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蛋白质能量营养不良改变黏膜 IgA 应答,降低小鼠黏膜疫苗的效力。

Protein energy malnutrition alters mucosal IgA responses and reduces mucosal vaccine efficacy in mice.

机构信息

International Vaccine Institute, SNU Research Park, Seoul, Republic of Korea.

Academy of Immunology and Microbiology, Institute for Basic Science, Pohang, Republic of Korea.

出版信息

Immunol Lett. 2017 Oct;190:247-256. doi: 10.1016/j.imlet.2017.08.025. Epub 2017 Aug 30.

Abstract

Oral vaccine responsiveness is often lower in children from less developed countries. Childhood malnutrition may be associated with poor immune response to oral vaccines. The present study was designed to investigate whether protein energy malnutrition (PEM) impairs B cell immunity and ultimately reduces oral vaccine efficacy in a mouse model. Purified isocaloric diets containing low protein (1/10 the protein of the control diet) were used to determine the effect of PEM. PEM increased both nonspecific total IgA and oral antigen-specific IgA in serum without alteration of gut permeability. However, PEM decreased oral antigen-specific IgA in feces, which is consistent with decreased expression of polymeric Immunoglobulin receptor (pIgR) in the small intestine. Of note, polymeric IgA was predominant in serum under PEM. In addition, PEM altered B cell development status in the bone marrow and increased the frequency of IgA-secreting B cells, as well as IgA secretion by long-lived plasma cells in the small intestinal lamina propria. Moreover, PEM reduced the protective efficacy of the mucosally administered cholera vaccine and recombinant attenuated Salmonella enterica serovar Typhimurium vaccine in a mouse model. Our results suggest that PEM can impair mucosal immunity where IgA plays an important role in host protection and may partly explain the reduced efficacy of oral vaccines in malnourished subjects.

摘要

口服疫苗的反应性在欠发达国家的儿童中通常较低。儿童期营养不良可能与对口服疫苗的免疫反应不良有关。本研究旨在探讨蛋白质能量营养不良(PEM)是否会损害 B 细胞免疫,从而最终降低小鼠模型中口服疫苗的效果。使用含有低蛋白(仅为对照饮食中蛋白质的 1/10)的等热量纯化饮食来确定 PEM 的影响。PEM 增加了血清中非特异性总 IgA 和口服抗原特异性 IgA,而不会改变肠道通透性。然而,PEM 减少了粪便中的口服抗原特异性 IgA,这与小肠中多聚免疫球蛋白受体(pIgR)的表达减少一致。值得注意的是,在 PEM 下,多聚 IgA 在血清中占优势。此外,PEM 改变了骨髓中的 B 细胞发育状态,并增加了 IgA 分泌 B 细胞的频率以及小肠固有层中长寿命浆细胞的 IgA 分泌。此外,PEM 降低了黏膜给予霍乱疫苗和重组减毒鼠伤寒沙门氏菌疫苗在小鼠模型中的保护效力。我们的研究结果表明,PEM 可损害 IgA 在宿主保护中起重要作用的黏膜免疫,这可能部分解释了营养不良人群中口服疫苗效果降低的原因。

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