Postexposure immunoprophylaxis of primary isolates by an antibody to HIV receptor complex

被引:35
作者
Wang, CY
Sawyer, LSW
Murthy, KK
Fang, XD
Walfield, AM
Ye, J
Wang, JJG
Chen, PD
Li, ML
Salas, MT
Shen, M
Gauduin, MC
Boyle, RW
Koup, RA
Montefiori, DC
Mascola, JR
Koff, WC
Hanson, CV
机构
[1] United Biomed Inc, Hauppauge, NY 11788 USA
[2] Calif Dept Hlth Serv, Viral & Rickettsial Dis Lab, Berkeley, CA 94704 USA
[3] SW Fdn Biomed Res, Dept Virol & Immunol, San Antonio, TX 78245 USA
[4] Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[5] Duke Univ, Med Ctr, Dept Surg, AIDS Res Ctr, Durham, NC 27710 USA
[6] Walter Reed Army Inst Res, Div Retrovirol, Rockville, MD 20850 USA
关键词
D O I
10.1073/pnas.96.18.10367
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
mAb B4 is a monoclonal antibody directed against HIV receptor complex. The antibody had broad neutralizing activity against HIV and provided postexposure prophylaxis to hu-peripheral blood leukocyte (PBL)-severe combined immunodeficient mice and chimpanzees. B4 recognized a complex receptor site for HIV on the T cell surface that includes CD4 and also may be influenced by interaction with HIV coreceptors. mAb B4 preferentially neutralized primary HIV-1 isolates compared with T cell line-adapted strains, including syncytium-inducing and non-syncytium-inducing phenotypes, representatives from HIV-1 subtypes A-G, as well as HIV-2, simian immunodeficiency virus, and chimeric simian/human immunodeficiency virus (SHIV). Neutralization was demonstrated in both pre- and postinfection models. The administration of mAb B4 after infectious challenge totally interrupted the infection of hu-PBL-severe combined immunodeficient mice by PBL-grown HIV-1 and the infection of chimpanzees by chimp-adapted HIV-1. This mode of protection suggested that the anti-HIV receptor antibody is efficacious for prophylaxis after exposure to HIV and for prevention of maternal transmission and may be an effective antiretroviral agent for treatment.
引用
收藏
页码:10367 / 10372
页数:6
相关论文
共 34 条
[1]   CC CKRS: A RANTES, MIP-1 alpha, MIP-1 beta receptor as a fusion cofactor for macrophage-tropic HIV-1 [J].
Alkhatib, G ;
Combadiere, C ;
Broder, CC ;
Feng, Y ;
Kennedy, PE ;
Murphy, PM ;
Berger, EA .
SCIENCE, 1996, 272 (5270) :1955-1958
[2]  
[Anonymous], 1998, MMWR Recomm Rep, V47, P1
[3]  
BURKLY LC, 1992, J IMMUNOL, V149, P1779
[4]   EFFICIENT NEUTRALIZATION OF PRIMARY ISOLATES OF HIV-1 BY A RECOMBINANT HUMAN MONOCLONAL-ANTIBODY [J].
BURTON, DR ;
PYATI, J ;
KODURI, R ;
SHARP, SJ ;
THORNTON, GB ;
PARREN, PWHI ;
SAWYER, LSW ;
HENDRY, RM ;
DUNLOP, N ;
NARA, PL ;
LAMACCHIA, M ;
GARRATTY, E ;
STIEHM, ER ;
BRYSON, YJ ;
CAO, YZ ;
MOORE, JP ;
HO, DD ;
BARBAS, CF .
SCIENCE, 1994, 266 (5187) :1024-1027
[5]  
CARMICHAEL J, 1987, CANCER RES, V47, P936
[6]   Human immunodeficiency virus type 1 coreceptors participate in postentry stages in the virus replication cycle and function in simian immunodeficiency virus infection [J].
Chackerian, B ;
Long, EM ;
Luciw, PA ;
Overbaugh, J .
JOURNAL OF VIROLOGY, 1997, 71 (05) :3932-3939
[7]   HIGH-CONCENTRATIONS OF RECOMBINANT SOLUBLE CD4 ARE REQUIRED TO NEUTRALIZE PRIMARY HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ISOLATES [J].
DAAR, ES ;
LI, XL ;
MOUDGIL, T ;
HO, DD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6574-6578
[8]  
FORNSGAARD A, 1992, EUR J IMMUNOL, V22, P2973
[9]   Effective ex vivo neutralization of human immunodeficiency virus type 1 in plasma by recombinant immunoglobulin molecules [J].
Gauduin, MC ;
Allaway, GP ;
Maddon, PJ ;
Barbas, CF ;
Burton, DR ;
Koup, RA .
JOURNAL OF VIROLOGY, 1996, 70 (04) :2586-2592
[10]   Passive immunization with a human monoclonal antibody protects hu-PBL-SCID mice against challenge by primary isolates of HIV-1 [J].
Gauduin, MC ;
Parren, PWHI ;
Weir, R ;
Barbas, CF ;
Burton, DR ;
Koup, RA .
NATURE MEDICINE, 1997, 3 (12) :1389-1393