Haemophilus influenzae pilus vaccines

BACKGROUND OF THE INVENTION
H.influenzae, a strict human pathogen, causes widespread and serious disease in both pediatric human populations (infants and children) and in adults and elderly. Pediatric diseases include mucosal surface diseases such as middle ear infections as well as invasive diseases such as meningitis, epiglottitis, septic arthritis and cellulitis. These diseases are leading causes of deafness and mental retardation and some of them can be fatal. While H.influenzae causes only about 30% of all otitis media, it is the most frequent cause of recurrent otitis media. Loss of hearing (and its accompanying retardation in learning) increases with the number of otitis episodes. Adult diseases are principally mucosal and include chronic bronchitis, sinusitis and pneumonia. H.influenzae is increasingly recognized as an important pathogen in adult and elderly populations.
Mucosal H.influenzae diseases are mainly caused by non-type b encapsulated and non-encapsulated (NT.sub.b H.influenzae) strains of the organism and invasive H.influenzae diseases are almost exclusively caused by type b encapsulated strains (H.influenzae b). No vaccine exists for NT.sub.b H.influenzae disease. A Type b capsular polysaccharide vaccine is available. The vaccine consisting of purified polyribitol phosphate (PRP), is partially effective but has several serious disadvantages. It is not antigenic or effective in the most susceptible group, that is children under the age of 18 months, and it is not completely effective in older children or in all populations. A new version of this vaccine has been recently licensed in which the polysaccharide is combined with a protein to enhance the polysaccharide's antigenicity. The conjugate vaccine appears more effective in younger populations. Neither of these vaccines gives any protection against mucosal H. influenzae diseases and neither of them prevents transmission of H.influenzae infection or colonization of the human nasopharynx.
We have discovered four morpholological and adhesion classes of pili on H.influenzae clinical isolates from different diseases, anatomical sites, ethnic groups and geographical areas. The principal pilus class, termed LKP pili, has been characterized in detail and evaluated as a purified pilus vaccine in a valid animal model of H.influenzae disease. LKP pili adhere to human erythrocytes, as do many of the pili used in other vaccines. Both NT.sub.b H.influenzae and H.influenzae b strains can express LKP pili of the same serotypes, opening the possibility that one purified LKP pilus vaccine consisting of mixed serotypes can protect against several H.influenzae diseases. Although at least eight different serotypes of LKP pili have been found, only a restricted number of them occur frequently on clinical isolates.
Purified LKP pilus vaccines have been tested in the chinchilla model of otitis media. A single pilus vaccine was safe, antigenic, and protected against both nasopharyngeal colonization and middle ear disease. Excellent protection was obtained irrespective of whether inoculation of the bacteria was directly into the middle ear or into the nasopharynx, and whether inoculation was with the piliated phase of the nonpiliated phase of H.influenzae bacteria. When inoculation was with the nonpiliated phase, a rapid shift to the piliated phase occurred in the nasopharynges and middle ears of the animals. This observation is consistent with an important role for LKP pili in colonization and virulence. Pilus vaccine immunization completely eliminated piliated phase bacteria from both anatomical sites. Protection was shown to be LKP pilus type specific.

BRIEF DESCRIPTION OF THE DRAWINGS
FIG. I is a graph of proportion of positive cultures against time after nasal instillation and barotrauma of Hemophilus influenzae into the bullae showing protection against bullar colonization in chinchillas by LKP pilus vaccine immunization. Intrabullar challenge.
FIG. II is a graph of proportion of otitis media disease signs (middle ear effusion) against time after inoculation of Hemophilus influenzae into the bullae showing protection against otitis media in chinchillas by LKP pilus vaccine immunization. Intrabullar challenge.
FIG. III is a graph of proportion of positive cultures against time after instillation of Hemophilus influenzae nasal colonization in chinchillas protected by LKP pilus vaccine immunization. Nasopharyngeal/barotrauma challenge.
FIG. IV is a graph of proportion of positive cultures against time after instillation of Hemophilus influenzae bullar colonization in chinchillas protected by LKP pilus vaccine immunization. Nasopharyngeal/barotrauma challenge.

