AU738824B2

AU738824B2 - Capsular polysaccharide immunomodulator

Info

Publication number: AU738824B2
Application number: AU13217/99A
Authority: AU
Inventors: Dennis L Kasper; Andrew B Onderdonk; Arthur O. Tzianabos
Original assignee: Brigham and Womens Hospital Inc
Current assignee: Brigham and Womens Hospital Inc
Priority date: 1994-09-02
Filing date: 1999-01-27
Publication date: 2001-09-27
Anticipated expiration: 2015-09-01
Also published as: AU1321799A

Description

AUSTRALIA

PATENTS ACT 1990

ORIGINAL

COMPLETE SPECIFICATION Name of Applicant: Address of Applicant: Actual Inventor(s): Brigham and Women's Hospital, Inc.

75 Francis Street, Boston, Massachusetts 02115, United States of America Arthur 0. Tzianabos; Andrew B. Onderdonk and Dennis L. Kasper.

DAVIES COLLISON CAVE, Patent Attorneys, 1 Little Collins Street, Melbourne, 3000.

Address for Service: Complete Specification for the invention entitled: Capsular polysaccharide immunomodulator The following statement is a full description of this invention, including the best method of performing it known to us: -1- 1A- CAPSULAR POLYSACCHARIE

IMMUNOMODULATOR

FIELD OF THE INVENTION This invention relates to immunomodulators and methods for protecting a subject against abscess formation associated with bacterial infection or contamination.

BACKGROUND

A commonly occurring complication associated with leakage of colonic bacteria into the peritoneum is intra-abdominal sepsis and abscess formation. An abscess is an encapsulated collection of bacteria, lymphocytes, macrophages, polymorphonuclear leukocytes and fibrin that forms in response to bacterial insult or contamination within the peritoneal cavity, such as occurs during a surgical procedure, trauma or diseases such as appendicitis or cancer.

Invasion of the exposed body area by the bacteria may occur in a localized area within the peritoneal cavity, retroperitoneal space, pelvis or other spaces or organs in the body. The S.:infected tissue area remains relatively immune to antibiotics which are unable to penetrate the tissue structures and effectively clear walled-off bacteria. If the abscess is left untreated, it may cause fever, prolonged hospitalization, and in some cases mortality. If the abscess ruptures, it will release its bacterial contents into the peritoneal cavity, which can in turn lead to recurring sepsis in these patients. Currently when abdominal surgeries are performed, antibiotics are administered prophylactically as well as post-operatively. However, once an abscess has formed, the major course of action is further surgical intervention to drain the offending abscess. The result is a time-consuming and costly procedure running on the average of $10,000 per patient.

It has been impractical to immunize patients against abscess formation such as in the case of intra-abdominal surgery. This traditional approach to treatment or prevention is not possible because there simply are too many strains of bacteria capable of causing abscess formation, J-and protection against one would not confer protection against another. It furthermore is -I y unsettled whether vaccination and consequent induction of an immune response would confer adequate protection against abscess formation by any particular bacterium. There also exist problems and dangers associated with administering live or attenuated strains of bacteria to humans, further discouraging efforts to produce vaccines containing a large number of different bacteria.

Capsular polysaccharides of bacteria can be found covering the surface of some bacteria pathogenic to humans. Polysaccharides have been characterized as T cell-independent antigens that elicit only humoral antibody responses. Although many polysaccharides have 10 been shown to be immunogenic, some are only weakly immunogenic at best.

Bacteroides fragilis is a predominant obligate anaerobe isolated from intra-abdominal abscesses. The capsular polysaccharide complex (CPC) has been identified as the region of fragilis which causes abscess formation. This carbohydrate complex covers the surface of B. fragilis. This isolated complex alone can interact with the host immune system, in the i: presence of adjuvant (sterile cecal contents and barium sulphate), to elicit a patho-biologic response that results in fully formed intraperitoneal abscesses in individuals injected intraperitoneally with the complex. Studies were preformed in rodent models in which B.

fragilis or its CPC were injected intraperitoneally. Both intact B. fragilis and CPC alone provoked abscess formation associated with intra-abdominal sepsis.

It was investigated whether the CPC of B. fragilis, in the presence of Freund's incomplete adjuvant, could be used to immunize subjects against subsequent infection and abscess formation by B. fragilis. It was by no means predictable that this would be possible based upon the property of CPC alone to provoke abscess formation since "immunity" and abscess formation are not known to result from remotely related immunological responses. When CPC was administered subcutaneously it was found to confer immunological protection against intraperitoneal CPC-mediated abscess induction in a rat model. Protection against abscess formation by this polysaccharide complex was determined to be mediated by a T cell-dependent host response.

U

S

-3- Although subcutaneous administration of either B. fragilis or CPC is sufficient to protect animals against abscess formation subsequent to challenge with B. fragilis or CPC, neither conferred immunity against other bacterial strains, as was expected. They therefore have no use as a "vaccine" for abscess formation caused by the multitude of organisms normally found in the colon.

The CPC consists of two distinct high molecular weight polysaccharides, termed A and B.

Each polysaccharide is composed of distinct oligosaccharide repeating units possessing uncommon constituent sugars with free amino, carboxyl and phosphonate groups.

10 Polysaccharide A has a tetrasaccharide repeating unit with a balanced positively charged amino group and negatively charged carboxyl group. Polysaccharide B has a hexasaccharide repeating unit, including an unusual substituent containing a free amino group and negatively charged phosphate group. The galacturonic acid residue contains an additional negatively charged carboxyl group. Ionic interaction between the two saccharide chains tightly links polysaccharides A and B into the high molecular weight CPC complex. The complex capsular motif is a conserved trait for all strains of B. fragilis that have thus far been examined.

It would be extremely desirable to have a pharmaceutical preparation that could protect a host organism against abscess formation associated with infection by multiple bacterial strains.

SUMMARY OF THE INVENTION Methods and products for protecting against abscess formation associated with surgery, trauma or diseases that predispose the host to abscess formation are provided. Methods for forming immunomodulators and pharmaceutical compositions relating thereto also are provided.

It has been discovered that polymers having a particular structural motif can protect animals 3 against challenge with abscess-inducing bacteria. This motif includes possession of a -I -4positively charged free amino group and a negatively charged group on a polysaccharide repeating unit. Such polymers are capable of inducing "cross-protection". That is, a single polymer can produce protection against abscess formation by a variety of bacteria.

According to one aspect of the invention a method for inducing protection against abscess formation associated with surgery, trauma or diseases that predispose the host to abscess formation is provided. A pharmaceutical preparation is administered to a subject in conjunction with intra-abdominal surgery or upon presentation of a predisposing condition.

i The preparation includes an effective amount for inducing protection against abscess S 10 formation of a polymer of repeating units of a charge motif characteristic of polysaccharide A of B. fragilis, the motif being a positively charged free amino moiety and a negatively charged moiety selected from the group consisting of carboxyl, phosphate, phosphonate, sulfate and sulfonate. The polymer can be a polysaccharide formed of repeating units of a i* maximum of ten saccharides, wherein each repeating unit includes at least one free amino 15 moiety and one negatively charged moiety selected from the group consisting of carboxyl, phosphate or phosphonate. The polymer is free from complexation as part of a B. fragilis capsular polysaccharide complex.

0 Preferably the polysaccharide is formed of repeating units of a maximum of five monosaccharides. Such polysaccharides occur in nature and may be isolated. One such polysaccharide, the most preferred, is capsular polysaccharide A of the B. fragilis capsular polysaccharide complex. In nature the polysaccharide A occurs only in complexed form, tightly bound to the B. fragilis capsular polysaccharide B. The A:B capsular polysaccharide complex is not capable of inducing cross-protection to infection with other bacteria. Thus, the invention contemplates administration of isolated capsular polysaccharide A, free from complexation as part of a B. fragilis capsular polysaccharide complex.

The polysaccharides useful according to the invention also may be synthesized from naturally occurring polysaccharides that do not possess the requisite motif. For example, certain naturally occurring polysaccharides have a negatively charged group and at least one N-acetyl moiety on each repeating unit. Such polysaccharides may be de-N-acetylated to convert the N-acetyl moiety to a free amino moiety, thereby creating the necessary structural motif for use according to the invention. Other naturally occurring polysaccharides include imine groups which can be reduced to form a free amino moiety, thereby creating together with a negatively charged group the necessary structural motif necessary for usefulness according to the invention.

Thus, the invention contemplates methods for preparing pharmaceuticals by selecting .i polysaccharides having repeating units of a maximum of ten saccharides, each unit having at least one negatively charged moiety selected from the group consisting of carboxyl, phosphate and phosphonate. Each repeating unit also includes a moiety that may be modified to form a free amino moiety. Such modified polysaccharides then are mixed with pharmaceutically acceptable carriers, preferably in amounts to form effective doses for protecting a subject against abscess formation associated with surgery, trauma or diseases that predispose the host 15 to abscess formation.

Pharmaceutical preparations also are provided. The pharmaceutical preparations include a polysaccharide formed of repeating units of a maximum of ten saccharides, each repeating unit including a free amino moiety and a negatively charged moiety selected from the group consisting of carboxyl, phosphate and phosphonate, together with a pharmaceutically acceptable carrier. The polysaccharide is free from complexation as part of a B. fragilis polysaccharide complex. Preferably the polysaccharide is a bacterial polysaccharide and most preferably the polysaccharide is a component of the B. fragilis capsular polysaccharide complex. The capsular polysaccharide A may also be modified, for example, to contain a hydroxymethyl group.

Exemplary pharmaceutical preparations include monomers that carry both the free amino group and the negatively charged group, dimers in a 1-4 linkage wherein the negatively charged group is on the first saccharide and trimers wherein the negatively charged group is S- RS n the first saccharide, wherein the free amino moiety is also on the first saccharide and/or -6wherein the third saccharide is free of any amino or negatively charged moiety. The most preferred preparation is a polysaccharide that has a repeating unit of a tetramer with a trimeric backbone, characteristic of B. fragilis capsular polysaccharide A.

