WO2001081380A2 - Immunogenic pneumococcal protein and vaccine compositions thereof - Google Patents
Immunogenic pneumococcal protein and vaccine compositions thereof Download PDFInfo
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- WO2001081380A2 WO2001081380A2 PCT/US2001/013828 US0113828W WO0181380A2 WO 2001081380 A2 WO2001081380 A2 WO 2001081380A2 US 0113828 W US0113828 W US 0113828W WO 0181380 A2 WO0181380 A2 WO 0181380A2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/315—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Streptococcus (G), e.g. Enterococci
- C07K14/3156—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Streptococcus (G), e.g. Enterococci from Streptococcus pneumoniae (Pneumococcus)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K2035/11—Medicinal preparations comprising living procariotic cells
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
- A61K2039/53—DNA (RNA) vaccination
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
Definitions
- This invention relates to the field of bacterial surface proteins and their use as components in vaccines and vaccine compositions for protection against bacterial infections.
- Streptococcus pneumoniae (S. pneumoniae; pneumococcus ⁇ is a gram positive bacterium that is also a major causative agent of invasive infections in animals and humans, including such diseases as sepsis, menningitis, otitis media, and lobar pneumonia.
- pneumococci readily bind to non-inflamed human epithelial cells of the upper and lower respiratory tract by binding to eukaryotic carbohydrates in a lectin-like manner (Cundell et al, Micro. Path. , 17:361 -374 ( 1 994)).
- Conversion to invasive pneumococcal infections for bound bacteria may involve the local generation of inflammatory factors that may activate the epithelial cells to change the number and type of receptors on their surfaces.
- inflammatory factors that may activate the epithelial cells to change the number and type of receptors on their surfaces.
- PAF platelet activating factor
- Certain soluble receptor analogs have been shown to prevent the progression of pneumococcal infections (Idanpaan-Heikkila et al, J. Inf. Dis. , 176:704-71 2 ( 1 997)).
- Other proteins have been suggested as being involved in the pathogenicity of S. pneumoniae, but the majority of the gene products have not been characterized.
- Such processes may include the production of recombinant vectors and cells comprising polynucleotides encoding the polypeptides disclosed herein.
- Figure 1 shows the results of experiments (Figs 1 A and 1 B, respectively) using the preparations of recombinant SP1 33 polypeptide of the invention.
- the experimental data show that active immunization with recombinant SP1 33 polypeptide derived from pneumococcal strain
- mice immunized with recombinant SP1 33 polypeptide showed a significant difference in the number of survivors compared to that of the sham immunized mice (P ⁇ 0.05).
- Figure 2 shows the detection of SP1 33 on the bacterial cell surface by immunolabeling and flow cytometry. The results demonstrate that immune sera raised against SP1 33 protein can label the cell surface of intact pneumococci (strain SJ2).
- Figure 3 is a western blot of whole-cell lysates prepared from each of the 23 serotypes included in currently available pneumococcal vaccine probed with antiserum raised against recombinant SP1 33 polypeptide. Nearly all of the S. pneumoniae strains tested detected a protein with molecular mass of approximately 32 kDa (that reacted with the anti- SP1 33 antiserum), consistent with the predicted molecular mass of SP1 33. Although SP1 33 protein was not detected in a lysate prepared from a serotype 3 strain (WU2) SP1 33 protein was detected in two other serotype 3 strains (ATCC3 and A66).
- Figure 4 is a western blot showing the reactivity of patient sera with SP1 33.
- the recombinant SP1 33 protein was separated by SDS- PAGE and transferred onto nitrocellulose.
- Sera were collected from 4 patients (indicated by the numeral at the top) at two different times. The first collection (denoted “A” for acute serum) was soon after onset of illness while the second collection (denoted “C” for "convalescent serum”) was made eight to thirty days later. These sera were used to probe the blots. The data show that for patients 1 and 2, convalescent serum reacted more strongly with SP1 33 than did the corresponding acute serum .
- the present invention relates generally to the field of bacterial antigens and their use, for example, as immunogenic agents in humans and animals to stimulate an immune response. More specifically, it relates to the vaccination of mammalian species with a polypeptide obtained from Streptococcus pneumoniae species as a mechanism for stimulating production of antibodies that protect the vaccine recipient against infection by a wide range of serotypes of pathogenic S. pneumoniae.
- the present invention further relates to antibodies against such polypeptides, which antibodies (whether polyclonal or monoclonal) find use in diagnosis and/or passive immune therapy of such pneumococcal infections.
- the present invention relates to the prevention and/or treatment of pneumococcal infections such as infections of the middle ear, nasopharynx, lung and bronchial areas, blood, cerebrospinal fluid, and others, that are caused by pneumococcal bacteria.
- pneumococcal infections such as infections of the middle ear, nasopharynx, lung and bronchial areas, blood, cerebrospinal fluid, and others, that are caused by pneumococcal bacteria.
- the present invention relates to a purified polypeptide comprising an amino acid sequence shown in SEQ ID NO: 4.
- the present invention is broad enough also to encompass polypeptides having at least about 80% identity to the amino acid sequence of SEQ ID NO: 4, preferably at least about 90% sequence identity, or homology, therewith, most preferably at least about 95% identity to the amino acid sequence of SEQ ID NO: 4, especially at least about 98% identity to the amino acid sequence of SEQ ID NO: 4, with a polypeptide having the amino acid sequence of SEQ ID NO: 4 being a preferred embodiment.