DESCRIPTION OF THE PREFERRED EMBODIMENTS
The following LKP strains of H. influenzae, deposited at the American Type Culture Collection, 12301 Parklawn Drive, Rockville, Md. 20852, on Jun. 15, 1988 are identified by LKP pilus type; Applicants' reference number and ATCC designation:
LKP type 1 pilus-86-0295-ATCC 53775
LKP type 2 pilus-81-0568-ATCC 53776
LKP type 3 pilus-KL/8434-1-ATCC 53777
LKP type 4 pilus-86-1249-ATCC 53778
LKP type 5 pilus-81-0384-ATCC 53779
LKP type 6 pilus-86-0612-ATCC 53780
LKP type 7 pilus-87-0297-ATCC 53781
LKP type 8 pilus-FIN 48-ATCC 53782
The pili may be administered orally--say, in capsule form--or by injection--that is to say, subcutaneous, intradermal, or intramuscular injections. Where the mode of administration is by injection, since the pili may be insoluble, any pharmaceutically acceptable suspending medium may be employed. It has been found especially useful to employ phosphate buffer, suitably containing merthiolate, as the vehicle or suspending medium. It is preferred to use 0.0005-0.1, most suitably 0.0004M phosphate buffer, at ionic strength containing 0.0005 to 0.1 u, and, suitably 0.01% merthiolate. The concentration of pili in the vehicle is not critical. The sole criterion of desirability being that the pili shall be sufficiently finely divided to provide a suspension which meets generally accepted standards of syringeability. A concentration of 1-30, preferably about 20 mg. of pilus protein per 10 ml. of suspending medium is especially suitable.
It is generally preferred to administer the vaccine composition in more than one dose separated by a predetermined time interval. This time interval is selected to permit the formation of an adequate titer of antibodies to the pili in the injected subject.
Since there are no local or systemic toxic effects engendered by the injection of vaccine, there appear to be no upper limits to the dosage administered. It has been found suitable, however, to administer between 1 and 100 micrograms of pili per kilogram of body weight, most suitably about 20 micrograms per kilogram of body weight per injection.
The foregoing amounts refer to total pilus protection. Thus, if 10 pilus types from each of the designated strains are used in a mixture, a certain measure of protection is provided by a vaccine containing at least one member of each pilus type.
In vivo testing by Intrabullar and Nasal challenge Barotrauma Bacterial Isolates and Cultures
A non-typable H.influenzae strain 86-0295 isolated from the middle ear of a child with acute otitis media were used in these experiments. Bacteria was grown overnight on Brain Heart Infusion Agar (DIFCO) supplemented with 10 ug. each of NAD (SIgma, N7004) and Hemin (Sigma H2250) (S-HBIA - Formula II) at 37.degree. C. with 80% relative humidity and 5% CO.sub.2. The original isolate contained no detectable (by hemagglutination and by Electron Microscopy) piliation and piliated phase bacteria were selected by hemasbsorption (A Hemabsorption Method for Detection of Colonies of Haemophilus Influenzae Type b Expressing Fimbriae, Connor. E.M. and M.R. Loeb, Journal of Infectious Diseases, Vol. 148, pp. 855-860 (1983) (incorporated herein by reference). Aliquots of piliated (P.sup.+) and non-piliated (P.sup.-) strain 86-0295 were stored at -70.degree. C. using 5.5% Dimethyl Sulfoxide (DMSO) in Tryptic Soy Broth (TSB) as cryo protectant.
Vaccine Preparation
Pilus vaccine was prepared from P.sup.+ 86-0295 grown on S-BHIA in aluminum cookie trays by methods set forth below in Examples I thru III.
Experimental Animals and Vaccination
Adult chinchillas obtained from local ranges and exmained by otoscopy and tympanometry to be free of prior ear diseases were used in the experiment. Each animal was identified by a number on a neck collar and on the external ear. A code assigning each animal as to vaccine or placebo was developed and kept by an uninterested colleague until all experimental observations were completed. One-half of the animals were assigned to the placebo (Phosphate Buffered Saline-PBS) group and the other half animals to the vaccine group. Each dose consisted of 0.5 ml. of the vaccine or the placebo contained in a syringe labeled only with the animal's identification number. Each animal was given 2 intramuscular injections 28 days apart.
Serological Assays
Immediately before the first immunization, 10 days after the booster injection and 14 days after barotrauma, 1 ml. of blood was taken from the heart of each animal. Serum samples were prepared by standard methods and antipilus antibody titers were determined by piliated bacteria agglutination assay (PBAA).
Overnight grown P.sup.+ 86-0295 bacteria were harvested into formalinized (0.5%) PBS for use as stock test antigen (STA). Working test antigen was prepared by diluting with PBS from STA to a standardized concentration of 0.5 optical density (OD) units as determined in a 13 mm. glass tube at 540 nm. 50 ul. aliquots of the test serum were two-fold serially diluted in PBS in a 96-well flat bottom micro titer plate. The diluted serum was mixed with 50 ul. of the standardized test antigen and the test plate shaken at 150 rpm at room temperature for 20 minutes. The reactions were observed under a 20.times.stereomicroscope. The titer of a test serum is defined as the reciprocal of the dilution factor under which a distinct bacterial agglutination can be observed.
Experimental Infection
10 days following the booster injection, each group of animals was randomly divided into two subgroups, equal in number by the vaccine code keeper. One subgroup of animals was infected with the P.sup.+ bacteria and the other P.sup.- bacteria.
10 ml. of Brain Heart Infusion broth supplemented with 10 ul. each of NAD and Hemin in a 15.times.160 mm. tube was inoculated with 20 ul. of either a P.sup.+ or a P.sup.- suspension. The liquid cultures were incubated unshaken at 37.degree. C. with 5% CO.sub.2 and 80% relative humidity for about 17 hours. Such cultures routinely attained approximately 1.times.10.sup.9 colony forming units (cfu) per ml. Immediately before use, the cultures were diluted 1:10 with sterile saline.
Before infection, each animal was examined for prior middle ear infection. 0.1 ml. of the appropriate bacterial suspension was inoculated into the bulla through a small hole pierced in the bony covering of the bulla. The hole was then covered with tape. Samples of the bullar contents were removed subsequently through the same hole. The challenge dose was 10 colony-forming units per ml.
Nasal/Barotrauma Challenge
0.5 ml. of the appropriate bacterial suspension was delivered to the right naris using a 18 gauge catheter tube. The challenge dose was 10.sup.8 colony forming units/ml.
One day following nasal infection, nasal samples were collected on a chocolate agar plate from each animal by transnasal instillation of saline. Then, each animal was placed under barotrauma by placement of a needle into the epitympanic bulla and application of 25 mm Hg of negative pressure for 5 minutes. After barotrauma, the animals were returned to their cages.
Culture and Clinical Observations
Samples for culture and clinical observations were made 3, 6, 9 and 14 days following challenge according to Table 1 below:
TABLE 1______________________________________Day Clinical Observation Sample for CultureFollowing (bilateral) BullarBarotrauma Otoscopy Tympanometry Nasal Left Right______________________________________3 + + + + -6 + + + + -9 + + + + +14 + + + + +______________________________________
The results of the intrabullar challenge are illustrated in FIGS. I and II. FIG. I data show that colonization of the chinchilla middle ear (bulla) can be effectively prevented by immunization with purified LKP pili. FIG. II data show that the disease signs of otitis media can be effectively prevented by immunization with purified LKP pili.
Serum Antibody Titers
Following primary and booster vaccination with the purified LKP pilus vaccine, 6 originally had no rise in piliated cell agglutination titer, 14 had titers in the 2 to 16 range, 10 had titers in the 17 to 64 range and 5 had titers of greater than 100. No non-immunized animal had a detectable titer.
The results of the nasopharyngeal barotrauma challenge are illustrated in FIG. III. FIG. III data show that pilus immunization protects when the route of infection is the natural one via the nasopharynx. Large inocula (10.sup.8 colony-forming units) of bacteria are necessary to infect by this route. However, pilus immunization is highly effective in spite of the large challenge dose. Pilus immunization protected equally well whether the inoculation was in the pilated or nonpiliated phase. The nonpiliated inoculum rapidly shifted to the piliated phase in the nasopharynx in non-immunized animals. FIG. IV data show that the rapid elimination of H.influenzae bacteria from the nasopharynx of pilus-immunized chinchillas. The significance of this result is great. The reservoir of H.influenzae bacteria causing disease is the human nasopharynx/throat (upper respiratory tract). H.influenzae infection is transmitted from one human respiratory tract to another. The H.influenzae bacteria that cause disease in an individual originate in that individual's upper respiratory tract. If pilus immunization can prevent transmission to and colonization of the upper respiratory tract, widespread use of a pilus vaccine could eradicate H.influenzae as a pathogen. Thus, our vaccine may provide epidemiological as well as individual disease control, and eventually eradicate H.influenzae disease.
