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慢性病毒感染会损害对另一种病原体的免疫记忆。

Chronic viral infection impairs immune memory to a different pathogen.

机构信息

Department of Infectious Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.

Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Pennsylvania, Philadelphia, United States of America.

出版信息

PLoS Pathog. 2024 Mar 28;20(3):e1012113. doi: 10.1371/journal.ppat.1012113. eCollection 2024 Mar.

Abstract

Chronic viral infections cause T cell dysfunction in both animal models and human clinical settings, thereby affecting the ability of the host immune system to clear viral pathogens and develop proper virus-specific immune memory. However, the impact of chronic viral infections on the host's immune memory to other pathogens has not been well described. In this study, we immunized mice with recombinant Listeria monocytogenes expressing OVA (Lm-OVA) to generate immunity to Lm and allow analysis of OVA-specific memory T (Tm) cells. We then infected these mice with lymphocytic choriomeningitis virus (LCMV) strain Cl-13 which establishes a chronic infection. We found that chronically infected mice were unable to protect against Listeria re-challenge. OVA-specific Tm cells showed a progressive loss in total numbers and in their ability to produce effector cytokines in the context of chronic LCMV infection. Unlike virus-specific T cells, OVA-specific Tm cells from chronically infected mice did not up-regulate the expression of inhibitory receptors, a hallmark feature of exhaustion in virus-specific T cells. Finally, OVA-specific Tm cells failed to mount a robust recall response after bacteria re-challenge both in the chronically infected and adoptively transferred naïve hosts. These results show that previously established bacteria-specific Tm cells become functionally impaired in the setting of an unrelated bystander chronic viral infection, which may contribute to poor immunity against other pathogens in the host with chronic viral infection.

摘要

慢性病毒感染可导致动物模型和人类临床环境中的 T 细胞功能障碍,从而影响宿主免疫系统清除病毒病原体并产生适当的病毒特异性免疫记忆的能力。然而,慢性病毒感染对宿主对其他病原体的免疫记忆的影响尚未得到很好的描述。在这项研究中,我们使用表达 OVA 的重组李斯特菌 monocytogenes(Lm-OVA)免疫小鼠,以产生对 Lm 的免疫力,并允许分析 OVA 特异性记忆 T(Tm)细胞。然后,我们用淋巴细胞性脉络丛脑膜炎病毒(LCMV)株 Cl-13 感染这些小鼠,该病毒建立了慢性感染。我们发现,慢性感染的小鼠无法抵抗李斯特菌的再次攻击。在慢性 LCMV 感染的情况下,OVA 特异性 Tm 细胞的总数和产生效应细胞因子的能力逐渐丧失。与病毒特异性 T 细胞不同,慢性感染小鼠的 OVA 特异性 Tm 细胞并未上调抑制性受体的表达,这是病毒特异性 T 细胞耗竭的一个标志特征。最后,在细菌再次攻击后,慢性感染和过继转移的幼稚宿主中的 OVA 特异性 Tm 细胞均无法引发强烈的回忆反应。这些结果表明,先前建立的细菌特异性 Tm 细胞在无关的旁观者慢性病毒感染的情况下功能受损,这可能导致慢性病毒感染宿主对其他病原体的免疫功能不佳。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/004e/11003680/4b705f5fb6b9/ppat.1012113.g001.jpg

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