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环孢素对表皮细胞的作用。I. 环孢素在体外抑制表皮朗格汉斯细胞的辅助细胞功能。

The effect of cyclosporine on epidermal cells. I. Cyclosporine inhibits accessory cell functions of epidermal Langerhans cells in vitro.

作者信息

Furue M, Katz S I

机构信息

Dermatology Branch, National Cancer Institute, Bethesda, MD 20892.

出版信息

J Immunol. 1988 Jun 15;140(12):4139-43.

PMID:3259608
Abstract

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.

摘要

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。

相似文献

1
The effect of cyclosporine on epidermal cells. I. Cyclosporine inhibits accessory cell functions of epidermal Langerhans cells in vitro.环孢素对表皮细胞的作用。I. 环孢素在体外抑制表皮朗格汉斯细胞的辅助细胞功能。
J Immunol. 1988 Jun 15;140(12):4139-43.
2
Cyclosporine A inhibits accessory cell and antigen-presenting cell functions of epidermal Langerhans cells.环孢素A抑制表皮朗格汉斯细胞的辅助细胞及抗原呈递细胞功能。
Transplant Proc. 1988 Apr;20(2 Suppl 2):87-91.
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Inhibition of Langerhans cell antigen-presenting function by IL-10. A role for IL-10 in induction of tolerance.白细胞介素-10对朗格汉斯细胞抗原呈递功能的抑制作用。白细胞介素-10在诱导耐受性中的作用。
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Epidermal cells as accessory cells in the generation of allo-reactive and hapten-specific cytotoxic T lymphocyte (CTL) responses.表皮细胞作为同种异体反应性和半抗原特异性细胞毒性T淋巴细胞(CTL)反应产生中的辅助细胞。
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Differential sensitivity of freshly isolated and cultured murine Langerhans cells to ultraviolet B radiation and chemical fixation.新鲜分离和培养的小鼠朗格汉斯细胞对紫外线B辐射和化学固定的差异敏感性。
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Dissection of human Langerhans cells' allostimulatory function: the need for an activation step for full development of accessory function.人类朗格汉斯细胞共刺激功能的剖析:辅助功能充分发挥需要激活步骤。
Eur J Immunol. 1993 Feb;23(2):376-82. doi: 10.1002/eji.1830230212.
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In vivo treatment with anti-I-A antibodies: differential effects on Ia antigens and antigen-presenting cell function of spleen cells and epidermal Langerhans cells.用抗I-A抗体进行体内治疗:对脾细胞和表皮朗格汉斯细胞的Ia抗原及抗原呈递细胞功能的不同影响
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Enhanced antigen-presenting capacity of cultured Langerhans' cells is associated with markedly increased expression of Ia antigen.培养的朗格汉斯细胞增强的抗原呈递能力与Ia抗原表达的显著增加相关。
J Immunol. 1987 Oct 15;139(8):2551-5.
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In vitro evidence that Langerhans cells can adopt two functionally distinct forms capable of antigen presentation to T lymphocytes.体外实验证据表明,朗格汉斯细胞可呈现两种功能不同的形式,能够将抗原呈递给T淋巴细胞。
J Immunol. 1989 Dec 15;143(12):3925-33.

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Lack of demonstrable effect of cyclosporin A on human epidermal Langerhans cell function.环孢菌素A对人表皮朗格汉斯细胞功能无明显作用。
Arch Dermatol Res. 1991;283(3):198-202. doi: 10.1007/BF00372062.