Kj. Hasenkrug et B. Chesebro, IMMUNITY TO RETROVIRAL INFECTION - THE FRIEND-VIRUS MODEL, Proceedings of the National Academy of Sciences of the United Statesof America, 94(15), 1997, pp. 7811-7816
Friend virus infection of adult immunocompetent mice is a well establi
shed model for studying genetic resistance to infection by an immunosu
ppressive retrovirus, This paper reviews both the genetics of immune r
esistance and the types of immune responses required for recovery from
infection, Specific major histocompatibility complex (MHC) class I an
d 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 cytotoxi
c T lymphocyte, T helper, and antibody responses, each of which provid
es essential nonoverlapping functions, The complexity of responses nec
essary for recovery from Friend virus infection has implications for b
oth immunotherapies and vaccines, For example, it is shown that succes
sful passive antibody therapy is dependent on MHC type because of the
requirement for T cell responses, For vaccines, successful immunizatio
n requires priming of both T cell and B cell responses, In vivo deplet
ion experiments demonstrate different requirements for CD8(+) T cells
depending on the vaccine used, The implications of these studies for h
uman retroviral diseases are discussed.