Passive Immunization
Bacterial Isolates and Cultures
Same as NP-Barotrauma Experiment above.
Antiserum Preparation
Vaccines prepared by methods detailed (in NP-Barotrauma experiment) previously. Matured young New Zealand rabbits were immunized subcutaneously with 200 ug. pilus protein mixed with Freund's incomplete adjuvent. 3 injections were given at 4-week intervals. After the last booster, animals were bled through the marginal ear vein and serum prepared by standard methods. The serum was titrated for antipilus antibodies using piliated bacteria agglutination as detailed previously. The preparation used in this experiment had an agglutination titer of 10,240.
Experimental Animals, Immunization and Challenge
40 adult chinchillas were obtained from local ranches. Before immunization, each was examined for prior middle ear infection by otoscopy and tympanometry. The animals were divided into 4 groups of 10 animals each, using a blind code. Code syringes containing 1 ml. of eitehr undiluted hyperimmune antipilus serum, 1 ml. of 1:10 diluted antipilus serum, 1 ml. of 1:100 diluted antipilus serum, or 1 ml. of non-immune serum. Each animal was given its coded injection intraperitoneally. One day following immunization, each animal was challenged into the right bulla with 10 cfu of piliated 86-0295.
Culture and Clinical Observations
Four and 8 days following bullar challenge, each animal was clinically observed by otoscopy and tympanometry. Samples for culture were taken through a surgically opened bullar by an alginate swab. Samples were streaked onto chocolate agar plates and incubated overnight at 37.degree. C. with 5% CO.sub.2 and 80% relative humidity. Individual isolated colonies were picked using sterile filter paper strips and resuspended in a drop of PBS on a ring slide. A drop of appropriately diluted antipilus serum was added and the slide shaken (150 rpm) at room temperature for 15 minutes. Positive agglutination indicates the colony contained piliated bacteria.
The results are shown in Table 4. Table 4 shows that protection against H. influenzae colonization and otitis media disease can also be obtained when LKP pilus antibodies are administered passively. The antibodies may be produced in a different species than the one protected. This result is important because patients at high risk of disease or with an overwhelming H. influenzae infection could be given immediate protection by the injection of LKP pilus antibodies as a passive immunoprophylactic or as an immunotherapeutic.
TABLE 2__________________________________________________________________________Protection of Chinchillas Against ExperimentalOtitis Media by The Passive Administration ofHomologous Antipilus Rabbit Serumintrabullar Challenge with 10 Colony-Forming Units. Fraction.sup.(3) Geometric Percent Fraction.sup.(5) Percent Fraction.sup.(6)Antibody Relative.sup.(2) with Mean Fraction.sup.(4) Protection Sympto- Protection with Pili-Dosage Serum Circulating Agglutina- Infected Against matic at Against ated PhaseGroup Dilution Antibody tion Titer at 4 Days Infection at 4 Days Symptoms at 4 Days__________________________________________________________________________High 1 .sup. 95/9.sup.(1) 3/8 63% 3/8 63% 1/8.sup.(1)Medium 1/10 8/8 99 3/8 63% 1/8 88% 0/8Low 1/100 7/7 7 2/7 86% 3/7 57% 0/7Control 0 0/10 0 10/10 0% 10/10 0% 10/10__________________________________________________________________________ .sup.(1) The single animal infected with piliated phase cells was also th single animal with no circulating antibody. .sup.(2) Animals injected IP with 1 ml serum; undiluted titer = 20,480. .sup.(3) Animals bled at time of challenge. .sup.(4) Determined by bullar culture. .sup.(5) Determined by direct observation of bulla. .sup.(6) Piliated phase bacteria determined by antiserum agglutination.
