MHC class I on target cells regulates CD4+ T cell-mediated immunity
Year: 2026
Type: article
Abstract: Major histocompatibility complex (MHC) class I and class II molecules present antigens to CD8 + and CD4 + T cells respectively. Here we uncover a previously unrecognized role for MHC class I in modulating CD4 + T cell-mediated immunity. In allogeneic graft-versus-host disease and tumor models, we demonstrate that the absence of MHC class I on target cells significantly increases their susceptibility to CD4 + T cell cytotoxicity. Transcriptomic and functional studies suggest that this was because of heightened sensitivity to enhanced ferroptosis of the target cells. In large human transcriptomic and sequencing datasets, a role for CD4 + T cells in enhancing immune checkpoint blocker-mediated responses in persons with melanoma and mismatch-repair-deficient colon cancers that have downregulated MHC class I was suggested. These findings revise and expand the known role of MHC class I in CD8 + T cell and natural killer cell immunity and demonstrate a previously unrecognized role in CD4 + T cell-mediated cancer and alloimmunity.
Source: Nature Immunology
Language: English
Topic: T-cell and B-cell Immunology
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $12,690
Awards: CyTOF XT with Hyperion XTi platform, Recruitment of Established Investigators, COPII dependent regulation of T cell alloimmunity, G9000014016, G9000108883, G9000170858, G9000258367, Baylor College of Medicine Cancer Center - Cancer Center Support Grant, BD FACSDiscover S8 Spectral and Imaging Cell Sorter
OpenAlex ID: W7140187132
