共 60 条
A Multivalent Clade C HIV-1 Env Trimer Cocktail Elicits a Higher Magnitude of Neutralizing Antibodies than Any Individual Component
被引:34
作者:

Bricault, Christine A.
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h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Kovacs, James M.
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Childrens Hosp, Div Mol Med, Sch Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Nkolola, Joseph P.
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h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Yusim, Karina
论文数: 0 引用数: 0
h-index: 0
机构:
Los Alamos Natl Lab, Los Alamos, NM USA
New Mexico Consortium, Los Alamos, NM USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Giorgi, Elena E.
论文数: 0 引用数: 0
h-index: 0
机构:
Los Alamos Natl Lab, Los Alamos, NM USA
New Mexico Consortium, Los Alamos, NM USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Shields, Jennifer L.
论文数: 0 引用数: 0
h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Perry, James
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h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Lavine, Christy L.
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h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Cheung, Ann
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h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Ellingson-Strouss, Katharine
论文数: 0 引用数: 0
h-index: 0
机构:
Seattle Biomed Res Inst, Seattle, WA 98109 USA
Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Rademeyer, Cecelia
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Cape Town, Div Med Virol, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Gray, Glenda E.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Witwatersrand, Fac Hlth Sci, Perinatal HIV Res Unit, Johannesburg, South Africa
South African Med Res Council, Cape Town, South Africa Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Williamson, Carolyn
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h-index: 0
机构:
Univ Cape Town, Div Med Virol, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Stamatatos, Leonidas
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h-index: 0
机构:
Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Seaman, Michael S.
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h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Korber, Bette T.
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h-index: 0
机构:
Los Alamos Natl Lab, Los Alamos, NM USA
New Mexico Consortium, Los Alamos, NM USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Chen, Bing
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Childrens Hosp, Div Mol Med, Sch Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA

Barouch, Dan H.
论文数: 0 引用数: 0
h-index: 0
机构:
Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA
Ragon Inst MGH & Harvard, Boston, MA USA Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA
机构:
[1] Beth Israel Deaconess Med Ctr, Ctr Virol & Vaccine Res, Boston, MA 02215 USA
[2] Harvard Univ, Childrens Hosp, Div Mol Med, Sch Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[4] Los Alamos Natl Lab, Los Alamos, NM USA
[5] New Mexico Consortium, Los Alamos, NM USA
[6] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[7] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[8] Univ Cape Town, Div Med Virol, Inst Infect Dis & Mol Med, ZA-7925 Cape Town, South Africa
[9] Univ Witwatersrand, Fac Hlth Sci, Perinatal HIV Res Unit, Johannesburg, South Africa
[10] South African Med Res Council, Cape Town, South Africa
[11] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[12] Ragon Inst MGH & Harvard, Boston, MA USA
基金:
美国国家卫生研究院;
关键词:
ENVELOPE GLYCOPROTEIN;
SUBTYPE-B;
MONOCLONAL-ANTIBODIES;
CRYSTAL-STRUCTURE;
DOUBLE-BLIND;
POTENT;
VACCINE;
BROAD;
IMMUNOGENICITY;
CONSENSUS;
D O I:
10.1128/JVI.03331-14
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
The sequence diversity of human immunodeficiency virus type 1 (HIV-1) presents a formidable challenge to the generation of an HIV-1 vaccine. One strategy to address such sequence diversity and to improve the magnitude of neutralizing antibodies (NAbs) is to utilize multivalent mixtures of HIV-1 envelope (Env) immunogens. Here we report the generation and characterization of three novel, acute clade C HIV-1 Env gp140 trimers (459C, 405C, and 939C), each with unique antigenic properties. Among the single trimers tested, 459C elicited the most potent NAb responses in vaccinated guinea pigs. We evaluated the immunogenicity of various mixtures of clade C Env trimers and found that a quadrivalent cocktail of clade C trimers elicited a greater magnitude of NAbs against a panel of tier 1A and 1B viruses than any single clade C trimer alone, demonstrating that the mixture had an advantage over all individual components of the cocktail. These data suggest that vaccination with a mixture of clade C Env trimers represents a promising strategy to augment vaccine-elicited NAb responses. IMPORTANCE It is currently not known how to generate potent NAbs to the diverse circulating HIV-1 Envs by vaccination. One strategy to address this diversity is to utilize mixtures of different soluble HIV-1 envelope proteins. In this study, we generated and characterized three distinct, novel, acute clade C soluble trimers. We vaccinated guinea pigs with single trimers as well as mixtures of trimers, and we found that a mixture of four trimers elicited a greater magnitude of NAbs than any single trimer within the mixture. The results of this study suggest that further development of Env trimer cocktails is warranted.
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收藏
页码:2507 / 2519
页数:13
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