Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1967 Oct;94(4):836–843. doi: 10.1128/jb.94.4.836-843.1967

Preparation and Effect of Different Adjuvants on the Immunogenic Activity of Mycobacterial Ribosomal Fraction

Anne S Youmans 1, Guy P Youmans 1
PMCID: PMC276741  PMID: 4963785

Abstract

Several emulsified and two nonemulsified incomplete adjuvants were examined for their adjuvant activity by use of mycobacterial ribosomal fractions as a substrate. A good adjuvant is defined as one which produces a high immunological response with the ribosomal fraction in mice to infection with virulent tubercle bacilli. Freund's incomplete adjuvant, consisting of Aquaphor and heavy mineral oil, and Arlacel A plus hexadecane were the best adjuvants tested. Aquaphor plus light mineral oil and Arlacel A plus 7-n-hexyloctadecane were not quite as effective. Peanut oil was not satisfactory when emulsified with either Aquaphor or Arlacel A. A moderate degree of immunity was produced in mice vaccinated with ribosomal fraction mixed with aluminum hydroxide gel. Sodium alginate mixed with ribosomal fraction produced a low degree of immunity only with the highest vaccinating dose. It was found that the effectiveness of the emulsified type of adjuvant depended upon the method of preparation. Careful standardization of technique to produce uniform and complete emulsification was essential for maximal adjuvant activity using minimal vaccinating doses. A rapid and practical method of preparing emulsified adjuvants is given. The mode of action of incomplete adjuvants as employed in these experiments is discussed, and it is thought that they acted primarily by protecting the ribosomes from being inactivated by host ribonuclease before they were engulfed by the macrophages.

Full text

PDF
837

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ALEXANDER H. E., KOCH G., MOUNTAIN I. M., VAN DAMME O. Infectivity of ribonucleic acid from poliovirus in human cell monolayers. J Exp Med. 1958 Oct 1;108(4):493–506. doi: 10.1084/jem.108.4.493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Freund J., Thomson K. J. A SIMPLE, RAPID TECHNIC OF PREPARING WATER-IN-OIL EMULSIONS OF PENICILLIN, DRUGS AND BIOLOGICS. Science. 1945 May 4;101(2627):468–469. doi: 10.1126/science.101.2627.468-a. [DOI] [PubMed] [Google Scholar]
  3. HERRIOTT R. M., CONNOLLY J. H., GUPTA S. Blood nucleases and infectious viral nucleic acids. Nature. 1961 Mar 11;189:817–820. doi: 10.1038/189817a0. [DOI] [PubMed] [Google Scholar]
  4. HILLEMAN M. R. A FORWARD LOOK AT VIRAL VACCINES: WITH SPECIAL REFERENCE TO A NEW IMMUNOLOGIC ADJUVANT. Am Rev Respir Dis. 1964 Nov;90:683–706. doi: 10.1164/arrd.1964.90.5.683. [DOI] [PubMed] [Google Scholar]
  5. HOYT A., THOMPSON M. A., MOORE F. J., SMITH C. R. THE EFFECT OF ADJUVANTS ON A NONVIABLE ANTITUBERCULOSIS VACCINE AND ON LIVE BCG. Am Rev Respir Dis. 1965 Apr;91:565–574. doi: 10.1164/arrd.1965.91.4.565. [DOI] [PubMed] [Google Scholar]
  6. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  7. Luttges M., Johnson T., Buck C., Holland J., McGaugh J. An examination of "transfer of learning" by nucleic Acid. Science. 1966 Feb 18;151(3712):834–837. doi: 10.1126/science.151.3712.834. [DOI] [PubMed] [Google Scholar]
  8. MCKINNEY R. W., DAVENPORT F. M. Studies on the mechanism of action of emulsified vaccines. J Immunol. 1961 Jan;86:91–100. [PubMed] [Google Scholar]
  9. PRIGAL S. J. Studies with medicated water-in-oil emulsions. I. The use of a high-speed shaker for the production of emulsions under sterile conditions. J Allergy. 1962 Jul-Aug;33:295–300. doi: 10.1016/0021-8707(62)90028-x. [DOI] [PubMed] [Google Scholar]
  10. ROTH J. S., MILSTEIN S. W. Ribonuclease. I. A new assay method with P32 labeled yeast ribonucleic acid. J Biol Chem. 1952 May;196(2):489–498. [PubMed] [Google Scholar]
  11. SCHWARZ M. R., RIEKE W. O. Appearance of radioactivity in mouse cells after administration of labeled macromolecular RNA. Science. 1962 Apr 13;136(3511):152–154. doi: 10.1126/science.136.3511.152. [DOI] [PubMed] [Google Scholar]
  12. SUTER E., RAMSEIAR H. CELLULAR REACTIONS IN INFECTION. Adv Immunol. 1964;27:117–173. doi: 10.1016/s0065-2776(08)60707-5. [DOI] [PubMed] [Google Scholar]
  13. Sved S. The metabolism of exogenous ribonucleic acids injected into mice. Can J Biochem. 1965 Jul;43(7):949–958. doi: 10.1139/o65-109. [DOI] [PubMed] [Google Scholar]
  14. UCHITEL I. Y., KHASMAN E. L. ON THE MECHANISM OF ADJUVANT ACTION OF NONSPECIFIC STIMULATORS OF ANTIBODY FORMATION. J Immunol. 1965 Apr;94:492–497. [PubMed] [Google Scholar]
  15. YOUMANS A. S., YOUMANS G. P. IMMUNOGENIC ACTIVITY OF A RIBOSOMAL FRACTION OBTAINED FROM MYCOBACTERIUM TUBERCULOSIS. J Bacteriol. 1965 May;89:1291–1298. doi: 10.1128/jb.89.5.1291-1298.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. YOUMANS G. P., YOUMANS A. S. The measurement of the response of immunized mice to infection with Mycobacterium tuberculosis va. hominis. J Immunol. 1957 May;78(5):318–329. [PubMed] [Google Scholar]
  17. Youmans A. S., Youmans G. P. Effect of trypsin and ribonuclease on the immunogenic activity of ribosomes and ribonucleic acid isolated from Mycobacterium tuberculosis. J Bacteriol. 1966 Jun;91(6):2146–2154. doi: 10.1128/jb.91.6.2146-2154.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Youmans A. S., Youmans G. P. Preparation of highly immunogenic ribosomal fractions of Mycobacterium tuberculosis by use of sodium dodecyl sulfate. J Bacteriol. 1966 Jun;91(6):2139–2145. doi: 10.1128/jb.91.6.2139-2145.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES