US 5,770,208 AGrant
Staphylococcus Aureus B-Linked Hexosamine Antigen
Issue Date:1998-06-23
•23 Claims
•4 Drawing Sheets
Abstract
A negatively-charged S. aureus antigen contains .beta.-hexosamine as a major carbohydrate component. S. aureus strains that carry the antigen account for nearly all of the clinically significant strains of S. aureus that are not Type 5 or Type 8 strains. The antigen can be used in combination with S. aureus Type 5 polysaccharide antigen and S. aureus Type 8 polysaccharide antigen to provide nearly 100% coverage of S. aureus infection.
Metadata
Assignee
- NABI
Inventors
- Ali Ibrahim Fattom
- Atulkumar Induprasad Patel
Application Information
Application Number:US 7124384
Filing Date:1996-09-11
Priority Date:1996-09-11
Art Unit:187
Classifications
IPC:
A61K 39085A61K 3940C07K 1612
Field of Search:
424530536514141.1;183.1;243.1;93.1;197.11;150.1;93.42;165.1388.1;388.2;388.4;389.5;402;403123.154
Patent Drawings (4 sheets)
Description
BACKGROUND OF THE INVENTION
The present invention relates to a novel Staphylococcus aureus antigen, and to a method for obtaining and using the antigen.
S. aureus causes several diseases by various pathogenic mechanisms. The most frequent and serious of these diseases are bacteremia and its complications in hospitalized patients. In particular, S. aureus can cause wound infections and infections associated with catheters and prosthetic devices. Serious infections associated with S. aureus bacteremia include osteomyelitis, invasive endocarditis and septicemia. The problem is compounded by multiple antibiotic resistance in hospital strains, which severely limits the choice of therapy.
A S. aureus vaccine would provide a solution for the problem of antibiotic resistance. Eight different serotypes of S. aureus have been identified using polyclonal and monoclonal antibodies to capsular polysaccharide (CPS). Karakawa et al., J. Clin. Microbiol. 22:445 (1985). The contents of this document and all others listed herein are incorporated herein by reference. Surveys have shown that approximately 85-90% of isolates are capsular polysaccharide Type 5 or Type 8. An individual vaccinated with a vaccine containing Type 5 and Type 8 CPS antigens would be protected from infection by 85-90% of S. aureus strains, but a significant risk of infection still would exist. A vaccine containing antigens from the other six serotypes theoretically could provide 100% protection, but would require production and purification of six additional components. This would be untenable from a practical standpoint. On the other hand, an antigen common to the isolates not typeable as Type 5 or Type 8 would enable production of a vaccine containing only three antigens.
SUMMARY OF THE INVENTION
It is therefore an object of the present invention to provide an antigen common to S. aureus strains of clinical significance that are not Type 5 or Type 8 strains.
It is a further object to provide a vaccine that contains an antigen common to S. aureus strains that are not Type 5 or Type 8 strains.
It is yet another object to provide a vaccine that contains S. aureus Type 5 antigen, S. aureus Type 8 antigen and an antigen common to S. aureus strains that are not Type 5 or Type 8 strains.
It is another object to provide a hyperimmune globulin composition that contains antibodies directed against Type 5 antigen, Type 8 antigen and an antigen common to S. aureus strains that are not Type 5 or Type 8 strains.
In accordance with these and other objects according to the invention, there is provided an isolated Staphylococcus aureus antigen that comprises .beta.-linked hexosamine. Also provided is a composition comprising the S. aureus antigen comprising .beta.-linked hexosamine, and at least one of a S. aureus Type 5 polysaccharide antigen and a S. aureus Type 8 polysaccharide antigen, and a sterile, pharmaceutically-acceptable carrier therefor. An immunotherapy method comprises a step of administering to a subject an immunostimulatory amount of such a composition.
A method of preparing an immunotherapeutic agent against S. aureus infection comprises steps of immunizing subjects with a composition according to the invention, collecting plasma from the immunized subjects, and harvesting a hyperimmune globulin that contains antibodies directed against S. aureus from the collected plasma. The hyperimmune globulin contains antibodies directed against the .beta.-linked hexosamine antigen, and additionally may contain antibodies directed against S. aureus Type 5 polysaccharide antigen and S. aureus Type 8 polysaccharide antigen. An immunotherapy method comprises a step of administering this hyperimmune globulin to a subject.