The following is a description of the general growth and purification procedures that were found to give acceptable yield and purity of protein. Exceptions to the general procedure are noted.
EXAMPLE I
General Outline of Purification of H. influenzae Pili. Inoculum Preparation, Growth and Harvest
Frozen p.sup.+ seed cultures of H. Influenza CHP 86-1249b were thawed and plated on supplemented brain-heart infusion agar. Plating was performed 18-20 hours before the anticipated tray inoculatin. The plates were incubated at 37.degree. C., with 80% relative humidity and 5% CO.sub.2. The percentage of the colonies having hemagglutinating activity was assessed. Generally, ten individual colonies were picked and assayed. In all cases at least nine out of 10 colonies were HA.sup.+ for human red cells.
Trays of GC base supplemented with DSF and hemin were inoculated with bacteria suspended in a culture transfer solution. The transfer solution was a potassium phosphate buffered saline solution containing 5mg/ml. beta-NAD. Bacteria were scraped from the plates with dacron swabs and suspended in the transfer solution until visibly turbid. Each tray was then inoculated with 2.5 ml. A glass spreader was used to distribute the inoculum evenly over the surface of the medium. Inoculated trays were incubated for 20 hours at 37.degree. C. with 5% CO.sub.2 and 80% relative humidity.
Growth was scraped from the agar using a metal scraper and 5-10 ml. of harvest buffer per tray. Since the cells were being washed before blending, the harvest buffer was at pH 5 to crystallize and recover any pili which had been shed.
EXAMPLE II
Blending and Initial Stages of Cycling
Each cell pellet from Example I, was resuspended in a volume of blending buffer such that the suspension volume was 150-200 ml., or about 5 ml. of buffer per gram of wet cell pellet. The pellet was not completely resuspended but instead broken up sufficiently so that it could be removed from the centrifuge bottle. Blending was performed using the large cup and unmodified blade assembly of the Omni mixer. Each resuspended pellet was blended for 3 minutes at a speed of 10-11 k rpm. After blending, "depiliated" cells were removed by centrifugation at 15,300.times.g. for 20 minutes. The supernatant was poured off and further clarified by another centrifugation at 15,300.times.g. for 20 minutes. The supernatant was poured off and the cell pellets discarded.
The first crystallization was performed by dialysis of the crude supernatant against a pH 5 acetate buffer. Dialysis was performed against 20 volumes of buffer overnight at 4.degree. C. Dialysis was performed against 20 volumes overnight at 4.degree. C. Crystalline pili, appearing as large chunky aggregates in the darkfield, were sedimented for 60 minutes at 4.degree. C. and 22,100.times.g. The supernatant was poured off and discarded. The pellets were inverted over paper towels to drain briefly. This point marked the end of the first cycle.
Solubilization of the pellets was performed by resuspension in 0.01M caps buffer, at half the original crude volume. The pellets were broken up by the use of a rubber policeman and by drawing the pellets into and out of a 10 ml. pipette. The pellets, brown in color, were then allowed to solubilize at 4.degree. C. with no stirring for several hours or overnight. The preparation was clarified by centrifugation at 22,100 x g for 60 minutes. The preparation was loaded into dialysis tubing then dialyzed against 50 mM sodium acetate buffer pH 5. Dialysis was performed in the cold overnight. Pilus aggregates were then collected and centrifugation of dialysis to the content. This point marked the end of the second cycle.
The third cycle was identical to the second, except that the volume of solubilizing buffer used was half of that used in the second cycle.
EXAMPLE III.
Final Stages of Cycling
After 3 cycles, the preparation still carried a faint yellow color, although it seemed fairly clean by SDS-PAGE. The following cycles were performed to remove additional impurities.
Crystalline pili were sedimented by centrifugation at 22,100.times.g. Pili were solubilized in a pH 10.5 phosphate buffer containing 5 m. M EDTA and 0.2% Triton X-100 (PBET). The same volume as in the previous cycle was used. Solubilization was performed at 4.degree. C. with occasional mild stirring and was usually completed within 4 hours. Clarification was performed by centrifugation at 22,100.times.g for 60 minutes. The supernatant was carefully poured off, leaving a clear gelatinous pellet.