- percent identity or “percent identical,” including percent (%) homology, when referring to a sequence, means that a sequence is compared to a claimed or described sequence after alignment of the sequence to be compared (the "Compared Sequence") with the described or claimed sequence (the "Reference Sequence”).
- the Percent Identity is then determined according to the following formula:
- C is the number of differences between the Reference Sequence and the Compared Sequence over the length of alignment between the Reference Sequence and the Compared Sequence wherein (i) each base or amino acid in the Reference Sequence that does not have a corresponding aligned base or amino acid in the Compared Sequence and (ii) each gap in the Reference Sequence and (iii) each aligned base or amino acid in the Reference Sequence that is different from an aligned base or amino acid in the Compared Sequence, constitutes a difference; and R is the number of bases or amino acids in the Reference Sequence over the length of the alignment with the Compared Sequence with any gap created in the Reference Sequence also being counted as a base or amino acid.
- the Compared Sequence has the specified minimum percent identity to the Reference Sequence even though alignments may exist in which the hereinabove calculated Percent Identity is less than the specified Percent Identity.
- the present invention further relates to a polypeptide which has the deduced amino acid sequence (SEQ ID NO:4), as well as fragments, analogs and derivatives of such polypeptide.
- fragment when referring to the polypeptide (SEQ ID NO:4), means a polypeptide which retains essentially the same biological function or activity as such polypeptide.
- an analog includes a proprotein which can be activated by cleavage of the proprotein portion to produce an active mature polypeptide.
- Such fragments, derivatives and analogs must have sufficient similarity to the polypeptide of SEQ ID NO:4 so that activity of the native polypeptide is retained.
- the polypeptide of the present invention may be a recombinant polypeptide, a natural polypeptide or a synthetic polypeptide, preferably a recombinant polypeptide.
- the fragment, derivative or analog of the polypeptide (SEQ ID NO:4) may be (i) one in which one or more of the amino acid residues are substituted with a conserved or non-conserved amino acid residue (preferably a conserved amino acid residue) and such substituted amino acid residue may or may not be one encoded by the genetic code, or (ii) one in which one or more of the amino acid residues includes a substituent group, or (iii) one in which the mature polypeptide is fused with another compound, such as a compound to increase the half-life of the polypeptide (for example, polyethylene glycol), or (iv) one in which the additional amino acids are fused to the mature polypeptide, such as a leader or secretory sequence or a sequence which is employed for purification of the mature polypeptide or a
- polypeptides and polynucleotides of the present invention are preferably provided in an isolated form, and preferably are purified to homogeneity.
- isolated means that the material is removed from its original environment (e.g., the natural environment if it is naturally occurring).
- a naturally-occurring polynucleotide or polypeptide present in a living animal is not isolated, but the same polynucleotide or polypeptide, separated from some or all of the coexisting materials in the natural system, is isolated.
- Such polynucleotides could be part of a vector and/or such polynucleotides or polypeptides could be part of a composition, and still be isolated in that such vector or composition is not part of its natural environment.
- the present invention relates to an isolated polypeptide comprising an amino acid sequence at least about 80% identical to the amino acid sequence of SEQ ID NO: 4, preferably at least about 90% identical to the amino acid sequence of SEQ ID NO: 4, most preferably at least about 95% identical to the amino acid sequence of SEQ ID NO: 4, especially where said isolated polypeptide has a sequence at least about 98 % identical to the amino acid sequence of SEQ ID NO: 4, and most especially where said isolated polypeptide comprises a polypeptide having the amino acid sequence of SEQ ID NO: 4, including all immunogenically active fragments of any of the aforementioned isolated polypeptides.
- similarity between two polypeptides is determined by comparing the amino acid sequence and its conserved amino acid substitutes of one polypeptide to the sequence of a second polypeptide.
- Fragments or portions of the polypeptides of the present invention may be employed for producing the corresponding full-length polypeptide by peptide synthesis; therefore, the fragments may be employed as intermediates for producing the full-length polypeptides. Fragments or portions of the polynucleotides of the present invention may be used to synthesize full-length polynucleotides of the present invention.
- the present invention further relates to an isolated and/or purified polynucleotide comprising the nucleotide sequence of SEQ ID NO: 3 as well as a polynucleotide having the nucleotide sequence of SEQ ID NO: 3.
- the polynucleotides of the present invention are defined sufficiently broadly to also encompass a nucleotide sequence at least 65% identical to a polynucleotide sequence encoding the polypeptide of SEQ ID NO 4, preferably a polynucleotide having a nucleotide sequence at least 80% identical to a nucleotide sequence encoding the polypeptide of SEQ ID NO:4, most preferably a polynucleotide having a nucleotide sequence at least 95% identical to a nucleotide sequence encoding the polypeptide of SEQ ID NO:4, especially where the polynucleotide has a nucleotide sequence at least about 98% identical to a nucleotide sequence encoding the amino acid sequence of SEQ ID NO:4, with a polynucleotide encoding the polypeptide of SEQ ID NO: 4 being especially preferred.
