Wang K M, Reichlin M
Veterans Administration Medical Center, Buffalo, NY.
Mol Immunol. 1988 Aug;25(8):795-8. doi: 10.1016/0161-5890(88)90115-0.
T-lymphocyte proliferative responses were determined with peripheral blood lymphocytes (PBL), peritoneal exudate lymphocytes (PEL) and lymph node lymphocytes (LNL) of guinea pigs immunized with horse cytochrome c (HCytc). The proliferative response of PBL activated by peptide 81-104 from animals immunized with HCytc was equal to or better than HCytc while the proliferative response activated by peptide 1-65 was small and no reactivity was seen when peptide 66-80 was tested. In contrast, the proliferative responses of PEL and LNL stimulated by peptide 1-65 approached those activated by HCytc, while peptide 81-104 was far less effective. The differences in the proliferative responses of PBL and PEL activated by peptide 81-104 and peptide 1-65 suggest that different lymphoid compartments may have T-cells directed to different T-cell epitopes displayed on the same antigen. The possible roles of different T-cell clones, antigen processing, and differential induction of suppressor cells are discussed in relation to these findings.
用马细胞色素c(HCytc)免疫豚鼠的外周血淋巴细胞(PBL)、腹腔渗出液淋巴细胞(PEL)和淋巴结淋巴细胞(LNL)来测定T淋巴细胞增殖反应。用HCytc免疫的动物来源的81 - 104肽激活的PBL增殖反应等于或优于HCytc,而1 - 65肽激活的增殖反应较小,测试66 - 80肽时未观察到反应性。相反,1 - 65肽刺激的PEL和LNL增殖反应接近HCytc激活的反应,而81 - 104肽的效果则差得多。81 - 104肽和1 - 65肽激活的PBL和PEL增殖反应的差异表明,不同的淋巴区室可能有针对同一抗原上不同T细胞表位的T细胞。结合这些发现讨论了不同T细胞克隆、抗原加工和抑制细胞差异诱导的可能作用。