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Requirements for the differentiation of innate T-bethigh memory-phenotype CD4+ T lymphocytes under steady state
by
Trinchieri, Giorgio
, Hilligan, Kerry
, Yamane, Hidehiro
, Kawajiri, Akihisa
, Zhu, Jinfang
, Jankovic, Dragana
, Ishii, Naoto
, Yi, Jaeu
, Kim, Kwang Soon
, Kawabe, Takeshi
, Fang, Difeng
, Sher, Alan
in
13/21
/ 13/31
/ 14/19
/ 631/250/1619/554/1898
/ 631/250/2152/1566/1571
/ 631/250/2504
/ 631/250/254
/ 64/60
/ Antigens
/ CD4 antigen
/ CD40 antigen
/ CD40L protein
/ Cell differentiation
/ Dendritic cells
/ Effector cells
/ Genotype & phenotype
/ Homeostasis
/ Humanities and Social Sciences
/ Immunological memory
/ Interleukin 12
/ Lymphocytes
/ Lymphocytes T
/ Memory cells
/ multidisciplinary
/ MyD88 protein
/ Phenotypes
/ Science
/ Science (multidisciplinary)
/ Self-recognition
/ Subpopulations
2020
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Requirements for the differentiation of innate T-bethigh memory-phenotype CD4+ T lymphocytes under steady state
by
Trinchieri, Giorgio
, Hilligan, Kerry
, Yamane, Hidehiro
, Kawajiri, Akihisa
, Zhu, Jinfang
, Jankovic, Dragana
, Ishii, Naoto
, Yi, Jaeu
, Kim, Kwang Soon
, Kawabe, Takeshi
, Fang, Difeng
, Sher, Alan
in
13/21
/ 13/31
/ 14/19
/ 631/250/1619/554/1898
/ 631/250/2152/1566/1571
/ 631/250/2504
/ 631/250/254
/ 64/60
/ Antigens
/ CD4 antigen
/ CD40 antigen
/ CD40L protein
/ Cell differentiation
/ Dendritic cells
/ Effector cells
/ Genotype & phenotype
/ Homeostasis
/ Humanities and Social Sciences
/ Immunological memory
/ Interleukin 12
/ Lymphocytes
/ Lymphocytes T
/ Memory cells
/ multidisciplinary
/ MyD88 protein
/ Phenotypes
/ Science
/ Science (multidisciplinary)
/ Self-recognition
/ Subpopulations
2020
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Do you wish to request the book?
Requirements for the differentiation of innate T-bethigh memory-phenotype CD4+ T lymphocytes under steady state
by
Trinchieri, Giorgio
, Hilligan, Kerry
, Yamane, Hidehiro
, Kawajiri, Akihisa
, Zhu, Jinfang
, Jankovic, Dragana
, Ishii, Naoto
, Yi, Jaeu
, Kim, Kwang Soon
, Kawabe, Takeshi
, Fang, Difeng
, Sher, Alan
in
13/21
/ 13/31
/ 14/19
/ 631/250/1619/554/1898
/ 631/250/2152/1566/1571
/ 631/250/2504
/ 631/250/254
/ 64/60
/ Antigens
/ CD4 antigen
/ CD40 antigen
/ CD40L protein
/ Cell differentiation
/ Dendritic cells
/ Effector cells
/ Genotype & phenotype
/ Homeostasis
/ Humanities and Social Sciences
/ Immunological memory
/ Interleukin 12
/ Lymphocytes
/ Lymphocytes T
/ Memory cells
/ multidisciplinary
/ MyD88 protein
/ Phenotypes
/ Science
/ Science (multidisciplinary)
/ Self-recognition
/ Subpopulations
2020
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Requirements for the differentiation of innate T-bethigh memory-phenotype CD4+ T lymphocytes under steady state
Journal Article
Requirements for the differentiation of innate T-bethigh memory-phenotype CD4+ T lymphocytes under steady state
2020
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Overview
CD4
+
T lymphocytes consist of naïve, antigen-specific memory, and memory-phenotype (MP) cell compartments at homeostasis. We recently showed that MP cells exert innate-like effector function during host defense, but whether MP CD4
+
T cells are functionally heterogeneous and, if so, what signals specify the differentiation of MP cell subpopulations under homeostatic conditions is still unclear. Here we characterize MP lymphocytes as consisting of T-bet
high
, T-bet
low
, and T-bet
−
subsets, with innate, Th1-like effector activity exclusively associated with T-bet
high
cells. We further show that the latter population depends on IL-12 produced by CD8α
+
type 1 dendritic cells (DC1) for its differentiation. Finally, our data demonstrate that this tonic IL-12 production requires TLR-MyD88 signaling independent of foreign agonists, and is further enhanced by CD40-CD40L interactions between DC1 and CD4
+
T lymphocytes. We propose that optimal differentiation of T-bet
high
MP lymphocytes at homeostasis is driven by self-recognition signals at both the DC and Tcell levels.
CD4
+
T cells contain a T-bet
high
memory-phenotype (MP) population with innate-like functions. Here the authors characterize the requirements for their differentiation at homeostasis and identify a function for IL-12 that is tonically produced by type 1 dendritic cells in an MyD88- and CD40-dependent, but foreign PAMP-independent manner.
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