Prud'homme G J, Fuks A, Colle E, Guttmann R D
Diabetes. 1984 Aug;33(8):801-3. doi: 10.2337/diab.33.8.801.
T-lymphocyte lines specific for islet cell antigens were isolated from the spleen and pancreas of newly diabetic BB rats or from the related strain BBUF. These cell lines were grown in continuous culture with interleukin-2 (IL-2) containing medium for greater than 60 days. Such T-lymphocytes responded by proliferation and IL-2 secretion in the combined presence of islet cell antigens and major histocompatibility (MHC)-matched antigen-presenting cells. By fluorescence-activated cell sorter (FACS) analysis the cells were W3/13+, W3/25+, and OX8-. Thus, both functionally and by cell-surface-marker analysis they appear to be of the T-helper phenotype. The long-term growth and study of anti-islet T-lymphocyte lines will permit a detailed analysis of the role of T-lymphocytes in the pathogenesis of IDDM.
从新患糖尿病的BB大鼠的脾脏和胰腺或相关品系BBUF中分离出对胰岛细胞抗原有特异性的T淋巴细胞系。这些细胞系在含有白细胞介素-2(IL-2)的培养基中连续培养超过60天。此类T淋巴细胞在胰岛细胞抗原和主要组织相容性(MHC)匹配的抗原呈递细胞共同存在的情况下,通过增殖和分泌IL-2作出反应。通过荧光激活细胞分选仪(FACS)分析,这些细胞为W3/13+、W3/25+和OX8-。因此,从功能和细胞表面标志物分析来看,它们似乎都具有T辅助细胞表型。对抗胰岛T淋巴细胞系的长期培养和研究将有助于详细分析T淋巴细胞在胰岛素依赖型糖尿病发病机制中的作用。