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在软骨毛发发育不全中,培养受损产生细胞毒性,同时自然杀伤细胞的自发活性得以保留。

Impaired culture generated cytotoxicity with preservation of spontaneous natural killer-cell activity in cartilage-hair hypoplasia.

作者信息

Pierce G F, Brovall C, Schacter B Z, Polmar S H

出版信息

J Clin Invest. 1983 Jun;71(6):1737-43. doi: 10.1172/jci110928.

Abstract

Recent studies of cartilage-hair hypoplasia (CHH), a form of short-limbed dwarfism, have shown that all affected individuals have a cellular proliferation defect that results in a cellular immunodeficiency. However, only a minority of CHH individuals suffer from severe, life-threatening infections. For this reason, relevant immune defense mechanisms that may be responsible for maintaining intact host defenses in the majority of CHH individuals were studied. Spontaneous and allogeneic culture-induced (mixed lymphocyte response-MLR) specific and nonspecific (NK-like) cytotoxic mechanisms were analyzed and correlated with lymphocyte subpopulations present in CHH and normal individuals. Spontaneous natural-killer (NK) activity was present at or above normal levels, but culture-induced specific cytotoxicity and NK-like cytotoxicity as well as NK-like activity by T cell lines were significantly reduced in CHH individuals. The generation of radiation-resistant cytotoxicity, which normally occurs during allogeneic MLR, was markedly diminished in CHH, and was correlated with the decreased proliferation observed in CHH cultures. Preservation of spontaneous NK activity and loss of all forms of culture-induced cytotoxicity was associated with an increase in the proportion of lymphocytes bearing a thymic independent NK phenotype (OKM1+ OKT3- Fc gamma + low-affinity E+), and a significant decrease in thymic derived OKT3+ cytolytic T cell sub-populations in CHH individuals. Therefore, an intact cellular cytotoxic effector mechanism has been identified in CHH (i.e., NK activity). Natural cytotoxicity may be of importance in maintaining host resistance to viral infections despite diminished thymic-derived effector mechanisms in cartilage-hair hypoplasia.

摘要

近期对软骨毛发发育不全(CHH)——一种短肢侏儒症——的研究表明,所有受影响个体都存在细胞增殖缺陷,进而导致细胞免疫缺陷。然而,只有少数CHH个体患有严重的、危及生命的感染。因此,对可能在大多数CHH个体中维持完整宿主防御的相关免疫防御机制进行了研究。分析了自发的和同种异体培养诱导的(混合淋巴细胞反应-MLR)特异性和非特异性(NK样)细胞毒性机制,并将其与CHH个体和正常个体中存在的淋巴细胞亚群相关联。自发自然杀伤(NK)活性处于或高于正常水平,但CHH个体中培养诱导的特异性细胞毒性、NK样细胞毒性以及T细胞系的NK样活性均显著降低。在同种异体MLR期间通常会出现的抗辐射细胞毒性的产生在CHH中明显减少,并且与CHH培养物中观察到的增殖减少相关。自发NK活性的保留以及所有形式的培养诱导细胞毒性的丧失与具有胸腺非依赖性NK表型(OKM1 + OKT3 - Fcγ + 低亲和力E +)的淋巴细胞比例增加以及CHH个体中胸腺来源的OKT3 + 溶细胞性T细胞亚群显著减少有关。因此,在CHH中已鉴定出一种完整的细胞毒性效应机制(即NK活性)。尽管软骨毛发发育不全中胸腺来源的效应机制有所减弱,但天然细胞毒性可能在维持宿主对病毒感染的抵抗力方面具有重要意义。

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