Hidden Memories: Frontline Memory T Cells and Early Pathogen Interception

被引:118
作者
Masopust, David [2 ]
Picker, Louis J. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Vaccine & Gene Therapy Inst, Beaverton, OR 97006 USA
[2] Univ Minnesota, Ctr Immunol, Dept Microbiol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
PERIPHERAL-TISSUES; PROMOTES DIFFERENTIATION; INTESTINAL EPITHELIUM; PROTECTIVE IMMUNITY; NONLYMPHOID TISSUE; VIRUS-INFECTIONS; RESIDENT MEMORY; CUTTING EDGE; EFFECTOR; PHENOTYPE;
D O I
10.4049/jimmunol.1102695
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunologic memory reflects the ability of a host to more effectively respond to a re-encounter with a particular pathogen than the first encounter, and when a vaccine mimics the first encounter, comprises the basis of vaccine efficacy. For T cells, memory is often equated with the anamnestic response, the ability of secondary lymphoid tissue-based (central) memory T cells to respond to pathogen exposure with a more rapid and higher magnitude production and infection-site delivery of pathogen-specific effector cells than observed in naive hosts. However, increasing evidence supports a fundamentally different kind of T cell memory in which differentiated, long-lived effector memory T cells, prepositioned in sites of potential pathogen invasion or rapidly mobilized to such sites from blood and marginated pools, intercept and potentially control/eliminate pathogen within hours of infection. In this article, we review the evidence for this "hidden" T cell memory and its implication for vaccine development. The Journal of Immunology, 2012, 188: 5811-5817.
引用
收藏
页码:5811 / 5817
页数:7
相关论文
共 66 条
[1]   Immunological memory and protective immunity: Understanding their relation [J].
Ahmed, R ;
Gray, D .
SCIENCE, 1996, 272 (5258) :54-60
[2]   Memory CD8+ T cells vary in differentiation phenotype in different persistent virus infections [J].
Appay, V ;
Dunbar, PR ;
Callan, M ;
Klenerman, P ;
Gillespie, GMA ;
Papagno, L ;
Ogg, GS ;
King, A ;
Lechner, F ;
Spina, CA ;
Little, S ;
Havlir, DV ;
Richman, DD ;
Gruener, N ;
Pape, G ;
Waters, A ;
Easterbrook, P ;
Salio, M ;
Cerundolo, V ;
McMichael, AJ ;
Rowland-Jones, SL .
NATURE MEDICINE, 2002, 8 (04) :379-385
[3]   Recall proliferation potential of memory CD8+ T cells and antiviral protection [J].
Bachmann, MF ;
Wolint, P ;
Schwarz, K ;
Oxenius, A .
JOURNAL OF IMMUNOLOGY, 2005, 175 (07) :4677-4685
[4]   Initial T cell receptor transgenic cell precursor frequency dictates critical aspects of the CD8+ T cell response to infection [J].
Badovinac, Vladimir P. ;
Haring, Jodie S. ;
Harty, John T. .
IMMUNITY, 2007, 26 (06) :827-841
[5]   CD69 Suppresses Sphingosine 1-Phosophate Receptor-1 (S1P1) Function through Interaction with Membrane Helix 4 [J].
Bankovich, Alexander J. ;
Shiow, Lawrence R. ;
Cyster, Jason G. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (29) :22328-22337
[6]   Endogenous naive CD8+ T cell precursor frequency regulates primary and memory responses to infection [J].
Bar, Joshua J. ;
Khanna, Kamal M. ;
Lefrancois, Leo .
IMMUNITY, 2008, 28 (06) :859-869
[7]   Memory T cells as an occupying force [J].
Bevan, Michael J. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2011, 41 (05) :1192-1195
[8]   Orchestrating the orchestrators: chemokines in control of T cell traffic [J].
Bromley, Shannon K. ;
Mempel, Thorsten R. ;
Luster, Andrew D. .
NATURE IMMUNOLOGY, 2008, 9 (09) :970-980
[9]   Chemokine receptor CCR7 guides T cell exit from peripheral tissues and entry into afferent lymphatics [J].
Bromley, SK ;
Thomas, SY ;
Luster, AD .
NATURE IMMUNOLOGY, 2005, 6 (09) :895-901
[10]   Lymphocyte homing and homeostasis [J].
Butcher, EC ;
Picker, LJ .
SCIENCE, 1996, 272 (5258) :60-66