Document 0806 DOCN M9590806 TI Induction of human immunodeficiency virus type 1 (HIV-1)-specific cytolytic T lymphocyte responses in seronegative adults by a nonreplicating, host-range-restricted canarypox vector (ALVAC) carrying the HIV-1MN env gene. DT 9509 AU Egan MA; Pavlat WA; Tartaglia J; Paoletti E; Weinhold KJ; Clements ML; Siliciano RF; Department of Medicine, School of Medicine, Johns Hopkins; University, Baltimore, Maryland 21205, USA. SO J Infect Dis. 1995 Jun;171(6):1623-7. Unique Identifier : AIDSLINE MED/95287062 AB CD8+ cytolytic T lymphocytes (CTL) are likely to be an important component of effective vaccines against human immunodeficiency virus type 1 (HIV-1). CTL can be induced most effectively with live virus vectors. However, because of concerns about the safety of such vectors, a nonreplicating canarypox vector (ALVAC) capable of expressing foreign genes in mammalian cells has been developed. This study evaluated the capacity of an ALVAC vector expressing the HIV-1MN envelope (env) glycoprotein to induce HIV-1-specific CTL in seronegative volunteers. Protocols were designed to determine whether immunization with ALVAC alone or in combination with subunit boosting could induce CTL in vaccinia-immune and -naive volunteers. A simple method for antigen-specific in vitro stimulation was used to detect CTL responses in HIV-1-seronegative vaccine recipients. The results indicate that low doses of a nonreplicating virus vector alone can elicit both CD4+ and CD8+ HIV-1-specific CTL in a subset of seronegative volunteers. DE Adult Avipoxvirus/*GENETICS AIDS Vaccines/*IMMUNOLOGY Cytotoxicity, Immunologic CD4-Positive T-Lymphocytes/IMMUNOLOGY CD8-Positive T-Lymphocytes/IMMUNOLOGY *Genes, env Genetic Vectors Human HIV-1/*IMMUNOLOGY Immunity, Cellular Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/IMMUNOLOGY T-Lymphocytes, Cytotoxic/*IMMUNOLOGY Time Factors Vaccines, Synthetic JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).