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Plasticity of CD4+ T Cell Lineage Differentiation
Open accessAbstract
The differentiation of naive CD4(+) T cells into lineages with distinct effector functions has been considered to be an irreversible event. T helper type 1 (Th1) cells stably express IFN-gamma, whereas Th2 cells express IL-4. The discovery and investigation of two other CD4(+) T cell subsets, induced regulatory T (iTreg) cells and Th17 cells, has led to a rethinking of the notion that helper T cell subsets represent irreversibly differentiated endpoints. Accumulating evidence suggests that CD4(+) T cells, particularly iTreg and Th17 cells, are more plastic than previously appreciated. It appears that expression of Foxp3 by iTreg cells or IL-17 by Th17 cells may not be stable and that there is a great degree of flexibility in their differentiation options. Here, we will discuss recent findings that demonstrate the plasticity of CD4(+) T cell differentiation and the biological implications of this flexibility.
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“The former group encompasses functionally distinct populations including T H 1 cells responsible for host defense against intracellular microbes and implicated in systemic autoimmunity, T H 2 cells that fight off extracellular parasites and are involved in anaphylactic reactions and T H 17 cells that mediate immunity against extracellular bacteria and fungi as well as organspecific autoimmunity (Z”
From Iron in infection and immunity (2020) · cites this paper as Zhou et al., 2009
In the citing paper
“However, the current view is that CD4 Th cell subsets are not separate lineages but have plasticity and form a continuum of mixed functional capacities [177, 178].”
From Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition) (2021) · cites this paper as [177]
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Metadata
- Authors
- Zhou, L., Chong, M. M. W., & Littman, D. R.
- Affiliations
- Howard Hughes Medical Institute (US)
- New York University (US)
- Corresponding author
- Littman, Dan R.
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2009-05
- Volume
- 30
- Issue
- 5
- Pages
- 646-655
- ISSN
- 1074-7613 (ISSN-L)
- OpenAlex
- W2016827757
- Cited by
- 1,551
- References
- 101
- Citations by year
- 2026: 33 · 2025: 48 · 2024: 51 · 2023: 61 · 2022: 73 · 2021: 96 · 2020: 73 · 2019: 61 · 2018: 68 · 2017: 77 · 2016: 90 · 2015: 99 · 2014: 110 · 2013: 145 · 2012: 134
- FWCI
- 11.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1574 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Keywords
- CD4+ T cell differentiation, T cell plasticity, Th1 cells, Th2 cells, induced regulatory T cells, Th17 cells, Foxp3, IL-17, T helper cell subsets
- MeSH terms
- Animals, Cell Differentiation, T-Lymphocytes, Helper-Inducer, Humans, T-Lymphocyte Subsets, Cytokines, Cell Lineage, T-Lymphocytes, Regulatory, Forkhead Transcription Factors
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