MN and IIIB recombinant glycoprotein 120 vaccine-induced binding antibodies to native envelope glycoprotein of human immunodeficiency virus type 1 primary isolates. National Institute of Allergy and Infectious Disease Aids Vaccine Evaluation Group. NLM AIDSLINE Important note: Information in this article was accurate in 1999. The state of the art may have changed since the publication date.

Click here to return to AIDSLINE main menu
DonateNow
Print this Article


MN and IIIB recombinant glycoprotein 120 vaccine-induced binding antibodies to native envelope glycoprotein of human immunodeficiency virus type 1 primary isolates. National Institute of Allergy and Infectious Disease Aids Vaccine Evaluation Group.

AIDS Res Hum Retroviruses. 1999 Jul 1;15(10):921-30. Unique Identifier : AIDSLINE MED/99335214
Gorse GJ; Patel GB; Mandava M; Berman PW; Belshe RB; St. Louis Department of Veterans Affairs Medical Center and Saint; Louis University School of Medicine, Missouri 63110, USA.; gorsegi@slu.edu


Abstract: The ability of antibody induced by MN and IIIB recombinant gp120 (rgp120) human immunodeficiency virus type 1 (HIV-1) vaccines to bind to oligomeric native HIV-1 envelope glycoproteins of primary isolates of HIV-1 was measured by flow cytometric indirect immunofluorescence assay (FIFA) in 25 uninfected, healthy adults. After three immunizations, MN rgp120 HIV-1 vaccine given alone and coadministered with IIIB rgp120 HIV-1 vaccine elicited antibody that bound to cells infected with each of a panel of six subtype B strains of HIV-1. Lower levels of vaccine-induced binding antibody were detected against envelope subtype A, D, and (EA) strains of HIV-1 than against subtype B strains. Priming immunization with IIIB rgp120 HIV-1 vaccine alone induced low levels of antibody capable of binding to envelope glycoprotein of primary isolate strains of HIV-1, and booster immunizations with MN rgp120 HIV-1 vaccine resulted in much higher antibody levels. We conclude that MN rgp120 HIV-1 vaccine was an effective inducer of antibody to native envelope glycoproteins of antigenically diverse primary isolates of HIV-1.
Keywords: CLINICAL TRIAL CLINICAL TRIAL, PHASE I JOURNAL ARTICLE RANDOMIZED CONTROLLED TRIAL Adolescence Adult Animal AIDS Vaccines/*IMMUNOLOGY CHO Cells Hamsters Human HIV Antibodies/BLOOD/*IMMUNOLOGY HIV Envelope Protein gp120/*IMMUNOLOGY HIV-1/*IMMUNOLOGY/ISOLATION & PURIF Middle Age Support, U.S. Gov't, P.H.S. Vaccination Vaccines, Synthetic/*IMMUNOLOGYKWDclinicaltrialclinicaltrial,phaseijournalarticlerandomizedcontrolledtrialadolescenceadultanimalaidsvaccines/KWDimmunologychocellshamstershumanhivantibodies/blood/KWDimmunologyhivenvelopeproteingp120/KWDimmunologyhiv-1/KWDimmunology/isolation&purifmiddleagesupport,uKWDsKWDgov't,pKWDhKWDsKWDvaccinationvaccines,synthetic/KWDimmunology
991130
A99B1081

Copyright © 1999 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

AEGiS is a 501(c)3, not-for-profit, tax-exempt, educational corporation. AEGiS is made possible through unrestricted funding from Boehringer Ingelheim, Bridgestone/Firestone Charitable Trust, Bristol-Myers Squibb Company, Elton John AIDS Foundation, Gill Foundation, the National Library of Medicine, Quest Diagnostics, Roche and Trimeris, and donations from users like you. Always watch for outdated information. This article first appeared in 1999. This material is designed to support, not replace, the relationship that exists between you and your doctor.

AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.

Copyright ©1980, 1999. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. .