytes, and 8 p.m for guinea pig macrophages.
Fifty thousand calceirt labellal cells were resuspended in RPMI medium containing 2 mg/ml BSA and placed in the upper wells. MDC or other test substances were diluted in RPMI
with BSA (e.g., final MDC concentrations of 25, 50, 100, 250 ng/ml) and placed in the lower wells. Following incubation at 37 °C for 2 hours, unmigrated cells remaining above the filter were removed by wiping; the filter was then air-dried. Controls in these assays were: RPMI with BSA as the negative control, and 50 ng/ml of MCP-1 and 1% zymosan activated serum (ZAS, prepared as described [Denholm and Lewis, Amer. J. Pathol., 126:464-474, (1987)]) were used as positive controls. lvfigration of cells was quantitated on a fluorescent plate reader (Cytofluor, Millipore Inc. Bedford, MA) and the number of cells migrated expressed as fluorescent units.
In assays of inhibitory activity, cells in the upper wells of the chambers were suspended in varying concentrations (0.005, 0.05, 0. 5, 5:0, and 50 ng/ml) of MDC. The lower wells of the chamber were filled with either medium alone or the chemotactic factors, MCP- I or zymosan activated serum (ZAS). Inhibition was assessed by comparing the number of cells that migrated to MCP-1 or ZAS, in the absence of MDC, to the number of cells that migrated with increasing concentrations ofMDC. Preparation of cells and quantitation of assays was performed exactly as described above for the chemotaxis assays. The number of cells migrated was 2 0 expressed as fluorescent units.
As indicated in Figure 2, IvIDC did not induce THP-I-derived mononuclear cell migration, but rather appeared to inhibit mononuclear cell migration, at concentrations between 10 and 100 ng/ml. Other C-C chemokines, such as MCP-1 and RANTES, typically induce maximal monocyte chemotaxis within this concentration range.
2 5 As shown in Figure 3, MDC, at concentrations of .001 to 100 ng/ml had no net effect on gcanulocyte migration. In respect to this lack of effect on granulocyte chemotaxis, MDC
is similar to other previously described C-C chemokines.
The response of both macrophage and monocyte THP-1 cells to MDC is shown in Figure 4. Macrophages (closed circles) migrated to MDC in a dose dependent manner, with 3 0 optimal activity at 50 ng/ml. The decrease in macrophage chemotactic response to MDC at higher concentrations (100 ng/ml) reflects a desensitization of cells which is typical of most WO 99/15666 PGT/US9$/20270 -chemotactic factors at high concentrations [Falk and Leonard, Infect.
Immunol., 32:464-468 (1981)]. Monocytic THP-1 cells (open circles) however, did not migrate to MDC.
The chemotactic activity of MDC for macrophages was further verified in experiments utilizing elicited guinea pig peritoneal macrophages. MDC induced a dose dependent migration of guinea pig macrophages {Figure 5), at concentrations between 100 and 500 ng/ml.
The concentrations necessary to induce the migration of guinea pig macrophages was approximately ten-.fold of that for human cells (fig. 4). Similar differences in concentrations necessary for peak biological activity of human chemokines in other species have been reported for MCP-1 by Yashimura, J. Immunol., 150:5025-5032 (1993}.
The results of these experiments suggest that the biological activities of MDC
are linked to the differentiation of monocytes to macrophages. In contrast to MCP-1 [Yoshimura, J. Immu»oZ, 150:5025-5032 (1993)], MDC induces macrophage but not monocyte chemotaxis.
The ability of MDC to attract macrophages indicates that this chemokine might act to induce the focal accumulation of tissue macrophages. The accumulation of tissue macrophages in specific areas is important in the formation of granulomas, in which lung macrophages act to surround and enclose foreign particulates or relatively nondestructible bacterial pathogens such as Mycobacterium sp. [Adams, Am.J. Pathol., 84:164-191 (1976)].
In certain conditions such as arthritis, the accumulation of macrophages is understood to be detrimental and destructive. The ability of MDC to promote macrophage 2 0 chemotaxis indicates a therapeutic utility for MDC inhibitors of the invention, to prevent, reduce, or eliminate macrophage accumulation in tissues.
The results of the chemotaxis assays with human mononuclear cells, presented in Figure Z, suggested that MDC might inhibit cell migration. In the absence of MDC, monocytic THP-I cells migrate to MCP-1, as shown in Figure 6 (MDC of 0 ng/ml). However, when cells are exposed to MDC, the chemotactic response to MCP-1 {closed circles) is decreased. MDC, at concentrations of 0.005-0.5 ng/ml, inhibited monocyte chemotactic response to MCP-1.
Although MDC inhibited the chemotactic response of monocytes to MCP-1, there was no significant effect of MDC on chemokinesis, or random migration, as reflected by the numbers of cells migrating to medium alone (open circles, RPMI with BSA), either in the presence of absence 3 0 of MDC.

The inhibitory activity of MDC on monocyte chemotaxis indicates therapeutic utility for MDC in the treatment of several chronic inflammatory conditions (atherosclerosis, arthritis, pulmonary fibrosis) in which monocyte chemotaxis appears to play an important pathogenic role. Enhancing the activity of MDC in such diseases might result in the decreased migration of monocytes into tissues, thereby lessening the severity of disease symptoms.
Tumor growth-inhibition properties of MDC are assayed, e.g., by modifying the protocol described by Laving et al., J. Immunol., 153: 4625-463 5 ( 1994) for assaying the tumor growth-inhibitory properties of murine TCA3. An MDC-encoding cDNA is transfected by electroporation into the myeloma-derived cell line J558 (American Type Culture Collection, Rockville, MD). Transfectants are screened for MDC production by standard techniques such as ELISA (enzyme-linked immunoadsorbant assay) using a monoclonal antibody generaxed against MDC as detailed in Example 18. A bolus of 10 million cells from an MDC-producing clone is injected subcutaneously into the lower right quadrant of BALB/c mice.
For comparison, 10 million non-transfected cells are injected into control mice. The rate and frequency of tumor formation in the two groups is compared to determine efficacy of MDC in inhibiting tumor growth. The nature of the cellular infiltrate subsequently associated with the tumor cells is 2 0 identified by histologic means. In addition, recombinant MDC (20 ng) is mixed with non-transfec~ed J558 cells and injected (20 ng/day) into tumors derived from such cells, to assay the effect of MDC administered exogenously to tumor cells.
2 5 Intraneritoneal Ini ec,~tion Assav The cells which respond to MDC in vivo are determined through injection of 1-1000 ng of purified MDC into the intraperitoneal cavity of mice or other mammals (e.g., rabbits or guinea pigs), as described by Luo et al., .I. Immunol., 153:4616-4624 (1994). Following injection, leukocytes are isolated from peripheral blood and from the peritoneal cavity and 3 0 identified by staining with the Diff Quick kit (Baxter, McGraw, IL). The profile of leukocytes is measured at various times to assess the kinetics of appearance of different cell types. In separate experiments, neuaalizing antibodies directed against MDC (Example 18) are injected along with MDC to confirm that the infiltration of leukocytes is due to the activity of MDC.
In vivo Activil~r - Subcutpnenna Tn; .rrin~
The chemoattractant properties of MDC are assayed in vivo by adapting the protocol described by Meurer et al., J. Exp. Med, 178:1913-1921 (1993).
Recombinant MDC
(10-500 pmol/site) is injintradennally into a suitable mammal, e.g., dogs or rabbits. At times of 4 to 24 hours, cell infiltration at the site of injection is assessed by histologic methods. The presence of MDC is confirmed by immunocytochemistry using antibodies directed against NJDC.
The nature of the cellular inf prate is identified by staining with Baxter's Diff Quick kit.
The myelosuppressive activity of MDC is assayed by injection of MDC into mice or another mammsi (e.g. rabbits, guinea pigs), e.g., as described by Maze et al., J. Immurrol., 149:1004-1009 (1992) for the measurement of the myelosuppressive action of MIP-1 a. A single dose of 0.2 to 10 ug of recombinant MDC is intravenously injected into C3H/HeJ
mice (Jackson Laboratories, Bar Harbor ME). The myelosuppressive effect of the chemokine is determined by 2 0 measuring the cycling rates of myeloid progenitor cells in the femoral bone marrow and spleen.
The suppression of growth and division of progenitor cells has clinical implications in the treatment of patients receiving chemotherapy or radiation therapy. The myeloprotective effect of such chemokine treatment has been demonstrated in pre-clinical models by Dunlop et al., Bloom 79:2221 (1992).
An in vitro assay also is employed to measure the effect of MDC on myelosuppression, in the same manner as described previously for derivatives of the chemokines interleukin-8 (a,-8) and platelet factor 4 (PF-4). See Daly ei al., J. Biol.
Chem., 270:23282 (1995). Briefly, low density (less than 1.077 g/cm) normal human bone marrow cells are plated in 0.3% agar culture medium with 10% fetal bovine serum (HyClone, Logan, tTT) with 100 3 0 units/ml recombinant human GM-CSF (R&D Systems, Minneapolis, MIA plus 50 ng/ml recombinant human Steel factor (Immunex Corp., Seattle, WA) in the absence (control) and presence of MDC for assessment of granulocyte-macrophage precursors. For assessment of granulocyte ersrthroid myeloid megakaryocyte colony forming units (CFU-GEMM) and erythroid burst forming units (BFU-E), cells are grown in 0.9% methylcellulose culture medium in the presence ofrecombinant human erythropoietin (1-~ units/ml) in combinationwith 50 nglml Steel factor. Plates are scored for colonies aftei incubation at 37 °C in lowered (5%) 02 for 14 days.
The combination of GM-CSF and Steel factor or erythropoietin and Steel factor allow detection of large colonies (usually > 1000 cells/colony) which come from early, more immature subsets of granulocyte myeloid colony forming units (CFU-G11~, CFU-GEMM, and BFU-E.
Eaam In a 18 A Monoclonal antibodies Recombinant MDC, produced by cleavage of a GST-lVmC fusion protein as described in Example 6, was used to immunize a mouse for generation of monoclonal antibodies.
In addition, a separate mouse was immunized with a chemically synthe~zed peptide corresponding to the N termunus of the mature form of Iv>DC (residues 1 to 12 of SEQ ID NO.
2). The peptide was synthesized on an Applied Biosystem Model 473A Peptide Synthesizer (Foster City, CA), and conjugated to Keyhole Lympet Hemocyanine (Pierce), according to the manufacturer's recommendations. For the initial injection to produce "Fusion 191" hybridomas, approximately 2 0 10 ltg of MDC protein or conjugated peptide was emulsified with Freund's Complete Adjuvant and injected subcutaneously. At intervals of two to three weeks, additional aliquots of 1V1DC
protein were emulsified with Freund's Incomplete Adjuvant and injected subcutaneously. Prior to the final prefusion boost, a sample of serum was taken from the immunized mice. These sera were assayed by western blot to confirm their reactivity with 1V1DC protein.
For a prefusion boost, the mouse was injected with I1~C in PBS, and four days later the mouse was sacrificed and its spleen removed.
For the production of "Fusion 252" hybridomas, a mouse was immunized with the 11~C(0-69) chemically syrnhesized peptide (See Example 11). On Day 0, the mouse was pre-bl~i and injected subcutaneously at two sites with 10 ug of IvmC(0-69) in 200 ul complete Freund's 3 0 adjuvant. On Day 22, the mouse was boosted with 30 ug of MDC(0-69) in 150 ul of incomplete Freund's adjuvant. On Day 40, the mouse was boosted with 20 ug IvIDC(0-69) in 100 ul of incomplete Freund's adjuvant. On day 54, blood was drawn and screened for anti-MDC
antibodies via western blot, and reactivity was observed against MDC. On days 127 through 130, the mouse was injected on each of four consecutive days with 10 ug of MDC(0-69) in a volume of 200 u( PBS. On day 131, the mouse was sacrificed and the spleen was removed for a fusion.
For the production of "Fusion 272" hybridomens, a mouse was treated in a similar fashion as the mouse for fusion 252, except, on day 356, the mouse was boosted with lVmC(0-69) in incomplete Freund's adjuvant. Test bleeds were taken on day 367 and screened by ELISA.
On days 385, 386, 387, and 388, the mouse was boosted with 5 pg injections of MDC(0-69). On day 389 the spleen was removed for a fusion.
The spleens were placed in 10 ml serum-free RPMI 1640, and single cell suspensions were formed by grinding the spleens between the frosted ends of two glass microscope slides submerged in serum-free RPMI 1640, supplemented with 2 mM L-glutamine, 1 mM sodium pyruvate, 100 units/ml penicillin, and 100 p.g/ml streptomycin (RPMI) (Gibco, Canada). The cell ions were filtered through a sterile 70-mesh Nitex cell strainer (Becton Dickinson, Parsippany, New Jersey), and were washed twice by centrifuging at 200 g for 5 minutes and resuspending the pellet in 10 ml serum-free RPMI. Thymocytes taken from three naive Balb/c mice were prepared in a similar manner and used as a Feeder Layer. NS-1 myeloma cells, kept in log phase in RPMI with 10~/o fetal bovine serum (FBS) (Hyclone Laboratories, Inc., Logan, Utah) for three days prior to fusion, were centrifuged at 200 g for 5 minutes, and the 2 0 pellet was washed twice as described above.
Spleen cells (2 x 10~ were combined with 4 x 10' NS-I cells and centrifuged, and the supernatant was aspirated. The cell pellet was dislodged by tapping the tube, and 2 ml of 37°C
PEG 1500 (50~/o in 75mM Hepes, pH 8.0) (Boehringer MaMheim) was added with stirring over the course of 1 minute, followed by the addition of 14 ml of serum-free RPMI
over 7 minutes.
2 5 An additional 16 ml RPMI was added and the cells were centrifuged at 200 g for 10 minutes.
After discarding the supernatant, the pellet was resuspended in 200 ml RPMI
containing 15%
FBS, 100 iiM sodium hypoxanthine, 0.4 pM aminopterin, 16 ~.M thymidine (HAT) (Gibco), 25 units/mI II,-6 (Boehringer Mannheim) and 1.5 x 106 thymocytes/ml and plated into 10 Corning flat-bottom 96-well tissue culture plates (Corning, Corning New York).
3 0 On days 2, 4, and 6, after the fusion, 100 pl of medium was removed from the wells of the fusion plates and replaced with fresh medium. On day 8, Fusion 191 was screened by ELISA, testing for the presence of mouse IgG binding to lVmC as follows.
Immulon 4 plates (Dynatech, Cambridge, MA) were coated for 2 hours at 37°C with 100 ng/well of MDC diluted in 25mM Tris, pH 7.5. The coating solution was aspirated and 200 ul/well of blocking solution [0.5% fish skin gelatin (Sigma) diluted in CMF-PBS] was added and incubated for 30 min. at 37°C. The blocking solution was aspirated and 50 ~1 culture supernatant was added. After incubation at 37°C for 30 minutes, and washing three times with PBS
containing 0.05% Tween 20 (PBST), 50 ul of horseradish peroxidase conjugated goat anti-mouse IgG(fc) (Jackson ImmunoResearch, West Grove, Pennsylvania) diluted 1:7000 in PBST was added.
Plates were incubated as above, washed four times with PBST, and 100 uL substrate, consisting of 1 mg/ml o-phenylene diamine (Sigma) and 0.1 ~1/ml 30% H2O2 m 100 mM Citrate, pH 4.5, was added.
The color reaction was stopped after 5 minutes with the addition of 50 pl of 15% HZS04. A,4~
was read on a plate reader (Dynatech). Fusions 252 and 272 were screened in a similar manner, except ELISA plates were coated with 50 ng/well of MDC.
Selected fusion wells wexe Boned twice by dilution into 96-well plates and visually scored for the number of colonies/well after 5 days. The monoclonal antibodies produced by hybridomas were isotyped using the Isostrip system (Boehringer Mannheim, Indianapolis, III.
Anti-MDC antibodies were characterized further by western blotting against recombinant MDC produced as desc~ed above in E. coli or mammalian CHO cells.
To prepare 2 o the blot, approximately 3 ltl of sedimented cells (transformed E. coli producing MDC; transfected CHO cells producing MDC; untransformed ~ toll (control); and untransfected CHO
cells (control)) were dissolved in standard sample preparation buffer containing SDS
(sodium dodecyl sulfate) and DTT (dithiolthreitol) (Sambrook et al.). After boiling, the lysates were fractionated via denaturing SDS-PAGE (18% acrylamide, Tris Glycine gel, NOVEL and electroblotted to 2 5 PVDF membranes (ll~~llipore, Bedford, MA). MDC monoclonal antibodies were diluted to 0.7 pg/ml in PBS for use in the western blotting, following standard techniques (Sambrook et al.).
As an additional control, the monoclonal antibodies were further tested for cross-reactivity on western blots of whole tissue lysates of human skin, tonsil, arid thymus.
One anti-MDC monoclonal antibody, designated monoclonal antibody l9iD, 3 0 reacted strongly with recombinant MDC produced by both bacteria and mammalian cells.
Further, this ant~ody displayed very little background reactivity in preliminary screening against bacteria, the CHO mammalian cell line, or the whole human tissues tested. In addition, this antibody showed the ability to immunoprecipitate recombinant CHO-derived MDC, following standard immunoprecipitation protocols (Sambrook et al.).
Some background reactivity was observed in subsequent western analyses using the anti-MDC monoclonal antibody 191D. further anti-MDC monoclonal antibodies designated 252Y and 2522 (derived from Fusion 252), used at a concentration of 4 ug/ml, showed less background and strong reactivity with synthetic MDC at a concentration of 0.5 ng. No band was seen on the western blot with human tissue lysates of either colon, skin or tonsil, and background reactivity was minimal. The hybridomas that produce monoclonals 252Y and 2522 have been designated "hybridoma 252Y" and "hybridoma 2522," respectively.
Monoclonal antibody 272D, at 1 ~.g/ml, recognized 200 ng of wild type MDC by western blot, although less strongly than antibody 252Y. Antibody 272D showed no background reactivity against lanes loaded with human thymus whole cell lysate or human skeletal muscle lysate.
The hybridoma cell line which produces monoclonal antibody 191D (designated hybridoma 19ID) has been deposited with the American Type Culture Collection (ATCC), 10801 University Blvd., Manassas, V'~rginia 20110-2209 (USA) pursuant to the provisions of the Budapest Treaty (ATCC Deposit date: June 04, 1996; ATCC Accession No. HB-12122). The hybridoma cell lines that produce monoclonal antibodies 252Y and 2522 (designated "hybridoma 2 0 252Y" and "hybridoma 252Z") were also deposited with the ATCC pursuant to the provisions of the Budapest Treaty {ATCC Deposit date: November 19, 1997; ATCC Accession Nos. HB-12433 and HB-12434, rvely). The hybridoma cell line that produces monoclonal antibody 272D was deposited with the ATCC pursuant to the provisions of the Budapest Treaty on March 27, 1998 (ATCC Accession No. HB-12498). Availability of the deposited materials is not to be 2 5 construed as a license to practice the invention in contravention of the rights granted under the authority of any government in accordance with its patent laws.
B. ~3iclonal_ antibodies.
Polyclonal antibodies against MDC were raised in rabbits following standard 3 0 protocols (Sambrook et al.). Recombinant MDC produced as a GST fusion protein as descn'bed above was diluted in PBS, emulsified with Freund's Complete Adjuvant, and injected INDICATIONS RELATING TO A DEPOSITED MICROORGANISM
(PC"T Rule 136is) A. The indications made below relate to the microorga~usm referred to in the description on page 72 , line 15-24 B. IDENTIFICATION OF DEPOSIT g~~
~si~ ~ i~fied on an additional sheet Name of depositary institution American Type Culture Collection (ATCC) Address of depositary institution including postal code and country) 10801 University Blvd.

