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The recent breakthrough in immunotherapy has emphasized the importance of stem-like CD4+ T cells as the cornerstone to impose anti-tumor immunity. Such self-renewing T cells mature into multiple distinct effector states, which are capable of maintaining long-term immune responses in tumors. Exhibiting distinctive surface proteins and transcriptional phenotypes, they enable T-cell transitions to maintain tumor control. This review covers their phenotypic and functional characteristics, state transition mechanisms, and interaction within the tumor microenvironment. We examine how tumor-reactive stem-like CD4+ T cells cause tumor regression, with particular focus on checkpoint inhibitors and CAR-T cell therapy, while addressing the prevention of immune resistance relapse and challenges to clinical translation. This review integrates novel evidence, signaling pathways, and potential interventions to highlight the pivotal role of stem-like CD4+ T cells in cancer immunotherapy.
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http://dx.doi.org/10.1016/j.intimp.2025.115432 | DOI Listing |
bioRxiv
August 2025
Laboratory of Mucosal Immunology, Rockefeller University, New York, NY 10063, USA.
Pathogen-specific CD4 T cells undergo dynamic expansion and contraction during infection, ultimately generating memory clones that shape the subsequent immune responses. However, the influence of distinct tissue environments on the differentiation and clonal selection of polyclonal T cells remains unclear, primarily because of the technical challenges in tracking these cells in vivo. To address this question, we generated Tracking Recently Activated Cell Kinetics (TRACK) mice, a dual-recombinase fate-mapping system that enables precise spatial and temporal labeling of recently activated CD4 T cells.
View Article and Find Full Text PDFiScience
September 2025
CHU Nantes, Nantes Université, INSERM, Center for Research in Transplantation and Translational Immunology, UMR 1064, ITUN, 44000 Nantes, France.
Pharmacological MEK inhibition might be an innovative approach to complete the immunosuppressive regimen that enables solid organ transplantation. While MEK inhibitors like trametinib are approved in oncology, their immunomodulatory properties remain poorly investigated in the context of organ transplantation, especially in human context. Using a human skin transplantation model in NSG mice reconstituted with third-party human PBMCs, we evaluated the effects of trametinib on graft survival and the human allogeneic immune response.
View Article and Find Full Text PDFInt Immunopharmacol
August 2025
Department of Biomedical Science, Alagappa University, Karaikudi 630003, Tamil Nadu, India.. Electronic address:
The recent breakthrough in immunotherapy has emphasized the importance of stem-like CD4+ T cells as the cornerstone to impose anti-tumor immunity. Such self-renewing T cells mature into multiple distinct effector states, which are capable of maintaining long-term immune responses in tumors. Exhibiting distinctive surface proteins and transcriptional phenotypes, they enable T-cell transitions to maintain tumor control.
View Article and Find Full Text PDFNat Aging
August 2025
Department of Medicine, Mayo Clinic Alix School of Medicine, Rochester, MN, USA.
Immune responses underlying autoimmune diseases follow the same principles that protect individuals from infection and malignancies. However, while protective immunity wanes with progressive age, the risk for autoimmune disease steadily increases; incidence rates for many autoimmune diseases peak in later life. Here, we discuss whether aging predisposes to autoimmunity, arguing that disease progression in the autoimmune vasculitis giant cell arteritis is driven by age-inappropriate sustenance of immune competence.
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