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韦格纳肉芽肿病中的淋巴细胞功能。

Lymphocyte functions in Wegener's granulomatosis.

作者信息

Niinaka T, Okochi T, Watanabe Y, Sakai S, Takahashi Y, Yamamura Y

出版信息

J Med. 1978;9(6):491-501.

PMID:287764
Abstract

Lymphocyte function was examined in Wegener's granulomatosis patients and the following results were obtained. 1) The T and B lymphocyte subpopulation was within the normal range. 2) Lymphocyte blast formation was examined with the use of PHA-P, Con A or TAP (tuberculin active peptide). A decrease in responsiveness against TAP was found in four out of ten patients, but no decrease was observed in responsiveness agains Con A or PHA-P. 3) Skin tests were carried out on seven patients with six different antigens. In two out of seven patients, the skin reactions were decreased against all the antigens used. In the other five patients, skin reactions were observed against only one or two of the antigens used. These results suggest that Wegener's granulomatosis may be associated with a partial deficiency in the cellular immune mechanism.

摘要

对韦格纳肉芽肿病患者的淋巴细胞功能进行了检测,结果如下:1)T和B淋巴细胞亚群在正常范围内。2)使用PHA-P、Con A或TAP(结核菌素活性肽)检测淋巴细胞的增殖。10名患者中有4名对TAP的反应性降低,但对Con A或PHA-P的反应性未观察到降低。3)对7名患者进行了6种不同抗原的皮肤试验。7名患者中有2名对所有使用的抗原的皮肤反应减弱。在其他5名患者中,仅对一两种使用的抗原观察到皮肤反应。这些结果表明,韦格纳肉芽肿病可能与细胞免疫机制的部分缺陷有关。

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