Manassas, VA 20110-2209 Date of deposit Accession Number 04 June 1998; 19 November 1997; ATCC HB-12122, -12433, -12434, -12498 27 March 1998 C. ADDITIONAL INDICATIONS (leave blank if not applfcwble) This information is continued on an additional sheet In respect of those designations in which a European patent or a patent in Norway is sought, a sample of the deposited microorganism will be made available until the publication of the mention of the grant of the European patent or the corresponding information concerning the patent in Norway or until the date on which the application has been refused or withdrawn or is deemed to be withdrawn, only by the issue of such a sample to an expert nominated by the person requesting the sample (Rule 28(4) EPC and the corresponding regulations !n Norway).

D. DESIGNATED STATES FOR WHICH
INDICATIONS ARE MADE ((j'the indications arse not for all desigrurted States) E. SEPARATE FURMSHING OF INDICATIONS
(leave blmrk if not applicable) The indications hated below will be submittod to the inttrnatrona Bureau later (specs t a genera nature t a indications e.g., "Accession Number ojDsposit") For receiving Office use only ~ For International Bureau use only This sheet was received with the international application D Thin sheet was received by the lnteanational Bureau a~n:
'~ ~ct~OW ~LL Author;ud officer _.., OGZOZ/86SflLLJd 999SI/66 OM

WO 99/15666 ._ - PCT/US98120270 INDICATIONS RELATING TO A DEPOSTTED MICROORGANISM
(PCT Rule 13 bis) A. The indications made below relate to the microorganism referred to in the description on page 72 , line 15-24 B. IDENTIFICATION OF DEPOSiiT Further deposits are identified ~ an additional sheet Name of depository institution American Type Culture Collection (ATCC) Address of depository institution (including postal code and country) 10801 University Blvd.

Mantissas, VA 20110-2209 Date of deposit Accession Number 04 June 1996; 19 November 1997; ATCC Hl3-12122, -12433, -12434, 27 March 1998 - 12498 C. ADDITIONAL >aVDICATIONS (leave blank ijnot applicable) This information is continued on an additional sheet When designating Australia, in accordance with regulation 3.25 of the Patents Regulations (Australia Statutory Rules 1991 No. 71 ), samples of materials deposited in accordance with the Budapest Treaty in relation to this Patent Request are only to be provided before:
the patent is granted on the application;
or the application has lapsed or been withdrawn or refused; to a person who is:
a skilled addressee without an interest in the invention; and nominated by a person who makes a request for the furnishing of those samples.

D. DESIGNATED STATES FOR WHICH INDICATIONS
ARE MADE (if the indications are not for all designated States) E. SEPARATE FURNISHING OF INDICATIONS
(leave blank if not applteable) The indications li ow will be submitted to the International Bureau later (specify general rusture o the icatior~s e.g.
"
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~ ~ ""' , Accession Number of DspoJitt ) ---~- For r~eiving Otlice use only Far laternational Bureau use only This sheet was received with the international application a This sheet was received by the International Bureau on:
Authorized o~~x"~ ~,~tG,~ ~ ''tai ALL Authorized ot~cer i'~
. _ ~a~.9 OLZOZl86Sf1hL7d 999SI/66 OM

subcutaneously into rabbits. At intervals of three and six weeks, additional MDC diluted in PBS
was emulsified with Freund's Incomplete Adjuvant and injected subcutaneously into the same rabbits. Ten days after the third immunization, serum was withdrawn from the rabbits and diluted ten-fold in Tris-buffered saline with 0.5% Tween 20 (TBS-T, Sambrook et al.) for characterization via western blotting against recombinant MDC as described above.
In a similar set of experiments, polyclonal antisera was generated in a rabbit against a 12-mer peptide corresponding to the amino-terniinus of mature MDC {SEQ ID
NO: 2, positions 1-12). The resultant antiserum was characterized in Western blot experiments using synthetic MDC (mature form, residues 1-69); MDC(0-69); MDC(9-69); MDC-eyfy; and MDC-wvas (see Example 11). The antiserum recognized all forms hut the MDC(9-69) peptide.
C. MDC Detection . eAv Monoclonal a~'bodies 252Y and 2522 were employed in an MDC detection assay as follows: Aliquots of the antibodies 252Y and 2522 were biotinylated using NHS-LC-Biotin (Pierce) according to menu's instructions. Immulon 4 ELISA plates were coated with one monoclonal ant~'body (252Y or 2522, unbiotinylated) overnight at 4°C.
The next day, the plates were blocked with 0.5% fish skin for 30 minutes at 37°C. Known quantities of MDC were loaded onto the plate for 30 minutes at 37°C. The plates were washed and coated with the other monoclonal antibody (biotinylated) for 30 minutes at 37°C. The plates were washed and loaded 2 0 with streptavidin-HRP for 30 minutes at 37°C. The plates were then developed and read on a Dynatech MR5000 plate reader. Preliminary results indicate that, by using the antibody pair 252Y
and 2522, MDC is detectable in the conceon range of low monograms to high picograms per milliliter.
In a related set of experiments, an ELISA format was employed to examine the relative affinity of antibodies 191D, 252Y, and 2522 for antigen. Antibodies were produced as ascites and purified over a protein A matrix (Prosep-A, Bioprocessing, LTD, Durham, England) according to manufacturer's instructions. Eluted antibody was dialyzed against PBS and antibody concentration was assessed by Ago measurements. MDC was coated onto Immulon 4 plates in four-fold dilutions ranging from 2000 to 0.4 ng/ml. After blocking and washing the plates as 3 0 described above, each antibody was added at a constant concentration of 250 ng/ml, and A~
measurements were taken to quantify antibody bound to the plates. The absorbance values for antibodies 252Y and 2522 were more than five-fold higher than those of antibody 191D (1.86 and 1.90 versus 0.34) at 2000 ng/ml MDC; more than seven-fold higher (1.22, 1.29, and 0.16, respectively) at 500 ng/ml, and more than three-fold higher (0.47, 0.47, and 0.13) at 125 ng/ml MDC. At 31 ng/ml MDC, the Ago measurements were at background levels for all three antibodies. -D. ~a_rarteri~tion of epi open reco, , ize~j bX antibodies 252Y a_nd 2527 The ability of monoclonal antibodies 252Y and 2522 to recognize synthetic MDC
(mature form, residues 1-69) and MDC variants (MDC(0-69); MDC(9-69); MDC-eyfy;
and MDGwvas (see Example 11 )) was analyzed via Western blot. One hundred to 500 nanograms of each synthetic peptide was electrophoresed on a denaturing polyacrylamide gel, transferred, and probed with antibody 252Y or antibody 2522 at a concentration of I pg/ml.
Immunoreactivity was visualized by incubating the probed blot with horseradish peroxidase-conjugated goat anti-mouse immunoglobulin G {Transduction Laboratories #M15345) at a concentration of 0.2 ug/ml or 1:5000 dilution in TRIS buffered saline with 0.1% Tween 20 (TBS
Tw20) and 1% bovine serum albumin for 30 minutes at room temperature. The blot was washed three times in the TRIS buffered salineJO.1% Tween 20 solution and detection of antibody binding was measured by autoradiography (Kodak Hyperfihn) using electro-chemiluminescence (NEN
Renaissance ECL # NEL 102). Both monoclonal antibodies were observed to recognize wildtype 2 0 1VIDC and the analogs MDC(0-69), MDC(9-69), and MDGeyfy. However, antibody 252Y and antibody 2522 both failed to recognize I~C-wvas, suggesting that the epitope(s) recognized by these antibodies includes) the wv motif near the carboxyl-terminus of lVmC.
This motif tends to be highly conserved in atl CC chemokines (see Fig. 1).
To further characterize the epitope(s) recognized by antibodies 252Y and 2522, 2 5 an Immulon 4 plate was coaxed with lVft7C at 1.0 pg/ml. After blocking the plate with fish skin as described above in part C, unlabeled antibody 252Y, 2522, or an isotype-matched control was added at 5 lcg/ml and incubated for 30 minutes at 37°C. Without washing, either biotinlyated antibody 252Y or 2522 was added at a concentration of 0.25 ~glml, and the plate was incubated an additional 30 minutes at 37°C. Thereafter, the plate was washed and developed with 3 0 streptavidin-HRP. The results showed that either 252Y or 2522 was capable of reducing the signal of either biotinlyated antibody ten-fold, as compared with the signal of either biotynilated antibody blocked with the control antibody. These results further indicate that antibodies 252Y
and 2522 recognize similar or overlapping epitopes.
In contrast, unpurified supernatant from hydriboma 272D was tested in a similar experiment for its ability to compete with biotynilated 252Y or biotynilated 2522, but was unable to reduce the signal of either antibody. Thus, monoclonal antibody 272D
recognizes an epitope different from that recognized by monoclonals 252Y and 2522.
E. A_n_tibodies 252Y nd 252Z mpWi for i m m~~,; a ine 1~~C
The following experiments were conducted which demonstrate a utility for antibodies 252Y and 2522 for immuprecipitation of MDC. Antibodies 252Y, 2522, and an irrelevant isotype-matched control were added separately at a concentration of 10 pg/ml to an extraction buffer (1% triton X-100, 10 mM Tris base, 5 mM EDTA, 10 mM NaCI, 30 mM Na pyrophospate, 50 mM NaF, 100 pM Na Orthovanadate, pH 7.6) containing 100 ng/ml MDC.
These samples were incubated on ice for 1 hour. To precipitate the immune complexes, 15 pl of protein G sepharose (Pharmacia Biotech # I7-0618-O1) were added to each sample and incubated on a rotation apparatus at 4°C for 30 minutes. The samples were then centrifuged to collect the protein G sepharoseJ'immune complexes, washed three times (1 ml each) in extraction buffer, boiled/solubilized in 2X SDS-PAGE buffer, electrophoresed on an 18% SDS-PAGE
gel, and western blotted to PVDF membrane (Novex # LC2002). Nonspecific binding sites on the PVDF
2 0 membrane were blocked with TBS Tw20/1% BSA for 30 minutes at room temperature. The blot was then probed with 1 pg/ml of antibody 252Y in TBS Tw20/1% BSA for 1 hour, washed three times with TBS Tvr~O, probed with horseradish peroxidase-conjugated goat anti-mouse 1gG in TBS Tw20/1% BSA for 30 minutes at room temperature, washed three times with TBS Tw20, and detected by autoradiography using ECL. Bands at approximately 8 kD were detected in the 2 5 252Y and 2522 lanes but not in the negative isotype-matched control lane.
Additionally, MDC
was immunprecipitated from cell culture supernatants containing RPMI (Rosell Park Memorial Institute - Gibco) medium with 10~/o fetal bovine serum spiked with 25 ng/ml MDC using the same conditions stated above.

F.
The activities of MDC as reported herein suggest numerous the~rap~tic indications for MDC inhibitors (antagonists). MDC-neutralizing antibodies (see Example 30) comprise one class of therapeutics useful as MDC antagonists. Following are protocols to improve the utility of anti-MDC monoclonal antibodies as therapeutics in humans, by "humanizing"
the monoclonal antibodies to improve their serum half life and render them less immunogenic in human hosts (i.e., to prevent human antibody response to non-human anti-MDC antibodies).
The principles of humanizaxion have been described in the literature and are facilitated by the modular arrangement of antibody proteins. To minimize the possibility of binding complement, a humanized antibody of the IgG4 isotype is preferred.
For example, a level of humanization is achieved by generating chimeric antibodies comprising the variable domains of non-human antibody proteins of interest with the constant domains of human antibody molecules. (See, e.g., Morrison and Oi, Adv.
Immunol., 44:65-92 (1989). The variable domains of MDC neutralizing anti-MDC antibodies are cloned from the genomic DNA of a B-cell hybridoma or from cDNA generated from mRNA isolated from the hybridoma of ingest. The V region gene fiagments are linked to exons encoding human antibody constant domains, and the resultant construct is expressed in suitable mammalian host cells (e.g., myeloma or CHO cells).
To achieve an even greater level of humanization, only those portions of the 2 0 variable region gene fragm~ts that encode antigen-binding complementarity determining regions ("CDR") of the non-human monoclonal antibody genes are cloned into human antibody sequences. [See, e.g., Jones et al., Nature, 321:522-525 (1986); Riechmann et al., Nature, 332:323-327 (1988); Verhoeyen et al., Science, 239:1534-36 (1988); and Tempest et al., BiolT'echnology, 9:266-71 (1991). If necessary, the ~i-sheet framework of the human antibody 2 5 surrounding the CDR3 regions also is modified to more closely mirror the three dimensional structure of the antigen binding domain of the original monoclonal antibody.
(See Kettleborough et al., Protein Engin., 4:773-783 (1991); and Foote et al., J. Mol. Biol., 224:487-499 (1992).) In an alternative approach, the surface of a non-human monoclonal antibody of interest is humanized by altering selected surface residues of the non-human antibody, e.g., by 3 0 site-directed mutagenesis, while retaining all of the interior and contacting residues of the non-human antibody. See Padlan, Molecular Immunol., 28(4/Sj:489-98 (1991).

The foregoing approaches are employed using MDC-neutralizing anti-MDC
monoclonal a~'bodies and the hybridomas that produce them, such as antibodies 252Y and 2522, to generate humanized MDC-neutralizing antibodies useful as therapeutics to treat or palliate conditions wherein MDC expression is detrimental.
G. Human MDC-Neutrali~ng t~n_tibodies from ~hage di~~lav Human lVmC-neutralizing antibodies are generated by phage display techniques such as those described in Aujame et a~, HumanAretibariies, 8(4):155-168 (1997); Hoogenboom, TTBTECH, 15:62-70 (199'n; and Ra,der et al., Curr. Opin. Biotechtio~, 8:503-508 (1997), all of which are incorporated by reference. For example, antibody variable regions in the form of Fab fragments or linked single chain Fv fragments are fused to the amino terminus of filamentous phage minor coat protein pIII. Expression of the fusion protein and incorporation thereof into the mature phage coat results in phage particles that present an antibody on their surface and contain the genetic material encoding the antibody. A phage library comprising such constructs is expressed in bacteria, and the library is panned (screened) for MDC-specific phage-antibodies using labelled or immobilized MDC as antigen-probe.
H. Humarn_ MDC-neutrat_i_~ng a_n_tibodie from ~r~enic min Human 1V)DC-neutralizing antibodies are generated in transgenic mice essentially as described in Bruggemann and N~berger, Immunol. Today, 17(8):391-97 (1996) and Bruggemann and Taussig, Cun: Opin. Biotechnol., 8:455-58 (1997). Transgenic mice carrying human V-gene segments in germline configuration and that express these transgenes in their lymphoid tissue are immunized with an IvmC composition using conventional immunization protocols. Hybridomas are generated using B cells from the immunized mice using conventional protocols and screened to identify hybridomas secreting anti-IVmC human antibodies (e.g., as described above).
I. FI,ISA for detecting and monito 'ng sen3m conc"-ntration of h"~C
The measurement of endogenous levels of MDC is useful to monitor the immune 3 0 state of a patient, especially a patient who is immunocompromized, in a hyperimmune state, or undergoing treatment with Nll~C neutralizing antibodies or other 1V>DC
antagonists.

_78_ A sensitive ELISA to measure MDC in biological fluids, for example serum, can be established using monoclonal antibodies, polyclonal antibodies, immuno-conjugates containing MDC ligands (for example heparin conjugates), or combinations thereof. For example, monoclonal antibodies 272D, 252Y and 2522 were employed in an MDC detection assay as described below. -Aliquots of the antibodies 252Y and 2522 were biotinyIated using NHS-LC-Biotin (Pierce) according to manufacturer's instructions. Immulon 4 ELISA plates were coated with antibody 272D overnight at 4°C. The next day, the plates were blocked with 0.5% fish skin for 30 minutes at 37°C. Known quantities of MDC(1-69) were loaded onto the plate for 30 minutes at 37°C. The plates were washed and coated with either 252Y or 2522 (biotinylated) for 30 minutes at 37°C. The plates were washed and loaded with streptavidin-HRP for 30 minutes at 37°C. The plates were then developed and read on a Dynatech MR5000 plate reader. Preliminary results indicate that MDC is detectable in the concentration range of low nanograms per milliliter in this ELISA format. It is expected that use of polyclonal antibodies for the capture antibody will lead to a still more sensitive ELISA assay.
Changes in intracellular calcium concentrations, indicative of cellular activation by 2 0 chemokines, were monitored in several cell lines by an art-recognized calcium flux assay. Cells were incubated in 1 ml complete media containing I uM Fura-2/AM (Molecular Probes, Eugene, OR) for 30 minutes at room temperature, washed once, and resuspended in D-PBS
at 106 cells/ml.
Two ml of suspended cells were placed in a continuously stirred cuvette at 37°C
2 5 in a fluorimeter (AMiNCO Bowman Series 2, Rochester, NY). The concentration of intracellular calcium was indicated by fluorescence, which was monitored at 510 nm emission wavelength while switching between excitation wavelengths of 340 nm and 380 nm every 0.5 seconds. The ratio ofthe emissions from the 340 nm relative to the 380 mn excitation wavelengths corresponds to the level of intracellular calcium.
3 0 Cell lines measured by this assay included the following: the human embryonic kidney cell line HEK-293 stably transfected with the putative chemokine receptor gene V28 [Report et al., Gene, 163:295-299 (1995)]; HEK 293 cells stably transfected with the chemokine receptor gene CCRS [Samson et al., Biochemisby, 35:3362-3367 (1996); see also co-owned, co-pending U.S. Patent Application Serial No. 08/575,967, filed December 20, 1995, incorporated herein by reference, disclosing chemokine receptor materials and methods, including CCRS
(identified therein as "88C")], the human manocytic cell line THP-1, the human lung epithelial cell line A 549; and the human fibroblast cell line ZIVVIR 90. None of these cell lines fluxed calcium in response to the recombinant MDC protein. As positive controls, the HEK-293 transfectants responded strongly to thrombin, indicating that the assay was valid. In addition, the THP-1 cells responded strongly to the commercially available chemokines MCP-1 and MCP-3 (Peprotech, Rocky Ifill, Nn at a final concentration of 2S ng/ml. No additional stimuli were tested on the A
549 or IZVIR 90 cell lines.
Several CC chemokines have been implicated in suppressing the proliferation of Human Immunodeficiency Virus (HiV), the causative agent of human Acquired Immune Deficiency Syndrome (AIDS). See Cocchi et al., Science, 270:1811 (I99S);
Winkler et al., Science, 279:389-393 (1998). The HIV antiproliferative activity of MDC is measured by means such as those described by Cocchi et al., in which a CD4+ T cell line is acutely infected with an 2 0 HIV strain and cultured in the presence of various concentrations of MDC.
After three days, a fresh dilution of MDC in the culture medium is added to the cells. At S to 7 days following infection, the level of HIV is measured by testing the culture supernatants for the presence of HIV
p24 antigen by a commercial ELISA test (Coulter, Miami, FI,).
One technical report teaches that MDC possesses an HIV antiproliferative activity.
2 5 See Pat et a~, Science, 278: 695-698 (1997). The agert used in the study consisted of purified polypeptides that had been secreted fi~om an immortalized cell line derived from CD8+ T cells from an HIV 1-infected individual. Pal et a~ reported that the purified "native MDC" from this cell line possessed an NH2-terminus corresponding to the tyrosine at position 3 of SEQ
ID NO: 1. A
"minor" sequence beginning with the proline at position 2 of SEQ 11? NO: 1 also was detected.
3 0 The authors did not detect a peptide beginning with the glycine at position I of SEQ ID NO: 1 in their "native MDC" composition. According to Pal et al., a reversed-phase HPLC fraction WO 99/15666 . PCT/US98/20270 containing the "native MDC" suppressed the acute infection of CD8+ cell-depleted PBMCs by HIV-1~ and various NSI HIV isolates in a concentration-dependent fashion.
Similar HIV
suppressor activity was not observed in supernatants from other cell lines that appeared (from Northern blot studies) to demonstrate equivalent MDC gene expression.
-A. IJse ofMDC an~agoniats to in_h~bit HIV~~roliferation An acute HIV 1H,, infectivity assay reported in Pal et al. was repeated (100 TCID~
units/well) using the macrophage cell line PM-1 (1 x 105 cells/well) and using purified mature MDC recombinantly expressed in CHO cells and having an amino acid sequence beginning at position 1 of SEQ ID NO: 1 (see Example I0). Interestingly, mature MDC was found to have no HIV suppressive activity. The same assay was performed with MDC(0-69) (See Example 11), an analog that exhibits properties of a partial MDC antagonist (see Example 19) in that it binds CCR4 with wild-type affinity, but exhibits substantially reduced capacity to induce a calcium flux or induce chemotaxis. At a concentration of 1 pg/ml, MDC(0-69) conferred a 58%
and 67%
reduction in the production of infectious particles (TCID~ units measured on days 5 and 7). The positive control RANTES produced greater than 95% inhibition at 5 ng/ml.
Without intending to be limited to a particular theory, one explanation for these results is that mature MDC (1-69) induces HIV proliferation, and that the anti-proliferative effects of MDC(0-69) results from this species competitively inhibiting the capacity of endogenous matiue MDC (1-69) to stimulate HIV-2 0 1 production.
The effects of mature MDC and of MDC-neutralizing antibodies were analyzed in Pal et al.'s acute HIV-1~ (0.01 MOI/well) infectivity assay using peripheral blood mononuclear cells (PBMC, 1 x 106 cells/well) depleted of CD8'" cells. The mature MDC (1-69) failed to inhibit p24 production, as compared to a control marine IgGl antibody. However, the marine monoclonal anti-MDC neutralizing antibodies 252Y (IgGl) and 2522 each inhibited p24 production when tested separately at a concentration of 2 pg/ml (37% and 28%
inhibition, respectively). Again, one explanation for these data is that PBMC contain and produce endogenous MDC (1-69) that acts to stimulate HTV 1 functions, and that IvB?C
antagonists inhibit this elect.
3 0 To confirm the apparent role of MDC as an HIV-1 agonist, an infectivity assay (such a~s that described in Pal et al.) is repeated using MDC neutralizing antibody and titrating exogenous mature 1~'?C(1-69) into the assay wells. If native MDC(1-69) exerts an agonistic effect on HIV 1 infectivity and/or proliferation, then it is expected that the antiviral effect of the neutralizing antibody will be reduced with increasing amounts of mature 11~C, and will be overwhelmed with the addition of a molar excess of MDC.
Collectively, these results provide a therapeutic indication for lVmC
antagonists for inhibiting proliferation of infectious retroviruses, especially HIV
retroviruses. Such therapeutic methods and uses are intended as an aspect of the invention. For use in this context, the term "MDC antagonist" includes any compound capable of inhibiting HIV-1 proliferation in a manner analogous to MDC neutralizing antibodies, or MDC(0-69), or MDC(3-69).
For example, anti-11~C amibodies (especially neutralizing antibodies, and preferably humanized antibodies) are highly preferred 1VIDC antagonists. Similarly, polypeptides that are capable of binding to MDC that comprise an antigen-binding fragment of an anti-lVmC
antibody are contemplated. Effective MDC analogs also are contemplated as MDC antagonists.
For example, N-terminal deletion analogs of IvmC are contemplated, especially deletion analogs having an amino acad sequence consisting of a portion of the amino acid sequence set forth in SEQ ID NO:
2 that is ~cient to bind to the chemokine receptor CCR4, the portion having an amino-ternunus between residues 3 and 12 of SEQ ID NO: Z. Likewise, analogs comprising a chemical addition to the amino terminus to render said polypeptide antagonistic to MDC are contemplated. The chemical addition may be added to the amino terminus of IvmC(1-69) to form the analog, or to 2 0 the amino terminus of an 11~C analog that has had amino acids deleted from its amino terminus (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 residues deleted).
Additional classes of MDC antagonists useful in anti-HIV therapeutic methods include antagonists derived from CCR4 or from other 1VIDC receptors. For example, a solubilized, NIDGbinding version of CCR4 or CCR4 fragment is contemplated.
Similarly, humanized antibodies that block but do not signal through CCR4 are contemplated as useful as anti-HIV th~ap~tics. Such antibodies are made using techniques described herein for making anti-MDC antibodies and/or techniques that have been described in the art, for generating antibodies to other seven transmembrane receptor proteins (e.g., using as an antigen CCR4 transfected cells that express CCR4 on their surface). See Wu et al., J. Fxp.
MeaC, 185:1681 3 0 1691 (1997).