According to another aspect of the invention, the products and methods of the invention may be administered with immunomodulators and/or antibiotics separately or as a part of the pharmaceutical preparations of the invention. Preferred immunomodulators are those that enhance protection against abscess formation. Useful immunomodulators include adjuvants; cytokine blockers such as antibodies to tumor necrosis factor, antibodies to interferon and 10 antibodies to interleukin-2 (all of which block abscess formation); and cytokines such as interleukin-10 (which also blocks abscess formation). Thus, the invention involves pharmaceutical preparations containing such immunomodulators and/or antibiotics together with the polymers useful according to the invention as described above. This includes Snaturally occurring bacterial polysaccharides that previously may have been used as 15 immunogens to stimulate a humoral B cell response, but have not before been used to protect against abscess formation and have not been used together with immunomodulators and/or antibiotics Streptococcus pneumoniae polysaccharide, Trypanosoma cruzi lipopeptidophosphoglycan and Shigella sonnei Phase I lipopolysaccharide O-antigen).

The methods and products of the invention are useful in protecting against abscess formation associated with infection by many different microorganisms, including but not limited to including protection against abscess formation by a microorganism selected from the group consisting of Bacteroides, Clostridia, Fusobacteria, Enterococcus, Prevotella, Porphyromonas, Staphylococcus, Proprionobacteria, Peptostreptococcus, Streptococcus, Veillonella, Actinomycetes, and Escherichia coli. The pharmaceutical preparations may be administered before and/or after exposure to the abscess-forming conditions. Parenteral administration is preferred.

It is believed that bacterial polysaccharides of the invention most likely act to stimulate T cell proliferation, which has not before been described in connection with bacterial r, -2 -7polysaccharides. The invention avoids the dangers associated with using live bacteria to stimulate an immune response and further provides cross-protection against a variety of strains of bacteria. The invention further can be used in connection with both planned and emergency surgeries, trauma or diseases that predispose the host to abscess formation.

These and other aspects of the invention are described in greater detail below.

DETAILED DESCRIPTION OF THE INVENTION 10 The invention is useful whenever it is desirable to prevent bacterial abscess formation in a subject. This includes prophylactic treatment to prevent such conditions in planned surgical e oo procedures as well as emergency situations. Elective surgeries include the following intraabdominal surgeries: right hemicolectomy; left hemicolectomy; sigmoid colectomy; subtotal colectomy; total colectomy; laparoscopic or open cholecystectomy (gall bladder); gastrectomy; etc. Emergency surgeries include those to correct the following conditions: perforated ulcer (duodenal or gastric); perforated diverticulitis; obstructive diverticulitis; perforated appendicitis; blunt abdominal trauma; penetrating abdominal trauma; second operation to drain abscess; etc. The invention also is useful with nonintra-abdominal surgeries such as cardiac surgeries and surgeries to correct wound infections. The invention also is useful in connection with diseases that predispose a subject to abscess formation such as pelvic inflammatory disease, inflammatory bowel disease, urinary tract infections and colon cancer. The invention thus is useful with abscesses of virtually any tissue or organ, including specifically but not limited to dermal abscesses such as acne. Those of ordinary skill in the art to which this invention pertains will recognize the range of conditions and procedures with which the invention is useful. A subject as used herein means; humans, primates, horses, cows, sheep, pigs, goats, dogs, cats and rodents.

It has been discovered that certain polysaccharides can be used to stimulate host T cells and induce protection against numerous bacteria. This protective effect is T cell-dependent and not mediated by a humoral antibody response. As such, administration of the preparations R.4 U~I ILLIII CLCV 1U~ IC~L(LVI -8of the invention is not "vaccination" and the preparations are not "vaccines" which mediate protection that is specific to bacteria expressing the immunizing antigen.

It was discovered that the B. fragilis capsular polysaccharide A (PSA), when separated from the polysaccharide A:B complex, was capable of conferring broad protection against abscess formation resulting from challenge with B. fragilis and other bacterial species. This was unexpected because PSA does not exist except as a complex with PSB in nature, and it therefore was not predictable that PSA would have any activity when separated from PSB.

What is more surprising is that this protection extends to abscess formation resulting from 10 infection by organisms other than B. fragilis because PSA does not exist on bacteria other than B. fragilis. Thus, the preparations of the invention represent the first "universal" immunomodulators capable of protecting against abscess formation that might result from infection/contamination by any number of bacteria. The invention thereby opens the door to pretreating abdominal surgical patients, trauma patients or patients with diseases that S 15 predispose the host to abscess formation with a safe immunomodulator to provoke a generalized immune response to protect against abscess formation.

g The protective effect described above was seen also using purified B. fragilis polysaccharide B (PSB), isolated and separated from polysaccharide A.

PSA has the following structure: H 0 H NHAc OO COD OHO HC

I

n4,6-pynvatc 3a-D-Su 3)-ft-D-Galp-(l--

Q

-9- PSB has the following structure:

HO

CH3 -0 0 3O

H-N

SOOH

OOH 0 H .C NHAcN rare particular structural features on polysacharide A and B removal of the charged amino or carboxyl group abrogated abscess induction by these polysaccharides. Polysaccharides from other organisms, such as the group antigen or capsular polysaccharide from Streptococcus pneumnoniae type 1 strains, that had different repeating unit structures but the same charged structural groups at least one free amino and one negatively charged group) also promoted abscess formation. Both the positively and negatively charged groups on these polysaccharides also modulate their ability to induce abscess formation and to protect animals against abscess formation. Treatment with either polysaccharide A or B protected animals against abscess formation subsequent to challenge with polysaccharide A, B or S. pneumoniae type 1 capsular polysaccharide. Both the positive and negative charges on polysaccharide A are essential to the ability of this polymer to confer protection against abscess formation, as neutralization of either charge abrogated the HO-* OH0 ,o °0 Itwsdtrie*htteeaepriua tutrlfaue nplschrd n whc*eit t blt oidc nr-boria bcse.Ceia etaiaino reoa ftecagdaioo*abxlgopargtdasesidcinb hs protection against abscess formation, as neutralization of either charge abrogated the protection. The ability of polysaccharide A or B to confer protection against abscess formation is mediated by T cells.

Polysaccharides useful according to the present invention include those naturally occurring polysaccharides that include the requisite charged groups. These polysaccharides may be derived from bacterial sources. Bacteria used as starting materials to obtain capsular polysaccharides can be obtained commercially from a number of sources. For example, the B. fragilis, NCTC 9343 and ATCC 23745 may be obtained from the National Collection of Type Cultures (London, England) and the American Type Culture Collection (Bethesda, Md).

10 Polysaccharide A and polysaccharide B can be purified from the above bacteria following the protocol of Pantosti et al., Infection and Immunity 59:2075-2082 (1991), the details of which are described briefly in Example 1.

In addition to the naturally occurring polysaccharides, polysaccharide repeating units that consist of at least one N-acetyl sugar and at least one uronic acid (sugar with a negatively charged carboxyl group) can be modified to produce the immune response of the present invention. A polysaccharide repeating unit containing at least one N-acetyl sugar and at least .one uronic acid can be de-N-acetylated to create a free amino group and thus will yield a polysaccharide with the correct charge motif. Molecules which may be de-N-acetylated include Salmonella typhi capsular polysaccharide (VI antigen), Escherichia coli K5 capsular polysaccharide, Staphylococcus aureus type 5 capsular polysaccharide, Group B Streptococcus type III capsular polysaccharide, and Rhizobium meliloti exopolysaccharide II (all described in greater detail below).

Bacterial polysaccharides which possess imine groups (C=NH) in addition to free carboxyl groups may be modified and used to produce the immune response of the present invention.

Many of the Pseudomonas aeruginosa O-specific side chains possess imine groups. Imine groups can be reduced with sodium borohydride (NaBH 4 to create free amino groups

(NH

3 An example of a compound which may be reduced with sodium borohydride to create free amino groups is Pseudomonas aeruginosa Fisher 7.

-11- The most preferred polysaccharide antigen is the capsular polysaccharide A from B. fragilis, modified slightly. Modification of polysaccharide A by oxidation with 0.01M Sodium metaperiodate (NaIO 4 by the procedure of Teleti et al., Journal of Clinical Investigation 89:203-209 (1992) enhances the biological activity.

HO O= (PSA). HOHC

(PSA)

:0 10 This modification selectively creates carbonyl groups on the galactofuranose side chain of the polysaccharide A repeating unit. This group is very amenable to reduction with a reducing agent such as sodium borohydride and will convert it to a hydroxymethyl group

(CH

2 OH) (see Example *oo The size of the polysaccharides useful according to the invention varies greatly.

Polysaccharides between 500 and 20,000,000 daltons will be typical. Polysaccharide A is about 2,000,000 daltons.

The polysaccharides useful in the invention may be delivered in mixtures of more than one polysaccharide. A mixture may consist of several polysaccharides.

As discussed above, naturally occurring polysaccharides can be modified to yield immunomodulators useful in the invention. Salmonella typhi has a capsular polysaccharide (Vi antigen) that is formed entirely of repeating monomers of galactosaminuronic acid. This acid includes a carboxylic moiety and an N-acetyl moiety. The N-acetyl moiety can be modified to yield a free amino group such that each monomeric repeating unit then has both a positively and negatively charged group.

Polysaccharides that are complexes exist and can be modified to yield immunomodulators useful in the invention. Esherichia coli K5 capsular polysaccharide is formed of repeat units 12of a complex of glucuronic acid and glucosamine linked together in 1-4 linkages. The glucuronic acid carries a carboxylic acid moiety and the glucosamine carries an N-acetyl group, which can be modified to form a free amino group. When so modified a complex repeat unit having both a negatively charged moiety (on the first sugar) and a free amino group (on the second sugar) is formed.

