Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1976 Oct 1;144(4):985–995. doi: 10.1084/jem.144.4.985

The analysis of the monoclonal immune response to influenza virus. II. The antigenicity of the viral hemagglutinin

PMCID: PMC2190443  PMID: 62020

Abstract

The antigenicity of the hemagglutinins (HA) of five influenza viruses of the A0 and A1 subtypes has been analyzed by means of monoclonal antibodies of murine origin produced in vitro. Secondary monoclonal anti-HA(PR8) antibodies were able to differentiate 14 antigenic determinants (or groups of determinants) on the HA of five influenza virus strains of the A0 and A1 subtypes. Taking into account that certain pairs of determinants delineated on heterologous HA may reflect the heterogeneity of the humoral immune response to a single homologous determinant, the presence of at least eight determinants (host cell- derived determinants not included) on the homologous HA of PR8 and probably on the HA of influenza viruses in general is postulated. Three types of HA-determinants of A0 and A1 influenza virus strains could be distinguished: strain-specific, partially shared, and determinant(s) common to all five virus strains tested. Roughly 40, 55, and 5%, respectively, of the secondary anti-PR8 antibodies of BALB/c mice were directed against determinants belonging to either of the three types.

Full Text

The Full Text of this article is available as a PDF (891.1 KB).

Selected References

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

  1. Aymard-Henry M., Coleman M. T., Dowdle W. R., Laver W. G., Schild G. C., Webster R. G. Influenzavirus neuraminidase and neuraminidase-inhibition test procedures. Bull World Health Organ. 1973;48(2):199–202. [PMC free article] [PubMed] [Google Scholar]
  2. Baker N., Stone H. O., Webster R. G. Serological cross-reactions between the hemagglutinin subunits of H0N1 and H1N1 influenza viruses detected with "monospecific" antisera. J Virol. 1973 Jan;11(1):137–140. doi: 10.1128/jvi.11.1.137-140.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Braciale T. J., Gerhard W., Klinman N. R. Analysis of the humoral immune response to influenza virus in vitro. J Immunol. 1976 Mar;116(3):827–834. [PubMed] [Google Scholar]
  4. Compans R. W., Dimmock N. J., Meier-Ewert H. Effect of antibody to neuraminidase on the maturation and hemagglutinating activity of an influenza A2 virus. J Virol. 1969 Oct;4(4):528–534. doi: 10.1128/jvi.4.4.528-534.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DE ST GROTH S. F., WITHELL J., LAFFERTY K. J. An improved assay method for neutralizing antibodies against influenza viruses. J Hyg (Lond) 1958 Sep;56(3):415–426. doi: 10.1017/s0022172400037906. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dowdle W. R., Coleman M. T., Gregg M. B. Natural history of influenza type A in the United States, 1957-1972. Prog Med Virol. 1974;17(0):91–135. [PubMed] [Google Scholar]
  7. Easterday B., Laver W. G., Pereira H. G., Schild G. C. Antigenic composition of recombinant virus strains produced from human and avian influenza A viruses. J Gen Virol. 1969 Jul;5(1):83–91. doi: 10.1099/0022-1317-5-1-83. [DOI] [PubMed] [Google Scholar]
  8. Fazekas de Saint Groth The antigenic subunits of influenza viruses. II. The spectrum of cross reactions. J Immunol. 1969 Nov;103(5):1107–1115. [PubMed] [Google Scholar]
  9. Fazekas de St Groth New criteria for the selection of influenza vaccine strains. Bull World Health Organ. 1969;41(3):651–657. [PMC free article] [PubMed] [Google Scholar]