Yet another class of MDC antagonists useful in anti-HIV therapeutic methods of the invention include agents that have the effect of transforming mature MDC(1-69) to antagonist forms irr viva, e.g., by modifying the amino terminus of MDC. For example, administration of a therapeutically effective amount of the dipeptidyl aminopeptidase CD26 is contemplated.
Therapeutically effective amounts of MDC antagonists (i.e., for inhibiting HIV
infectivity and/or proliferation) are readily determined using standard dose-response studies.
Moreover, determination of proper dose and dosing is facilitated by anti-MDC
antibodies of the invention (Example 18), which can be used in an ELISA or other standard assays to monitor serum MDC levels in subjects receiving treatment. A therapeutic MDC
neutralizing antibody should be administered in su~aent quantity and with sufficient frequency so as to maintain serum concentrations ofMDC below detectable levels. Doses of an MDC neutralizing antibody on the order of 0.1 to 100 mg antibody per kilogram body weight, and more preferably 1 to 10 mg/kg, are specifically contemplated. For humanized antibodies, which typically exhibit a long circulating half life, dosing at intervals ranging from daily to every other month, and more preferably every week, or every other week, or every third week, are specifically contemplated.
Use of an IgG4 type humanized MDC-neutralizing antibody is highly preferred, to minimize or eliminate the possibility of inducing a complement reaction.
Moreover, determination of therapeutically effecEive MDC antagonists, doses, and dosing schedules is faalitated by dose-response studies in art-recognized in viva models for HIV
2 0 infection and proliferation, such as studies in appropriate mice jPettoello-Mantovani et al., J.
Irfec~ Diseases, 177:337 (1998); J.M. McCune et al., "The Hematophtology ofHIV-1 Disease:
Experimental Analysis in viva," in Huma~ee Hematopoiesis in SLID Mice, M.
Roncarolo et al.
(eds.), Landes Publishing Co., New York, NY, pp. 129-156 (1995); and McCune et al., "The SCID-hu mouse: a small animal model for HIV infection and antiviral testing,"
in Progress in Immurtol., Yol. Yll, Melchers et al. (eds.), Springer-Verlag Berlin Heidelberg, pp. 1046-1049 ( 1989)] or primate models.
B. Use of TA_RC ~n~gonQts to inhibit HIV~rofferation The foregoing experiments also suggest further analysis wherein an HIV-1 3 0 infectiv'rty assay is repeated using neutralizing antibodies directed against other beta chemokines.
For those (i-chemokines lacking an activity towards TH2 cells (analogous to MDC's activity toward such cells), it is expected that chemokine-specific n~trali~ng antibodies will behave much like the marine control IgGl antibody above. However, for those ~3 chemokines that possess an activity toward TH2 cells that is comparable to that of MDC (i.e., TARC), it is expected that chemokine-specific neutralizing antibodies will behave much like MDC-neutralizing antibodies and inhibit HIV-1 infectivity and/or proliferation. The use of TARC-neutralizing antibodies and/or other TARC inhibitors to suppress the infeetivity and/or proliferation of immunodeficiency viruses is specifically contemplated as an aspect of the invention.
The nucleotide and deduced amino acid sequences of TARC have been reported in the literature and are set forth herein in SEQ m NOs: 42 and 43. See Imai et al., J. Biol.
Chem. 271: 21514-21521 (1996); GENBANK ACCESSION NO. D43767. TARC golypeptides and anti-TARC antibodies are synthesized using procedures essentially as described herein for making MDC and anti-MDC antibodies, or using procedures described in the literature for TARC.
[See Imai et al., J. Biol. Cltem., 272: 15036-15042 (1997); and Imai et al., J. Bio~ Chem., 271:
21514-21521 (1996).] The HIV-proliferativeJanti-proliferative effects of TARC
polypeptides (e.g., native mature TARC and TARC analogs, especially amino-terminal deletion and addition analogs) and TARC-neutralizing antibodies are assayed essentially as described in Pal et al. or Cocchi et al.
Based on the theory that the HIV antiproliferative e$ycacy of 1VIDC
antagonists is mediated by blocking the signaling of MDC through CCR4 in target cells that express CCR4, 2 0 it is further contemplated that antibodies to any other chemokine that known or is discovered to signal through CCR4 will be useful as anti-HIV therapeutics of the invention.
In addition to their ability to attract and activate leukocytes, some chemokines, such as IL-8, have been shown to be capable of affecting the proliferation of non-leukocytic cells [see Tuschil, J. Invest. Dermatol., 99:294-298 (1992)]. Fibroblasts throughout the body are important to the structural integrity of most tissues. The proliferation of fibroblasts is essential to wound heating and response to injury but can be deleterious as well, as in the case of chronic inflammatory diseases, such as pulmonary fibrosis [Phan, in: ImmunoloQV of nflamma inn Elsevier (1983), pp. 121-162].

In vitro ceU proliferation assays were utilized to assess the effects of MDC
on the proliferation of fibroblasts. Human fibroblasts (CRL-1635) were obtained from ATCC and maintained in culture in DMEM with 10% FBS and 1% antibiotics. Proliferation assays were performed and quantitated as previously described in the art by Denholm and Phan, Amer. J.
Pathol., 134:355-363 (1989). Briefly, on day 1, 2.5 x 103 cells/well were plated into 96 well plates in DMEM with 10% FBS. Day 2: twenty-four hours after plating, medium on cells was changed to serum-free DMEM. Day 3: medium was removed finm cells and replaced with MDC
diluted in DMEM comaining 0.4% FBS. Day 5: one microCurie of 3H-thymidine was added per well and incubation continued for an additional 5 hours. Cells were harvested onto glass fiber filters. Cell proliferation was expressed as cpm of ~i-thymidine incorporated into fibroblasts.
Controls for this assay included the basal medium for this assay, DMEM with 0.4% FBS as the negative control, and DMEM with 10% FB S as the positive control.
As shown in Figure 7, MDC treatment decreased the proliferation of fibroblasts in a dose dep~dent manner. Similar inhibition of fibroblast proliferation was observed with both MDC purified from CHO cells (closed circles} and chemically synthesized MDC
(open circles}.
The fibroblast-antiproliferative effect of MDC indicates a therapeutic utility for MDC in the treatment of diseases such as pulmonary fibrosis and tumors, in which enhanced or uncontrolled cell proliferation is a major feature.
The effects of MDC upon the proliferation of epithelial cells, T cells, fibroblasts, endothelial cells, macrophages, antl tumor cells are assayed by methods known in the art, such as those described in Denholm et al., Amer. J. Paihol., 134:355-363 (1989), and "In Vitro Assays 2 5 of Lymphocyte Functions," in: Current Protocols Immunology, Sections 3-4, Whey and Sons (1992), for the assay of growth factor activities. In these methods, enhancement or inhibition of cell growth and the release of growth factors are measured:
MDC effects on the proliferation of epithelial cells and endothelial cells are assayed using the same procedures as those described above for fibroblasts (Example 21).
3 0 The effects on the proliferation of T cells are determined using peripheral blood lymphocytes. Mononuclear cells are isolated from peripheral blood as described in Denholm et -8$-al., Amer. J. Pathol., 135:571-580 (1989); cells are resuspended in RPMI with 10% FBS and incubated overnight in plastic tissue culture flasks. Lymphocytes remain in suspension in these cultures and are obtained by centrifugation of culture medium. One hundred thousand lymphocytes are plated into each well of a 96 well plate and incubated for three days in medium {RPMI plus 10% FBS) containing 1 pg/ml PHA with or without 50, 125, 250 or 500 ng/ml of MDC. One microCurie of 3H-thymidine is added during the last 18 hours of incubation. Cells are harvested and proliferations expressed as described for fibroblasts in Example 21.
The effects of MDC on macrophage proliferation are determined using elicited guinea pig peritoneat macrophages, obtained as described above in Example 13.
Macrophages are plated into 96 well plates at a density of one hundred thousand cells per well in RPMI with 10% FBS, and incubated 2 hours to allow cells to adhere. Medium is then removed and replaced with fresh medium with or without 50, 125, 250 or 500 ng/ml of MDC. Cells with MDC are incubated three days, and proliferation is determined as described above for lymphocytes.
Chemokine-mediated control of the proliferation of these cell types has therapeutic implications in enhancing tissue repair following injury, and in limiting the proliferation of these cells in chronic inflammatory reactions such as psoriasis, fibrosis, and atherosclerosis, and in neoplastic conditions.
2 0 In Pivo FibrQblast Proliferation Aesav The anti-proliferative effects of MDC upon fibroblasts are determined in vivo by the methods known in the art, such as those reported by Phan and Fantone, Amer. J. Pathol., 50:587-591 (1984), which utilize a rat model of pulmonary fibrosis in which the disease is induced by bleomycin. This model is well-characterized and allows for the assessment of fibroblast 2 5 proliferation and collagen synthesis during all stages of this disease.
Briefly, rats are divided into four treatment groups: 1) controls, given intratracheal injections of normal saline; 2) saline-injected rats which also receive a daily intraperitoneal injection of 500 ng ofMDC in saline; 3) bleomycin-treated, given an intratracheal injection of 1.5 mg/kg bleomycin (Calbiochem, Palo Alto, CA); and 4) bleomycin-treated rats which also are 3 0 given a daily intraperitoneal injection of 500 ng of MDC.

WO 99/15b66 PCTIUS98/Z0270 Three rats per group are sacrificed at 4, 7, 14, 21, and 28 days after the initial intratracheal injections. Lungs are removed and samples of each lobe taken for histological examination and assays of collagen content.
~aam In a 24 A 20 kb genomic fragment containing the human MDC gene was labelled with digoxigenin by nick translation and used as a probe for fluorescence in situ hybridization of human chromosomes (Genome Systems, Inc., St. Louis, MO). The labelled probe was hybridized to normal metaphase chromosomes derived from PHA-stimulated peripheral blood lymphocytes.
Reactions were carried out in the presence of sheared human DNA in 50%
fonmamide, 10%
dextran sulfate, 30 mM sodium chloride, 3 mM sodium citrate, and 0.1% sodium dodecyl sulphate. Hybridization signals were detected by treating slides with fluoresceinated anti-digoxigenin antibodies, followed by counter-staining with 4,6-diamidino-2-phemrlindole. An initial hybridization experiment localized the gene to the q terminus of a group E chromosome.
A genomic probe that specifically hybridizes to the short arm of chromosome 16 was used to demonstrate co-hybridization of chromosome 16 with the MDC probe.
A total of 80 metaphase cells were analyzed with 61 biting specific labeling. The lVmC
probe hybridized to a region immediately adjacent to the heterochromaticJeuchromatic boundary, corresponding 2 0 to band 16q13. The gene encoding TARC also is localized in this region.
See Nomiyama et al., Genomics, 40: 211-213 (1997).
These chromosomal mapping data indicate a utility of lVmC-encoding polynucleotides as a chromosomal marker. Contiguous fragments of SEQ m NO: 1 of at least 15 nucleotides, and more preferably at least 20, 25, 50, 75, 100, 150, 200, 500, or more 2 5 nucleotides, and the complements of such fragments, are specifically contemplated as probes of the invention. Moreover, probes having partial degeneracy from SEQ m NO: 1 are contemplated as being useful as well. Probes having preferably at least 90%, and more preferably 95%, 96%, 97%, 98%, 99%, or more similarity to SEQ B7 NO: 1 are preferred as probes of the invention.