Polysaccharides that are trimers exist and can be modified to yield immunomodulators useful in the invention. Staphylococcus aureus type 5 capsular polysaccharide is formed of repeat units of a trimer of mannosaminuronic acid-fucosamine-fucosamine. The mannosaminuronic 10 acid carries a carboxylic acid moiety and the fucosamines carry N-acetyl moieties which can be modified to form free amino moieties. When so modified, a trimeric repeat unit having a negatively charged moiety (on the first sugar) and at least one positively charged moiety (on 0* the second and third sugars) is formed. In a similar manner, Pseudomonas aeruginosa S O-antigens can be modified to yield immunomodulators useful in the invention. Examples include trimers that carry carboxylic acid moieties and imine moieties which can be modified to yield free amino groups. Fisher immunotype 7, Lanyi-Bergan 02a, 02b and Lanyi-Bergan 02d and 2f have polysaccharides formed of trimeric repeat units with carboxylic acid moieties on the first and second sugars and an imine moiety on the first sugar. (The third sugar is free of a charged moiety; all sugars also carry an N-acetyl moiety). For example, the first sugar can be modified so as to carry both a free amino moiety and the carboxylic acid moiety.

Likewise the N-acetyl groups could be modified to yield a different arrangement useful according to the invention.

Polysaccharides that have longer repeat units such as tetramers and pentamers also can be modified as described above. It is believed that repeat units up to decimers are useful according to the invention. In addition, repeat units including side chain sugars also are useful, including those wherein-one or both of the free amino and negatively charged moieties are located on such side chains. Furthermore, such side chains carrying the charged moieties need not be sugars, although it is preferred that at least the backbone of the repeat unit is -r-made up of only sugars.

13 It is preferred that the repeat unit have no more than three free amino groups, and preferably no more than two such groups. It also is preferred that there be at least one negatively charged group for each free amino group.

The starting materials further need not be derived from bacterial origin. Any polysaccharides carrying carboxylic acid moieties and N-acetyl or imine groups may be modified as described above.

Specific examples together with chemical names and structural formulas are as follows. The 10 invention, however, is by no means limited to the following examples. In the chemical formulas, use is made of the following abbreviations: S AAT =2-acetamido-4-amino-2,4,6-tridoxy-D-galactose A=uronic acid NAc= N-acetyl group p=pyranose :::AEP 2-aminoethylphosphonate OAc= O-acetyl group Polysaccharides having N-acetyl moieties: Salmonella typhi capsular polysaccharide (Vi antigen) Cco- o If- i SdaCM°mkMU11aid The N-acetyl group structure and its modification to a free amino group are illustrated for the above polysaccharide only. N-acetyl groups will be abbreviated as NHAc in the structural formulas of the subsequent examples.

14 Esherichia ccli K5 capsular polysaccharide COO- 0CHzOH 0 HO- OH 0 H H4 Staphylococcus aureus type 5 capsular polysaccharide 0OCH 3 C 0 Coo-00 0 4 j N H A c 0NA.

H

-4I-OAc--D-MnNAcA(1 3).a4L-PucHAc- Rhizobium meliloti exopolysaccharide 11 RhiWbia neULi eboolysacchanid Ul COO-, l 3

C

gluainmine -5I ->3H 44AYmCt( \c A 4 15 group B streptococcus type III capsular polysaceharide

OH

OH0

OH

HOOC 0

O

S 4 HO ,OH 6)-P-Gkcp-NAc[f -Ga -3 j 2)- Cx-NeupACX1 3"--GaI-p-(I 0 glXCos---> gluWD=MiDC---- e&1 6 c 341ki acid) placbms Polysaccharide having an imine moiety: P Pseudomonas aeruginosa Fisher 7 0 cooOO- *415\0 C 0 N NHCNA ~>4).aOul(2NAc3N[CH3,C=NMA-(1 -e 4)gutmnki 9cid mmaunk acid--> fuomlne De-N-acetylation can be accomplished by conventional chemistry techniques well known to those of ordinary skill in the art. One suitable method involves the use of alkali with or without sodium borohydride. Twenty mng of polysaccharide is dissolved in 2M NaOH (3m1) and sodium borohydride is added (50mg). The solution is heating to 100 0 C for 5 h.

Following neutralization with acid, the solution is dialyzed against distilled water in the cold and freeze-dried. DiFabio Michon Briss Jennings Wessels Benedi Kasper Structure of the capsular polysaccharide antigen of type IV group B Streptococcus. 1989. Canadian Journal of Chemistry, 67:877-882.

For those polysaccharides that contain imine moieties free amino groups can be RI~9.formed by conventional chemistry techniques known to those of ordinary skill in the art. One 16suitable method involves the use of sodium borohydride. The imine group can be reduced with sodium borohydride to create a free amino group. This is done by adding in excess of of borohydride to polysaccharide dissolved in distilled water while stirring at room temperature for 2 hours. The mixture is then dialyzed against water and freeze dried. The reference from the reduction procedure above applies here as well.

Naturally occurring polysaccharides also may be used without modification in the methods of the invention and in forming the pharmaceutical preparations of the invention.

Non-limiting examples are as follows: Shigella sonnei Phase I lipopolysaccharide O-antigen CH 0O COO- 0 OH NHAc 15 P p

W

2--ft-Wi 2.4,A6-rY-D-cac 2-accmiddo2AeZz7LayItZIflTnjJ acid Streptococcus pneumoniae type 1 capsular polysaccharide 0 0O NHAA COO- o 0 o H 2 -acziapmido~4aa~m 4 7 lSsua~tta ni c ->~iatumuic aii -fp~ m M~OCH2 N 3 CH011 CH AM4CH3 HO0

OC

0 4(COH) 3 OH

PO+J

6) P-D-Ghqql 3AAATp_(I 4)-a4)_G.NA-kj 3).P (sphtidykholic ubsfttimt I i-dbitlphosph2± 2-ft-do-2D4,v-kmy gaj -m ac W pbctac 17- A polysaccharide that does not have solely a sugar backbone but still is believed to be useful according to the invention is Trypanosoma cruzi lipopeptidophosphoglycan: Galf-P-(1-3)-a- Manp(12)-a-Manp(16)[Galf]-a-, Manp(14)GlcpNH2[2-AEP]-Inositol-phospate-ceramide.

The naturally occurring polysaccharides that may be used without modification also may be modified to selectively add, subtract or modify various moieties, including free amino moieties, negatively charged moieties or other moieties. Examples include adding free amino moieties by modifying existing N-acetyl groups or imine groups or forming hydroxymethyl groups from alcohol groups.

Polysaccharides useful according to the invention may be obtained from commercial sources or may be isolated and derived from natural sources such as bacteria, fungi, seaweed and the like. The following is a list of bacterial polysaccharides and references which detail the isolation and preparation of such polysaccharides.

Salmonella typhi capsule (Vi antigen), Szu Li Stone A.L. and Robbins, J.B., Relation between structure and immunologic properties of the Vi capsular polysaccharide, Infection and Immunity 59:4555-4561 (1991).

E. coli K5 capsule, Vann Schmidt, Jann B. and Jann The structure of the capsular polysaccharide (K5 antigen) of urinary tract infective Esherichia coli, 010:K5:H4, A polymer similar to desulfo-heparin, European Journal of Biochemistry. 116:359-364 (1981).

Staphylococcus aureus type 5 capsule, Fournier Hannon Moreau Karakawa W.W. and Vann Isolation of type 5 capsular polysaccharide from Staphylococcus aureus, Ann. Inst. Pasteur/Microbiol. (Paris) 138:561-567 (1987).

Rhizobium meutoti expolysaccharide II, Glazebrook, J. and Walker a novel ,j\RA,430 expolysaccharide can function in place of the calcofluor-binding expolysaccharide in 18nodulation of alfalfa by Rhizobium, meliloti, Cell 65:661-672 (1989).

Group B streptococcus type III, Wessels Pozsgay Kasper D.L. and Jennings H.J., Structure and immunochemistry of an oligosaccharide repeating unit of the capsular polysaccharide of type III group B Streptococcus, Journal of Biological Chemistry, 262:8262- 8267 (1987).

Pseudomonas aeruginosa Fisher 7 O-specific side-chain, Knirel Paramonov N.A., Vinogradov Shashkow Kochetkov Stanislavsky E.S. and Kholodkova S 10 Somatic antigens of Pseudomonas aeruginosa, The structure of O-specific polysaccharide chains of lipopolysaccharides of P. aeruginosa 03(Lanyi), 025(Wokatsch) and Fisher immunotypes 3 and 7, European Journal of Biochemistry 167:549 (1987).

Shigella sonnei O-specific side chain, Kenne Lindberg B. and Petersson Structural 15 studies of the O-specific side-chains of the Shigella sonnei phase I lipopolysaccharide, Carbohydrate Research, 78:119-126 (1980).

pneumoniae type I capsule, Lindbert Lindqvist Lonngren Powell D.A., Structural studies of the capsular polysaccharide from Streptococcus pneumoniae type 1, Carbohydrate Research, 78:111-117 (1980).

Streptococcus pneumoniae group antigen, Jennings Lugowski C. and Young N.M., Structure of the complex polysaccharide C-substance from Streptococcus pneumoniae type 1, Biochemistry, 19:4712-4719 (1980).

When administered, the formulations of the invention are applied in pharmaceutically acceptable solutions. Such preparations may routinely contain pharmaceutically acceptable concentrations of salt, buffering agents, preservatives, compatible carriers, adjuvants, and optionally other therapeutic ingredients.