Other objects, features and advantages of the present invention will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.
BRIEF DESCRIPTION OF THE DRAWINGS
FIGS. 1A-C show the NMR spectra for Type 336 (FIG. 1A), Type 8 (FIG. 1B), and Type 5 S. aureus antigens (FIG. 1C).
FIG. 2 is a bar graph showing the ability of 336 conjugate IgG to mediate opsonophagocytosis of a representative strain of S. aureus that carries the 336 antigen.
DESCRIPTION OF PREFERRED EMBODIMENTS
It has been discovered that virtually all strains of S. aureus that are not typeable as Type 5 or Type 8 have in common an antigen, here denoted "the 336 antigen." When combined with Type 5 and Type 8 antigens, the 336 antigen represents the basis for a vaccine that provides almost complete protection against infection by clinically significant S. aureus isolates. In this regard, a "clinically significant" isolate is an isolate that is pathogenic.
More particularly, typing of isolates obtained from various sources has shown that approximately 60% of isolates are Type 8, approximately 30% are Type 5 and that nearly all of the remaining 10% of isolates are Type 336, as shown in Table 1. Less than 1% of the isolates are not typeable as one of these three types.
Notably, the present inventors obtained 27 clinical isolates that were not typeable as either Type 5 or Type 8 strains of S. aureus, and that were characterized as being methicillin-resistant strains. All of the 27 strains reacted very strongly with 336 antigen conjugate antibody sera, and thus were typeable as strains that contain 336 antigen.
Antibodies to the 336 antigen do not cross-react with polysaccharides isolated from any of S. aureus Type 5, Type 8, Type 4, K73 (a Type 5 variant strain) or S. epidermidis. The 336 antigen therefore is type-specific, that is, it produces a single band with only the homologous-type antiserum.
The 336 antigen can be obtained in recoverable amount, from certain S. aureus isolates cultured pursuant to the protocols described herein, in substantially pure form. In particular, purified antigen contains less than 1% protein and less than 1% nucleic acids. A "recoverable" amount in this regard means that the isolated amount of the antigen is detectable by a methodology less sensitive than radiolabeling, such as immunoassay, and can be subjected to further manipulations involving transfer of the antigen per se into solution.
To obtain the 336 antigen, a 336 isolate according to the invention first is grown on a Columbia Broth agar plate supplemented with MgCl.sub.2 /CaCl.sub.2 and then transferred to a 2% NaCl/Columbia starter flask. A 50-liter fermentor that contains the same medium is inoculated with the starter flask. Cells are fermented for 16-24 hours. Following fermentation, cells are killed with 2% final concentration of phenol to ethanol (1:1) and then centrifuged to separate the cells from the supernatant. Antigen is extracted from cell paste. Some 336 antigen is present in the supernatant, but the amount is insignificant as compared to the amount found in the cell paste. Because of the low yield, and the risk of hexose contamination from the media, extraction from supernatant is not preferred.
Enzyme treatments of cell paste with lysostaphin, DNase, RNase and protease, followed by sequential precipitation with 25-75% cold ethanol/CaCl.sub.2, results in a crude antigen extraction. The crude material is redissolved in water, dialyzed and lyophilized. The lyophilized material is dissolved in buffer and loaded onto a separatory column equilibrated with the same buffer. The column is washed with 0.15M NaCl loading buffer and then eluted with a 0.15-0.4M NaCl gradient. Most of the antigen according to the invention elutes at 0.32 to 0.35M NaCl. Fractions containing antigen are pooled, dialyzed, concentrated, and lyophilized. The separation can be repeated to obtain better purification. The crude antigen is treated with lysozyme and purified by size on a suitable column and the 336 positive fractions are then pooled, concentrated, dialyzed and lyophilized.
Analysis of purified 336 antigen by gas liquid chromatography (GLC) shows the presence of glucosamine as a major glycosyl component. This is confirmed by sugar analysis on a Dionex system. 1 H-NMR spectroscopy of the 336 antigen indicates the presence of .beta.-linked hexosamine as a major carbohydrate component. The antigen additionally comprises a component that is responsible for an observed negative charge displayed by the 336 antigen.
