Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm
ABSTRACT Ebola virus (EBOV) disease (EVD) results from an exacerbated immunological response that is highlighted by a burst in the production of inflammatory mediators known as a “cytokine storm.” Previous reports have suggested that nonspecific activation of T lymphocytes may play a central role in...
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American Society for Microbiology
2017
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oai:doaj.org-article:48b879ffa3974e9c88d3f79502e915e82021-11-15T15:51:50ZEbola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm10.1128/mBio.00845-172150-7511https://doaj.org/article/48b879ffa3974e9c88d3f79502e915e82017-11-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.00845-17https://doaj.org/toc/2150-7511ABSTRACT Ebola virus (EBOV) disease (EVD) results from an exacerbated immunological response that is highlighted by a burst in the production of inflammatory mediators known as a “cytokine storm.” Previous reports have suggested that nonspecific activation of T lymphocytes may play a central role in this phenomenon. T-cell immunoglobulin and mucin domain-containing protein 1 (Tim-1) has recently been shown to interact with virion-associated phosphatidylserine to promote infection. Here, we demonstrate the central role of Tim-1 in EBOV pathogenesis, as Tim-1−/− mice exhibited increased survival rates and reduced disease severity; surprisingly, only a limited decrease in viremia was detected. Tim-1−/− mice exhibited a modified inflammatory response as evidenced by changes in serum cytokines and activation of T helper subsets. A series of in vitro assays based on the Tim-1 expression profile on T cells demonstrated that despite the apparent absence of detectable viral replication in T lymphocytes, EBOV directly binds to isolated T lymphocytes in a phosphatidylserine–Tim-1-dependent manner. Exposure to EBOV resulted in the rapid development of a CD4Hi CD3Low population, non-antigen-specific activation, and cytokine production. Transcriptome and Western blot analysis of EBOV-stimulated CD4+ T cells confirmed the induction of the Tim-1 signaling pathway. Furthermore, comparative analysis of transcriptome data and cytokine/chemokine analysis of supernatants highlight the similarities associated with EBOV-stimulated T cells and the onset of a cytokine storm. Flow cytometry revealed virtually exclusive binding and activation of central memory CD4+ T cells. These findings provide evidence for the role of Tim-1 in the induction of a cytokine storm phenomenon and the pathogenesis of EVD. IMPORTANCE Ebola virus infection is characterized by a massive release of inflammatory mediators, which has come to be known as a cytokine storm. The severity of the cytokine storm is consistently linked with fatal disease outcome. Previous findings have demonstrated that specific T-cell subsets are key contributors to the onset of a cytokine storm. In this study, we investigated the role of Tim-1, a T-cell-receptor-independent trigger of T-cell activation. We first demonstrated that Tim-1-knockout (KO) mice survive lethal Ebola virus challenge. We then used a series of in vitro assays to demonstrate that Ebola virus directly binds primary T cells in a Tim-1–phosphatidylserine-dependent manner. We noted that binding induces a cytokine storm-like phenomenon and that blocking Tim-1–phosphatidylserine interactions reduces viral binding, T-cell activation, and cytokine production. These findings highlight a previously unknown role of Tim-1 in the development of a cytokine storm and “immune paralysis.”Patrick YounanMathieu IampietroAndrew NishidaPalaniappan RamanathanRodrigo I. SantosMukta DuttaNdongala Michel LubakiRichard A. KoupMichael G. KatzeAlexander BukreyevAmerican Society for Microbiologyarticlecytokine stormT lymphocytestranscriptomecytokinesEbola virusviral pathogenesisMicrobiologyQR1-502ENmBio, Vol 8, Iss 5 (2017) |
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cytokine storm T lymphocytes transcriptome cytokines Ebola virus viral pathogenesis Microbiology QR1-502 |
