TY - JOUR
T1 - Passive immunization against oral AIDS virus transmission
T2 - An approach to prevent mother-to-infant HIV-1 transmission?
AU - Hofmann-Lehmann, Regina
AU - Rasmussen, Robert A.
AU - Vlasak, Josef
AU - Smith, Beverly A.
AU - Baba, Timothy W.
AU - Liska, Vladimir
AU - Montefiori, David C.
AU - McClure, Harold M.
AU - Anderson, Daniel C.
AU - Bernacky, Bruce J.
AU - Rizvi, Tahir A.
AU - Schmidt, Russell
AU - Hill, Lori R.
AU - Keeling, Michale E.
AU - Katinger, Hermann
AU - Stiegler, Gabriela
AU - Posner, Marshall R.
AU - Cavacini, Lisa A.
AU - Chou, Ting Chao
AU - Ruprecht, Ruth M.
PY - 2001
Y1 - 2001
N2 - 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.
AB - 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.
KW - Human immunodeficiency virus (SHIV)
KW - Neutralizing human anti-HIV monoclonal antibodies
KW - Primate model
KW - Rhesus monkeys
KW - Simian
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U2 - 10.1034/j.1600-0684.2001.d01-52.x
DO - 10.1034/j.1600-0684.2001.d01-52.x
M3 - Article
C2 - 11555137
AN - SCOPUS:0034837873
SN - 0047-2565
VL - 30
SP - 190
EP - 196
JO - Journal of Medical Primatology
JF - Journal of Medical Primatology
IS - 4
ER -