A comparison of the NMR spectra for each of the 336, Type 5 and Type 8 S. aureus antigens, as shown in FIG. 1, confirms that the 336 antigen is chemically distinct from both the Type 5 and Type 8 S. aureus antigens. The structures of Types 5 and 8 polysaccharide antigens have been elucidated by Moreau et al., Carbohydr. Res. 201:285 (1990); and Fournier et al., Infect. Imm. 45:87 (1984). Both have FucNAcp in their repeat unit as well as ManNAcA which can be used to introduce a sulfhydryl group. The structures are as follows: ##STR1## By contrast, the main carbohydrate component of the 336 antigen is .beta.-linked hexosamine.
Induction of bacteremia in mammals requires extremely high numbers of organisms or some previous maneuver to lower the host resistance. In vitro phagocytosis, however, can be studied as a correlate of protective immunity in vivo. In this model, the ability of 336 antigen-specific monoclonal and polyclonal antibodies to opsonize S. aureus in vitro is measured by phagocytosis, according to the method described in Kojima et al., Infect. Dis. Immun. 58:2367-2374 (1990).
Antibodies induced by a 336 antigen vaccine facilitate type-specific phagocytosis. The in vitro phagocytosis assays thus indicate that antibodies to the 336 antigen are protective against infection by S. aureus strains that carry the 336 antigen. Vaccines based on Type 5 and Type 8 antigens previously have been shown to be protective against infection by Type 5 and Type 8 strains of S. aureus, respectively. Fattom et al. Inf. and Imm. 58:2367-2374 (1990) and Fattom et al., Inf. and Imm. 64:1659-1665 (1996). A vaccine based on a combination of Type 5, Type 8 and 336 antigen can be used to protect against infection from the majority of clinical S. aureus strains.
A composition of the 336 antigen according to the present invention "consists essentially of" the 336 antigen, which means that the composition does not contain any material that interferes with elicitation of an immune response to the 336 antigen (and to other antigens, if present) when the composition is administered to a subject as a vaccine. In a preferred embodiment, the composition contains Type 336, Type 5 and Type 8 S. aureus antigens.
For use in a vaccine, it is preferable to conjugate the 336 antigen to an immunocarrier, usually a polypeptide or protein, to improve the interaction between T and B cells for the induction of an immune response against the antigen. This is particularly important for vaccines intended for use in patients with reduced resistance. An immunocarrier enhances immunogenicity both for active immunization and for preparing high-titered antisera in volunteers for passive immunization. Suitable immunocarriers according to the present invention include tetanus toxoid, diphtheria toxoid, Pseudomonas aeruginosa Exotoxin A or its derivatives, recombinantly-produced non-toxic mutant strains of exotoxin A, as described, for example, in Fattom et al., Inf. and Imm. 61:1023-1032 (1993), as well as other proteins commonly used as immunocarriers.
Preferably the antigen or antigen conjugate is administered without an adjuvant in order to avoid adjuvant-induced toxicity. If an adjuvant is used, it is preferred to use one which promotes the protective IgG subtype 2 antibodies. Typical adjuvants include complete Freund's adjuvant (CFA) and incomplete Freund's adjuvant (IFA). Dextran sulfate has been shown to be a potent stimulator of IgG.sub.2 antibody against staphylococcal cell surface antigens, and also is suitable as an adjuvant.
The present invention also relates to the use of the 336 antigen to produce polyclonal antibodies or monoclonal antibodies (mouse or human) that bind to or neutralize S. aureus strains that carry the 336 antigen. Protocols for producing these antibodies are described in Ausubel, et al. (eds.), Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.)., Chapter 11; in METHODS OF HYBRIDOMA FORMATION 257-271, Bartal & Hirshaut (eds.), Humana Press, Clifton, N.J. (1988); in Vitetta et al., Immunol. Rev. 62:159-83 (1982); and in Raso, Immunol. Rev. 62:93-117 (1982).
Inoculum for polyclonal antibody production typically is prepared by dispersing the antigen-immunocarrier in a physiologically-tolerable diluent such as saline, to form an aqueous composition. An immunostimulatory amount of inoculum, with or without adjuvant, is administered to a mammal and the inoculated mammal is then maintained for a time period sufficient for the antigen to induce protecting anti-336 antigen antibodies. Boosting doses of the antigen-immunocarrier may be used in individuals that are not already primed to respond to the antigen.
