Document 3193 DOCN M94A3193 TI SIVmac chimeric viruses having HIV-1 env useful for HIV-1 vaccine evaluation using macaque monkeys. DT 9412 AU Kuwata T; Igarashi T; Okada M; Ido E; Ami Y; Komatsu T; Jin M; Adachi A; Hayami M; Institute for Virus Research, Kyoto University, Japan. SO Int Conf AIDS. 1994 Aug 7-12;10(1):131 (abstract no. PA0144). Unique Identifier : AIDSLINE ICA10/94369382 AB OBJECTIVE: By constructing SIVmac chimeric viruses having HIV-1 env more efficient in macaque infection, we attempts to establish an experimental infection system using macaque monkeys instead of chimpanzees. METHODS: The chimeric viruses having LTRs, gag, pol, vif and vpx of SIVmac and tat, rev, vpu and env of HIV-1 and additionally vpr and/or nef of either HIV-1 or SIVmac were constructed. Growth of chimeras was examined in human and macaque PBMC, and one of them was inoculated to macaques. RESULTS: Growth potential of each chimera was different depending on whether vpr and nef were from HIV-1, SIVmac or defective. When NM-3rN carrying HIV-1 vpr and SIVmac nef was inoculated to two cynomolgus and two rhesus monkeys, viruses were reisolated from all monkeys at 2 through 14 weeks post inoculation constantly. DISCUSSION AND CONCLUSIONS: The results indicate the infection with NM-3rN is more efficient than that with previously constructed chimeric viruses, and suggest usefulness of NM-3rN as challenging virus for the HIV-1 vaccine evaluation in macaque monkeys. Now, macaques immunized with live-attenuated vaccine candidates were challenged with NM-3rN. DE Animal AIDS Vaccines/*PHARMACOLOGY Chimera Chimpansee troglodytes Comparative Study Drug Evaluation *Genes, env *Genes, Viral HIV-1/*GENETICS/IMMUNOLOGY Lymphocytes/MICROBIOLOGY Macaca Repetitive Sequences, Nucleic Acid SIV/GROWTH & DEVELOPMENT/*GENETICS MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).