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Cited by 1,798

The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.

CD4 T cells: fates, functions, and faults

Open access
Zhu, Jinfang, Paul, William E.·2008·Blood

Abstract

In 1986, Mosmann and Coffman identified 2 subsets of activated CD4 T cells, Th1 and Th2 cells, which differed from each other in their pattern of cytokine production and their functions. Our understanding of the importance of the distinct differentiated forms of CD4 T cells and of the mechanisms through which they achieve their differentiated state has greatly expanded over the past 2 decades. Today at least 4 distinct CD4 T-cell subsets have been shown to exist, Th1, Th2, Th17, and iTreg cells. Here we summarize much of what is known about the 4 subsets, including the history of their discovery, their unique cytokine products and related functions, their distinctive expression of cell surface receptors and their characteristic transcription factors, the regulation of their fate determination, and the consequences of their abnormal activation.

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Crossref · 10.1182/blood-2008-05-078154

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Metadata

Authors
Zhu, J., & Paul, W. E.
Venue
Blood
Published
2008-09-01
Volume
112
Issue
5
Pages
1557-1569
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W1965734808
Cited by
1,798
References
35
FWCI
45.18
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: CD4 T cells: fates, functions, and faults. https://app.cochat.ai/papers/10.1182/blood-2008-05-078154
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Zhu, J., & Paul, W. E. (2008). CD4 T cells: fates, functions, and faults. Blood. https://doi.org/10.1182/blood-2008-05-078154

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.