These findings provide a compelling rationale for utilizing NLRC5 overexpression in "cold" tumor models to enhance tumor susceptibility to T-cell recognition and elimination by boosting the presentation of endogenous tumor antigens. This approach holds promise for improving antitumoral immune responses in OC.
Taken together, our findings demonstrated that NLRC5 potentiates anti-tumor CD8 T cells responses by activating interferon-β in EC, suggesting that genetically escalated NLRC5 and IFN-β may act as potential candidates for the clinical translation of adjuvant immunotherapies to patients with EC.
over 1 year ago
Journal • IO biomarker
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CD8 (cluster of differentiation 8) • NLRC5 (NLR Family CARD Domain Containing 5) • IFNB1 (Interferon Beta 1)