WO2000038711A2

WO2000038711A2 - Purification of polysaccharide-protein conjugate vaccines by ultrafiltration with ammonium sulfate solutions

Info

Publication number: WO2000038711A2
Application number: PCT/US1999/030109
Authority: WO
Inventors: Ronald P. Mcmaster
Original assignee: Connaught Laboratories Ltd; Connaught Laboratories Inc
Current assignee: Sanofi Pasteur Ltd; Sanofi Pasteur Inc
Priority date: 1998-12-29
Filing date: 1999-12-16
Publication date: 2000-07-06
Anticipated expiration: 2001-06-29
Also published as: HK1106999A1; PT1140156E; CA2358022A1; CA2358022C; EP1140156B1; EP1762245A3; EP1762245A2; DK1762245T3; DK1140156T3; DE06025470T1; PT1762245E; EP2292261A1; ES2277462T3; EP1140156A2; AU2367500A; ATE347906T1; US6146902A; DE69934434D1; CY2200152T2; CY1111375T1

Abstract

The present invention relates to the removal of unbound polysaccharides from conjugated polysaccharide-protein vaccines using the method of ultrafiltration whereby the diafiltration solution contains saturating levels of ammonium sulfate.

Description

TITLE OF THE INVENTION

Purification of Polysaccharide-Protein Conjugate Vaccines by Ultrafiltration with

Ammonium Sulfate Solutions.

FIELD OF THE INVENTION

The present invention relates to the removal of unbound polysaccharides from

conjugated polysaccharide-protein vaccines using the method of ultrafiltration whereby the

diafiltration solution contains saturating levels of ammonium sulfate.

Several publications are referenced in this application. Full citation to these publications

is found where cited or at the end of the specification, immediately preceding the claims; and

each of these publications is hereby incorporated by reference. These publications relate to

the state of the art to which the invention pertains; however, there is no admission that any of

these publications is indeed prior art.

BACKGROUND OF THE INVENTION

In recent years, a number of polysaccharide-protein conjugate vaccines have been

developed for use in protection against bacterial infections. One such vaccine, the

Haemophilus influenzae type B conjugate vaccine is now licensed for use in humans

throughout the world. This vaccine is administered to infants along with their other routine

pediatric vaccines. The Haemophilus influenzae type B conjugate vaccine has proven to be

quite effective in protecting against Haemophilus influenzae type B disease (Santosham, M.,

1993). The polysaccharide-protein conjugate vaccines are prepared by covalently attaching

purified bacterial capsular polysaccharides to protein molecules using a variety of chemical

methods. Upon completion of the conjugation reactions, the unreacted polysaccharide molecules are separated from the polysaccharide-protein conjugates using an assortment of

separation techniques. The techniques that have been proven to be most effective in purifying

the polysaccharide-protein conjugates include gel filtration chromatography, hydrophobic

interaction chromatography, ultracentrifugation, liquid-liquid extraction, and ammonium

sulfate precipitation/fractionation.

The reason for the interest in developing conjugate vaccines is that these vaccines are

capable of eliciting an anti-polysaccharide specific immune response that protects against

disease. These polysaccharide-conjugate vaccines protect against pathogens that contain an

outer polysaccharide shell. These vaccines have proven to be effective in protecting infants

and young children against disease. The reason why these vaccines are effective in younger

populations is due to the conversion of the purified bacterial capsular polysaccharides, which

are classified as t-cell independent antigens, into t-cell-like antigens when they are covalently

attached to certain protein molecules. T-cell antigens are capable of eliciting an immune

response that can be boosted upon subsequent vaccination thereby allowing one to establish a

level of protection in the vaccinated subject. These T-cell antigens normally confer long

lasting immunity against disease. The purified bacterial capsular polysaccharides are capable

of eliciting an immune response in man, however, the immune response can be of limited

duration, especially in younger populations. The immune response in younger populations is

normally very low, and is considered not to be of a protective level. Subsequent vaccinations

with polysaccharide does not normally yield a higher, or boosted, antibody response, because

there is no T-cell help, or memory antibody. For this reason, the polysaccharide vaccines

have not been recommended for use in infant populations, and children younger than 2 years

of age. In preparation of the polysaccharide-protein conjugate vaccines, steps are normally

taken to remove the unbound polysaccharide from these preparations because the unbound

polysaccharide does not provide any benefit to the vaccinated subject. In addition, there has

been an increased effort to develop well-characterized vaccines that are of a higher degree of

purity for licensure.

OBJECTS AND SUMMARY OF THE INVENTION

Ultrafiltration, like dialysis, is based on the principle of separating molecules according

to size using a semipermeable membrane of a defined range of pore sizes. Ultrafiltration is

widely used in protein and polysaccharide purification for concentrating protein and

polysaccharide molecules and for changing the composition of the buffer solution.

Ultrafiltration is also used in polysaccharide and protein purification for removing low-

molecular-weight solutes from these sample solutions. This process technique is routinely

applied in small laboratory experiments and in manufacturing scale process steps.

The object of this invention is to provide a method of separating unreacted or unbound

polysaccharide from polysaccharide-protein conjugate preparations based upon the difference

in molecular size. The unreacted or unbound polysaccharide, although relatively large in

molecular size, 1,000 to 50,000 daltons, are much smaller than the molecular size of the

polysaccharide-protein conjugate molecules, that range from 100,000 to 1,000,000 daltons in

molecular size. In developing this method for polysaccharide-protein conjugate purification, the invention provides the opportunity for ease of scale-up to industrial size reaction

preparations.

Polysaccharide and protein molecules do not behave the same with respect to their

relative ease of passing through semipermeable membranes. One reason for this is that

polysaccharides exist as molecular size distributions whereas proteins are normally of a

defined molecular size. Proteins exist in solution as bead-like structures, whereas

polysaccharides may adopt a variety of conformations (e.g. helical coils) or they can exist as

random string-like structures. As a result of the various geometric forms that polysaccharides

can adopt in solution, some polysaccharides may pass through semipermeable membranes

more easily than others. The chemical make up of the semipermeable can be either

hydrophobic (e.g. polyether sulfone) or hydrophilic (e.g. regenerated cellulose) in nature. The

chemical make-up of the semipermeable membrane can influence the ease with which

proteins and polysaccharide pass through the pores. Polysaccharides of molecular size 1 to

50,000 can pass through semipermeable membranes whose pore size has a molecular size

cutoff of 30,000 using 0.15M sodium chloride solution as the diafiltration buffer. When a

mixture of the same polysaccharide and polysaccharide-protein conjugates are subjected to the

same ultrafiltration experimental conditions, very little of the unbound polysaccharide will

pass through the semipermeable membrane. However, when the diafiltration buffer is

changed to 40% (of saturation) ammonium sulfate, then the unbound polysaccharide freely

passes through the membrane pores.

The ammonium sulfate does not affect the size of the membrane pores. The level of

saturation does play an important role in allowing the unbound polysaccharide to freely pass through the semipermeable membrane. Below 40% (of saturation) very little unbound

polysaccharide will pass through the membrane, however, above 40% (of saturation) the

polysaccharide freely elutes through the membrane pores. This invention does not require

that the polysaccharide-protein conjugate precipitate out of solution for it to work. The

method works equally well whether or not the polysaccharide-protein conjugate is fully

solubilized or precipitated from solution. Proper selection of the appropriate membrane pore

size and percent saturation of ammonium sulfate, allows for high yield recovery of the desired

polysaccharide-protein conjugate while allowing for the removal of unreacted polysaccharide.

The present invention provides a gentle means for the purification of polysaccharide-

protein conjugates that is readily scaleable to any size reaction volume. One method of

purification that can be performed at large scale volumes is to precipitate the polysaccharide-

protein conjugate from solution using ammonium sulfate. In this process, the unbound

polysaccharide remains in solution, however, there are certain drawbacks with this approach.

In order to achieve the same level of purity that is provided by the present invention, one

needs to perform repetitive ammonium sulfate precipitations due to some partitioning of the

polysaccharide with the precipitated polysaccharide-protein conjugate. Certain

polysaccharide-protein conjugates are difficult to resolubilize once they are precipitated from

solutions. In the present invention, the method does not require that the polysaccharide-

protein conjugate be precipitated out of solution. The ammonium sulfate diafiltration solution

disrupts any potential interaction or association between the unbound polysaccharide and the

polysaccharide-protein conjugate. The invention provides a method for purifying polysaccharide-protein conjugates to a

level that contain less than 1 % unbound polysaccharide by weight.

The invention provides a method for purifying polysaccharide-protein conjugates that

have been prepared from bacterial capsular polysaccharides from Streptococcus pneumoniae

serotypes 1, 3, 5, 6B, 7F, 9V, 14, 18C, 19F, 23F and from Neisseria meningitidis serogroups

A, C, W-135 and Y.