19- The capsular polysaccharide antigen may be administered per se (neat) or in the form of a pharmaceutically acceptable salt. When used in medicine the salts should be pharmaceutically acceptable, but non-pharmaceutically acceptable salts may conveniently be used to prepare pharmaceutically acceptable salts thereof and are not excluded from the scope of the invention. Such pharmacologically and pharmaceutically acceptable salts include, but are not limited to, those prepared from the following acids: hydrochloric, hydrobromic, sulphuric, nitric, phosphoric, maleic, acetic, salicylic, p-toluene sulphonic, tartaric, citric, methane sulphonic, formic, malonic, succinic, naphthalene-2-sulphonic, and benzene sulphonic. Also i pharmaceutically acceptable salts can be prepared as alkaline metal or alkaline earth salts, such as sodium, potassium or calcium salts of the carboxylic acid group.

Suitable buffering agents include: acetic acid and a salt citric acid and a salt 1 boric acid and a salt and phosphoric acid and a salt (0.8-2% Suitable preservatives include benzalkonium chloride (0.003-0.03% W/V); 15 chlorobutanol parabens (0.01-0.25% W/V) and thimerosal (0.004-0.02%

W/V).

The immune stimulating polysaccharide preparation of the present invention may be a pharmaceutical composition having an effective amount of a polysaccharide optionally included in a pharmaceutically-acceptable carrier. The term "pharmaceutically-acceptable carrier" as used herein, and described more fully below, means one or more compatible solid or liquid filler, dilutants or encapsulating substances which are suitable for administration to a human or other animal.

In the present invention, the term "carrier" denotes an organic or inorganic ingredient, natural or synthetic, with which the active ingredient is combined to facilitate the application. The components of the pharmaceutical compositions also are capable of being commingled with the polysaccharides of the present invention, and with each other, in a manner such that there is no interaction which would substantially impair the desired pharmaceutical efficiency.

Compositions suitable for parenteral administration conveniently comprise sterile aqueous preparations of the polysaccharide, which can be isotonic with the blood of the recipient.

Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono or di-glycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables. Carrier formulations suitable for subcutaneous, intramuscular, intraperitoneal, intravenous, etc. administrations may be found in Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, PA.

The term "adjuvant" is intended to include any substance which is incorporated into or administered simultaneously with the polysaccharide of the invention which potentiates the immune response in the subject. Adjuvants include aluminum compounds, e.g. gels, aluminum hydroxide and aluminum phosphate, and Freund's complete or incomplete adjuvant (in which the polysaccharide antigen is incorporated in the aqueous phase of a stabilized water in paraffin oil emulsion). The paraffin oil may be replaced with different types of oils, e.g.

squalene or peanut oil. Other materials with adjuvant properties include BCG (attenuated Mycobacterium tuberculosis), calcium phosphate, levamisole, isoprinosine, polyanions (e.g.

poly lentinan, pertussis toxin, lipid A, saponins, peptides muramyl dipeptide).

Rare earth sales lanthanum and cerium) may also be used as adjuvants. The amount of adjuvant depends on the subject and the particular polysaccharide used and can be readily determined by one skilled in the art without undue experimentation. Preferred adjuvants are those that selectively stimulate T cells. It is desirable to avoid adjuvants that might suppress a T cell response.

Other immunomodulators such as cytokines may be delivered in conjunction with the polymers of the invention, and "cocktails" including the polymers and the cytokines are contemplated. The cytokines contemplated are those that will enhance the beneficial effects that result from administering the polymers according to the invention. Cytokines are factors _30 that support the growth and maturation of cells, including lymphocytes. Important to the A -21 invention herein is modulating T cell development, as the methods of the invention appear to be T cell-mediated. The cytokines may act directly on T cells or indirectly on T cells through other cells. It is believed that the addition of cytokines will augment cytokine activity stimulated in vivo by carrying out the methods of the invention. The preferred cytokine is Other immunomodulators useful with the polymers of the invention are those that block cytokine activity associated with abscess formation. Certain cytokines such as tumor necrosis factor, interferon and interleukin-2 may participate in abscess formation, since antibodies 10 specific for such substances can help block abscess formation. Such antibodies therefore can be used to supplement the activity of the polymers of the invention. In general,, any immunomodulator which supplements the protective activity of the polymers of the invention can be used.

15 The precise amounts of the foregoing immunomodulators used in the invention will depend upon a variety of factors, including the polymer selected, the dose and dose-timing selected,

S

the mode of administration, the nature of any surgery contemplated and the characteristics of the subject. Where local administration is carried out, it will be understood that very small amounts may be required (nanograms and possibly picograms) in the case of cytokines since physiological levels of cytokines are correspondingly low. The precise amounts selected can be determined without undue experimentation, particularly since a threshold amount will be any amount which will favorably enhance the immune response. Thus, it is believed that picogram to milligram amounts are possible, depending upon the mode of delivery, but that nanogram to microgram amounts are likely to be most useful.

It will also be appreciated by those of ordinary skill in the art that the polysaccharides of the present invention have adjuvant properties by themselves. To the extent that the polysaccharides described herein potentiate human immune responses, they can be used as adjuvants in combination with other materials.

-22- Thus, the present invention also provides pharmaceutical compositions, for medical use, which comprise polymers of the invention together with one or more pharmaceutically acceptable carriers and optionally other therapeutic ingredients.

The polymers useful in the invention may be delivered separately with another anti-bacterial antibiotic drug or in the form of anti-bacterial antibiotic cocktails. An anti-bacterial antibiotic cocktail is a mixture of any of a polysaccharide useful with this invention with another antibacterial, antibiotic drug and/or supplementary potentiating agent. The use of antibiotics in the treatment of bacterial infection is routine. In this embodiment, a common administration vehicle tablet, implant, injectable solution, etc.) could contain both the polysaccharide antigen useful in this invention and the anti-bacterial antibiotic drug and/or supplementary potentiating agent. Alternatively, the anti-bacterial, antibiotic drug, can be separately dosed.

Anti-bacterial antibiotic drugs are well known and include: penicillin G, penicillin V, 15 ampicillin, amoxicillin, bacampicillin, cyclacillin, epicillin, hetacillin, pivampicillin, methicillin, nafcillin, oxacillin, cloxacillin, dicloxacillin, flueloxacillin, carbenicillin, ticarcillin, avlocillin, mezlocillin, piperacillin, amdinocillin, cephalexin, cephradine, .cefadoxil, cefaclor, cefazolin, cefuroxime axetil, cefamandole, cefonicid, cefoxitin, cefotzaxime, ceftizoxime, cefmenoxine, ceftriaxone, moxalactam, cefotetan, cefoperazone, 20 ceftazidme, imipenem, clavulanate, timentin, sulbactam, neomycin, erythromycin, metronidazole, chloramphenicol, clindamycin, lincomycin, vancomycin, trimethoprim-sulfamethoxazole, aminoglycosides, quinolones, tetracyclines and refampin.

(See Goodman and Gilman's Pharmacological Basics of Therapeutics, 8th Ed. 1993, McGraw Hill Inc.).

The polymers of the invention, when used in combinations, are administered in therapeutically effective amounts. A therapeutically effective amount will be determined by the parameters discussed below; but in any event, is that amount which establishes a level of antibacterial reaction effective in inhibiting the abscess formation.

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23 The preparations of the invention are administered "in conjunction with" infection. This means close enough in time with the surgery, trauma or diseases that predispose the host to abscess formation so that a protective effect against abscess formation is obtained. The preparations may be administered long before surgery in the case of elective surgery (i.e.

weeks or even months) preferably with booster administrations closer in time to (and even after) the surgery. Particularly in emergency situations, the preparations may be administered immediately before (minutes to hours) and/or after the trauma or surgery. It is important only that the preparation be administered close enough in time to the surgery so as to enhance the subject's immune response against bacterial infection/contamination, thereby increasing the chances of a successful host response and reducing the likelihood of abscess formation.

Multiple administrations in the days and weeks before the surgery as well as after the surgery have been shown to be effective, as discussed in greater detail below.

*o The preparations of the invention are administered in effective amounts. An effective amount 15 is that amount of a polysaccharide that will alone, or together with further doses, inhibit or prevent the formation of abscess resulting from infection by a particular bacteria. It is believed that doses ranging from 1 nanogram/kilogram to 100 milligrams/kilogram, i depending upon the mode of administration, will be effective. The preferred range is believed to be between 500 nanograms and 500 micrograms/kilograms, and most preferably between 1 microgram and 100 micrograms/kilogram. The absolute amount will depend upon eee.

a variety of factors including whether the administration is in conjunction with elective surgery or emergency surgery, concurrent treatment, number of doses and individual patient parameters including age, physical condition, size and weight. These are factors well known to those of ordinary skill in the art and can be determined with no more than routine experimentation. It is preferred generally that a maximum dose is used, that is the highest safe dose according to sound medical judgement.

Multiple doses of the pharmaceutical compositions of the invention are contemplated. The invention has been shown to be effective with multiple doses administered over a three week period preceding surgery, over a two week period preceding surgery, over a one week period <pAL, 3u ~9) -24preceding surgery, when the first dose was administered only 24 hours preceding surgery and even when given only after exposure to bacteria. Further doses may be administered postsurgery as well. Any regimen that results in an enhanced immune response to bacterial infection/contamination and subsequent abscess formation may be used, although optimum doses and dosing regimens are those that would not only inhibit the development of abscess formation, but also would result in a complete protection against abscess formation by a particular or a variety of bacterial organisms. Desired time intervals for delivery of multiple doses of a particular polysaccharide can be determined by one of ordinary skill in the art employing no more than routine experimentation.

A variety of administration routes are available. The particular mode selected will depend, of course, upon the particular polysaccharide selected, the particular condition being treated 0: 00 and the dosage required for therapeutic efficacy. The methods of this invention, generally speaking, may be practised using any mode of administration that is medically acceptable, 15 meaning any mode that produces effective levels of an immune response without causing S clinically unacceptable adverse effects. Preferred modes of administration are parenteral 0 routes. The term "parenteral" includes subcutaneous injections, intravenous, intramuscular, i intraperitoneal, intrasternal injection or infusion techniques.

The compositions may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing the polymer into association with a carrier which constitutes one or more accessory ingredients. In general, the compositions are prepared by uniformly and intimately bringing the polymer into association with a liquid carrier, a finely divided solid carrier, or both, and then, if necessary, shaping the product. The polymer may be stored lyophilized.

