Researchers suggested a previously unidentified method for xenogenizing tumors by using fusogenic exosomes to introduce fusogenic viral antigens onto the tumor cell surface.
The authors revealed a TGFβ–SKI–Smad4 pathway that critically and specifically directed resident CD103+CD8+ T cell generation for protective immunity against primary and secondary viral infection.
In all human cells, human leukocyte antigen (HLA) class I glycoproteins assemble with a peptide and takes it to the cell surface for surveillance by lymphocytes.
Researchers showed that IL-18BP, a high-affinity IL-18 decoy receptor, was frequently upregulated in diverse human and mouse tumors and limited the anti-tumor activity of IL-18 in mice.
Zhou, T., Damsky, W., Weizman, O.-E., McGeary, M. K., Hartmann, K. P., Rosen, C. E., … Ring, A. M. (2020). IL-18BP is a secreted immune checkpoint and barrier to IL-18 immunotherapy. Nature, 1–6. https://doi.org/10.1038/s41586-020-2422-6Cite
Investigators discuss how the role of NK cells evolves with tumor progression, presenting new opportunities to target NK cell function to enhance cancer immunotherapy response rates across a more diverse range of cancers.
Scientists describe the thymic development of NK T cells, mucosal-associated invariant T (MAIT) cells and γδ T cells and highlight some of the key differences between conventional and unconventional T cell development.
Researchers showed that peripheral infections generated antigen-specific CD8+ memory T cells in the brain that adopted a unique tissue resident memory signature.
Using a syngeneic hepatoceullar carcinoma (HCC) mouse model, the authors demonstrated that treatment with apatinib resulted in attenuation of tumor growth and increased tumor vessel normalization. Results indicated that NK cells, but not CD4+ or CD8+ T cells mediated the therapeutic efficacy of apatinib in HCC mouse models.