IL41902A - Immunogenic substance,its production,vaccine preparations containing it and their preparation - Google Patents

Immunogenic substance,its production,vaccine preparations containing it and their preparation

Info

Publication number
IL41902A
IL41902A IL41902A IL4190273A IL41902A IL 41902 A IL41902 A IL 41902A IL 41902 A IL41902 A IL 41902A IL 4190273 A IL4190273 A IL 4190273A IL 41902 A IL41902 A IL 41902A
Authority
IL
Israel
Prior art keywords
vaccine
substance
immunogenic substance
multocida
immunogenic
Prior art date
Application number
IL41902A
Other versions
IL41902A0 (en
Original Assignee
Wellcome Found
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Wellcome Found filed Critical Wellcome Found
Publication of IL41902A0 publication Critical patent/IL41902A0/en
Publication of IL41902A publication Critical patent/IL41902A/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/102Pasteurellales, e.g. Actinobacillus, Pasteurella; Haemophilus

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Medicinal Chemistry (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Claims (9)

1. A386 PI What we claim is:- 1. An immunogenic substance suitable for use in conferring immunity in a mammal or bird against pasturellosis arising from infection with Pasteurella multocida or Pasteurella haemolytica which substance is obtainable from an encapsulated variant of a serotype selected from P.multocida and P .haemolytica serotypes , said serotype corresponding to the serotype against which immunity is to be conferred by said substance; is nontoxic in mammals and birds at the immunising dose of said substance; is antigenically stable after 10 minutes in water at 100°C; is non-dialysable; is water soluble; and is substantially absent from non-capsulated variants of P .multocida and .haemolytica.
2. An immunogenic substance as claimed in claim 1 wherein an immunising dose of the substance has a toxicity less than one tenth of the toxicity associated with an immunising dose of a culture of encapsulated P.multocida or P .haemolytica from which endotoxin has not been removed.
3. An immunogenic substance as claimed in claim 1 wherein an immunising dose of the substance has a toxicity less than one hundredth of the toxicity associated with an immunising dose of a culture of encapsulated P .multocida or P. haemolytica from which endotoxin has not been removed.
4. An immunogenic substance as claimed in either of claims 1 and 2 wherein the substance has an LD50 of more than 5 yg. in chick embryos by the method of Milner and Finkelstein; a reactive dose of more than 100 yg. in the localised Schwartzman reaction; a pyrogenic index in rabbits of less than 20 by the method of Milner and Finkelstein when using a dose of 5 yg; or a lethal dose for rabbits when administered intravenously of more than A386 PI 1 mg.
5. An immunogenic substance as claimed in any of claims 1 to 4 wherein the substance has a molecular weight of from 4 7 10 to 10 .
6. An immunogenic substance as claimed in any of claims 1 to 5 wherein the encapsulated variant is of P.multocida Type A (Carter) or Type D (Carter) .
7. An immunogenic substance as claimed in any of claims 1 to 5 wherein the encapsulated variant is a serotype selected from P.multocida Types B and E (Carter).
8. An immunogenic substance as claimed in any of claims 1 to 5 wherein the encapsulated variant is a P.haemolytlea serotype.
9. An immunogenic substance as claimed in any of claims 1 to 8 wherein the immunogenic substance has a solubility in distilled water of at least 20 mg/ml. A 386 P2 10. A sterile vaccine suitable for immunisation of a mammal or bird against pasteurellosis arising from infection with P. multocida or P. haemolytica comprising an immunogenic substance according to any of Claims 1 to 9 in association with a physiologically acceptable carrier, said vaccine being sterile and isotonic with blood of the mammal or bird to be immunised. 11 . A vaccine according to Claim 10 characterised in that the vaccine is in a freeze-dried form for reconstitution with pyrogen-free water. 12. A vaccine according to Claim 10 characterised in that the carrier comprises pyrogen-free water. 13· A vaccine according o any of Claims 10 to 12 characterised in that the vaccine includes an adjuvant. 1 . A vaccine according to Claim 13 characterised in that the adjuvant is an aluminium salt or base. 15. A vaccine according to any of Claims 10 and 12 to 14 characterised in that the vaccine comprises a water-in-oil emulsion wherein the immunogenic substance is present in the aqueous phase. 16. A vaccine according to Claim 15 characterised in that the and/ vaccine includes a lipophilic/or hydrophilic emulsifier. 17. A vaccine according to any of Claims 10 to 16 characterised in that it is presented in unit dosage form. 18. A vaccine according to Claim 17 characterised in that . '■ — —: — · the- unit dosage contains from A 386 P2 1 to 100 mg. of dialysed and i'reeze-dried immunogenic substance. 19. A vaccine according to Claim 18 characterised in that dialysed and freeze-dried the unit dosage contains from 2 to 20 mg. of / immunogenic substance. 20. A vaccine according to any of Claims 10 to 19 characterised in that the vaccine contains an additional immunising substance of bacterial or viral origin. 21. A vaccine according to Claim 20 characterised in that the other active ingredient is of a Clostridium chauvoei vaccine. 22. A vaccine according to Claim 20 characterised in that the encapsulated variant is of P. multocida Type B or E (Carter) cells and the other active ingredient is of an Anthrax spores vaccine . . 23. A vaccine according to Claim 20 characterised in that the encapsulated variant is of P. multocida Type A or D (Carter) cells and the other active ingredient is of a Clostridium septicum vaccine. 24-. A method of preparing a vaccine according to any of Claims 10 to 23, suitable for the immunisation of a mammal or bird against pasteurellosis characterised in that one brings an immunogenic substance according to any of Claims 1 to 9 into association with a physiologically acceptable carrier and renders the vaccine sterile and isotonic with the blood of the mammal or bird to be immunised. A 386 P3 25· An immunogenic substance substantially as described herein with reference to Examples 1, 2, 3 and 6. 26. A method of preparing an immunogenic substance substantial! as described herein with reference to Examples 1, 2, 3 and 6. 2 · A vaccine substantially as described herein with reference to Example 4. 28. A method of preparing a vaccine substantially as described herein with reference to Example 4-, 41902/2 - 45 - 29. A method of inraamisation of non-humans and birds against pasteurellosis comprising administration of an effective dosage of a sterile vaccine according to any Claims 10 to 24. 30. A method of immunisation of non-human mammals against shipping fever, according to Claim 29, characterized in that th encapsulated variant is of P. multocida Type A or D (Carter) serotype. 31. A method of immunisation of non-human mammals against Haemorrhagic septicaemia according to Claiji 29 characterized in that the encapsulated variant is of a P. Multocida Type B or E (Carter) serotype. 32. , A method of immunisation of non-human mammals against pneumonic pasteurellosis, according to Claim 29 characterized in that the encapsulated variant is of a P. Haamolytica serotype. 33. A method according to any of Claim 29 to 32 characterized in that the vaccine is administered intramuscularly or subcutaneously. 34. A method according to any of Claims 29 to 33 characterized in that the dosage is from 1 to loo rag. of dialysed and freeze-dried immunogenic substance. 35. A method according to Claim 34 characterized in that the dosage is from 2 to 20 mg. of dialysed and freeze-dried immunogenic substance. 36. A method according to any of Claims 29 to 33 characterized in that the amount of immunogenic substance per dose corresponds 6 to the amount of immunogenic substance obtainable from, from 10 to 1011 cells of said encapsulated variant. Ppr tJhe Applicants
IL41902A 1972-03-29 1973-03-28 Immunogenic substance,its production,vaccine preparations containing it and their preparation IL41902A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB1491072 1972-03-29
GB593573*[A GB1441098A (en) 1972-03-29 1973-02-07 Biological preparations

