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常见可变免疫缺陷中的T细胞和B细胞缺陷

T and B cell defects in common variable immunodeficiency.

作者信息

Farrant J

机构信息

Immune Deficiency Diseases Research Group, Clinical Research Centre, Harrow, UK.

出版信息

Immunol Invest. 1991 Apr;20(2):143-50. doi: 10.3109/08820139109050782.

Abstract

More than 50 patients with common variable immunodeficiency have been classified into 5 groups representing different blocks in B cell function. To do this, B cells were assessed in vitro by secretion of IgM or IgG in response to anti-IgM and IL-2 or to EBV alone. Some clinical features and the patients' sex ratio correlated with this B cell classification. In vitro attempts were made to identify and overcome these blocks using physiological ligands (e.g. cytokines), and agents that induce transcription (e.g. retinoic acid). The patient group with the most severely affected B cells also contained some patients whose T cells showed depressed DNA synthesis in response to mitogens. In vitro data indicate that the abnormality may be in the T cell itself rather than in monocytes failing to provide essential cytokines (e.g. IL-6). In 3 patients, splenic B cells were able to secrete IgM more effectively than circulating B cells, but still they produced no IgG.

摘要

50多名常见可变免疫缺陷患者已被分为5组,代表B细胞功能的不同障碍。为此,通过体外检测B细胞对抗IgM和白细胞介素-2或单独对EB病毒的反应中IgM或IgG的分泌情况来进行评估。一些临床特征和患者的性别比例与这种B细胞分类相关。体外尝试使用生理配体(如细胞因子)和诱导转录的试剂(如视黄酸)来识别和克服这些障碍。B细胞受影响最严重的患者组中也有一些患者,其T细胞对有丝分裂原的反应显示DNA合成受抑制。体外数据表明,异常可能存在于T细胞本身,而非单核细胞未能提供必需的细胞因子(如白细胞介素-6)。在3名患者中,脾脏B细胞比循环B细胞更有效地分泌IgM,但仍不产生IgG。

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