Antibodies can include antibody preparations from a variety of commonly used animals, e.g., goats, primates, donkeys, swine, rabbits, horses, hens, guinea pigs, rats, and mice, and even human antibodies after appropriate selection, fractionation and purification. Animal antisera may also be raised by inoculating the animals with formalin-killed 336 strains of S. aureus, by conventional methods, bleeding the animals and recovering serum or plasma for further processing.
The antibodies induced in this fashion can be harvested and isolated to the extent desired by well known techniques, such as by alcohol fractionation and column chromatgraphy, or by immunoaffinity chromatography; that is, by binding antigen to a chromatographic column packing like Sephadex.TM., passing the antiserum through the column, thereby retaining specific antibodies and separating out other immunoglobulins (IgGs) and contaminants, and then recovering purified antibodies by elution with a chaotropic agent, optionally followed by further purification, for example, by passage through a column of bound blood group antigens or other non-pathogen species. This procedure may be preferred when isolating the desired antibodies from the sera or plasma of humans that have developed an antibody titer against the pathogen in question, thus assuring the retention of antibodies that are capable of binding to the antigen. They can then be used in preparations for passive immunization against 336 strains of S. aureus.
A monoclonal antibody composition contains, within detectable limits, only one species of antibody combining site capable of effectively binding to the 336 antigen. Suitable antibodies in monoclonal form can be prepared using conventional hybridoma technology.
To form hybridomas from which a monoclonal antibody composition of the present invention is produced, a myeloma or other self-perpetuating cell line is fused with lymphocytes obtained from peripheral blood, lymph nodes or the spleen of a mammal hyperimmunized with the 336 antigen. It is preferred that the myeloma cell line be from the same species as the lymphocytes. Splenocytes are typically fused with myeloma cells using polyethylene glycol 1500. Fused hybrids are selected by their sensitivity to HAT. Hybridomas secreting the antibody molecules of this invention can be identified using an ELISA.
A Balb/C mouse spleen, human peripheral blood, lymph nodes or splenocytes are the preferred materials for use in preparing murine or human hybridomas. Suitable mouse myelomas for use in the present invention include the hypoxanthine-aminopterin-thymidine-sensitive (HAT) cell lines, a preferred myeloma being P3X63-Ag8.653. The preferred fusion partner for human monoclonal antibody production is SHM-D33, a heteromyeloma available from ATCC, Rockville, Md. under the designation CRL 1668.
A monoclonal antibody composition of the present invention can be produced by initiating a monoclonal hybridoma culture comprising a nutrient medium containing a hybridoma that secretes antibody molecules of the appropriate specificity. The culture is maintained under conditions and for a time period sufficient for the hybridoma to secrete the antibody molecules into the medium. The antibody-containing medium is then collected. The antibody molecules then can be isolated further by well known techniques.
Media useful for the preparation of these compositions are both well known in the art and commercially available, and include synthetic culture media, inbred mice and the like. An exemplary synthetic medium is Dulbecco's Minimal essential medium supplemented with 20% fetal calf serum. An exemplary inbred mouse strain is the Balb/c.
Other methods of preparing monoclonal antibody compositions are also contemplated, such as interspecies fusions, since it is primarily the antigen specificity of the antibodies that affects their utility in the present invention. Human lymphocytes obtained from infected individuals can be fused with a human myeloma cell line to produce hybridomas which can be screened for the production of antibodies that recognize the 336 antigen. More preferable in this regard, however, is a process that does not entail the use of a biological sample from an infected human subject. For example, a subject immunized with a vaccine as described herein can serve as a source for antibodies suitably used in an antibody composition within the present invention.
In a particularly preferred embodiment, monoclonal antibodies are produced to the 336 antigen using methods similar to those described for type-specific antibodies to S. aureus Type 5 and Type 8. The purified monoclonal antibodies are characterized by bacterial agglutination assays using a collection of clinical isolates.