The invention provides a method for purifying a polysaccharide-protein conjugate so as

to preserve an epitope of interest, a biological response modulator, and/or a growth factor,

such that the present invention provides an immunological and/or vaccine or therapeutic

agent.

The invention further provides a purified polysaccharide-protein conjugate vaccine that

may be administered to an animal or human in order to obtain an immunological or protective

immune response or for treatment or therapy.

DETAILED DESCRIPTION OF THE INVENTION

The invention has been applied to purify a number of distinctly different polysaccharide-

protein conjugates that are derived from a variety of bacterial capsular polysaccharides,

although the invention need not be limited to only these polysaccharide-protein conjugates.

The bacterial capsular polysaccharide-protein conjugates that have been purified by this

process include Streptococcus pneumoniae serotypes 1, 3, 5, 6B, 7F, 9V, 14, 18C, 19F, and

23F, and Neisseria meningitidis serogroups A, C, W-135 and Y. According to the method of the present invention, the derivatized polysaccharide, which

are prepared by the method described in patent application 454312-2500, is first mixed with

the protein carrier of choice in a solution of physiological saline (0.85% sodium chloride), and

the pH of the mixture is adjusted to 5.0±0.1. The conjugation reaction is initiated by adding

1 -ethyl-3-(3-dimehtylaminopropyl) carbodiimide (ED AC) which serves to activate the

carboxyl groups on the carrier protein allowing for reaction from a nucleophilic site that is

present on the polysaccharide chain. The pH of the reaction is maintained at 5.0±0.1 during

the course of the reaction, normally for two hours at 18 to 25°C. After the reaction time is

complete, the pH of the reaction mixture is adjusted to 7.0±0.1, and the reaction is allow to

stand for 12 to 18 hours at 2 to 8°C to allow for hydrolysis of the unreacted EDAC.

The polysaccharide-protein conjugate is purified by first allowing the mixture to

equilibrate to 18 to 25°C. The mixture is connected to a spiral wound ultrafiltration unit that

is equipped with a Millipore Prep/Scale 30,000MWCO regenerated cellulose membrane.

Ammonium sulfate is added to the reaction mixture at a specified level of saturation (in

general, 50 to 60% of saturation). The conjugate mixture is diafiltered against 20 volume

exchanges of 50 to 60% (of saturation) ammonium sulfate solution. The ammonium sulfate is

removed from the polysaccharide-protein solution by diafiltration against 10 volume

exchanges of physiological saline (0.85% sodium chloride). The purified conjugate is filtered

through 1.2 and 0.45 micron membranes, and then sterilized by filtration through a 0.22

micron membrane. The invention is dependent upon the presence of ammonium sulfate in the diafiltration

wash buffer. This invention was discovered from the following set of experiments that are

described below.

A conjugation reaction was performed using purified Neisseria meningitidis serogroup

C that had been derivatized with adipic acid dihydrazide with diphtheria toxoid protein. A

portion of this reaction mixture was purified by three successive ammonium sulfate

precipitations using at 50% of saturation. The precipitations were performed by first adjusting

the pH of the mixture to 7.0±0.1 using dilute sodium hydroxide. Solid ammonium sulfate was

added slowly over a 10 minute interval to reach a final concentration of 50% of saturation.

The solution was allowed to stand at room temperature for 15 minutes. The precipitated

polysaccharide-protein conjugate was collected by centrifugation, using a Beckman JA-20

rotor, at 10,000rpm at 4°C. The supernatant containing solubilized unreacted polysaccharide

was removed, and the protein pellet was dissolved into physiological saline, 0.85% sodium

chloride. The pH was adjusted to 7.0+0.1 and the polysaccharide-protein conjugate was

precipitated as above. Following the third ammonium sulfate precipitate, the polysaccharide-

protein conjugate was dialyzed against physiological saline, 0.85% sodium chloride. The

purified conjugate was filtered through 1.2 and 0.45 micron membranes, and then sterilized by

filtration through a 0.22 micron membrane. This sample was analyzed for protein, sialic acid

content, and for the content of unbound polysaccharide. The remaining portion of the reaction

mixture was subjected to a number of ultrafiltration methods of purification. The summary of

these purification methods is reported in Table 1. In the first approach, the remaining reaction mixture was connected to a screen channel

minisette ultrafiltation unit equipped with a Filtron 30,000 MWCO polyether sulfone

membrane. The conjugation reaction mixture was diafiltered against 10 volumes of

physiological saline, 0.85% sodium chloride. A sample of this material was analyzed for

protein and sialic acid content, see Table 1.

