Kim Y T, Deblasio T, Thorbecke G J, Weksler M E, Siskind G W
Department of Medicine, Cornell University Medical College, New York.
Immunology. 1989 Jun;67(2):191-6.
We have previously shown that that idiotype (Id) repertoire expressed by old mice is different from that of young mice after immunization with trinitrophenylated Ficoll. Older mice also produce more auto-anti-Id antibodies than do young mice. Mice surviving a normally lethal dose of radiation (800 rads) as result of partial shielding of their bone marrow slowly recover immune function, after the repopulation of their peripheral lymphoid system by bone marrow precursor cells. Aged mice subjected to such a procedure produce low auto-anti-Id responses, like those of young mice. However, transfer of splenic T cells from old donors into such mice increases the magnitude of the auto-anti-Id response. In the present studies, we show that the age-related shift in Id expression is also determined by the age of the donor T cells. Furthermore, we show in serial cell transfer studies that the peripheral T-cell population of old mice modifies the level of the auto-anti-Id response in the absence of antigen. The results thus provide evidence for the normal, in vivo, operation of an Id-anti-Id network between B and T lymphocytes.
我们之前已经表明,在用三硝基苯基化的菲可诱导免疫后,老年小鼠表达的独特型(Id)库与年轻小鼠不同。老年小鼠产生的自身抗独特型抗体也比年轻小鼠多。由于骨髓部分屏蔽而在正常致死剂量辐射(800拉德)下存活的小鼠,在骨髓前体细胞重新填充其外周淋巴系统后,免疫功能会缓慢恢复。接受这种处理的老年小鼠会产生与年轻小鼠相似的低自身抗独特型反应。然而,将老年供体的脾T细胞转移到此类小鼠中会增加自身抗独特型反应的强度。在本研究中,我们表明Id表达中与年龄相关的变化也由供体T细胞的年龄决定。此外,我们在系列细胞转移研究中表明,在没有抗原的情况下,老年小鼠的外周T细胞群体可改变自身抗独特型反应的水平。因此,这些结果为B淋巴细胞和T淋巴细胞之间Id-抗Id网络在体内的正常运作提供了证据。