Details

Autor(en) / Beteiligte

• Grunst, Michael W
• Gil, Hwi Min
• Grandea, 3rd, Andres G
• Snow, Brian J
• Andrabi, Raiees
• Nedellec, Rebecca
• Burton, Iszac
• Clark, Natasha M
• Janaka, Sanath Kumar
• Keles, Nida K
• Moriarty, Ryan V
• Weiler, Andrea M
• Capuano, 3rd, Saverio
• Fennessey, Christine M
• Friedrich, Thomas C
• O'Connor, Shelby L
• O'Connor, David H
• Broman, Aimee T
• Keele, Brandon F
• Lifson, Jeffrey D
• Hangartner, Lars
• Burton, Dennis R
• Evans, David T
• Johnson, Welkin E.

Titel

Potent antibody-dependent cellular cytotoxicity of a V2-specific antibody is not sufficient for protection of macaques against SIV challenge

Ist Teil von

• PLoS pathogens, 2024-01, Vol.20 (1), p.e1011819-e1011819

Ort / Verlag

United States: Public Library of Science

Erscheinungsjahr

2024

Link zum Volltext

Quelle

EZB Electronic Journals Library

Beschreibungen/Notizen

• Fc-mediated antibody effector functions, such as antibody-dependent cellular cytotoxicity (ADCC), can contribute to the containment HIV-1 replication but whether such activities are sufficient for protection is unclear. We previously identified an antibody to the variable 2 (V2) apex of the HIV-1 Env trimer (PGT145) that potently directs the lysis of SIV-infected cells by NK cells but poorly neutralizes SIV infectivity. To determine if ADCC is sufficient for protection, separate groups of six rhesus macaques were treated with PGT145 or a control antibody (DEN3) by intravenous infusion followed five days later by intrarectal challenge with SIVmac239. Despite high concentrations of PGT145 and potent ADCC activity in plasma on the day of challenge, all animals became infected and viral loads did not differ between the PGT145- and DEN3-treated animals. To determine if PGT145 can protect against a neutralization-sensitive virus, two additional groups of six macaques were treated with PGT145 and DEN3 and challenged with an SIVmac239 variant with a single amino acid change in Env (K180S) that increases PGT145 binding and renders the virus susceptible to neutralization by this antibody. Although there was no difference in virus acquisition, peak and chronic phase viral loads were significantly lower and time to peak viremia was significantly delayed in the PGT145-treated animals compared to the DEN3-treated control animals. Env changes were also selected in the PGT145-treated animals that confer resistance to both neutralization and ADCC. These results show that ADCC is not sufficient for protection by this V2-specific antibody. However, protection may be achieved by increasing the affinity of antibody binding to Env above the threshold required for neutralization.