In a second approach, a portion of the retentate from the physiological saline diafiltered

reaction mixture was connected to a screen channel minisette ultrafiltration unit that was

equipped with a Filtron 30,000 MWCO polyether sulfone membrane. The mixture was

diafiltered against 10 volumes of 1M sodium chloride, followed by 10 volumes of

protein and sialic acid content, see Table 1.

In a third approach, a second portion of the retentate from the physiological saline

diafiltered reaction mixture was connected to a screen channel minisette ultrafiltration unit

that was equipped with a Filtron 30,000 MWCO polyether sulfone membrane. To this

mixture was added solid ammonium sulfate to a concentration of 20% of saturation. The

mixture was diafiltered against 7 volumes of 20% (of saturation) ammonium sulfate, followed

by 6 volumes of physiological saline, 0.85% sodium chloride. A sample of this material was

analyzed for protein and sialic acid content see Table 1.

In a fourth approach, the retentate from the 20% (of saturation) ammonium sulfate

diafiltration reaction mixture was connected to a open channel minisette ultratilftrafion unit

that was equipped with a Filtron 30,000 MWCO polyether sulfone membrane. To this mixture was added solid ammonium sulfate to a concentration of 50% of saturation. The

mixture was diafiltered against 5 volumes of 50% (of saturation) ammonium sulfate, followed

analyzed for protein and sialic acid content, see Table 1.

In a fifth approach, the retentate from the 50% (of saturation) ammonium sulfate

diafiltration reaction mixture was connected to a spiral wound ultrafiltration unit that was

equipped with a Millipore Prep/Scale 30,000 MWCO regenerated cellulose membrane. The

Prep/Scale spiral wound filter cartridge allows one to perform this operation at a higher flux

than is obtained with the flat sheet minisette ultrafiltration system. The mixture was

diafiltered against 10 volumes of 50% (of saturation) ammonium sulfate, followed by 10

volumes of physiological saline, 0.85% sodium chloride. A sample was analyzed for protein,

sialic acid content, and for the content of unbound polysaccharide, see Table 1.

The results from the fourth and fifth experiments showed that inclusion of ammonium sulfate

in the diafiltration wash solution allowed for the wash out of the unbound polysaccharide.

These experiments were confirmed by performing a follow-up experiment using a new

reaction mixture of Neisseria meningitidis serogroup C with diphtheria toxoid protein. The

conjugation reaction mixture was performed as described above. After overnight incubation

at 2-8°C, the reaction mixture was connected to a spiral wound ultrafiltration unit that was

mixture was diafiltered against 10 volumes of 50% (of saturation) ammonium sulfate. The

permeate was tested for sialic acid content on each volume wash. The kinetic profile for the

unbound polysaccharide removed is shown in Figure 1. Following the diafiltration against 50% (of saturation) ammonium sulfate, the polysaccharide-protein conjugate was diafiltered

against 10 volumes of physiological saline, 0.85% sodium chloride. The sample was analyzed

for protein, sialic acid content, and for the content of unbound polysaccharide, see Table 2.

This invention has been applied in the purification of a number of different

polysaccharide-protein conjugate vaccines of which a non-inclusive listing is presented in

Table 3. A better understanding of the present invention and of its many advantages will be

had form the following non-limiting Examples, given by way of illustration.

EXAMPLES

Example 1 - Ultrafiltration purification of Neisseria meningitidis serogroup A diphtheria

toxoid protein conjugate.

Materials used in the conjugation reaction and the ultrafiltration purification of the

polyaccharide-protein conjugate include adipic acid dihydrazide derivatized serogroup A

polysaccharide, diphtheria toxoid protein, l-ethyl-3-(3-dimehtylaminopropyl) carbodiimide

(EDAC), physiological saline (0.85% sodium chloride), 0.1N hydrochloric acid, 0.1 N sodium

hydroxide, and ammonium sulfate.

The adipic acid dihydrazide derivatized serogroup A polysaccharide (at 6.5mg/ml) was

mixed with diphtheria toxoid protein (at 5mg/ml) and the pH of the mixture was adjusted to

5.0+0.1 using 0.1N hydrochloric acid. The reaction was initiated by adding

l-ethyl-3-(3-dimehtylaminopropyl) carbodiimide (EDAC) to a concentration of 3mg/ml. The

of the reaction mixture was maintained at 5.0±0.1 for two hours. After two hours, the pH of the reaction mixture was adjusted to 7.0±0.1 using 0. IN sodium hydroxide. The reaction

mixture was incubated at 2-8°C for 18 hours.

