» Articles » PMID: 21362141

Tec Family Kinases: Itk Signaling and the Development of NKT αβ and γδ T Cells

Overview
Journal FEBS J
Specialty Biochemistry
Date 2011 Mar 3
PMID 21362141
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

The Tec family tyrosine kinase interleukin-2 inducible T-cell kinase (Itk) is predominantly expressed in T cells and has been shown to be critical for the development, function and differentiation of conventional αβ T cells. However, less is known about its role in nonconventional T cells such as NKT and γδ T cells. In this minireview, we discuss evidence for a role for Itk in the development of invariant NKT αβ cells, as well as a smaller population NKT-like γδ T cells. We discuss how these cells take what could be the same signaling pathway regulated by Itk, and interpret it to give different outcomes with regards to development and function.

Citing Articles

Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis.

Chiang S, Covill L, Tesi B, Campbell T, Schlums H, Nejati-Zendegani J Blood. 2024; 144(8):873-887.

PMID: 38958468 PMC: 11375501. DOI: 10.1182/blood.2024024499.


Natural Killer T Lymphocytes Integrate Innate Sensory Information and Relay Context to Effector Immune Responses.

Joyce S, Okoye G, Van Kaer L Crit Rev Immunol. 2022; 41(4):55-88.

PMID: 35381143 PMC: 11078124. DOI: 10.1615/CritRevImmunol.2021040076.


TCR Signal Strength and Antigen Affinity Regulate CD8 Memory T Cells.

Solouki S, Huang W, Elmore J, Limper C, Huang F, August A J Immunol. 2020; 205(5):1217-1227.

PMID: 32759295 PMC: 8104072. DOI: 10.4049/jimmunol.1901167.


The Role of Adaptor Proteins in the Biology of Natural Killer T (NKT) Cells.

Gerth E, Mattner J Front Immunol. 2019; 10:1449.

PMID: 31293596 PMC: 6603179. DOI: 10.3389/fimmu.2019.01449.


Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells.

Eken A, Cansever M, Somekh I, Mizoguchi Y, Zietara N, Okus F J Clin Immunol. 2019; 39(4):391-400.

PMID: 31025232 DOI: 10.1007/s10875-019-00632-5.