Killen J A, Swanborg R H
J Neuroimmunol. 1982 Oct;3(2):159-66. doi: 10.1016/0165-5728(82)90049-2.
Suppressor cells that regulate experimental allergic encephalomyelitis (EAE) are present in lymph nodes of Lewis rats that have recovered from the disease, as demonstrated by adoptive transfer of suppression for at least 108 days following challenge of donor rats with myelin basic protein (BP) in complete Freund's adjuvant (CFA). These suppressor lymph node cells (LNC) inhibit the occurrence of active, but not passive EAE in recipients, suggesting that they function early in the inductive phase of the response to BP. The suppressor cells are nylon-adherent, and suppression can be partially abrogated by depletion of B cells with anti-immunoglobulin (ig) and complement (C). Serum from recovered donors has, at best, only a modest suppressive effect when transfused into syngeneic recipients. These findings suggest that the B cells do not mediate suppression on EAE via production of blocking antibody, but may function directly, perhaps by triggering T cells to become suppressor cells.
调节实验性变应性脑脊髓炎(EAE)的抑制细胞存在于已从该疾病中恢复的Lewis大鼠的淋巴结中,这一点通过在完全弗氏佐剂(CFA)中用髓磷脂碱性蛋白(BP)攻击供体大鼠后进行至少108天的抑制性过继转移得以证明。这些抑制性淋巴结细胞(LNC)抑制受体中主动型而非被动型EAE的发生,这表明它们在对BP的反应诱导期早期发挥作用。抑制细胞能黏附于尼龙,用抗免疫球蛋白(Ig)和补体(C)清除B细胞可部分消除抑制作用。当将康复供体的血清输注到同基因受体中时,其至多只有适度的抑制作用。这些发现表明,B细胞并非通过产生封闭抗体来介导对EAE的抑制作用,而是可能直接发挥作用,或许是通过触发T细胞成为抑制细胞。