Pryjma J, Kowalczyk D, Ruggiero I, Zembala M
Department of Clinical Immunology and Microbiology, Copernicus Medical School, Cracow, Poland.
Arch Immunol Ther Exp (Warsz). 1992;40(2):139-43.
The aim of this study was to analyze phenotypes of T cells activated by mitogen (PWM) and antigen (PPD) in the presence of FcR+ or FcR- monocytes. It was found that CD4+ and CD8+ lymphocytes are preferentially activated in the presence of different monocyte subpopulations. Expression of HLA-DR and CD25 on CD4+ lymphocytes was greater in cultures activated in the presence of FcR-. CD8+ lymphocytes were more efficiently activated (expression of HLA-DR) when FcR+ monocytes were added to culture. In the presence of FcR+ monocytes an increased expression of CD45RA antigen on CD4+ cells was also observed. These data support our previous functional studies which showed that "suppressor" T cells of CD8+ phenotype are activated in the presence of FcR+ monocytes.
本研究的目的是分析在存在FcR+或FcR-单核细胞的情况下,由丝裂原(PWM)和抗原(PPD)激活的T细胞的表型。结果发现,在不同单核细胞亚群存在的情况下,CD4+和CD8+淋巴细胞优先被激活。在FcR-存在的情况下激活的培养物中,CD4+淋巴细胞上HLA-DR和CD25的表达更高。当将FcR+单核细胞添加到培养物中时,CD8+淋巴细胞被更有效地激活(HLA-DR的表达)。在FcR+单核细胞存在的情况下,还观察到CD4+细胞上CD45RA抗原的表达增加。这些数据支持了我们之前的功能研究,该研究表明CD8+表型的“抑制性”T细胞在FcR+单核细胞存在的情况下被激活。