- DNA segment refers to a DNA polymer, in the form of a separate fragment or as a component of a larger DNA construct, which has been derived from DNA isolated at least once in substantially pure form, i.e., free of contaminating endogenous materials and in a quantity or concentration enabling identification, manipulation, and recovery of the segment and its component nucleotide sequences by standard biochemical methods, for example, using a cloning vector.
- segments are provided in the form of an open reading frame uninterrupted by internal nontranslated sequences, or introns, which are typically present in eukaryotic genes. Sequences of non-translated DNA may be present downstream from the open reading frame, where the same do not interfere with manipulation or expression of the coding regions.
- nucleic acids and polypeptide expression products disclosed according to the present invention may be in "enriched form.”
- enriched means that the concentration of the material is at least about 2, 5, 10, 100, or 1000 times its natural concentration (for example), advantageously 0.01 %, by weight, preferably at least about 0.1 % by weight. Enriched preparations of about 0.5%, 1 %, 5%, 1 0%, and 20% by weight are also contemplated.
- sequences, constructs, vectors, clones, and other materials comprising the present invention can advantageously be in enriched or isolated form.
- isolated in the context of the present invention with respect to polypeptides (or polynucleotides) means that the material is removed from its original environment ⁇ e.g. , the natural environment if it is naturally occurring).
- a naturally-occurring polynucleotide or polypeptide present in a living organism is not isolated, but the same polynucleotide or polypeptide, separated from some or all of the co-existing materials in the natural system, is isolated.
- Such polynucleotides could be part of a vector and/or such polynucleotides or polypeptides could be part of a composition, and still be isolated in that such vector or composition is not part of its natural environment.
- the polypeptides and polynucleotides of the present invention are preferably provided in an isolated form, and preferably are purified to homogeneity.
- polynucleotides, and recombinant or immunogenic polypeptides, disclosed in accordance with the present invention may also be in "purified” form.
- the term “purified” does not require absolute purity; rather, it is intended as a relative definition, and can include preparations that are highly purified or preparations that are only partially purified, as those terms are understood by those of skill in the relevant art.
- individual clones isolated from a cDNA library have been conventionally purified to electrophoretic homogeneity. Purification of starting material or natural material to at least one order of magnitude, preferably two or three orders, and more preferably four or five orders of magnitude is expressly contemplated.
- a claimed polypeptide which has a purity of preferably 0.001 %, or at least 0.01 % or 0.1 %; and even desirably 1 % by weight or greater is expressly contemplated.
- coding region refers to that portion of a gene which either naturally or normally codes for the expression product of that gene in its natural genomic environment, i.e., the region coding in vivo for the native expression product of the gene.
- the coding region can be from a normal, mutated or altered gene, or can even be from a DNA sequence, or gene, wholly synthesized in the laboratory using methods well known to those of skill in the art of DNA synthesis.
- nucleotide sequence refers to a heteropolymer of deoxyribonucleotides.
- DNA segments encoding the proteins provided by this invention are assembled from cDNA fragments and short oligonucleotide linkers, or from a series of oligonucleotides, to provide a synthetic gene which is capable of being expressed in a recombinant transcriptional unit comprising regulatory elements derived from a microbial or viral operon.
- the forward and reverse primers for polymerase chain reaction synthesis are given as SEQ ID NOs.: 1 and 2, respectively.
- expression product means that polypeptide or protein that is the natural translation product of the gene and any nucleic acid sequence coding equivalents resulting from genetic code degeneracy and thus coding for the same amino acid(s).
- fragment when referring to a coding sequence, means a portion of DNA comprising less than the complete coding region whose expression product retains essentially the same biological function or activity as the expression product of the complete coding region.
- primer means a short nucleic acid sequence that is paired with one strand of DNA and provides a free 3'-OH end at which a DNA polymerase starts synthesis of a deoxyribonucleotide chain.
- promoter means a region of DNA involved in binding of RNA polymerase to initiate transcription.
- ORF open reading frame
- reference to a DNA sequence includes both single stranded and double stranded DNA.
- specific sequence unless the context indicates otherwise, refers to the single strand DNA of such sequence, the duplex of such sequence with its complement (double stranded DNA) and the complement of such sequence.
- portion, “segment, “ and “fragment,” when used in relation to polypeptides, refer to a continuous sequence of residues, such as amino acid residues, which sequence forms a subset of a larger sequence.
- the oligopeptides resulting from such treatment would represent portions, segments or fragments of the starting polypeptide.
- such terms refer to the products produced by treatment of said polynucleotides with any of the common endonucleases.
- the present invention also relates to a vaccine, or a vaccine composition, comprising a polypeptide, including immunogenic fragments thereof, selected from the polypeptides, and immunogenic fragments thereof, disclosed according to the present invention and wherein said polypeptides and fragments are in a pharmaceutically acceptable carrier and wherein said polypeptide and/or fragments are present in an amount effective to elicit antibodies, preferably protective antibodies, in an animal against an organism of the genus Streptococcus.
- the vaccine compositions of the present invention may, as stated, comprise immunogenically active fragments of the polypeptides disclosed herein, such as the polypeptide of SEQ ID NO: 4, and, where this is the case, such fragments will commonly be of varying sizes but will commonly be immunogenic fragments at least about 200 amino acid residues in length, plus or minus 5 residues, preferably at least about 250 amino acid residues in length, and most preferably at least 270 amino acid residues in length, plus or minus about 5 residues.
