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软骨毛发发育不全的体外T细胞和B细胞反应性

In vitro T- and B-cell reactivity in cartilage hair hypoplasia.

作者信息

Ranki A, Perheentupa J, Andersson L C, Häyry P

出版信息

Clin Exp Immunol. 1978 May;32(2):352-60.

Abstract

We have investigated and parameters of cellular immunity in ten patients with cartilage hair hypoplasia, CHH. All ten patients displayed a negative skin test to 1 Tu tuberculin, eight patients did not respond to 10 Tu and seven not even to 100 Tu. Six patients were skin test-negative to 1:50 oidiomycin; and three were negative to even 1:10 oidiomycin. The absolute and relative distribution of blood T lymphocytes was normal. The absolute distribution of blood B lymphocytes was slightly decreased in three patients, but all patients had normal levels of IgM, IgG and IgA. Major changes were observed in the proliferative responses of blood leucocytes to mitogens and antigens. Five patients responded suboptimally to phytohaemagglutinin (PHA), two to concanavalin A, three patients were hyporesponsive to strain Cowan I bacteria, six to tuberculin (PPD) and six to oidiomycin. The responses of two patients were entirely normal. Except for three patients responding suboptimally to PPD or oidiomycin only, the reduced responses were all confined to the five patients responding suboptimally to PHA. The suboptimally responding patients displayed normal dose–response profiles to both PHA and Con A. The hyporeactivity was a persistent phenomenon, as the pattern of PHA and Con A reactivity was essentially similar when the same patients had been tested to the same mitogens 5 years earlier. Except for the skin test hyporeactivity, none of these patients displayed any detectable clinical handicap, suggesting that the Finnish variant of the syndrome is dissimilar from the Amish variant, where the deficiency to mitogens and antigens is related to susceptibility to severe and often fatal infections, especially to varicella and vaccinia.

摘要

我们对10例软骨毛发发育不全(CHH)患者的细胞免疫参数进行了研究。所有10例患者对1结核菌素单位(Tu)结核菌素皮肤试验均呈阴性,8例患者对10 Tu无反应,7例甚至对100 Tu也无反应。6例患者对1:50放线菌酮皮肤试验呈阴性;3例对甚至1:10放线菌酮也呈阴性。血液T淋巴细胞的绝对和相对分布正常。3例患者血液B淋巴细胞的绝对分布略有下降,但所有患者的IgM、IgG和IgA水平均正常。观察到血液白细胞对有丝分裂原和抗原的增殖反应有重大变化。5例患者对植物血凝素(PHA)反应欠佳,2例对刀豆球蛋白A反应欠佳,3例患者对考恩I菌菌株反应低下,6例对结核菌素(PPD)反应低下,6例对放线菌酮反应低下。2例患者的反应完全正常。除3例仅对PPD或放线菌酮反应欠佳的患者外,反应降低均局限于对PHA反应欠佳的5例患者。反应欠佳的患者对PHA和Con A均表现出正常的剂量反应曲线。低反应性是一种持续现象,因为当同一患者在5年前接受相同有丝分裂原检测时,PHA和Con A反应模式基本相似。除皮肤试验低反应性外,这些患者均未表现出任何可检测到的临床缺陷,这表明该综合征的芬兰变种与阿米什变种不同,在阿米什变种中,对有丝分裂原和抗原的缺陷与对严重且往往致命感染的易感性有关,尤其是对水痘和牛痘。

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