Human Anti-HIV-1 gp120 Monoclonal Antibodies with Neutralizing Activity Cloned from Humanized Mice Infected with HIV-1

被引:5
|
作者
Gawron, Melissa A. [1 ]
Duval, Mark [1 ]
Carbone, Claudia [2 ]
Jaiswal, Smita [2 ]
Wallace, Aaron [1 ]
Martin, Joseph C., III [1 ]
Dauphin, Ann [2 ]
Brehm, Michael A. [2 ]
Greiner, Dale L. [2 ]
Shultz, Leonard D. [3 ]
Luban, Jeremy [2 ]
Cavacini, Lisa A. [1 ]
机构
[1] Univ Massachusetts, Sch Med, MassBiol, 460 Walk Hill St, Boston, MA 02126 USA
[2] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01655 USA
[3] Jackson Lab, 600 Main St, Bar Harbor, ME 04609 USA
来源
JOURNAL OF IMMUNOLOGY | 2019年 / 202卷 / 03期
基金
美国国家卫生研究院;
关键词
MOUSE MODEL; IMMUNE-RESPONSES; B-CELLS; VIRUS; FRAMEWORK; VRC01; BROAD;
D O I
10.4049/jimmunol.1801085
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Broadly neutralizing, anti-HIV-1 gp120 mAbs have been isolated from infected individuals, and there is considerable interest in developing these reagents for Ab-based immunoprophylaxis and treatment. As a means to identify potentially new anti-HIV Abs, we exploited humanized NOD-scid IL2r gamma(null) mice systemically infected with HIV-1 to generate a wide variety of Ag-specific human mAbs. The Abs were encoded by a diverse range of variable gene families and Ig classes, including IgA, and several showed significant levels of somatic mutation. Moreover, the isolated Abs not only bound target Ags with similar affinity as broadly neutralizing Abs, they also demonstrated neutralizing ability against multiple HIV-1 clades. The use of humanized mice will allow us to use our knowledge of HIV-1 gp120 structure and function, and the immune response targeting this protein, to generate native human prophylactic Abs to reduce the infection and spread of HIV-1.
引用
收藏
页码:799 / 804
页数:6
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