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Hem-1 通过 B 细胞特异性方式调节保护性体液免疫和限制自身抗体产生。

Hem-1 regulates protective humoral immunity and limits autoantibody production in a B cell-specific manner.

机构信息

The Department of Comparative Medicine, University of Washington, Seattle, Washington, USA.

Seattle Children's Research Institute, Seattle, Washington, USA.

出版信息

JCI Insight. 2022 May 9;7(9):e153597. doi: 10.1172/jci.insight.153597.

Abstract

Hematopoietic protein-1 (Hem-1) is a member of the actin-regulatory WASp family verprolin homolog (WAVE) complex. Loss-of-function variants in the NCKAP1L gene encoding Hem-1 were recently discovered to result in primary immunodeficiency disease (PID) in children, characterized by poor specific Ab responses, increased autoantibodies, and high mortality. However, the mechanisms of how Hem-1 deficiency results in PID are unclear. In this study, we utilized constitutive and B cell-specific Nckap1l-KO mice to dissect the importance of Hem-1 in B cell development and functions. B cell-specific disruption of Hem-1 resulted in reduced numbers of recirculating follicular (FO), marginal zone (MZ), and B1 B cells. B cell migration in response to CXCL12 and -13 were reduced. T-independent Ab responses were nearly abolished, resulting in failed protective immunity to Streptococcus pneumoniae challenge. In contrast, T-dependent IgM and IgG2c, memory B cell, and plasma cell responses were more robust relative to WT control mice. B cell-specific Hem-1-deficient mice had increased autoantibodies against multiple autoantigens, and this correlated with hyperresponsive BCR signaling and increased representation of CD11c+T-bet+ age-associated B cell (ABC cells) - alterations associated with autoimmune diseases. These results suggest that dysfunctional B cells may be part of a mechanism explaining why loss-of-function Hem-1 variants result in recurring infections and autoimmunity.

摘要

造血蛋白-1(Hem-1)是肌动蛋白调节 Wiskott-Aldrich 综合征蛋白(WASP)家族 verprolin 同源物(WAVE)复合物的成员。编码 Hem-1 的 NCKAP1L 基因的功能丧失变异最近被发现导致儿童原发性免疫缺陷病(PID),其特征是特异性 Ab 反应差、自身抗体增加和死亡率高。然而,Hem-1 缺乏导致 PID 的机制尚不清楚。在这项研究中,我们利用组成型和 B 细胞特异性 Nckap1l-KO 小鼠来剖析 Hem-1 在 B 细胞发育和功能中的重要性。B 细胞特异性 Hem-1 缺失导致循环滤泡(FO)、边缘区(MZ)和 B1 B 细胞数量减少。对 CXCL12 和 -13 的 B 细胞迁移减少。T 细胞非依赖性 Ab 反应几乎被废除,导致对肺炎链球菌挑战的保护性免疫失败。相比之下,T 细胞依赖性 IgM 和 IgG2c、记忆 B 细胞和浆细胞反应相对于 WT 对照小鼠更为强劲。B 细胞特异性 Hem-1 缺陷小鼠产生针对多种自身抗原的自身抗体增加,这与 BCR 信号的过度反应和 CD11c+T-bet+年龄相关 B 细胞(ABC 细胞)的增加相关 - 与自身免疫性疾病相关的改变。这些结果表明,功能失调的 B 细胞可能是解释为什么功能丧失的 Hem-1 变体导致反复感染和自身免疫的机制的一部分。

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