Publications (2)

Publication Number Publication Date
IL41902A0 IL41902A0 (en) 1973-05-31
IL41902A true IL41902A (en) 1976-03-31

Family

ID=26240265

Family Applications (1)

Application Number Title Priority Date Filing Date
IL41902A IL41902A (en) 1972-03-29 1973-03-28 Immunogenic substance,its production,vaccine preparations containing it and their preparation

Country Status (9)

Country Link
JP (1) JPS496118A (en)
DE (1) DE2315563A1 (en)
ES (1) ES413100A1 (en)
FR (1) FR2182909B1 (en)
GB (1) GB1441098A (en)
HU (1) HU171383B (en)
IL (1) IL41902A (en)
IT (1) IT1035061B (en)
NL (1) NL7304320A (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2964721D1 (en) * 1978-08-24 1983-03-17 Nat Res Dev Pasteurellosis vaccines
US4328210A (en) 1980-03-31 1982-05-04 Norden Laboratories, Inc. Modified Pasteurella bacteria and vaccines prepared therefrom
US4335106A (en) 1980-03-31 1982-06-15 Norden Laboratories Inc. Processes for the growth of a modified Pasteurella multocida bacteria and preparation of a vaccine therefrom
US4388299A (en) 1980-03-31 1983-06-14 Norden Laboratories, Inc. Modified pasteurella bacteria and vaccines prepared therefrom
US4293545A (en) 1980-03-31 1981-10-06 Norden Laboratories, Inc. Modified Pasteurella multocida bacteria vaccines
US4506017A (en) * 1981-04-17 1985-03-19 Norden Laboratories, Inc. Modified Pasteurella haemolytica bacteria
US4626430A (en) * 1981-04-17 1986-12-02 Norden Laboratories, Inc. Processes for growth of modified Pasteurella haemolytica bacteria and preparation of a vaccine therefrom
US4559306A (en) * 1981-04-17 1985-12-17 Norden Laboratories, Inc. Modified Pasteurella multocida bacteria
NL8200392A (en) * 1982-02-03 1983-09-01 Duphar Int Res PROCESS FOR PREPARING AN IMMUNOGEN OF PASTEURELLA MULTOCIDA
JPH0662433B2 (en) * 1984-04-23 1994-08-17 財団法人日本生物科学研究所 Method for producing powdered vaccine of Haemophilus paragarinarum
EP0287206B2 (en) * 1987-03-24 1999-11-24 BTG INTERNATIONAL LIMITED (Company No. 2664412) Vaccine against pasteurella
MX9301736A (en) * 1992-03-30 1994-01-31 Smithkline Beecham Corp PASTEURELLA HAEMOLYTICA TYPE A-1 BACTERINE-TOXOID VACCINE.

Also Published As

Publication number Publication date
ES413100A1 (en) 1976-06-01
HU171383B (en) 1977-12-28
GB1441098A (en) 1976-06-30
DE2315563A1 (en) 1973-10-11
JPS496118A (en) 1974-01-19
IT1035061B (en) 1979-10-20
FR2182909B1 (en) 1976-04-09
NL7304320A (en) 1973-10-02
IL41902A0 (en) 1973-05-31
FR2182909A1 (en) 1973-12-14

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