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February 14, 2026Frontiers in Immunology1 citationsOpen Access

NKG2D CAR-T cells for solid tumor immunotherapy: advances, challenges, and future directions

CLChen LiuZWZhiqiang WangWZWentao Zhang

Key Points

  • This review aims to evaluate the effectiveness of NKG2D CAR-T cells in treating solid tumors against the challenges posed by the tumor microenvironment.
  • Reviewed recent literature on NKG2D CAR-T cell advancements.
  • Analyzed innovations in CAR architecture and signaling pathways.
  • Examined combination immunotherapy approaches and armored CAR constructs.
  • NKG2D CAR-T cells target stress-induced ligands on tumor cells effectively.
  • Advancements in CAR architecture enhance T-cell function in the tumor microenvironment.
  • Combination therapies show promise in addressing immunosuppressive barriers.

Abstract

Chimeric antigen receptor (CAR) T-cell therapy has achieved significant success in hematologic malignancies, but its efficacy in solid tumors remains limited, primarily due to the immunosuppressive tumor microenvironment (TME) that hinders CAR-T cell trafficking and function. NKG2D CAR-T cells, which target stress-induced NKG2D ligands (NKG2DLs) broadly expressed on tumor cells, have shown promising potential in overcoming the immunosuppressive barriers of the solid TME. This review highlights recent advances in NKG2D CAR-T cell strategies for solid tumors, including innovations in CAR architecture, signaling pathway engineering, combination immunotherapy, and the development of armored CAR constructs. We further discuss the therapeutic potential, current challenges, and future directions of these approaches to inform the design of more effective and durable CAR-T cell therapies for solid tumors.

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Cite This Study

Liu et al. (2026) studied this question.

synapsesocial.com/papers/699010382ccff479cfe56ba1https://doi.org/10.3389/fimmu.2026.1763843
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