Meyer-Olson Dirk, Brady Kristen W, Blackard Jason T, Allen Todd M, Islam Sabina, Shoukry Naglaa H, Hartman Kelly, Walker Christopher M, Kalams Spyros A
Partners AIDS Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129, USA.
J Immunol. 2003 Apr 15;170(8):4161-9. doi: 10.4049/jimmunol.170.8.4161.
Chimpanzees are used for a variety of disease models such as hepatitis C virus (HCV) infection, where Ag-specific T cells are thought to be critical for resolution of infection. The variable segments of the TCR alphabeta genes are polymorphic and contain putative binding sites for MHC class I and II molecules. In this study, we performed a comprehensive analysis of genes that comprise the TCR beta variable gene (TCRBV) repertoire of the common chimpanzee Pan troglodytes. We identified 42 P. troglodytes TCRBV sequences representative of 25 known human TCRBV families. BV5, BV6, and BV7 are multigene TCRBV families in humans and homologs of most family members were found in the chimpanzee TCRBV repertoire. Some of the chimpanzee TCRBV sequences were identical with their human counterparts at the amino acid level. Notably four successfully rearranged TCRBV sequences in the chimpanzees corresponded to human pseudogenes. One of these TCR sequences was used by a cell line directed against a viral CTL epitope in an HCV-infected animal indicating the functionality of this V region in the context of immune defense against pathogens. These data indicate that some TCRBV genes maintained in the chimpanzee have been lost in humans within a brief evolutionary time frame despite remarkable conservation of the chimpanzee and human TCRBV repertoires. Our results predict that the diversity of TCR clonotypes responding to pathogens like HCV will be very similar in both species and will facilitate a molecular dissection of the immune response in chimpanzee models of human diseases.
黑猩猩被用于多种疾病模型,如丙型肝炎病毒(HCV)感染,在这种模型中,抗原特异性T细胞被认为对感染的清除至关重要。TCRαβ基因的可变区具有多态性,并且包含MHC I类和II类分子的假定结合位点。在本研究中,我们对构成普通黑猩猩黑猩猩指名亚种TCRβ可变基因(TCRBV)库的基因进行了全面分析。我们鉴定出42个黑猩猩指名亚种TCRBV序列,它们代表了25个已知的人类TCRBV家族。BV5、BV6和BV7是人类中的多基因TCRBV家族,并且在黑猩猩TCRBV库中发现了大多数家族成员的同源物。一些黑猩猩TCRBV序列在氨基酸水平上与其人类对应序列相同。值得注意的是,黑猩猩中四个成功重排的TCRBV序列对应于人类假基因。这些TCR序列之一被一个针对HCV感染动物中病毒CTL表位的细胞系所使用,这表明该V区在针对病原体的免疫防御背景下具有功能。这些数据表明,尽管黑猩猩和人类的TCRBV库有显著的保守性,但在短暂的进化时间框架内,黑猩猩中保留的一些TCRBV基因在人类中已经丢失。我们的结果预测,对HCV等病原体作出反应的TCR克隆型的多样性在这两个物种中非常相似,并且将有助于在人类疾病的黑猩猩模型中对免疫反应进行分子剖析。