Neutralizing antibody response during acute and chronic hepatitis C virus infection

被引:327
|
作者
Logvinoff, C
Major, ME
Oldach, D
Heyward, S
Talal, A
Balfe, P
Feinstone, SM
Alter, H
Rice, CM
McKeating, JA
机构
[1] Rockefeller Univ, Ctr Study Hepatitis C, New York, NY 10021 USA
[2] US FDA, Lab Hepatitis Viruses, Div Viral Prod, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
[3] Univ Maryland, Sch Med, Inst Human Virol, Baltimore, MD 21201 USA
[4] Cornell Univ, Weill Med Coll, Dept Med, New York, NY 10021 USA
[5] Cornell Univ, Weill Med Coll, Ctr Study Hepatitis C, New York, NY 10021 USA
[6] Columbia Univ, Div Infect Dis, New York, NY 10032 USA
[7] NIH, Dept Transfus Med, Ctr Clin, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.0403519101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Little is known about the role of Abs in determining the outcome of hepatitis C virus (HCV) infection. By using infectious retroviral pseudotypes bearing HCV glycoproteins, we measured neutralizing Ab (nAb) responses during acute and chronic HCV infection. in seven acutely infected health care workers, only two developed a nAb response that failed to associate with viral clearance. In contrast, the majority of chronically infected patients had nAbs. To determine the kinetics of strain-specific and crossreactive nAb emergence, we studied patient H, the source of the prototype genotype 1a H77 HCV strain. An early weak nAb response, specific for the autologous virus, was detected at seroconversion. However, neutralization of heterologous viruses was detected only between 33 and 111 weeks of infection. We also examined the development of nAbs in 10 chimpanzees infected with H77 clonal virus. No nAb responses were detected in three animals that cleared virus, whereas strain-specific nAbs were detected in six of the seven chronically infected animals after approximate to50 weeks of infection. The delayed appearance of high titer crossreactive nAbs in chronically infected patients suggests that selective mechanism(s) may operate to prevent the appearance of these Abs during acute infection. The long-term persistence of these nAbs in chronically infected patients may regulate viral replication.
引用
收藏
页码:10149 / 10154
页数:6
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