Innate Memory T cells

被引:92
作者
Jameson, Stephen C. [1 ]
Lee, You Jeong [1 ]
Hogquist, Kristin A. [1 ]
机构
[1] Univ Minnesota, Sch Med, Ctr Immunol, Minneapolis, MN 55455 USA
来源
ADVANCES IN IMMUNOLOGY, VOL 126 | 2015年 / 126卷
关键词
TEC KINASE ITK; LYMPHOPENIA-INDUCED PROLIFERATION; CLASS-II MOLECULES; CD8(+) T; HOMEOSTATIC PROLIFERATION; CUTTING EDGE; NAIVE CD4; NEGATIVE REGULATION; POSITIVE SELECTION; RECEPTOR SIGNALS;
D O I
10.1016/bs.ai.2014.12.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory T cells are usually considered to be a feature of a successful immune response against a foreign antigen, and such cells can mediate potent immunity. However, in mice, alternative pathways have been described, through which naive T cells can acquire the characteristics and functions of memory T cells without encountering specific foreign antigen or the typical signals required for conventional T cell differentiation. Such cells reflect a response to the internal rather the external environment, and hence such cells are called innate memory T cells. In this review, we describe how innate memory subsets were identified, the signals that induce their generation and their functional properties and potential role in the normal immune response. The existence of innate memory T cells in mice raises questions about whether parallel populations exist in humans, and we discuss the evidence for such populations during human T cell development and differentiation.
引用
收藏
页码:173 / 213
页数:41
相关论文
共 157 条
  • [1] Derivation and Maintenance of Virtual Memory CD8 T Cells
    Akue, Adovi D.
    Lee, June-Yong
    Jameson, Stephen C.
    [J]. JOURNAL OF IMMUNOLOGY, 2012, 188 (06) : 2516 - 2523
  • [2] Development of Promyelocytic Zinc Finger and ThPOK-Expressing Innate γδ T Cells Is Controlled by Strength of TCR Signaling and Id3
    Alonzo, Eric S.
    Gottschalk, Rachel A.
    Das, Joy
    Egawa, Takeshi
    Hobbs, Robin M.
    Pandolfi, Pier Paolo
    Pereira, Pablo
    Nichols, Kim E.
    Koretzky, Gary A.
    Jordan, Martha S.
    Sant'Angelo, Derek B.
    [J]. JOURNAL OF IMMUNOLOGY, 2010, 184 (03) : 1268 - 1279
  • [3] T-Cell Signaling Regulated by the Tec Family Kinase, Itk
    Andreotti, Amy H.
    Schwartzberg, Pamela L.
    Joseph, Raji E.
    Berg, Leslie J.
    [J]. COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (07): : a002287
  • [4] The Transmembrane Adaptor Protein SIT Inhibits TCR-Mediated Signaling
    Arndt, Boerge
    Krieger, Tina
    Kalinski, Thomas
    Thielitz, Anja
    Reinhold, Dirk
    Roessner, Albert
    Schraven, Burkhart
    Simeoni, Luca
    [J]. PLOS ONE, 2011, 6 (09):
  • [5] T cell regulation as a side effect of homeostasis and competition
    Barthlott, T
    Kassiotis, G
    Stockinger, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (04) : 451 - 460
  • [6] The biology of NKT cells
    Bendelac, Albert
    Savage, Paul B.
    Teyton, Luc
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 : 297 - 336
  • [7] CD4+ T cell division in irradiated mice requires peptides distinct from those responsible for thymic selection
    Bender, J
    Mitchell, T
    Kappler, J
    Marrack, P
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (03) : 367 - 373
  • [8] Signalling through TEC kinases regulates conventional versus innate CD8+ T-cell development
    Berg, Leslie J.
    [J]. NATURE REVIEWS IMMUNOLOGY, 2007, 7 (06) : 479 - 485
  • [9] TCR-MHC class II interaction is required for peripheral expansion of CD4 cells in a T cell-deficient host
    Beutner, U
    MacDonald, HR
    [J]. INTERNATIONAL IMMUNOLOGY, 1998, 10 (03) : 305 - 310
  • [10] Selective stimulation of T cell subsets with antibody-cytokine immune complexes
    Boyman, O
    Kovar, M
    Rubinstein, MP
    Surh, CD
    Sprent, J
    [J]. SCIENCE, 2006, 311 (5769) : 1924 - 1927