Sodium chloride and polyethylene glycol were used as the crystallizing agent in the 4th cycle. However, to facilitate crystallization, it was necessary to first lower the pH from 10.5 to 7.5-8.0 by titration with HCl. The pili, still soluble at this stage, were crystallized by adding 5M sodium chloride to a final concentration of 0.5M and 30% PEG to a 3% final concentration. Streaming birefringence was visible immediately. The preparation was held at 4.degree. C. for 1 hour and then the crystalline pili sedimented by centrifugation at 22,100.times.g for 60 minutes. This point marked the end of the 4th cycle.
The yellow supernatant was poured off and discarded and the pellets inverted to drain. Solubilization was performed again in the PBET, followed by clarification by centrifugation at 22,100.times.g for 60 minutes. Again, after removal of the supernatant, a clear gelatinous pellet remained. This point marked the end of the 5th cycle.
The 6th cycle was identical to the 5th, except that the pH 10.5 phosphate buffer used for solubilization did not contain EDTA or Triton X-100.
The preparation is stored soluble, in the final pH 10.5 phosphate buffer, with 0.02% sodium azide as a preservative.
EXAMPLE IV
In accordance with the procedures of Examples I thru III, but in place of strain CHP 86-1249, there were prepared all of the pili of the strains set forth in Table 3. Slight variations in solubility may occur. For example, LKP3 pili are less soluble at pH 6 than at pH 5. Also, LKP2 pili are less soluble at pH 4 than pH 5. However, all 8 types can be purified using the described procedure.
The following formulas were used in all of the foregoing standard preparations.
FORMULA I
Hemin Stock 10 mg.ml.
Hemin is dissolved at a concentration of 10 mg./ml. in 0.05N NaOH. The hemin is usually autoclaved to sterilize, but filter sterilization through a 0.2u. filter is possible if care is taken to thoroughly dissolve the hemin. The stock may be stored at 4.degree. C. for up to 1 week or at -20.degree. C. indefinitely.
(For 40 trays: 0.6 gm. hemin in 60 ml. 0.05N NaOH)
FORMULA II
NAD Stock 5 mg./ml.
Beta-nicotinamide adenine dinucleotide is dissolved in a potassium phosphate buffered saline solution. The lab standard 20.times.k.sub.2 /KH.sub.2 PO.sub.4 media stock solution is diluted 1:20 with 0.85% NaCl to make the appropriate volume of buffer. The NAD is dissolved and then filter sterilized through a 0.2 u. filter. The stock may be stored at 4.degree. C. for up to 1 month or frozen at -20.degree. C. indefinitely.
FORMULA III
Hemin-NAD Stock for Plate Media
Combine 1 part sterile Hemin Stock with 2 parts sterile NAD Stock. Dispense into freezing vials, 3.5 ml. per vial. Store frozen at -20.degree. C. To use, thaw and add 3 ml./liter of sterile medium at no higher than 52.degree. C. The medium will be 10 ug./ml. hemin, 10 ug./ml. NAD.
FORMULA IV
Supplemented Brain-Heart Infusion Agar (S-BHIA)
To a 2-liter flask, add:
1 stir bar
37 gm. DIFCO brain-heart infusion
20 gm. DIFCO Bacto agar
1 L dH.sub.2 O
Autoclave 25 minutes to sterilize. Cool to 50.degree.-52.degree. C. With stirring, add 3 ml. of Hemin-NAD stock. Pour.
FORMULA V
DSF Supplement
______________________________________Dextrose 600 gm.1-Glutamine 15 gm.Ferric Nitrate 0.75 gm.dH.sub.2 O 1.5 L.______________________________________
Dissolve by stirring with mild heating. Dispense into 1 liter bottles, 500 ml./bottle. Autoclave 20 minutes to sterilize. Store at 42.degree. .sub.C.
FORMULA VI
GC Tray Medium
For each 4.0 L flask or 4 trays:
90 gm. DIFCO GC Base
2.5 L dH.sub.2 O
Autoclave 40 minutes to sterilize.
Add 25 ml. DSF supplement and 5 ml. sterile Hemin Stock, 10 mg./ml. Swirl to mix, then pour. This medium should contain approximately 20 ug./ml. Hemin.
