Literature DB >> 17433873

Requirements for CD8 T-cell priming, memory generation and maintenance.

Martin Prlic1, Matthew A Williams, Michael J Bevan.   

Abstract

Immunological memory is characterized by the ability to provide protection from secondary exposure to pathogens. CD8(+) memory T cells provide protection from cell-associated antigens owing to their elevated frequency, rapid response and localization to sites of infection. Events occurring during primary exposure to antigen can impact not only the magnitude and quality of the initial cytotoxic T lymphocyte response but also the efficacy and longevity of the ensuing CD8(+) memory pool. Recent advances shed light on the relative roles of TCR signals and environmental cues in guiding the development of CD8(+) effector T cells into CD8(+) memory T cells and supporting CD8(+) memory T-cell maintenance.

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Year:  2007        PMID: 17433873     DOI: 10.1016/j.coi.2007.04.010

Source DB:  PubMed          Journal:  Curr Opin Immunol        ISSN: 0952-7915            Impact factor:   7.486


  65 in total

Review 1.  Nature and nurture: T-cell receptor-dependent and T-cell receptor-independent differentiation cues in the selection of the memory T-cell pool.

Authors:  Chulwoo Kim; Matthew A Williams
Journal:  Immunology       Date:  2010-08-25       Impact factor: 7.397

Review 2.  The persistence of T cell memory.

Authors:  Mark A Daniels; Emma Teixeiro
Journal:  Cell Mol Life Sci       Date:  2010-04-04       Impact factor: 9.261

3.  Manipulating Memory CD8 T Cell Numbers by Timed Enhancement of IL-2 Signals.

Authors:  Marie T Kim; Samarchith P Kurup; Gabriel R Starbeck-Miller; John T Harty
Journal:  J Immunol       Date:  2016-07-20       Impact factor: 5.422

4.  Rapid culling of the CD4+ T cell repertoire in the transition from effector to memory.

Authors:  Matthew A Williams; Eugene V Ravkov; Michael J Bevan
Journal:  Immunity       Date:  2008-03-20       Impact factor: 31.745

5.  Exploring regulatory mechanisms of CD8+ T cell contraction.

Authors:  Martin Prlic; Michael J Bevan
Journal:  Proc Natl Acad Sci U S A       Date:  2008-10-22       Impact factor: 11.205

6.  CD69 guides CD4+ T cells to the seat of memory.

Authors:  Stephen P Schoenberger
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-21       Impact factor: 11.205

7.  CD8 memory T cells have a bioenergetic advantage that underlies their rapid recall ability.

Authors:  Gerritje J W van der Windt; David O'Sullivan; Bart Everts; Stanley Ching-Cheng Huang; Michael D Buck; Jonathan D Curtis; Chih-Hao Chang; Amber M Smith; Teresa Ai; Brandon Faubert; Russell G Jones; Edward J Pearce; Erika L Pearce
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-12       Impact factor: 11.205

8.  The proteosomal degradation of fusion proteins cannot be predicted from the proteosome susceptibility of their individual components.

Authors:  Petr O Ilyinskii; Anatoli B Meriin; Vladimir L Gabai; Evgeny V Usachev; Alexei G Prilipov; Galini Thoidis; Alexander M Shneider
Journal:  Protein Sci       Date:  2008-04-14       Impact factor: 6.725

9.  The magnitude of CD4+ T cell recall responses is controlled by the duration of the secondary stimulus.

Authors:  Eugene V Ravkov; Matthew A Williams
Journal:  J Immunol       Date:  2009-07-15       Impact factor: 5.422

10.  Stability and function of secondary Th1 memory cells are dependent on the nature of the secondary stimulus.

Authors:  Chulwoo Kim; David C Jay; Matthew A Williams
Journal:  J Immunol       Date:  2012-07-27       Impact factor: 5.422

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