Strigård K, Olsson T, Larsson P, Holmdahl R, Höjeberg B, Klareskog L
Department of Neurology, Huddinge University Hospital, Sweden.
Scand J Immunol. 1988 Sep;28(3):325-30. doi: 10.1111/j.1365-3083.1988.tb01456.x.
The role of CD8+ T 'cytotoxic/suppressor' T cells in induced immunospecific tolerance and during recovery after actively induced disease was examined by means of elimination of CD8+ cells from Lewis rats using in vivo treatment by Ox8 monoclonal antibodies, in experimental allergic neuritis (EAN). Animals depleted of CD8+ T cells after recovery from EAN did not show any clinical signs of relapse. Other animals were pretreated with the peripheral nerve basic protein P2 and thereby rendered resistant to disease induction with a potentially neuritogenic emulsion. The elimination of CD8+ T cells did not result in EAN here either. Thus, the CD8+ T-cell population does not seem to participate in the suppression of this autoimmune disease under these experimental conditions.
通过使用Ox8单克隆抗体对Lewis大鼠进行体内治疗以消除CD8⁺细胞,在实验性变态反应性神经炎(EAN)中研究了CD8⁺“细胞毒性/抑制性”T细胞在诱导免疫特异性耐受以及主动诱导疾病后的恢复过程中的作用。从EAN恢复后耗尽CD8⁺ T细胞的动物未表现出任何复发的临床症状。其他动物用周围神经碱性蛋白P2进行预处理,从而使其对用潜在致神经炎乳剂诱导疾病具有抗性。在这里,CD8⁺ T细胞的消除也未导致EAN。因此,在这些实验条件下,CD8⁺ T细胞群体似乎不参与这种自身免疫性疾病的抑制。