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cytokine storm T lymphocytes transcriptome cytokines Ebola virus viral pathogenesis Microbiology QR1-502 Patrick Younan Mathieu Iampietro Andrew Nishida Palaniappan Ramanathan Rodrigo I. Santos Mukta Dutta Ndongala Michel Lubaki Richard A. Koup Michael G. Katze Alexander Bukreyev Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm |
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ABSTRACT Ebola virus (EBOV) disease (EVD) results from an exacerbated immunological response that is highlighted by a burst in the production of inflammatory mediators known as a “cytokine storm.” Previous reports have suggested that nonspecific activation of T lymphocytes may play a central role in this phenomenon. T-cell immunoglobulin and mucin domain-containing protein 1 (Tim-1) has recently been shown to interact with virion-associated phosphatidylserine to promote infection. Here, we demonstrate the central role of Tim-1 in EBOV pathogenesis, as Tim-1−/− mice exhibited increased survival rates and reduced disease severity; surprisingly, only a limited decrease in viremia was detected. Tim-1−/− mice exhibited a modified inflammatory response as evidenced by changes in serum cytokines and activation of T helper subsets. A series of in vitro assays based on the Tim-1 expression profile on T cells demonstrated that despite the apparent absence of detectable viral replication in T lymphocytes, EBOV directly binds to isolated T lymphocytes in a phosphatidylserine–Tim-1-dependent manner. Exposure to EBOV resulted in the rapid development of a CD4Hi CD3Low population, non-antigen-specific activation, and cytokine production. Transcriptome and Western blot analysis of EBOV-stimulated CD4+ T cells confirmed the induction of the Tim-1 signaling pathway. Furthermore, comparative analysis of transcriptome data and cytokine/chemokine analysis of supernatants highlight the similarities associated with EBOV-stimulated T cells and the onset of a cytokine storm. Flow cytometry revealed virtually exclusive binding and activation of central memory CD4+ T cells. These findings provide evidence for the role of Tim-1 in the induction of a cytokine storm phenomenon and the pathogenesis of EVD. IMPORTANCE Ebola virus infection is characterized by a massive release of inflammatory mediators, which has come to be known as a cytokine storm. The severity of the cytokine storm is consistently linked with fatal disease outcome. Previous findings have demonstrated that specific T-cell subsets are key contributors to the onset of a cytokine storm. In this study, we investigated the role of Tim-1, a T-cell-receptor-independent trigger of T-cell activation. We first demonstrated that Tim-1-knockout (KO) mice survive lethal Ebola virus challenge. We then used a series of in vitro assays to demonstrate that Ebola virus directly binds primary T cells in a Tim-1–phosphatidylserine-dependent manner. We noted that binding induces a cytokine storm-like phenomenon and that blocking Tim-1–phosphatidylserine interactions reduces viral binding, T-cell activation, and cytokine production. These findings highlight a previously unknown role of Tim-1 in the development of a cytokine storm and “immune paralysis.” |
format |
article |
author |
Patrick Younan Mathieu Iampietro Andrew Nishida Palaniappan Ramanathan Rodrigo I. Santos Mukta Dutta Ndongala Michel Lubaki Richard A. Koup Michael G. Katze Alexander Bukreyev |
author_facet |
Patrick Younan Mathieu Iampietro Andrew Nishida Palaniappan Ramanathan Rodrigo I. Santos Mukta Dutta Ndongala Michel Lubaki Richard A. Koup Michael G. Katze Alexander Bukreyev |
author_sort |
Patrick Younan |
title |
Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm |
title_short |
Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm |
title_full |
Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm |
title_fullStr |
Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm |
title_full_unstemmed |
Ebola Virus Binding to Tim-1 on T Lymphocytes Induces a Cytokine Storm |
title_sort |
ebola virus binding to tim-1 on t lymphocytes induces a cytokine storm |
publisher |
American Society for Microbiology |
publishDate |
2017 |
url |
https://doaj.org/article/48b879ffa3974e9c88d3f79502e915e8 |
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