The monoclonal and polyclonal antibody compositions produced according to the present description can be used by passive immunization to induce an immune response for the prevention or treatment of infection by strains of S. aureus that carry the 336 antigen. In this regard, the antibody preparation can be a polyclonal composition. Such a polyclonal composition includes antibodies that bind to the 336 antigen, and additionally may include antibodies that bind to the antigens that characterize Type 5 and Type 8 strains of S. aureus. The polyclonal antibody component can be a polyclonal antiserum, preferably affinity purified, from an animal which has been challenged with the 336 antigen, and preferably also with Type 5 and Type 8 antigens. Alternatively, an "engineered oligoclonal" mixture may be used, which is a mixture of monoclonal antibodies to the 336 antigen, and monoclonal antibodies Type 5 and/or Type 8 antigens.
In both types of mixtures, it can be advantageous to link antibodies together chemically to form a single polyspecific molecule capable of binding to the 336 antigen and one or both of Type 5 and Type 8 antigens. One way of effecting such a linkage is to make bivalent F(ab').sub.2 hybrid fragments by mixing two different F(ab').sub.2 fragments produced, e.g., by pepsin digestion of two different antibodies, reductive cleavage to form a mixture of Fab' fragments, followed by oxidative reformation of the disulfide linkages to produce a mixture of F(ab').sub.2 fragments including hybrid fragments containing a Fab' portion specific to each of the original antigens. Methods of preparing such hybrid antibody fragments are disclosed in Feteanu, LABELED ANTIBODIES IN BIOLOGY AND MEDICINE 321-23, McGraw-Hill Int'l Book Co. (1978); Nisonoff, et al., Arch Biochem. Biophys. 93:470 (1961); and Hammerling, et al., J. Exp. Med. 128:1461 (1968); and in U.S. Pat. No. 4,331,647.
Other methods are known in the art to make bivalent fragments that are entirely heterospecific, e.g., use of bifunctional linkers to join cleaved fragments. Recombinant molecules are known that incorporate the light and heavy chains of an antibody, e.g., according to the method of Boss et al., U.S. Pat. No. 4,816,397. Analogous methods of producing recombinant or synthetic binding molecules having the characteristics of antibodies are included in the present invention. More than two different monospecific antibodies or antibody fragments can be linked using various linkers known in the art.
An antibody component produced in accordance with the present invention can include whole antibodies, antibody fragments, or subfragments. Antibodies can be whole immunoglobulin of any class, e.g., IgG, IgM, IgA, IgD, IgE, chimeric antibodies or hybrid antibodies with dual or multiple antigen or epitope specificities, or fragments, e.g., F(ab').sub.2, Fab', Fab and the like, including hybrid fragments, and additionally includes any immunoglobulin or any natural, synthetic or genetically engineered protein that acts like an antibody by binding to a specific antigen to form a complex. In particular, Fab molecules can be expressed and assembled in a genetically transformed host like E. coli. A lambda vector system is available thus to express a population of Fab's with a potential diversity equal to or exceeding that of subject generating the predecessor antibody. See Huse, W. D., et al., Science 246:1275-81 (1989).
The 336 antigen according to the present invention can be the active ingredient in a composition, further comprising a pharmaceutically acceptable carrier for the active ingredient, which can be used as a vaccine to induce a cellular immune response and/or production in vivo of antibodies which combat S. aureus infection. In this regard, a pharmaceutically acceptable carrier is a material that can be used as a vehicle for administering a medicament because the material is inert or otherwise medically acceptable, as well as compatible with the active agent, in the context of vaccine administration. In addition to a suitable excipient, a pharmaceutically acceptable carrier can contain conventional vaccine additives like diluents, adjuvants, antioxidants, preservatives and solubilizing agents.
Pursuant to the present invention, such a vaccine can be administered to a subject not already infected with S. aureus, thereby to induce a S. aureus-protective immune response (humoral or cellular) in that subject. Alternatively, a vaccine within the present invention can be administered to a subject in which S. aureus infection already has occurred but is at a sufficiently early stage that the immune response produced to the vaccine effectively inhibits further spread of infection.
By another approach, a vaccine of the present invention can be administered to a subject who then acts as a source for globulin, produced in response to challenge from the specific vaccine ("hyperimmune globulin"), that contains antibodies directed against S. aureus. A subject thus treated would donate plasma from which hyperimmune globulin would then be obtained, via conventional plasma-fractionation methodology, and administered to another subject in order to impart resistance against or to treat S. aureus infection. Hyperimmune globulins according to the invention are particularly useful for immune-compromised individuals, for individuals undergoing invasive procedures or where time does not permit the individual to produce his own antibodies in response to vaccination.
