ABSTRACT
Group 2 innate lymphoid cells (ILC2s) are essential for orchestrating type 2 immune responses during allergic airway inflammation and infection. ILC2s have been reported to play a regulatory role in tumors; however, this conclusion is controversial. In this study, we showed that IL-33-activated ILC2s could boost CD8+ T-cell function through direct antigen cross-presentation. After activation by IL-33, ILC2s showed an enhanced potential to process antigens and prime CD8+ T cell activation. Activated ILC2s could phagocytose exogenous antigens in vivo and in vitro, promoting antigen-specific CD8+ T cell function to enhance antitumor immune responses. Administration of OVA-loaded ILC2s induces robust antitumor effects on the OVA-expressing tumor model. These findings suggested that the administration of tumor antigen-loaded ILC2s might serve as a potential strategy for cancer treatment.
Disclosure statement
No potential conflict of interest was reported by the authors.
Author contributions
Wen and Zhang designed the experiments and prepared the figures. J. Wen, R. Wang, Y. Zhang, S. Cheng, Y. Huang, and L. Xu performed experiments. J.Wen, Y. Zhang, and S. Cheng analyzed the data. L. Ma and Z. Ling provided material support. Wen, Sun, and Zhang interpreted the results and wrote the manuscript. B. Sun, Y. Zhang, D. Zhao and J. Xu supervised the project.
Data availability statement
The data that support the findings of this study are available from the corresponding author, B. Sun, upon reasonable request.
Supplementary material
Supplemental data for this article can be accessed online at https://doi.org/10.1080/2162402X.2023.2243112