FORMULA VII
______________________________________Harvest Buffer -- PBS, 0.15 u., pH 5.0______________________________________Sodium phosphate, monobasic 5.6 gm.monohydrateSodium chloride 3.2 gm.dH.sub.2 O 800 ml.______________________________________
Adjust pH to 5.0, then bring to 1 L with dH.sub.2 O.
FORMULA VIII
______________________________________Blending Buffer -- TBS, pH 10-10.3______________________________________TRIS 12.1 gm.Sodium Chloride 8.5 gm.______________________________________
Adjust pH to 10-10.3, then bring to 1 L with dH.sub.2 O.
FORMULA IX
______________________________________Dialysis Buffer -- M Acetate Buffer______________________________________Sodium Acetate, 17.23 gm.AnhydrousGlacial Acetic Acid 5.14 ml.d.H.sub.2 O 5 L______________________________________
Adjust pH to 5.0 with acetic acid, then bring to 6 L with d.H.sub.2 O (distilled H.sub.2 O).
FORMULA X
______________________________________Solubilizing Buffer -- 0.01M CAPS, pH 10.4______________________________________CAPS (3-[cyclohexylaminol]-1-propane 2.21 gm.sulfonic acid)dH.sub.2 O 800 ml.______________________________________
Adjust pH to 10.4 with NaOH, then bring to 1 L with dH.sub.2 O.
FORMULA XI
______________________________________Solubilizing Buffer -- 0.1 u. Phosphate Buffer + 5m M EDTA+0.2% Triton X-100 (PBET).______________________________________Sodium phosphate 7.92 gm.dibasicTertiary sodium 0.08 gm.phosphate .multidot.12H.sub.2 ODisodium ethylene- 1.86 gm.diaminetetraacetateTriton X-100 2 ml.dH.sub.2 O 800 ml.______________________________________
Titrate to pH 10.3-10.5 with NaOH. Bring to 1 L with dH.sub.2 O.
FORMULA XII
______________________________________Solubilizing Buffer -- 0.1 u. Phosphate Buffer______________________________________Sodium phosphate 7.92 gm.dibasicTertiary sodium 0.08 gm.phosphate.12H.sub.2 OdH.sub.2 O 800 ml.______________________________________
Titrate to pH 10.3-10.5. Bring to 1 L with dH.sub.2 O.
FORMULA XIII
5M Sodium Chloride
______________________________________Sodium Chloride 292.2 gm.dH.sub.2 O 1 L______________________________________
Filter through a 0.45 u. filter to sterilize.
FORMULA XIV
______________________________________Polyethylene Glycol, 30%______________________________________PEG-8000 (Fisher 300 gm.Carbowax)dH.sub.2 O 700 ml.______________________________________
Filter through a 0.45 u. filter to sterilize.
TABLE 3__________________________________________________________________________FREQUENCY OF LKP PILUS TYPES ON INDEPENDENTCLINICAL ISOLATES OF HAEMOPHILUS INFLUENZAE Purified Pilus Typing Serum (Rabbit, Unabsorbed) LKP1 LKP2 LKP4 LKP5 LKP6 LKP7 LKP8Pilus Disease (86- (81- LKP3 (86- (81- (86- (87- (FIN (LKP) (EM)Type Strain/Capsule Source* 0295) 0568) (Eagan) 1249) 0384) 0612) 0297 48) HA+.sup.# P+.sup.