- the vaccine compositions of the present invention may also comprise polynucleotides as disclosed herein.
- vaccines are prepared as injectables, in the form of aqueous solutions or suspensions. Vaccines in an oil base are also well known such as for inhaling. Solid forms which are dissolved or suspended prior to use may also be formulated.
- Pharmaceutically acceptable carriers, diluents and excipients are generally added that are compatible with the active ingredients and acceptable for pharmaceutical use.
- compositions useful herein also contain a pharmaceutically acceptable carrier, including any suitable diluent or excipient, which includes any pharmaceutical agent that does not itself induce the production of antibodies harmful to the individual receiving the composition, and which may be administered without undue toxicity.
- a pharmaceutically acceptable carrier including any suitable diluent or excipient, which includes any pharmaceutical agent that does not itself induce the production of antibodies harmful to the individual receiving the composition, and which may be administered without undue toxicity.
- Pharmaceutically acceptable carriers include, but are not limited to, liquids such as water, saline, glycerol and ethanol, and the like, including carriers useful in forming sprays for nasal and other respiratory tract delivery or for delivery to the ophthalmic system.
- liquids such as water, saline, glycerol and ethanol, and the like, including carriers useful in forming sprays for nasal and other respiratory tract delivery or for delivery to the ophthalmic system.
- Vaccine compositions may further incorporate additional substances to stabilize pH, or to function as adjuvants, wetting agents, or emulsifying agents, which can serve to improve the effectiveness of the vaccine.
- Vaccines are generally formulated for parenteral administration and are injected either subcutaneously or intramuscularly. Such vaccines can also be formulated as suppositories or for oral administration, using methods known in the art, or for administration through nasal or respiratory routes.
- the amount of vaccine sufficient to confer immunity to pathogenic bacteria, viruses, or other microbes is determined by methods well known to those skilled in the art. This quantity will be determined based upon the characteristics of the vaccine recipient and the level of immunity required. Typically, the amount of vaccine to be administered will be determined based upon the judgment of a skilled physician. Where vaccines are administered by subcutaneous or intramuscular injection, a range of .5 to 500 ⁇ g purified protein may be given.
- such dosages are commonly sufficient to provide about 1 ⁇ g, possibly 10 ⁇ g, even 50 ⁇ g, and as much as 100 ⁇ g, up to 500 ⁇ g of immunogenic protein, or immunogenic polypeptide, or immunogenically active fragments thereof.
- more than one such active material may be present in the vaccine.
- more than one antigenic structure may be used in formulating the vaccine, or vaccine composition to use in the methods disclosed herein. This may include two or more individually immunogenic proteins or polypeptides, proteins or polypeptides showing immunogenic activity only when in combination, either quantitatively equal in their respective concentrations or formulated to be present in some ratio, either definite or indefinite.
- a vaccine composition for use in the processes disclosed herein may include one or more immunogenic proteins, one or more immunogenic polypeptides, and/or one or more immunogenically active immunogens comprising antigenic fragments of said immunogenic proteins and polypeptides, the latter fragments being present in any proportions selected by the use of the present invention.
- the exact components, and their respective quantities, making up the vaccines, and vaccine compositions, useful in the methods of the present invention are determined, inter alia, by the nature of the disease to be treated or prevented, the severity of such condition where it already exists, the age, sex, and general health of the recipient, as well the personal and professional experience and inclinations of the researcher and/or clinician utilizing these methods.
- the present invention also contemplates use of a vaccine composition
- a vaccine composition comprising a polynucleotide encoding a polypeptide, including immunogenic fragments thereof, selected from any of the polypeptides disclosed according to the invention and wherein said polynucleotide is suspended in a pharmaceutically acceptable carrier and wherein said polynucleotide is present in an amount effective to elicit protective antibodies in an animal against an organism of the genus Streptococcus.
- the present invention further relates to an isolated antibody that binds specifically to a polypeptide selected from the group consisting of the polypeptides, and immunogenic fragments thereof, disclosed herein.
- Such an isolated antibody may be either a polyclonal or a monoclonal antibody.
- Still another aspect of the present invention relates to a method of using one or more antibodies (monoclonal or polyclonal, natural or recombinant, and regardless of how prepared, i.e., by purification from a natural source, or generated by cloning or by direct chemical synthesis), preferably, but not necessarily, specific for one or more antigenic determinants present in the vaccine, or vaccine composition selected for use in the methods of the present invention.
- one or more antibodies monoclonal or polyclonal, natural or recombinant, and regardless of how prepared, i.e., by purification from a natural source, or generated by cloning or by direct chemical synthesis
- specific for one or more antigenic determinants present in the vaccine, or vaccine composition selected for use in the methods of the present invention preferably, but not necessarily, specific for one or more antigenic determinants present in the vaccine, or vaccine composition selected for use in the methods of the present invention.
- the present invention also relates to a composition
- a composition comprising one or more of the isolated antibodies disclosed herein wherein said antibody is suspended in a pharmaceutically acceptable carrier, including all suitable and equivalent diluents or excipients as described hereinabove and wherein said antibody is present in said composition in a therapeutically effective amount so as to protect an animal against an organism of the genus Streptococcus.
