Literature DB >> 19786545

De novo recruitment of antigen-experienced and naive T cells contributes to the long-term maintenance of antiviral T cell populations in the persistently infected central nervous system.

Jingxian Zhao1, Jincun Zhao, Stanley Perlman.   

Abstract

Mice infected with attenuated strains of mouse hepatitis virus, strain JHM, develop a chronic infection in the brain and spinal cord characterized by low levels of viral Ag persistence and retention of virus-specific CD4 and CD8 T cells at the site of infection. It is not known whether these cells are maintained by proliferation of T cells that entered the CNS during acute infection or are newly recruited from Ag-experienced or naive T cell pools. In this study, using adoptive transfer experiments and bone marrow chimeras, we show that at least some of these cells are recruited from the periphery, predominantly from the viral Ag-experienced T cell pool. Both virus-specific CD4 and CD8 T cells are functional, as assessed by cytokine expression and degranulation after peptide exposure. In addition, populations of virus-specific CD4 T cells undergo dynamic changes in the infected CNS, as previously shown for CD8 T cells, because ratios of cells responding to two CD4 T cell epitopes change by a factor of five during the course of persistence. Collectively, these results show that maintenance of T cell responses in the virus-infected CNS is a dynamic process. Further, virus-specific T cell numbers at this site of infection are maintained by recruitment from peripheral Ag-experienced and naive T cell pools.

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Year:  2009        PMID: 19786545      PMCID: PMC2811315          DOI: 10.4049/jimmunol.0902164

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  34 in total

1.  Role of viral persistence in retaining CD8(+) T cells within the central nervous system.

Authors:  N W Marten; S A Stohlman; C C Bergmann
Journal:  J Virol       Date:  2000-09       Impact factor: 5.103

2.  Cutting edge: rapid in vivo killing by memory CD8 T cells.

Authors:  Daniel L Barber; E John Wherry; Rafi Ahmed
Journal:  J Immunol       Date:  2003-07-01       Impact factor: 5.422

3.  Dynamics of blood-borne CD8 memory T cell migration in vivo.

Authors:  Kimberly D Klonowski; Kristina J Williams; Amanda L Marzo; David A Blair; Elizabeth G Lingenheld; Leo Lefrançois
Journal:  Immunity       Date:  2004-05       Impact factor: 31.745

4.  Costimulation blockade, busulfan, and bone marrow promote titratable macrochimerism, induce transplantation tolerance, and correct genetic hemoglobinopathies with minimal myelosuppression.

Authors:  A B Adams; M M Durham; L Kean; N Shirasugi; J Ha; M A Williams; P A Rees; M C Cheung; S Mittelstaedt; A W Bingaman; D R Archer; T C Pearson; E K Waller; C P Larsen
Journal:  J Immunol       Date:  2001-07-15       Impact factor: 5.422

5.  Pathogenicity of antigenic variants of murine coronavirus JHM selected with monoclonal antibodies.

Authors:  J O Fleming; M D Trousdale; F A el-Zaatari; S A Stohlman; L P Weiner
Journal:  J Virol       Date:  1986-06       Impact factor: 5.103

6.  Selection of CTL escape mutants in mice infected with a neurotropic coronavirus: quantitative estimate of TCR diversity in the infected central nervous system.

Authors:  L Pewe; S B Heard; C Bergmann; M O Dailey; S Perlman
Journal:  J Immunol       Date:  1999-12-01       Impact factor: 5.422

7.  High-magnitude, virus-specific CD4 T-cell response in the central nervous system of coronavirus-infected mice.

Authors:  J S Haring; L L Pewe; S Perlman
Journal:  J Virol       Date:  2001-03       Impact factor: 5.103

8.  Analysis of JHM central nervous system infections in rats.

Authors:  D Parham; A Tereba; P J Talbot; D P Jackson; V L Morris
Journal:  Arch Neurol       Date:  1986-07

9.  Differential T cell function and fate in lymph node and nonlymphoid tissues.

Authors:  Nicola L Harris; Victoria Watt; Franca Ronchese; Graham Le Gros
Journal:  J Exp Med       Date:  2002-02-04       Impact factor: 14.307

10.  IL-15 independent maintenance of virus-specific CD8(+) T cells in the CNS during chronic infection.

Authors:  Jun Zuo; Stephen A Stohlman; Gabriel I Parra; Cornelia C Bergmann
Journal:  J Neuroimmunol       Date:  2008-12-23       Impact factor: 3.478

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  20 in total

Review 1.  T cell-driven initiation and propagation of autoimmune diabetes.

