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X连锁高IgM综合征中缺乏IgD-CD27(+)记忆B细胞群体。

Absence of IgD-CD27(+) memory B cell population in X-linked hyper-IgM syndrome.

作者信息

Agematsu K, Nagumo H, Shinozaki K, Hokibara S, Yasui K, Terada K, Kawamura N, Toba T, Nonoyama S, Ochs H D, Komiyama A

机构信息

Department of Pediatrics, Shinshu University School of Medicine, Matsumoto 390, Japan.

出版信息

J Clin Invest. 1998 Aug 15;102(4):853-60. doi: 10.1172/JCI3409.

Abstract

The present study analyzed peripheral blood B cell populations separated by IgD and CD27 expression in six males with X-linked hyper-IgM syndrome (XHIM). Costimulation of mononuclear cells from most of the patients induced no to low levels of class switching from IgM to IgG and IgA with Staphylococcus aureus Cowan strain (SAC) plus IL-2 or anti-CD40 mAb (anti-CD40) plus IL-10. Measurable levels of IgE were secreted in some of the patients after stimulation with anti-CD40 plus IL-4. Costimulation with SAC plus IL-2 plus anti-CD40 plus IL-10 yielded secretion of significant levels of IgG in addition to IgM, but not IgA. The most striking finding was that peripheral blood B cells from all of the six patients were composed of only IgD+ CD27(-) and IgD+ CD27(+) B cells; IgD- CD27(+) memory B cells were greatly decreased. IgD+ CD27(+) B cells from an XHIM patient produced IgM predominantly. Our data indicate that the low response of IgG production in XHIM patients is due to reduced numbers of IgD- CD27(+) memory B cells. However, the IgG production can be induced by stimulation of immunoglobulin receptors and CD40 in cooperation with such cytokines as IL-2 and IL-10 in vitro.

摘要

本研究分析了6名患有X连锁高IgM综合征(XHIM)男性患者外周血中通过IgD和CD27表达分离的B细胞群体。大多数患者的单核细胞经金黄色葡萄球菌考恩菌株(SAC)加白细胞介素-2(IL-2)或抗CD40单克隆抗体(抗CD40)加IL-10共刺激后,从IgM向IgG和IgA的类别转换诱导水平为无至低水平。部分患者在用抗CD40加IL-4刺激后可分泌可测量水平的IgE。SAC加IL-2加抗CD40加IL-10共刺激除产生IgM外,还产生显著水平的IgG,但不产生IgA。最显著的发现是,6名患者的外周血B细胞均仅由IgD+CD27(-)和IgD+CD27(+)B细胞组成;IgD-CD27(+)记忆B细胞大大减少。一名XHIM患者的IgD+CD27(+)B细胞主要产生IgM。我们的数据表明,XHIM患者IgG产生反应低是由于IgD-CD27(+)记忆B细胞数量减少。然而,体外通过免疫球蛋白受体和CD40与IL-2和IL-10等细胞因子协同刺激可诱导IgG产生。

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