Effros R B, Walford R L
Cell Immunol. 1984 Oct 15;88(2):531-9. doi: 10.1016/0008-8749(84)90184-9.
We have utilized limiting dilution analysis (LDA)2 to compare the intrinsic precursor cytotoxic T lymphocyte (pCTL) frequency for influenza-plus-self in young and old C57BL/6 mice. Under conditions of excess interleukin 2 (IL-2) and antigen presenting cells (APC) derived from spleens of mice matched in age to those being tested, we found more than a twofold difference in pCTL frequency between young and old animals. However, there was no difference in pCTL frequency between the two age groups if antigen was presented to the old responder cells on spleen cells derived from young mice. The apparent decrease in pCTL frequency in old mice by standard LDA may in fact be due to a defect in the antigen processing and/or presentation mechanism of old spleen cells. We conclude that the age-associated defective CTL activity previously reported by us and by others may be due at least in part to a defect in the antigen presentation mechanism of aging mice.
我们运用有限稀释分析(LDA)2 来比较年轻和年老的 C57BL/6 小鼠中流感病毒加自身抗原的内在前体细胞毒性 T 淋巴细胞(pCTL)频率。在过量白细胞介素 2(IL-2)以及来自与受试小鼠年龄匹配的小鼠脾脏的抗原呈递细胞(APC)的条件下,我们发现年轻和年老动物之间的 pCTL 频率存在两倍多的差异。然而,如果用来自年轻小鼠的脾细胞向年老的应答细胞呈递抗原,两个年龄组之间的 pCTL 频率没有差异。标准 LDA 显示年老小鼠中 pCTL 频率明显降低,实际上可能是由于年老脾细胞的抗原加工和/或呈递机制存在缺陷。我们得出结论,我们和其他人之前报道的与年龄相关的 CTL 活性缺陷可能至少部分归因于衰老小鼠抗原呈递机制的缺陷。