Stites D P, Brecher G, Schmidt L, Berger F M
Immunopharmacology. 1979 Dec;2(1):39-49. doi: 10.1016/0162-3109(79)90019-5.
The immunosuppressive action of chlorphenesin was investigated in a wide variety of in vitro assays for cellular immunity in humans and mice. Chlorphenesin, at doses of 20-50 micrograms/ml, inhibited mitogenic responses of both mouse and human B and T cells. These doses did not kill cells exposed to the drug for 72 hr. Mixed lymphocyte reactions in inbred strains of mice and in unrelated humans were also inhibited at concentrations of about 50 micrograms/ml. However, the generation of cytotoxic T cells in cell-mediated lympholysis assays was not inhibited to the same degree as proliferation in mixed lymphocyte reaction and the cytotoxic potential of presensitized mouse T cells for allogeneic targets was totally unaffected. These studies suggest that chlorphenesin may have a broad spectrum of suppressive effects both on T and B cells and that the predominant inhibition of proliferative responses in these cells may reduce the expansion of clones of immunocompetent cells in vivo.
在多种针对人类和小鼠细胞免疫的体外试验中,对氯苯甘醚的免疫抑制作用进行了研究。氯苯甘醚在20 - 50微克/毫升的剂量下,抑制小鼠和人类B细胞及T细胞的有丝分裂反应。这些剂量在72小时内不会杀死接触该药物的细胞。在近交系小鼠和无关人类中的混合淋巴细胞反应,在浓度约为50微克/毫升时也受到抑制。然而,在细胞介导的淋巴细胞溶解试验中,细胞毒性T细胞的生成并未像混合淋巴细胞反应中的增殖那样受到同等程度的抑制,并且预致敏小鼠T细胞对同种异体靶标的细胞毒性潜力完全未受影响。这些研究表明,氯苯甘醚可能对T细胞和B细胞都具有广泛的抑制作用,并且这些细胞中增殖反应的主要抑制可能会减少体内免疫活性细胞克隆的扩增。