Broadly Neutralizing Antibody Mediated Clearance of Human Hepatitis C Virus Infection

被引:76
作者
Kinchen, Valerie J. [1 ]
Zahid, Muhammad N. [2 ,3 ]
Flyak, Andrew I. [4 ]
Soliman, Mary G. [1 ]
Learn, Gerald H. [2 ]
Wang, Shuyi [2 ,3 ]
Davidson, Edgar [5 ]
Doranz, Benjamin J. [5 ]
Ray, Stuart C. [1 ,6 ]
Cox, Andrea L. [1 ,6 ]
Crowe, James E., Jr. [7 ,8 ,9 ]
Bjorkman, Pamela J. [4 ]
Shaw, George M. [2 ,3 ]
Bailey, Justin R. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
[4] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[5] Integral Mol Inc, Philadelphia, PA 19104 USA
[6] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[7] Vanderbilt Univ, Dept Pathol Microbiol & Immunol, Med Ctr, Nashville, TN 37232 USA
[8] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
[9] Vanderbilt Univ, Vanderbilt Vaccine Ctr, Med Ctr, Nashville, TN 37232 USA
关键词
HUMAN MONOCLONAL-ANTIBODIES; POLYCLONAL SERA; VIRAL CLEARANCE; CELL RESPONSES; ENVELOPE; REPLICATION; RESISTANCE; EVOLUTION; SELECTION; EPITOPES;
D O I
10.1016/j.chom.2018.10.012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The role that broadly neutralizing antibodies (bNAbs) play in natural clearance of human hepatitis C virus (HCV) infection and the underlying mechanisms remain unknown. Here, we investigate the mechanism by which bNAbs, isolated from two humans who spontaneously cleared HCV infection, contribute to HCV control. Using viral gene sequences amplified from longitudinal plasma of the two subjects, we found that these bNAbs, which target the front layer of the HCV envelope protein E2, neutralized most autologous HCV strains. Acquisition of resistance to bNAbs by some autologous strains was accompanied by progressive loss of E2 protein function, and temporally associated with HCV clearance. These data demonstrate that bNAbs can mediate clearance of human HCV infection by neutralizing infecting strains and driving escaped viruses to an unfit state. These immunopathologic events distinguish HCV from HIV-1 and suggest that development of an HCV vaccine may be achievable.
引用
收藏
页码:717 / +
页数:19
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