Furue M, Katz S I
Dermatology Branch, National Cancer Institute, Bethesda, MD 20892.
J Immunol. 1988 Jun 15;140(12):4139-43.
Although the precise mechanism of action of cyclosporine (CS) is unknown, there is substantial evidence that CS preferentially acts on T cells by impairing lymphokine production. Recent studies have demonstrated that CS may also inhibit the functions of accessory cells and APC. Since topically applied CS inhibits contact sensitivity and epidermal Langerhans cells (LC) are very effective accessory cells and APC, we determined whether CS directly affects their accessory cell functions. Murine LC were pulsed with solvent control or with various doses of CS (up to 10 micrograms/ml) and then Con A-induced T cell proliferation was assayed. CS pulsing of LC caused, when compared with solvent control-pulsed LC, a dose-dependent decrease in T cell stimulation (up to 93%). LC fixed with paraformaldehyde after 2-h CS pulsing showed a similar degree of decreased accessory cell function, indicating that the immunosuppressive action is established by 2 h. The inhibitory capacity of CS pulsing on LC is not likely to be related to diminished IL-1 production, enhanced PG biosynthesis, or decreased surface Ia Ag intensity. The possibility of carryover of CS into the culture supernatants was ruled out by adding CS-pulsed LC or their supernatants to other T cell proliferative assays. Thus, these studies indicate that CS directly inhibits accessory cell functions of LC.
虽然环孢素(CS)的确切作用机制尚不清楚,但有大量证据表明,CS通过损害淋巴因子的产生而优先作用于T细胞。最近的研究表明,CS也可能抑制辅助细胞和抗原呈递细胞(APC)的功能。由于局部应用的CS可抑制接触敏感性,且表皮朗格汉斯细胞(LC)是非常有效的辅助细胞和APC,因此我们确定CS是否直接影响它们的辅助细胞功能。用溶剂对照或不同剂量的CS(高达10微克/毫升)处理小鼠LC,然后检测伴刀豆球蛋白A诱导的T细胞增殖。与用溶剂对照处理的LC相比,用CS处理的LC导致T细胞刺激呈剂量依赖性降低(高达93%)。用CS处理2小时后用多聚甲醛固定的LC显示出相似程度的辅助细胞功能降低,表明免疫抑制作用在2小时内就已确立。CS处理对LC的抑制能力不太可能与白细胞介素-1产生减少、前列腺素生物合成增强或表面Ia抗原强度降低有关。通过将用CS处理的LC或其培养上清液加入其他T细胞增殖试验中,排除了CS残留于培养上清液中的可能性。因此,这些研究表明,CS直接抑制LC的辅助细胞功能。