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Antibody 10-1074 suppresses viremia in HIV-1-infected individuals

Authors :
Caskey, Marina
Schoofs, Till
Gruell, Henning
Settler, Allison
Karagounis, Theodora
Kreider, Edward F.
Murrell, Ben
Pfeifer, Nico
Nogueira, Lilian
Oliveira, Thiago Y.
Learn, Gerald H.
Cohen, Yehuda Z.
Lehmann, Clara
Gillor, Daniel
Shimeliovich, Irma
Unson-O'Brien, Cecilia
Weiland, Daniela
Robles, Alexander
Kuemmerle, Tim
Wyen, Christoph
Levin, Rebeka
Witmer-Pack, Maggi
Eren, Kemal
Ignacio, Caroline
Kiss, Szilard
West, Anthony P., Jr.
Mouquet, Hugo
Zingman, Barry S.
Gulick, Roy M.
Keler, Tibor
Bjorkman, Pamela J.
Seaman, Michael S.
Hahn, Beatrice H.
Faetkenheuer, Gerd
Schlesinger, Sarah J.
Nussenzweig, Michel C.
Kleine, Florian
Caskey, Marina
Schoofs, Till
Gruell, Henning
Settler, Allison
Karagounis, Theodora
Kreider, Edward F.
Murrell, Ben
Pfeifer, Nico
Nogueira, Lilian
Oliveira, Thiago Y.
Learn, Gerald H.
Cohen, Yehuda Z.
Lehmann, Clara
Gillor, Daniel
Shimeliovich, Irma
Unson-O'Brien, Cecilia
Weiland, Daniela
Robles, Alexander
Kuemmerle, Tim
Wyen, Christoph
Levin, Rebeka
Witmer-Pack, Maggi
Eren, Kemal
Ignacio, Caroline
Kiss, Szilard
West, Anthony P., Jr.
Mouquet, Hugo
Zingman, Barry S.
Gulick, Roy M.
Keler, Tibor
Bjorkman, Pamela J.
Seaman, Michael S.
Hahn, Beatrice H.
Faetkenheuer, Gerd
Schlesinger, Sarah J.
Nussenzweig, Michel C.
Kleine, Florian
Publication Year :
2017

Abstract

Monoclonal antibody 10-1074 targets the V3 glycan supersite on the HIV-1 envelope (Env) protein. It is among the most potent anti-HIV-1 neutralizing antibodies isolated so far. Here we report on its safety and activity in 33 individuals who received a single intravenous infusion of the antibody. 10-1074 was well tolerated and had a half-life of 24.0 d in participants without HIV-1 infection and 12.8 d in individuals with HIV-1 infection. Thirteen individuals with viremia received the highest dose of 30 mg/kg 10-1074. Eleven of these participants were 10-1074-sensitive and showed a rapid decline in viremia by a mean of 1.52 logic copies/ml. Virologic analysis revealed the emergence of multiple independent 10-1074-resistant viruses in the first weeks after infusion. Emerging escape variants were generally resistant to the related V3-specific antibody PGT121, but remained sensitive to antibodies targeting nonoverlapping epitopes, such as the anti-CD4-binding-site antibodies 3BNC117 and VRC01. The results demonstrate the safety and activity of 10-1074 in humans and support the idea that antibodies targeting the V3 glycan supersite might be useful for the treatment and prevention of HIV-1 infection.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1364919525
Document Type :
Electronic Resource