Similarly, monoclonal or polyclonal anti-S. aureus antibodies produced according to the present invention can be conjugated to an immunotoxin, and administered to a subject in whom S. aureus infection has already occurred but has not become widely spread. To this end, antibody material produced pursuant to the present description would be administered in a pharmaceutically acceptable carrier, as defined herein.
The present invention is further described by reference to the following, illustrative examples.
EXAMPLE 1
Fermentation of S. aureus
A strain of S. aureus that carries the 336 antigen was cultivated in Columbia broth supplemented with 2% NaCl in an 80-liter fermentor containing 60 liters of broth medium at 37.degree. . The fermentation was started with one liter of a 16 hour old seed culture. The cells were grown with agitation at 200 rpm for 24 hours, to an A.sub.650nm of 20.0.
Cells to be used as a vaccine to prepare whole cell antiserum were formalin fixed overnight at room temperature. Cells for purification of antigen were killed by adding phenol-ethanol (1:1, vol/vol) to the fermentor to a final concentration of 2%, and mixing slowly for 2 hours at 15.degree.-20.degree. C. No viable cells were detected after this treatment. The cells then were harvested by centrifugation at 14,500.times.g and stored at -70.degree. C. until use. Approximately 800-900 grams of cell paste (net weight) was obtained from a 60-liter fermentation.
EXAMPLE 2
Preparation of Whole Cell Antiserum
Formalin-fixed cells from Example 1 were adjusted at OD.sub.540nm =1 and were injected intravenously into rabbits. No adjuvant was used. Rabbits were bled at weekly and positive whole cell serum was collected and pooled. IgG was purified from whole cell serum by a protein G affinity column. The purified material contained 23 mg/ml total IgG (280 UV scan) and substantially less 336 antigen-specific IgG.
EXAMPLE 3
Purification of Antigen
The cell paste was suspended at 0.5 g (wet weight) per ml in 0.05M Tris-2mM MgSo.sub.4, pH 7.5. Lysostaphin (100 to 150 .mu.g/ml) was added and incubated at 37.degree. C. for 3 hours with mixing. Thereafter, DNase and Rnase were added to final concentrations of 50 .mu.g/ml each, and the incubation was continued for an additional 4 hours. The reaction mixture was precipitated sequentially with 25 and 75% ethanol in the presence of 10 mM CaCl.sub.2.
The 75% ethanol precipitate was pelleted by centrifugation at 12,000.times.g for 30 minutes, or at a lower rpm for a longer time. The supernatant was transferred to dialysis tubing. The reaction mixture was filtered through a 0.45 .mu.m pore-size membrane and precipitated sequentially with 25 and 75% ethanol in the presence of 10 mM CaCl.sub.2. The 75% ethanol precipitate was dialyzed extensively against water at 3.degree. to 8.degree. C. and freeze-dried. The powder was dissolved in 0.2M NaCl/0.05M Tris HCl, pH 7.0. The resulting crude material was loaded onto a Q Sepharose column in 0.2M NaCl/0.05M Tris HCl, pH 7.0, and eluted with a 0.2-0.4M NaCl linear gradient. Fractions that contained antigen, as detected by capillary precipitation with antiserum from Example 2, were pooled, dialyzed, and freeze-dried. Most of the antigen eluted at 0.32-0.35M NaCl/0.05M Tris HCl.
The crude antigen thus obtained was treated with 1 mg lysozyme per 10 mg crude antigen in 10 mM CaCl.sub.2 to digest residual peptidoglycan contamination. The lysozyme-treated crude antigen then was further purified on a Sephacryl S-300 gel filtration column in 0.2M NaCl/PBS 1.times. to obtain substantially pure antigen. All reactive material was screened using whole antiserum.
