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在一名患有蕈样肉芽肿综合征且表现出大量高免疫球蛋白血症E的患者中,存在IgE类特异性辅助性T细胞恶性增殖的证据。

Evidence for a malignant proliferation of IgE-class specific helper T cells in a patient with Sézary syndrome exhibiting massive hyperimmunoglobulinemia E.

作者信息

Mitsuya H, Sato M, Hirano T, Fujimoto K, Kawano F, Kishimoto S

出版信息

Clin Immunol Immunopathol. 1983 Feb;26(2):171-83. doi: 10.1016/0090-1229(83)90135-6.

Abstract

Peripheral blood mononuclear cells (PBM) from a patient with Sézary syndrome exhibiting massive hyperimmunoglobulinemia E were examined in vitro. The patient's PBM and B cells (Bp) but not normal individuals' PBM and B cells (Bn) produced spontaneously large amounts of IgE. The addition of pokeweed mitogen (PWM) did not affect IgE production by both the patient's and normal individuals' PBM. The IgE production by PWM-stimulated Bp was depressed when cocultured with normal T cells but not depressed with the patient's T cells (Tp). When Tp were cocultured with Bn, significantly larger than expected quantities of IgE were produced. Ig assay of the same supernates showed that Tp had significantly less helper activities for IgG, IgA, and IgM production. Almost all Tp possessed the Leu3a and Leu3b antigens which are expressed on the helper/inducer T cell subset. These results indicate that the neoplastic cells in this patient originated from a subset of T cells programmed not for IgG, IgA, and IgM, but for IgE synthesis.

摘要

对一名患有蕈样肉芽肿综合征且表现出大量高免疫球蛋白E血症的患者的外周血单个核细胞(PBM)进行了体外研究。该患者的PBM和B细胞(Bp)能自发产生大量IgE,而正常个体的PBM和B细胞(Bn)则不能。加入商陆有丝分裂原(PWM)后,患者和正常个体的PBM产生IgE的情况均未受影响。PWM刺激的Bp与正常T细胞共培养时,其IgE产生受到抑制,但与患者的T细胞(Tp)共培养时则未受抑制。当Tp与Bn共培养时,产生的IgE量显著高于预期。对相同上清液进行的Ig检测显示,Tp对IgG、IgA和IgM产生的辅助活性显著较低。几乎所有Tp都具有在辅助/诱导性T细胞亚群上表达的Leu3a和Leu3b抗原。这些结果表明,该患者的肿瘤细胞起源于一个不是针对IgG、IgA和IgM编程,而是针对IgE合成编程的T细胞亚群。

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