Williams B R, Read S E, Gelfand E W
Clin Exp Immunol. 1984 Apr;56(1):34-8.
Interferon (IFN) treatment of peripheral blood mononuclear cells from seven children with severe combined immunodeficiency (SCID) failed, with one exception, to induce the IFN-dependent enzyme, 2-5A synthetase or enhance natural killer cell activity. In one patient this hyporeactivity was demonstrated in both T cell enriched and T cell depleted lymphocyte preparations. These results may reflect the absence of an IFN reactive lymphocyte subpopulation or of the IFN receptor. This defect in SCID patients may be partly responsible for their increased susceptibility to viral infections and may contribute to the regulatory imbalances in T lymphocyte subpopulations.
用干扰素(IFN)治疗7名重症联合免疫缺陷病(SCID)患儿的外周血单个核细胞,除1例例外,均未能诱导出IFN依赖性酶2-5A合成酶,也未能增强自然杀伤细胞活性。在1例患者中,这种低反应性在富含T细胞和去除T细胞的淋巴细胞制剂中均得到证实。这些结果可能反映出缺乏IFN反应性淋巴细胞亚群或IFN受体。SCID患者的这一缺陷可能部分导致了他们对病毒感染易感性增加,并可能导致T淋巴细胞亚群的调节失衡。