Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps

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Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps. / Ma, Junjie; Tibbitt, Christopher A; Georén, Susanna Kumlien; Christian, Murray; Murrell, Ben; Cardell, Lars-Olaf; Bachert, Claus; Coquet, Jonathan M.

In: Science immunology, Vol. 6, No. 62, 13.08.2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ma, J, Tibbitt, CA, Georén, SK, Christian, M, Murrell, B, Cardell, L-O, Bachert, C & Coquet, JM 2021, 'Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps', Science immunology, vol. 6, no. 62. https://doi.org/10.1126/sciimmunol.abg6356

APA

Ma, J., Tibbitt, C. A., Georén, S. K., Christian, M., Murrell, B., Cardell, L-O., Bachert, C., & Coquet, J. M. (2021). Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps. Science immunology, 6(62). https://doi.org/10.1126/sciimmunol.abg6356

Vancouver

Ma J, Tibbitt CA, Georén SK, Christian M, Murrell B, Cardell L-O et al. Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps. Science immunology. 2021 Aug 13;6(62). https://doi.org/10.1126/sciimmunol.abg6356

Author

Ma, Junjie ; Tibbitt, Christopher A ; Georén, Susanna Kumlien ; Christian, Murray ; Murrell, Ben ; Cardell, Lars-Olaf ; Bachert, Claus ; Coquet, Jonathan M. / Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps. In: Science immunology. 2021 ; Vol. 6, No. 62.

Bibtex

@article{9832b9929180497a86cf76eb2e527f6a,
title = "Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps",
abstract = "Chronic rhinosinusitis with nasal polyps (CRSwNP) is characterized by a chronic inflammatory process often associated with comorbid asthma. In this study, we analyzed the transcriptomes of single T helper (TH) cells from nasal polyps of patients with CRSwNP and validated these findings using multiparameter flow cytometry. Polyp tissue contained suppressive T regulatory (Treg) cells, TH2 cells, type 2 innate lymphoid cells, and three transcriptionally distinct subsets of cytotoxic CD4+ T cells (CD4+ CTL). GATA3 expression was a feature of polyp Treg cells, whereas TH2 cells highly expressed TCN1, CD200R, and HPGDS and were enriched for genes involved in lipid metabolism. Only a portion of polyp TH2 cells expressed the prostaglandin D2 receptor CRTH2, whereas a subpopulation of CD109+CRTH2- TH2 cells expressed mRNA for common inhibitor receptors including LAG3 and TIM3 and produced IL-10. Together, we resolved the complexity of TH cells in patients with CRSwNP, identifying several distinct clusters of CD4+ CTL and a population of CD109+CRTH2- TH2 cells with putative regulatory potential.",
keywords = "Antigens, CD/immunology, CD4-Positive T-Lymphocytes/immunology, GPI-Linked Proteins/immunology, Humans, Interleukin-10/immunology, Nasal Polyps/immunology, Neoplasm Proteins/immunology, Single-Cell Analysis, T-Lymphocytes, Cytotoxic/immunology, Th2 Cells/immunology",
author = "Junjie Ma and Tibbitt, {Christopher A} and Geor{\'e}n, {Susanna Kumlien} and Murray Christian and Ben Murrell and Lars-Olaf Cardell and Claus Bachert and Coquet, {Jonathan M}",
note = "Copyright {\textcopyright} 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.",
year = "2021",
month = aug,
day = "13",
doi = "10.1126/sciimmunol.abg6356",
language = "English",
volume = "6",
journal = "Advances in Immunology",
issn = "0065-2776",
publisher = "American Association for the Advancement of Science",
number = "62",

}

RIS

TY - JOUR

T1 - Single-cell analysis pinpoints distinct populations of cytotoxic CD4+ T cells and an IL-10+CD109+ TH2 cell population in nasal polyps

AU - Ma, Junjie

AU - Tibbitt, Christopher A

AU - Georén, Susanna Kumlien

AU - Christian, Murray

AU - Murrell, Ben

AU - Cardell, Lars-Olaf

AU - Bachert, Claus

AU - Coquet, Jonathan M

N1 - Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

PY - 2021/8/13

Y1 - 2021/8/13

N2 - Chronic rhinosinusitis with nasal polyps (CRSwNP) is characterized by a chronic inflammatory process often associated with comorbid asthma. In this study, we analyzed the transcriptomes of single T helper (TH) cells from nasal polyps of patients with CRSwNP and validated these findings using multiparameter flow cytometry. Polyp tissue contained suppressive T regulatory (Treg) cells, TH2 cells, type 2 innate lymphoid cells, and three transcriptionally distinct subsets of cytotoxic CD4+ T cells (CD4+ CTL). GATA3 expression was a feature of polyp Treg cells, whereas TH2 cells highly expressed TCN1, CD200R, and HPGDS and were enriched for genes involved in lipid metabolism. Only a portion of polyp TH2 cells expressed the prostaglandin D2 receptor CRTH2, whereas a subpopulation of CD109+CRTH2- TH2 cells expressed mRNA for common inhibitor receptors including LAG3 and TIM3 and produced IL-10. Together, we resolved the complexity of TH cells in patients with CRSwNP, identifying several distinct clusters of CD4+ CTL and a population of CD109+CRTH2- TH2 cells with putative regulatory potential.

AB - Chronic rhinosinusitis with nasal polyps (CRSwNP) is characterized by a chronic inflammatory process often associated with comorbid asthma. In this study, we analyzed the transcriptomes of single T helper (TH) cells from nasal polyps of patients with CRSwNP and validated these findings using multiparameter flow cytometry. Polyp tissue contained suppressive T regulatory (Treg) cells, TH2 cells, type 2 innate lymphoid cells, and three transcriptionally distinct subsets of cytotoxic CD4+ T cells (CD4+ CTL). GATA3 expression was a feature of polyp Treg cells, whereas TH2 cells highly expressed TCN1, CD200R, and HPGDS and were enriched for genes involved in lipid metabolism. Only a portion of polyp TH2 cells expressed the prostaglandin D2 receptor CRTH2, whereas a subpopulation of CD109+CRTH2- TH2 cells expressed mRNA for common inhibitor receptors including LAG3 and TIM3 and produced IL-10. Together, we resolved the complexity of TH cells in patients with CRSwNP, identifying several distinct clusters of CD4+ CTL and a population of CD109+CRTH2- TH2 cells with putative regulatory potential.

KW - Antigens, CD/immunology

KW - CD4-Positive T-Lymphocytes/immunology

KW - GPI-Linked Proteins/immunology

KW - Humans

KW - Interleukin-10/immunology

KW - Nasal Polyps/immunology

KW - Neoplasm Proteins/immunology

KW - Single-Cell Analysis

KW - T-Lymphocytes, Cytotoxic/immunology

KW - Th2 Cells/immunology

U2 - 10.1126/sciimmunol.abg6356

DO - 10.1126/sciimmunol.abg6356

M3 - Journal article

C2 - 34389612

VL - 6

JO - Advances in Immunology

JF - Advances in Immunology

SN - 0065-2776

IS - 62

ER -

ID: 356968049