EXAMPLE 4
Characterization of Antigen
Analysis of purified 336 antigen by gas liquid chromatography (GLC) shows the presence of glucosamine as a major glycosyl component. This is confirmed by sugar analysis on the Dionex system. 1H-NMR spectroscopy of the 336 antigen shows one anomeric proton at 4.751 ppm, corresponding to .beta.-linked hexosamine. In addition, the NMR spectrum shows well separated signals at 4.229 ppm (2 H), 3.649 (1 H), 3.571 ppm (2 H), 2.19 ppm (3 H). Signals corresponding to O-acetyl groups are not found. This indicates the absence of O-acetylation, and is clearly distinguished from the 20-80% O-acetylation found on other S. aureus type isolates, such as Type 5 and Type 8. The 13C-NMR spectrum shows one signal in the anomeric region at 102.396 ppm. This confirms the presence of monosaccharide as a major component. Other C13-NMR spectrum signals appear at 81.865, 76.641, 74.950, 71.841, 71.051, 70.775, 67.665, 67.142, 61.716, 56.552, 50.355, 43.408 and 23.246 ppm, respectively.
The mobility of purified antigen in immunoelectrophoresis (IEF) indicates the presence of negatively-charged groups. The purified antigen does not contain neutral sugars as detected by the phenol sulfuric assay. The K.sub.d of purified antigen was 0.3 on Superose 12 HR column, which is a smaller molecular size material in comparison with Type 5 (K.sub.d of 0.017), Type 8 (K.sub.d of 0.061) and teichoic acid (K.sub.d of 0.18).
EXAMPLE 5
Antigen-Immunocarrier Conjugates
Purified antigen was derivatized with 0.5M adipic acid dihydrazide (ADH) using 100 mM 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDAC) at pH 5.6. Percentage derivatization was achieved in the range of 2 to 7% (w/w). Derivatized purified antigen was conjugated to recombinantly-produced, non-toxic mutant strain of Pseudomonas aeruginosa exotoxin A using 50 mM EDAC at 1:1 (antigen:protein), as described in Fattom et al., Inf. and Imm. 60:584-589 (1992). The conjugation yield was 50-70%, determined by measurement of protein. The Kd of the conjugate was 0.2 on the Superose 12 HR column.
The conjugate was injected into rabbits with adjuvant (CFA followed by IFA) at a 1:1 ratio. Positive bleeds were combined and IgGs were purified on a protein G column. Conjugate-raised IgG showed identity with antibodies induced by whole cell IgG against the antigen in an immunodiffusion assay. Purified conjugate sera IgG was shown to contain 12.2 mg/ml total IgG by a 280 nm UV scan and 0.7 mg/ml antigen-specific IgG by ELISA. Whole cell serum, whole cell IgG, and conjugate IgG were used in opsonophagocytosis assays and animal models.
EXAMPLE 6
In vitro Opsonophagocytosis Assays
Polymorphonuclear leukocytes (PMNs) were obtained from HL-60 cells adjusted to a concentration of 1.0.times.10.sup.7 cells per ml in MEM supplemented with 10% fetal bovine serum (FBS). S. aureus was grown overnight in Columbia broth supplemented with MgCl.sub.2 /CaCl.sub.2. The concentration of bacteria was adjusted spectrophotometrically to an OD of 0.02 at 540 nm (4.times.10.sup.6 cells/ml) then adjusted to 1.times.10.sup.6 cells/ml in MEM supplemented with 10% FBS. Purified antigen-specific or control non-reactive IgGs were added to facilitate opsonization by PMNs. Baby rabbit complement, diluted 1:8 in MEM supplemented with 10% FBS was used as the negative control.
The reaction mixture contained 25 .mu.l S. aureus (concentration 1.times.10.sup.6 cells/ml), 25 .mu.l PMNs (concentration 1.times.10.sup.7 cells/ml), 25 .mu.l complement, 100 .mu.l sera or antibodies, and sufficient MEM/10% FBS to bring the total reaction volume to 250 .mu.l. At 0 hours, 1 hours and 2 hours, 25 .mu.l of sample were serially diluted. 25 .mu.l of the 10.sup.-2, 10.sup.-3, 10.sup.-4 and 10.sup.-5 dilutions were plated onto TSA agar plates, and incubated overnight at 37.degree. C.
The results are shown in FIG. 2, and show that antibody to conjugate mediates opsonophagocytosis of a representative strain of S. aureus that carries the 336 antigen. The results are reported as percent killing by amounts of 336 antigen-specific IgG ranging from 300 .mu.g to 128 .mu.g. For comparison, percent killing by an equivalent amount of non-reactive IgG is also reported. PMNs plus complement was used as a control.
