Skip to main content
Book cover

H-2 Antigens pp 757–767Cite as

Expression of H-2 Genes and Susceptibility to Parasitic Infection

  • Chapter
  • 94 Accesses

Part of the book series: NATO ASI Series ((NSSA,volume 144))

Abstract

The term parasitism is difficult to define. Many infectious organisms such as bacteria or fungi, live at the expense of their hosts, yet are not usually regarded as parasites. In contrast, certain protozoans or helminths which live in close association with their hosts, but cause no demonstrable disease, are called parasites nonetheless. For present purposes, the discussion of immunity to parasites will be restricted to immune responses induced in vertebrate hosts following exposure to protozoan, helminth, or arthropod “parasites”. While such a distinction is arbitrary, it follows conventional practice. Following a brief discussion of immunity to parasitic infections in very general terms, results from studies of Trichinella spiralis-infected mice will be reviewed to provide specific examples of how H-2 genes may influence the outcome of such host-parasite interactions.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   84.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Flood, P.M., Benoist, C., Mathis, D., and Murphy, D.B.: Altered I-J phenotype in Ea transgenic mice. Proc Natl Acad Sci, 83: 8308–8312, 1986.

    Article  PubMed  CAS  Google Scholar 

  • Hayes, C.E., Klyczek, K.K., Krum, D.D., Whitcomb, R.M., Hullett, D.A., and Cantor, H.: Chromosome 4 Jt gene controls murine T cell surface I-J expression. Science, 223: 559–563.

    Google Scholar 

  • Moeller, G. ed.: I-J. Immunol Rev vol 83, 1985.

    Google Scholar 

  • Müller, V., Jongeneel, C.V., Nedospasov, S.A., Fischer-Lindahl, K., and Steinmetz, M.: Tumor necrosis factor and lymphotoxin genes map close to H-2D in the mouse major histocompatibility complex. Nature, 325: 265–267, 1987.

    Article  PubMed  Google Scholar 

  • Ruddle, N.H.: Tumor necrosis factor and related cytotoxins. Immunol Today, 8: 129–130, 1987.

    Article  Google Scholar 

  • Shapiro, L.H., Dugan, E.S., and Neiderhuber, J.E.: Monoclonal antibody characterization of a unique immune response control locus between H-2 S and D. J Exp Med, 162: 1477–1493, 1985.

    Article  PubMed  CAS  Google Scholar 

  • Silberstein, D.S., and David, J.R.: Tumor necrosis factor enhances eosinophil toxicity to Schistosoma mansoni Larvae. Proc Natl Acad Sci, 83: 1055–1059, 1986.

    Article  PubMed  CAS  Google Scholar 

  • Sumida, T., Sado, T., Kojima, M., Ono, K., Kamisaku, H., and Taniguchi, M.: I-J as an idiotype of the recognition component of antigen-specific suppressor T-cell factor. Nature, 316: 738–741, 1985.

    Article  PubMed  CAS  Google Scholar 

  • Taverne, J., Tavernier, J., Fiers, W., and Playfair, J.H.L.: Recombinant tumor necrosis factor inhibits malaria parasites in vivo but not in vitro. Clin Exp Immunol, 67: 1–4, 1987.

    PubMed Central  PubMed  CAS  Google Scholar 

  • Uracz, W., Asano, Y., Abe, R., and Tada, T.: I-J epitopes are adaptively acquired by T cells differentiated in the chimaeric condition. Nature, 316: 741–743, 1985.

    Article  PubMed  CAS  Google Scholar 

  • Waltenbaugh, C., Sun, L., and Lei, H.-Y.: Regulation of immune responses by I-J gene products. VI. Recognition of I-E molecules by I-J-bearing suppressor factors. J. Exp. Med., 163: 797–811, 1986.

    Article  PubMed  CAS  Google Scholar 

  • Wassom, O.L., David, C.S., and Gleich, G.J.: Genes within the major histocompatibility complex influence susceptibility to Trichinella spiralis in the mouse. Immunogenetics, 9: 491–496, 1979.

    Article  Google Scholar 

  • Wassom, D.L., David, C.S., and Gleich, G.J.: MHC-linked genetic control of the immune response to parasites: Trichinella spiralis in the mouse. In Skamene E, Kongshavn, P.A.L., and Landy, M. (eds.) “Genetic Control of Natural Resistance to Infection and Malignancy.” New York Academic Press pp 75–82, 1980.

    Chapter  Google Scholar 

  • Wassom, D.L., Brooks, 8.0., Babish, J.G., and David, C.S.: A gene mapping between the S and D regions of the H-2 complex influences resistance to Trichinella spiralis infections of mice. J Immunogenetics, 10: 371–378, 1983.

    CAS  Google Scholar 

  • Wassom, D.L., Krco, C.J., and David, C.S.: I-E expression and susceptibility to parasite infection. Imnunol Today, 8: 39–43, 1987.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1987 Springer Science+Business Media New York

About this chapter

Cite this chapter

Wassom, D.L., Krco, C.J., David, C.S. (1987). Expression of H-2 Genes and Susceptibility to Parasitic Infection. In: David, C.S. (eds) H-2 Antigens. NATO ASI Series, vol 144. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-0764-9_73

Download citation

  • DOI: https://doi.org/10.1007/978-1-4757-0764-9_73

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-0766-3

  • Online ISBN: 978-1-4757-0764-9

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics