Precursor central memory versus effector cell fate and naïve CD4+ T cell heterogeneity Journal Article


Authors: Deep, D.; Gudjonson, H.; Brown, C. C.; Rose, S. A.; Sharma, R.; Iza, Y. A. P.; Hong, S. H.; Hemmers, S.; Schizas, M.; Wang, Z. M.; Chen, Y.; Wesemann, D. R.; Pascual, V.; Pe'er, D.; Rudensky, A. Y.
Article Title: Precursor central memory versus effector cell fate and naïve CD4+ T cell heterogeneity
Abstract: Upon antigenic stimulation, naive CD4(+) T cells can give rise to phenotypically distinct effector T helper cells and long-lived memory T cells. We computationally reconstructed the in vivo trajectory of CD4(+) T cell differentiation during a type I inflammatory immune response and identified two distinct differentiation paths for effector and precursor central memory T cells arising directly from naive CD4(+) T cells. Unexpectedly, our studies revealed heterogeneity among naive CD4(+) T cells, which are typically considered homogeneous save for their diverse T cell receptor usage. Specifically, a previously unappreciated population of naive CD4(+) T cells sensing environmental type I IFN exhibited distinct activation thresholds, suggesting that naive CD4(+) T cell differentiation potential may be influenced by environmental cues. This population was expanded in human viral infection and type I IFN response-lined autoimmunity. Understanding the relevance of naive T cell heterogeneity to beneficial and maladaptive T cell responses may have therapeutic implications for adoptive T cell therapies in cancer immunotherapy and vaccination.
Keywords: transcription factor; quiescence; expression; responses; helper; set; signals
Journal Title: Journal of Experimental Medicine
Volume: 221
Issue: 10
ISSN: 0022-1007
Publisher: Rockefeller University Press  
Date Published: 2024-09-01
Start Page: e20231193
Language: English
ACCESSION: WOS:001320409200001
DOI: 10.1084/jem.20231193
PROVIDER: wos
PMCID: PMC11448869
PUBMED: 39321257
Notes: Erratum issued, see DOI: 10.1084/jem.2023119310182024c -- The MSK Cancer Center Support Grant (P30 CA008748) is acknowledged in the PubMed record and PDF. Corresponding MSK authors are Chrysothemis C. Brown and Alexander Y. Rudensky -- Source: Wos
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MSK Authors
  1. Alexander Rudensky
    156 Rudensky
  2. Michail Schizas
    27 Schizas
  3. Dana Pe'er
    110 Pe'er
  4. Roshan Sharma
    24 Sharma
  5. Zhongmin Wang
    12 Wang
  6. Chrysothemis Celia Margaret Brown
    17 Brown
  7. Deeksha Deep
    4 Deep
  8. Samuel Adam Rose
    3 Rose