Cited by 189T-cell and B-cell ImmunologyPsoriasis: Treatment and PathogenesisImmunotherapy and Immune Responses

Human CD4+ T cell recent thymic emigrants are identified by protein tyrosine kinase 7 and have reduced immune function

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Haines, Christopher J., Giffon, Thierry D., Lu, Li-Sheng, Lu, Xiaowei, Tessier-Lavigne, Marc, Ross, Douglas T., Lewis, David B.·2009·Journal of Experimental Medicine

Abstract

CD4+ recent thymic emigrants (RTEs) comprise a clinically and immunologically important T cell population that indicates thymic output and that is essential for maintaining a diverse αβ–T cell receptor (TCR) repertoire of the naive CD4+ T cell compartment. However, their frequency and function are poorly understood because no known surface markers distinguish them from older non-RTE naive CD4+ T cells. We demonstrate that protein tyrosine kinase 7 (PTK7) is a novel marker for human CD4+ RTEs. Consistent with their recent thymic origin, human PTK7+ RTEs contained higher levels of signal joint TCR gene excision circles and were more responsive to interleukin (IL)-7 compared with PTK7− naive CD4+ T cells, and rapidly decreased after complete thymectomy. Importantly, CD4+ RTEs proliferated less and produced less IL-2 and interferon-γ than PTK7− naive CD4+ T cells after αβ-TCR/CD3 and CD28 engagement. This immaturity in CD4+ RTE effector function may contribute to the reduced CD4+ T cell immunity observed in contexts in which CD4+ RTEs predominate, such as in the fetus and neonate or after immune reconstitution. The ability to identify viable CD4+ RTEs by PTK7 staining should be useful for monitoring thymic output in both healthy individuals and in patients with genetic or acquired CD4+ T cell immunodeficiencies.

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  • Protein tyrosine kinase 7 and CD31 are expressed on a subpopulation of naive cells in children and young adults, are lost with homeostatic proliferation, and decline with age.

    “The cell surface molecules protein tyrosine kinase 7 and CD31, expressed on a subpopulation of naive cells in children and young adults, are lost with homeostatic proliferation and decline with age”

    From Successful and Maladaptive T Cell Aging (2017) · cites this paper as Haines et al., 2009

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Authors
Haines, C. J., Giffon, T. D., Lu, L.-S., Lu, X., Tessier-Lavigne, M., Ross, D. T., & Lewis, D. B.
Affiliations
  • Howard Hughes Medical Institute (US)
  • Department of Pediatrics and the Immunology Program 1 , 2 , and 3
Corresponding author
Lewis, David B.
Venue
Journal of Experimental Medicine
Published
2009-01-26
Volume
206
Issue
2
Pages
275-285
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2112729981
Cited by
189
References
30
Citations by year
2026: 5 · 2025: 7 · 2024: 9 · 2023: 6 · 2022: 6 · 2021: 8 · 2020: 8 · 2019: 7 · 2018: 22 · 2017: 10 · 2016: 10 · 2015: 14 · 2014: 9 · 2013: 22 · 2012: 17
FWCI
6.61
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • The Journal of Experimental Medicine (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
National Institute of Allergy and Infectious Diseases (T32AI007290)
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 › Immunotherapy and Immune Responses
Keywords
recent thymic emigrants, CD4+ T cells, PTK7, naive T cells, thymic output, IL-7, T cell proliferation, interleukin-2, interferon-gamma, thymectomy, T cell deficiency, immune reconstitution
MeSH terms
Age Factors, Animals, Cell Movement, Cricetulus, Flow Cytometry, Cricetinae, Humans, Immunity, Cellular, Thymus Gland, Biomarkers, CD4-Positive T-Lymphocytes, Cell Adhesion Molecules, Immunophenotyping, CHO Cells, DNA Primers, Receptor Protein-Tyrosine Kinases

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