WO1996017868A1 - A novel chemokine expressed in inflamed adenoid, its production and uses - Google Patents

Abstract

The present invention provides nucleotide and amino acid sequences that identify and encode a novel expressed chemokine (ADEC) from inflamed adenoid tissue. The present invention also provides for antisense molecules to the nucleotide sequences which encode ADEC, expression vectors for the production of purified ADEC, antibodies capable of binding specifically to ADEC, hybridization probes or oligonucleotides for the detection of ADEC-encoding nucleotide sequences, genetically enginered host cells for the expression of ADEC, diagnostic tests for inflammation or disease based on ADEC-encoding nucleic acid molecules or antibodies capable of binding specifically to ADEC.

Description

A NOVEL CHEMOKINE EXPRESSED IN INFLAMED ADENOID, ITS PRODUCTION AND USES

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is related to co-pending United States Patent Application Serial No. 08/ 194,317 entitled Novel Human Adenoid Cell-Derived Polypeptides, Their Production and Uses, filed February 4, 1994.

BACKGROUND ART

Leukocytes including monocytes, macrophages, basophils, and eosinophils play important roles in the pathological mechanisms initiated by T and/or B lymphocytes. Macrophages, in particular, produce powerful oxidants and proteases which contribute to tissue destruction and secrete a range of cytokines which recruit and activate other inflammatory cells.

The investigation of the critical, regulatory processes by which white cells proceed to their appropriate destination and interact with other cells is underway. The current model of leukocyte movement or trafficking from the blood to injured or inflamed tissues comprises the following steps. The first step is the rolling adhesion of the leukocyte along the endothelial cells of the blood vessel wall. This movement is mediated by transient interactions between selectins and their ligands. A second step involves cell activation which promotes a more stable leukocyte-endothelial cell interaction mediated by the integrins and their ligands. This stronger, more stable adhesion precipitates the final steps of leukocyte diapedesis and extravasation into the tissues.

The chemokine family of polypeptide cytokines, also known as intercrines, possesses the cellular specificity required to explain leukocyte trafficking in different inflammatory situations. First, chemokines mediate the expression of particular adhesion molecules on endothelial cells; and second, they generate gradients of chemoattractant factors which activate specific cell types. In addition, the chemokines stimulate the proliferation of specific cell types and regulate the activation of cells which bear specific receptors. Both of these activities demonstrate a high degree of target cell specificity.

The chemokines are small polypeptides, generally about 70-100 amino acids (aa) in length, 8-11 kD in molecular weight and active over a 1-100 ng ml concentration range. Initially, they were isolated and purified from inflamed tissues and characterized relative to their bioactivity. More recently, chemokines have been discovered through molecular cloning techniques and characterized by structural as well as functional analysis. The chemokines are related through a four cysteine motif which is based primarily on the spacing of the first two cysteine residues in the mature molecule. Currently the chemokin are assigned to one of two families, the C-X-C chemokines (α) and the C-C chemokines (β). Although exceptions exist, the C-X-C chemokines generally activate neutrophils and fibroblast while the C-C chemokines act on a more diverse group of target cells which include monocytes macrophages, basophils, eosinophils, T lymphocytes and others. The known chemokines of both families are synthesized by many diverse cell types as reviewed in Thomso A. (1994) The Cytokine Handbook, 2d Ed. Academic Press, NY. The two groups of chemokines will be described in turn.

The archetypal and most extensively studied C-X-C chemokine is platelet factor 4 (PF4). This 70 aa protein displays the definitive four cysteines and is released along with platelet derived growth factor (PDGF), transforming growth factor β (TGF-β) and β- thromboglobulin (β-TG) from the granules of stimulated platelets. This homotetrameric molecule shares structural similarity with interleukin-8 (IL-8), induces the migration of fibroblasts, neutrophils and monocytes, and binds heparin. PF4 provides the biological model for a link among thrombosis, inflammation, and wound healing.

Other chemokines found in the platelet a granule include β-TG, connective tissue activating protein III (CTAP-III) and neutrophil activating peptide 2 (NAP-2). All three peptides are derived from the differential processing of a precursor molecule, platelet basic protein (PBP). β-TG is an 81 aa, highly basic protein which influences the migration of fibroblasts but has no effect on neutrophils or monocytes. CTAP-III is 85 aa long, and aa 4-85 are identical to β-TG. Since CTAP-III is the primary protein in the a granule and its role as a purified protein has not elucidated, it may be a secondary precursor, inactive until further processed. NAP-2 appears to attract neutrophils but not monocytes.

Nonplatelet C-X-C chemokines include IL-8, γ interferon inducible protein (IP-10), melanocyte growth stimulatory activity (MGSA or gro) proteins, epithelial derived neutrophil attractant-78 (ENA-78), granulocyte chemotactic protein-2 (GPC-2) and stromal cell- derived f actors- 1α and 1β (SDF-1α and -1β). IL-8 (also know as NAP-1) is secreted by monocytes/macrophages, neutrophils, fibroblasts, endothelial cells, keratinocytes and T lymphocytes in response to proinflammatory cytokines, IL-1 and 3, IFN-γand TNF, as well as endotoxin, mitogens, particulates, bacteria and viruses. IL-8 stimulates acute inflammation including the upregulation of both neutrophil adhesion and keratinocyte growth and the downregulation of histamine production by basophils.

IP-10 is a 10 kD protein of undefined function whose mRNA has been found in monocytes, fibroblasts and endothelial cells. Monocytes, keratinocytes and activated T cells secrete IP-10 protein which has been localized to sites of delayed hypersensitivity reactions. The cDNA of MGSA/gro a produces a 15 kD protein which appears in fibroblasts. Its transcription is growth related, and it functions as an autocrine growth factor. The distinct and non-allelic forms, gro β and gro g are 90% and 86% identical to gro a, respectively. Recombinant gro a proteins attract and activate neutrophils. ENA-78 was purified from supematants of lung alveolar cells. Like gro γ , it attracts and activates neutrophils in vitro.

GCP-2 is a 6 kD protein isolated from the supematants of osteosarcoma cells. GCP-2 exists in various N-terminally truncated forms, and it attracts and activates neutrophils in vitro and causes granulocyte accumulation in vivo. SDF-1 and -1β are newly isolated cDNAs which encode secreted molecules and type I membrane proteins.

Strieter et al. (1995) Journal of Leukocyte Biology. 57:752-762 ("Strieter A") and Strieter et al. (1995) The Journal of Biological Chemistry. 270:27348-27357 ("Strieter B"), demonstrate that the C-X-C family of chemokines displays disparate angiogenic activity depending upon the presence or absence of the NH2-terminal ELR (Glu-Leu-Arg) motif that procedes the first cysteine amino acid residue of the C-X-C chemokine family member. For example, IL-8, an ELR C-X-C chemokine, has been shown to exhibit angiogenic properties whereas PF4, a non-ELR, has been shown to inhibit angiogenesis. Angiogenesis, characterized by the neoformation of blood vessels, is an essential biological event in embryogenesis, wound healing, chronic inflammation and the growth of malignant solid tumors. Strieter B suggest that a biological imbalance in the production of angiogenic and angiostatic factors contributes to the pathogenesis of several angiogenesis-dependent disorders, including rheumatoid arthritis, scleroderma, psoriasis and tumorigenesis. Strieter A further suggest that non ELR C-X-C chemokines, such as IP-10 and PF4, will have a negative effect on tumorgenesis through a reduction in tumor-derived angiogenic activity. Current techniques for diagnosis of abnormalities in the inflamed or diseased tissues mainly rely on observation of clinical symptoms or serological analyses of body tissues or fluids for hormones, polypeptides or various metabolites. Patients often manifest no clinical symptoms at early stages of disease or tumor development. Furthermore, serological analyses do not always differentiate between invasive diseases and genetic syndromes which have overlapping or very similar ranges. Thus, development of new diagnostic techniques comprisi small molecules such as the expressed chemokines are important to provide for early and accurate diagnoses, to give a better understanding of molecular pathogenesis, and to use in the development of effective therapies. The chemokine molecules were reviewed in Schall TJ (1994) Chemotactic Cytokines:

Targets for Therapeutic Development. International Business Communications, Southborough, MA, pp 180-270; and in Paul WE (1993) Fundamental Immunology, 3rd Ed. Raven Press, NYC, pp 822-826.

DISCLOSURE OF THE INVENTION

The subject invention provides a nucleotide sequence which uniquely encodes a novel human protein from inflamed adenoid. The new gene, which is known as adenoid expressed chemokine, or adec (Incyte Clone No. 20293), encodes a polypeptide designated ADEC, of the C X-C chemokine family. The invention also comprises diagnostic tests for inflammatory conditions which include steps for testing a sample or an extract thereof with adec DNA, fragments or oiigomers, thereof. Aspects of the invention include adec antisense molecules; cloning or expression vectors containing nucleic acid encoding ADEC; host cells or organisms transformed with expression vectors containing nucleic acid encoding ADEC; purified ADEC and methods for the production and recovery of purified ADEC from host cells.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 displays the nucleotide sequence for adenoid expressed chemokine (adec) and t predicted amino acid (aa) sequence of ADEC (SEQ ID NO: 1 and SEQ ID NO -2).

Figure 2 shows the amino acid alignment of ADEC with other human chemokines of the X-C family. Alignments shown were produced using the multisequence alignment program of

DNASTAR software (DNASTAR Inc, Madison Wl).

Figure 3 shows a .elatedness tree of human C-X-C chemokines. The phylogenetic tree was generated by phylogenetic tree program of DNASTAR software (DNASTAR, Inc, Madison, using the Clustal method with the PAM250 residue weight table. Figure 4 displays an analysis of hydrophobicity and immunogenic characteristics of

ADEC based on the predicted amino acid sequence and composition.

