TY - JOUR
T1 - CD8+ tissue-resident memory T-cell development depends on infection-matching regulatory T-cell types
AU - Barros, Leandro
AU - Piontkivska, Daryna
AU - Figueiredo-Campos, Patrícia
AU - Fanczal, Júlia
AU - Ribeiro, Sofia Pereira
AU - Baptista, Marta
AU - Ariotti, Silvia
AU - Santos, Nuno
AU - Amorim, Maria João
AU - Pereira, Cristina Silva
AU - Veldhoen, Marc
AU - Ferreira, Cristina
N1 - Funding Information:
We would like to thank the excellent contributions from the iMM flow cytometry, rodent, and microscopy facilities. The project that gave rise to these results has received funding from the following sources:”la Caixa” Foundation under the grant agreement LCF/PR/HR19/52160005; European Union’s Horizon 2020 Research and Innovation Programme under grant agreements No 667824; FCT - Portuguese Foundation for Science and Technology under grant agreements (PD/BD/138847/2018) (COVID/BD/152538/2022) (L.B.) SFRH/BD/131605/2017 (P.F-C), COMPETE LISBOA-01-0145-FEDER-028003, and 2021.01136.CEECIND (C.F), FCT - Fundação para a Ciência e a Tecnologia, I.P., under the project LA/P/0082/2020, for work in the Veldhoen laboratory: and FCT PD/BD/135481/2018 (D.P.), UIDB/04612/2020, UIDP/04612/2020 and LA/P/0087/2020 for work in the Silva Pereira laboratory; FCG - Fundação Calouste Gulbenkian within the Post-Graduation Programme for Science and Development (N.S.), FCT CEECIND/02373/2020 and FCG, FCT and ”la Caixa” Foundation under the grant agreement HR22-00722 for work in the Amorim laboratory. The authors wish to acknowledge Brian Chan and Pedro Papotto, Lydia Becker Institute for Immunology & Inflammation, Faculty of Biology, Medicine & Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom for the delivery of N. brasiliensis.
Funding Information:
We would like to thank the excellent contributions from the iMM flow cytometry, rodent, and microscopy facilities. The project that gave rise to these results has received funding from the following sources:”la Caixa” Foundation under the grant agreement LCF/PR/HR19/52160005; European Union’s Horizon 2020 Research and Innovation Programme under grant agreements No 667824; FCT - Portuguese Foundation for Science and Technology under grant agreements (PD/BD/138847/2018) (COVID/BD/152538/2022) (L.B.) SFRH/BD/131605/2017 (P.F-C), COMPETE LISBOA-01-0145-FEDER-028003, and 2021.01136.CEECIND (C.F), FCT - Fundação para a Ciência e a Tecnologia, I.P., under the project LA/P/0082/2020, for work in the Veldhoen laboratory: and FCT PD/BD/135481/2018 (D.P.), UIDB/04612/2020, UIDP/04612/2020 and LA/P/0087/2020 for work in the Silva Pereira laboratory; FCG - Fundação Calouste Gulbenkian within the Post-Graduation Programme for Science and Development (N.S.), FCT CEECIND/02373/2020 and FCG, FCT and ”la Caixa” Foundation under the grant agreement HR22-00722 for work in the Amorim laboratory. The authors wish to acknowledge Brian Chan and Pedro Papotto, Lydia Becker Institute for Immunology & Inflammation, Faculty of Biology, Medicine & Health, Manchester Academic Health Science Centre, University of Manchester, United Kingdom for the delivery of N. brasiliensis.
Publisher Copyright:
© 2023, Springer Nature Limited.
PY - 2023/12
Y1 - 2023/12
N2 - Immunological memory is critical for immune protection, particularly at epithelial sites, which are under constant risk of pathogen invasions. To counter invading pathogens, CD8+ memory T cells develop at the location of infection: tissue-resident memory T cells (TRM). CD8+ T-cell responses are associated with type-1 infections and type-1 regulatory T cells (TREG) are important for CD8+ T-cell development, however, if CD8+ TRM cells develop under other infection types and require immune type-specific TREG cells is unknown. We used three distinct lung infection models, to show that type-2 helminth infection does not establish CD8+ TRM cells. Intracellular (type-1) and extracellular (type-3) infections do and rely on the recruitment of response type-matching TREG population contributing transforming growth factor-β. Nevertheless, type-1 TREG cells remain the most important population for TRM cell development. Once established, TRM cells maintain their immune type profile. These results may have implications in the development of vaccines inducing CD8+ TRM cells.
AB - Immunological memory is critical for immune protection, particularly at epithelial sites, which are under constant risk of pathogen invasions. To counter invading pathogens, CD8+ memory T cells develop at the location of infection: tissue-resident memory T cells (TRM). CD8+ T-cell responses are associated with type-1 infections and type-1 regulatory T cells (TREG) are important for CD8+ T-cell development, however, if CD8+ TRM cells develop under other infection types and require immune type-specific TREG cells is unknown. We used three distinct lung infection models, to show that type-2 helminth infection does not establish CD8+ TRM cells. Intracellular (type-1) and extracellular (type-3) infections do and rely on the recruitment of response type-matching TREG population contributing transforming growth factor-β. Nevertheless, type-1 TREG cells remain the most important population for TRM cell development. Once established, TRM cells maintain their immune type profile. These results may have implications in the development of vaccines inducing CD8+ TRM cells.
UR - http://www.scopus.com/inward/record.url?scp=85170632511&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-41364-w
DO - 10.1038/s41467-023-41364-w
M3 - Article
C2 - 37696824
AN - SCOPUS:85170632511
SN - 2041-1723
VL - 14
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 5579
ER -