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使用利妥昔单抗进行B细胞清除疗法可逆转特发性血小板减少性紫癜患者T细胞亚群的异常。

Response to B-cell depleting therapy with rituximab reverts the abnormalities of T-cell subsets in patients with idiopathic thrombocytopenic purpura.

作者信息

Stasi Roberto, Del Poeta Giovanni, Stipa Elisa, Evangelista Maria Laura, Trawinska Margherita M, Cooper Nichola, Amadori Sergio

机构信息

Department of Medical Sciences, Ospedale Regina Apostolorum, Albano Laziale, Italy.

出版信息

Blood. 2007 Oct 15;110(8):2924-30. doi: 10.1182/blood-2007-02-068999. Epub 2007 Jun 4.

Abstract

Rituximab, an anti-CD20 monoclonal antibody, has been used to treat autoimmune disorders such as idiopathic thrombocytopenic purpura (ITP). However, its mechanisms of action as well as the effects on cellular immunity remain poorly defined. We investigated the changes of different peripheral blood T-cell subsets, the apoptosis profile, as well as the changes of T-cell receptor (TCR) beta-variable (VB) region gene usage of CD4+ and CD8+ T-cell subpopulations following rituximab therapy. The study involved 30 patients with chronic ITP who received rituximab, of whom 14 achieved a durable (> 6 months) response. Compared with the control group, pretreatment abnormalities of T cells in ITP patients included an increase of the Th1/Th2 ratio and of the Tc1/Tc2 ratios (P < .001), increased expression of Fas ligand on Th1 and Th2 cells (P < .001), increased expression of Bcl-2 mRNA (P = .003) and decreased expression of bax mRNA (P = .025) in Th cells, and expansion of oligoclonal T cells with no preferential use of any TCR VB subfamily. These abnormalities were reverted in responders at 3 and 6 months after treatment, whereas they remained unchanged in nonresponders. Our findings indicate that in patients with ITP, response to B-cell depletion induced by rituximab is associated with significant changes of the T-cell compartment.

摘要

利妥昔单抗是一种抗CD20单克隆抗体,已被用于治疗自身免疫性疾病,如特发性血小板减少性紫癜(ITP)。然而,其作用机制以及对细胞免疫的影响仍不清楚。我们研究了利妥昔单抗治疗后不同外周血T细胞亚群的变化、细胞凋亡情况以及CD4+和CD8+ T细胞亚群的T细胞受体(TCR)β可变区(VB)基因使用情况的变化。该研究纳入了30例接受利妥昔单抗治疗的慢性ITP患者,其中14例获得了持久(>6个月)缓解。与对照组相比,ITP患者治疗前T细胞异常包括Th1/Th2比值和Tc1/Tc2比值升高(P<.001),Th1和Th2细胞上Fas配体表达增加(P<.001),Th细胞中Bcl-2 mRNA表达增加(P=.003)和bax mRNA表达降低(P=.025),以及寡克隆T细胞扩增,且无任何TCR VB亚家族的优先使用。这些异常在治疗后3个月和6个月时在缓解者中恢复正常,而在无反应者中保持不变。我们的研究结果表明,在ITP患者中,对利妥昔单抗诱导的B细胞耗竭的反应与T细胞区室的显著变化有关。

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