MODES FOR CARRYING OUT THE INVENTION Definitions As used herein, "adenoid expressed chemokine" or ADEC, refers to a polypeptide disclosed in SEQ ID NO:2, or a fragment thereof, which is encoded by an mRNA transcribed from the nucleic acid of SEQ ID NO:1. ADEC may be naturally occurring or chemically synthesized. As used herein, the lower case "adec" refers to a nucleic acid sequence while the upper case "ADEC" refers to a protein, peptide or amino acid sequence.

As used herein, the term "active" refers to those forms of ADEC which retain the biologic and/or immunologic activities of naturally occurring ADEC.

As used herein, the term "naturally occurring ADEC" refers to ADEC produced by human cells that have not been genetically engineered and specifically contemplates various ADEC forms arising from post-translational modifications of the polypeptide including but not limited to acetylation, carboxylation, glycosylation, phosphorylation, lipidation and acylation.

As used herein, the term "derivative" refers to polypeptides derived from naturally occurring ADEC by chemical modifications such as ubiquitination, labeling (e.g., with radionuclides, various enzymatic modifications), pegylation (derivatization with polyethylene glycol) or by insertion or substitution by chemical synthesis of aa such as omithine, which do not normally occur in human proteins.

As used herein the term "variant" or "mutant" or "recombinant variant" refers to any polypeptide differing from naturally occurring ADEC by amino acid insertions, deletions, and substitutions, created using recombinant DNA techniques. Guidance in determining which amino acid residues may be replaced, added or deleted without abolishing activities of interest, cell adhesion and chemotaxis, may be found by comparing the sequence of the particular ADEC with that of homologous cytokines and minimizing the number of amino acid sequence changes made in regions of high homology.

Preferably, amino acid substitutions are the result of replacing one amino acid with another amino acid having similar structural and or chemical properties, such as the replacement of a leucine with an isoleucine or valine, an aspartate with a glutamate, or a threonine with a serine, i.e., conservative aa replacements. Insertions or deletions are typically in the range of about 1 to 5 amino acids. The variation allowed may be experimentally determined by systematically making insertions, deletions, or substitutions of amino acids in ADEC using recombinant DNA techniques and assaying the resulting recombinant variants for activity.

Where desired, ADEC or an ADEC variant can be genetically engineered to contain a "signal or leader sequence" that can direct the polypeptide through the membrane of a cell. Such a sequence may be naturally present on the polypeptides of the present invention or provided from heterologous protein sources by recombinant DNA techniques.

As used herein, an ADEC "fragment," "portion," or "segment" refers to any stretch of amino acids which has sufficient length to display biologic and/or immunologic activity and in preferred embodiments will contain at least about 5 amino acids, at least about 7 amino acids, least about 8 to 13 amino acids and in additional embodiemtns about 17 or more amino acids.

As used herein, an "oligonucleotide" or polynucleotide "fragment", "portion", or "segment" refers to any stretch of nucleic acids encoding ADEC which is of sufficient length to use as a primer in polymerase chain reaction (PCR), or various hybridization procedures known to those of skill in the art, for the purpose of identifying or amplifying identical or related nucleic acids.

The present invention includes purified ADEC polypeptides from natural or recombinan sources, vectors and host cells transformed with recombinant nucleic acid molecules encoding ADEC. Various methods for the isolation of the ADEC polypeptides may be accomplished by procedures known to those of skill in the art. For example, such polypeptides may be purified by immunoaffinity chromatography by employing the antibodies provided by the present invention. Various other methods of protein purification well known in the art include those described in Deutscher M (1990) Methods in Enzymology Vol. 182, Academic Press, San Diego and Scopes R (1982) Protein Purification: Principles and Practice. Springer- Veriag, NYC, both incorporated herein by reference. As used herein the term "recombinant" refers to a polynucleotide which encodes ADEC that is prepared using recombinant DNA techniques. The DNA which encodes ADEC may also include allelic or recombinant variants and mutants thereof.

As used herein, the term "probe" or "nucleic acid probe" or "polynucleotide probe" o "oligonucleotide probe" refers to a portion, fragment, or segment of ADEC that is capable of being hybridized to a desired target sequence. A probe can be used to detect, amplify or quantif cDNAs or endogenous nucleic acid encoding ADEC by employing conventional techniques in molecular biology. A probe may be of variable length, preferably from about 10 nucleotides u to several hundred nucleotides. As will be understood by those of skill in the art, hybridization conditions and probe design will vary depending upon the intended use. For example, a probe intended for use in PCR will be from about 15 to 30 nucleotides in length and may be part of a pool of degenerate probes, i.e., oligonucleotides which tolerate nucleotide mismatch but accommodate binding to an unknown sequence; whereas a probe for use in Southern or northern hybridizations may be a single, specific nucleotide sequence that is several hundred nucleotides in length. Accordingly, a preferred probe for the specific detection of ADEC will comprise a polynucleotide or oligonucleotide fragment from a non-conserved nucleotide region of SEQ ID NO:1. As used herein the term "non-conserved nucleotide region" refers to a nucleotide region that is unique to SEQ ID NO:1 and does not comprise a region that is conserved in the family of C- X-C chemokines. Probes may be single-stranded or double-stranded and may have specificity in solution, cell, tissue or membrane-based hybridizations including in situ and ELISA-iike technologies. The present invention encompasses oligonucleotides, fragments or portions of the polynucieotides disclosed herein, or their complementary strands used as probes.

Oligonucleotides" of "oligonucleotide probes" are prepared based on the nucleotide sequences disclosed herein which encode ADEC. Oligonucleotides comprise portions of the nucleotide sequence disclosed herein and contain at least about 15 nucleotides, and usually at least about 20 nucleotides and may include up to 60 nucleotides. Nucleic acid probes may comprise portions of the sequence having fewer nucleotides than about 6kb, usually fewer than about 1kb. The oligonucleotides and nucleic acid probes of the present invention may be used to determine whether nucleic acid encoding ADEC is present in a cell or tissue or to isolate similar nucleic acid sequences from chromosomal DNA as described by Walsh PS et al (1992) PCR Methods Appl. 1:241-250.

Nucleic acid probes of the present invention may be derived from naturally occurring or recombinant single- or double-stranded nucleic acids or be chemically synthesized. They may be labeled by nick translation, Klenow fill-in reaction, PCR or other methods well known in the art. Probes of the present invention, their preparation and/or labeling are elaborated in

Sambrook J et al (1989) Molecular Cloning: A Laboratory Manual, 2d Ed, Cold Spring Harbor, NY; or Ausubel FM et al (1989) Current Protocols in Molecular Biology, Vol 2, John Wiley & Sons, both incorporated herein by reference.

Alternatively, recombinant variants encoding the polypeptides of the present invention or related polypeptides may be synthesized or identified through hybridization techniques known to those of skill in the art by making use of the "redundancy" in the genetic code. Various codon substitutions, such as the silent changes which produce various restriction sites, may be introduced to optimize cloning into a plasmid or viral vector or expression in a particular prokaryotic or eukaryotic system. Mutations may also be introduced to modify the properties of the polypeptide, to change ligand-binding affinities, interchain affinities, or polypeptide degradation or turnover rate.

Detailed Description of the Invention

The present invention provides a nucleotide sequence uniquely identifying a novel chemokine of the C-X-C family, referred to herein as ADEC. Nucleotide sequences encoding ADEC have been identified in a cDNA library made from inflamed adenoid tissue, in a cDNA library made from fetal spleen tissue and in a cDNA library made from hip derived rheumatoid synovium. Nucleotide sequences encoding ADEC have also been identified in adherent monocyte cultured for 3 hours and in cultured T-cells. Nucleotide sequences encoding ADEC have not bee found in adherent monocytes cultured for 72 hours or in T-cells treated with phorbol myristic acid (PMA).

It would be useful to have a diagnostic test for detection of the expression of ADEC in tissues where it is identified. Activation of neutrophils and fibroblasts which respond by producing abundant proteases and other molecules which can lead to tissue damage or destruction. Therefore, a diagnostic test for excess expression of ADEC can accelerate diagnosis and proper treatment of the inflammation before extensive tissue damage or destruction occurs

Recent evidence suggests that while the C-X-C chemokine family of chemotatic cytokine appear to have inflammatory activities, they display disparate effects in mediating angiogenesi as a function or the presence or absence of the ELR domain (Strieter A and B supra ). The non- ELR C-X-C chemokines have been shown to inhibit angiogenesis. Accordingly, ADEC, or fragments thereof, may be used to prevent or treat angiogenesis-dependent disorders, such as tumorgenesis, rheumatoid arthritis, scleroderma, and psoriasis.

Nucleotide sequences encoding ADEC, or their complements, have numerous applications in techniques known to those skilled in the art of molecular biology. These techniques include use as hybridization probes, use as oligomers for PCR, use for chromosome and gene mapping, use in the recombinant production of ADEC, and use in generation of anti-sense DNA or RNA, their chemical analogs and the like. Uses of nucleotides encoding ADEC disclosed herein are exemplary of known techniques and are not intended to limit their use in any technique known t a person of ordinary skill in the art. Furthermore, the nucleotide sequences disclosed herein may be used in molecular biology techniques that have not yet been developed, provided the new techniques rely on properties of nucleotide sequences that are currently known, e.g., the triple genetic code, specific base pair interactions.

It will be appreciated by those skilled in the art that as a result of the degeneracy of the genetic code, a multitude of ADEC-encoding nucleotide sequences, some bearing minimal nucleotide sequence homology to the nucleotide sequence of any known and naturally occurring gene may be produced as long as the nucleotide sequence encodes ADEC. The invention has specifically contemplated each and every possible variation of nucleotide sequence that could be made by selecting combinations based on possible codon choices. These combinations are made i accordance with the standard triplet genetic code as applied to the nucleotide sequence of naturally occurring ADEC, and all such variations are to be considered as being specifically disclosed.