Other delivery systems include timed-release, delayed release or sustained release delivery systems. Such systems can avoid repeated administrations of the polysaccharides of the invention, increasing convenience to the subject and the physician. Many types of release 3 livery systems are available and known to those of ordinary skill in the art. They include polymer-based systems such as polylactic and polyglycolic acid, polyanhydrides and polycaprolactone; nonpolymer systems that are lipids including sterols such as cholesterol, cholesterol esters and fatty acids or neutral fats such as mono-, di and triglycerides; hydrogel release systems; silastic systems; peptide based systems; wax coatings, compressed tablets using conventional binders and excipients, partially fused implants and the like. Specific examples include, but are not limited to: erosional systems in which the polysaccharide is contained in a form within a matrix, found in US Patent Nos. 4,452,775 (Kent); 4,667,014 (Nestor et and 4,748,034 and 5,239,660 (Leonard) and diffusional systems in which an active component permeates at a controlled rate through a polymer, found in US Patent Nos.3,832,253 (Higuchi et al.) and 3,854,480 (Zaffaroni). In addition, a pump-based hardware delivery system can be used, some of which are adapted for implantation.

In other embodiments, compositions of the invention can be used as reagents in immunoassays to detect T cell response against polysaccharide antigens such as B. fragilis capsular 15 polysaccharide A and B. Immunoassays can be any of the conventional assay types.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps 20 but not the exclusion of any other integer or step or group of integers or steps.

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\l I uj)~~ -26- EXAMPLE 1 Source of Bacteria, Isolation and Modification of Polysaccharides, and Preparation of Inoculum B. fragilis NCTC 9343 and ATCC 23745, B. distasonis ATCC 8503 and Fusobacterium varium ATCC 8501 were originally obtained from the National Collection of Type Cultures (London, England) or the American Type Culture Collection (Bethesda, MD).

B. thetaiotaomicron 5482 and Enterococcusfaecalis 2603 strains were obtained from stock culture collections of the Channing Laboratory, Brigham and Women's Hospital (Boston, MA). Microorganisms were stored at -80oF in peptone-yeast or brain heart infusion broth until used, and grown anaerobically as previously described. Pantosti et al., Infection and Immunity 59:2075-2082 (1991). The CPC from B. fragilis NCTC 9343 or ATCC 23745 was isolated by hot phenol/water extraction and subsequent purification of PSA and PSB 15 performed as previously described. Tzianabos et al., Journal of Biological Chemistry 267:18230-18235 (1992).

The S. pneumoniae type 1 capsular polysaccharide (CP) and other pneumococcal polysaccharides were obtained in pure form from the ATCC (MD).

Chemical modifications of polysaccharides to produce molecules with altered charges have Sbeen described perviously. L. Taylor and H. Conrad, Biochem 11:1383 (1972) (reduction) and Baumann, A. et al., Biochem 31:4081 (1992) (N-acetylation and deamination).

Inocula contained a 1:1 mixture of the challenge organism(s) and an adjuvant solution containing sterile rate cecal contents and 10% barium sulfate as previously described.

Onderdonk, A. et al., Infection and Immunity 13:22-26 (1976). Bacteria were grown anaerobically and, unless otherwise indicated, adjusted to the following concentrations (as determined by colony forming units on solid agar) per gelatin capsule: Bacteroides fragilis §4jx107, B. distasonis-5xl0 7 F. varium-2.5x10 7 B. thetaiotaomicron-5x10 7 and E. faecalis- B. OB<' -27- 1.3x10 7 For some experiments, a cecal content inoculum containing faeces procured from the ceca of meat-fed rats was used to challenge animals. Onderdonk A. et al., Infection and Immunity 10:1256-1259 (1974). Quantitative and qualitative bacteriology, of the inoculum was performed and the results were as follows: (CFU/ml -logo): Facultative organisms: Escherichia coli group D Streptococcus and alpha hemolytic Streptococcus Obligate Anaerobes: Clostridium perfringes Bacteroides thetaiotaomicron Clostridium sordellii Bacteroides vulgatus Bacteroides caccae (6.30); and Bacteroides fragilis (6.00).

10 The cecal contents inoculum was mixed with barium sulfate (10% final concentration, w/v) and titered in the rat model to yield approximately 50% mortality in a given group of rats with 100% rate of abscess formation in survivors.

EXAMPLE 2 15 Abscess Formation and Immune Response Abscess Induction The rat model of intra-abdominal sepsis used in this study has been described previously.

Onderdonk, A. et al. J. Infect. Diseases 136:82-89 (1977) and Tzianabos, A. et al., Science 20 262:416-419 (1993). Briefly, male Wistar rats (Charles River Laboratories, Wilmington, Mass.) weighing between 180 and 200g were housed separately and received chow (Ralston Purina, St. Louis, Mo.) and water ad libitum. Animals were anaesthetized with a single intraperitoneal injection of 0.15ml of Nembutal (50mg/ml; Abbott Laboratories, North Chicago, Ill.) and their abdomens were shaved and swabbed with a Tincture of iodine. An anterior midline incision (0.5-1.0cm) was made through the abdominal wall and peritoneum, and a gelatin capsule containing 0.5ml of inoculum was inserted into the pelvis. The incisions were closed with interrupted 3.0 silk sutures, and the animals were returned to the cages.

Alternatively, in some experiments animals were directly injected with polysaccharide. Six days later animals were necropsied in a blinded fashion and examined for the formation of /ne or more intra-abdominal abscesses by an observer blinded to the experimental groups.

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-28 The inoculum contained at 1:1 mixture of the test polysaccharide and an adjuvant solution containing sterile rate cecal contents and 10% barium sulfate as previously described.

Onderdonk, A. et al., Infection and Immunity 13:22-26 (1976). Rats were administered fold dilutions of each polysaccharide.

A mathematical model was used to compare the biologic activities of modified and unmodified polysaccharides over a range of three doses (200, 20 and 2 and to calculate a dose of each polysaccharide that induced abscesses in 50% of the animals (AD 5 Reed.

L. and H. Muench, Am. J. Hyg. 27:493 (1938). Abscesses induced by these polysaccharides 10 were generally uniform in size and those rats that possessed one or more fully formed abscesses were scored as positive. Animals that did not have any fully formed abscesses were scored as negative. Two control groups were included in all experiments; positive controls were challenged with intact B. fragilis mixed with adjuvant solution, while negative controls received adjuvant solution alone. In all cases 100% of the positive control group and none 15 of the negative control group developed abscesses. Data were accumulated from two separate trials.

Different polysaccharides were compared for abscess-forming ability in several experiments.

In Table 1 native polysaccharide A was compared with native polysaccharide B and the CPC.

Polysaccharide A was an order of magnitude more active (AD 50 =0.67gg) than polysaccharide B (ADso=0.25Mg) or the CPC (AD 5 s=0.22k/g) Table 1 Fraction of rats with abscesses in a dose of ADso Polysaccharide 200/zg 20/.g 2pg 0.2gg 0.02gg (Cg) P A (native) 31/38 18/25 21/38 7/18 2/19 0.67 B 23/29 14/30 5/28 ND ND CPC 23/28 10/19 6/20 ND ND 22 3 /L u -29- .0.

0 0 0 0 0 0 0..0.

0 In Table 2 the abscess-forming ability of native polysaccharides A and B were compared with chemically modified versions of polysaccharides A and B.

Table 2 Abscess Induction by Unmodified and Modified PSA and PSB from B. fragilis Fraction of rats with abscesses at indicated dose Type of PS 2 00 ,g 20/tg 2p/g ADs 0 (Ag) P value* B (native) 18/19 13/18 7/19 4 B (reduced) 17/18 15/20 9/19 3 NS (Modification I) B (N-acetylated) 4/20 5/20 1/20 200 0.005 (Modification II) B (De-N-acetylated) 9/20 2/20 1/20 >200 <0.005 (Modification III) A (native) 16/20 14/20 10/19 1.3 A (reduced) 5/20 2/19 2/19 >200 <0.0005- A (N-acetylated) 7/20 3/19 1/17 200 <0.0005 A (deaminated) 7/20 6/18 3/19 200 <0.0005 *As comparted with polysaccharide A or B (native).

The AD 5 o of unmodified B. fragilis polysaccharide A was less than 2gg (Table 2).

Conversion of the negatively charged carboxyl group associated with the pyruvate substituent to a neutral hydroxymethyl group by carbodiimide reduction (reduced) created a polysaccharide with no negative charge. This modificaiton resulted in an increase in AD 5 o to greater than 2 0 0/g. N-acetylation of the free amino group on the trideoxyfucosamine (Nacetylated) and removal of the same free amino group by nitrous deamination (deaminated) created a polysaccharide with one negative charge and no positive charges per repeat unit.

These modifications also signficantly reduced the abscess induction by these polymers so that 0 1 N they displayed at AD 5 0 of greater than 200pg. Modification of the charged groups reduced the biologic potency by at least two orders of magnitude suggesting that polysaccharide A requires both amino (positive) and carboxyl (negative) groups to promote abscess induction in this animal model. Each of the modifications yielded a significant reduction in abscessinducing ability as compared with that of unmodified polysaccharide A 0.0005).

The ADso of unmodified B. fragilis polysaccharide B was 44g (Table Conversion of the negatively charged carboxyl group on the galacturonic acid of the polysaccharide B to a hydroxymethyl group via carbodiimide reduction (reduced) created a polysaccharide with one free amino group and one phosphonate group per repeating unit (a positive to negative charge ratio of This modification did not alter the ability of polysaccharide B to induce S. abscesses as can be evidenced by the AD 5 o value of 3pg. N-acetylation of the free amino group associated with the 2-aminoethylphosphonate substituent (N-acetylated) created a polysaccharide with two negatively charged groups (carboxyl and phosphonate) and no 15 positive charges. This modification of the free amino group to a secondary amine i significantly reduced the abscess induction by this polymer, so that is displayed at ADso of greater than 200g. Modification of the positive group reduced the biologic potency by at *least two orders of magnitude suggesting that polysaccharide B requires at least one positive group to promote abscess induction in this animal model but that both negative groups are not 20 required.

