Li Yangqiu, Geng Suxia, Du Xin, Chen Shaohua, Yang Lijian, Wu Xiuli, Li Bo, Schmidt Christian A, Przybylski Grzegorz K
Institute of Hematology, Medical College, Jinan University, Guangzhou, China.
Hematology. 2011 Jan;16(1):43-9. doi: 10.1179/102453311X12902908411634.
T-cell immunodeficiency is a common feature in cancer patients, which may relate to initiation and development of tumor. In expanding our previous observations in this area, we studied the repertoire of T-cell receptor beta variable region (TRBV) and T-cell proliferative history in CD4+ and CD8+ T cells from chronic myeloid leukemia (CML) patients. The expression and clonality analysis were performed by reverse transcription-polymerase chain reaction (RT-PCR) and GeneScan technique in peripheral blood mononuclear cells (PBMCs), CD4+ and CD8+ subsets of T cells. Nineteen CML cases in chronic phase were selected for this study and 17 healthy individuals served as controls. Marked restriction of TRBV repertoire was observed in both CD4+ and CD8+ T cells from CML. In most CML samples, clonally expanded T cells were identified in CD4+ and CD8+ T cells, predominantly in TRBV19 and TRBV21 (5/19) subfamilies. In conclusion, the restricted expression of TRBV subfamilies indicates the T-cell immunodeficiency in CML patients; however, clonally expanded T cells suggest a specific immune response to leukemia associated antigens.
T细胞免疫缺陷是癌症患者的常见特征,这可能与肿瘤的发生和发展有关。为了扩展我们之前在该领域的观察结果,我们研究了慢性髓性白血病(CML)患者CD4+和CD8+ T细胞中T细胞受体β可变区(TRBV)的 repertoire 以及T细胞增殖历史。通过逆转录聚合酶链反应(RT-PCR)和基因扫描技术在外周血单核细胞(PBMC)、T细胞的CD4+和CD8+亚群中进行表达和克隆性分析。本研究选取了19例慢性期CML病例,17名健康个体作为对照。在CML患者的CD4+和CD8+ T细胞中均观察到TRBV repertoire的明显受限。在大多数CML样本中,在CD4+和CD8+ T细胞中鉴定出克隆性扩增的T细胞,主要存在于TRBV19和TRBV21(5/19)亚家族中。总之,TRBV亚家族的受限表达表明CML患者存在T细胞免疫缺陷;然而,克隆性扩增的T细胞提示对白血病相关抗原存在特异性免疫反应。