Although nucleotide sequences which encode ADEC and/or ADEC variants are preferably capable of hybridizing to the nucleotide sequence of the naturally occurring ADEC gene under stringent conditions, it may be advantageous to produce nucleotide sequences encoding ADEC or ADEC derivatives possessing a substantially different codon usage. Codons can be selected to increase the rate at which expression of the peptide occurs in a particular prokaryotic or eukaryotic expression host in accordance with the frequency with which particular codons are utilized by the host. Other reasons for substantially altering the nucleotide sequence encoding ADEC and/or ADEC derivatives without altering the encoded amino acid sequence include the production of RNA transcripts having more desirable properties, e.g., a greater half-life, than transcripts produced from the naturally occurring nucleotide sequence.

Nucleotide sequences encoding ADEC may be joined to a variety of other nucleotide sequences by means of well established recombinant DNA techniques (cf Sambrook J et al.

(1989) Molecular Cloning: A Laboratory Manual, 2d Ed, Cold Spring Harbor, NY).

Useful nucleotide sequences for joining to adec include an assortment of cloning vectors, e.g., plasmids, cosmids, lambda phage derivatives, phagemids, and the like, that are known in the art. Vectors of interest include expression vectors, replication vectors, probe generation vectors, sequencing vectors, and the like. In general, vectors of interest may contain an origin of replication functional in at least one organism, convenient restriction endonuclease sensitive sites, and selectable markers for the host cell.

Another aspect of the subject invention is to provide for adec-specific nucleic acid hybridization probes capable of hybridizing with naturally occurring nucleotide sequences encoding ADEC. Such probes for the detection of ADEC encoding sequences should preferably contain a nucleotide fragment from a non-conserved region of SEQ ID NO: 1. Such probes for the detection of related chemokine encoding sequences should preferably contain at least 50% of the nucleotides from a C-X-C or C-C encoding sequence. The hybridization probes of the subject invention may be derived from the nucleotide sequences of the SEQ ID NO: 1 or from genomic sequences including promoters, enhancer elements and introns of naturally occurring adec.

Hybridization probes may be labeled by a variety of reporter groups, including radionuclides such as 32p or 35s, or enzymatic labels such as alkaline phosphatase, coupled to the probe via avidin/biotin coupling systems, and the like through techniques known to those of skill in the art. PCR as described U.S. Patents 4,965,188 and 4,683,195 and 4,800,195 provides additional uses for oligonucleotides based upon the nucleotide sequences which encode ADEC. Such probes used in PCR may be of recombinant origin, may be chemically synthesized, or a mixture of both and comprise a discrete nucleotide sequence for diagnostic use or a degenerate pool of possible sequences for identification of closely related genomic sequences.

Other means of producing adec-specific hybridization probes include the cloning of nucleic acid sequences encoding ADECs and ADEC derivatives into vectors for the production of mRNA probes. Such vectors are known in the art and are commercially available and may be used to synthesize RNA probes in vitro by means of the addition of the appropriate RNA polymerase as T7 or SP6 RNA polymerase and the appropriate radioactively labeled nucleotide

It is now possible to produce a DNA sequence, or portions thereof, encoding ADEC and ADEC derivatives entirely by synthetic chemistry, after which the gene can be inserted into an of the many available DNA vectors using reagents, vectors and cells that are known in the art at the time of the filing of this application. Moreover, synthetic chemistry may be used to introduce mutations into the adec polynucleotide sequence or any portion thereof.

Methods for DNA sequencing are well known in the art. Conventional enzymatic methods employed DNA polymerase Klenow fragment, SEQUENASE® (US Biochemical Corp, Cleveland, OH) or Taq polymerase to extend DNA chains from an oligonucleotide primer annealed to the DN template of interest. Methods have been developed for the use of both single- and double- stranded templates. The chain termination reaction products were electrophoresed on urea- acryiamide gels and detected either by autoradiography (for radionuclide-labeled precursors) or by fluorescence (for fluorescent-labeled precursors). Recent improvements in mechanized reaction preparation, sequencing and analysis using the fluorescent detection method have permitted expansion in the number of sequences that can be determined per day (using machine such as the Catalyst 800 and the Applied Biosystems 373 DNA sequencer).

The nucleotide sequence can be used to construct an assay to detect inflammation and disease associated with abnormal levels of expression of ADEC. The nucleotide sequence can be labeled by methods known in the art and added to a fluid or tissue sample from a patient under hybridizing conditions. After an incubation period, the sample is washed with a compatible flui which optionally contains a dye (or other label requiring a developer) if the nucleotide has bee labeled with an enzyme. After the compatible fluid is rinsed off, the dye is quantitated and compared with a standard. If the amount of dye is significantly elevated, the nucleotide sequenc has hybridized with the sample. If adec is present at an abnormal level, the assay indicates the presence of inflammation and/or disease. The nucleotide sequence for adec can be used to construct hybridization probes for mapping that gene. The nucleotide sequence provided herein may be mapped to a chromosome and specific regions of a chromosome using well known genetic and/or chromosomal mapping techniques. These techniques include in situ hybridization, linkage analysis against known chromosomal markers, hybridization screening with libraries or flow-sorted chromosomal preparations specific to known chromosomes, and the like. The technique of fluorescent in situ hybridization of chromosome spreads has been described, among other places, in Verma et al (1988) Human Chromosomes: A Manual of Basic Techniques, Pergamon Press, NYC.

Fluorescent in_silu hybridization of chromosomal preparations and other physical chromosome mapping techniques may be correlated with additional genetic map data. Examples of genetic map data can be found in O'Brien (1990) Genetic Maps: Locus Maps of Complex Genomes, Book 5: Human Maps, Cold Spring Harbor Laboratory, NY. Correlation between the location of adec on a physical chromosomal map and a specific disease (or predisposition to a specific disease) can help delimit the region of DNA associated with that genetic disease. The nucleotide sequence of the subject invention may be used to detect differences in gene sequence between normal, carrrier and affected individuals, i.e. Individuals subject to a disease or condition.

Nucleotide sequences encoding ADEC may be used to produce purified ADEC using well known methods of recombinant DNA technology. Among the many publications that teach methods for the expression of genes after they have been isolated is Goeddel (1990) Gene Expression Technology, Methods and Enzymology. Vol 185, Academic Press, San Diego. ADEC may be expressed in a variety of host cells, either prokaryotic or eukaryotic. Host cells may be from species either the same or different from the species in which adec nucleotide sequences are endogenous. Advantages of producing ADEC by recombinant DNA technology include obtaining highly enriched sources of the proteins for purification and the availability of simplified purification procedures.

ADEC may be expressed as a chimeric protein with one or more additional polypeptide domains added to facilitate protein purification. Such purification facilitating domains include, but are not limited to, metal chelating peptides such as histidine-tryptophan modules that allow purification on immobilized metals, protein A domains that allow purification on immobilized immunoglobulin, and the domain utilized in the FLAGS extension/affinity purification system (Immunex Corp, Seattle, WA). The inclusion of a cleavable linker sequence (such as Factor XA or enterokinase) between the purification domain and the ADEC-encoding sequence may be useful to facilitate production of ADEC. Cells transformed with DNA encoding ADEC may be cultured under conditions suitable f the expression of the ADEC and the recovery of the protein from the cell culture. ADEC produc by a recombinant cell may be secreted or may be contained intracellulariy, depending on the particular genetic construction used. In general, it is more convenient to prepare recombinan proteins in secreted form. Purification steps depend on the nature of the production process used and the particular ADEC produced.

Translation of the adec cDNA of the present invention into protein may be accomplished by subcloning the cDNA into an appropriate expression vector and transfecting this vector into an appropriate expression host. As described in -Example VII, a preferred expression vector f the expression and purification of ADEC is one which provides for expression of a fusion protei comprising ADEC and contains nucleic acid encoding 6 histidine residues followed by thioredoxi and an enterokinase cleavage site. The histidine residues facilitate purification on IMIAC (immobilized metal ion affinity chromatography as described in Porath et al. (1992) Protein Expression and Purification 3:263:281) while the enterokinase cleavage site provides a mean for purifying the chemokine from the fusion protein.

The expression vector used for the generation of the cDNA libraries described herein, which provides a promoter for β-galactosidase upstream of the cloning site, followed by a nucleotide sequence containing the amino-terminal Met and the subsequent 7 residues of β- galactosidase followed by a bacteriophage promoter useful for artificial priming and transcription and a number of unique restriction sites (including Eco RI). can also be used for expression of the chemokines of the present invention, induction of the isolated bacterial strai with IPTG using standard methods will produce a fusion protein corresponding to the first seve residues of β-galactosidase, about 15 residues of linker, and ADEC encoded within the cDNA. Since cDNA clone inserts are generated by an essentially random process, there is one chance i three that the included cDNA will lie in the correct frame for proper translation. If the cDNA i not in the proper reading frame, it can be obtained by deletion or insertion of the appropriate number of bases by well known methods including jn vitro mutagenesis, digestion with exonuclease III or mung bean nuclease, or oligonucleotide linker inclusion. ADEC will be expressed in the bacterial system as described. An ADEC encoding nucleotide sequence of the present invention can be shuttled to vectors known to be useful for expression of protein in specific hosts. Oligonucleotide amplimers containing cloning sites as well as a segment of DNA sufficient to hybridize to stretches at both ends of the target cDNA (25 bases) can be synthesized chemically by standard methods. These primers can then be used to amplify the desired gene segments by PCR. The resulting new gene segments can be digested with appropriate restriction enzymes Under standard conditions and isolated by gel electrophoresis. Alternately, similar gene segments can be produced by digestion of the nucleotide sequence with appropriate restriction enzymes and filling in the missing gene segments with chemically synthesized oligonucleotides. Segments of the coding sequence from more than one gene can be iigated together and cloned in appropriate vectors to optimize expression of recombinant sequence.