The chemokine receptor designated CCR4 has been characterized previously [Power et al., J. Biol Chem., 270: 19495-19500 (1995)], and shown to bind the CC chemokine TARC ('I'l~nus and Activation-Regulated Chemokine, Genbank Accession No.
043767). See Imai et al., J. Biol. Chem., 272: 15036-15042 (1997); and Imai et al., J.
Biol. Chem., 271: 21514-21521 (1996). The cDNA and deduced amino acid sequences of human CCR4 are set forth in SEQ ID NOs: 33 and 34, and are deposited with Genbank (Accession No. X85740).
The following experiments were performed that demonstrate that MDC is a high affinity ligand for CCR4.
A. prgpsytion of CCR4-transfected cells The murine pre-B cell line L1.2 [See, e.g., Gallatin et al., Nature, 304:30-34 (1983)] maintained in RPMI 1640 media supplemented with 10% fetal calf serum, was selected for transformation with the CCR4 expression vector described in Imai et al., J. Biol. Chem., 272:
15036-15042 (1997), incorporated herein by reference. L1.2 cells were stably transfected as descn'bed previously by elecrroporation with 10 pg linearized plasmid at 260 V, 960 microfarads using a Gene Pulser (BioRad). See Imai et a1, J. Biol. Chem., 272: 15036-15042 (1997). It will be apparent that other cell lines in the art are suitable for CCR4 transfection for the following 2 0 assays. For example, 293 cell lines have been transfected with CCR4 cDNA
and employed effectively in calcium Flux assays.
B. Preparation of Recombinant Chemokines The mature sequences of both 1V11?C and TARC were chemically synthesized by Gryphon Sciences (South San Francisco CA) using t-butyl-oxycarbonyl chemistries on a peptide synthesizer (430A; Applied Biosyste<ns). Lyophilized protein was dissolved at 10 mgrml in 4 mM
HCl and immediately diluted to 0.1 mglml in phosphate-buffered saline plus 0.1% bovine serum albumin (BSA) for storage at -80° C.
Recombinant 11~C also was expressed as a fusion protein with the secreted form 3 0 of placental alkaline phosphatase (SEAP) in the expression vector pcDNA3 (Clontech, Palo Alto CA). A similar TARO-SEAP fusion protein is described in Imai et al. (1997).
Briefly, the coding -88_ region ofMDC, followed by a sequence encoding a five amino acid linker (Ser-Arg-Ser-Ser-Gly), was fused in-frame to a sequence encoding mature SEAP, followed by a sequence encoding a (His)6 tag. The MDC-SEAP expression plasmid was transfected into COS cells by the DEAF
Dextran method. See Sambrook et al., Molecular Ctonireg: A LaboratoryMamral, Cold Spring Harbor Laboratory, Cold Spring Harbor; NY (1989). The transfected cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal calf serum.
Twenty-four hours after transfection, the serum levels were reduced from 10% to 1 %. After 3-4 days, the culture supernatants were collected, centrifuged, filtered through a 0.45 micron membrane, and stored at 4 ° C. The concentration of MDC-SEAP in the filtered supernatant was determined by comparison with the reported specific activity of secreted placental alkaline phosphatase [Berger et al., Gene, 66: 1-10 (1988)], and confirmed using known concentrations of TARC-SEAP [Imai et al., (1997)] as an internal reference standard.
C. CCR4 Binding The 1V1DC-SEAP was used as a probe to examine MDC binding to CCR4-transfected L 1.2 cells. For displacement and saturation experiments, transfected L 1.2 cells (approx. 3 X I03) were incubated for one hour ax 16'C in the presence of 0.5 nM MDC-SEAP
in the presence or absence of various concentrations of unlabeled chemokines in 200 ~tI binding buffer (RPMI 1640 media containing 25 mM HEPES, pH 7.4, 1% BSA, and 0.02%
sodium 2 0 azide). Following incubation, the cells were washed four times in binding buffer and lysed in 50 pl of 10 mM Tris-HCI, pH 8.0, and 1% Triton X-100. Samples were heated at bS~C
for 15 minutes to inactivate cellular phosphatases, centrifuged, and stored at -20 ° C until assayed.
Alkaline phosphatase activity in 10 ~1 of sample was determined by a chemiluminescence assay using the Great Escape Detection kit (Clontech, Palo Alto, CA) 2 5 according to the manufacturer's instructions. The saturation binding curve was fitted (Table G~uveT~ using the Ill equation y = a(~)l(~ + b'), where y is the amount of ligand bound, a is the maximum amount of ligand bound, x is the concentration of ligand, b is the concentration of Iigand at which 50% of receptor sites are occupied (KD), and c is the I~11 coeffcient. Binding competition curves were fitted (TabIeCurveTM) using a three-parameter logistic model described 3 0 by the equation y = al(I + (xlb)'J, where y is the amount of labelled ligand bound, a is the maximum amount of labelled ligand bound; x is the concentration of the competitive chemokine, b is the ICso, and c is a parameter that determines the slope of the curve at the ICso.
These binding assays demonstrated that MDC-SEAP bound to CCR4-expressing cells. This binding was to a single high affinity site with a ICd of 0.18 nM, as demonstrated by Scatchard analysis. Binding of MDGSEAP was competitively inhibited with increasing concons of unlabeled MDC or TARC. The ICso for 1V1DC was 0.65 nM, while the ICS for TARC was 2.1 nM. These data suggest that both MDC and TARC recognize a common binding site on CCR4, and that MDC has more than three-fold higher affinity than TARC
for CCR4.
To examine the specificity of MDC binding to CCR4, six additional chemokines (MCP-1, MCP-3, MCP-4, RANTES, MIP-la, and MIP-lp) were tested for competition of MDC-SEAP binding. A 200-fold molar excess of each chemokine was tested for competition with a constant quantity of MDC-SEAP (0.5 nM). The additional chemokines did not compete for binding of MDC-SEAP to CCR4. In contrast, unlabeled MDC and TARC both blocked binding of MDC-SEAP to CCR4 transfectants.
D. Calcium mobiI'~tion ascav Imai et al. (1997 showed that TARC signals through CCR4 by inducing calcium mobilization. To determine the ability of MDC to cause signaling through chemokine receptors, we eacamined calcium mobilization in L1.2 cells recombinantly expressing CCRI, CCR2B, CCR3, 2 0 CCR4, CCRS, CCR6, or CCR7.
Transfected L1.2 cells were suspended at a concentration of 3 x 106 cells/ml in Hank's balanced salt solution supplemented with 1 mg/ml BSA and 10 mM HEPES, pH 7.4. Cells were incubated with 1 pM fore-PE3-AM (Texas Fluorescence Labs) at room temperature for 1 hour in the dark. After washing twice, cells were resuspended at a concentration of 2.5 x 106 cells/mI. To measure intracellular calcium, 2 ml of cells were placed in a quartz cuvette in a Perkin-Elmer LS SOB spectrofluorimeter. Fluorescence was monitored at 340 nm (excitation wavelength 1), 380 nm (excitation wavelength 2), and 510 nm (emission wavelength) every 200 ms.
In these experiments, MDC did not cause calcium flux in Ll .2 cells transfected 3 0 with CCRI, CCR2B, CCR3, CCRS, CCR6, or CCR7, whereas each of these transfected cell lines responded to its known cognate ligand. In contrast, L1.2 cells transfected with CCR4 produced a strong calcium flux when stimulated with 10 nM MDC. Similar to other G
protein-coupled receptors, CCR4 was refractory to subsequent stimulation with the same concentration of MDC.
Ten nanomolar 1~C also completely desensitized CCR4 transfectants to subsequent 10 nM
TARC treatment. However, pre-treatment of CCR4-transfected L1.2 cells with TARC did not desensitize the receptor to subsequent stimulation with lvIDC. The signal produced by initial TARC stimulation was of lower intensity than both the primary MDC signal and the MDC signal secondary to TARC stimulation. These results further confirm that N117C is a ligand for CCR4.
E. Chemotaxis assay . We next examined the ability of lViDC and TARC to induce migration of CCR4-transfected L1.2 cells. Approximately 106 CCR4-transfected L1.2 cells, resuspended in 0.1 ml RPMI 1640 media with 0.5% BSA, were loaded in the upper wells of a transwell chamber (3 pm pore size, Costar). Untransfected L1.2 cells were used as a control. Test chemolcines were added to the lower wells at a concentration of 0-100 nM in a volume of 0.6 ml. After 4 hours at 37°C, cells in the lower chamber were collected and counted by FACS.
Both lViDC and TARC induced migration of CCR4-transfected L1.2 cells. Both chemolcines produced classic bell-shaped migration responses with maximal migration at about 10 nM. The migration observed with MDC was significantly higher than that for TARC, with N117C inducing migration of greater than 7% of input cells versus less than 3%
migration for 2 0 TARC. Untransfected L1.2 cells failed to migrate when treated with Iv)DC.
These chemotaxis results fizrther confirm that both IvmC and TARC are functional Iigands for CCR4.
F. Conclusion Collectively, the foregoing experiments provide compelling evidence that MDC
2 5 acts as a high affinity ligand for the chemoldne receptor CCIt4.
As described below in Example 32, CCR4 has been found to be abundantly and nearly exclusively expressed on antigen-specific TH2 helper T cells. Such cells are particularly susceptible to HIV-1 infection. (See Maggi et al., Science, 265:244-252 (1994).) The identification herein of a high affinity 1VZDC receptor on HIV-susceptible T
cells indicates a 3 0 putative mechanism/pathway through which 1VIDC(1-69) exerts its agonistic activity relating to enhanced HIV-1 infectivity and or viral production in infected cells (see Example 20), and likewise indicates a target for therapeutic intervention. Without intending to be limited to a particular theory, MDC-mediated activation of TH2 cells, through the CCR4 receptor, is postulated to enhance infectivity and/or production of HIV-1 vines, in a manner analogous to the increased infectivity that has previously been observed for activated target cells. See Woods et al., Blood 89: 1635-1641 (199'x; and Roederer et al., J. Clin. Invest., 99(7):
1555-1564 (1997).
Modulators of MDC activity may be useful for the treatment of diseases or symptoms of diseases wherein MDC plays a role. Such modulators may be either agonists or antagonists of MDC binding. The following receptor binding assays provide procedures for identifying such MDC modulators.
MDC is labelled with a detectable label such as "~I, 3H, '4C, biotin, or Europium. A
preparation of cell membranes containing MDC receptors is prepared from natural cells that respond to MDC, such as human macrophages, phorbol ester-stimulated THP-1 cells, human fibroblasts, human fibroblast cell lines, or guinea pig macrophages.
(Alternatively, a recombinant receptor preparation is made from cells transfected with an MDC receptor cDNA, such as a mammalian cell line transfected with a cDNA encoding CCR4 and expressing CCR4 on its surface.) The membrane preparation is exposed to'~I-labelled MDC, for example, and incubated 2 0 under suitable conditions (e.g., ten minutes at 37°C). The membranes, with any bound'uI-MDC, are then collected on a filter by vacuum filtration and washed to remove unbound'~I-MDC. The radioactivity associated with the bound MDC is then quantitated by subjecting the filters to liquid scintillation spectrophotometry.
The specificity of MDC binding may be confirmed by repeating the foregoing assay 2 5 in the presence of incxeasing quantities of unlabeled MDC, and measuring the level of competition for binding to the receptor. These binding assays also can be employed to identify modulators of MDC receptor binding.
The foregoing receptor binding assay also may be performed with the following modification: in addition to labelled MDC, a potential MDC modulator is exposed to the 3 0 membrane preparation. In this assay variation, an increased level (quantity) of membrane-associated label indicates the potential modulator is an activator of MDC
binding; a decreased level (quantity) of membrane-associated label indicates the potential modulator is an inhibitor of MDC receptor binding. This assay can be utilized to identify specific activators and inhibitors of MDC binding from large libraries of chemical compounds or natural products.
Rapid screening of multiple modulator candidate compounds simultaneously is specifically contemplated.
-The discovery that CCR4 acts as an MDC receptor prompted the development of the following additional assays to identify modulators of the interaction between MDC and CCR4.
Such assays are intended as aspects of the present invention.
A. Direct Assav In one embodiment, the invention comprehends a direct assay for modulation (potentiation or inhibition) of MDC-receptor binding. In one direct assay, membrane preparations preseribng the chemokine receptor CCR4 in a functional conformation are exposed to either MDC
alone or MDC in combination with potential modulators.
For suitable meanbrane preparations, tissue culture cells, such as 293 or K-562 cells (ATCC CRL-1573 and CCL-243, respectively), are transfected with an expression vehicle encoding the MDC receptor CCR4. Cells that express the receptor are selected and cultured, and 2 0 a membrane preparation is made from the transfected cells expressing the chemokine receptor.
By way of example, suitable membrane preparations are made by homogenizing cells in TEM
buffer (25 mM Tris-HCI, pH 7.4, I mM EDTA, 6 mM MgC h 10 pM PMSF, 1 pg/ml leupeptin).
The homogenate is centrifuged at 800 x g for 10 minutes. The resulting pellet is homogenized again in TEM and re-pelleted. The combined supernatants are then centrifuged at 100,000 x g 2 5 for one hour. The pellets containing the membrane preparations are resuspended in TEM at 1.5 mg/ml.
Membrane preparations are exposed to labelled MDC (e.g., MDC labelled with h~ or other isotope,.MDC prepared as an MDC-secreted alkaline phosphatase fusion protein, or MDC labelled in some other manner) either in the presence (experimental) or absence (control) 3 0 of one or more compounds to be tested for the ability to modulate MDC-receptor binding activity.
To practice the assay in standard 96-well plates, an exemplary reaction would include 2 pg of the membrane preparation, 0.06 nM of radio-labelled MDC, and 0.01 to 100 ~M of one or more test compounds, in a reaction buffer comprising 50 mM HEPES, pH 7.4, 1 mM CaCl2, 5 mM MgCl2, and 0.1% BSA. The reactions are then incubated under suitable conditions (e.g., for I-120 minutes, or more preferably 10-60 minutes, at a temperature from about room temperature to about 37°C).
After incubation, the membranes, with any bound MDC and test compounds, are collected on a filter by vacuum filtration and washed to remove any unbound ligand and test compound. Thereafter, the amount of labelled MDC associated with the washed membrane preparation is quantified. In an ~nbodiment wherein the label is a radioisotope, then bound MDC
preferably is quantified by subjecting the filters to liquid scintillation spectrophotornetry. In an embodiment wherein an MDC-alkaline phosphatase fixsion protein is employed, alkaline phosphatase activity is measured using, for example, the "Great Escape"
detection kit (Clontech, Palo Alto, California) according to the manufacturer's instructions. The amount of label (e.g., scintillation counts or alkaline phosphatase activity) associated with the membranes is proportional to the amount of labelled MDC bound thereto. If the quantity of bound, labelled MDC observed in an experimental reaction is greater than the amount observed in the corresponding control, then the experimental reaction is scored as containing one or more putative agonists (i.e., activators, potentiators) of MDC receptor binding. If the quantity of bound, labelled MDC
observed in an experimental reaction is less than the amount observed in the corresponding control, then the 2 0 experimental reaction is scored as containing one or more putative antagonists (inhibitors) of MDC receptor binding.
The specificity of modulator binding may be confirmed by repeating the foregoing assay in the presence of increasing quantities of unlabeled test compound and noting the level of competition for binding to the receptor. The assay may also be repeated using labelled modulator 2 5 compounds, to determine whether the modulator compound operates by binding with the MDC
receptor.
B. Tndirect GT~P aceav In another embodiment, the invention comprehends indirect assays for identifying 3 0 modulations of MDC receptor binding that exploit the coupling of chemokine receptors to G
proteins. As reviewed in Linder et al., Sci. Am., 267: 56-65 (1992), during signal transduction, an activated receptor interacts with and activates a G protein. The G protein is activated by exchanging GDP for GTP. Subsequent hydrolysis of the G protein-bound GTP
deactivates the G protein. Therefore, one can indirectly assay for G protein activity by monitoring the release of 3zp; from ['y 3zP]-GTP.
For example, approximatelg 5 x 10' HEK-293 cells that have been transformed or transfected (e.g., with a CCR4 expression vector) to express CCR4 are grown in MEM + 10%
fetal calf serum (FCS). The growth medium is supplemented with 5 mCi/ml [~PJ-sodium phosphate for 2 hours to uniformly label nucleotide pools. The cells are subsequently washed in a low-phosphate isotonic buffer.
An experimental aliquot of washed cells is exposed to MDC in the presence of one or more test compounds, while a control aliquot of cells is exposed to MDC, but without exposure to the test compound. Following an incubation period (e.g., 10 minutes, 37°C); cells are pelleted and lysed, and nucleotide compounds are fractionated using, e.g., thin layer chromatography (TLC) developed with 1 M LiCI. Labelled GTP and GDP are identified in the TLC by developing known GTP and GDP standards in parallel. The labelled GTP
and GDP are then quantified by autoradiographic techniques that are standard in the art.
In this assay, the extent of MDC irneraction with its receptor is proportional to the levels of~P-labelled GDP that are observed, thereby permitting the identification of modulators of MDC-CCR4 binding. An intensified signal resulting from a relative increase in GTP hydrolysis, 2 0 producing 3zP-labelled GDP, indicates a relative increase in receptor activity. The intensified signal therefore identifies the potential modulator as an activator of MDC-CCR4 activity, or possibly as an MDC mimetic. Conversely, a diminished relative signal for ~P-labelled GDP, indicative of decreased rector activity, identifies the pot~tial modulator as an inhibitor of MDC
receptor binding or an inhibitor of MDC-induced CCR4 signal transduction.
C. ~8,~
The ales of G protein effector molecules (e.g., adenylyl cycdase, phospholipase C, ion channels, and phosphodiesterases) are also amenable to assay. Assays for the activities of these effector molecules have been previously described. For example, adenylyl cyclase, which 3 0 catalyzes the synthesis of cyclic adenosine monophosphate (CAMP), is activated by G proteins.
Therefore, MDC binding and activation of CCR4 that activates a G protein, which in turn activates adenylyl cyclase, can be detected by monitoring cAMP levels in a host cell that recombinantly expresses CCR4.
Host cells that recombinarnly express CCR4 are prefeixed for use in the assay.
The host cells are incubated in the presence of either MDC alone or MDC plus one or more test compounds as descn'bed above. The cells are lysed, and the concentration of cAMP is measured by a suitable assay, such as a commercial enzyme immunoassay. For example, the BioTrak Kit (Amersham, Inc., Arlington Heights, IL) provides reagents for a suitable competitive immunoassay for cAMP.
An elevated level of intracellular cAMP in a test reaction relative to a control reaction is attributed to the presence of one or more test compounds that increase or mimic MDC-induced CCR4 activity, thereby identifying a potential activator compound. A
relative reduction in the concentration of CAMP would indirectly identify an inhibitor of MDC-induced CCR4 activity.
It will be apparent to those in the art that the foregoing assays may be performed using MDC analogs described herein. Moreover, variations of the foregoing assays will be apparent to those in the art. Any variations that utilize both 1V>DC and CCR4, and especially those variations which utilize MDC and cells that recombinantly express CCR4, are intended as aspects of the invention.
While the use of human MDC and CCR4 comprises a highly preferred 2 0 embodiment, it will be apparent that the source organism for 1V>DC and CCR4 is not a limiting factor, and the foregoing assays may be practiced effectively with MDC and/or with CCR4 that are derived from non-human organisms. By way of example, rat and mouse MDC are taught herein; and a Mus musculus chemokine receptor 4 sequence has been reported in the art. See Hoogewerf et al., Biochem. Biophy~ Res Comm., 218(1): 337-343, and GenBank Accession No.
2 5 X90862. Moreover, the methods used herein to obtain rat and mouse MDC are employable to obtain MDC or CCR4 from other organisms.
Moreover, evidence exists thlK there is at least one additional receptor that recognizes MDC. For example, MDC stimulates migration of dendritic cells and IIr2 activated natural killer cells. Godiska et al., J. Fxp. Med, 185: 1595-1604 (1997), incorporated herein by 3 0 reference. This migration is not likely to be mediated by CCR4, since CCR4 appears to be expressed primarily on T cells, but not on monocytes or NK cells. See Imai et al. (1997).

Consistent with this, CCR4 clones were represented very rarely in a human macrophage cDNA
library (less than one in a million clones). Variations of the assays reported herein that utilize MDC with other MDC receptors also are intended as aspects of the invention.
Additionally, it will be apparent that the protocols described in preceding examples for assaying MDC biological activities (in-vivo or with respect to specific cell types in vitro) are useful as assays for MDC modulators. In a highly preferred embodiment, a compound is first identified as a candidate MDC modulator using any of the assays described in Examples 26 and 27. Compounds that modulate MDC-receptor activity in one or more of these initial assays are further screened in any of the protocols described in preceding examples, to determine the ability of the compounds to modulate the MDC biological activities to which those examples specifically relate.
A Isc~1_ation of cl~NA Encoding Rat and Mouse MDC Pnp~ein_s Knowledge of the human MDC gene sequence described herein was used as described below to isolate and clone putative rat and mouse MDC cDNAs, which are intended as aspects of the invention.
To clone a rat MDC cDNA, a labelled probe was prepared using standard random 2 0 primer extension techniques. A fragment of the human MDC cDNA was generated by PCR, which fi~nent includes the MDC coding region plus approximately 300 bases of 3' untranslated sequence. This fi-agment was labelled with ~P-deoxyribonucleotides using the Random Primed DNALabeling kit (Boehringer Mannhein, Indianapolis, IN). The labelled MDC
probe was used to screen approximately 106 bacteriophage lambda clones from a commercially-available rat 2 5 thymus cDNA fbrary (Stratagene, La. Jolla, California, Cat. No. 936502).
Three positive clones were obtained. Sequencing of one of the positive clones, designated RT3, provided an approximately 958 base pair sequence (SEQ m NO: 37) that included an MDC open reading fi~ame (SEQ ID NO: 38) and about 0.5 kb of 3' untranslated sequence. The open reading frame included sequence encoding the putative mature MDC protein (SEQ ID NO: 38, residues 1 to 69) 3 0 plus 13 amino acids of the putative signal peptide sequence; it lacked the initiator methionine codon and sequence encoding the amino terminus of the signal peptide. A
complete rat MDC

cDNA or genomic clone is obtainable using all or a portion of the RT3 sequence as a labelled probe to re-probe the Stratagene rat cDNA library, and/or other rat cDNA
libraries, and/or a rat genomic DNA library.
To clone a mouse MDC cDNA, approximately 106 bacteriophage lambda clones of a commercially-available mouse thymes cDNA library (Stratagene, Cat. No.
935303) were scxeened with a radiolabeled fragment of the above-described rat MDC cDNA. The probe was generated using overlapping primers in a primer extension reaction. The primer extension reaction comprised: partially overlapping primers corresponding to nucleotides 41 to 164 of SEQ
ID NO: 37 (and to nucleotides 92-215 of SEQ ID NO: 1); 32P-labelled deoxyribonucleotides; and the Klenow fragment of E. coli DNA polymerase. Twelve positive clones were isolated.
One positive clone, designated MT3, was sequenced and found to contain a 1.8 kb cDNA insert that included the entire putative murine MDC coding region and about 1507 bases of3' uMranslated sequence. The cDNA and deduced amino acid sequences for this murine MDC clone are set forth in SEQ m NOs: 35 and 36, respectively. The mouse MDC
has a I5 putative 24 amino acid signal sequence followed by a 68 amino acid A~II3C
sequence.
Comparisons of the human, rat, and mouse MDC protein and DNA (coding region) sequences reveal the following levels of similarity:
Human vs. rat protein: 65% identity;
Human vs. rat DNA: 74% identity;
2 0 Human vs. mouse protein: 64% identity;
Human vs. mouse DNA: 72% identity;
Rat vs. mouse protein: 88% identity;
Rat vs. mouse DNA: 92% identity.
The four cysteines characteristic of C-C chemokines are conserved in all three MDC proteins.
2 5 It is contemplated that the encoded rat and mouse lVmC polypeptides corresponding to SEQ ll? NOs: 38 and 36 are processed into mature mouse MDC
proteins, in a manner analogous to the processing of the human lVlDC precursor, by cleavage of a signal peptide. The signal peptides for both human and murine 1VIDC are 24 amino acids. The exact length of the rat MDC signal peptide will be readily apparent upon isolation of a full length rat 3 0 MDC cDNA. It will be appreciated that these proteins can be synthesized recombinantly or synthetically and assayed for NIDC biological activities as described herein for human 1VIDC.

_98_ Likewise, it will be appreciated that any analogs descn'bed herein for human MDC can be similarly prepared for these other mammalian MDC proteins.
The foregoing results demonstrate the utility of polynucleotides of the invention for identifying and isolating polynucleotides encoding other vertebrate MDC
proteins, especially other mammalian or avian MDC proteins- Such identified and isolated polynucieotides, in turn, can be expressed (using procedures similar to those described in preceding examples) to produce recombinant polypeptides corresponding to other vertebnite forms of MDC, which proteins would be useful in the same manners that human MDC is useful, including therapeutic veterinary applications. Polynucleotides encoding vertebrate (and especially mammalian or avian) MDC
proteins, the proteins themselves, and analogs thereof are all contemplated to be aspects of the present invention.
B. SSmthesis of mLrine MDC and demon~ration of biological activit~
The inteniction between marine MDC and human CCR4 was demonstrated using synthetic marine MDC in a chemotaxis assay. Marine L1.2 cells transfected with human CCR4 (Example 25) were tested to determine if such cells would migrate towards synthetic full-length mature marine MDC (SEQ ID NO: 36, residues 1 to b8) (Gryphon Sciences and Ian Clark-Lewis), and/or toward a synthetic marine MDC analog designated "Lea-MDC" which consists of a l~cine residue attached to the amino terminus of mature marine MDC.
(Marine Leu-MDC
is thus analogous to 'W.DC(n+1)" described in Example 11. Costar Transwells with 3 pm filters were used for the assay.
Varying amounts of the synthetic I193C polypeptides (ten-fold dilutions from 10000 to 1 ng/ml final concentrations) were added to 600 pl RPMI/0.5% BSA
(endotoxin-free) in the lower wells and 106 cells in 100 ~.l RPMI/0.5% BSA (endotoxin-free) were added to the uppex chambers. After incubating the transwells at 37°C for 4 hours, the upper chambers were transferred to 500 p.l ice-cold PBS/0.5 mM EDTA to release any migrated cells still clinging to the underside of the filter. Cells which had migrated to the lower chambers were harvested by combining the 600 lil medium from the lower chamber with the 500 pl PBS/EDTA
for each well.
Cells were centrifuged, resuspended in 200 pl of 1% formaldehyde, and then counted for 30 3 0 seconds on the FACSCAN (Becton-Dickinson).

wo ~ns~ . rcTnrs9sno2~o _99_ The number of Ll.2/huCCR4 cells that were observed to have migrated toward full-length mature marine MDC showed a characteristic dose-response curve, with chemotaxis observed at 1 ng/ml MDC and with peak chemotaxis occurring at 100 ng/mI marine MDC. The same number of cells migrated towards the 100 ng/ml full-lenght mature marine MDC from Gryphon Sciences and Ian Clark-Lewis,-indicating that the two preparations had equivalent activity. The responses of Ll.Z/huCCR4 cells to marine Leu-MDC were approximately 20%
lower than to full-length MDC.
C. brine MDC comyetes with human MDC for binding to uma_n CCR4.
In duplicate, 5 x lOs L1.2/huCCR4 cells were incubated with 0.1 nM'ZSI-labeled human mature MDC, alone or with unlabeled human mature MDC ( 10 nM or 100 nMJ, marine mature MDC (100 nM), or the the chemokine LARC (100 nM, control), for one hour in 200 pl binding buffer (50 mM HEPES, pH 7.5, 1 mM CaCl2, 5 mM MgCh, 0.5% BSA, and 0.05%
azide). Cells were spun down at slow speed and washed twice with binding buffer plus 0.5 M
NaCI. Fifty microliters of scintillant fluid was added and samples were counted with a beta counter. Unlabeled human and marine MDC both substantially reduced the amount of labeled MDC that bound to the CCR4-expressing cells (approx. 4000 cpm versus less than 500 cpm), with 100 nM marine MDC displaying a level of competition imermediate to that of 10 nM and 100 nM human MDC. The contol chemokine LARC (which specifically binds CCR6) diplayed substantially no competitive binding ability (approx. 3800 cpm).
The foregosng assay results demonstrate that a nonhuman form of MDC (marine MDC) is capable of binding and stimulating cells expressing a human MDC
receptor. This data demonstrates an indication for vertebrate MDC, MDC fi~agtnents and analogs, and MDC
modulators for human treatments and treatment formulations, as described elsewhere herein for human MDC, MDC fragments and analogs, and MDC modulators.
D. M~que MDC cDNA and po~y~gptide sequences.
Polymerise chain reaction (PCR), using oligonucleotides died from the human MDC cDNA as primers, was performed in order to amplify and isolate a cDNA
encoding 3 0 macaque MDC from a macaque thymus cDNA library. The macaque MDC amino acid sequence with sec~ory signal sequence is 93 amino acids and shares about 94% amino acid identity with human MDC. Referring to SEQ m NO: 2, the macaque MDC amino acid sequence is identical to that ofthe human sequence, with the following variations: valine at position -18; phenylalanine at position -17; glycine at position -15; isoleucine at position -12;
methionine at position 21; and serine at position 46. The macaque cDNA and deduced amino acid sequences are set forth in SEQ m NOs: 45 and 46.
E. Use of multiple vertebrate MDC syuences to desjgn h~G a_nal_oqc_ The amino acid sequences for human, macaque, mouse, rat and/or other animals can be aligned using any alignment algorithm known in the art. Such an alignment will identify positions and regions within the MDC sequences that are highly conserved (e.g., that are identical in different species), moderately conserved (e.g., identical in some species with substitutions in other species of amino acids of similar character (e.g., acidic, basic, aliphatic, aromatic)), or variable (e.g., different in most or all species, including substitutions of amino acids of different character). Such an alignment provides significant guidance for the design of 1V1DC analogs that will act as MDC mimetics as well as analogs that may act as 11~C inhibitors.
Substitution or deletion of variable residues is more likely to result in analogs that retain MDC biological activities, whereas highly conserved residues are targets for alteration or deletion to design analogs having different activities or having MDC inhibitory activity.
~~~pile 29 Using procedures essentially as described in Example 25, selected IVmC analogs descn'bed in Example 11 were for the ability to bind CCR4 and/or induce calcium (Ca'"") flux and chemotaxis in Ll .2 cells transfected with CCR4.
The analog lVmC{n+1) bound CCR4 with similar affnity to lva3C, but induced calcium 8ux and chemotaxis in L1.2/CCR4 cells with a slightly Lower potency than MDC. For example, in chemotaxis, the peak activity for lVmC(n+1) was observed at 100 ng/ml rather than 10 ng/ml, and the maximum number of cells migrating was 5000, compared to 9000 for lVmC.
MDC(9-69) bound CCR4 with reduced amity relative to that of MDC (0-69).
lVmC(9-69) did not induce calcium flux in L1.2/CCR4 cells, and it was much less potent in chemotaxis. The fact that MDC(9-69) binds CCR4 but does not signal through CCR4 indicates a utility of MDC(9-69) as an MDC inhibitor.
Collectively, the activities of MDC (n+1) and MDC (9-69) indicate that amino-terminal additions and deletions and other modifications may result in useful MDC inhibitors.
The analog "MDC-wvas"-hound CCR4 with 500-fold less amity than MDC, induced only a very small calcium flux, and did not induce any chemotaxis. The analog "MDC-eyfy" acted similar to lVmC in CCR4-binding, chemotaxis, and calcium flux assays.
Monoclonal Antibodies 252Y & 2522 Inhibit CCR4-Mediated Cellular Resnonsrs to MDC
Using procedures similar to those described in Example 25, the monoclonal antibodies 252Y and 2522 described in Example 18 were screened for the ability to modulate MDC-CCR4 binding and modulate the CCR4-mediated biological activities of MDC.
A. Antibodies 252Y and 2522 inhibit MDC binding to CCR4 The fusion protein MDC-SEAP (Example 25) was employed to evaluate the ability of the antt'bodies to inhibit MDC binding to its receptor CCR4. MDC-SEAP at a concentration of 0.5 nM was incubated for fifteen minutes at room temperature with varying concentrations 2 0 (0.01-10 pg/ml, shown in Fig. I 1) of antibody 252Y, antibody 2522, or an isotype control (final reaction volume 100 pl). Thereafter, the mixtures were added to CCR4-expressing L1.2 cells (100 ul, 4000 cells per ul), and incubated at 4 ° C for an additional 60 minutes. The extent of MDC-SEAP binding to the CCR4-expressing cells was determined by alkaline phosphatase chemiluminescent assay as described in Example 25. A baseline Level of non-specific binding 2 5 (defined as the amount of binding that could not be competed by a 200-fold molar excess of native MDC) was detennined and subtracted from experimental measurements. Figure 11 presents the experimental results in graphical form, wherein each data point represents a percentage of maximum binding. (Maximum binding was defined as the amount of MDC-SEAP bound to the cells in the absence of antibody, minus non-specific binding.) As shown in Figure 11, both 3 0 antt'body 252Y and arnx'body 2522 (but not the isotype control) inhibited MDC-SEAP binding to CCR4-infected cells in a dose-dependem manner. Fifty percent inhibition of binding was observed for both antibodies at an a~'body concentration of about 2 pglml.

WO 99/15666 PCT/US98l20270 B. Antibodies 252Y and 2522 irLh_ibit MDC-indLC.~d chemotaxis To confnm that antibodies 252Y and 2522 also were capable of inhibiting CCR4-mediated cellular responses to MDC, both calcium flux and chemotaxis assays were performed using the CCR4-transfected L1.2 cells.
For the calaum flux assay, the transfected L1.2 cells were labelled with Fura-(see Example 19) and monitored for Ca~-induced fluorescence changes using an AMINCO-Bowman Series 2 fluorimeter. Addition of 75 nM MDC to the cells induced a rapid, transient increase in intracellular Ca''~* levels. This Ca''+ flux response was completely inhibited when either antibody 252Y or antibody 2522 were added to the cells at a concentration of 10 lig/ml one minute before contacting the cells with the MDC solution. An isotype-matched control antibody had no effect on the MDC-induced Ca** flux. Thus, both antibodies blocked the calcium flux response to MDC in CCR4-transfected L1.2 cells.
For the chemotaxis assay, CCR4 transferred L1.2 cells (approx. 10 million cellslml in a volume of 0.1 ml) were preincubated with antibody 252Y, antibody 2522, or an isotype-matched control in RPMI-1640 media (Cribco) at various concentrations ranging from 0.5 to 50 lig/ml for 30 minutes at room temperature. Thereafter, the cells were exposed to 100 nglml 11~C (i.e., the peak concentration for maximum chemotaxis) for 4 hours in a Costar Transwell apparatus. The number of cells migrating toward MDC was counted using a Becton-Dickinson FACScan apparatus. As shown in Figure 12, MDC-induced chemotaxis of these cells was totally 2 0 inhibited by either antibody 252Y or antibody 2522 at concentrations of 2 -5 ~,g/ml, but not by the isotype-matched control. The ICS antibody concentration (required to inhibit 50% migration) was 1 lig/ml. The same antibodies did not inhibit chemotaxis ofthe CCR4/L1.2 cells toward the C-C chemokine TARC, indicating that the inhibitory effect was specific for MDC.
In a similar set of experiments, antibody 272D was sfor its ability to inhibit MDC stimulated chemotaxis. Ten ~g/ml of antibody 272D was required to inhibit chemotaxis toward recombinant MDC (30 ng/ml) by greater than 90%. Only 2 pg/ml of antibody 2522 was required to achieve a similar level of inhibition, indicating that antibody 2522 is a more potent inhibitor of 1V1DC induced chemotaxis.

A transendothelial migation assay was performed essentially as described in the art [Ponath, et al., J. Clin. Invest., 97: 604-612 (1996); Ponath et al., J.
Exp. Mec~, 183: 2437-2448 (1996); and Imai, et al., Cell, 91: 521-530 (1997)] to determine the presence and the phenotype of T cells that migate toward the chemokines TARC and MDC. Briefly, about 2 x 10' cells of the endothelial cell line ECV304 (ATCC CRL-1998 or European Cell Culture Colleckion, Portions Down, LJK) were added to Transwell inserts (Coaster) with a 5 pm pore size and cultured at 37°C for 48-96 hours in M199 medium (GIBCOBRL) supplemented with 10%
FCS. Chemokines were diluted (serial dilutions of 0.1 to 100 nM) in a migration medium (a 1:1 mixture of RPMI-1640:M199, supplemented with 0.5% BSA, 20 mM HEPES, pH 7.4) and added to 24-well tissue culture plates in a final volume of 600 pl. Endothelial cell-coated inserts were placed in each well and 106 peripheral blood mononuclear cells (PBMC) or T
cell lines in 100 pl were added to the upper chambers. The cells were allowed to migrate through the endothelial cells into the lower chambers at 37°C for 4 hours (PBMC) or 90 minutes (T cell lines). The migated cells in the lower chambers were stained with FITC- or PE- conjugated monoclonal antibodies (mAb) for indicated cell surface makers and counted by flow cytometry.
In the tru~sendothelial cell migration assay, both TARC and MDC induced dose-dependent vigorous migration of CD14' lymphocytes but not of CD14+ monocytes, with MDC
2 0 consistently inducing cell migration about 2 times more e~ciently than TARC. IVfigration activity was detected with chemolane conons as low as 1 nM. Significant migration occurred with 10 nM TARC and 10 nM MDC. Analysis of the migating lymphocytes revealed that 10 nM of either TARC or MDC attracted predominantly CD4'' T cells. Neither TARC nor MDC
induced migarion of CD19+ B calls or CD16+ NK cells. Furthermore; TARC and NmC
attracted almost 2 5 exclusively CD45RA /CD45R0+ effectorlmemory T cells. This observation was consistent with the observation that a murine {IgG) monoclonal antibody to CCR4 stained highly selectively a fraction 020~/0) of CD45R0+CD4+ memory helper T cells.
Effector/memory helper T cells represent a population of cells that have encountered cognate antigens irm vivo and have differentiated into THl or TH2 cells. Since CCR4 3 0 is expressed on about 20% of effector/memory helper T cells, additional experiments were conducted to determine whether CCR4 is selectively expressed on certain subsets of helper T
cells.
First, CD4+CD45R0+ T cells (obtained from PBMC by negative selection with Dynabeads (Dynal) after incubation with anti-CD 16, anti-CD 14, anti-CD20, anti-CDB, and anti-CD45RA antibodies) were fractionated into CCR4+ and CCR4' subpopulations by staining with the anti-CCR4 mAb and cell sorting. The cell subpopulations were expanded as polyclonal cell lines by culturing for 9 - 14 days at 37 ° C in RPMI medium supplemented with PHA (diluted 1:100) and 100 U/ml IL-2. Expanded cells were subjected to a second round of enrichment by staining with anti-CCR4 monoclonal antibody and sorting. Sorted cells were immediately l0 activated with 50 ng/ml PMA (Sigma) and 1000 ng/ml ionomycin (Sigma) for 24 hours, at which time the culture medium was analyzed by ELISA (R&D) to determine each population's pattern of cytolcine production. Since helper T cells are classified into THI and TH2 subsets based on their profiles of cytoIcine production [Mosmann et al., Immunol. Today, 17: 138-146 (1996)], this analysis permitted determination of whether CCR4 is selectively expressed in one or the other subpopulation.
Analysis of the culture medium revealed that the CCR4+ T cells produced significantly larger amounts of IL-4 and IL-5 than the cultured CCR4' T cells (>12 ng/ml for CCR4+ T cells versus < 2.5 ng/ml for CCR4' T cells for each cytokine).
Conversely, CCR4' T
cells produced IFN-Y at levels much higher than CCR4+ T cells (> 300 ng/ml vs.
< 25 ng/ml).
2 0 These cytolane acpression patterns indicate that the CCR4'" population of cells contained almost exclusively TH2 cells, whereas CCR4' cells were enriched for THl cells.
To support the conclusion that CCR4+ T cells are predominantly TH2 cells, the CD4+CD45R0+ T cells that had been attracted by TARC or NmC in the transendothelial migration assay were expanded by wlturing in PHA and ILr2 and then examined for their pattern 2 5 of cytoldne production as described above. Compared to total CD4*CD45R0+ T
cells, the cells attracted by TARC or MDC were enriched for producers of IL-4 and IL-5 and depleted of producers of IFN-y.
To further confirm the observed selective expression of CCR4 on TH2 cells, experiments were performed to polarize CD4+CD45RA+ naive T cells in vitro, and the artificially 3 0 polarized cell populations were acamined for CCR4 expression. The naive T
cells (obtained from PBMC by negative selection with Dynabeads after incubation with anti-CD 16, anti-CD 14, anti-CD20, anti-CDB, and anti-CD45R0 antibodies) were polarized into THl cells by culturing in the presence of PHA (1:100), 2 ng/ml IL-12, and 200 ng/ml anti-IL-4 monoclonal antibodies (Pharmingen); or into TH2 cells by culturing with PHA ( 1:100), 10 ng/ml IL-4, and 2 ~glml anti-IG 12 monoclonal antibodies. After 3 - 4 days, 100 U/ml IL,-2 was added to the cultures. CCR4 expression and transmigration were analyzed at day 9 - 14.
Analysis of the cultured cells with an anti-CCR4 monoclonal antibody revealed that 60% of cells polarized into TH2 cells expressed CCR4, compared to only 4%
of cells polarized into THl cells. Northern blot analysis of the RNA isolated from these cell populations also demonstrated that TH2 cells expressed CCR4 mRNA at levels much higher than TH1 cells.
As controls, CCR7 mRNA was expressed in both types of cells whereas CCR3 mRNA
was not detected in either type of cell.
In the endothelial transmigration assay, the artificially polarized TH2 cells, but not those polarized into THl, migrated vigorously toward TARC and MDC, whereas both types of cells migrated toward SLC. (See Nagira, et al., "Molecular cloning of a novel human CC
chemoldne secondary lymphoid-tissue chemolcine that is a potent chemoatrcactant for lymphocytes and mapped to chromosome 9p13," J. Biol. Chem., 272: 19518-19524 (1997).) Neither population of cells migrated toward eotaxin, a ligand for CCR3.
Collectively, the foregoing experiments demonstrate that a significant population of TH2 cells express the chemolcine receptor CCR4, and that the chemolcines TARC and MDC
2 0 represent selective chemoattractants of TH2 cells, an effect that presumably is mediated at least in part through CCR4. Tissues of allergic inflammation are infiltrated by TH2 cells, as well as by eosinophils, another cell type selectively attracted by MDC {see Example 12).
Furthermore, T
calls migrating into tissues after antigen challenge have been reported to be involved in localized production of the TH2 cytolW es, IL.-4 and TL-5, and in accumulation of eosinophils. (See Garlisi et al., Clin. Immunol. Immunopathol., 75: 75-83 (1995).) Additionally, TARC
and MDC are abundantly produced by dendritic cells whose close interactions with migrating lymphocytes constitute essential parts in initiation and promotion of immune responses.
(See Steinman, R.M., Armu. Reu Immunol., 9: 271-296 (1991).) Enhanced TARC and MDC production from antigen presenting cells in TH2 responses would be expected to lead to further recruitment of TH2 cells 3 0 via CCR4. Thus, the discoveries herein relating to the biological effects of MDC indicate that the effects may be deeply intertwined and involved in multiple aspects of an immunological or allergic cascade, a factor of direct clinical importance. For example, agents that interfere with the interactions of TARC or MDC with the receptor CCR4 (and/or that interfere with the interactions of TARC or MDC with TH2 cells or eosinophils in cell-based assays) have therapeutic indications for reducing allergic inflammatory responses. The use of such agents in the treatment of asthma, a conditions characterized by eosinophilic infiltration and probable involvement of presentation of sensitizing antigen by mucosal dendritic cells to TH2 T cells, is specifically contemplated.
, Use of MDC aid MDG antagonists to modLlate,platelet aaggL~ga ion The following experimental data indicates that 11~C promotes platelet aggregation, and suggests a therapeutic indication for MDC and lvmC
antagonists to modulate platelet aggregation.
Female Lewis rats, six to eight weeks old, were administered 0.5 pg of synthetic mature human IvmC(1-69) intravenously in a saline solution, via the tail vein.
At various time points, the animals (4) were anesthetized with 100 lcl ACE cocktail (Ketamine, ACE promazine and Rompon) and blood samples were collected into Nficrocontainers containing EDTA
(Beckton Dickinson). Samples (300-400 pl) were stored overnight at 4-8 °C. A CBC with Differential analysis was conducted to identify changes in cell number in the rats compared to 2 0 control rats that had been administered only phosphate-buffered saline. In all four animals treated, marked platelet aggregation was observed. This aggregation was most pronounced at the time oflvmC administration and dissipated with time after the bolus. A
similar phenomenon was observed in mice using an analogous protocol.
Receptor analyses have indicated that platelets express detectable levels of the 2 5 1~C receptor CCR4. These experiments suggest a receptor through which 11~C
may exert its platelet-aggregating effects.
The foregoing observations suggest that mature MDC stimulates platelet aggregation, and suggests that Iv~C antagonists are useful for inhibiting coagulation. Such use is indicated, e.g., in myocardial infarction patients to prevent further inappropriate blood clotting, 3 0 and in patients for the therapeutic or prophylactic treatment of stroke.

The concentrations at which MDC induces platelet aggregation and at which lVmC antagonists prevent platelet aggregation are determined in vitro using purified platelets and serial dilutions of MDC and NmC antagonists and procedures that are well known in the art.
See, e.g., Jeske et al., Thromb. Res, 88(3):271-281 (1997); Herault et al., Thromb. Haemost., 79(2):383-388 (1998); and Furakawa et a~f.Jpn. J. Phmmaco~, 75(3):295-298 (1997). Putative MDC antagonists for screening in such assays include all of the putative IvR7C
antagonists identified above, e.g., in Example 20. Those MDC analogs that inhibit platelet aggregation and those that promote aggregation are determined by such dose response studies and/or by mouse studies as described above.
Similarly, since TARC also signals through CCR4, the use of TARC and TARC
antagonists to modulate platelet aggregation also is intended as an aspect of the invention.
The following procedures are performed to demonstrate that MDC antagonists, such as MDC neutralizing antibodies, are capable of modulating an immune respone in a mammalian host.
A. Antigen-induced asthma model Laboratory animals (e.g., BaIb/C mice) are challenged with ovalbumin using the following regimen: Day 0: 100 pg ovalbumin (Sigma), 4.5 mg alum (Lnject~, Pierce), administered by 200 ~1 intraperitoneal injection; Day 14: 100 pg ovaibumin, 4.5 mg alum administered by 200 gl intraperitoneal injection, plus 100 p.g ovalbumin in 50 ul saline, administered infra-nasally, days 25, 26, and 27: 50 pg ovalbumin in 50 gl saline, administered 2 5 infra-nasally. As a contol, saline is administered to animals in lieu of ovalbumin. To test the effect of a putative ABC modulator (such as an MDC-neutralizing antibody) on the animal's allergio-type response to the ovalbumen, the modulator (or a control, e.g., saline) is administered to test animals intraperitoneally on days 25, 26, and 27, one hour prior to challenge with ovalbumin. Exemplary dosing of an anti-MDC antibody is 0.1 to 5 mg/kg body weight.
3 0 On day 28, the mice are sacrificed, blood is collected, and bronchioalveolar lavage is performed. Cells from the lavage fluid are collected and counted, and a white blood cell differential is performed. Reduction in eosinophils and/or neutrophils in the lavage fluid of treated animal versus contol animals is indicative of the therapeutic efl~cacy of the MDC