- the present invention further relates to methods of using the vaccine compositions and antibody compositions disclosed herein in prophylactically and therapeutically effective manner to present and/or treat disease.
- the present invention is also directed to a method of preventing or attenuating an infection caused by a member of the genus Streptococcus in an animal, most preferably where said animal is a human patient, infected therewith, or at risk of infection therewith, comprising administering to said animal a therapeutically effective amount of a vaccine composition as disclosed herein according to the present invention.
- the present invention further relates to a method of preventing or attenuating an infection caused by a member of the genus Streptococcus in an animal infected therewith, or at risk of infection therewith, comprising administering to said animal, most preferably where said animal is a human patient, a therapeutically effective amount of the one or more of the antibodies disclosed herein according to the present invention, wherein said antibody is administered in an amount effective to prevent or attenuate said infection.
- the vaccine compositions of the present invention that are useful for treating disease, especially pneumococcal disease, are not limited to those containing purified, or isolated, polypeptides, and immunogenically active fragments thereof, as disclosed herein but also include compositions formed of microorganisms wherein the microorganism expresses and presents the immunogenic polypeptide, or fragment thereof, to the immune system.
- Such microorganisms to find use in the methods of the present invention, may be suitably attenuated so as to avoid other complications, or possible superinfection.
- the present invention includes a vaccine composition
- a vaccine composition comprising a microbial organism transformed with polynucleotides, and thereby expressing the polypeptides, or immunogenic fragments thereof, selected from the group consisting of the polypeptides disclosed herein, such as the polypeptide, and homologous polypeptides thereof, of SEQ ID NO: 4.
- the microorganisms finding most use for the methods of the present invention include, but are not necessarily limited to, the group consisting of Salmonella, Mycobacteria, Streptococcus, poxviruses, and adenoviruses.
- the present invention also relates to vectors comprising the polynucleotides disclosed herein.
- the present invention further relates to recombinant cells comprising within their genomes, or within vectors or other extrachromasomal polynucleotides incorporated into said cells, wherein said polynucleotides have sequences selected from the sequences disclosed herein.
- Such cells find use as a means of expressing, and secreting, the polypeptides of the present invention and include mammalian cells genetically engineered to produce such polypeptides, the latter commonly being encoded by polynucleotides of the invention present within such recombinant cells.
- expressing may or may not include secretion of said protein.
- a recombinant cell synthesizes the polypeptide only internally, which polypeptide must then be collected by lysing the cells and isolating the polypeptide from the lysate, this process would be encompassed by the term "expressing” or "expression.”
- the present invention also relates to vectors which include polynucleotides of the present invention, host cells which are genetically engineered with vectors of the invention and the production of polypeptides of the invention by recombinant techniques.
- Host cells are genetically engineered (transduced or transformed or transfected) with the vectors of this invention which may be, for example, a cloning vector or an expression vector.
- the vector may be, for example, in the form of a plasmid, a viral particle, a phage, etc.
- the engineered host cells can be cultured in conventional nutrient media modified as appropriate for activating promoters, selecting transformants or amplifying the genes of the present invention.
- the culture conditions such as temperature, pH and the like, are those previously used with the host cell selected for expression, and will be apparent to the ordinarily skilled artisan.
- the polynucleotides of the present invention may be employed for producing polypeptides by recombinant techniques.
- the polynucleotide may be included in any one of a variety of expression vectors for expressing a polypeptide.
- Such vectors include chromosomal, nonchromosomal and synthetic DNA sequences, e.g., derivatives of SV40; bacterial plasmids; phage DNA; baculovirus; yeast plasmids; vectors derived from combinations of plasmids and phage DNA, viral DNA such as vaccinia, adenovirus, fowl pox virus, and pseudorabies.
- any other vector may be used as long as it is replicable and viable in the host.
- the appropriate DNA sequence may be inserted into the vector by a variety of procedures.
- the DNA sequence is inserted into an appropriate restriction endonuclease site(s) by procedures known in the art. Such procedures and others are deemed to be within the scope of those skilled in the art.
- the DNA sequence in the expression vector is operatively linked to an appropriate expression control sequence(s) (promoter) to direct mRNA synthesis.
- promoter for example, LTR or SV40 promoter, the E. coli. lac or trp, the phage lambda P L promoter and other promoters known to control expression of genes in prokaryotic or eukaryotic cells or their viruses.
- the expression vector also contains a ribosome binding site for translation initiation and a transcription terminator.
- the vector may also include appropriate sequences for amplifying expression.
- the expression vectors preferably contain one or more selectable marker genes to provide a phenotypic trait for selection of transformed host cells such as dihydrofolate reductase or neomycin resistance for eukaryotic cell culture, or such as tetracycline or ampicillin resistance in E. coli.
- the vector containing the appropriate DNA sequence as hereinabove described, as well as an appropriate promoter or control sequence, may be employed to transform an appropriate host to permit the host to express the protein.
- bacterial cells such as E. coli, Streptomyces, Salmonella typhimurium
- fungal cells such as yeast
- insect cells such as Drosophila S2 and Spodoptera Sf9
- animal cells such as CHO, COS or Bowes melanoma
- adenoviruses plant cells, etc.
