Document 0883 DOCN M9550883 TI Vertical Transmission of HIV-1. Correlation with maternal viral load and plasma levels of CD4 binding site anti-gp120 antibodies. DT 9505 AU Khouri YF; McIntosh K; Cavacini L; Posner M; Pagano M; Tuomala R; Marasco WA; Dana-Farber Cancer Institute, Division of Human Retrovirology,; Boston, Massachusetts 02115. SO J Clin Invest. 1995 Feb;95(2):732-7. Unique Identifier : AIDSLINE MED/95164706 AB Almost all childhood HIV-1 is now acquired through vertical transmission. Identifying factors that affect the rate of transmission may lead to the initiation of specific preventive strategies. In this study, antibody levels against different neutralizing epitopes on the envelope glycoprotein of HIV-1 (gp120) were measured in HIV-1-infected pregnant women that either transmitted HIV-1 to their infants (18 women) or did not (29 women). Differences in levels of antibodies directed against the monomeric gp120 molecule and against the V3 loop region of gp120 were not significantly different between the two groups studied. However, significant differences were observed in the levels of CD4 binding site antibodies, as determined by the ability of diluted maternal plasma to inhibit binding of the CD4 binding site monoclonal antibody F105 (mAb F105) to monomeric gp120. In addition, more nontransmitting mothers had low viral load as defined by having two or more negative HIV-1 viral cultures during pregnancy compared with transmitters. This pilot study suggests that in addition to higher viral load, low levels of CD4 binding site antibodies correlate with increased risk of HIV-1 vertical transmission. Passive immunotherapy with broadly neutralizing CD4 binding site antibodies should be considered as a strategy to reduce this risk. DE Acquired Immunodeficiency Syndrome/BLOOD/IMMUNOLOGY/*TRANSMISSION Adult Analysis of Variance Biological Markers/BLOOD Comparative Study CD4 Lymphocyte Count *Disease Transmission, Vertical Female Human HIV Antibodies/*BLOOD HIV Envelope Protein gp120/*IMMUNOLOGY HIV Seropositivity/BLOOD/IMMUNOLOGY/*TRANSMISSION HIV-1/*ISOLATION & PURIF Pregnancy Pregnancy Complications, Infectious/BLOOD/IMMUNOLOGY/*VIROLOGY Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. CLINICAL TRIAL CONTROLLED CLINICAL TRIAL JOURNAL ARTICLE MULTICENTER STUDY SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).