Suitable expression hosts for such chimeric molecules include but are not limited to mammalian cells such as Chinese Hamster Ovary and human 293 cells, insect cells such as Sf9 cells, yeast cells such as Saccharomyces cerevisiae. and bacteria such as £ G&li- For each of these cell systems, a useful expression vector may also include an origin of replication to allow propagation in bacteria and a selectable marker, such as the β-iactamase antibiotic resistance gene, to allow selection in bacteria. In addition, the vectors may include a second selectable marker, such as the neomycin phosphotransferase gene, to allow selection in transfected eukaryotic host cells. Vectors for use in eukaryotic expression hosts may require RNA processing elements such as 3' polyadenylation sequences if such are not part of the cDNA of interest.

Additionally, the vector may contain promoters or enhancers which increase gene expression. Such promoters are host specific and include MMTV, SV40, or metallothionine promoters for CHO cells; tip, lac, tac or T7 promoters for bacterial hosts, or alpha factor, alcohol oxidase or PGH promoters for yeast. Transcription enhancers, such as the RSV enhancer, may be used in mammalian host cells. Once homogeneous cultures of recombinant cells are obtained through standard culture methods, large quantities of recombinantly produced ADEC can be recovered from the conditioned medium and analyzed using chromatographic methods known in the art. In addition to recombinant production, ADEC fragments may be produced by direct peptide synthesis using solid-phase techniques (cf Stewart et al (1969) Solid-Phase Peptide Synthesis, WH Freeman Co. San Francisco; Merrifield R (1963) J Am Chem Soc 85:2149- 2154. In vitro protein synthesis may be performed using manual techniques or by automation. Automated synthesis may be achieved, for example, using Applied Biosystems 431 A Peptide Synthesizer (Foster City, California) in accordance with the instructions provided by the manufacturer. Various fragments of ADEC may be chemically synthesized separately and combined using chemical methods to produce full length ADEC.

ADEC for use in the induction of antibodies must have immunogenic activity. Peptides for use in the induction of ADEC-specific antibodies will comprise an amino acid sequence consisting of at least five amino acids and preferably at least 10 amino acids such that the peptide retains the three-dimensional configuration of a portion of the naturally occurring ADEC and may contain the entire amino acid sequence of the naturally occurring ADEC. Short stretches of ADE amino acids may be fused with those of another protein such as keyhole limpet hemocyanin and the chimeric molecule used for antibody production.

Various methods are known to those of skill in the art for preparing monoclonal and polyclonal antibodies to ADECs of the present invention. In one approach, denatured ADEC fro the reverse phase HPLC separation is obtained and used to immunize mice or rabbits using techniques known to those of skill in the art. About 100 micrograms are adequate for immunization of a mouse, while up to 1 mg can be used for immunization of a rabbit. For identifying mouse hybridomas, the denatured protein can be radioiodinated and used to screen potential murine B-cell hybridomas for those which produce antibody. This procedure requir only small quantities of protein, such that 20 mg would be sufficient for labeling and screenin of several thousand clones. In another approach, the amino acid sequence of ADEC, as deduced from the cDNA seque analyzed to determine regions of high immunogenicity. Polypeptides comprising these regions synthesized and used in suitable immunization protocols to raise antibodies. Analysis to select appropriate epitopes is described by Ausubel FM et al (1989, Current Protocols in Molecular Biology, Vol 2. John Wiley & Sons). The optimal amino acid sequences for immunization are usually at the C-terminus, the N-terminus and those intervening, hydrophilic regions of the polypeptide which are likely to be exposed to the external environment when the protein is in natural conformation.

Typically, selected peptides, about 15 residues in length, are synthesized using an Applied Biosystems Peptide Synthesizer Model 431 A using fmoc-chemistry and coupled to keyhole limpet hemocyanin (KLH, Sigma) by reaction with M- maieimidobenzoyl-N- hydroxysuccinimide ester (MBS; cf. Ausubel FM et al, supra). If necessary, a cysteine may b introduced at the N-terminus of the peptide to permit coupling to KLH and animals are immunized with the peptide-KLH complex in complete Freund's adjuvant. The resulting antisera are tested for antipeptide activity by binding the peptide to plastic, blocking with 1% BSA, reacting with antisera, washing and reacting with labeled (radioactive or fluorescent), affinity purified, specific goat anti-rabbit IgG.

Hybridomas may also be prepared and screened using standard techniques. Hybridomas of interest are detected by screening with labeled ADEC to identify those fusions producing the monoclonal antibody with the desired specificity. For example, in a typical protocol, wells of plates (FAST, Becton-Dickinson, Palo Alto, CA) are coated with affinity purified, specific rabbit-anti-mouse (or suitable anti-species Ig) antibodies at about 10 mg/ml. The coated wells are blocked with 1% BSA, washed and exposed to supematants from hybridomas. After incubation the wells are exposed to labeled ADEC at a concentration of about 1 mg/ml. Clones producing antibodies will bind a quantity of labeled ADEC which is detectable above background. Such clones are expanded and subjected to 2 cycles of cloning at limiting dilution (1 cell/3 wells). Cloned hybridomas are injected into pristane-treated mice to produce ascites, and monoclonal antibody is purified from mouse ascitic fluid by affinity chromatography using Protein A. Monoclonal antibodies with affinities of at least 108 M-1, preferably 109 to 10"> or stronger, will typically be made by standard procedures as described in Harlow and Lane

(1988) Antibodies: A Laboratory Manual_* Cold Spring Harbor Laboratory, NY, or Goding (1986) Monoclonal Antibodies: Principles and Practice, 2d Ed. Academic Press New York City, both incorporated herein by reference.

Antibodies specific for a particular ADEC sequence may be produced by inoculation of an appropriate animal with the ADEC sequence. An antibody is specific for ADEC if the antibody is produced against all or part of the ADEC polypeptide as disclosed in SEQ ID NO:2 and binds to all or part of the protein. Induction of antibodies includes not only the stimulation of an immune response by injection into animals, but also analogous steps in the production of synthetic antibodies or other specific-binding molecules such as the screening of recombinant immunoglobulin libraries (cf Orlandi et al (1989) PNAS 86:3833-3837, or Huse et al

(1989) Science 256:1275-1281) or the in vitro stimulation of lymphocyte populations. Current technology (Winter and Milstein (1991) Nature 349:293-299) provides for a number of highly specific binding reagents based on the principles of antibody formation. These techniques may readily be adapted to produce molecules capable of specifically binding ADEC. An ADEC encoding polynucleotide may be useful in the treatment of various abnormal conditions associated with angiogenesis, such as for example, tumorgenesis, rheumatoid arthritis, scleroderma, and psoriasis. By introducing ADEC gene sequences into cells, gene therapy can be used to treat conditions characterized by underexpression of ADEC or overexpression of sequences that are associated with angiogenesis-associated disease states. In some instances, the polynucleotide encoding ADEC is intended to replace or act in the place of a functionally deficient endogenous gene. Alternatively, ADEC, or fragments thereof, may be used in the treatment of diseases or conditions associated with angiogenesis.

Expression vectors derived from viruses such as retroviruses, vaccinia virus, adeno- associated virus, herpes viruses, or bovine papilloma virus, may be used for delivery of nucleotide sequences encoding ADEC into the targeted cell population. Methods which are well known to those skilled in the art can be used to construct recombinant viral vectors containing an ADEC polynucleotide sequence. See, for example, the techniques described in Maniatis et al., 1989, Molecular Cloning A Laboratory Manual, Cold Spring Harbor Laboratory, N.Y. and Ausubel βt al., 1989, Current Protocols in Molecular Biology, Greene Publishing Associates an Wiley Interscience, N.Y. Alternatively, recombinant ADEC molecules can be reconstituted into liposomes for delivery to target cells. Accordingly, the present invention provides a pharmaceutical composition for treating disease states associated with angiogenesis comprisin an effective amount of the polynucleotide sequence encoding ADEC and a pharmaceutically acceptable carrier. The present invention further provides a method of treating a patient subject to a disease state associated with angiogenesis comprising administering an effective amount of the polynucleotide encoding ADEC to said patient. Alternatively, abnormal conditions characterized by over expression of ADEC, such as conditions associated with inflammation, ca be treated by using gene therapy techniques to introduce anti-sense nucleic acid into cells to inhibit the translation of ADEC mRNA.

Antibodies, inhibitors, antisense molecules, receptors or analogs of ADEC (treatments for excessive ADEC production, hereafter abbreviated TEC") can provide different effects when administered therapeutically. The TECs will be formulated in a nontoxic, inert, pharmaceutically acceptable aqueous carrier medium preferably at a pH of about 5 to 8, more preferably 6 to 8, although the pH may vary according to the characteristics of the antibody, inhibitor, receptor or analog being formulated and the condition to be treated. Characteristics of the TEC include solubility of the molecule, half-life and antigenicity/immunogenicity and may aid in defining an effective carrier. Naturally occurring human proteins are preferred as TECs, but organic molecules resulting from drug screens may be equally effective in particula situations.

TECs may be delivered by known routes of administration including but not limited to topical creams or gels; transmucosa! spray or aerosol, transdermal patch or bandage; injectable, intravenous or lavage formulations; or orally administered liquids or pills. The particular formulation, exact dosage, and route of administration will be determined by the attending physician and will vary according to each specific situation.

Such determinations are made by considering multiple variables such as the condition t be treated, the TEC to be administered, and the pharmacokinetic profile of the particular TEC. Additional factors which may be taken into account include the severity of the disease state, the patient, age, weight, gender, diet, time of administration, drug combination, reaction sensitivities, and tolerance/response to therapy. Long acting TEC formulations might be administered every 3 to 4 days, every week, or once every two weeks depending on half-life and clearance rate of the particular TEC.

