Thomson Michael, Nascimbeni Michelina, Havert Michael B, Major Marian, Gonzales Sophia, Alter Harvey, Feinstone Stephen M, Murthy Krishna K, Rehermann Barbara, Liang T Jake
Liver Diseases Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Virol. 2003 Jan;77(2):862-70. doi: 10.1128/jvi.77.2.862-870.2003.
Clearance of hepatitis C virus (HCV) infection in humans and chimpanzees is thought to be associated with the induction of strong T-cell responses. We studied four chimpanzees infected with HCV derived from an infectious full-length HCV genotype 1b cDNA. Two of the chimpanzees cleared the infection to undetectable levels for more than 12 months of follow-up; the other two became persistently infected. Detailed analyses of HCV-specific immune responses were performed during the courses of infection in these chimpanzees. Only weak and transient T helper responses were detected during the acute phase in all four chimpanzees. A comparison of the frequency of gamma interferon (IFN-gamma)-producing CD4(+) and CD8(+) T cells in peripheral blood by ELISpot assay did not reveal any correlation between viral clearance and T-cell responses. In addition, analyses of IFN-gamma, IFN-alpha, and interleukin-4 mRNA levels in liver biopsies, presumably indicative of intrahepatic T-cell responses, revealed no distinct pattern in these chimpanzees with respect to infection outcome. The present study suggests that the outcome of HCV infection in chimpanzees is not necessarily attributable to HCV sequence variation and that chimpanzees may recover from HCV infection by mechanisms other than the induction of readily detectable HCV-specific T-cell responses.
人类和黑猩猩丙型肝炎病毒(HCV)感染的清除被认为与强烈的T细胞反应的诱导有关。我们研究了四只感染源自感染性全长HCV 1b基因型cDNA的HCV的黑猩猩。其中两只黑猩猩在超过12个月的随访中清除感染至检测不到的水平;另外两只则持续感染。在这些黑猩猩的感染过程中对HCV特异性免疫反应进行了详细分析。在所有四只黑猩猩的急性期仅检测到微弱和短暂的T辅助反应。通过ELISpot试验比较外周血中产生γ干扰素(IFN-γ)的CD4(+)和CD8(+) T细胞的频率,未发现病毒清除与T细胞反应之间存在任何相关性。此外,对肝活检中IFN-γ、IFN-α和白细胞介素-4 mRNA水平的分析(可能指示肝内T细胞反应)显示,这些黑猩猩在感染结果方面没有明显模式。本研究表明,黑猩猩中HCV感染的结果不一定归因于HCV序列变异,并且黑猩猩可能通过诱导易于检测的HCV特异性T细胞反应以外的机制从HCV感染中恢复。