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Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge

Immunological memory to a previously encountered pathogen can influence the outcome of a sequential infection, which is called heterologous immunity. Lymphocytic choriomeningitis virus (LCMV) immune mice develop a NP205-specific T cell response that is cross-reactive to Pichinde virus infection (PIC...

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Autores principales: Mischke, Jasmin, Klein, Sebastian, Seamann, Austin, Prinz, Immo, Selin, Liisa, Ghersi, Dario, Cornberg, Markus, Kraft, Anke R.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612015/
https://www.ncbi.nlm.nih.gov/pubmed/36298848
http://dx.doi.org/10.3390/v14102293
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author Mischke, Jasmin
Klein, Sebastian
Seamann, Austin
Prinz, Immo
Selin, Liisa
Ghersi, Dario
Cornberg, Markus
Kraft, Anke R.M.
author_facet Mischke, Jasmin
Klein, Sebastian
Seamann, Austin
Prinz, Immo
Selin, Liisa
Ghersi, Dario
Cornberg, Markus
Kraft, Anke R.M.
author_sort Mischke, Jasmin
collection PubMed
description Immunological memory to a previously encountered pathogen can influence the outcome of a sequential infection, which is called heterologous immunity. Lymphocytic choriomeningitis virus (LCMV) immune mice develop a NP205-specific T cell response that is cross-reactive to Pichinde virus infection (PICV). So far, limited data are available if cross-reactive T cell responses appear also during chronic infections with exhausted T cell responses. Exhaustion in chronic viral infections can be treated with checkpoint inhibitors, which might affect heterologous outcomes unexpectedly. The aim of this study was to investigate the cross-reactive immune response in chronic LCMV clone 13 (LCMVcl13) infection during primary PICV infection at phenotypic, functional, and T cell receptor (TCR) level. Moreover, the influence of checkpoint inhibitor therapy with αPD-L1 was investigated. Cross-reactive NP205-specific responses were present and functional in the chronic environment. Additionally, chronically infected mice were also protected from PICV mediated weight loss compared to naive PICV mice. An altered phenotype of NP205-specific T cells was detectable, but no major differences in the clonality and diversity of their TCR repertoire were observed. Checkpoint inhibitor treatment with αPD-L1 did alter chronic LCMV infection but had no major effect on heterologous immunity to PICV. Our study demonstrated that cross-reactive CD8(+) T cells also exist in the setting of chronic infection, indicating a clinically relevant role of cross-reactive T cells in chronic infections.
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spelling pubmed-96120152022-10-28 Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge Mischke, Jasmin Klein, Sebastian Seamann, Austin Prinz, Immo Selin, Liisa Ghersi, Dario Cornberg, Markus Kraft, Anke R.M. Viruses Article Immunological memory to a previously encountered pathogen can influence the outcome of a sequential infection, which is called heterologous immunity. Lymphocytic choriomeningitis virus (LCMV) immune mice develop a NP205-specific T cell response that is cross-reactive to Pichinde virus infection (PICV). So far, limited data are available if cross-reactive T cell responses appear also during chronic infections with exhausted T cell responses. Exhaustion in chronic viral infections can be treated with checkpoint inhibitors, which might affect heterologous outcomes unexpectedly. The aim of this study was to investigate the cross-reactive immune response in chronic LCMV clone 13 (LCMVcl13) infection during primary PICV infection at phenotypic, functional, and T cell receptor (TCR) level. Moreover, the influence of checkpoint inhibitor therapy with αPD-L1 was investigated. Cross-reactive NP205-specific responses were present and functional in the chronic environment. Additionally, chronically infected mice were also protected from PICV mediated weight loss compared to naive PICV mice. An altered phenotype of NP205-specific T cells was detectable, but no major differences in the clonality and diversity of their TCR repertoire were observed. Checkpoint inhibitor treatment with αPD-L1 did alter chronic LCMV infection but had no major effect on heterologous immunity to PICV. Our study demonstrated that cross-reactive CD8(+) T cells also exist in the setting of chronic infection, indicating a clinically relevant role of cross-reactive T cells in chronic infections. MDPI 2022-10-18 /pmc/articles/PMC9612015/ /pubmed/36298848 http://dx.doi.org/10.3390/v14102293 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mischke, Jasmin
Klein, Sebastian
Seamann, Austin
Prinz, Immo
Selin, Liisa
Ghersi, Dario
Cornberg, Markus
Kraft, Anke R.M.
Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge
title Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge
title_full Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge
title_fullStr Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge
title_full_unstemmed Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge
title_short Cross-Reactive T Cell Response Exists in Chronic Lymphocytic Choriomeningitis Virus Infection upon Pichinde Virus Challenge
title_sort cross-reactive t cell response exists in chronic lymphocytic choriomeningitis virus infection upon pichinde virus challenge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612015/
https://www.ncbi.nlm.nih.gov/pubmed/36298848
http://dx.doi.org/10.3390/v14102293
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