Following incubation at 2-8°C, the reaction mixture was allowed to equilibrate to 15 to

30°C, and the pH was adjusted to 7.0±0.1, if necessary. To the reaction mixture was added

solid ammonium sulfate over a 10 minute interval to attain a concentration of 60% of

saturation. The mixture was connected to a spiral wound ultrafiltration unit that was equipped

with a Millipore Prep/Scale 30,000MWCO regenerated cellulose membrane. The conjugate

mixture was diafiltered against 20 volumes of 60% (of saturation) ammonium sulfate solution.

The ammonium sulfate was removed from the polysaccharide-protein solution by diafiltration

against 10 volume exchanges of physiological saline, 0.85% sodium chloride. The purified

conjugate was filtered through 1.2 and 0.45 micron membranes, and then sterilized by

filtration through a 0.22 micron membrane.

The quantity of polysaccharide was determined by assaying for phosphorus by the method of

Bartlett, G.R.J. (1959) Journal of Biological Chemistiy, 234, 466. The quantity of protein

was determined by the method of Lowry, O.H., et. al. (1951) Journal of Biological Chemistry

193, 265. The quantity of unbound polysaccharide was measured by passage of the

polysaccharide-protein conjugate through a phenyl sepharose CL-6B resin using 1M

ammonium sulfate solution, and by quantitating the amount the unbound and bound

polysaccharide by the phosphorus method.

The same method has been used to purify polysaccharide-protein conjugates prepared from

Neisseria meningitidis serogroups C, W-135 and Y, and from Streptococcus pneumoniae serotypes 1, 6B, 7F, 14, and 18C. The difference in the methods used for these other

polysaccharide-protein conjugates is the amount of ammonium sulfate that is added to the

conjugate reaction mixture, and the concentration of ammonium sulfate in the diafiltration

wash buffer.

REFERENCES

1. Santosham, M. (1993) Vaccine JT : 552-557.

2. Bartlett, G.R.J. (1959) Journal of Biological Chemistry 234: 466.

3. Lowry, O.H., et.al. (1951) Journal of Biological Chemistry 193: 265.

TABLE 1

Purification assessment of Neisseria mengiditis serogroup C polysaccharide-protein conjugates by ultrafiltration versus the method of ammonium sulfate precipitation.

* Note: scm = screen channel minisette, ocm = open channel minisette, and spw = spiral wound cartridge.

TABLE 2

Purification of a Nesseria meningitidis Serogroup C Polysaccharide Protein Conjugate using a spiral wound ultrafiltration unit equipped with a Millipore Prep/Scale 30,000 MWCO regenerated cellulose membrane

TABLE 3

Purification results on polysaccharide-protein conjugates using a spiral wound ultrafiltration unit equipped with a Millipore Prep/Scale 30,000 MWCO regenerated cellulose membrane against 20 volumes of saturated ammonium sulfate solutions, followed by 10 volume exchanges against physiological saline, 0.85% sodium chloride.

Claims

We claim

1 A method foi lemoval of unbound polysaccharide from protein-polysacchaπde con^jugate ^\ accines in a mixture of protein-polysaccharide con_jugate and unbound polysacchaⁱide, the method comprising adding saturating amounts of a salt solution to the mι^\tuιe followed by filtration of the mixture through a semi-permeable membrane

- The method of claim 1 , wherein the semi-permeable membrane is hydrophobic

3 The method of claim 2, wherein the hydrophobic membrane is comprised of polyether sulfone

4 The method of claim 3, w herein the polyether sulfone membrane has a molecular weight cutoff of 30,000

⁵ The method of claim 1 , wherein the semi-permeable membrane is hydrophilic

6 The method of claim 5, wherein the hydrophilic membrane is comprised of regenerated cellulose

7 The method of claim 6, wherein the regenerated cellulose has a molecular weight cutoff of 30.000

S The me^thod of claim 1. wherein the salt solution is compπsed of ammonium sulfate

9 The me^thod of claim 8, wherein the ammonium sulfate is present at from 20 to 60% of saturation

10 The method of claim 1 , wherein the protein is diphtheπa toxoid

1 The method of claim 1 , wherein the polysacchaπde is capsular polysacchande from bactena selected from the group consisting of Sit eptococcus pneumoniae serotypes

1 ,3.5.6B.7F.9\ 14 18C,19F,23F and Neisseria meningitidis serogroups A,C, W-135 and Y