- the selection of an appropriate host is deemed to be within the scope of those skilled in the art from the teachings herein. More particularly, the present invention also includes recombinant constructs comprising one or more of the sequences as broadly described above.
- the constructs comprise a vector, such as a plasmid or viral vector, into which a sequence of the invention has been inserted, in a forward or reverse orientation.
- the construct further comprises regulatory sequences, including, for example, a promoter, operably linked to the sequence.
- regulatory sequences including, for example, a promoter, operably linked to the sequence.
- Bacterial pQE70, pQE60, pQE-9 (Qiagen), pBS, pD10, phagescript, psiX1 74, pBluescript SK, pBSKS, pNH8A, pNH16a, pNH18A, pNH46A (Stratagene); pTRC99a, pKK223-3, pKK233-3, pDR540, pRIT5 (Pharmacia); Eukaryotic: pWLNEO, pSV2CAT, pOG44, pXT1 , pSG (Stratagene) pSVK3, pBPV, pMSG, pSVL (Pharmacia). However, any other plasmid or vector may be used as long as they are replicable and viable in the host.
- Promoter regions can be selected from any desired gene using CAT (chloramphenicol transferase) vectors or other vectors with selectable markers.
- Two appropriate vectors are pKK232-8 and pCM7.
- Particular named bacterial promoters include lacl, lacZ, T3, T7, gpt, lambda P R , P L and trp.
- Eukaryotic promoters include CMV immediate early, HSV thymidine kinase, early and late SV40, LTRs from retrovirus, and mouse metallothionein-l. Selection of the appropriate vector and promoter is well within the level of ordinary skill in the art.
- the present invention relates to host cells containing the above-described constructs.
- the host cell can be a higher eukaryotic cell, such as a mammalian cell, or a lower eukaryotic cell, such as a yeast cell, or the host cell can be a prokaryotic cell, such as a bacterial cell.
- Introduction of the construct into the host cell can be effected by calcium phosphate transfection, DEAE-Dextran mediated transfection, or electroporation (Davis, L., Dibner, M., Battey, I., Basic Methods in Molecular Biology, (1 986)).
- constructs in host cells can be used in a conventional manner to produce the gene product encoded by the recombinant sequence.
- the polypeptides of the invention can be synthetically produced by conventional peptide synthesizers.
- Mature proteins can be expressed in mammalian cells, yeast, bacteria, or other cells under the control of appropriate promoters. Cell-free translation systems can also be employed to produce such proteins using RNAs derived from the DNA constructs of the present invention. Appropriate cloning and expression vectors for use with prokaryotic and eukaryotic hosts are described by Sambrook, et al., Molecular Cloning: A Laboratory Manual, Second Edition, Cold Spring Harbor, N.Y., (1989), the disclosure of which is hereby incorporated by reference.
- Enhancers are cis-acting elements of DNA, usually about from 10 to 300 bp that act on a promoter to increase its transcription. Examples include the SV40 enhancer on the late side of the replication origin bp 1 00 to 270, a cytomegalovirus early promoter enhancer, the polyoma enhancer on the late side of the replication origin, and adenovirus enhancers.
- recombinant expression vectors will include origins of replication and selectable markers permitting transformation of the host cell, e.g., the ampicillin resistance gene of E. coli and S. cerevisiae Trp1 gene, and a promoter derived from a highly-expressed gene to direct transcription of a downstream structural sequence.
- promoters can be derived from operons encoding glycolytic enzymes such as 3-phosphoglycerate kinase (PGK), ⁇ -factor, acid phosphatase, or heat shock proteins, among others.
- the heterologous structural sequence is assembled in appropriate phase with translation initiation and termination sequences, and preferably, a leader sequence capable of directing secretion of translated protein into the periplasmic space or extracellular medium.
- the heterologous sequence can encode a fusion protein including an N-terminal identification peptide imparting desired characteristics, e.g., stabilization or simplified purification of expressed recombinant product.
- Useful expression vectors for bacterial use are constructed by inserting a structural DNA sequence encoding a desired protein together with suitable translation initiation and termination signals in operable reading phase with a functional promoter.
- the vector will comprise one or more phenotypic selectable markers and an origin of replication to ensure maintenance of the vector and to, if desirable, provide amplification within the host.
- Suitable prokaryotic hosts for transformation include E. coli. Bacillus subtilis, Salmonella typhimurium and various species within the genera Pseudomonas, Streptomyces, and Staphylococcus, although others may also be employed as a matter of choice.
- useful expression vectors for bacterial use can comprise a selectable marker and bacterial origin of replication derived from commercially available plasmids comprising genetic elements of the well known cloning vector pBR322 (ATCC 3701 7).
- cloning vector pBR322 ATCC 3701 7
- Such commercial vectors include, for example, pKK223-3 (Pharmacia Fine Chemicals, Uppsala, Sweden) and GEM1 (Promega Biotec, Madison, Wl, USA). These pBR322 "backbone" sections are combined with an appropriate promoter and the structural sequence to be expressed.
- the selected promoter is induced by appropriate means (e.g., temperature shift or chemical induction) and cells are cultured for an additional period.
- Cells are typically harvested by centrifugation, disrupted by physical or chemical means, and the resulting crude extract retained for further purification.
