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Antibody 10-1074 suppresses viremia in HIV-1-infected individuals
被引:373
|作者:
Caskey, Marina
[1
]
Schoofs, Till
[1
]
Gruell, Henning
[2
,3
,4
]
Settler, Allison
[1
]
Karagounis, Theodora
[1
]
Kreider, Edward F.
[5
,6
]
Murrell, Ben
[7
]
Pfeifer, Nico
[8
]
Nogueira, Lilian
[1
]
Oliveira, Thiago Y.
[1
]
Learn, Gerald H.
[5
,6
]
Cohen, Yehuda Z.
[1
]
Lehmann, Clara
[3
,4
]
Gillor, Daniel
[3
]
Shimeliovich, Irma
[1
]
Unson-O'Brien, Cecilia
[1
]
Weiland, Daniela
[2
,3
,4
]
Robles, Alexander
[9
]
Kuemmerle, Tim
[3
]
Wyen, Christoph
[3
]
Levin, Rebeka
[1
]
Witmer-Pack, Maggi
[1
]
Eren, Kemal
[10
,11
]
Ignacio, Caroline
[7
]
Kiss, Szilard
[12
]
West, Anthony P., Jr.
[13
]
Mouquet, Hugo
[14
]
Zingman, Barry S.
[15
,16
]
Gulick, Roy M.
[17
]
Keler, Tibor
[18
]
Bjorkman, Pamela J.
[13
]
Seaman, Michael S.
[9
]
Hahn, Beatrice H.
[5
,6
]
Faetkenheuer, Gerd
[3
,4
]
Schlesinger, Sarah J.
[1
]
Nussenzweig, Michel C.
[1
,19
]
Klein, Florian
[2
,3
,4
]
机构:
[1] Rockefeller Univ, Lab Mol Immunol, 1230 York Ave, New York, NY 10021 USA
[2] Univ Cologne, Expt Immunol Lab, Ctr Mol Med Cologne, Cologne, Germany
[3] Univ Hosp Cologne, Dept Internal Med 1, Cologne, Germany
[4] German Ctr Infect Res, Partner Site Bonn Cologne, Cologne, Germany
[5] Univ Penn, Dept Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Microbiol, Perelman Sch Med, Philadelphia, PA 19104 USA
[7] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[8] Max Planck Inst Informat, Dept Computat Biol & Appl Algorithm, Saarbrucken, Germany
[9] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA USA
[10] Univ Calif San Diego, Dept Biomed Informat, San Diego, CA USA
[11] Univ Calif San Diego, Bioinformat & Syst Biol, San Diego, CA 92103 USA
[12] Cornell Univ, Weill Carnell Med Coll, Dept Ophthalmol, New York, NY 10021 USA
[13] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[14] Inst Pasteur, Dept Immunol, Lab Humoral Response Pathogens, Paris, France
[15] Montefiore Med Ctr, Albert Einstein Coll Med, Div Infect Dis, Bronx, NY 10467 USA
[16] Einstein Rockefeller CUNY Ctr AIDS Res, Bronx, NY USA
[17] Weill Cornell Med, Div Infect Dis, New York, NY USA
[18] Celldex Therapeut, Hampton, VA USA
[19] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
基金:
欧洲研究理事会;
美国国家卫生研究院;
关键词:
BROADLY NEUTRALIZING ANTIBODIES;
HUMAN MONOCLONAL-ANTIBODIES;
HIV-1;
VACCINE;
GLYCAN RECOGNITION;
PASSIVE TRANSFER;
IN-VIVO;
POTENT;
VRC01;
THERAPY;
PHARMACOKINETICS;
D O I:
10.1038/nm.4268
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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页码:185 / 191
页数:7
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