CD4+T Cells: Differentiation and Functions

Author:

Luckheeram Rishi Vishal12,Zhou Rui123,Verma Asha Devi4,Xia Bing1235ORCID

Affiliation:

1. Department of Gastroenterology, Zhongnan Hospital, Wuhan University School of Medicine, Wuhan 430071, China

2. Center for Clinical Study of Intestinal Diseases, Zhongnan Hospital, Wuhan University School of Medicine, Wuhan 430071, China

3. Key Laboratory of Allergy and Immune-Related Diseases, Wuhan University School of Medicine, Wuhan 430071, China

4. Department of Paediatrics, Renmin Hospital, Wuhan University School of Medicine, Wuhan 430071, China

5. Clinical Centre of Intestinal and Colorectal diseases, Hubei, Wuhan 430071, China

Abstract

CD4+T cells are crucial in achieving a regulated effective immune response to pathogens. Naive CD4+T cells are activated after interaction with antigen-MHC complex and differentiate into specific subtypes depending mainly on the cytokine milieu of the microenvironment. Besides the classical T-helper 1 and T-helper 2, other subsets have been identified, including T-helper 17, regulatory T cell, follicular helper T cell, and T-helper 9, each with a characteristic cytokine profile. For a particular phenotype to be differentiated, a set of cytokine signaling pathways coupled with activation of lineage-specific transcription factors and epigenetic modifications at appropriate genes are required. The effector functions of these cells are mediated by the cytokines secreted by the differentiated cells. This paper will focus on the cytokine-signaling and the network of transcription factors responsible for the differentiation of naive CD4+T cells.

Publisher

Hindawi Limited

Subject

General Medicine,Immunology,Immunology and Allergy

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