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      Cytotoxic CD4 T Cells: Differentiation, Function, and Application to Dengue Virus Infection

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          Abstract

          Dengue virus (DENV) has spread through most tropical and subtropical areas of the world and represents a serious public health problem. The control of DENV infection has not yet been fully successful due to lack of effective therapeutics or vaccines. Nevertheless, a better understanding of the immune responses against DENV infection may reveal new strategies for eliciting and improving antiviral immunity. T cells provide protective immunity against various viral infections by generating effector cells that cooperate to eliminate antigens and memory cells that can survive for long periods with enhanced abilities to control recurring pathogens. Following activation, CD8 T cells can migrate to sites of infection and kill infected cells, whereas CD4 T cells contribute to the elimination of pathogens by trafficking to infected tissues and providing help to innate immune responses, B cells, as well as CD8 T cells. However, it is now evident that CD4 T cells can also perform cytotoxic functions and induce the apoptosis of target cells. Importantly, accumulating studies demonstrate that cytotoxic CD4 T cells develop following DENV infections and may play a crucial role in protecting the host from severe dengue disease. We review our current understanding of the differentiation and function of cytotoxic CD4 T cells, with a focus on DENV infection, and discuss the potential of harnessing these cells for the prevention and treatment of DENV infection and disease.

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          Most cited references73

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          T cell metabolism drives immunity

          Buck et al. discuss the role of lymphocyte metabolism on immune cell development and function.
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            Efficacy and Long-Term Safety of a Dengue Vaccine in Regions of Endemic Disease.

            A candidate tetravalent dengue vaccine is being assessed in three clinical trials involving more than 35,000 children between the ages of 2 and 16 years in Asian-Pacific and Latin American countries. We report the results of long-term follow-up interim analyses and integrated efficacy analyses.
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              Granzyme B and perforin are important for regulatory T cell-mediated suppression of tumor clearance.

              Granzyme B is important for the ability of NK cells and CD8(+) T cells to kill their targets. However, we showed here that granzyme B-deficient mice clear both allogeneic and syngeneic tumor cell lines more efficiently than do wild-type (WT) mice. To determine whether regulatory T (Treg) cells utilize granzyme B to suppress immune responses against these tumors, we examined the expression and function of granzyme B in Treg cells. Granzyme B was not expressed in naive Treg cells but was highly expressed in 5%-30% of CD4(+)Foxp3(+) Treg cells in the tumor environment. Adoptive transfer of WT Treg cells, but not granzyme B- or perforin-deficient Treg cells, into granzyme B-deficient mice partially restored susceptibility to tumor growth; Treg cells derived from the tumor environment could induce NK and CD8(+) T cell death in a granzyme B- and perforin-dependent fashion. Granzyme B and perforin are therefore relevant for Treg cell-mediated suppression of tumor clearance in vivo.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                07 December 2016
                2016
                : 7
                : 531
                Affiliations
                [1] 1Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology , La Jolla, CA, USA
                Author notes

                Edited by: John Zaunders, University of New South Wales, Australia

                Reviewed by: John J. Miles, Queensland Institute of Medical Research, Australia; Karin Schilbach, University of Tübingen, Germany

                *Correspondence: Daniela Weiskopf, dweiskopf@ 123456lji.org

                Specialty section: This article was submitted to T Cell Biology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2016.00531
                5141332
                28003809
                2ba69005-80c5-4287-b844-ac82cc18ca95
                Copyright © 2016 Tian, Sette and Weiskopf.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 September 2016
                : 10 November 2016
                Page count
                Figures: 2, Tables: 0, Equations: 0, References: 96, Pages: 9, Words: 7685
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: HSN272200900042C, HHSN27220140045C
                Categories
                Immunology
                Review

                Immunology
                cd4 t cells,cytotoxicity,dengue virus,protection,vaccines
                Immunology
                cd4 t cells, cytotoxicity, dengue virus, protection, vaccines

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