Claims
What we claim is:
1. An isolated Staphylococcus aureus antigen that comprises .beta.-linked hexosamine, wherein said antigen contains no O-acetyl groups detectable by nuclear magnetic resonance spectroscopy and specifically binds with antibodies to Staphylococcus aureus Type 336 deposited under ATCC 55804.
2. An antigen-carrier conjugate, comprising an antigen as claimed in claim 1 conjugated to an immunocarrier.
3. An antigen-carrier conjugate as claimed in claim 2, wherein said immunocarrier is a recombinantly-produced, non-toxic mutant strain of Pseudomonas aeruginosa exotoxin A.
4. A composition consisting essentially of an antigen as claimed in claim 1, and a sterile, pharmaceutically-acceptable carrier therefor.
5. A composition consisting essentially of an antigen-immunocarrier conjugate as claimed in claim 2, and a sterile, pharmaceutically-acceptable carrier therefor.
6. A composition as claimed in claim 5, wherein said immunocarrier is a recombinantly-produced, non-toxic mutant of Pseudomonas aeruginosa exotoxin A.
7. A composition comprising: an isolated S. aureus antigen that comprises .beta.-linked hexosamine, wherein said antigen contains no O-acetyl groups detectable by nuclear magnetic resonance spectroscopy and specifically binds with antibodies to Staphylococcus aureus Type 336 deposited under ATCC 55804; S. at least aureus Type 5 polysaccharide antigen or S. aureus Type 8 polysaccharide antigen; and a sterile pharmaceutically acceptable carrier therefor.
8. A composition as claimed in claim 7, comprising both said Type 5 and Type 8 polysaccharide antigens.
9. A composition as claimed in claim 8, wherein each of said antigens is conjugated to an immunocarrier.
10. A composition as claimed in claim 9, wherein each of said antigens is conjugated to the same immunocarrier.
11. A composition as claimed in claim 9, wherein said immunocarrier is a recombinantly-produced, non-toxic mutant strain of Pseudomonas aeruginosa exotoxin A.
12. An immunotherapy method comprising a step of administering to a subject an immunostimulatory amount of a composition as claimed in claim 5.
13. An immunotherapy method comprising a step of administering to a subject an immunostimulatory amount of a composition as claimed in claim 9.
14. A method of preparing an immunotherapeutic agent against S. aureus infection, comprising steps of immunizing subjects with a composition according to claim 5, collecting plasma from said immunized subjects, and harvesting antibodies directed against S. aureus from said collected plasma.
15. A method of preparing an immunotherapeutic agent against S. aureus infection, comprising steps of immunizing subjects with a composition according to claim 9, collecting plasma from said immunized subjects, and harvesting antibodies directed against S. aureus from said collected plasma.
16. A composition containing antibodies directed against S. aureus Type 5 polysaccharide antigen, S. aureus Type 8 polysaccharide antigen, and an antigen as claimed in claim 1.
17. A hyperimmune globulin containing antibodies directed against S. aureus Type 5 polysaccharide antigen, S. aureus Type 8 polysaccharide antigen, and an antigen as claimed in claim 1.
18. A composition containing a monoclonal antibody directed against S. aureus Type 5 polysaccharide antigen, a monoclonal antibody directed against S. aureus Type 8 polysaccharide antigen, and a monoclonal antibody directed against an antigen as claimed in claim 1.
19. An immunotherapy method comprising a step of administering to a subject the isolated antibodies as claimed in claim 16.
20. An immunotherapy method comprising a step of administering to a subject the isolated antibodies as claimed in claim 17.
21. A monoclonal antibody to the antigen of claim 1.
22. A composition comprising (a) a monoclonal antibody as claimed in claim 21, (b) at least one of a monoclonal antibody to S. aureus Type 5 polysaccharide antigen and a monoclonal antibody to S. aureus Type 8 polysaccharide antigen, and (c) a sterile, pharmaceutically-acceptable carrier therefor.
23. A composition as claimed in claim 22, comprising a monoclonal antibody to S. aureus Type 5 polysaccharide antigen and a monoclonal antibody to S. aureus Type 8 polysaccharide antigen.
Patent Citations (2)
Non-Patent Literature (15)
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