TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection

T follicular helper (TFH) and T helper 1 (Th1) cells generated after viral infections are critical for the control of infection and the development of immunological memory. However, the mechanisms that govern the differentiation and maintenance of these two distinct lineages during viral infection r...

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Published in:Cell Reports
Main Authors: Tuoqi Wu, Hyun Mu Shin, E. Ashley Moseman, Yun Ji, Bonnie Huang, Christelle Harly, Jyoti M. Sen, Leslie J. Berg, Luca Gattinoni, Dorian B. McGavern, Pamela L. Schwartzberg
Format: Article
Language:English
Published: Elsevier 2015-09-01
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124715009468
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author Tuoqi Wu
Hyun Mu Shin
E. Ashley Moseman
Yun Ji
Bonnie Huang
Christelle Harly
Jyoti M. Sen
Leslie J. Berg
Luca Gattinoni
Dorian B. McGavern
Pamela L. Schwartzberg
author_facet Tuoqi Wu
Hyun Mu Shin
E. Ashley Moseman
Yun Ji
Bonnie Huang
Christelle Harly
Jyoti M. Sen
Leslie J. Berg
Luca Gattinoni
Dorian B. McGavern
Pamela L. Schwartzberg
author_sort Tuoqi Wu
collection DOAJ
container_title Cell Reports
description T follicular helper (TFH) and T helper 1 (Th1) cells generated after viral infections are critical for the control of infection and the development of immunological memory. However, the mechanisms that govern the differentiation and maintenance of these two distinct lineages during viral infection remain unclear. We found that viral-specific TFH and Th1 cells showed reciprocal expression of the transcriptions factors TCF1 and Blimp1 early after infection, even before the differential expression of the canonical TFH marker CXCR5. Furthermore, TCF1 was intrinsically required for the TFH cell response to viral infection; in the absence of TCF1, the TFH cell response was severely compromised, and the remaining TCF1-deficient TFH cells failed to maintain TFH-associated transcriptional and metabolic signatures, which were distinct from those in Th1 cells. Mechanistically, TCF1 functioned through forming negative feedback loops with IL-2 and Blimp1. Our findings demonstrate an essential role of TCF1 in TFH cell responses to viral infection.
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spelling doaj-art-3c3cfee35705436eae052daf1f1a14152025-08-19T20:58:53ZengElsevierCell Reports2211-12472015-09-0112122099211010.1016/j.celrep.2015.08.049TCF1 Is Required for the T Follicular Helper Cell Response to Viral InfectionTuoqi Wu0Hyun Mu Shin1E. Ashley Moseman2Yun Ji3Bonnie Huang4Christelle Harly5Jyoti M. Sen6Leslie J. Berg7Luca Gattinoni8Dorian B. McGavern9Pamela L. Schwartzberg10National Human Genome Research Institute (NHGRI), NIH, Bethesda, MD 20892, USADepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USANational Institute of Neurological Disorders and Stroke (NINDS), NIH, Bethesda, MD 20892, USANational Cancer Institute (NCI), NIH, Bethesda, MD 20892, USANational Human Genome Research Institute (NHGRI), NIH, Bethesda, MD 20892, USANational Cancer Institute (NCI), NIH, Bethesda, MD 20892, USANational Institute on Aging (NIA), NIH, Baltimore, MD 21224, USADepartment of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USANational Cancer Institute (NCI), NIH, Bethesda, MD 20892, USANational Institute of Neurological Disorders and Stroke (NINDS), NIH, Bethesda, MD 20892, USANational Human Genome Research Institute (NHGRI), NIH, Bethesda, MD 20892, USAT follicular helper (TFH) and T helper 1 (Th1) cells generated after viral infections are critical for the control of infection and the development of immunological memory. However, the mechanisms that govern the differentiation and maintenance of these two distinct lineages during viral infection remain unclear. We found that viral-specific TFH and Th1 cells showed reciprocal expression of the transcriptions factors TCF1 and Blimp1 early after infection, even before the differential expression of the canonical TFH marker CXCR5. Furthermore, TCF1 was intrinsically required for the TFH cell response to viral infection; in the absence of TCF1, the TFH cell response was severely compromised, and the remaining TCF1-deficient TFH cells failed to maintain TFH-associated transcriptional and metabolic signatures, which were distinct from those in Th1 cells. Mechanistically, TCF1 functioned through forming negative feedback loops with IL-2 and Blimp1. Our findings demonstrate an essential role of TCF1 in TFH cell responses to viral infection.http://www.sciencedirect.com/science/article/pii/S2211124715009468
spellingShingle Tuoqi Wu
Hyun Mu Shin
E. Ashley Moseman
Yun Ji
Bonnie Huang
Christelle Harly
Jyoti M. Sen
Leslie J. Berg
Luca Gattinoni
Dorian B. McGavern
Pamela L. Schwartzberg
TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection
title TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection
title_full TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection
title_fullStr TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection
title_full_unstemmed TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection
title_short TCF1 Is Required for the T Follicular Helper Cell Response to Viral Infection
title_sort tcf1 is required for the t follicular helper cell response to viral infection
url http://www.sciencedirect.com/science/article/pii/S2211124715009468
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