Griswold D E, Alessi S, Badger A M, Poste G, Hanna N
J Immunol. 1984 Jun;132(6):3054-7.
The effect of histamine type 2 (H2) receptor antagonists, cimetidine and ranitidine, on the induction and expression of hapten-specific suppressor T cells was studied. The activity of DNBSO3 -induced suppressor cells was evaluated after adoptive transfer to naive syngeneic recipients. Treatment with cimetidine or ranitidine markedly inhibited suppressor T cell activity in a dose-related manner and enhanced the contact sensitivity response to DNFB. Both H2 antagonists were effective in inhibiting the expression and, to a lesser extent, the induction of suppressor T cells. In contrast, norburimamide , a non-H2 antagonist structurally related to cimetidine, was inactive. The relevance of these findings to the clinical observation of cimetidine-induced reversal of acquired tolerance to dinitrochlorobenzene in anergic patients is discussed.
研究了组胺2型(H2)受体拮抗剂西咪替丁和雷尼替丁对半抗原特异性抑制性T细胞诱导和表达的影响。将二硝基苯磺酸盐(DNBSO3)诱导的抑制性细胞过继转移至同基因未致敏受体后,评估其活性。西咪替丁或雷尼替丁治疗以剂量相关方式显著抑制抑制性T细胞活性,并增强对二硝基氟苯(DNFB)的接触敏感性反应。两种H2拮抗剂均能有效抑制抑制性T细胞的表达,且在较小程度上抑制其诱导。相比之下,与西咪替丁结构相关的非H2拮抗剂诺布酰胺则无活性。讨论了这些发现与临床观察到的西咪替丁诱导无反应性患者对二硝基氯苯获得性耐受性逆转之间的相关性。