  10. Fazekas de St Groth, Webster R. G. Disquisitions of Original Antigenic Sin. I. Evidence in man. J Exp Med. 1966 Sep 1;124(3):331–345. doi: 10.1084/jem.124.3.331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gerhard W., Braciale T. J., Klinman N. R. The analysis of the monoclonal immune response to influenza virus. I. Production of monoclonal anti-viral antibodies in vitro. Eur J Immunol. 1975 Oct;5(10):720–725. doi: 10.1002/eji.1830051013. [DOI] [PubMed] [Google Scholar]
  12. Kilbourne E. D., Laver W. G., Schulman J. L., Webster R. G. Antiviral activity of antiserum specific for an influenza virus neuraminidase. J Virol. 1968 Apr;2(4):281–288. doi: 10.1128/jvi.2.4.281-288.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Klinman N. R. Regain of homogeneous binding activity after recombination of chains of "mono- focal" antibody. J Immunol. 1971 May;106(5):1330–1337. [PubMed] [Google Scholar]
  14. Laver W. G., Downie J. C., Webster R. G. Diversity of the antibody response to the different antigenic determinants on the hemagglutinin subunits of influenza viruses. J Immunol. 1976 Feb;116(2):336–341. [PubMed] [Google Scholar]
  15. Laver W. G., Downie J. C., Webster R. G. Studies on antigenic variation in influenza virus. Evidence for multiple antigenic determinants on the hemagglutinin subunits of A-Hong Kong-68 (H3 N2) virus and the A-England-72 strains. Virology. 1974 May;59(1):230–244. doi: 10.1016/0042-6822(74)90218-9. [DOI] [PubMed] [Google Scholar]
  16. Laver W. G., Webster R. G. Selection of antigenic mutants of influenza viruses. Isolation and peptide mapping of their hemagglutination proteins. Virology. 1968 Feb;34(2):193–202. doi: 10.1016/0042-6822(68)90230-4. [DOI] [PubMed] [Google Scholar]
  17. Michaelides M. C., Eisen H. N. The strange cross-reaction of menadione (vitamin K3) and 2,4-dinitrophenyl ligands with a myeloma protein and some conventional antibodies. J Exp Med. 1974 Sep 1;140(3):687–702. doi: 10.1084/jem.140.3.687. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Schild G. C., Oxford J. S., Dowdle W. R., Coleman M., Pereira M. S., Chakraverty P. Antigenic variation in current influenza A viruses: evidence for a high frequency of antigenic 'drift' for the Hong Kong virus. Bull World Health Organ. 1974;51(1):1–11. [PMC free article] [PubMed] [Google Scholar]
  19. Schild G. C. Studies with antibody to the purified haemagglutinin of an influenza Ao virus. J Gen Virol. 1970 Dec;9(3):191–200. doi: 10.1099/0022-1317-9-3-191. [DOI] [PubMed] [Google Scholar]
  20. Varga J. M., Konigsberg W. H., Richards F. F. Antibodies with multiple binding functions. Induction of single immunoglobin species by structurally dissimilar haptens. Proc Natl Acad Sci U S A. 1973 Nov;70(11):3269–3274. doi: 10.1073/pnas.70.11.3269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Virelizier J. L., Postlethwaite R., Schild G. C., Allison A. C. Antibody responses to antigenic determinants of influenza virus hemagglutinin. I. Thymus dependence of antibody formation and thymus independence of immunological memory. J Exp Med. 1974 Dec 1;140(6):1559–1570. doi: 10.1084/jem.140.6.1559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Webster R. G., Laver W. G. Antigenic variation in influenza virus. Biology and chemistry. Prog Med Virol. 1971;13:271–338. [PubMed] [Google Scholar]
  23. Webster R. G., Laver W. G. Preparation and properties of antibody directed specifically against the neuraminidase of influenza virus. J Immunol. 1967 Jul;99(1):49–55. [PubMed] [Google Scholar]
  24. Webster R. G., Laver W. G., Tumova B. Studies on the origin of pandemic influenza viruses V. Persistence of Asian influenza virus hemagglutinin (H2) antigen in nature? Virology. 1975 Oct;67(2):534–543. doi: 10.1016/0042-6822(75)90453-5. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES