Document 0570 DOCN M9650570 TI A multistep procedure for the chemical inactivation of human immunodeficiency virus for use as an experimental vaccine. DT 9605 AU Race E; Stein CA; Wigg MD; Baksh A; Addawe M; Frezza P; Oxford JS; Department of Academic Virology, London Hospital Medical College,; UK. SO Vaccine. 1995 Nov;13(16):1567-75. Unique Identifier : AIDSLINE MED/96164473 AB The kinetics of inactivation of four different strains of HIV-1 (RF, MN, SF2 and IIIB) by beta-propiolactone (BPL) and binary ethylenimine (BEI) were studied under various conditions. The conditions that would be required for the reduction of virus infectivity by at least 10(20) TCID50 ml-1 were estimated on the basis of the experimental rates of inactivation obtained. A multiple step procedure including treatment with 0.2% BPL, 0.05% sodium cholate, 10 mM BEI and 0.02% formaldehyde was designed to inactivate HIV-1 for use as an experimental vaccine. Complete inactivation of virus infectivity was confirmed by prolonged cell culture. The experimental vaccine preparation was analysed for the presence of HIV-1 proviral DNA utilizing the polymerase chain reaction. After treatment with both BPL and BEI proviral DNA was detected in one of four samples using primers encoding a 244 bp segment of the pol region of the viral genome. Proviral DNA could not be detected in any of the four samples using primers encoding segments of > 400 bp in the gag and reverse transcriptase region. DE Aziridines/*PHARMACOLOGY AIDS Vaccines/*PHARMACOLOGY Comparative Study DNA, Viral/DRUG EFFECTS Enzyme-Linked Immunosorbent Assay Human HIV Antigens/ANALYSIS/IMMUNOLOGY HIV Core Protein p24/ANALYSIS/IMMUNOLOGY HIV Envelope Protein gp120/ANALYSIS/IMMUNOLOGY/PHARMACOLOGY HIV-1/*DRUG EFFECTS/GROWTH & DEVELOPMENT/*IMMUNOLOGY Propiolactone/*PHARMACOLOGY Support, Non-U.S. Gov't Vaccines, Inactivated/PHARMACOLOGY Virus Activation/*DRUG EFFECTS JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).