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用8-巯基鸟苷恢复xid B细胞对TNP-菲可的体外反应性。

Restoration of in vitro responsiveness of xid B cells to TNP-Ficoll by 8-mercaptoguanosine.

作者信息

Ahmad A, Mond J J

出版信息

J Immunol. 1986 Feb 15;136(4):1223-6.

PMID:3511143
Abstract

8-Mercaptoguanosine (8sGuo) has been reported to enhance responses of normal mice to the type 2 antigen trinitrophenol (TNP)-Ficoll. In this report, we demonstrate that this immune adjuvant restores the immune responsiveness of B cells from mice with the x-linked immune defect (xid), which are nonresponsive to the type 2 antigen TNP-Ficoll. The data demonstrate that TNP-Ficoll, which by itself cannot stimulate anti-TNP responses in CBA/N mice, is able to initiate the initial steps of cell activation in xid B cells and render them sensitive to the subsequent differentiative effects of 8sGuo. We propose that the unresponsiveness of xid B cells to type 2 antigens reflects not the inability of these antigens to stimulate xid B cells from G0 to G1, but rather the inability of these antigen-activated cells to respond to a second signal to which these immune defective B cells are poorly responsive and can be substituted for by 8sGuo.

摘要

据报道,8-巯基鸟苷(8sGuo)可增强正常小鼠对2型抗原三硝基苯酚(TNP)-菲可的反应。在本报告中,我们证明这种免疫佐剂可恢复具有X连锁免疫缺陷(xid)的小鼠B细胞的免疫反应性,这些小鼠对2型抗原TNP-菲可不产生反应。数据表明,TNP-菲可本身不能刺激CBA/N小鼠产生抗TNP反应,但能够启动xid B细胞的细胞活化初始步骤,并使其对8sGuo随后的分化作用敏感。我们提出,xid B细胞对2型抗原无反应并非反映这些抗原无法将xid B细胞从G0期刺激至G1期,而是反映这些抗原激活的细胞无法对第二种信号作出反应,而这些免疫缺陷B细胞对该信号反应较差,8sGuo可替代该信号。

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