- Microbial cells employed in expression of proteins can be disrupted by any convenient method, including freeze-thaw cycling, sonication, mechanical disruption, or use of cell lysing agents, such methods are well known to those skilled in the art.
- mammalian cell culture systems can also be employed to express recombinant protein.
- mammalian expression systems include the COS-7 lines of monkey kidney fibroblasts, described by Gluzman, Cell, 23: 1 75 (1 981 ), and other cell lines capable of expressing a compatible vector, for example, the C1 27, 3T3, CHO, HeLa and BHK cell lines.
- Mammalian expression vectors will comprise an origin of replication, a suitable promoter and enhancer, and also any necessary ribosome binding sites, polyadenylation site, splice donor and acceptor sites, transcriptional termination sequences, and 5' flanking nontranscribed sequences. DNA sequences derived from the SV40 splice, and polyadenylation sites may be used to provide the required nontranscribed genetic elements.
- the polypeptide can be recovered and purified from recombinant cell cultures by methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Protein refolding steps can be used, as necessary, in completing configuration of the mature protein. Finally, high performance liquid chromatography (HPLC) can be employed for final purification steps.
- HPLC high performance liquid chromatography
- polypeptides of the present invention may be a naturally purified product, or a product of chemical synthetic procedures, or produced by recombinant techniques from a prokaryotic or eukaryotic host (for example, by bacterial, yeast, higher plant, insect and mammalian cells in culture). Depending upon the host employed in a recombinant production procedure, the polypeptides of the present invention may be glycosylated or may be non-glycosylated. Polypeptides of the invention may also include an initial methionine amino acid residue.
- buffers, media, reagents, cells, culture conditions and the like are not intended to be limiting, but are to be read so as to include all related materials that one of ordinary skill in the art would recognize as being of interest or value in the particular context in which that discussion is presented. For example, it is often possible to substitute one buffer system or culture medium for another and still achieve similar, if not identical, results. Those of skill in the art will have sufficient knowledge of such systems and methodologies so as to be able, without undue experimentation, to make such substitutions as will optimally serve their purposes in using the methods and procedures disclosed herein.
- the genomic DNA used as the target for amplification was isolated from Streptococcus pneumoniae (strain N4), the same strain used for genomic sequencing.
- the nucleotide sequence of the gene fragment encoding SP1 33 is contained in SEQ ID NO:3 and the corresponding amino acid sequence for polypeptide SP1 33 in SEQ ID NO: 4.
- Primers (SEQ ID NOS: 1 and 2) were designed so as to amplify the SP1 33 gene fragment and facilitate cloning thereof into the expression vector pQE10 with, for example, subsequent expression of a histidine-tagged protein product for purification by Nickel-affinity chromatography.
- mice 50 ⁇ l PBS emulsified in 50 ⁇ l complete Freund's adjuvant [CFA]).
- Groups of 10 or 1 9 sham-immunized mice received PBS (phosphate buffered saline) with adjuvant only.
- a second immunization of 1 5 ⁇ g protein with incomplete Freund's adjuvant (IFA) was administered 3 weeks later.
- the sham groups received PBS with IFA.
- Blood was drawn (by retro-orbital bleed) at week 7.
- Sera from each group were pooled for analysis of anti- SP1 33 antibody by ELISA.
- Mice were challenged at week 8 by an intraperitoneal (i.p.) injection of approximately 800 colony forming units (CFU) or 340 CFU of S.
- CFU colony forming units
- pneumoniae strain SJ2 (serotype 6B; provided by P. Flynn, St. Jude Children's Research Hospital, Memphis, TN).
- the LD 50 of this strain was determined to be about 10 CFU. Mice were monitored for 1 5 days for survival. A two-sample Log-rank test was used to evaluate the protection against death in a mouse model of systemic disease.
- Pneumococci (strain SJ2) were cultured in Todd Hewitt broth supplemented with 0.5% yeast extract (THY) medium at 37°C to mid- logarithmic phase. Bacteria were harvested and washed once in PBS containing 5% heat inactivated fetal calf serum (FCS; BioWhittaker, Walkersville, MD) at 4,000 x g for 10 minutes. Bacterial cell numbers were adjusted to 5 x 10 6 bacteria in 0.1 ml/tube. Pooled sera from mice immunized with SP1 33 (as already described for Example 1 ) diluted to 1 : 100 was added to each tube and placed on ice for 1 hr.
- FCS heat inactivated fetal calf serum
- the pneumococcal strains used in this experiment were obtained from the American Type Culture Collection (10801 University Boulevard., Manassas, VA 201 1 0-2209) and include one isolate from each of the serotypes in the multivalent pneumococcal carbohydrate vaccine.
- several laboratory strains and various primary clinical isolates including N4 (Serotype 4) and SJ2 (serotype 6B) were examined for SP1 33 expression.
- N4 Serotype 4
- SJ2 serotype 6B
- mice anti-SP1 33 sera detected a major band with an apparent molecular weight of 32 kDa in all pneumococcal lysates tested (except for strain WU2; see Figure 3).
- Lanes labeled C were probed with serum collected either one month (patients 1 and 2) or eight days after the first serum collection (patients 3 and 4). For patients 1 and 2, reactivity of the convalescent sera with SP1 33 was stronger than that of the corresponding acute sera.