Normal dosage amounts may vary from 0.1 to 100,000 micrograms, up to a total dose of about 1 g, depending upon the route of administration. Guidance as to particular dosages for the TECs is provided in the literature; see U.S. Patents 4,657,760; 5,206,344; or 5,225,212. It is anticipated that different formulations will be effective for different TECs and that administration targeting the liver may necessitate delivery in a manner different from that for delivery targeted to the pituitary gland. It is contemplated that a condition associated with inflamed adenoid or disease which activates leukocytes, particularly monocytes and macrophages, and precipitates permanent damage may be treatable with TECs. These conditions or diseases may be specifically diagnosed by the diagnostic tests discussed inlra. such testing should be performed, for example, in patients suspected of being subject to Epstein-Barr virus, Hodgkin's disease, and various neoplasms or nonspecific pharyngitis.

The examples below are provided to illustrate the subject invention. These examples are provided by way of illustration and are not included for the purpose of limiting the invention.

EXAMPLES

I Isolation of mRNA and construction of cDNA libraries

The adec cDNA sequence was initially identified among the polynucleotide sequences comprising the inflamed adenoid library. This library was constructed from mixed adenoid and tonsil lymphoid tissue surgically removed from a child during a tonsiiectomy. The adenoid tissue was obtained from University of California at Los Angeles and frozen for future use. The frozen tissue was ground in a mortar and pestle and lysed immediately in buffer containing guanidinium isothiocyanate (cf Chirgwin JM et al (1979) Biochemistry 18:5294). Lysis was followed by several phenol-chloroform extractions and ethanol precipitations. Poly-A-t- mRNA was isolated using biotinylated oligo d(T) and streptavidin coupled to paramagnetic particles (Poly(A) Tract Isolation System; Promega, Madison, Wl).

The poly A mRNA from the inflamed adenoid tissue was used by Stratagene Inc (11011 N. Torrey Pines Rd., La Jolla, CA 92037) to construct a cDNA library. cDNA synthesis was primed using oligo dT and or random hexamers. Synthetic adapter oligonucleotides were ligated onto cDNA ends enabling its insertion into the UNI-ZAP™ vector system (Stratagene Inc). This allows high efficiency unidirectional (sense orientation) lambda library construction and the convenience of a plasmid system with blue/white color selection to detect clones with cDNA insertions.

The quality of the each cDNA library was screened using either DNA probes or antibody probes, and then the pBluescript® phagemid (Stratagene inc) was rapidly excised in living cells. The phagemid allows the use of a plasmid system for easy insert characterization, sequencing, site-directed mutagenesis, the creation of unidirectional deletions and expression fusion proteins. Phage particles from each library were infected into the E. coli host strain XL1-BLUE® (Stratagene Inc.). The high transformation efficiency of XL1-BLUE increases th probability of obtaining rare, under-represented clones from the cDNA library.

II Isolation of cDNA Clones The phagemid forms of individual cDNA clones were obtained by the in vivo excision process, in which XL1-BLUE was coinfected with an f1 helper phage. Proteins derived from both lambda phage and f 1 helper phage initiated new DNA synthesis from defined sequences on the lambda target DNA and created a smaller, single stranded circular phagemid DNA molecule that included all DNA sequences of the pBluescript plasmid and the cDNA insert. The phagemid DNA was released from the ceils and purified, then used to re-infect fresh bacterial host cells

(SOLR, Stratagene Inc.), where the double stranded phagemid DNA was produced. Because the phagemid carries the gene for β-lactamase, the newly transformed bacteria were selected on medium containing ampicillin.

Phagemid DNA was purified using the QIAWELL-8 Plasmid Purification System from QIAGEN® DNA Purification System (QIAGEN Inc., 9259 Eton Ave., Chatsworth, CA 91311). This technique provides a rapid and reliable high-throughput method for lysing the bacterial cells and isolating highly purified phagemid DNA. The DNA eluted from the purification resin was suitable for DNA sequencing and other analytical manipulations.

III Sequencing of cDNA Clones

The cDNA inserts from random isolates of the inflamed adenoid library were sequenced part. The cDNAS were sequenced by the method of Sanger F. And AR Coulson (1975; J. Mol. Bi 94:441 f), using a Hamilton Micro Lab 2200 (Hamilton, Reno NV) in combination with four Peltier Thermal Cyclers (PTC200 from MJ Research, Watertown MA) and Applied Biosystems 377 or 373 DNA Sequencing Systems (Perkin Elmer) and reading frame determined.

ιv Homology Searching of cDNA Clones and Deduced Protein

Each cDNA was compared to sequences in GenBank using a search algorithm developed by Applied Biosystems and incorporated into the INHERIT™ 670 Sequence Analysis System. In this algorithm, Pattern Specification Language (TRW Inc, Los Angeles CA) was used to determine regions of homology. The three parameters that determine how the sequence comparisons run were window size, window offset, and error tolerance. Using a combination of these three parameters, the DNA database was searched for sequences containing regions of homology to the query sequence, and the appropriate sequences were scored with an initial value. Subsequently, these homologous regions were examined using dot matrix homology plots to distinguish regions of homology from chance matches. Smith-Waterman alignments were used to display the results of the homology search.

Peptide and protein sequence homoiogies were ascertained using the INHERIT™ 670 Sequence Analysis System in a way similar to that used in DNA sequence homoiogies. Pattern

Specification Language and parameter windows were used to search protein databases for sequences containing regions of homology which were scored with an initial value. Dot-matrix homology plots were examined to distinguish regions of significant homology from chance matches. BLAST, which stands for Basic Local Alignment Search Tool (Altschul SF (1993) J Mol

Evol 36:290-300; Altschul, SF et al (1990) J Mol Biol 215:403-10), was used to search for local sequence alignments . BLAST produces alignments of both nucleotide and amino acid sequences to determine sequence similarity. Because of the local nature of the alignments, BLAST is especially useful in determining exact matches or in identifying homologs. BLAST is useful for matches which do not contain gaps. The fundamental unit of BLAST algorithm output is the High-scoring Segment Pair (HSP).

An HSP consists of two sequence fragments of arbitrary but equal lengths whose alignment is locally maximal and for which the alignment score meets or exceeds a threshold or cutoff score set by the user. The BLAST approach is to look for HSPs between a query sequence and a database sequence, to evaluate the statistical significance of any matches found, and to report only those matches which satisfy the user-selected threshold of significance. The parameter E establishes the statistically significant threshold for reporting database sequence matches. E is interpreted as the upper bound of the expected frequency of chance occurrence of an HSP (or set of HSPs) within the context of the entire database search. Any database sequence whose match satisfies E is reported in the program output.

The nucleotide and amino acid sequences for the adenoid expressed chemokine, ADEC are shown in SEQ ID NO:1 and SEQ ID NO:2, respectively.

V Identification and Full Length Sequencing of the Gene

From all of the randomly picked and sequenced clones of the inflamed adenoid library, adec sequences were homologous to but clearly different from any known C-X-C chemokine molecule. The nucleotide sequence for adec was found within Incyte clone 20293. When all three possible predicted translations of the sequence were searched against protein databases such as SwissProt and PIR, no exact matches were found to the possible translations of adec. Figure 2 shows the comparison of ADEC with other a chemokine molecules; substantial regions of homology including the C-X-C motif are shaded. The phylogenetic analysis, however, show that ADEC is not very closely related to other well characterized human C-X-C chemokines (Figure 3). The most related of these molecules cluster together at the right hand side of the figure. It appears that ADEC may represent a new subfamily or variant of the C-X-C chemokines.

VI Antisense anelvela

Knowledge of the correct, complete cDNA sequences of ADEC enables its use in antisense technology in the investigation of gene function. Either oligonucleotides, genomic or cDNA fragments comprising the antisense strand of polynucleotide sequences encoding ADEC can be used either in vitro or in vivo to inhibit expression of the specific protein. Such technology i now well known in the art, and probes can be designed at various locations along the nucleotide sequence. By treatment of cells or whole test animals with such antisense sequences, the gene interest can be effectively turned off. Frequently, the function of the gene can be ascertained observing behavior at the cellular, tissue or organismal level (e.g. lethality, loss of differentiated function, changes in morphology, etc.).

In addition to using sequences constructed to interrupt transcription of the open readin frame, modifications of gene expression can be obtained by designing antisense sequences to intron regions, promoter/enhancer elements, or even to trans-acting regulatory genes.

Similarly, inhibition can be achieved using Hogeboom base-pairing methodology, also known a "triple helix" base pairing.

VII Expression of ADEC The nucleotide sequences encoding ADEC were cloned into an expression vector that comprises a T7 promoter followed by an initiating methionine codon (ATG), followed by six histidine codons, followed by the TrxA gene of J fi--li (which encodes thioredoxin), followed by a sequence coding for an enterokinase cleavage site and nucleotide sequences encoding ADEC. For ADEC, the N-terminal residue of the expressed protein is residue 24, Leu, of SEQ ID NO:2.

The expression vectors described above containing the 6 histidine codons were used to transform a host cell, the host cell culture was induced with IPTG and the expressed protein was subjected to denaturing SDS poly acrylamide gel electrophoresis. Nucleic acid from the expression vector was partially purified using the miniprep procedure of Sambrook supra which produced super-coiled DNA. About 100 ng of DNA were used to transform the host bacterial cell, W3110/DE3. W3110/DE3 was constructed using W3110 from the ATCC and the lambda DE3 lysogenization kit commerically available from Novagen. DE3 lysogens are often less competent than their parent, W3110, and are adapted to use super-coiled DNA for efficient transformation. A single transformant from each chemokine transformation was selected and used to inoculate a 5 ml culture of L-broth containing ampicillin. Each 5 ml culture was grown overnight (12-15 hours) at 37 degrees C. with shaking. The next day, 1 ml of the overnight culture was used to inoculate a 100 ml culture of L-broth with ampicillin in a 500 ml flask and allowed to grow at 37 degrees C. with shaking until the OD600 of the culture reached 0.4-0.6. If inoculated cells are allowed to grow past an OD600 of 0.6, they will begin to reach stationary phase and induction levels will be reduced.

