| Literature DB >> 11555137 |
R Hofmann-Lehmann1, R A Rasmussen, J Vlasak, B A Smith, T W Baba, V Liska, D C Montefiori, H M McClure, D C Anderson, B J Bernacky, T A Rizvi, R Schmidt, L R Hill, M E Keeling, H Katinger, G Stiegler, M R Posner, L A Cavacini, T C Chou, R M Ruprecht.
Abstract
To develop immunoprophylaxis regimens against mother-to-child human immunodeficiency virus type 1 (HIV-1) transmission, we established a simian-human immunodeficiency virus (SHIV) model in neonatal macaques that mimics intrapartum mucosal virus exposure (T.W. Baba, J. Koch, E.S. Mittler et al: AIDS Res Hum Retroviruses 10:351-357, 1994). We protected four neonates from oral SHIV-vpu+ challenge by ante- and postpartum treatment with a synergistic triple combination of immunoglobulin (Ig) G1 human anti-HIV-1 neutralizing monoclonal antibodies (mAbs) (T.W. Baba, V. Liska, R. Hofmann-Lehmann et al: Nature Med 6:200-206, 2000), which recognize the CD4-binding site of Env, a glycosylation-dependent gp120, or a linear gp41 epitope. Two neonates that received only postpartum mAbs were also protected from oral SHIV-vpu+ challenge, indicating that postpartum treatment alone is sufficient. Next, we evaluated a similar mAb combination against SHIV89.6P, which encodes env of primary HIV89.6. One of four mAb-treated neonates was protected from infection and two maintained normal CD4+ T-cell counts. We conclude that the epitopes recognized by the three mAbs are important determinants for achieving protection. Combination immunoprophylaxis with synergistic mAbs seems promising to prevent maternal HIV-1 transmission in humans.Entities:
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Year: 2001 PMID: 11555137 DOI: 10.1034/j.1600-0684.2001.d01-52.x
Source DB: PubMed Journal: J Med Primatol ISSN: 0047-2565 Impact factor: 0.667