Human AIDS presents a mysterious problem, whose understanding at the biologic level would benefit from study of a reasonable animal model. To date, however, human AIDS has not proven transmissable to animals, so access to a spontaneous AIDS-like animal disease would be all the more helpful. We have described the recurrent outbreaks of an AIDS-like problem (called SAIDS for simian AIDS) occurring spontaneously in rhesus monkeys at the California Primate Center (CPRC). More recently we have found that SAIDS, including Kaposi-like skin lesions, is experimentally transmissable to monkeys at both the CPRC and NIH. Inocula giving rise to the disease include, not only tissue extracts, but also whole blood and filtered plasma. Although infectious CMV is present in the donor and recipient monkeys, purified SAIDS-CMV has not as yet induced the disease nor has CMV been isolated from the infective plasma. Thus, as with human AIDS, there may be another etiologic agent acting synergistically or independently of CMV. The ready transmissability of SAIDS, both under natural cage exposure conditions and after inoculation, affords the opportunity to identify and characterize the etiologic agent(s) (specific aim #1), to work out the natural history and pathogenesis (specific aim #2) and to develop effective means of treatment and prevention (specific aim #3). Knowledge gained from this animal model system may have direct applicability to the human situation and should lead to an improved understanding of the primate immune system and its functional impairment by this type of acquired infection.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01CA037467-02
Application #
3548411
Study Section
(SSS)
Project Start
1984-03-01
Project End
1987-02-28
Budget Start
1985-03-01
Budget End
1986-02-28
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Davis
Department
Type
DUNS #
094878337
City
Davis
State
CA
Country
United States
Zip Code
95618
Lackner, A A; Moore, P F; Marx, P A et al. (1990) Immunohistochemical localization of type D retrovirus serotype 1 in the digestive tract of rhesus monkeys with simian AIDS. J Med Primatol 19:339-49
Lackner, A A; Marx, P A; Lerche, N W et al. (1989) Asymptomatic infection of the central nervous system by the macaque immunosuppressive type D retrovirus, SRV-1. J Gen Virol 70 ( Pt 7):1641-51
Schiodt, M; Lackner, A; Armitage, G et al. (1988) Oral lesions in rhesus monkeys associated with infection by simian AIDS retrovirus, serotype-I (SRV-1). Oral Surg Oral Med Oral Pathol 65:50-5
Lackner, A A; Rodriguez, M H; Bush, C E et al. (1988) Distribution of a macaque immunosuppressive type D retrovirus in neural, lymphoid, and salivary tissues. J Virol 62:2134-42
Marx, P A; Munn, R J; Joy, K I (1988) Computer emulation of thin section electron microscopy predicts an envelope-associated icosadeltahedral capsid for human immunodeficiency virus. Lab Invest 58:112-8
Marx, P A; Lowenstine, L J (1987) Mesenchymal neoplasms associated with type D retroviruses in macaques. Cancer Surv 6:101-15
Thayer, R M; Power, M D; Bryant, M L et al. (1987) Sequence relationships of type D retroviruses which cause simian acquired immunodeficiency syndrome. Virology 157:317-29
Heidecker, G; Lerche, N W; Lowenstine, L J et al. (1987) Induction of simian acquired immune deficiency syndrome (SAIDS) with a molecular clone of a type D SAIDS retrovirus. J Virol 61:3066-71
Lerche, N W; Marx, P A; Osborn, K G et al. (1987) Natural history of endemic type D retrovirus infection and acquired immune deficiency syndrome in group-housed rhesus monkeys. J Natl Cancer Inst 79:847-54
Kwang, H S; Pedersen, N C; Lerche, N W et al. (1987) Viremia, antigenemia, and serum antibodies in rhesus macaques infected with simian retrovirus type 1 and their relationship to disease course. Lab Invest 56:591-7

Showing the most recent 10 out of 22 publications