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Cell host & microbe:人类巨细胞病毒和自身免疫性疾病有关联

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发布时间: 2016-4-16 15:52

正文摘要:

一个由中国科学家做的研究把鲜为人知的病毒和自身免疫性疾病关联起来。该工作刊载在Cell Host & Microbe。 你可能没听过它,不过人类巨细胞病毒(CMV)可能是你遇到过最普遍的病毒。人类群体大约60到90百分比都被其 ...

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ipsvirus 发表于 2016-4-16 15:54:03
A Cytomegalovirus Peptide-Specific Antibody Alters Natural Killer Cell Homeostasis and Is Shared in Several Autoimmune Diseases

Yu Liu1, 2, 7, Rong Mu3, 7, Ya-Ping Gao1, 2, 7, Jie Dong1, Lei Zhu3, Yuyuan Ma4, Yu-Hui Li3, He-Qiu Zhang1, Dong Han1, 2, Yu Zhang5, Iain B. McInnes6, Jingang Zhang4, Beifen Shen1, 2, Guang Yang1, 2, , , Zhan-Guo Li3, ,

Highlights
•An antibody against the hCMV Pp150 protein is shared in patients with autoimmune diseases
•Anti-Pp150 recognizes CIP2A on CD56bright NK cells and induces cell death
•The percentage of circulating CD56bright NK cells is reduced in autoimmune disease patients
•CD56bright NK cell number is negatively correlated with anti-Pp150 levels

Summary
Human cytomegalovirus (hCMV), a ubiquitous beta-herpesvirus, has been associated with several autoimmune diseases. However, the direct role of hCMV in inducing autoimmune disorders remains unclear. Here we report the identification of an autoantibody that recognizes a group of peptides with a conserved motif matching the Pp150 protein of hCMV (anti-Pp150) and is shared among patients with various autoimmune diseases. Anti-Pp150 also recognizes the single-pass membrane protein CIP2A and induces the death of CD56bright NK cells, a natural killer cell subset whose expansion is correlated with autoimmune disease. Consistent with this finding, the percentage of circulating CD56bright NK cells is reduced in patients with several autoimmune diseases and negatively correlates with anti-Pp150 concentration. CD56bright NK cell death occurs via both antibody- and complement-dependent cytotoxicity. Our findings reveal that a shared hCMV-induced autoantibody is involved in the decrease of CD56bright NK cells and may thus contribute to the onset of autoimmune disorders.

http://www.sciencedirect.com/sci ... i/S1931312816300464

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