@__________________________________________________________________________LKP1(86-0295) CB/86-0295/nt OM + + + JR/Henderson/b NP + + + KL/8418-1/b epigl + + + KL/8430-1/b men + + +LKP2(81-0568) CB/81-0568/e OM + + + CB/85-0911/e OM + + + CB/86-0779/e OM + + + CB/86-1067/e OM + + + CB/86-1454/nt OM + + + CB/87-0199/e OM + + +LKP3(Eagan) JR/Eagan/b men + + + JR/1147/b epigl + + + JR/Madigan/b men + + + KL/8434-1/b epigl< + + + KL/8440-1/b epigl + + +LKP4(86-1249) CB/86-1249/nt OM + + + KL/8405-1/b men + + + KL/8408/b PC + + + KL/8410-1/b men + + + KL/8411-1/b SA + + + KL/8414-1/b BC + + + KL/8415-1/b SA + + + KL/8417-1/b men + + + KL/8419-1/b BC + + + KL/8420-1/b men + + + KL/8429/b men + + + KL/8433/b men + + + KL/8436-1/b men + + + KL/8448-1/b men + + + KL/8453/b men + + + KL/8501-1/b men + + + KL/8502-1/b men + + + KL/8503-1/b men + + + KL/8504-1/b epigl + + + KL/8505-1/b men + + KL/8507-1/b men + + +LKP4 +(86-1249) EH/AT102/b + + EH/CH100/b + + EH/COLNY10/b + + EH/DV102/b + + EH/NA100/b + + EH/NO100/b + + EH/NO105/b, + + EH/DL42/b + + EH/DL166/b + + EH/OC104/b + + RM/P2047/b SA + + RM/SP1468/b men + + RM/B536/b men + + RM/B5379/b BC + + RM/P4488/b SA + + RM/B2917/b SA + + RM/B3813/b men + + RM/B1565/b men + + RW/82 men + + RW/< men +LKP5 + +(81-0384) CB/81-0384/nt OM + + + CB/86-1814/nt OM + + + CB/87-0944/nt OM + + + KL/8458-1/b SA +LKP6 + +(86-0612) CB/86-0612/f OM + + + CB/88-0349/nt Thr + + +LKP7(87-0297) CB/87-0297/f OM +LKP8 +(FIN 48) FIN 48 OM__________________________________________________________________________ NOTE: *OM, otitis media; NP, nasopharyngeal; epigl., epiglottitis; men, meningitis PC, periorbital cellulitis; SA, septic arthritis; BC, buccal cellutitis. # Hemagglutination of human erythrocytes. @ LKP piliation by electron microscopy.
__________________________________________________________________________Reverse Phase HPLC Amino Acid Compositions and Molecular Weights ofEightHemophilus influenzae LKP Pilus Preparations Strain and/or Preparation 86-0295 Eagan 86-1067 Mix Lot 001 Lot 001 86-0295 86-0297 Lot 001 86-1249b Lot 001 81-0384 LKP1, LKP2,Amino acid (n.sub.i) LKP1 LKP1 LKP1 LP3 LKP4 LKP2 LKP5 and LKP3__________________________________________________________________________Aspartic acid or Asparagine 45.8 46.5 47.2 35.4 32.4 33.8 38.7 38.2Glutamic acid or Glutamine 22.7 22.5 22.3 18.4 22.0 21.6 20.6 21.4Serine 14.8 14.5 14.3 15.4 13.2 9.4 17.2 13.0Glycine 16.2 15.6 15.5 16.6 16.8 19.3 22.1 17.8Histidine 5.0 5.2 5.2 5.6 6.5 3.6 4.5 4.8Arginine 2.7 2.3 2.3 1.1 4.5 8.5 5.8 4.4Threonine 32.6 33.2 33.0 27.6 24.2 20.4 24.1 26.2Alanine 23.3 23.5 23.4 17.7 17.7 22.0 24.1 21.3Proline 5.3 5.3 4.3 3.7 6.5 4.0 6.4 3.7Tyrosine 9.0 9.2 9.4 5.4 6.5 6.3 11.1 6.6Valine 21.4 21.4 21.7 17.5 17.1 19.1 17.3 19.1Methionine 2.0 2.0 1.8 1.8 3.3 0.8 1.8 1.81/2 Cystine 2.1 2.5 2.1 1.7 1.8 2.1 2.1 2.0Isoleucine 9.8 9.7 9.7 7.3 9.5 11.4 12.3 9.6Leucine 9.9 9.7 9.4 15.4 14.9 14.6 13.9 13.9Phenylalanine 8.7 8.5 8.6 9.5 8.5 4.3 7.1 7.3Tryptophan 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0Lysine 18.8 18.3 19.7 16.8 16.6 16.0 15.7 16.9Total (N) 250.1 249.9 249.9 216.9 222.0 217.2 244.8 228.0Daltons 26934.3 26937.0 27001.0 23223.6 24105.9 23263.7 26168.8 24460.5.mu.g/tube 7.8 5.9 6.6 9.2 33.4 8.8 6.1 8.8__________________________________________________________________________

Haemophilus influenzae pilus vaccines

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