Study of the relation between the clinical pulmonary condition of children with cystic fibrosis and the lymphoblastic response to the antigen Pseudomonas aeruginosa.

Annales d'immunologie Pub Date : 1982-11-01
R Van Geffel, E Hubert, M Josse
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Abstract

This study was performed on four sibling pairs affected by cystic fibrosis. Of each sibling pair, one was more affected than the other. The results show that the lymphoblastic response to the antigen Pseudomonas aeruginosa of the most affected patient was strongly reduced in comparison to the response of the less affected one. The plasma from the most affected patient contains an inhibitory factor which reduces the lymphoblastic response of the less affected one. On the other hand, plasma from the less affected patient improves the lymphoblastic response of the most affected one (although not significantly). One notes a better lymphoblastic response when the most affected patient's lymphocytes are put in the presence of the less affected one's antigens and plasma. These findings suggest a phenomenon of lymphocyte tolerance in the most affected patient towards P. aeruginosa.

囊性纤维化患儿临床肺部状况与淋巴细胞对抗原铜绿假单胞菌反应关系的研究。
这项研究是在四对患有囊性纤维化的兄弟姐妹中进行的。在每一对兄弟姐妹中,一个比另一个受影响更大。结果表明,与感染较轻的患者相比,感染最严重的患者淋巴细胞对抗原铜绿假单胞菌的反应明显降低。受影响最严重的患者的血浆中含有一种抑制因子,可减少受影响较轻的患者的淋巴细胞反应。另一方面,受影响较小的患者的血浆改善了受影响最严重的患者的淋巴细胞反应(尽管不明显)。人们注意到,当受影响最严重的病人的淋巴细胞与受影响较轻的病人的抗原和血浆放在一起时,淋巴细胞的反应会更好。这些发现表明,在最严重的患者淋巴细胞耐受铜绿假单胞菌的现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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