Godfrey H P
Immunology. 1976 May;30(5):685-94.
Hapten-specific sensitivity of guinea-pigs sensitized to dinitrophenyl (DNP) contactants and to DNP-protein conjugates was investigated by skin test and by antigen-induced elaboration of migration inhibition (MIF) and macrophage agglutination factors (MAF) From lymph node cells. The delayed contact reaction was highly specific for low doses of contactant and markedly less so for conjugates; lymph node cells elaborted both lymphokines in response to brief exposures to dinitrofluorobenzene (DNFB) or prolonged exposures to DNP conjugates. Elicitation of MAF by DNFB or DNP conjugate was inhibited in the presence of DNP glycine; the activity of MAF induced by DNP conjugate (but not that induced by DNFB) was inhibited in the presence of DNP-glycine as well. These results suggest that contact sensitivity to DNP conjugates reflect two different types of hapten-specific cellular sensitivity mediated by populations of cells with different antigen receptors and possibly, functionally different lymphokines.
通过皮肤试验以及抗原诱导淋巴结细胞产生迁移抑制因子(MIF)和巨噬细胞凝集因子(MAF),研究了对二硝基苯基(DNP)接触剂和DNP-蛋白质偶联物致敏的豚鼠的半抗原特异性敏感性。迟发性接触反应对低剂量接触剂具有高度特异性,而对偶联物的特异性则明显较低;淋巴结细胞在短暂暴露于二硝基氟苯(DNFB)或长期暴露于DNP偶联物后会产生这两种淋巴因子。在存在DNP甘氨酸的情况下,DNFB或DNP偶联物诱导的MAF产生受到抑制;在存在DNP-甘氨酸的情况下,DNP偶联物诱导的MAF活性(但不是DNFB诱导的MAF活性)也受到抑制。这些结果表明,对DNP偶联物的接触敏感性反映了由具有不同抗原受体的细胞群体介导的两种不同类型的半抗原特异性细胞敏感性,并且可能是功能不同的淋巴因子。