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Chronic viral infection impairs immune memory to a different pathogen.
Yang, Cheng; Liu, Zhicui; Yang, Ying; Cocka, Luis J; Li, Yongguo; Zeng, Weihong; Shen, Hao.
Affiliation
  • Yang C; Department of Infectious Diseases, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • Liu Z; Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Pennsylvania, Philadelphia, United States of America.
  • Yang Y; Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Pennsylvania, Philadelphia, United States of America.
  • Cocka LJ; Department of Dermatology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, China.
  • Li Y; Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Pennsylvania, Philadelphia, United States of America.
  • Zeng W; Hainan Academy of Medical Sciences, Hainan Medical University, Hainan, China.
  • Shen H; Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Pennsylvania, Philadelphia, United States of America.
PLoS Pathog ; 20(3): e1012113, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38547316
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Diseases / Lymphocytic Choriomeningitis Limits: Animals / Humans Language: En Journal: PLoS Pathog Year: 2024 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virus Diseases / Lymphocytic Choriomeningitis Limits: Animals / Humans Language: En Journal: PLoS Pathog Year: 2024 Document type: Article Affiliation country: China Country of publication: United States