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Laboratory of Persistent Viral Diseases, Rocky Mountain
Laboratories, National Institute of Allergy and Infectious Diseases,
National Institutes of Health, Hamilton, MT 59840
Friend virus infection of adult immunocompetent mice is a
well established model for studying genetic resistance to infection by
an immunosuppressive retrovirus. This paper reviews both the genetics
of immune resistance and the types of immune responses required for
recovery from infection. Specific major histocompatibility complex
(MHC) class I and II alleles are necessary for recovery, as is a
non-MHC gene, Rfv-3, which controls virus-specific antibody responses.
In concordance with these genetic requirements are immunological
requirements for cytotoxic T lymphocyte, T helper, and antibody
responses, each of which provides essential nonoverlapping functions.
The complexity of responses necessary for recovery from Friend virus
infection has implications for both immunotherapies and vaccines. For
example, it is shown that successful passive antibody therapy is
dependent on MHC type because of the requirement for T cell responses.
For vaccines, successful immunization requires priming of both T cell
and B cell responses. In vivo depletion experiments
demonstrate different requirements for CD8+ T cells
depending on the vaccine used. The implications of these studies for
human retroviral diseases are discussed.
Proc. Natl. Acad. Sci. USA
Vol. 94,
pp. 7811-7816,
July 1997
Review
Immunity to retroviral infection: The Friend virus model
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