Process for the preparation of purified bacterial membranal proteoglycans

Abstract

This invention relates to a process for the preparation of purified bacterial membranal proteoglycans. The process comprises at least one step in which crude proteoglycans are treated in aqueous medium with a base or a hypobromite, followed by elimination of the excess reactant and the insoluble residue, the purified proteoglycans being present in aqueous solution. The thus obtained purified proteoglycans may be used as immunity adjuvants in vaccines without causing side-effects such as pyrogenic reactions.

Description

The present invention relates to purified and detoxified bacterial membranal proteoglycans, to a process for their preparation and to their use as immunity adjuvants in vaccines.

Vaccines are generally formed by one or more immunogenic elements, i.e. elements capable of producing an immunity reaction, but in some cases the immunogenic elements are incapable of developing their immunogenic power on their own or only develop it to a minimal extent, so that it is necessary in such cases to use products known as "immunity adjuvants".

Conventionally, immunity adjuvants are products which have an immunostimulating activity without being immunogenic themselves. One example is the immunity adjuvant known as incomplete Freund's adjuvant (IFA) which consists of 85% paraffin and 15% naphthalene.

The present invention relates to immunity adjuvants for use in vaccines and, more particularly, for use in so-called ribosomal vaccines or vaccines based on RNA. Ribosomal vaccines of this type are described, in particular, in French Pat. No. 73 43 957.

The vaccines in question contain as their immunogenic compound either bacterial ribosomes or bacterial RNA's emanating from pathogenic bacteria against which it is desired to obtain immunity. However, as described in the above-mentioned French Patent, these immunogenic compounds are only capable of developing their full activity in the presence of immunity adjuvants formed by membranal proteoglycans extracted from membranes of bacteria.

Conventional processes for the preparation of these proteoglycans do not, however, enable these proteoglycans to be completely purified and detoxified, and in some cases this can give rise to vaccinal or pyrogenic reactions which reactions it is advantageous to be able to avoid.

More particularly therefore, the present invention relates to a process for purifying such proteoglycans to obtain bacterial membranal proteoglycans which are soluble in water. This represents a considerable advantage because the proteoglycans thus obtained may be sterilised simply by filtration and this obviates the need to use heat which, hitherto, has been in danger of denaturing their properties. It is for this reason that, in the context of the present invention, purified proteoglycans are understood to be proteoglycans which are soluble in water.

Accordingly, the present invention provides a process for the preparation of purified, soluble, bacterial membranal proteoglycans which comprises at least one step in which the crude proteoglycans are treated in an aqueous medium with a base or a hypobromite, followed by removal of excess reactant and insoluble residues, the purified proteoglycans being present in aqueous solution.

In one embodiment of the process according to the present invention, the crude proteoglycans are treated with an aqueous alkali hydroxide, particularly sodium hydroxide solution having a molarity of from 0.05 to 2 M, preferably a molarity 0.1 M, the treatment being continued for a few hours, for example 24 l hours, at a temperature which is close to ambient temperature, for example 25.degree. C. The treatment is preferably carried out with stirring. The effect of the above treatment is to hydrolyse the proteoglycans in controlled manner in order to extract the soluble fraction therefrom.

In order to eliminate the excess reactant in this embodiment, the hydrolysate is neutralised with an acid, such as hydrochloric acid, and the salt thus formed is eliminated, for example by dialysis against distilled water. This leaves an insoluble residue which may be eliminated by precipitation and, more advantageously, by centrifuging, for example for 45 minutes at 30,000 g and at 4.degree. C.

The supernatant phase obtained constitutes the purified soluble proteoglycans.

In a second embodiment of the process according to the present invention, the crude proteoglycans in water are treated with an alkali hypobromite for a period of the order of a few tens of minutes, preferably at ambient temperature and with stirring, after which time the excess hypobromite may be eliminated, preferably by dialysis for 24 hours against running water and then against distilled water. The insoluble residue may be eliminated as described above.

In addition, the process according to the present invention preferably further comprises a step in which the lipids A are eliminated by acid hydrolysis in an aqueous medium, preferably at a temperature in the range of from 70.degree. to 100.degree. C. and in the presence of approximately 1% of glacial acetic acid for a period of the order of 90 minutes, followed by elimination of the thus formed precipitate.

The present invention also provides purified, water-soluble bacterial membranal proteoglycans as an immunity adjuvant in vaccines, having the following composition by weight:

______________________________________hexoses 24-42%proteins 31-53%lipids 12-18%hexosamines 2-6%RNA <0.5%DNA <0.2%LPS <0.001%______________________________________

Of these proteoglycans, particular reference is made to those having the following compositions:

______________________________________hexoses 37 .+-. 5%proteins 36.5 .+-. 5%lipids 15 .+-. 3%hexosamines 5 .+-. 2%RNA <0.5%DNA <<0.2%LPS <0.001%______________________________________ and which may be obtained in particular by the above-described process using an alkali hydroxide.

Among the proteoglycans according to the present invention, reference is also made to those having the following composition:

______________________________________hexoses 29 .+-. 5%proteins 48 .+-. 5%lipids 15 .+-. 3%hexosamines 4 .+-. 2%RNA <0.5%DNA <<0.2%LPS <0.001%______________________________________ which may be obtained in particular by the above-described process using a hypobromite.

The various fractions may be characterised by the following analytical methods:

Hexoses: by the reaction with anthrone according to SCOTT (T. A.), MELVIN (E. H.), 1953, Analyt. Chem. 25, 1956. Proteins: by the biuret reaction according to GORNALL (A. G.), BARDAXILL (C. A.), DAVID (V. V.), 1949, J. Biol. Chem. 177,751 Lipids: by a gravimetric method based on global extraction with organic solvents. Hexosamines: by their reaction with p-dimethyl amino benzaldehyde according to MORGAN (W. T. S.), RONDELL (C. J. M.), 1955, Biochem. J.61 RNA (ribonucleic acid): by direct UV spectrophotometry at 260 nm and by the orcinol reaction according to LUSENA (C. V.), 1951, Canad. J. Biochem. 29, 107-108 DNA (desoxy ribonucleic acid): by the coloured diphenyl amine reaction according to BURTON (K.), 1956, Biochem. J. 62,315. LPS (lipopolysaccharides): by the coloured carboncyanine reaction described by JANDA (J.), WORK (E.), 1971, FEBS Letters, Vol. 16, number 4, pages 343-345. Residual water: by the Karl FISCHER reaction.

In general, the crude membranal proteoglycans to be purified may be prepared by any known process and, more particularly, by the process described in the above-mentioned French Patent or by fractional centrifuging from a ground bacterial biomass in order to sediment successively the cell debris at an acceleration of preferably from 7000 to 8000 g for a few minutes and then the membranes at an acceleration of from 20,000 to 40,000 g for a few tens of minutes, followed by separation of the proteoglycans from the membranes by fractional centrifugation in saline solution and in water.

The following scheme is one example of how purified proteoglycans are obtained from a bacterial biomass.

______________________________________Schematic Illustration of the Preparation of Proteoglycans:______________________________________ ##STR1## ##STR2## ##STR3## ##STR4## ##STR5##______________________________________

Those membranal proteoglycans according to the present invention which are of particular interest are extracted from membranes of gram-negative bacteria, more particularly from those of the geni Klebsiella, Serratia and Escherichia and, above all, Klebsiella pneumoniae, Serratia marcescens and Escherichia coli.

The present invention also relates to vaccines containing the membranal proteoglycans described above, and, more particularly, to vaccines containing as immunogenic fraction ribosomes or RNA's extracted from pathogenic bacteria against which it is desired to obtain immunity.

The RNA's and ribosomes suitable for use in the vaccines according to the present invention may be prepared by known processes and, in particular, by the processes described in French Pat. Nos. 73 43957, 75 10252 and 76 24124.

In one embodiment of this aspect of the present invention, the ratio by weight between the immunogenic fraction and the proteoglycans according to the present invention amounts to between 1.4 and 1.6 and preferably to 1.5.

Reference is made in particular to the following vaccines:

______________________________________(1) Broncho-ORL vaccines(a) Ribosome/proteoglycan associationribosomes of Klebsiella pneumoniae 3.5 .mu.gribosomes of Streptococcus pneumoniae 3.0 .mu.gribosomes of Streptococcus pyogenes A.sub.12 3.0 .mu.gribosomes of Hemophilus influenzae 0.5 .mu.gproteoglycans of Klebsiella pneumoniae 15.0 .mu.g(b) Ribosomal RNA/proteoglycan association:ribosomal RNA of Klebsiella pneumoniae 2.45 .mu.gribosomal RNA of Streptococcus pneumoniae 2.10 .mu.gribosomal RNA of Streptococcus pyogenes A.sub.12 2.10 .mu.gribosomal RNA of Hemophilus influenzae 0.35 .mu.gproteoglycans of Klebsiella pneumoniae 10.50 .mu.g(2) Anti-pyorrhoeal vaccines(a) Ribosomes/proteoglycans associationribosomes of Rothia dentocariosus 1.2 .mu.gribosomes of Actinomyces viscosus 1.2 .mu.gribosomes of Streptococcus mutans 0.8 .mu.gribosomes of Streptococcus salivarius 2.0 .mu.gribosomes of Lactobacillus casei 1.2 .mu.gproteoglycans of Klebsiella pneumoniae 9.6 .mu.g(b) Ribosomal RNA/proteoglycan association:ribosomal RNA of Rothia dentocariosus 0.84 .mu.gribosomal RNA of Actinomyces viscosus 0.84 .mu.gribosomal RNA of Streptococcus mutans 0.56 .mu. gribosomal RNA of Streptococcus salivarius 1.40 .mu.gribosomal RNA of Lactobacillus casei 0.84 .mu.gproteoglycans of Klebsiella pneumoniae 6.72 .mu.g(3) Dermatological anti-acne vaccine(a) Ribosome/proteoglycan association:ribosomes of Corynebacterium acnes 2 .mu.gribosomes of Corynebacterium parvum 2 .mu.gribosomes of Streptococcus pyogenes 2 .mu.gribosomes of Staphylococcus epidermidis 2 .mu.gproteoglycans of Serratia marcescens 12 .mu.g(b) Ribosomal RNA/proteoglycan association:ribosomal RNA of Corynebacterium acnes 1.4 .mu.gribosomal RNA of Corynebacterium parvum 1.4 .mu.gribosomal RNA of Streptococcus pyogenes 1.4 .mu.gribosomal RNA of Staphylococcus epidermidis 1.4 .mu.gproteoglycans of Serratia marcescems 8.4.mu.g(4) Gynaecological vaccine(a) Ribosome/proteoglycan associationribosomes of Escherichia coli 2 .mu.gribosomes of Streptococcus faecalis 2 .mu.gribosomes of Streptococcus H 2 .mu.gribosomes of Staphylococcus epidermidis 2 .mu.gribosomes of Candida albicans 2 .mu.gproteoglycans of Escherichia coli 15 .mu.g(b) Ribosomal RNA/proteoglygan associationribosomal RNA of Escherichia coli 1.4 .mu. gribosomal RNA of Streptococcus faecalis D 1.4 .mu.gribosomal RNA of Streptococcus H 1.4 .mu.gribosomal RNA of Staphylococcus epidermidis 1.4 .mu.gribosomal RNA of Candida albicans 1.4 .mu.gproteoglycans of Escherichia coli 10.5 .mu.g(5) Intestinal anti-typhus vaccine(a) Ribosome/proteoglycan associationribosomes of Bacterium coli .mu.gribosomes of Salmonella paratyphi A 2 .mu.gribosomes of Salmonella paratyphi B 2 .mu.gribosomes of Shigella dysenteria 2 .mu.gribosomes of Enterococcus 2 .mu.gproteoglycans of Serratia marcescens 15 .mu.g(b) Ribosomal RNA/proteoglycan associationribosomal RNA of Bacterium coli 1.4 .mu.gribosomal RNA of Salmonella paratyphi A 1.4 .mu.gribosomal RNA of Salmonella paratyphi B 1.4 .mu.gribosomal RNA of Shigella dysenteriae 1.4 .mu.gribosomal RNA of Enterococcus 1.4 .mu.gproteoglycans of Serratia marcescens 10.5 .mu.g______________________________________

EXAMPLE 1

Preparation of crude membranal proteoglycans of K. pneumoniae

The strain of K. pneumoniae is cultured on a medium containing (per liter):

Meat extract: 5 g Yeast extract: 5 g Sucrose: 2 g Disodium phosphate: 2.5 g

After culturing the cells are separated from the culture medium by centrifuging, washed with a saline solution (NaCl), dried and optionally stored at -20.degree. C.

The biomass obtained by fermentation is concentrated and washed by continuous centrifuging. The bacterial concentrate thus obtained is dispersed in physiological serum to a final concentration of dry cells of 50 g per liter (as measured by spectrophotometry).

The bacterial suspension is subjected to cell grinding by passing through an APV-Manton Gaulin homogeniser equipped with special disintegration valves. During this operation, the temperature of the suspension is kept below 10.degree. C.

The crude proteoglycans are isolated from this cell suspension by a series of differential centrifuging operations carried out under the following conditions:

Centrifuging for 10 minutes at 7500 g and 4.degree. C. enables the unground cells and cell debris to be eliminated. The supernatant phase is then centrifuged for 45 minutes at 30,000 g and 4.degree. C. to sediment the crude membranal fraction.

The 30,000 g deposit is dispersed by means of a homogeniser in 1 volume of cold 0.15 M NaCl and then subjected to the same cycle of centrifuging operations at 7500 g and 30,000 g as described above.

The 30,000 g deposit is then taken up this time in 1 volume of distilled water and dispersed to complete homogeneity.

The suspension in distilled water is again subjected to a cycle of centrifuging operations at 7500 g and 30,000 g, after which the deposit is taken up this time in one quarter of the initial volume of distilled water. The suspension is centrifuged for 10 minutes at 7500 g and the supernatant phase containing the crude proteoglycans is conserved.

EXAMPLE 2

To the preceding supernatant phase obtained in Example 1 containing the crude proteoglycans is added 1 ml of sodium hydroxide (10 N) per 100 ml of supernatant phase so as to obtain a final molarity of 0.1 M of NaOH.

The whole is then incubated for 24 hours at 25.degree. C. with moderate stirring in order to extract the soluble fraction from the proteoglycans by controlled hydrolysis.

The hydrolysate is then neutralised with a 3 N solution of hydrochloric acid and the sodium chloride formed is eliminated by dialysis against distilled water.

The insoluble residue is eliminated after dialysis by centrifuging for 45 minutes at 30,000 g and 4.degree. C. and the supernatant phase containing the soluble proteoglycans is conserved.

EXAMPLE 3

Preparation of purified proteoglycans

To the supernatant phase obtained in Example 1 containing the crude proteoglycans is added 2 ml of sodium hypobromite (10 ml of bromine+60 ml of concentrated sodium hydroxide) per 100 ml of supernatant phase.

The suspension is then stirred for 30 minutes at ambient temperature, and after this time the excess hypobromite is eliminated by dialysis for 24 hours against running water and then against distilled water.

The insoluble residue is eliminated after dialysis by centrifuging for 45 minutes at 30,000 g and 4.degree. C. and the supernatant phase containing the soluble proteoglycans is conserved.

EXAMPLE 4

The proteoglycans prepared in accordance with Example 2 are not completely detoxified, since they still contain small quantities of lipopolysaccharides having a hyperthermal effect. It is for this reason that the proteoglycans of Example 2 are treated as follows:

1 ml of glacial acetic acid is added to 100 ml of dialysed supernatant phase containing the soluble proteoglycans, followed by heating for 90 minutes to a temperature of 90.degree. C.

This hydrolysis quantitatively separates the lipid A from the LPS and cooling in ice causes it to precipitate.

The precipitate of lipid A is eliminated by centrifuging for 20 minutes at 30,000 g and 0.degree. C.

The supernatant phase is collected and then dialysed against distilled water for 24 hours to eliminate the acetic acid.

The dialysate is sterilised by filtration on a 0.22.mu. membrane and the filtrate is conserved in either frozen or freeze-dried form.

Its composition is as follows:

______________________________________Hexoses 37 .+-. 5%Proteins 36.5 .+-. 5%Lipids 15 .+-. 3%Hexosamines 5 .+-. 2%RNA <0.5%DNA <<0.2%LPS <0.001%______________________________________

EXAMPLE 5

Proteoglycans having the following composition are obtained as in Example 4 from the purified proteoglycans of Example 3:

______________________________________Hexoses 29 .+-. 5%Proteins 48 .+-. 5%Lipids 15 .+-. 3%Hexosamines 4 .+-. 2%RNA 0.5%DNA 0.2%LPS 0.001%______________________________________

The purified and detoxified proteoglycans are of course obtainable in analogous fashion from Serratia marcescens and Escherichia coli and may be used in the composition described above.

The vaccine formulations according to the present invention may of course be packaged with the supports and excipients known in the art according to their mode of application. The compositions described above are preferably injectable types.

The vaccines according to the present invention were tested for immunogenic activity and were found to have a considerably better activity than the vaccines described in French Pat. No. 73 43957 due to the replacement of the membranal proteoglycans by purified and detoxified membranal proteoglycans. However, the most advantageous aspect of the vaccines according to the present invention is that they have no pyrogenic effect.

A study of the pyrogenic effect was conducted as follows:

A dose of vaccine in 1 ml of water is injected intravenously into rabbits weighing from 2 to 2.5 kg and their rectal temperature is observed by thermocouple probe. The results obtained are set out in Table 1 below.

It can be seen that the vaccines according to the present invention are free from any pyrogenic effects.

______________________________________PYROGENIC EFFECT______________________________________.DELTA..degree.C.Batch Lot 15' 30' 45' 1 h 1 h 15'______________________________________GN 153 -0,03 0 0 -0,016 -0,05GN 155 +0,06 +0,50 +0,83 +1,05 +1,16GN 156 +0,06 -0,04 -0,06 -0,16 -0,20______________________________________CONT'D.DELTA..degree.C.Batch Lot 1 h 30' 1 h 45' 2 h 2 h 30' 3 h______________________________________GN 153 -0,03 -0,03 -0,03 -0,10 -0,10GN 155 +1,16 +1,11 +1,06 +1,43 +1,66GN 156 -0,26 -0,26 -0,30 -0,40 -0,46______________________________________CONT'D.DELTA..degree.C.Batch Lot 3 h 30' 4 h 4 h 30' 5 h 5 h 30'______________________________________GN 153 0 -0,16 -0,15 -0,16 -0,18GN 155 +1,90 +1,48 +1,1 +0,71 +0,36GN 156 -0,20 -0,50 -0,44 -0,46 -0,46______________________________________ GN 153 Antipyorrhoeal vaccines 2a, the proteoglycans being prepared by process described in Example 4. GN 156 Same vaccines except that the proteoglycans were prepared by the process described in Example 5. GN 155 Same vaccines as before except that the proteoglycans were subjected only to complete delipidation with chloroform.

Claims

1. A process for the preparation of purified water soluble bacterial membranal proteoglycans which comprises at least one step in which crude proteoglycans are treated in an aqueous medium with a reactant selected from the group consisting of bases and hypobromites, followed by removal of the excess reactant and the insoluble residue, the purified proteoglycans being present in aqueous solution.

2. A process as set forth in claim 1, wherein the base used is an alkali hydroxide having a molarity of from 0.05 to 2 M and the treatment time is a few hours at a temperature of about ambient temperature.

3. A process as set forth in claim 1, wherein the hypobromite used is an alkali hypobromite and the treatment time is a few tens of minutes at ambient temperature.

4. A process as set forth in claim 1 wherein the excess reactant is eliminated by dialysis and the insoluble residue is eliminated by centrifuging.

5. A process as claimed in claim 1, which further comprises at least one step in which the membranal proteoglycans are hydrolysed with acetic acid in an aqueous medium at a temperature of from 70.degree. to 100.degree. C. and the thus formed insoluble fraction is eliminated.

6. A process as claimed in claim 5, wherein the acid hydrolysis step is carried out with 1% by volume glacial acetic acid.

7. A process as claimed in claim 1, wherein the proteoglycans are extracted from a gram-negative bacteria.

8. A process as claimed in claim 1, wherein the proteoglycans are extracted from gram-negative bacteria selected from the group consisting of Klebsiella pneumoniae, Serratia marcesens and Escherichia coli.