At the time of inoculation, a 5 ml sample was removed, placed on ice and used as a pre- induction (or 0 hour) sample. When the cell culture reached an OD600 of 0.6, 400μl of an 100mM IPTG stock solution was added for a final concentration of 0.4mM. The cultures were allowed to grow for 3 hours at 37 degrees C. with shaking. Analysis of induction was determined by sampling 5 ml aiiquots of the culture at 1 hour intervals up to 6 hours and analysing on a denaturing SDS poly acrylamide gel electrophoresis. The fusion protein appeared to accumulate in the insoluble fraction of the cells.

Maximal induction of ADEC occurred by 2 hours. Growth beyond 4 hours resulted in lysis in the culture and overall reduced yields of the desired protein due to proteolysis. Five ml aiiquots of the cell cultures were obtained at 0, 1 and 2 hours and centrifuged for 5 minutes at 3000 RPM at 4 degrees C. The supernatant was aspirated and the pellets were subjected to a freeze-thaw step to help lyse the cells. The pellet was resuspended in TE [10mM Tris-HCL pH 8.0, 1mM EDTA pH 8.0] at 4 degrees C. at a volume calculated as: vol TE(μl) = (OD600)(250), and an equivalent volume of 2X SDS Sample Loading Buffer (Novex) was adde to each sample. The samples were boiled for 5 minutes and 10μl of each sample was loaded pe lane. The results of the gel electrophoresis show that the ADEC fusion protein migrated at 24 KD molecular weight (with an expected weight of 24093 Daltons) on a denaturing SDS gel.

VIM Isolation of Recombinant APEC

ADEC was expressed as a chimeric protein having six histidines followed by the thioredoxin (TrxA) gene of ] _CQli with an enterokinase cleavage site between the TrxA protein and ADEC. The histidines were added to facilitate protein purification. The presence of the histidines allows for purification on I Ml AC chromatography (Porath supra).

IX Production of ADEC-Speclfic Antibodies Polyclonal antibodies to PGEC were prepared by injecting rabbits with about 100 micrograms of electrophoresis purified PGEC fusion protein as described in Section VII. At about 8 weeks after injection of primary antigen, potyclonal antisera was collected. Polyclon antibodies to a peptide of ADEC, consisting of ADEC residues 25 through 42 of SEQ ID NO:2, we prepared by standard methods.

X Diagnoatic Test Using ADEC-Speclfic Antibodies

Particular ADEC antibodies are useful for the diagnosis of prepathologic conditions, and chronic or acute diseases which are characterized by differences in the amount or distribution of ADEC. ADEC is likely to be specific for abnormalities or pathologies of particular tissues from which it has been identified.

Diagnostic tests for ADEC include methods utilizing the antibody and a label to detect ADEC in human body fluids, tissues or extracts of such tissues. The polypeptides and antibodie of the present invention may be used with or without modification. Frequently, the polypeptid and antibodies will be labeled by joining them, either covalently or noncovalently, with a substance which provides for a detectable signal. A wide variety of labels and conjugation techniques are known and have been reported extensively in both the scientific and patent literature. Suitable labels include radionuclides, enzymes, substrates, cofactors, inhibitors, fluorescent agents, chemiluminescent agents, magnetic particles and the like. Patents teaching the use of such labels include U.S. Patent Nos. 3,817,837; 3,850,752; 3,939,350; 3,996,345; 4,277,437; 4,275,149; and 4,366,241. Also, recombinant immunoglobulins may be produced as shown in U.S. Patent No. 4,816,567, incorporated herein by reference. A variety of protocols for measuring soluble or membrane-bound ADEC, using either potyclonal or monoclonal antibodies specific for that ADEC are known in the art. Examples include enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA) and fluorescent activated cell sorting (FACS). A two-site monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering epitopes on ADEC is preferred, but a competitive binding assay may be employed. These assays are described, among other places, in Maddox, DE et al (1983, J Exp Med 158:1211).

XI Purification of Native ADEC Using Specific Antibodies

Native or recombinant ADEC was purified by immunoaffinity chromatography using ADEC-specific antibodies. In general, an immunoaffinity column is constructed by covalently coupling the anti-ADEC antibody to an activated chromatographic resin. Polyclonal immunoglobulins are prepared as in Example IX and monoclonal antibodies are prepared from mouse ascites fluid by ammonium sulfate precipitation or chromoatorgraphy on imrnobililzed Protein A. Partially purified immunoglobulin is covalently attached to a chromatographic resin such as CnBr-activated Sepharose (Pharmacia LKB Biotechnology). The antibody is coupled to the resin, the resin is blocked, and the derivative resin is washed according to the manufacturer's instructions.

Such an immunoaffinity column is utilized in the purification of ADEC by preparing a fraction from cells containing ADEC in a soluble form. Soluble ADEC is derived by solubilizing the whole cell or of a subcellular fraction obtained via differential centrifugation by the addition of detergent or by other methods well known in the art. Alternatively, soluble ADEC containing a signal sequence may be secreted in useful quantity into the medium in which the cells are grown.

A soluble ADEC-containing preparation is passed over an immunoaffinity column, and the column is washed under conditions that allow the preferential absorbance of ADEC (eg, high ionic strength buffers in the presence of detergent). ADEC is eluted from the column under conditions that disrupt antibody/ADEC binding (e.g., a buffer of pH 2-3 or a high concentration of a chaotrope such as urea or thiocyanate ion), and the ADEC was collected.

X I I Determination of ADEC-lnduced Chemotaxis or Cell Activation

The chemotactic activity of ADEC is measured in a 48-well microchemotaxis chamber (Falk WR et al (1980) J Immunol Methods 33:239). In each well, two compartments are separated by a filter that allows the passage of cells in response to a chemical gradient. Cell culture medium such as RPMI 1640 containing ADEC is placed on one side of a filter, usually polycarbonate, and cells suspended in the same media are placed on the opposite side of the filt Sufficient incubation time is allowed for the cells to traverse the filter in response to the concentration gradient across the filter. Filters are recovered from each well, and cells adhering to the side of the filter facing ADEC are typed and quantified.

The specificity of the chemoattraction is determined by performing the chemotaxis ass on specific populations of cells. First, blood cells obtained from venipuncture are fractionate by density gradient centrifugation and the chemotactic activity of ADEC is tested on enriched populations of neutrophils, peripheral blood mononuclear cells, monocytes and lymphocytes. Optionally, such enriched cell populations are further fractionated using CD8+ and CD4+ specific antibodies for negative selection of CD4+ and CD8+ enriched T-cell populations, respectively.

Another assay elucidates the chemotactic effect of ADEC on activated T-cells. There, unfractionated T-cells or fractionated T-cell subsets are cultured for 6 to 8 hours in tissue culture vessels coated with CD-3 antibody. After this CD-3 activation, the chemotactic activ of ADEC is tested as described above. Many other methods for obtaining enriched cell populatio are known to those of skill in the art.

Some chemokines also produce a non-chemotactic cell activation of neutrophils and monocytes. This is tested via standard measures of neutrophil activation such as actin polymerization, increase in respiratory burst activity, degranulation of the azurophilic gran and mobilization of Ca++ as part of the signal transduction pathway. The assay for mobilizati of Ca++ involves preloading neutrophils with a fluorescent probe whose emission characteristics have been altered by Ca++ binding. When the cells are exposed to an activatin stimulus, Ca++ flux is determined by observation of the cells in a fluorometer. The measurement of Ca++ mobilization has been described in Grynkievicz G et al. (1985) J Biol Chem 260:3440, and McColl S et al. (1993) J Immunol 150:4550-4555, incorporated her by reference.

Degranulation and respiratory burst responses are also measured in monocytes (Zachariae COC et al. (1990) J Exp Med 171: 2177-82). Further measures of monocyte activation are regulation of adhesion molecule expression and cytokine production (Jiang Y et (1992) J Immunol 148: 2423-8). Expression of adhesion molecules also varies with lymphocyte activation (Taub D et al. (1993) Science 260: 355-358). XIII Drug Screening

ADEC, or fragments thereof, are particularly useful for screening compounds in any of a variety of drug screening techniques. The ADEC polypeptide or fragment employed in such a test may either be free in solution, affixed to a solid support, borne on a cell surface or located intracellularly. One method of drug screening utilizes eukaryotic or prokaryotic host cells which are stably transformed with recombinant nucleic acids expressing the polypeptide or fragments thereof. Drugs are screened against such transformed cells in competitive binding assays. Such cells, either in viable or fixed form, can be used for standard binding assays. One may measure, for example, the formation of complexes between ADEC or fragment and the agent being tested or examine the diminution in complex formation between ADEC and a neutrophil or fibroblast caused by the agent being tested.

Thus, the present invention provides methods of screening for drugs or other agents which can affect inflammation and disease. These methods comprise contacting such an agent with an ADEC polypeptide or fragment thereof and assaying (i) for the presence of a complex between the agent and the ADEC polypeptide or fragment, or (ii) for the presence of a complex between the ADEC polypeptide or fragment and the cell, by methods well known in the art. In such competitive binding assays, the ADEC polypeptide or fragment is typically labeled. After suitable incubation, free ADEC polypeptide or fragment is separated from that present in bound form, and the amount of free or uncomplexed label is a measure Of the ability of the particular agent to bind to ADEC or to interfere with the ADEC/cell complex.

