Broadly neutralizing antibodies and monoclonal V2 antibodies derived from RV305 inhibit capture and replication of HIV-1

被引:0
|
作者
Kim, Jiae [1 ,2 ]
Villar, Zuzana [1 ,2 ]
Jobe, Ousman [1 ,2 ]
Rerks-Ngarm, Supachai [3 ]
Pitisuttithum, Punnee [4 ]
Nitayaphan, Sorachai [5 ]
O'Connell, Robert J. [6 ]
Ake, Julie A. [7 ]
Vasan, Sandhya [1 ]
Rao, Venigalla B. [8 ]
Rao, Mangala [2 ]
机构
[1] US Mil HIV Res Program, Henry M Jackson Fdn Advancement Mil Med, 6720A Rockledge Dr, Bethesda, MD 20817 USA
[2] US Mil HIV Res Program, Walter Reed Army Inst Res, Ctr Infect Dis Res, Lab Adjuvant & Antigen Res, Silver Spring, MD 20910 USA
[3] Minist Publ Hlth, Dept Dis Control, Nonthaburi, Thailand
[4] Mahidol Univ, Fac Trop Med, Vaccine Trial Ctr, Salaya, Thailand
[5] Armed Forces Res Inst Med Sci, Bangkok, Thailand
[6] United States Army Med Component, Armed Forces Res Inst Med Sci, Bangkok, Thailand
[7] US Mil HIV Res Program, Walter Reed Army Inst Res, Ctr Infect Dis Res, Silver Spring, MD 20910 USA
[8] Catholic Univ Amer, Bacteriophage Med Res Ctr, Dept Biol, 620 Michigan Ave,NE, Washington, DC 20064 USA
关键词
Virus capture; Broadly neutralizing antibodies; V2; region; Monoclonal antibodies; Primary virus; HIV-1; vaccine; RV144; RV305; PBMCs; qRT-PCR; EFFICACY; INFECTION; AIDSVAX; REVEAL; BINDS; ALVAC;
D O I
10.1016/j.virol.2024.110158
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
An important approach to stopping the AIDS epidemic is the development of a vaccine that elicits antibodies that block virus capture, the initial interactions of HIV-1 with the target cells, and replication. We utilized a previously developed qRT-PCR-based assay to examine the effects of broadly neutralizing antibodies (bNAbs), plasma from vaccine trials, and monoclonal antibodies (mAbs) on virus capture and replication. A panel of bNAbs inhibited primary HIV-1 replication in PBMCs but not virus capture. Plasma from RV144 and RV305 trial vaccinees demonstrated inhibition of virus capture with the HIV-1 subtype prevalent in Thailand. Several RV305 derived V2-specific mAbs inhibited virus replication. One of these RV305 derived V2-specific mAbs inhibited both virus capture and replication, demonstrating that it is possible to elicit antibodies by vaccination that inhibit virus capture and replication. Induction of a combination of such antibodies may be the key to protection from HIV-1 acquisition.
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