Replacement of acetyl groups from the three amino sugars present in the repeating unit with three free amino groups created a net positive charge on polysaccharide B with a 4:2 ratio of positively to negatively charged groups (de-N-acetylated). The de-N-acetylation of polysaccharide B significantly reduced abscess-forming potential of this saccharide (ADs greater than 200pg). This result indicated that increasing the density of the charged amino groups on this polysaccharide is necessary but not sufficient to confer this biological activity.

It is apparent that the density of these charged groups per repeating unit may be another critical variable regulating the ability of these polysaccharides to induce abscesses. Perhaps the increased number of positively charge amino groups on this polysaccharide prevents -31 0 0

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critical interactions with cell receptors (possibly present on T cells) that initiate the cascade of cellular events resulting in abscess formation.

Some other naturally existing and chemically modified polysaccharides were also assessed for abscess-forming ability. The results of these experiments are depicted in Table 3.

Table 3 Fraction of rats with abscess at indicated dose of ADso 0 Polysaccharide 200,ug 20/g 2p/g P C substance 17/18 12/18 6/19 C substance (N-acetylated) 5/10 1/10 1/10 200 <0.05* S. pneumoniae Type 1 17/20 7/18 2/18 31 5 S. pneumoniae Type 1 6/19 6/20 3/20 >200 0.018* (N-acetylated) S. pneumoniae Type 3 0/15 2/10 1/9 >200 <0.005* Group B meningococcal 1/10 ND ND Group B streptococcal 0/10 ND ND 0 Type la Group B streptococcal 1/10 ND ND Type III S. pneumoniae Type 14 2/10 ND ND Vi antigen 3/20 ND ND Vi antigen (De-N-acetylated) 15/20 9/18 7/20 16 <0.005T The naturally occurring polysaccharides which have oppositely charged groups include, C substance, the group B polysaccharide from Streptococcus pneumoniae, and the capsular polysaccharide of S. pneumoniae strains. C substance has a tetrasaccharide repeating unit L with a total of three positive charges (conferred by a phosphatidylcholine substituent and two Ru -32free amino groups) and two negative charges (conferred by phosphate groups). The capsule of S. pneumoniae type 1 has a trisaccharide repeating unit with one positive charge (free amino group) and two negative charges (carboxyl groups). Each was a potent inducer of abscesses, with AD 50 values of 5 and 31 g respectively. However, when each molecule was N-acetylated to neutralize the free amino group, the result was a marked reduction in abscessinducing activity. This result was expected for the capsule of S. pneumoniae type 1 based on the results obtained in Table 2. However, it was unexpected that C substance would exhibit such a dramatic reduction in activity because it still has a positive charge (conferred by a phosphatidylcholine substituent) and two negative charges. This result indicated that free S 10 amino groups on these polysaccharides are necessary for abscess-inducing activity. A Sdifferent type of positive charge could not be substituted. No structural requirement exists, however, for a negatively charged group on these polymers.

Naturally occurring bacterial polysaccharides that have repeating unit structures devoid of 15 charged groups or that have one negatively charged group per repeating unit were tested for *i ability to form abscesses and the results are shown in Table 3. The capsular polysaccharide of S. pneumoniae type 14 is a disaccharide repeating unit with no charged groups at all. The capsular polysaccharide of S. pneumoniae type 3, capsular polysaccharides of group B Neisseria meningitidis or of types Ia and III of group B streptococci all have one negative 20 charge per repeating unit. Each of the above polysaccharides is poor inducer of abscesses.

Finally, in order to determine whether an inactive polysaccharide which naturally has only a negative charge could be activated, a positive charge was added to the Vi antigen (a homopolymer of galactaminuronic acid from Salmonella typhi). Vi antigen, which has an Nacetyl group at the C-2 position of the pyranose ring and a negatively charged carboxyl group at the C-6 position, was modified by alkali treatment to produce a positively charge free amino group and a negatively charged carboxyl group. This chemical modification transformed the antigen into an abscess-inducing polysaccharide.

-33 The data presented in Tables 1-3 reveal that abscess induction in the peritoneal cavity of rodents is mediated by oppositely charged groups on bacterial polysaccharides and that a positively charged amino group is required.

Immune Response Animals were treated with bacterial polysaccharides by subcutaneous injection of 10pg of polysaccharide in 0. Iml of phosphate buffered saline three times a week for three weeks.

Animals received a single treatment on week five and were available for challenge on week six.

The immune response conferring protection against abscess induction was measured after challenge of previously treated animal with homologous and heterologous B. fragilis species well as other homologous and heterologous bacterial polysaccharides. The results are shown in Table 4. Previous studies have shown that the 9343 CPC and 23745 CPC are 15 distinct polysaccharide complexes. Pantosi et al., Infect. Immun. 59:2075-2082 (1991). Immunochemical studies have demonstrated that like 9343 CPC. the 23745 CPC :consists of at least two distinct polysaccharides possessing positively and negatively charged groups, although the constituent monosaccharides of the CPC found on the two strains are distinct. Pantosi et al., Infect. Immun. 59:2075-2082 (1991) and Kasper et al., 20 J. Bacter. 153:991-997 (1983). Heterologous and homologous B. fragilis species were used to challenge rats previously treated with either purified 9343 CPC or 23745 CPC. In both cases, treatment with CPC protected rates against abscess formation following challenge with either B. fragilis, 9343 or 23745.

-34- 0: 0 0 .00* 0 000.6 .:00 0 Table 4 Polysaccharide-mediated cross-protection against abscess formation by B. fragilis polysaccharides Polysaccharide Challenge Number of rats Treatment Polysaccharide w/abscesses/ (200g/g) total P value saline PSA 8/8 saline PSB 9/9 saline S. pneumoniae type 1 PS 8/9 saline 9343 4/4 saline 23745 3/3 PSA PSA 3/10 0.005 PSA PSB 1/10 <0.005 PSA S. pneumoniae type 1 PS 3/10 <0.05 PSB PSA 1/8 0.005 PSB PSB 2/10 <0.005 PSB S. pneumoniae type 1 PS 4/10 <0.05 S. pneumoniae type 1 CP PSA 2/10 0.005 S. pneumoniae type 1 CP PSB 2/10 <0.005 S. pneumoniae type 1 CP S. pneumoniae type 1 PS 0/10 <0.005 9343 CPC 9343 1/10 9343 CPC 23745 1/10 23745 CPC 9343 1/10 23745 CPC 23745 1/10 As described above it has been established that particular structural features (free amino and negatively charged groups) on polysaccharides mediate abscess formation. To test whether these polysaccharides confer protection against abscess induction, animals were treated with either polysaccharide A or B, or the S. pneumoniae type 1 CP and challenged with heterologous and homologous polymers. Each polymer resulted in protection against abscess formation (Table 4).

In order to determine if the charged groups on these polysaccharides were responsible for mediating protection to abscess formation, chemical modifications of polysaccharide A were performed. Specific chemical modifications to polysaccharide A were performed to neutralize both the positively and negatively charged groups (as described in the above section on abscess induction) and the modified polysaccharide used to treat animals for protection studies. Animals were treated with N-acetylated polysaccharide A or reduced polysaccharide A and challenged with a native, unmodified polysaccharide A. In each case the chemically modified polysaccharides failed to protect animals against polysaccharide-induced abscess formation (Table 5. P is less than 0.05 compared with animals treated with native polysaccharide A and challenged with polysaccharide This experiment demonstrated that the free amino and carboxyl groups in polysaccharide A are essential for polysaccharidemediated protection against abscess formation.

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Table Effect of chemical modifications to PSA on induction of protection against abscess caused by B. fragilis polysaccharides Number Polysaccharide Challenge of rats Treatment Polysaccharide with (200/g) abscesses/ total P value+ PSA PSA 1/8 PSA:N-acetylated (eliminates PSA 8/10 <0.005 positive charge) PSA: reduced PSA 7/10 <0.05 (eliminates negative charge) GBS type 3 CP PSA 7/9 <0.05 GBS type 3 CP PSB 8/9 GBS type 3 CP S. pneumoniae type 1 CP 7/9 S. pneumoniae type 3 CP PSA 6/9 S. pneumoniae type 14 CP PSA 6/7 each group was compared with animals immunized with modified PSA and challenged with this same 20 polysaccharide.

Another experiment was performed testing bacterial polysaccharides that either completely lacked charged groups or have only negatively charged substituents. Animals were treated with the type 3 Group B streptococcal (GBS) CP and challenged with either polysaccharide A, polysaccharide B or the S. pneumoniae type 1 CP. The type 3 GBS CP, which has one negatively charged group per repeating unit in a terminal sialic acid residue, failed to protect animals against challenge with each of the abscess inducing polymers (Table Animals treated with the type 3 S. pneumoniae CP (one negatively charged group per repeating unit) or the type 14 S. pneumoniae CP (no charged substituents in its repeating unit) also failed to protect against abscess formation induced by polysaccharide A (Table -37- EXAMPLE 3 Immune Response is T Cell-Dependent T Cell-Mediated Protection to Polysaccharide-Induced Abscesses Animals were treated as described above and were available for adoptive transfer experiments on week 6. Cell transfer experiments were performed as previously described. Shapiro M., et al., J. Immunol. 137:341-346 (1986) and Shapiro et al., J. Exp. Med. 154:1188-1197 (1982). Briefly, spleens were removed from treated or naive rats and gently teased in RPMI medium supplemented with 5% fetal calf serum. Cells were counted using a Coulter FN Counter (Coulter Electronics Inc., Hialeah, Fl.) and were examined for viability by trypan blue exclusion. The preparation was enriched for T cells by passage over nylon wool columns. Purified T cells were then counted and adjusted to the appropriate cell number (Ixl0 7 /animal) prior to intra-cardiac transfer to animals (0.2ml volume). Animals were challenged twenty-four hours later.

