TY - JOUR
T1 - Anti-HIV antibody development up to 1 year after antiretroviral therapy initiation in acute HIV infection
AU - Mitchell, Julie L.
AU - Pollara, Justin
AU - Dietze, Kenneth
AU - Whitney Edwards, R.
AU - Nohara, Junsuke
AU - N’guessan, Kombo F.
AU - Zemil, Michelle
AU - Buranapraditkun, Supranee
AU - Takata, Hiroshi
AU - Li, Yifan
AU - Muir, Roshell
AU - Kroon, Eugene
AU - Pinyakorn, Suteeraporn
AU - Jha, Shalini
AU - Manasnayakorn, Sopark
AU - Chottanapund, Suthat
AU - Thantiworasit, Pattarawat
AU - Prueksakaew, Peeriya
AU - Ratnaratorn, Nisakorn
AU - Nuntapinit, Bessara
AU - Fox, Lawrence
AU - Tovanabutra, Sodsai
AU - Paquin-Proulx, Dominic
AU - Wieczorek, Lindsay
AU - Polonis, Victoria R.
AU - Maldarelli, Frank
AU - Haddad, Elias K.
AU - Phanuphak, Praphan
AU - Sacdalan, Carlo P.
AU - Rolland, Morgane
AU - Phanuphak, Nittaya
AU - Ananworanich, Jintanat
AU - Vasan, Sandhya
AU - Ferrari, Guido
AU - Trautmann, Lydie
N1 - Funding Information:
We thank our study participants and staff of the Thai Red Cross AIDS Research Centre (TRC-ARC), Chulalongkorn University, and the Armed Forces Research Institute of Medical Sciences (AFRIMS) for their valuable contributions to this study. We are grateful to the Thai Government’s Pharmaceutical Organization, Gilead, Merck, and ViiV Healthcare for providing the antiretroviral agents for these studies. We thank the members of the RV254 and RV304 Study Groups (see the Supplemental Acknowledgments for study group details). This study was supported by the NIH (grant R01AI108433) and a cooperative agreement (WW81XWH-18-2-0040) between the Henry M. Jackson Foundation for the Advancement of Military Medicine Inc. and the US Department of Defense, and by an intramural grant from the Thai Red Cross AIDS Research Centre. The RV254/SEARCH 010 was funded in part by the DAIDS, NIAID, NIH (grant AAI20052001). The views expressed are those of the authors and should not be construed to represent the positions of the US Army, the Department of Defense, the NIH, the Department of Health and Human Services, or the Henry M. Jackson Foundation for the Advancement of Military Medicine Inc. The investigators adhered to the policies for the protection of human subjects as prescribed in Army Regulation 70-25.
Publisher Copyright:
Copyright: © 2022, Mitchell et al.
PY - 2022/1/4
Y1 - 2022/1/4
N2 - Early initiation of antiretroviral therapy (ART) in acute HIV infection (AHI) is effective at limiting seeding of the HIV viral reservoir, but little is known about how the resultant decreased antigen load affects long-term Ab development after ART. We report here that Env-specific plasma antibody (Ab) levels and Ab-dependent cellular cytotoxicity (ADCC) increased during the first 24 weeks of ART and correlated with Ab levels persisting after 48 weeks of ART. Participants treated in AHI stage 1 had lower Env-specific Ab levels and ADCC activity on ART than did those treated later. Importantly, participants who initiated ART after peak viremia in AHI developed elevated cross-clade ADCC responses that were detectable 1 year after ART initiation, even though clinically undetectable viremia was reached by 24 weeks. These data suggest that there is more germinal center (GC) activity in the later stages of AHI and that Ab development continues in the absence of detectable viremia during the first year of suppressive ART. The development of therapeutic interventions that can enhance earlier development of GCs in AHI and Abs after ART initiation could provide important protection against the viral reservoir that is seeded in individuals treated early in the disease.
AB - Early initiation of antiretroviral therapy (ART) in acute HIV infection (AHI) is effective at limiting seeding of the HIV viral reservoir, but little is known about how the resultant decreased antigen load affects long-term Ab development after ART. We report here that Env-specific plasma antibody (Ab) levels and Ab-dependent cellular cytotoxicity (ADCC) increased during the first 24 weeks of ART and correlated with Ab levels persisting after 48 weeks of ART. Participants treated in AHI stage 1 had lower Env-specific Ab levels and ADCC activity on ART than did those treated later. Importantly, participants who initiated ART after peak viremia in AHI developed elevated cross-clade ADCC responses that were detectable 1 year after ART initiation, even though clinically undetectable viremia was reached by 24 weeks. These data suggest that there is more germinal center (GC) activity in the later stages of AHI and that Ab development continues in the absence of detectable viremia during the first year of suppressive ART. The development of therapeutic interventions that can enhance earlier development of GCs in AHI and Abs after ART initiation could provide important protection against the viral reservoir that is seeded in individuals treated early in the disease.
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U2 - 10.1172/JCI150937
DO - 10.1172/JCI150937
M3 - Article
C2 - 34762600
AN - SCOPUS:85122779591
SN - 0021-9738
VL - 132
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 1
M1 - e150937
ER -