Victorino R M, Ryan P, Hughes G R, Hodgson H J
Clin Exp Immunol. 1982 Apr;48(1):121-8.
Lymphocyte responsiveness to mitogens (phytohaemagglutinin (PHA), concanavalin A (Con A), and pokeweed mitogen (PWM)), T-cell subsets (T mu and T gamma) and short-lived suppressor cell activity were investigated in the peripheral blood of seven patients with Behçet's syndrome and compared to normal individuals and patients with systemic lupus erythematosus (SLE). Amongst patients with Behçet's syndrome, responses to mitogens PHA and Con A were normal or slightly reduced; numbers of circulating T gamma cells were unaltered whereas T mu cells were reduced (P less than 0 . 05) compared with normal individuals. This was in contrast to SLE where a marked reduction in responses to PHA and Con A was found with reduced T gamma cell but normal T mu cell numbers. Although the mean suppressor cell activity in the Behçet's group was significantly reduced, all patients had values within the normal range, in contrast with SLE where the reduction was much more marked and most patients had values below the normal range. In conclusion, the pattern of alteration in T mu and T gamma cells in Behçet's syndrome is distinct from that in SLE, and the reduction of short-lived suppressor cell activity is only mild in Behçet's syndrome but marked in SLE.
研究了7例白塞氏综合征患者外周血中淋巴细胞对丝裂原(植物血凝素(PHA)、刀豆球蛋白A(Con A)和商陆丝裂原(PWM))的反应性、T细胞亚群(Tμ和Tγ)以及短期抑制细胞活性,并与正常个体和系统性红斑狼疮(SLE)患者进行了比较。在白塞氏综合征患者中,对丝裂原PHA和Con A的反应正常或略有降低;循环Tγ细胞数量未改变,而与正常个体相比,Tμ细胞减少(P<0.05)。这与SLE形成对比,在SLE中发现对PHA和Con A的反应明显降低,Tγ细胞减少但Tμ细胞数量正常。虽然白塞氏组的平均抑制细胞活性显著降低,但所有患者的值均在正常范围内,而SLE的降低更为明显,大多数患者的值低于正常范围。总之,白塞氏综合征中Tμ和Tγ细胞的改变模式与SLE不同,白塞氏综合征中短期抑制细胞活性的降低仅为轻度,而在SLE中则很明显。