Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Cancer Invest. 2013 Feb;31(2):121-31. doi: 10.3109/07357907.2012.756110. Epub 2013 Jan 3.
Little is known regarding the immunobiology of regulatory T (Treg) cells in hematopoietic malignancies, particularly in chronic lymphocytic leukemia (CLL). In the present study, we showed that the frequencies of CD8(+) and CD4(+) Treg cells were significantly increased in progressive as compared with indolent CLL patients and normal subjects. Enriched CD4(+) Treg cells induced a similar level of inhibition in polyclonally activated B cells and effector T cells from CLL patients and normal subjects. Our results suggest that the increase in circulating Treg cells may result in downregulation of tumor-specific immune response, leading to tumor expansion and disease progression.
关于调节性 T(Treg)细胞在血液恶性肿瘤中的免疫生物学特性,尤其是在慢性淋巴细胞白血病(CLL)中,目前知之甚少。在本研究中,我们发现与惰性 CLL 患者和正常对照者相比,进展期 CLL 患者的 CD8(+)和 CD4(+)Treg 细胞频率显著增加。富含 CD4(+)Treg 细胞可诱导来自 CLL 患者和正常对照者的多克隆活化 B 细胞和效应 T 细胞产生相似水平的抑制作用。我们的结果表明,循环 Treg 细胞的增加可能导致肿瘤特异性免疫反应下调,从而导致肿瘤扩张和疾病进展。