Another technique for drug screening provides high throughput screening for compounds having suitable binding affinity to the ADEC polypeptides and is described in detail in European Patent Application 84/03564, published on September 13, 1984, incorporated herein by reference. Briefly stated, large numbers of different small peptide test compounds are synthesized on a solid substrate, such as plastic pins or some other surface. The peptide test compounds are reacted with ADEC polypeptide and washed. Bound ADEC polypeptide is then detected by methods well known in the art. Purified ADEC can also be coated directly onto plates for use in the aforementioned drug screening techniques, in addition, non-neutralizing antibodies can be used to capture the peptide and immobilize it on the solid support. This invention also contemplates the use of competitive drug screening assays in which neutralizing antibodies capable of binding ADEC specifically compete with a test compound for binding to ADEC polypeptide or fragments thereof. In this manner, the antibodies can be used to detect the presence of any peptide which shares one or more antigenic determinants with ADEC. XIV Rational Drug Design

The goal of rational drug design is to produce structural analogs of biologically active polypeptides of interest or of small molecules with which they interact, e.g., agonists, antagonists, or inhibitors. Any of these examples can be used to fashion drugs which are more active or stable forms of the polypeptide or which enhance or interfere with the function of a polypeptide in vivo (cf. Hodgson J (1991) Bio/Technology 9:19-21 , incorporated herein by reference).

In one approach, the three-dimensional structure of ADEC, or of an ADEC-inhibitor complex, is determined by x-ray crystallography, by computer modeling or, most typically, a combination of the two approaches. Both the shape and charges of the polypeptide must be ascertained to elucidate the structure and to determine active site(s) of the molecule. Less often, useful information regarding the structure of a polypeptide may be gained by modeling based on the structure of homologous proteins. In both cases, relevant structural information used to design analogous chemokine-like molecules or to identify efficient inhibitors. Useful examples of rational drug design may include molecules which have improved activity or stability as shown by Braxton S and Wells JA (1992 Biochemistry 31 :7796-7801) or whic act as inhibitors, agonists, or antagonists of native peptides as shown by Athauda SB et al (19 J Biochem 113:742-746), incorporated herein by reference.

It is also possible to isolate a target-specific antibody, selected by functional assay, as described above, and then to solve its crystal structure. This approach, in principle, yields a pharmacore upon which subsequent drug design can be based. It is possible to bypass protein crystallography altogether by generating anti-idiotypic antibodies (anti-ids) to a functional, pharmacologically active antibody. As a mirror image of a mirror image, the binding site of th anti-ids would be expected to be an analog of the original receptor. The anti-id could then be used to identify and isolate peptides from banks of chemically or biologically produced peptides

The isolated peptides would then act as the pharmacore.

By virtue of the present invention, sufficient amount of polypeptide may be made available to perform such analytical studies as X-ray crystallography. In addition, knowledge the ADEC amino acid sequence provided herein will provide guidance to those employing computer modeling techniques in place of or in addition to x-ray crystallography.

XV Identification of ADEC Receptors

Purified ADEC is useful for characterization and purification of specific cell surface receptors and other binding molecules. Cells which respond to ADEC by chemotaxis or other specific responses are likely to express a receptor for ADEC. Radioactive labels may be incorporated into ADEC by various methods known to those of skill in the art. A preferred embodiment is the labeling of primary amino groups in ADEC with ¹²⁵l Bolton-Hunter reagent (Bolton, AE and Hunter, WM (1973) Biochem J 133: 529), which has been used to label other chemokines without concomitant loss of biological activity (Hebert CA et al (1991) J Biol Chem 266: 18989; McColl S et al (1993) J Immunol 150:4550-4555). Receptor-bearing cells are incubated with labeled ADEC. The cells are then washed to removed unbound ADEC, and receptor-bound ADEC is quantified. The data obtained using different concentrations of ADEC are used to calculate values for the number and affinity of receptors. Labeled ADEC is useful as a reagent for purification of its specific receptor. ADEC is covalently coupled to a chromatography column. Receptor-bearing cells are extracted, and the extract is passed over the column. The receptor binds to the column by virtue of its biological affinity for ADEC. The receptor is recovered from the column and subjected to N-terminal protein sequencing. This amino acid sequence is then used to design degenerate oligonucleotide probes for cloning the receptor gene.

In an alternate method, expression cloning, mRNA is obtained from receptor-bearing cells and made into a cDNA expression library. The library is transfected into a population of cells, and those cells in the population which express the receptor are selected using fluorescently labeled ADEC. The receptor is identified by recovering and sequencing recombinant DNA from highly labeled cells.

In another alternate method, monoclonal antibodies are raised against the surface of receptor-bearing ceils and are screened to identify those which inhibit the binding of labeled ADEC. These monoclonal antibodies are then used in affinity purification or expression cloning of the receptor. Soluble receptors or other soluble binding molecules are identified in a similar manner.

Labeled ADEC is incubated with extracts or other appropriate materials derived from inflamed adenoid. After incubation, ADEC complexes larger than the size of purified ADEC are identified by a sizing technique such as size exclusion chromatography or density gradient centrifugation and are purified by methods known in the art. The soluble receptors or binding protein(s) are subjected to N-terminal sequencing to obtain information sufficient for database identification, if the soluble protein is known, or cloning, if the soluble protein is unknown.

All publications and patents mentioned in the above specification are herein incorporated by reference. The foregoing written specification is considered to be sufficient to enable one skilled in the art to practice the invention. Indeed, various modifications of the above describ modes for carrying out the invention which are obvious to those skilled in the field of molecul biology or related fields are intended to be within the scope of the following claims.

SEQUENCE LISTING

(1) GENERAL INFORMATION:

(i) APPLICANT: INCYTE PHARMACEUTICALS, INC.

(ii) TITLE OF INVENTION: A NOVEL CHEMOKINE EXPRESSED IN INFLAMED

ADENOID, ITS PRODUCTION AND USES

(iii) NUMBER OF SEQUENCES: 9

(iv) CORRESPONDENCE ADDRESS:

(A) ADDRESSEE: INCYTE PHARMACEUTICALS, INC.

(B) STREET: 3174 Porter Drive

(C) CITY: Palo Alto

(D) STATE: CA

(E) COUNTRY: USA

(F) ZIP: 94304

(v) COMPUTER READABLE FORM:

(A) MEDIUM TYPE: Floppy disk

(B) COMPUTER: IBM PC compatible

(C) OPERATING SYSTEM: PC-DOS/MS-DOS

(D) SOFTWARE: WordPefect 6.1/MS-DOS 6.2

(vi) CURRENT APPLICATION DATA:

(A) PCT APPLICATION NO. To Be Assigned

(B) FILING DATE: 07-DEC-1995

(C) CLASSIFICATION:

(vii) PRIOR APPLICATION DATA:

(A) APPLICATION SERIAL NO: US 08/352,324

(B) FILING DATE: 07-DEC-1994

(viii) ATTORNEY/AGENT INFORMATION:

(A) NAME: LUTHER, BARBARA J.

(B) REGISTRATION NUMBER: 33954

(C) REFERENCE/DOCKET NUMBER: PF-0025 PCT

(ix) TELECOMMUNICATION INFORMATION:

(A) TELEPHONE: 415-855-0555

(B) TELEFAX: 415-852-0195

(2) INFORMATION FOR SEQ ID NO:l:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 330 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: CDNA

(vii) IMMEDIATE SOURCE:

(A) LIBRARY: Inflamed Adenoid

(B) CLONE: 20293

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:l:

ATGAAGTTCA TCTCGACATC TCTGCTTCTC ATGCTGCTGG TCAGCAGCCT CTCTCCAGTC 60

CAAGGTGTTC TGGAGGTCTA TTACACAAGC TTGAGGTGTA GATGTGTCCA AGAGAGCTCA 120

GTCTTTATCC CTAGACGCTT CATTGATCGA ATTCAAATCT TGCCCCGTGG GAATGGTTGT 180

CCAAGAAAAG AAATCATAGT CTGGAAGAAG AACAAGTCAA TTGTGTGTGT GGACCCTCAA 240

GCTGAATGGA TACAAAGAAT GATGGAAGTA TGAGAAAAA GAAGTTCTTC AACTCTACCA 300

GTTCCAGTGT TTAAGAGAAA GATTCCCTGA 330

(2) INFORMATION FOR SEQ ID NO:2:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 109 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: polypeptide

(vii) IMMEDIATE SOURCE:

(A) LIBRARY: Inflamed Adenoid

(B) CLONE: 20293

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:

Met Lys Phe lie Ser Thr Ser Leu Leu Leu Met Leu Leu Val Ser Ser 1 5 10 15

Leu Ser Pro Val Gin Gly Val Leu Glu Val Tyr Tyr Thr Ser Leu Arg 20 25 30

Cys Arg Cys Val Gin Glu Ser Ser Val Phe lie Pro Arg Arg Phe lie 35 40 45

Asp Arg lie Gin lie Leu Pro Arg Gly Asn Gly Cys Pro Arg Lys Glu 50 55 60 lie lie Val Trp Lys Lys Asn Lys Ser lie Val Cys Val Asp Pro Gin

65 70 75 80

Ala Glu Trp lie Gin Arg Met Met Glu Val Leu Arg Lys Arg Ser Ser 85 90 95

Ser Thr Leu Pro Val Pro Val Phe Lys Arg Lys lie Pro 100 105

(2) INFORMATION FOR SEQ ID NO:3:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 114 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:

Met Ser Leu Leu Ser Ser Arg Ala Ala Arg Val Pro Gly Pro Ser Ser 1 5 10 15

Ser Leu Cys Ala Leu Leu Val Leu Leu Leu Leu Leu Thr Gin Pro Gly 20 25 -30

Pro lie Ala Ser Ala Gly Pro Ala Ala Ala Val Leu Arg Glu Leu Arg 35 40 45

Cys Val Cys Leu Gin Thr Thr Gin Gly Val His Pro Lys Met lie Ser 50 55 60

Asn Leu Gin Val Phe Ala He Gly Pro Gin Cys Ser Lys Val Glu Val 65 70 75 80

Val Ala Ser Leu Lys Asn Gly Lys Glu He Cys Leu Asp Pro Glu Ala 85 90 95

Pro Phe Leu Lys Lys Val He Gin Lys He Leu Asp Gly Gly Asn Lys 100 105 110

Glu Asn

(2) INFORMATION FOR SEQ ID NO:4:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 107 amino acids

(B) TYPE: amino acid (C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:

Met Ala Arg Ala Thr Leu Ser Ala Ala Pro Ser Asn Pro Arg Leu Leu 1 5 10 15

Arg Val Ala Leu Leu Leu Leu Leu Leu Val Ala Ala Ser Arg Arg Ala 20 25 30

Ala Gly Ala Pro Leu Ala Thr Glu Leu Arg Cys Gin Cys Leu Gin Thr 35 40 45

Leu Gin Gly He His Leu Lys Asn He Gin Ser Val Lys Val Lys Ser 50 55 60

Pro Gly Pro His Cys Ala Gin Thr Glu Val He Ala Thr Leu Lys Asn 65 70 75 80

Gly Gin Lys Ala Cys Leu Asn Pro Ala Ser Pro Met Val Lys Lys He 85 90 95

He Glu Lys Met Leu Lys Asn Gly Lys Ser Asn 100 105

(2) INFORMATION FOR SEQ ID NO:5:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 106 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:

Met Ala His Ala Thr Leu Ser Ala Ala Pro Ser Asn Pro Arg Leu Leu 1 5 10 15

Arg Val Ala Leu Leu Leu Leu Leu Leu Val Gly Ser Arg Arg Ala Ala 20 25 30

Gly Ala Ser Val Val Thr Glu Leu Arg Cys Gin Cys Leu Gin Thr Leu 35 40 45

Gin Gly He His Leu Lys Asn He Gin Ser Val Asn Val Arg Ser Pro 50 55 60 Gly Pro His Cys Ala Gin Thr Glu Val He Ala Thr Leu Lys Asn Gly

65 70 75 80

Lys Lys Ala Cys Leu Asn Pro Ala Ser Pro Met Val Gin Lys He He 85 90 95

Glu Lys He Leu Asn Lys Gly Ser Thr Asn 100 105

(2) INFORMATION FOR SEQ ID NO:6:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 99 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:

Met Thr Ser Lys Leu Ala Val Ala Leu Leu Ala Ala Phe Leu He Ser 1 5 10 15

Ala Ala Leu Cys Glu Gly Ala Val Leu Pro Arg Ser Ala Lys Glu Leu 20 25 30

Arg Cys Gin Cys He Lys Thr Tyr Ser Lys Pro Phe His Pro Lys Phe 35 40 45

He Lys Glu Leu Arg Val He Glu Ser Gly Pro His Cys Ala Asn Thr 50 55 60

Glu He He Val Lys Leu Ser Asp Gly Arg Glu Leu Cys Leu Asp Pro 65 70 75 80

Lys Glu Asn Trp Val Gin Arg Val Val Glu Lys Phe Leu Lys Arg Ala 85 90 95

Glu Asn Ser

(2) INFORMATION FOR SEQ ID NO:7:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 107 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single (D) TOPOLOGY: linear (ii) MOLECULE TYPE: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:

Met Ala Arg Ala Ala Leu Ser Ala Ala Pro Ser Asn Pro Arg Leu Leu 1 5 10 15

Arg Val Ala Leu Leu Leu Leu Leu Leu Val Ala Ala Gly Arg Arg Ala 20 25 30

Ala Gly Ala Ser Val Ala Thr Glu Leu Arg Cys Gin Cys Leu Gin Thr 35 40 45

Leu Gin Gly He His Pro Lys Asn He Gin Ser Val Asn Val Lys Ser 50 55 60

Pro Gly Pro His Cys Ala Gin Thr Glu Val He Ala Thr Leu Lys Asn 65 70 75 80

Gly Arg Lys Ala Cys Leu Asn Pro Ala Ser Pro He Val Lys Lys He 85 90 95

He Glu Lys Met Leu Asn Ser Asp Lys Ser Asn 100 105

(2) INFORMATION FOR SEQ ID NO:8:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 101 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS : single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:

Met Ser Ser Ala Ala Gly Phe Cys Ala Ser Arg Pro Gly Leu Leu Phe 1 5 10 15

Leu Gly Leu Leu Leu Leu Pro Leu Val Val Ala Phe Ala Ser Ala Glu 20 25 30

Ala Glu Glu Asp Gly Asp Leu Gin Cys Leu Cys Val Lys Thr Thr Ser 35 40 45

Gin Val Arg Pro Arg His He Thr Ser Leu Glu Val He Lys Ala Gly 50 55 60 Pro His Cys Pro Thr Ala Gin Leu He Ala Thr Leu Lys Asn Gly Arg 65 70 75 80

Lys He Cys Leu Asp Leu Gin Ala Pro Leu Thr Lys Lys He He Lys 85 90 95

Lys Leu Leu Glu Ser 100

(2) INFORMATION FOR SEQ ID NO:9:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 109 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(xi) SEQUENCE DESCRIPTION: SEQ ID NO: :

Met Lys Phe He Ser Thr Ser Leu Leu Leu Met Leu Leu Val Ser Ser 1 5 10 15

Leu Ser Pro Val Gin Gly Val Leu Glu Val Tyr Tyr Thr Ser Leu Arg 20 25 30

Cys Arg Cys Val Gin Glu Ser Ser Val Phe He Pro Arg Arg Phe He 35 40 45

Asp Arg He Gin He Leu Pro Arg Gly Asn Gly Cys Pro Arg Lys Glu 50 55 60

He He Val Trp Lys Lys Asn Lys Ser He Val Cys Val Asp Pro Gin 65 70 75 80

Ala Glu Trp He Gin Arg Met Met Glu Val Leu Arg Lys Arg Ser Ser 85 90 95

Ser Thr Leu Pro Val Pro Val Phe Lys Arg Lys He Pro 100 105

Claims

£LΔ1M&

1. A purified polynucleotide comprising a polynucleotide sequence encoding the polypeptide having the sequence as depicted in SEQ ID NO: 2 or its complement.

2. The polynucleotide of Claim 1 wherein the polynucleotide sequence consists of SEQ ID NO: 1.

3. A purified polynucleotide capable of hybridizing to the polynucleotide of Claim 2 under stringent conditions.

4. An expression vector comprising the purified polynucleotide of Claim 2.

5. A host cell comprising the expression vector of Claim 4.

6. A polynucleotide probe comprising a non-conserved fragment of the polynucleotide of Claim 2.

7. An antisense molecule comprising a polynucleotide sequence complementary to at least a portion of the polynucleotide of Claim 2.

8. A method for producing a polypeptide comprising the sequence as depicted in SEQ ID NO:2, said method comprising: a) culturing the host cells of Claim 5 under conditions suitable for the expression of the polypeptide, and b) recovering said polypeptide from the cell culture.

9. A diagnostic test for the detection of nucleotide sequences encoding adenoid expressed chemokine in a biological sample, comprising the steps of: a) combining the biological sample with a first nucleotide sequence which comprises the nucleotide sequence of SEQ ID NO: 1 , or a fragment thereof, under conditions suitable for the formation of a nucleic acid hybridization complex, b) detecting said hybridization complex, wherein the presence of said complex correlates with the presence of a second nucleotide sequence encoding adenoid expressed chemokine 1 in said biological sample, and c) comparing the amount of the second nucleotide sequence in said sample with a standard thereby determining whether the amount of said second nucleotide quence varies from said standard, wherein the presence of an abnormal level of said second nucleotide sequence correlates positively with a condition associated with inflammation.

10. The diagnostic test of Claim 9 wherein said first nucleotide sequence is labeled with a reporter molecule and the hybridization complex is detected by measuring said reporter molecule.

11. A diagnostic test for the detection of nucleotide sequences encoding adenoid expressed chemokine in a biological sample, comprising the steps of: a) combining the biological sample with polymerase chain reaction primers under conditions suitable for nucleic acid amplification, wherein said primers comprise fragments of the nucleotide sequence of SEQ ID NO:1 , c) detecting amplified nucleotide sequences, and d) comparing the amount of amplified nucleotide sequences in said biological sample with a standard thereby determining whether the amount of said nucleotide sequence varies from said standard, wherein the presence of an abnormal level of said nucleotide sequence correlates positively with a condition associated with inflammation.

12. A purified polypeptide wherein the polypeptide sequence comprises SEQ ID NO:

13. An antibody specific for the purified polypeptide of Claim 12.

14. Purified adenoid expressed chemokine having an N-terminal amino acid residue of residue 24, leucine, of SEQ ID NO: 2.

15. Purified adenoid expressed chemokine having an N-terminal amino acid residue of residue 25, glutamic acid, of SEQ ID NO: 2.

16. A purified peptide of adenoid expressed chemokine consisting of amino acid residues 25 to 42 of SEQ ID NO:2.

17. A pharmaceutical composition for treating disease states associated with angiogenesis comprising an effective amount of the polynucleotide sequence of Claim 1 and a pharmaceutically acceptable carrier.

18. A method of treating a patient subject to a disease state associated with angiogenesis comprising administering an effective amount of the pharmaceutical composition of Claim 17 to said patient.