It was previously demonstrated that treatment with the purified CPC protects against abscess formation following challenge with viable B. fragilis by a T cell-dependent mechanism.

Onderdonk, J. Clin. Investigation 69:9-16.(1982). In the present experiments, we tested whether protection against polysaccharide-induced abscesses is also T lymphocyte-dependent.

20 Naive rats were administered purified T cells (1x10 7 cells/animal) obtained from animals previously treated with polysaccharide A. T cell recipients were then challenged with abscess-inducing polysaccharides B or the type I S. pneumoniae CP. In each case, T cells from polysaccharide A-treated animals protected naive animals against abscesses formed subsequent to homologous and heterologous polysaccharide challenge (Table 6. P is less than 0.05 compared with animals given T cells from saline-treated animals and challenged with native polysaccharide Rats receiving T cells obtained from animals immunized with type 3 GBS CP (no positively charged group) were not protected against abscesses following challenge with polysaccharide A (Table 6).

-38- Table 6 T cell-mediated protection against abscess formation by native and chemically modified polysaccharides Number Polysaccharide Challenge of rats w/ Treatment Polysaccharide abscesses/ (200pg) total P value saline PSA 7/8 type III GBS PSA PSA PSA 0/8 <0.05 PSA PSB 1/8 <0.05 PSA S. pneumoniae type 1 PS 0/7 <0.05 PSA (N-acetylated) PSA 7/9 <0.005* PSA (reduced) PSA 6/9 <0.05* Vi PSA 7/9 Vi (de-N-acetylated) PSA 2/8 <0.051 9* 9 9 9 9 9 15 I1 compared with animals given T cells from saline-treated rats and the challenged with PSA.

compared with animals given T cells from PSA-treated rats and then challenged with PSA.

compared with animals given T cells from Vi polysaccharide-treated rats and then challenged with PSA.

Chemical Modification to Eliminate Oppositely Charged Groups on Polysaccharides that Induce T Cell-Dependent Protection against Abscess Induction To assess the role of the oppositely charged groups on polysaccharide A in T cell-mediated protection against abscess induction, animals were treated with either N-acetylated polysaccharide A or carbodiimide-reduced polysaccharide A and T cells from these animals administered to naive rats. T cells taken from animals treated with the chemically modified versions of polysaccharide A failed to confer protection against challenge with unmodified polysaccharide A (Table 6. P is less than 0.05).

-39- 00 0 0 0 0**0 0000 000 00.

T Cell-Mediated Protection by a Polysaccharide Created to Contain Oppositely Charged Groups Additional adoptive T cell transfer experiments were performed in order to confirm that the presence of both positively and negatively charged groups in polysaccharides are required for protection to polysaccharide-mediated abscess formation. Chemical de-N-acetylation of the Vi capsular polysaccharide of S. typhi, a homo-polymer of galactaminuronic acid, was employed to convert this polysaccharide from a polymer that possessed one negatively charged carboxyl group per repeating unit to a saccharide that possessed one positively charged amino group and one negatively charged carboxyl group per repeating unit. In this experiment, T cells were harvested from the spleens of animals treated with the unmodified or de-N-acetylated Vi polysaccharides and transferred to separate groups of naive rats. Each group of rats that received T cells was challenged with B. fragilis polysaccharide A. Rats receiving T cells from animals treated with the unmodified Vi polysaccharide were not protected against abscess induction by polysaccharide A, while animals receiving T cells from rats treated with de-N-acetylated Vi polysaccharide were protected against abscess induction by polysaccharide A (Table 6. P is less than 0.05).

EXAMPLE 4 Temporal Administration Experiment Animals were treated via the subcutaneous route with B. fragilis PSA lot p. 7 according to four different time sequences.

Group 1: Time schedule A: 3 times per week for three weeks (MWF), with two Group 2: Group 3: Group 4:

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Time schedule B: Time schedule C: Time schedule D: single treatments 7 and 10 days later.

3 times per week for two weeks, with two single treatments 7 and 10 days later.

3 times per week for one week, with two single treatments 7 and 10 days later.

24h before, 4 and 24h after challenge.

Single treatments were administered on Friday following treatment (7 days) and Monday prior to challenge on Wednesday. Animals were challenged with an abscess-inducing dose of B.

fragilis (108 cfu/animal).

Animals treated via all four time schedules did not form abscesses following challenge with an abscess inducing amount of B. fragilis in this experiment.

EXAMPLE Providing a Hydroxymethyl Group This entails first oxidizing the polymer with 0.01M sodium metaperiodate (NaIO 4 as previously described. Jennings Lugowski Immunochemistry of groups A, B and C meningococcal polysaccharide-tetanus toxoid conjugates, The Journal of Immunology, 123:1011-1018 (1981). This accomplishes selective creation of carbonyl groups on 15 the galactofurnase side-chain of the PSA repeating unit. The polysaccharide is treated for minutes at room temperature in the dark. Ethylene glycol is then added to stop the reaction.

The polysaccharide is then dialyzed against distilled water at 4°C to remove excess glycol and periodate. This group is very amenable to reduction with a reducing agent such as sodium borohydride (NaBH 4 and will convert it to a hydroxymethyl group (CHO2H). Approximately 20 2mg of borohydride is added to this mixture following dialysis and incubated for two hours while stirring at room temperature. This mixture is then dialyzed against water as above to remove the excess borohydride.

EXAMPLE 6 PSA Mediated Protection Against B. fragilis Effect of Regimen Several regimens were tested that varied the duration of PSA administration on protection against abscess formation. Animals were administered designated concentrations of B. fragilis 43"PSA by the subcutaneous route in 0.lml of PBS. For some experiments, animals were lKIJ -41treated with PSA three times a week for three weeks with an additional dose 24 hours prior to challenge (Regimen To determine the effect of shortening this treatment regimen, further experiments were performed in which Regimen 1 was reduced by one week (Regimen 2) and by two weeks (Regimen A fourth regimen (Regimen 4) included treatment with PSA 24 hours prior to challenge as well as 4 and 24 hours following challenge. With each regimen, groups of animals were given 10/g/injection of PSA, challenged with B. fragilis and six days later examined for abscess formation. This study shows that PSA protects against B. fragilis infection-mediated abscesses. Irrespective of the length of time animals were treated, fewer animals in each group possessed abscesses when compared to the salinetreated control group (P In addition, the protective activity was comparable in each of these groups. For Regimens 1 through 4 the abscess rates were 26%, 18%, 32% and 12%, 15 A dose response experiment was performed using the briefest of the four treatment regimens (Regimen Groups of animals receiving 10, 1 or 0.1 g/injection of PSA and were challenged with B. fragilis. In this experiment, significantly fewer animals receiving 10 or 1 ug/injection had abscesses compared with saline-treated control animals (Table 7).

However, animals receiving 0. l1g/injection of PSA were not significantly protected against 20 abscess formation.

Effect of Treatment Initiated Post-Contamination To assess the ability of PSA to inhibit abscess induction following intraperitoneal contamination, animals were first challenged with B. fragilis and then treated with varying doses of PSA 1, 24 and 48 hours post-challenge (Regimen Results from this experiment also are shown in Table 7. The 10 and 25g dose failed to protect a significant number of animals compared with the saline-treated control group. However, treatment of infected animals with 500g/injection of PSA yielded a significant level of protection against abscess ,u ,k/0 -42- 0@

C

S

0

C

5

S

Table 7 Abscess Formation (No.

Treatment Dose Challenge rats with abscesses/No. P value Regimen Inoculum tested) Saline B. fragilis 8/10(80%) Regimen 4 10 B. fragilis 5/19 0.02 Regimen 4 1 B. fragilis 6/19 0.02 Regimen 4 0.1 B. fragilis 10/20 NS Regimen 5 50 B. fragilis 3/19 0.001 10 Regimen 5 25 B. fragilis 9/17 NS Regimen 5 10 B. fragilis 6/10 NS EXAMPLE 7 PSA-Mediated Protection Against Abscess-Inducing Heterologous Bacterial Species Following administration of 10 /g doses of PSA according to Regimen 1, animals were challenged via the intraperitoneal route with various inocula containing bacteria commonly associated with abscesses found in humans. Groups of animals were challenged with a monomicrobial culture of B. fragilis, or mixed inocula consisting of combination of B.

20 distasonis and E. faecalis, B. thetaiotaomicron and E. faecalis or F. varium and E. faecalis.

In each case, fewer animals treated with PSA prior to bacterial challenge had abscesses than the saline-treated control group (Table 8).

3 Rnl~ i\,ul ~nn aCc -43 Table 8 PSA-mediated protection against abscess formation Abscess formation Treatment Challenge (No. rats with Inoculum abscesses/No. tested P value Saline B. fragilis 15/18 (83%) Saline B. distasonis E. faecalis 16/18 (89%) Saline B. thetaiotaomicron E. faecalis 15/19 (79%) Saline F. varium E. faecalis 13/15 (87%) PSA B. fragilis 1/19(5%) <0.0001 PSA B. distasonis E. faecalis 4/18(22%) <0.001 PSA B. thetaiotaomicron E. Faecalis 2/19(11%) <0.0001 PSA F. varium E. faecalis 5/17 <0.002 S. pneumoniae B. fragilis 9/10(90%) NS type 3 CP__ EXAMPLE 8 Protection Against Challenge with Cecal Contents To stimulate fecal contamination of the human peritoneal cavity, an inoculum of cecal contents was surgically implanted into the peritoneal cavity of rats. Although isolated from the ceca of rats, this inoculum contained a microbial flora similar to that found in the human colon. This inocula yielded approximately 50% mortality with all the survivors developing abscesses. Initially, the efficacy of PSA (50/g/injection according to Regimen 4) against abscess formation by the cecal inoculum was tested. However, only a small reduction in the rate of abscess formation in treated animals was observed. Therefore, another treatment regimen was devised to increase the number of treatments with PSA following implantation of the cecal contents inoculum. In these experiments, animals were treated with 50tg of PSA aA4,hours prior to surgery as well as 4, 24, 48 and 96 hours following surgery. Following this treatment, significantly fewer animals developed abscesses compared with animals treated -44with saline (12/25 versus 18/18, 48% versus 100%, P<0.0001). This establishes that PSA shows broad protection against multiple organisms found in cecal contents.

