scholarly journals Bronchiolitis and recurrent wheezing are distinguished by type 2 innate lymphoid cells and immune response

2020 ◽  
Vol 32 (1) ◽  
pp. 51-59
Author(s):  
Beatriz Sastre ◽  
María Luz García‐García ◽  
José Antonio Cañas ◽  
Cristina Calvo ◽  
José Manuel Rodrigo‐Muñoz ◽  
...  
2020 ◽  
Author(s):  
Beatriz Sastre ◽  
María Luz García-García ◽  
José Antonio Cañas ◽  
Cristina Calvo ◽  
José Manuel Rodrigo-Muñoz ◽  
...  

2018 ◽  
Vol 138 (9) ◽  
pp. 1962-1972 ◽  
Author(s):  
David A. Rafei-Shamsabadi ◽  
Saskia van de Poel ◽  
Britta Dorn ◽  
Stefanie Kunz ◽  
Stefan F. Martin ◽  
...  

2016 ◽  
Vol 136 (9) ◽  
pp. S228
Author(s):  
D. Rafei-Shamsabadi ◽  
S. Kunz ◽  
S. Martin ◽  
C. Klose ◽  
Y. Tanriver ◽  
...  

Cancers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 3452
Author(s):  
Enrico Maggi ◽  
Irene Veneziani ◽  
Lorenzo Moretta ◽  
Lorenzo Cosmi ◽  
Francesco Annunziato

Group 2 Innate Lymphoid Cells (ILC2s) belong to the family of helper ILCs which provide host defense against infectious agents, participate in inflammatory responses and mediate lymphoid organogenesis and tissue repair, mainly at the skin and mucosal level. Based on their transcriptional, phenotypic and functional profile, ILC2s mirror the features of the adaptive CD4+ Th2 cell subset, both contributing to the so-called type 2 immune response. Similar to other ILCs, ILC2s are rapidly activated by signals deriving from tissue and/or other tissue-resident immune cells. The biologic activity of ILCs needs to be tightly regulated in order to prevent them from contributing to severe inflammation and damage in several organs. Indeed, ILC2s display both enhancing and regulatory roles in several pathophysiological conditions, including tumors. In this review, we summarize the actual knowledge about ILC2s ability to induce or impair a protective immune response, their pro- or antitumor activity in murine models, human (children and adults) pathologies and the potential strategies to improve cancer immunotherapy by exploiting the features of ILC2s.


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