antagonist treatment. Reduction in anti-ovalbumen antibodies (especially IgE
antibodies) in the blood {assayed by ELISA, for example) is further indicative of the therapeutic efficacy of the MDC antagonist.
B. Modulation of a Ta ~ r~.cnonse To demonstrate the ability of an MDC antagonist to suppress an immune response, laboratory animals are immunized subcutaneously or intraperitoneally with a suitable antigen, such as ovalbumin or tetanus toxoid, or with a saline control.
Aluminum hydroxide (alum), which preferentially promotes a TH2 response, or Freund's complete adjuvant, which tends to drive a THl response, are used as adjuvants in some of the animals.
Animals are immunized on day 0 (e.g., with 100 pg ovalbumin + 4.5 mg alum), followed by booster immunizations at, e.g., days 14 and 28. The antibody titer against the selected antigen is permitted to drop to normal levels in the animals, e.g., for 1-2 months, monitored via ELISA.
After arna'body levels have dropped to normal, the animals are re-challenged with the selected antigen. An MDC antagonist, such as a an MDC-neutralizing antibody, is administered contemporaneously with the antigen, two, six, and/or twenty-four hours later. One week later, blood from the animals is drawn, white blood cells are analyzed, and antibodies to 2 0 the antigen are titered and isotyped. Reduced levels of IgGI antibody, IgE
antibody, and TH2 cells in the treated animals versus the control animals is indicative of a therapeutically effective MDC antagonist, where immunosuppression is desired. A more pronounced thereapeutic effect in the alum-administered animals than the animals injected with Freund's aduvant is expected.
C. Murine lupus model The therapeutic e~cacy of an MDC antagonist for the treatment of Iupus erythematosus is demonstrated in animal models, such as NZB/NZW Fl mice, that are known in the art and have been described in the literature. See, e.g., Wofsy, D. et al., J. Immu»ol., 138(10): 3247-3253 (May, 1987); and Daikh et al., J. Immunol., 159(7): 3104-3108 (Oct., 3 0 1997).

D. Use of a_n- MDC antrgorist to treat huma_n_ lupLS ervt-h_emAtosus An MDC antagonist such as a humanized or human anti-MDC antibody or anti-CCR4 antibody is employed in a standard dose-escalation study to demonstrate efficacy in the treatment of lupus erythematosus in affected human individuals. Exemplary dosing regimens for an antibody range from 0.01 to 50 mg/kg body weight, and preferably 0.1 to 5 mg/kg, administered weekly, or bi-weekly, or monthly. Treatment e~cacy is detenmined by monitoring standard indices. See, e.g., Bombardier et al., "Derivation of the SLEDAI: a disease activity index for lupus patients," Arthritis Rheum, 35: 630-640 (1992); Liang et al., "Measurement of systemic lupus erythematosus activity in clinical research," ArthritisRheum., 31: 817-825 (1988).
Optimal dosing is determined by standard dose-response studies after eff cacy is demonstrated.
E. Use of an MDC a_ntagoni_st to treat huma_n_ multiple sclerosis An MDC antagonist such as a humanized or human anti-MDC antibody or anti-CCR4 antibody is employed in a standard dose-escalation study to demonstrate efficacy in the treatment of multiple sclerosis in affected human individuals. Exemplary dosing regimens for an antibody-based therapeutic are as set forth in Seciton D, above. Treatment efficacy is determined by monitoring standard MS indices. See, e.g., Kurtzke, J.F., "Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS)," Neurology, 33: 1444 (1983).
The biological functions of MDC, elucidated as described above, suggest several clinical applications.
Chemokines in general attract and activate monocytes and macrophages (Baggiolini et al., supra), and MDC in particular attracts macrophages and inhibits monocyte chemotaxis. Thus, MDC expression in a pathogenic inflammatory setting may exacerbate disease states by recruiting additional macrophages or other leukocytes to the disease site, by activating the leukocytes that are already there, or by inducing leukocytes to remain at the site. Thus, inhibiting the chemoattractant activity of MDC may be expected to alleviate deleterious inflammatory processes. Significantly, the potential benefits of such an approach have been 3 0 directly demonstrated in experiments involving 13,,-8, a C-X-C chemokine that attracts and activates neutrophils. Antibodies directed against IL-8 have a profound ability to inhibit inflammatory disease mediated by neutrophils [Harada et al., J. Leukoc. Biol., 56:559 (1994)].
Inhibition of MDC is expected to have a similar effect in diseases in which macrophages are presumed to play a role, e.g., Crohn's disease, rheumatoid arthritis, or atherosclerosis.
Alternatively, augmenting the effect of MDC may have a beneficial role in such diseases, as chemokines have also been shown to have a positive effect in wound healing and angiogenesis. Thus, exogenous NIDC or MI7C agonists may be beneficial in promoting recovery from such diseases.
In addition, the myelosuppressive effect demonstrated for the C-C chemokine MIP-la (Maze et al., supra) suggests that MDC may have a similar activity.
Such activity, provided by 1VIDC or 11~C agonists, may yield substantial benefits for patients receiving chemotherapy or radiation therapy, reducing the deleterious effects of the therapy on the patient's myeloid progenitor cells.
MDC or MDC agonists may also prove to be clinically important in the treatment of tumors, as suggested by the ability of the C-C chemokine TCA3 to inhibit tumor formation in mice (see Laving et al., supra). MDC may act directly or indirectly to inhibit tumor formation, e.g., by attracting and activating various non-specific effector cells to the tumor site or by stimulating a specific anti-tumor immunity. The fibroblast-antiproliferative effect of MDC
indicates a therapeutic utility for MDC in the treatment of diseases such as pulmonary fibrosis and tumors, in which enhanced or uncontrolled cell proliferation is a major feature.
2 0 While the present invention has been described in terms of specific embodiments, it is understood that variations and modifications will occur to those skilled in the art.
Accordingly, only such limitations as appear in the appended claims should be placed on the invention.

SEQUENCE LISTING
<110> ICOS Corporation, et al.
<120> MACROPHAGE DERIVED CHEMOKINE (MDC), MDC ANALOGS, MDC
INHIBITOR SUBSTANCES, AND USES THEREOF
<130> 27866/34810PCT
<140>
<141>
<150> 09/067,447 <151> 1998-04-28 <150> 08/939,107 <151> 1997-09-26 <150> 08/660,542 <151> 1996-06-07 <150> 08/558,658 <151> 1995-11-16 <150> 08/479,620 <151> 1995-06-07 <160> 46 <170> PatentIn Ver. 2.0 <210> 1 <211> 2923 <212> DNA
<213> Homo sapiens - human MDC cDNA
<220>
<221> CDS
<222> (20)..(298) <220>
<221> mat~eptide <222> (92)..(298) <400> 1 gagacataca ggacagagc atg get cgc cta cag act gca ctc ctg gtt gtc 52 Met~Ala Arg Leu Gln Thr Ala Leu Leu Val Val ctc gtc ctc ctt get gtg gcg ctt caa gca act gag gca ggc ccc tac 100 Leu Val Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Pro Tyr SUBSTfTUTE SHEET (RULE 26) ggcgcc aacatggaa gacagc gtctgctgc cgtgat tacgtccgt tac 148 GlyAla AsnMetGlu AspSer ValCysCys ArgAsp TyrValArg Tyr cgtctg cccctgcgc gtggtg aaacacttc tactgg acctcagac tcc 196 ArgLeu ProLeuArg ValVal LysHisPhe TyrTrp Thr'SerAsp Ser tgcccg aggcctggc gtggtg ttgctaacc ttcagg gataaggag atc 244 CysPro ArgProGly ValVal LeuLeuThr PheArg AspLysGlu Ile tgtgcc gatcccaga gtgccc tgggtgaag atgatt ctcaataag ctg 292 CysAla AspProArg ValPro TrpValLys MetIle LeuAsnLys Leu agccaa tgaagagcct ggaaggctca 348 actctgatga ccgtggcctt ggctcctcca SerGln ggagccctac ctccctgcca ttatagctgc tccccgccag aagcctgtgc_caactctctg 408 cattccctga tctccatccc tgtggctgtc acccttggtc acctccgtgc tgtcactgcc 468 atctcccccc tgacccctct aacccatcct ctgcctccct ccctgcagtc agagggtcct 528 gttcccatca gcgattcccc tgcttaaacc cttccatgac tccccactgc cctaagctga 588 ggtcagtctc ccaagcctgg catgtggccc tctggatctg ggttccatct ctgtctccag 648 cctgcccact tcccttcatg aatgttgggt tctagctccc tgttctccaa acccatacta 708 cacatcccac ttctgggtct ttgcctggga tgttgctgac actcagaaag tcccaccacc 768 tgcacatgtg tagccccacc agccctccaa ggcattgctc gcccaagcag ctggtaattc 828 catttcatgt attagatgtc ccctggccct ctgtcccctc ttaataaccc tagtcacagt 888 ctccgcagat tcttgggatt tgggggtttt ctcccccacc tctccactag ttggaccaag 948 gtttctagct aagttactct agtctccaag cctctagcat agagcactgc agacaggccc 1008 tggctcagaa tcagagccca gaaagtggct gcagacaaaa tcaataaaac taatgtccct 1068 cccctctccc tgccaaaagg cagttacata tcaatacaga gactcaaggt cactagaaat 1128 gggccagctg ggtcaatgtg aagccccaaa tttgcccaga ttcacctttc ttcccccact 1188' cccttttttt tttttttttt tttgagatgg agtttcgctc ttgtcaccca cgctggagtg 1248 caatggtgtg gtcttggctt attgaagcct ctgcctcctg ggttcaagtg attctcttgc 1308 ctcagcctcc tgagtagctg ggattacagg ttcctgctac cacgcccagc taatttttgt 1368 atttttagta gagacgaggc ttcaccatgt tggccaggct ggtctcgaac tcctgtcctc 1428 SUBSTITUTE SHEET (RULE 26) aggtaatccg cccacctcag cctcccaaag tgctgggatt acaggcgtga gccacagtgc 1488 ctggcctctt ccctctcccc actgcccccc ccaacttttt tttttttttt atggcagggt 1548 ctcactctgt cgcccaggct ggagtgcagt ggcgtgatct cggctcacta caacctcgac 1608 ctcctgggtt caagtgattc tcccacccca gcctcccaag tagctgggat tacaggtgtg 1668 tgccactacg gctggctaat ttttgtattt ttagtagaga caggtttcac catattggcc 1728 aggctggtct tgaactcctg acctcaagtg atccaccttc cttgtgctcc caaagtgctg 1788 agattacagg cgtgagctat cacacccagc ctcccccttt ttttcctaat aggagactcc 1848 tgtacctttc ttcgttttac ctatgtgtcg tgtctgctta catttccttc tcccctcagg 1908 ctttttttgg gtggtcctcc aacctccaat acccaggcct ggcctcttca gagtaccccc 1968 cattccactt tccctgcctc cttccttaaa tagctgacaa tcaaattcat gctatggtgt 2028 gaaagactac ctttgacttg gtattataag ctggagttat atatgtattt gaaaacagag 2088 taaatactta agaggccaaa tagatgaatg gaagaatttt aggaactgtg agagggggac 2148 aaggtgaagc tttcctggcc ctgggaggaa gctggctgtg gtagcgtagc gctctctctc 2208 tctgtctgtg gcaggagcca aagagtaggg tgtaattgag tgaaggaatc ctgggtagag 2268 accattctca ggtggttggg ccaggctaaa gactgggagt tgggtctatc tatgcctttc 2328 tggctgattt ttgtagagac ggggttttgc catgttaccc aggctggtct caaactcctg 2388 ggctcaagcg atcctcctgg ctcagcctcc caaagtgctg ggattacagg cgtgaatcac 2448 tgcgcctggc ttcctcttcc tcttgagaaa tattcttttc atacagcaag tatgggacag 2508 cagtgtccca ggtaaaggac ataaatgtta caagtgtctg gtcctttctg agggaggctg 2568 gtgccgctct gcagggtatt tgaacctgtg gaattggagg aggccatttc actccctgaa 2628 cccagcctga caaatcacag tgagaatgtt caccttatag gcttgctgtg gggctcaggt 2688 tgaaagtgtg gggagtgaca ctgcctaggc atccagctca gtgtcatcca gggcctgtgt 2748 ccctcccgaa cccagggtca acctgcctgc cacaggcact agaaggacga atctgcctac 2808 tgcccatgaa cggggccctc aagcgtcctg ggatctcctt ctccctcctg tcctgtcctt 2868 gcccctcagg actgctggaa aataaatcct ttaaaatagt aaaaaaaaaa aaaaa 2923 <210> 2 <211> 93 <212> PRT
<213> Homo sapa.ens - human NmC
SUBSTITUTE SHEET (RULE 26) II

<400> 2 Met Ala Arg Leu Gln Thr Ala Leu Leu Val Val Leu Val Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Pro Tyr Gly Ala Asn Met Glu Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp Ser Cys Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro,Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 3 <211> 18 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer JHSP6 <400> 3 gacactatag aatagggc lg <210> 4 <211> 17 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer M13 <400> 4 gtaaaacgac ggccagt <210> 5 <211> 20 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer T3.1 <400> 5 aattaaccct cactaaaggg 20 SUBSTITUTE SHEET (RULE 26) CA 02302806 2000-03-08 n <210> 6 <211> 22 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer T7.1 <400> 6 gtaatacgac tcactatagg gc 22 <210> 7 <211> 35 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-1F
<400> 7 tctatctaga ggcccctacg gcgccaacat ggaag 35 <210> 8 <211> 33 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-2R
<400> 8 caccggatcc tcattggctc agcttattga gaa 33 <210> 9 <211> 29 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-4R
<400> 9 aatggatcca cagcacggag gtgaccaag 29 <210> 10 <211> 31 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-3R
SUBSTITUTE SHEET (RULE 26) i <400> to agtcaagctt agggcactct gggatcggca c 31 <210> 11 <211> 45 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-FX2 <400> 11 tatcggatcc tggttccgcg tggcccctac ggcgccaaca tggaa 45 <210> 12 c211> 22 <212> DNA
c213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer GEX5 <400> 12 gaaatccagc aagtatatag ca 22 <210> 13 <211> 36 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-Pel <400> 13 attgccatgg ccggccccta cggcgccaac atggaa 36 <210> 14 <211> 30 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390RcFI
<400> 14 gaccaagctt gagacataca ggacagagca 30 <210> 15 <211> 29 <212> DNA
SUBSTITUTE SHEET (RULE 26) ~~
__ "",.~"~, _'7_ <213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390RcX
<400> 15 tggatctaga agttggcaca ggcttctgg 29 <210> 16 <211> 20 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer DC03 <400> 16 cgaaattaat acgactcact 20 <210> 17 <211> 67 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390mycRX
<400> 17 tggatctaga tcaattcaag tcctcctcgc tgatcagctt ctgctcttgg ctcagcttat 60 tgagaat 67 <210> 18 <211> 99 <212> PRT
<213> Homo sapiens - Hu MCP-3 <220>
<400> 18 Met Lys Ala Ser Ala Ala Leu Leu Cys Leu Leu Leu Thr Ala Ala Ala Phe Ser Pro Gln Gly Leu Ala Gln Pro Val Gly Ile Asn Thr Ser Thr Thr Cys Cys Tyr Arg Phe Ile Asn Lys Lys Ile Pro Lys Gln Arg Leu Glu Ser Tyr Arg Arg Thr Thr Ser Ser His Cys Pro Arg Glu Ala Val SUBSTITUTE SH~B'~ (RUtE2S~

_g_ Ile Phe Lys Thr Lys Leu Asp Lys Glu Ile Cys Ala Asp Pro Thr Gln Lys Trp Val Gln Asp Phe Met Lys His Leu Asp Lys Lys Thr Gln Thr Pro Lys Leu <210> 19 <211> 99 <212> PRT
<213> Homo spapiens - Hu MCP-1 <400> 19 Met Lys Val Ser Ala Ala Leu Leu Cys Leu Leu Leu Ile Ala Ala Thr Phe Ile Pro Gln Gly Leu Ala Gln Pro Asp Ala Ile Asn Ala Pro Val Thr Cys Cys Tyr Asn Phe Thr Asn Arg Lys Ile Ser Val Gln Arg Leu Ala Ser Tyr Arg Arg Ile Thr Ser Ser Lys Cys Pro Lys Glu Ala Val Ile Phe Lys Thr Ile Val Ala Lys Glu Ile Cys Ala Asp Pro Lys Gln Lys Trp Val Gln Asp Ser Met Asp His Leu Asp Lys Gln Thr Gln Thr Pro Lys Thr <210> 20 <211> 76 <212> PRT
<213> Homo sapiens - Hu MCP-2 <220>
<400> 20 Gln Pro Asp Ser Val Ser Ile Pro Ile Thr Cys Cys Phe Asn Val Ile Asn Arg Lys Ile Pro Ile Gln Arg Leu Glu Ser Tyr Thr Arg Ile Thr Asn Ile Gln Cys Pro Lys Glu Ala Val Ile Phe Lys Thr Lys Arg Gly Lys Glu Val Cys Ala Asp Pro Lya Glu Arg Trp Val Arg Asp Ser Met SUBSTITUTE SHEET (RULE 26) Lys His Leu Asp Gln Ile Phe Gln Asn Leu Lys Pro <210> 21 <211> 91 <212> PRT
<213> Homo sapiens - RANTES
<220>
<400> 21 Met Lys Val Ser Ala Ala Ala Leu Ala Val Ile Leu Ile Ala Thr Ala Leu Cys Ala Pro Ala Ser Ala Ser Pro Tyr Ser Ser Asp Thr Thr Pro Cys Cys Phe Ala Tyr Ile Ala Arg Pro Leu Pro Arg Ala His Ile Lya Glu Tyr Phe Tyr Thr Ser Gly Lys Cys Ser Asn Pro Ala Val Val Phe Val Thr Arg Lys Asn Arg Gln Val Cys Ala Asn Pro Glu Lys Lys Trp Val Arg Glu Tyr Ile Asn Ser Leu Glu Met Ser <210> 22 <211> 9I
<212> PRT
<213> Homo sapiens - MIP-1 beta <220>
<400> 22 Met Lys Leu Cys Val Thr Val Leu Ser Leu Leu Met Leu Val Ala Ala Phe Cys Ser Pro Ala Leu Ser Ala Pro Met Gly Ser Asp Pro Pro Thr Ala Cys Cys Phe Ser Tyr Thr Arg Glu Ala Ser Ser Asn Phe Val Val Asp Tyr Tyr Glu Thr Ser Ser Leu Cys Ser Gln Pro Ala Val Val Phe Gln Thr Lys Arg Ser Lys Gln Val Cys Ala Asp Pro Ser Glu Ser Trp Val Gln Glu Tyr Val Tyr Asp Leu Glu Leu Asn SUBSTITUTE SI-~~ET RULE ~~) <210> 23 <211> 92 <212> PRT
<213> Homo sapiens - MIP-1 alpha <220>
<400> 23 Met Gln Val Ser Thr Ala Ala Leu Ala Val Leu Leu Cys Thr Met Ala Leu Cys Asn Gln Phe Ser Ala Ser Leu Ala Ala Asp Thr Pro Thr Ala Cys Cys Phe Ser Tyr Thr Ser Arg Gln Ile Pro Gln Asn Phe Ile Ala Asp Tyr Phe Glu Thr Ser Ser Gln Cys Ser Lys Pro Gly Val Ile Phe Leu Thr Lys Arg Ser Arg Gln Val Cys Ala Asp Pro Ser Glu Glu Trp Val Gln Lys Tyr Val Ser Asp Leu Glu Leu Ser Ala <210> 24 <211> 96 <212> PRT
<213> Homo sapiens - I-309 <220>
<400> 24 Met Gln Ile Ile Thr Thr Ala Leu Val Cys Leu Leu Leu Ala Gly Met Trp Pro Glu Asp Val Asp Ser Lys Ser Met Gln Val Pro Phe Ser Arg Cys Cys Phe Ser Phe Ala Glu Gln Glu Ile Pro Leu Arg Ala Ile Leu Cys Tyr Arg Asn Thr Ser Ser Ile Cys Ser Asn Glu Gly Leu Ile Phe Lys Leu Lys Arg Gly Lys Glu Ala Cys Ala Leu Asp Thr Val Gly Trp Val Gln Arg His Arg Lys Met Leu Arg His Cys Pro Ser Lys Arg Lys SUBSTITUTE SHEET (RUtE 26) <210> 25 <211> 93 <212> PRT
<213> Artificial Sequence - Human MDC analog <220>
<223> The amino acid at position 24 is selected from the group consisting of arg, gly.~ ala, val, leu, ile, pro, ser, thr, phe, tyr, trp, aspartate, glutamate, asn, gln, cys, and met <220>
<223> The amino acid at position 27 is independently selected from the group consisting of lys, gly, ala, val, leu, ile, pro, ser, thr, phe, tyr, trp, aspartate, glutamate, asn, gln, cys, and met <220>
<223> The amino acid at position 30 is independently selected from the group consisting of tyr, ser, lys, arg, his, aspartate, glutamate, asn, gln, and cys <220>
<223> The amino acid at position 50 is independently selected from the group consisting of glu, lys, arg, his, gly, and ala <220>
<223> The amino acid at position 59 is independently selected from the group consisting of trp, ser, lys, arg, his, aspartate, glutamate, asn, gln, and cys <220>
<223> The amino acid at position 60 is independently selected from the group consisting of val, ser, lys, arg, his, aspartate, glutamate, asn, gln, and cys <400> 25 Met Ala Arg Leu Gln Thr Ala Leu Leu Val Val Leu Val Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Pro Tyr Gly Ala Asn Met Glu Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Xaa val Val Xaa His Phe Xaa Trp Thr Ser Asp Ser Cys Pro Arg Pro Gly SUBSTITUTE SHEET (RULE 26) ni Val Val Leu Leu Thr Phe Arg Asp Lys Xaa Ile Cys Ala Asp Pro Arg Val Pro Xaa Xaa Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 26 <211> 30 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-7F
<400> 26 tattggatcc gttctagctc cctgttctcc 30 <210> 27 <211> 31 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer 390-8R
<400> 27 ccaagaattc ctgcagccac tttctgggct c 31 <210> 28 <211> 20 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer ARA1 <400> 28 gcgactctct actgtttctc 2p <210> 29 <211> 20 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Primer ARA2 <400> 29 cacaggaaac agctatgacc 20 SUBSTITUTE SHEET (RULE 26) <210> 30 <211> 70 <212> PRT
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Human MDC analog <400> 30 Leu Gly Pro Tyr Gly Ala Asn Met Glli Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp See Cys Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 31 <211> 69 <212> PRT
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Human MDC analog <400> 31 Gly Pro Tyr Gly Ala Asn Met Glu Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp Ser Cys Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro Tyr Leu Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 32 <211> 69 <212> PRT
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: Human MDC analog <400> 32 SUBSTI~'UTE SIi~EET (RULE 26) Gly Pro Tyr Gly Ala Asn Met Glu Asp Ser Val Cys Cys Arg Asp Tyr 1 ' 5 10 15 Val Arg Tyr Arg Leu Pro Leu Arg Val Val Lys Glu Tyr Phe Tyr Thr Ser Asp Ser Cys Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 33 <211> 1677 <212> DNA
<213> Homo sapiens - human CCR4 cDNA
<220>
<221> CDS
<222> (183)..(1262) <400> 33 cgggggtttt gatcttcttc cccttctttt cttccccttc ttctttcctt cctccctccc 60 tctctcattt cccttctcct tctccctcag tctccacatt caacattgac aagtccattc 120 agaaaagcaa gctgcttctg gttgggccca gacctgcctt gaggagcctg tagagttaaa 180 as atg aac ccc acg gat ata gca gat acc acc ctc gat gaa agc ata 227 Met Asn Pro Thr Asp Ile Ala Asp Thr Thr Leu Asp Glu Ser Ile tac agc aat tac tat ctg tat gaa agt atc ccc aag cct tgc acc aaa 275 Tyr Ser Asn Tyr Tyr Leu Tyr Glu Ser Ile Pro Lys Pro Cys Thr Lys 20 25 30, gaa ggc atc aag gca ttt ggg gag ctc ttc ctg ccc cca ctg tat tcc 323 Glu Gly Ile Lys Ala Phe Gly Glu Leu Phe Leu Pro Pro Leu Tyr Ser ttg gtt ttt gta ttt ggt ctg ctt gga aat tct gtg gtg gtt ctg gtc 371 Leu Val Phe Val Phe Gly Leu Leu Gly Asn Ser Val Val Val Leu Val ctg ttc aaa tac aag cgg ctc agg tcc atg act gat gtg tac ctg ctc 419 Leu Phe Lys Tyr Lys Arg Leu Arg Ser Met Thr Asp Val Tyr Leu Leu aac ctt gcc atc tcg gat ctg ctc ttc gtg ttt tcc ctc cat ttt tgg 467 Asn Leu Ala Ile Ser Asp Leu Leu Phe Val Phe Ser Leu Pro Phe Trp SUBST'1TUTE SHEET (RULE 26) ggc tac tat gca gca gac cag tgg gtt ttt ggg cta ggt ctg tgc aag 515 Gly Tyr Tyr Ala Ala Asp Gln Trp Val Phe Gly Leu Gly Leu Cys Lys atg att tcc tgg atg tac ttg gtg ggc ttt tac agt ggc ata ttc ttt 563 Met Ile Ser Trp Met Tyr Leu Val Gly Phe Tyr Ser Gly Ile Phe Phe gtc atg ctc atg agc att gat aga tac ctg gcg ata gtg cac gcg gtg 611 Val Met Leu Met Ser Ile Asp Arg Tyr Leu Ala Ile Val His Ala Val ttt tcc ttg agg gca agg acc ttg act tat ggg gtc atc acc agt ttg 659 Phe Ser Leu Arg Ala Arg Thr Leu Thr Tyr Gly Val Ile Thr Ser Leu get aca tgg tca gtg get gtg ttc gcc tcc ctt cct ggc ttt ctg ttc 707 Ala Thr Trp Ser Val Ala Val Phe Ala Ser Leu Pro Gly Phe Leu Phe agc act tgt tat act gag cgc aac cat acc tac tgc aaa acc aag tac 755 Ser Thr Cys Tyr Thr Glu Arg Asn His Thr Tyr Cys Lya Thr Lys Tyr tct ctc aac tcc acg acg tgg aag gtt ctc agc tcc ctg gaa atc aac 803 Ser Leu Asn Ser Thr Thr Trp Lys Val Leu Ser Ser Leu Glu Ile Asn att ctc gga ttg gtg atc ccc tta ggg atc atg ctg ttt tgc tac tcc 851 Ile Leu Gly Leu Val Ile Pro Leu Gly Ile Met Leu Phe Cys Tyr Ser atg atc atc agg acc ttg cag cat tgt aaa aat gag aag aag aac aag 899 Met Ile Ile Arg Thr Leu Gln His Cys Lys Asn Glu Lys Lys Asn Lys gcg gtg aag atg atc ttt gcc gtg gtg gtc ctc ttc ctt ggg ttc tgg 947 Ala VaI Lys Met Ile Phe Ala Val Val Val Leu Phe Leu Gly Phe Trp aca cct tac aac ata gtg ctc ttc cta gag acc ctg gtg gag cta gaa 995 Thr Pro Tyr Asn Ile Val Leu Phe Leu Glu Thr Leu Val Glu Leu Glu gtc ctt cag gac tgc acc ttt gaa aga tac ttg gac tat gcc atc cag 1043 Val Leu Gln Asp Cys Thr Phe Glu Arg Tyr Leu Asp Tyr Ala Ile Gln gcc aca gaa act ctg get ttt gtt cac tgc tgc ctt aat ccc atc atc 1091 Ala Thr Glu Thr Leu Ala Phe Val His Cys Cys Leu Asn Pro Ile Ile tac ttt ttt ctg ggg gag aaa ttt cgc aag tac atc cta cag ctc ttc 1139 Tyr Phe Phe Leu Gly Glu Lys Phe Arg Lys Tyr Ile Leu Gln Leu Phe SUBSTITUTE SHEET (RULE 26) WO 99/1566b PCT/US98/20270 aaa acc tgc agg ggc ctt ttt gtg ctc tgc caa tac tgt ggg ctc ctc 1187 Lys Thr Cys Arg Gly Leu Phe Val Leu Cys Gln Tyr Cys Gly Leu Leu caa att tac tct get gac acc ccc agc tca tct tac acg cag tcc acc 1235 Gln Ile Tyr Ser Ala Asp Thr Pro Ser Ser Ser Tyr Thr Gln Ser Thr atg gat cat gat ctt cat gat get ctg taggaaaaat gaaatggtga 1282 Met Asp His Asp Leu His Asp Ala Leu aatgcagagt caatgaactt ttccacattc agagcttact ttaaaattgg tatttttagg 1342 taagagatcc ctgagccagt gtcaggagga aggcttacac ccacagtgga aagacagctt 1402 ctcatcctgc aggcagcttt ttctctccca ctagacaagt ccagcctggc aagggttcac 1462 ctgggctgag gcatccttcc tcacaccagg cttgcctgca ggcatgagtc agtctgatga 1522 gaactctgag cagtgcttga atgaagttgt aggtaatatt gcaaggcaaa gactattccc 1582 ttctaacctg aactgatggg tttctccaga gggaattgca gagtactggc tgatggagta 1642 aatcgctacc ttttgctgtg gcaaatgggc ccccg 1677 <210> 34 <211> 360 <212> PRT