EXAMPLE 9 T Cell-Mediated Protection against Abscess Formation It was investigated whether cell-mediated immune mechanisms controlled the broadly protective activity exhibited by PSA in abrogating abscess formation by heterologous organisms commonly associated with intra-abdominal sepsis. Animals were treated with PSA 10 (10g/injection) according to Regimen 3 and T cells isolated 24 hours after last treatment.

T cells (1x10 7 from PSA-treated or saline-treated animals were administered to naive recipients 24 hours prior to challenge with B. fragilis or with a mixed inoculum of F. varium and E. faecalis. Results from these experiments are shown in Table 9. Animals receiving T cells from saline-treated rats and challenged with B. fragilis or the F. varium and E.

15 faecalis combination developed abscesses (75% and 87%, respectively). However, transfer of T cells from PSA-treated animals to naive recipients yielded significant protection against abscess formation following challenge with B. fragilis (13% abscess rate) or F. varium and E. faecalis (21 abscess rate).

Table 9 Abscess formation Treatment Challenge (No. rats with Inoculum abscesses/No. tested P value Saline B. fragilis 11/13(85%) Saline F. varium and E. faecalis 13/15 (87%) PSA B. fragilis 1/8(13%) <0.005 PSA F. varium and E. faecalis 3/14 <0.005 Those skilled in the art will be able to recognize or ascertain with no more than routine experimentation numerous equivalents to the specific products and processes described above.

Such equivalents are considered to be within the scope of the invention and are intended to S be covered by the following claims in which we claim: 4

Claims

1. A polymer for use as a medicament, said polymer being formed of a plurality of a repeating unit, each repeating unit having a charge motif characteristic of polysaccharide A, the motif being a positively charged free amino moiety and a negatively charged moiety selected from the group consisting of carboxyl, phosphate, phosphonate, sulfate and sulfonate, wherein the polymer is free from complexation as part of a B. fragilis capsular polysaccharide complex and is not selected from the group consisting of S. pneumoniae polysaccharide, T. cruzi 10 lipopeptidophosphoglycan, S. sonnei Phase I lipopolysaccharide O-antigen, B. fragilis capsular polysaccharide A and B. fragilis capsular polysaccharide B.

2. A polymer as claimed in claim 1, wherein the polymer is a polysaccharide. S 15

3. A polymer as claimed in claim 2, wherein the negatively charged moiety is selected from the group consisting of carboxyl, phosphate and phosphonate. o

4. A polymer as claimed in claims 2 or 3, wherein each repeating unit is a •oligosaccharide of a maximum often monosaccharides.

A polymer as claimed in claim 4, wherein the repeating unit is selected from the group consisting of: a monosaccharide carrying both the free amino group and the negatively charged group; a dimer of a first and a second covalently linked monosaccharide in a 1-4 linkage and wherein the negatively charged group is on the first saccharide; a trimer of a first, second and third saccharide and wherein the negatively charged moiety is on the first monosaccharide; a trimer of a first, second and third saccharide and wherein the third saccharide is free of any amino or negatively charged moiety; a pentamer with a trimeric backbone, characteristic of B. fragilis capsular 13 A %polysaccharide A; and P:'OPER'JMSl13217-99 cl.doc-1306 01 o -46- a hexamer with a trimeric backbone, characteristic of B. fragilis capsular polysaccharide B.

6. A polymer as claimed in claim 4, wherein each repeating unit is a oligosaccharide of a maximum of five monosaccharides.

7. A polymer as claimed in claim 2, wherein the polymer is a bacterial polysaccharide. 10

8. A polymer as claimed in claim 7, wherein the polymer is a bacterial capsular polysaccharide.

9. A polymer as claimed in claim 8, wherein the polymer is modified B. fragilis capsular polysaccharide A, modified to contain a hydroxymethyl group.

A polymer as claimed in claim 2, wherein the polymer is a polysaccharide formed by the process of de-N-acetylation of a precursor polysaccharide.

11. A polymer as claimed in claim 2, wherein the polymer is a polysaccharide formed by the process of reducing an imine group of a precursor polysaccharide.

12. A pharmaceutical preparation for inducing protection against abscess formation caused by infection by live heterologous microorganisms, said preparation containing a polymer as claimed in any of claims 1-11.

13. A pharmaceutical preparation as claimed in claim 12, further comprising a pharmaceutically acceptable carrier. t A

14. A pharmaceutical preparation comprising a polymer formed of a plurality of a repeating unit, each repeating unit having a charge motif characteristic of polysaccharide A, the motif being a positively charged free amino moiety and a negatively charged moiety selected from the group consisting of carboxyl, P.'PERJMSN13217-99 cl doc.- 306,01 -47- phosphate, phosphonate, sulfate and sulfonate; and a pharmaceutically acceptable carrier, wherein the polymer is free from complexation as part of a B. fragilis capsular polysaccharide complex and is not selected from the group consisting of S. pneumoniae polysaccharide, T. cruzi lipopeptidophosphoglycan and S. sonnei Phase I lipopolysaccharide O-antigen.

A pharmaceutical preparation as claimed in claims 13 or 14, wherein the pharmaceutically acceptable carrier is constructed and arranged as a sustained S.release delivery system.

16. A pharmaceutical preparation as claimed in any of claims 12-15, wherein the polymer is a polysaccharide and said preparation induces protection against abscess formation by a microorganism selected from the group consisting of Bacteroides, Clostridia, Fusobacteria, Enterococcus, Prevotella, Porphyromonas, Staphylococcus, Proprionobacteria, Peptostreptococcus, Streptococcus, Veillonella, Actinomycetes and E. coli.

17. A pharmaceutical preparation as claimed in claim 16, wherein the preparation *i induces protection against abscess formation by at least two members of said group.

18. The use of a polymer for the manufacture of a medicament for use in a method of inducing protection against abscess formation caused by infection with live heterologous microorganisms, said polymer formed of a plurality of a repeating unit, each repeating unit having a charge motif characteristic of polysaccharide A, the motif being positively charged free amino moiety and a negatively charged moiety selected from the group consisting of carboxyl, phosphate, phosphonate, sulfate and sulfonate, wherein the polymer is free from complexation as part of a B. fragilis capsular polysaccharide complex and wherein the polymer is present in the medicament in an amount effective for inducing protection against abscess formation by live microorganisms. P:OPER'JMS13217-99 elm doc- 13001 -48-

19. The use of claim 18, wherein the medicament is for inducing protection against abscess formation by a microorganism selected from the group consisting of Bacteroides, Clostridia, Fusobacteria, Enterococcus, Prevotella, Porphyromonas, Staphylococcus, Proprionobacteria, Peptostreptococcus, Streptococcus, Veillonella, Actinomycetes and E. coli. The use of claim 19, wherein the medicament is for inducing protection against abscess formation by at least two members of said group.

S 10

21. The use of any of claims 18-20, wherein the medicament is administered to a subject who is in need of surgery.

22. The use of any of claims 18-21, wherein the method of inducing protection against abscess formation further comprises co-administering to the subject an amount of 15 an antimicrobial drug or an immunomodulator effective for enhancing the f induction of protection against abscess formation.

23. The use of any of claims 18-22, wherein the polymer is as claimed in any of claims 1-11.

24. A method for preparing a pharmaceutical preparation comprising selecting a polymer formed of a plurality of a repeating unit, the repeating units joined to one another, each repeating unit being formed of a maximum of ten subunits, each repeating unit having at least one negatively charged moiety selected from the group consisting of carboxyl, phosphate, phosphonate, sulfonate and sulfate, and having at least one moiety capable of being modified to produce a positively charged amino moiety; modifying the polymer to produce at least one free positively charged amino moiety on each repeating unit, and combining the modified polymer with a pharmaceutically acceptable carrier to form a pharmaceutical preparation for protecting a subject against abscess formation .associated with infection.

P: OPER'JMS\13217-99 cldoc.13 0601 -49- A method as claimed in claim 24, wherein the polymer is a polysaccharide, the subunits are monosaccharides and the at least one moiety is an N-acetyl moiety, and wherein the polysaccharide is modified by de-N-acetylation to convert the at least one N-acetyl moiety of each repeating unit to a free amino a moiety.

26. A method as claimed in claims 24 or 25, wherein the polymer is a polysaccharide, the subunits are monosaccharides and the at least one moiety is an imine group, and wherein the polysaccharide is modified by reduction to convert the at least one 1 imine group of each repeating unit to a free amino moiety.

27. A method as claimed in any of claims 24-26, wherein the polymer is a bacterial capsular polysaccharide.

28. A method as claimed in any of claims 24-27, further comprising combining the 15 modified polysaccharide with an immunomodulator for enhancing the induction of protection against abscess formation or with an antimicrobial drug.

29. A pharmaceutical preparation prepared by a method as claimed in any of claims 24- 28, with the proviso that the modified polymer is not selected from the group consisting of B. fragilis capsular polysaccharide complex, B. fragilis capsular polysaccharide A, B. fragilis capsular polysaccharide B, S. pneumoniae polysaccharide, T. cruzi lipopeptidophosphoglycan and S. sonnei Phase I lipopolysaccharide 0-antigen. Dated this 13 th day of June 2001. Brigham and Women's Hospital, Inc. By its Patent Attorneys Davies Collison Cave .F-A SC T