在常见可变免疫缺陷患者中,记忆B细胞数量的减少与该细胞群的凋亡增加有关。一种检测全血样本细胞凋亡的新方法的发展

Fernanda Gabriela Silva-Carreras, Santiago Sobrecasas, Inmaculada Toboso de Lamo, José Luis Castañer Alabau, Ernesto Roldán Santiago
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引用次数: 0

摘要

共同性可变免疫缺陷(CVID)是一种异质性疾病,其特征是外周血(PB)记忆性B细胞计数低。虽然以前的报道将记忆性CD27+ B细胞减少归因于可能的生发中心发育缺陷,但这种缺陷的原因基本上仍然未知。另一方面,细胞凋亡的增加与多种疾病的发病机制有关,可能是解释记忆性B细胞减少的另一个因素。然而,CVID患者记忆B细胞凋亡/存活之间的负平衡仍未被证实。因此,我们想知道细胞凋亡的增加是否与CVID有关。为了验证这一概念,我们用流式细胞术研究了CVID患者和健康对照者的总B细胞和记忆B细胞,以确定自发和诱导的凋亡。用和不加抗cd95促凋亡单克隆抗体培养24小时后,Annexin-V表达量测定细胞凋亡。利用7-氨基放线菌素D (7-AAD)检测全PB中极少量的凋亡细胞,建立了一种灵敏的新方法。我们的研究结果清楚地表明,CVID患者的记忆B细胞绝对计数比健康对照组减少,凋亡增加(P <. 01)。此外,我们还证明CD95与调节记忆性B细胞凋亡无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
El descenso del número de linfocitos B de memoria en pacientes con inmunodeficiencia variable común está asociado a una apoptosis aumentada de esta población celular. Desarrollo de un método nuevo para la detección de la apoptosis en muestras de sangre completa

Common Variable Immunodeficiency (CVID) is a heterogeneous disease characterised by low memory B cell counts in peripheral blood (PB). Although previous reports have attributed memory CD27+ B cell decrease to a possible defective germinal centre development, the cause of this defect remains basically unknown. On the other hand, increased apoptosis has been implicated in the pathogenesis of several diseases, and could be another factor that contributes to explain memory B cell reduction. However, a negative balance between apoptosis/survival of memory B cells in CVID patients has still not been documented. Therefore, we asked whether increased apoptosis was relevant in CVID. To test this concept, total and memory B cells from CVID patients and healthy controls were studied by flow cytometry to determine spontaneous and induced apoptosis. Apoptosis was measured by Annexin-V expression after a 24 hour culture with and without anti-CD95 proapoptotic monoclonal antibody. We also developed a new and sensitive method that uses 7-amino-actinomycin D (7-AAD) to measure very low numbers of apoptotic cells in whole PB. Our results clearly indicate diminished absolute counts and higher apoptosis in memory B cells from CVID patients than in healthy controls (P < .01). Moreover, we also demonstrate that CD95 is not implicated in regulating memory B cell apoptosis.

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