Thomas W R, Watkins M C, Asherson G L
J Immunol. 1979 Jun;122(6):2300-3.
Previous reports have shown that picryl sulfonic acid (PSA) induces suppressor T cells that inhibit the effector phase of contact sensitivity, whereeas its DNP counterpart, dinitrobenzenesulfonate (DNBS) induces cells that inhibit the afferent phase of sensitization. Accordingly, cells from mice injected with DNBS, but not PSA, could be shown to inhibit the DNA synthesis in the lymph nodes that occurs during sensitization. It is now shown that PSA does induce T cells that suppress DNA synthesis but this can only be detected with enriched T cells or by using a regimen of PSA injection different frm previously used to induce suppressor cells for the effector phase. The T cells did not affect responses to oxazolone or dinitrofluorobenzene (DNFB) and were distinguishable from suppressors of the efferent phase in that they could be produced in adult thymectomized but not cyclophosphamide-treated mice. T cells from mice injected with DNBS that inhibited DNA synthesis to DNFB had the same properties.
先前的报告表明,苦味酸磺酸(PSA)可诱导抑制性T细胞,这些细胞会抑制接触敏感性的效应阶段,而其对应的二硝基苯磺酸(DNBS)则诱导抑制致敏传入阶段的细胞。因此,注射了DNBS而非PSA的小鼠的细胞可被证明能抑制致敏过程中淋巴结内发生的DNA合成。现在研究表明,PSA确实能诱导抑制DNA合成的T细胞,但这只能在富集的T细胞中检测到,或者通过采用与先前用于诱导效应阶段抑制细胞的PSA注射方案不同的方案来检测。这些T细胞不影响对恶唑酮或二硝基氟苯(DNFB)的反应,并且与传出阶段的抑制细胞不同,因为它们可以在成年胸腺切除但未用环磷酰胺处理的小鼠中产生。注射了DNBS且能抑制对DNFB的DNA合成的小鼠的T细胞具有相同的特性。