<213> Homo sapiens - human CCR4 <400> 34 Met Asn Pro Thr Asp Ile Ala Asp Thr Thr Leu Asp Glu Ser Ile Tyr Ser Asn Tyr Tyr Leu Tyr Glu Ser Ile Pro Lys Pro Cys Thr Lys Glu Gly Ile Lys Ala Phe Gly Glu Leu Phe Leu Pro Pro Leu Tyr Ser Leu Val Phe Val Phe Gly Leu Leu Gly Asn Ser Val Val Val Leu Val Leu Phe Lys Tyr Lys Arg Leu Arg Ser Met Thr Asp Val Tyr Leu Leu Asn Leu Ala Ile Ser Asp Leu Leu Phe Val Phe Ser Leu Pro Phe Trp Gly SUBSTITUTE SHEET (RULE 26) Tyr Tyr Ala Ala Asp Gln Trp Val Phe Gly Leu Gly Leu Cys Lys Met Ile Ser Trp Met Tyr Leu Val Gly Phe Tyr Ser Gly Ile Phe Phe Val Met Leu Met Ser Ile Asp Arg Tyr Leu Ala Ile Val His Ala Val Phe Ser Leu Arg Ala Arg Thr Leu Thr Tyr Gly Val Ile Thr Ser Leu Ala Thr Trp Ser Val Ala Val Phe Ala Ser Leu Pro Gly Phe Leu Phe Ser Thr Cys Tyr Thr Glu Arg Asn His Thr Tyr Cys Lys Thr Lys Tyr Ser Leu Asn Ser Thr Thr Trp Lys Val Leu Ser Ser Leu Glu Ile Asn Ile Leu Gly Leu Val Ile Pro Leu Gly Ile Met Leu Phe Cys Tyr Ser Met Ile Ile Arg Thr Leu Gln His Cys Lys Asn Glu Lys Lys Asn Lys Ala Val Lys Met Ile Phe Ala Val Val Val Leu Phe Leu Gly Phe Trp Thr Pro Tyr Asn Ile Val Leu Phe Leu Glu Thr Leu Val Glu Leu Glu Val Leu Gln Asp Cys Thr Phe Glu Arg Tyr Leu Asp Tyr Ala Ile Gln Ala Thr Glu Thr Leu Ala Phe Val His Cys Cys Leu Asn Pro Ile Ile Tyr Phe Phe Leu Gly Glu Lys Phe Arg Lys Tyr Ile Leu Gln Leu Phe Lys Thr Cys Arg Gly Leu Phe Val Leu Cys Gln Tyr Cys Gly Leu Leu Gln Ile Tyr Ser Ala Asp Thr Pro Ser Ser Ser Tyr Thr Gln Ser Thr Met Asp His Asp Leu His Asp Ala Leu <210> 35 <211> 1784 SUBSTITUTE SHEET (RULE 2fi) <212> DNA
<213> murine MDC cDNA
<220>

<221>
CDS

<222> (276) (1) . .

<220>

<221>
mat~eptide <222>
(73)..(276) <400>

atg aatctg cgtgtccca ctcctggtg getctcgtc cttctt get 48 tct Met AsnLeu ArgValPro LeuLeuVal AlaLeuVal LeuLeu Ala Ser gtg attcag acctctgat gcaggtccc tatggtgcc aatgtg gaa 96 gca Val IleGln ThrSerAsp AlaGlyPro TyrGlyAla AsnVal Glu Ala gac atctgc tgccaggac tacatccgt caccctctg ccatca cgt 144 agt Asp IleCys CysGlnAsp TyrIleArg HisProLeu ProSer Arg Ser tta aaggag ttcttctgg acctcaaaa tcctgccgc aagcct ggc 192 gtg Leu LysGlu PhePheTrp ThrSerLys SerCysArg LysPro Gly Val gtt ttgata accgtcaag aaccgagat atctgtgcc gatccc agg 240 gtt Val LeuIle ThrValLys AsnArgAsp IleCyaAla AspPro Arg Val cag tgggtg aagaagcta ctccataaa ctgtcctagggaggag 286 gtc Gln TrpVal LysLysLeu LeuHisLys LeuSer Val gacctgatga ccatgggtct ggtgtggtcc agggaggctc agcaagccct attcttctgc 346 cattccagca agagccttgc caacgacgcc acctttactc acctccatcc cctgggctgt 406 cactctgtca ggctctggtc cctctacctc ccctctatcc cttccagctt ateccccttc 466 aatgtggcag ctgggaaaca cattcaggcc agccttaccc aatgcctact ccccactgct 526 ttagatgaga ccagcgtcct tgttttgatg ccctgatcct atgatgcctt ccccatcccc 586 agccttggcc cccttctctt cttgcatgta gggaaggccc ataggtttca aatatgtgct 646 acctacttcc ctttctgggg ggttctaata cccagcatgt ttttcctgct gcaggcacct 706 atccagtgcc acacacctcc caagtttcta tcagtcccag tgggcatcca ccaagcccca 766 aacttcagac ttccttggcc tccacctact ctcagtagaa ttctgggagt ttcaggctgg 826 tccaccaggc cccccagggt taggccaagg tccccaccag agctcctcct gtttcttggt 886 SUBSTITUTE SH~~T (RULE 28) WO 991156b6 PCT/US98/Z0270 ctgcagcacg gggcagggag caaggagcag gctcagaatc agatttctta aaggagctgc 946 agactccatc agtaaaagga atctttctcc catccctgaa tataaggcag ttttctgtca 1006 acacagagac tcaggttgtt agaaatggcc acatagatca actgtgaaac cctaaattta 1066 ccaagaatca acttccaccc ctcttcaacc acatgctagg gtcttttact ttctctgccc 1126 cacacctttg actccttgcc tgtgtagctg atagtcgaag ttatgctatg gtgtcagtga 1186 ctgccacagt ttgtttggta ttataagcta tagttatatt tatataggaa agaggataaa 1246 tatatgtggg ccaaatagac gaactggaga gttttaggat ctgggggcag gaagggccat 1306 acaaagtgat acctcagaaa atagatggtt gtgggagctg ctgccagtgg cagagttaac 1366 ttaaagaact taattgaaat tattcttgag tggctgaggc caagacaaga atatagaacc 1426 cattcttgct tccctggaga caacagtggt cccaggggaa ggaataaacc ttcttgctcc 1486 tctggaggga gcatggcctg rcttagccga gtgactggac tgtgtgagat tgggggcatc 1546 gcttttccty tctgagcctc agctgacagc atatgggacc acaaagggct tgatccaaac 1606 cacagggatt gacagtgcca gccacagctg tgtccagggc tcgtgttctg ccagaaggag 1666 cacctggacg accagggcca ccactagtgc tactttgctc actgcccatg catgtcctga 1726 aggtccctcc ccctcctctc ctacttctgg gaaaataaat gctcgccaat aatacctg 1784 <210> 36 <211> 92 <212> PRT

<213> murine MDC

<400> 36 Met Ser Asn ArgVal ProLeu Leu Ala Leu Val Leu Leu Val Leu Ala Val Ala Ile ThrSer AspAla Gly Tyr Gly Ala Val Gln Pro Asn Glu Asp Ser Ile CysGln AspTyr Ile His Pro Leu Ser Cys Arg Pro Arg Leu Val Lys PhePhe TrpThr Ser Ser Cys Arg Pro Glu Lys Lys Gly Val Val Leu ThrVal LysAsn Arg Ile Cys Ala Pro Ile Asp Asp Arg Gln Val Trp LysLys LeuLeu His Leu Ser Val Lys SUBSTITUTE SHEET (RULE 26) <210> 37 <211> 958 <212> DNA
<213> rat MDC cDNA
<220>
<221> CDS
<222> (1) .. (243) <220>
<221> mat~eptide <222> (40)..(243) <400> 37 ctc gtc ctt ctt get gtg gca ctt cag acc tcc gat gca ggt ccc tat 48 Leu Val Leu Leu Ala Val Ala Leu Gln Thr Ser Asp Ala Gly Pro Tyr ggt gcc aat gtg gaa gac agt atc tgc tgc cag gac tac atc cgt cac 96 Gly Ala Asn Val Glu Asp Ser Ile Cys Cys Gln Aap Tyr Ile Arg His cct ctg cca cca cgt ttc gtg aag gag ttc tac tgg acc tca aag tcc 144 Pro Leu Pro Pro Arg Phe Val Lys Glu Phe Tyr Trp Thr Ser Lys Ser tgc cgc aag cct ggc gtc gtt ttg ata acc atc aag aac cga gat atc 192 Cys Arg Lys Pro Gly Val Val Leu Ile Thr Ile Lys Asn Arg Asp Ile tgt get gac ccc ang atg etc tgg gtg aag aag ata ctc cac aag ttg 240 Cys Ala Asp Pro Xaa Met Leu Trp Val Lys Lys Ile Leu His Lys Leu gcc tagggagaag ggcctgatga ccacgggtct ggtgtctcca caaggctcag 293 Ala caaaccctat ccttctgcca tccagcaaga gccttgccaa caactccacc tttgctcacc 353 tccatcccct gggttgtcac tctgtgaagc ctcgggtccc tgtacttcct gtccgtcccc 413 tccagctcat tctcttccaa cgtggcagcc gggaagcact tctggctagc cttacccaat 473 actactcccc actgctttaa atgagaccag ggtccttgtt ttggtgcctt tggatcctat 533 gatgccttcc cagtctccag ccttggcccc cttctcttct tacatgtagg gaacaccaat 593 atctttcaag tatgtgctac ccaattcctc ttcctcggag gctgctggga cccggaatat 653 tatcccctgc tgcaggcctc tccaagcacc actcacctcc caggctttcc atccgtccca 713 gtcccaagcc ccatgcttca gaacttccct tggccccccc ctacactcca caaattctgg 773 ggaagtctca cnaactgggt cccctcaggc ccccacggga aggaaggtcc cccnccaaca 833 SUBSTITUTE SHEET (RULE 26) acntcctcct gttttccccg gtctcccncc nccgggantt gggcncccna atccccaatt 893 tctgaanang aacngcecat tcntcccntt aaaattaacc tttccccccc tccctgangt 953 tagga 958 <210> 38 <211> 81 <212> PRT
<213> rat <400> 38 Leu Val Leu Leu Ala Val Ala Leu Gln Thr Ser Asp Ala Gly Pro Tyr Gly Ala Asn val Glu Asp Ser Ile Cys Cys Gln Asp Tyr Ile Arg His Pro Leu Pro Pro Arg Phe Val Lys Glu Phe Tyr Trp Thr Ser Lys Ser Cys Arg Lys Pro Gly Val Val Leu Ile Thr Ile Lys Asn Arg Asp Ile Cys Ala Asp Pro Xaa Met Leu Trp Val Lys Lys Ile Leu His Lys Leu Ala <210> 39 <211> 506 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: S. cerevisiae alpha factor pre-pro/human MDC cDNA chimeric construct <221> CDS
<222> (15)..(476) <220>
<221> mat_peptide <222> (270)..(476) <400> 39 atctcgagct cacg atg aga ttt cct tca att ttt act gca gtt tta ttc 50 Met Arg Phe Pro Ser Ile Phe Thr Ala Val Leu Phe gca gca tcc tcc gca tta get get cca gtc aac act aca aca gaa gat 98 Ala Ala Ser Ser Ala Leu Ala Ala Pro Val Asn Thr Thr Thr Glu Asp SUBSTITUTE SHEET (RULE 26) gaa acg gca caa att ccg get gaa get gtc atc ggt tac tta gat tta 146 Glu Thr Ala Gln Ile Pro Ala Glu Ala Val Ile Gly Tyr Leu Asp Leu gaa ggg gat ttc gat gtt get gtt ttg cca ttt tcc aac agc aca aat 194 Glu Gly Asp Phe Asp Val Ala Val Leu Pro Phe Ser Asn Ser Thr Asn aac ggg tta ttg ttt ata aat act act att gcc agc att get get aaa 242 Asn Gly Leu Leu Phe Ile Asn Thr Thr Ile Ala Ser Ile Ala Ala Lys gaa gaa ggg gta cct ttg gat aaa aga ggc ccc tac ggc gcc aac atg 290 Glu Glu Gly VaI Pro Leu Asp Lys Arg Gly Pro Tyr Gly Ala Asn Met gaa gac agc gtc tgc tgc cgt gat tac gtc cgt tac cgt ctg ccc ctg 338 Glu Asp Ser Val Cys Cys Arg Asp_Tyr Val Arg Tyr Arg Leu Pro Leu cgc gtg gtg aaa cac ttc tac tgg acc tca gac tcc tgc ccg agg cct 386 Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp Ser Cys Pro Arg Pro ggc gtg gtg ttg cta acc ttc agg gat aag gag atc tgt gcc gat ccc 434 Gly Val Val Leu Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro aga gtg ccc tgg gtg aag atg att ctc aat aag ctg agc caa 476 Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln tgaaggcctt ctagagcggc cgcatcgata 506 <210> 40 <211> 154 <212> PRT
<213> CDNA
<400> 40 Met Arg Phe Pro Ser Ile Phe Thr Ala Val Leu Phe Ala Ala Ser Ser Ala Leu Ala Ala Pro Val Asn Thr Thr Thr Glu Asp Glu Thr Ala Gln Ile Pro Ala Glu Ala Val Ile Gly Tyr Leu Asp Leu Glu Gly Asp Phe Asp Val Ala Val Leu Pro Phe Ser Asn Ser Thr Asn Asn Gly Leu Leu Phe Ile Asn Thr Thr Ile Ala Ser Ile Ala Ala Lys Glu Glu Gly Val SUBSTITUTE SHEET (RULE 26) WO 99/15666 . PCT/US98/20270 Pro Leu Asp Lys Arg Gly Pro Tyr Gly Ala Asn Met Glu Asp Ser VaI

Cys Cys Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp Ser Cys Pro Arg Pro Gly Val Val Leu-Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 41 <211> 93 <212> PRT
<213> Artificial Human MDC analog <220>
<223> The amino acid at position 2 is not proline <220>
<400> 41 Met Ala Arg Leu Gln Thr Ala Leu Leu Val Val Leu Val Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Xaa Tyr Gly Ala Asn Met Glu Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr Arg Leu Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp Ser Cys Pro Arg Pro Gly Val Val Leu Leu Thr Phe Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln <210> 42 <211> 538 <212> DNA
<213> Homo sapiems <220>
<221> CDS
<222> {53)..(334) <220>
SUBS1lTUTE SHfET (RULE 26) WO 99/15666 . PCT/US98f20270 <221> mat_peptide <222> (122)..(334) <400> 42 ccctgagcag agggacctgc acacagagac tccctcctgg gctcctggca cc atg gcc 58 Met Ala cca ctg aag atg ctg gcc ctg gtc arc ctc ctc ctg ggg get tct ctg 106 Pro Leu Lys Met Leu Ala Leu Val Thr Leu Leu Leu Gly Ala Ser Leu cag cac atc cac gca get cga ggg acc aat gtg ggc cgg gag tgc tgc 154 Gln His Ile His Ala Ala Arg Gly Thr Asn Val Gly Arg Glu Cys Cys ctg gag tac ttc aag gga gcc att ccc ctt aga aag ctg aag acg tgg 202 Leu Glu Tyr Phe Lys Gly Ala Ile Pro Leu Arg Lys Leu Lys Thr Trp tac cag aca tct gag gac tgc tcc agg gat gcc atc gtt ttt gta act 250 Tyr Gln Thr Ser Glu Asp Cys Ser Arg Asp Ala Ile Val Phe Val Thr gtg cag ggc agg gcc atc tgt tcg gac ccc aac aac aag aga gtg aag 298 Val Gln Gly Arg Ala Ile Cys Ser Asp Pro Asn Asn Lys Arg Val Lys aat gca gtt aaa tac ctg caa agc ctt gag agg tct tgaagcctcc 344 Asn Ala Val Lys Tyr Leu Gln Ser Leu Glu Arg Ser tcaccccaga ctcctgactg tctcccggga ctacctggga cctccaccgt tggtgttcac 404 cgcccccacc ctgagcgcct gggtccaggg gaggccttcc agggacgaag aagagccaca 464 gtgagggaga tcccatcccc ttgtctgaac tggagccatg ggcacaaagg gcccagatta 524 aagtctttat cctc 538 <210> 43 <211> 94 <212> PRT
<213> Homo sapiens <400> 43 Met Ala Pro Leu Lys Met Leu Ala Leu Val Thr Leu Leu Leu Gly Ala Ser Leu Gln His Ile His Ala Ala Arg Gly Thr Asn Val Gly Arg Glu Cys Cys Leu Glu Tyr Phe Lys Gly Ala Ile Pro Leu Arg Lys Leu Lys SUBSTITUTE, SHEET (RULE 26) WO 99/15666 . PCT/US98/20270 Thr Trp Tyr Gln Thr Ser Glu Asp Cys Ser Arg Asp Ala Ile Val Phe Val Thr Val Gln Gly Arg Ala Ile Cys Ser Asp Pro Asn Asn Lys Arg Val Lys Asn Ala Val Lys Tyr Leu Gln Ser Leu Glu Arg Ser 60 65 , 70 <210> 44 <211> 33 <212> DNA
<213> Artificial Sequence <220>
<223> Description of Artificial Sequence: primer <400> 44 atgggaccat atggagcaaa tatggaagat agt 33 <210> 45 <211> 335 <212> DNA
<213> Macaque MDC
<220>
<221> CDS
<222> (19)..(297) <400> 45 agacatacag gacagagc atg get cgc cta cag act gtg ttc ctg ggt gtc 51 Met Ala Arg Leu Gln Thr Val Phe Leu Gly Val ctc atc ctc ctt get gtg gcg ctt caa gca act gag gca ggc ccc tat 99 Leu Ile Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Pro Tyr ggc gcc aac atg gaa gac agc gtc tgc tgc cgt gat tac gtc cgt tac 147 Gly Ala Asn Met Glu Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr cgt atg ccc ctg cgt gtg gtg aaa cac ttc tac tgg acc tca gac tcc 195 Arg Met Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Asp Ser tgc ccg agg cct ggc gtg gtg ttg cta acc tcc agg gat aag gag atc 243 Cys Pro Arg Pro Gly Val Val Leu Leu Thr Ser Arg Asp Lys Glu Ile tgt gcc gat ccc aga gtg ccc tgg gtg aag atg att ctc aat aag ctg 291 Cys Ala Asp Pro Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu SUBSTITUTE SHEET (RULE 26~

agc caa tgaagagcct actatgatga ccgtggccta agcaagcc 335 Ser Gln <210> 46 <211> 93 <212> PRT
<213> Macaque MDC
<400> 46 Met Ala Arg Leu Gln Thr Val Phe Leu Gly Val Leu Ile Leu Leu Ala Val Ala Leu Gln Ala Thr Glu Ala Gly Pro Tyr Gly Ala Aan Met Glu Asp Ser Val Cys Cys Arg Asp Tyr Val Arg Tyr Arg Met Pro Leu Arg Val Val Lys His Phe Tyr Trp Thr Ser Aap Ser Cys Pro Arg Pro Gly Val Val Leu Leu Thr Ser Arg Asp Lys Glu Ile Cys Ala Asp Pro Arg Val Pro Trp Val Lys Met Ile Leu Asn Lys Leu Ser Gln SUBSTITUTE SHEET (RULE 26)

Claims

14. A method far identifying a modulator of binding between Macrophage Derived Chemokine (MDC) and am MDC receptor, comprising the steps of:
a) contacting an MDC receptor composition and a vertebrate Macrophage Derived Chemokine (MDC) polypeptide in the presence and in the absence of a putative modulator compound, wherein said receptor composition comprises easinaphil cell manbranes;
b) detecting binding between the receptor composition and the polypeptide; and c) identifying a putative modulator compound in vew of decreased or increased binding between the receptor composition and the polypeptide in the presence of the pulative modulator, as compared to binding in the absence of the putative modulator.

15. A method according to claim 73 or 14 wherein the polypeptide is a vertebrate MDC polypeptide.

16. A method according to claim any one of claims 13-15, wherein said contacting step comprises contacting said cell membranes with, said polypeptide, and wherein said method further composes stops of recovering said cell membranes afrer said contacting step; and washing said cell membranes prior to said detecting step to remove unbound polypoptide.

17. A method according to any one of claims 13-16 wherein said polypoptide comprises a detectable label, and wherein in step (b) binding between the receptor composition and the polypeptide is detected by detecting labeled polypeptide bound to the receptor composition.

18. A method according to any onr of claims 13-16, wherein the receptor composition comprises a whole cell expressing an MDC receptor an its surface, and wherein, in step (b), binding between the receptor composition and the polypeptide is detected by measuring a binding-induced physiological change in said cell.

19. A method according claim 18 wherein the binding-induced physiological change is selected from the group consisting of:
(a) the conversion of GTP to GDP in said host cell; and (b) a change in the concentration of cAMP in said host cell.

20. A purified compound that is a modulator of binding between the chemokine MDC and an MDC receptor, said compound identified by a method according to any of claims 13-19.

21. The use of an MDC antagonist or TARC antagonist compound for preparation of a medicament for inhibiting platelet aggregation in a mammalian subject.

22. The use of an MDC antagonist or TARC antagonist compound for preparation of a medicament for the treatment or palliation of lupus crythematosus in a mammalian subject.

23. The use of un MDC antagonist compound for preparation of a medicament for inhibiting MDC-induced activation, chemotaxis, or proliferation of cells that express the chemokine receptor CCR4.

24. The use of an MDC antagonist or TARC antagonist compound for preparation of a medicament for inhibiting an allergic reaction in a mammalian host.

25. The use of an MDC antagonist or TARC antagonist compound for preparation of a medicament for the treatment of asthma.

26. A method of palliating an allergic reaction in a mammalian subject, comprising the steps of:

identifying a mammalian subject in need of treatment for an allergic reaction that is characterized by eosinophil accumnulation, and administering to said mammalian subject a composition comprising an MDC
antagonist compound or TARC antagonist compound in an amount effective to palliate the allergic reaction.

27. A method of treating a disease state characterized by aggregation of platelets in a mammalian subject, comprising the steps of:
identifying a mammalian subject in need of treatment for said disease state, and administering to said mammalian subject a composition comprising an MDC
antagonist compound or TARC antagonist compound in an amount effective to prevent platelet aggregation in said mammalian subject.

28. A method of treating lupus erythemutosus in a mammalian subjet, comprising the steps of:
identifying a mammalian subject in need of treatment for lupus erythematosus, and administering to said mammalian subject a composition comprising an N1DC
antagonist compound or TARC antagonist compound in au amount effective to treat lupus crythcmatosus or Palliate its symptoms.
29. A method of treating a disease state characterized by activation, chemotaxis, or praliicration of cells that express flag chemokine receptor CCR4 in a ma~nalian subject, comprising the steps of identifying a mammalian subject in need of treatment for said disease state, and admittisterutg to said mammalian subject a composition comprising an MDC
azztagonist compound or TARC antagonist compound in an tunount effective to prevent at least one of activation, chemotaxis, and prolifaration of cells that express the chemokine receptor CCR4 in said mammalian subject.

30. A use according to any of claims 21-35 or a method according to any of claims 26-29 wherein the MDC antagonist compound is selected from the group consisting of:
(a) a polypeptide fragment or analog of a vertebrate MDC that inhibits MDC
activation of an MDC: receptor;
(b) an antibody that specifically binds a vertebrate MDC polypeptide;
(c) an MDC antagonist according to claim 20;
(d) a polypeptide capable of binding to a vertebrate MDC polypeptide and comprising an antigen-binding fragment of an anti-MDC antibody;
(e) a polypeptide comprising the C-C chemokine receptor 4 (CCR4) amino acid sequence set forth in SEQ ID NO: 34 or comprising a continuous fragment thereof that is capable of binding to MDC; and (f) combinations of (a)-(e).

31. A use according to any of claims 21-25 or a method according to any of claims 26-29 wherein said MDC antagonist compound comprises an antibody substance that binds MDC, said antibody substance selected from tho group consisting of monoclonal antibodies, polyclonal antibodies, single chain antibodies, chimeric, antibodies, and humanized antibodies.

32. In a vaccine composition, the improvement wherein a polypeptide is included in the vaccine composition, said polypeptide comprising a vertebrate MDC
polypeptide or biologically active fragment or analog thereof.

33. A method of stimulating en immune response in a human or animal comprising the step of administering a vaccine composition according to claim 32 to a human or animal in an amount effective to stimulate an immune response in the human or animal.

34. A method of screening a patient suspected of suffering from, or undergoing treatment for, a disorder characterized by MDC-induced T H2 cell migration or activation, comprising the steps of:
obtaining a fluid sample from a patient suspected of suffering from a disorder characterized by MDC-induced T H2 cell migration or activation; and determining the concentration of MDC in the fluid sample.

35. A method according to claim 34, wherein the fluid comprises serum, and wherein the MDC concentration is determined via ELISA assay.

36. A method according to claim 34, wherein the patient is suspected of suffering from the disease state, and wherein an elevated MDC concentration is considered diagnostic of the disease state.

37. A method according to claim 34, wherein the patient is undergoing treatment for the disease state, and MDG concentration in the fluid sample is used to monitor dosing or efficacy of treatment.