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B细胞上肿瘤坏死因子(TNF)家族受体表达降低与幼儿对肺炎链球菌感染的体液免疫反应减弱有关。

Decreased TNF family receptor expression on B-cells is associated with reduced humoral responses to Streptococcus pneumoniae infections in young children.

作者信息

Basha Saleem, Pichichero Michael E

机构信息

Center for Infectious Diseases and Immunology, Rochester General Hospital Research Institute, Rochester, NY 14621, USA.

Center for Infectious Diseases and Immunology, Rochester General Hospital Research Institute, Rochester, NY 14621, USA.

出版信息

Cell Immunol. 2017 Oct;320:11-19. doi: 10.1016/j.cellimm.2017.07.004. Epub 2017 Jul 21.

DOI:10.1016/j.cellimm.2017.07.004
PMID:28947093
Abstract

An underdeveloped or impaired immune response in young children is associated with increased susceptibility to Streptococcus pneumonia (Spn) infections. We determined serum antibody titers against 3 Spn vaccine candidate proteins and vaccine serotype polysaccharide antigens in a group of Spn infection prone 9-18months old and found lower IgG antibody titers to all tested antigens compared to age-matched non-infection-prone children. We also found the children had significantly reduced percentages of total memory B-cells, switched memory B-cells and plasma cells. We sought a mechanistic explanation for that result by examination of TNF family receptors (TNFRs) TACI, BCMA, and BAFFR receptor expression on B-cells and found significantly lower BAFFR and TACI expression; significantly lower proliferation of B-cells stimulated with exogenous BAFF; and diminished expression of co-stimulatory receptors B7-1 and B7-2 among infection prone vs. non-prone children. We conclude that lower expression of TNFRs, lower proliferation of B-cells in response to BAFF and lower expression of B7-1 and B7-2 by B-cells may contribute to reduced antibody responses to Spn and consequent infection proneness in young children.

摘要

幼儿免疫反应发育不全或受损与肺炎链球菌(Spn)感染易感性增加有关。我们测定了一组9至18个月易感染Spn的儿童针对3种Spn疫苗候选蛋白和疫苗血清型多糖抗原的血清抗体滴度,发现与年龄匹配的不易感染儿童相比,所有检测抗原的IgG抗体滴度均较低。我们还发现这些儿童的总记忆B细胞、转换记忆B细胞和浆细胞百分比显著降低。我们通过检查B细胞上的TNF家族受体(TNFRs)TACI、BCMA和BAFFR受体表达来寻找该结果的机制解释,发现BAFFR和TACI表达显著降低;外源性BAFF刺激的B细胞增殖显著降低;与不易感染儿童相比,易感染儿童中协同刺激受体B7-1和B7-2的表达减少。我们得出结论,TNFRs表达降低、B细胞对BAFF反应的增殖降低以及B细胞B7-1和B7-2表达降低可能导致幼儿对Spn的抗体反应降低以及随之而来的感染易感性。

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