- SP1 33 is recognized by the human immune system and suggest that antibodies able to bind the SP1 33 protein may be produced during natural S. pneumoniae infection in humans. Since the patients were infected with a variety of pneumococcal strains, these data also support a conclusion that SP1 33 is antigenically conserved.
Abstract
Description
Claims
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AU5577201A AU5577201A (en) | 2000-04-27 | 2001-04-27 | Immunogenic pneumococcal protein and vaccine compositions thereof |
JP2001578467A JP2003530872A (en) | 2000-04-27 | 2001-04-27 | Immunogenic S. pneumoniae proteins and vaccine compositions thereof |
CA002407455A CA2407455A1 (en) | 2000-04-27 | 2001-04-27 | Immunogenic pneumococcal protein and vaccine compositions thereof |
AU2001255772A AU2001255772B2 (en) | 2000-04-27 | 2001-04-27 | Immunogenic pneumococcal protein and vaccine compositions thereof |
EP01928972A EP1278856A2 (en) | 2000-04-27 | 2001-04-27 | Immunogenic pneumococcal protein and vaccine compositions thereof |
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Cited By (15)
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US7384775B2 (en) | 2001-04-16 | 2008-06-10 | Wyeth | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
WO2009111337A1 (en) | 2008-03-03 | 2009-09-11 | Irm Llc | Compounds and compositions as tlr activity modulators |
WO2010144734A1 (en) | 2009-06-10 | 2010-12-16 | Novartis Ag | Benzonaphthyridine-containing vaccines |
WO2011027222A2 (en) | 2009-09-02 | 2011-03-10 | Novartis Ag | Immunogenic compositions including tlr activity modulators |
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WO2011049677A1 (en) | 2009-09-02 | 2011-04-28 | Irm Llc | Compounds and compositions as tlr activity modulators |
WO2011057148A1 (en) | 2009-11-05 | 2011-05-12 | Irm Llc | Compounds and compositions as tlr-7 activity modulators |
WO2011084549A1 (en) | 2009-12-15 | 2011-07-14 | Novartis Ag | Homogeneous suspension of immunopotentiating compounds and uses thereof |
WO2011119759A1 (en) | 2010-03-23 | 2011-09-29 | Irm Llc | Compounds (cystein based lipopeptides) and compositions as tlr2 agonists used for treating infections, inflammations, respiratory diseases etc. |
WO2012072769A1 (en) | 2010-12-01 | 2012-06-07 | Novartis Ag | Pneumococcal rrgb epitopes and clade combinations |
EP2572726A1 (en) | 2007-08-01 | 2013-03-27 | Novartis AG | Compositions comprising pneumococcal antigens |
WO2013131983A1 (en) | 2012-03-07 | 2013-09-12 | Novartis Ag | Adjuvanted formulations of streptococcus pneumoniae antigens |
WO2014118305A1 (en) | 2013-02-01 | 2014-08-07 | Novartis Ag | Intradermal delivery of immunological compositions comprising toll-like receptor agonists |
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US6800744B1 (en) * | 1997-07-02 | 2004-10-05 | Genome Therapeutics Corporation | Nucleic acid and amino acid sequences relating to Streptococcus pneumoniae for diagnostics and therapeutics |
US6858706B2 (en) * | 1998-04-07 | 2005-02-22 | St. Jude Children's Research Hospital | Polypeptide comprising the amino acid of an N-terminal choline binding protein a truncate, vaccine derived therefrom and uses thereof |
KR20060126844A (en) * | 1998-04-07 | 2006-12-08 | 메디뮨 인코포레이티드 | Derivatives of pneumococcal choline binding proteins for vaccines |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998006734A1 (en) * | 1996-08-16 | 1998-02-19 | Smithkline Beecham Corporation | Novel prokaryotic polynucleotides, polypeptides and their uses |
WO1998018931A2 (en) * | 1996-10-31 | 1998-05-07 | Human Genome Sciences, Inc. | Streptococcus pneumoniae polynucleotides and sequences |
-
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- 2001-04-27 US US09/844,124 patent/US6689369B2/en not_active Expired - Lifetime
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- 2001-04-27 WO PCT/US2001/013828 patent/WO2001081380A2/en not_active Application Discontinuation
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Publication number | Priority date | Publication date | Assignee | Title |
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WO1998006734A1 (en) * | 1996-08-16 | 1998-02-19 | Smithkline Beecham Corporation | Novel prokaryotic polynucleotides, polypeptides and their uses |
WO1998018931A2 (en) * | 1996-10-31 | 1998-05-07 | Human Genome Sciences, Inc. | Streptococcus pneumoniae polynucleotides and sequences |
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US8241642B2 (en) | 2001-04-16 | 2012-08-14 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
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US9408907B2 (en) | 2009-12-15 | 2016-08-09 | Glaxosmithkline Biologicals Sa | Homogenous suspension of immunopotentiating compounds and uses thereof |
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US6689369B2 (en) | 2004-02-10 |
US20030166844A1 (en) | 2003-09-04 |
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EP1278856A2 (en) | 2003-01-29 |
CA2407455A1 (en) | 2001-11-01 |
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AU5577201A (en) | 2001-11-07 |
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