Authors:  Maria Bettini; Dario A A Vignali
Journal:  Curr Opin Immunol       Date:  2011-11-04       Impact factor: 7.486

2.  T cells facilitate recovery from Venezuelan equine encephalitis virus-induced encephalomyelitis in the absence of antibody.

Authors:  Christopher B Brooke; Damon J Deming; Alan C Whitmore; Laura J White; Robert E Johnston
Journal:  J Virol       Date:  2010-02-24       Impact factor: 5.103

3.  Regulatory T cells inhibit T cell proliferation and decrease demyelination in mice chronically infected with a coronavirus.

Authors:  Kathryn Trandem; Daniela Anghelina; Jingxian Zhao; Stanley Perlman
Journal:  J Immunol       Date:  2010-03-05       Impact factor: 5.422

4.  Structural and functional correlates of enhanced antiviral immunity generated by heteroclitic CD8 T cell epitopes.

Authors:  Jonathan A Trujillo; Stephanie Gras; Kelly-Anne Twist; Nathan P Croft; Rudragouda Channappanavar; Jamie Rossjohn; Anthony W Purcell; Stanley Perlman
Journal:  J Immunol       Date:  2014-05-02       Impact factor: 5.422

5.  Highly activated cytotoxic CD8 T cells express protective IL-10 at the peak of coronavirus-induced encephalitis.

Authors:  Kathryn Trandem; Jingxian Zhao; Erica Fleming; Stanley Perlman
Journal:  J Immunol       Date:  2011-02-11       Impact factor: 5.422

6.  Oligodendrocytes that survive acute coronavirus infection induce prolonged inflammatory responses in the CNS.

Authors:  Ruangang Pan; Qinran Zhang; Scott M Anthony; Yu Zhou; Xiufen Zou; Martin Cassell; Stanley Perlman
Journal:  Proc Natl Acad Sci U S A       Date:  2020-06-22       Impact factor: 11.205

7.  Age-Associated Resident Memory CD8 T Cells in the Central Nervous System Are Primed To Potentiate Inflammation after Ischemic Brain Injury.

Authors:  Rodney M Ritzel; Joshua Crapser; Anita R Patel; Rajkumer Verma; Jeremy M Grenier; Anjali Chauhan; Evan R Jellison; Louise D McCullough
Journal:  J Immunol       Date:  2016-03-09       Impact factor: 5.422

8.  The cellular redox environment alters antigen presentation.

Authors:  Jonathan A Trujillo; Nathan P Croft; Nadine L Dudek; Rudragouda Channappanavar; Alex Theodossis; Andrew I Webb; Michelle A Dunstone; Patricia T Illing; Noah S Butler; Craig Fett; David C Tscharke; Jamie Rossjohn; Stanley Perlman; Anthony W Purcell
Journal:  J Biol Chem       Date:  2014-08-18       Impact factor: 5.157

9.  The nsp3 macrodomain promotes virulence in mice with coronavirus-induced encephalitis.

Authors:  Anthony R Fehr; Jeremiah Athmer; Rudragouda Channappanavar; Judith M Phillips; David K Meyerholz; Stanley Perlman
Journal:  J Virol       Date:  2014-11-26       Impact factor: 5.103

10.  A T Cell Receptor Locus Harbors a Malaria-Specific Immune Response Gene.

Authors:  Natalija Van Braeckel-Budimir; Stephanie Gras; Kristin Ladell; Tracy M Josephs; Lecia Pewe; Stina L Urban; Kelly L Miners; Carine Farenc; David A Price; Jamie Rossjohn; John T Harty
Journal:  Immunity       Date:  2017-11-14       Impact factor: 31.745

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