Tschudy D P, Hess R A, Frykholm B C, Blaese R M
J Lab Clin Med. 1982 Apr;99(4):526-32.
SA, an inhibitor of ALA dehydrase, the second enzyme of the heme biosynthetic pathway, has been shown to exert immunosuppressive activity in several systems. When the Walker 256 tumor was grown subcutaneously in outbred Sprague-Dawley rats, SA prevented rejection of the tumor by the host. Human peripheral blood lymphocyte transformation in response to mitogens and antigens in vitro was markedly impaired by addition of SA to the medium. Addition of hematin to the medium did not reverse the SA-mediated inhibition of transformation. This finding suggests that SA may exert immunosuppressive activity by a mechanism separate from inhibition of heme biosynthesis. Continuous administration of SA to Fisher 344 rats profoundly suppressed hemolytic antibody production after immunization with SRBC. Administration of large doses (equivalent to the highest dose of Sa given to tumor-bearing animals) for a month produced a 20% decrease of hemoglobin concentration, a 12% decrease in hematocrit, and no significant effect on leukocyte or erythrocyte concentration. There were no significant changes in tissue histology, including marrow cellularity.
SA是血红素生物合成途径中第二种酶——δ-氨基-γ-酮戊酸脱水酶的抑制剂,已证实在多个系统中具有免疫抑制活性。当Walker 256肿瘤在远交系Sprague-Dawley大鼠皮下生长时,SA可阻止宿主对肿瘤的排斥。在体外培养基中添加SA可显著损害人外周血淋巴细胞对有丝分裂原和抗原的转化反应。向培养基中添加血红素并不能逆转SA介导的转化抑制作用。这一发现表明,SA可能通过一种与抑制血红素生物合成无关的机制发挥免疫抑制活性。持续给Fisher 344大鼠施用SA可显著抑制用绵羊红细胞免疫后的溶血抗体产生。连续一个月给予大剂量(相当于给予荷瘤动物的最高剂量的SA)可使血红蛋白浓度降低20%,血细胞比容降低12%,对白细胞或红细胞浓度无显著影响。包括骨髓细胞在内的组织组织学无显著变化。