{
  "abstract": "Background & aims: Mucosal-associated invariant T (MAIT) cells are innate-like T lymphocytes with cytotoxic capacity and emerging roles in tumour immunity. While MAIT cells express a diverse repertoire of natural killer (NK) receptors, the functional significance of these receptors in gastrointestinal (GI) cancers remains poorly understood.\n\nMethods: We characterized the NK receptor repertoire and effector function of MAIT cells across five human GI tumour entities: hepatocellular carcinoma (HCC; n = 30), colorectal liver metastases (CRLM; n = 15), colorectal cancer (CRC; n = 17), pancreatic ductal adenocarcinoma (PDAC; n = 17), and gastric cancer (GC; n = 18), and examined the functional phenotype and cytotoxic potential of primary HCC-derived MAIT cells.\n\nResults: MAIT cell frequencies varied across tumour entities and anatomical compartments, with significant intratumoral depletion in HCC compared with matched peritumoral tissue. Across all tumour entities, tumour-infiltrating MAIT cells consistently exhibited a pronounced downregulation of the activating NK receptor NKG2D. This reduction was also evident in peripheral blood MAIT cells but notably reversed following tumour resection and correlated with clinical outcomes. Functionally, IL-15-induced cytotoxicity was impaired in HCC-derived MAIT cells independently of receptor expression, suggesting additional mechanisms of dysfunction. Mechanistically, we report the expression of the endoplasmic reticulum stress-responsive transcription factor X-box binding protein 1 XBP1s (spliced form of XBP1) in circulating and tissue-resident MAIT cells. XBP1s expression was induced by IL-15 and ER stress but was attenuated in tumour-derived compared with peritumoral MAIT cells, indicating defective ER stress signalling.\n\nConclusions: Together, these findings define a distinct dysfunctional state of tumour-resident MAIT cells in HCC, characterized by defective ER stress responses, and identify impaired NK receptor expression across GI cancers that may contribute to impaired antitumour immunity.",
  "abstract_shown": true,
  "affiliations": [
    "Department of General and Visceral Surgery, Charité - Universitätsmedizin Berlin, Campus Benjamin Franklin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.",
    "Department of Hepatobiliary Surgery and Visceral Transplantation, Clinic for Visceral, Transplant, Thoracic and Vascular Surgery, Leipzig University Medical Center, Leipzig, Germany.",
    "Department of Radiology, Charité - Universitätsmedizin Berlin, Campus Benjamin Franklin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.",
    "Department of Pathology, Vivantes Klinikum Neukölln, Berlin, Germany.",
    "Department of Visceral Surgery, Vivantes Klinikum Neukölln, Berlin, Germany.",
    "Department of Pathology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.",
    "Department of Anesthesiology and Intensive Care Medicine, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Campus Benjamin Franklin, Berlin, Germany.",
    "Department of Urology, Evangelisches Krankenhaus Königin Elisabeth Herzberge, Berlin, Germany.",
    "Medical Department, Division of Gastroenterology, Infectious Diseases and Rheumatology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.",
    "Department of Traumatology and Reconstructive Surgery, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.",
    "Department of Internal Medicine I, University Hospital Tübingen, Eberhard Karls University of Tübingen, Tübingen, Germany.",
    "Center of Digital Health, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany."
  ],
  "article_type": "research support, non u.s. gov't",
  "arxiv": null,
  "author_total": 24,
  "authors": [
    {
      "affs": [
        0
      ],
      "name": "Vanessa Proß"
    },
    {
      "affs": [
        0
      ],
      "name": "Annkathrin Helena Ruhm"
    },
    {
      "affs": [
        0
      ],
      "name": "Linda Marie Laura Thole"
    },
    {
      "affs": [
        0
      ],
      "name": "Laura Tóth"
    },
    {
      "affs": [
        0
      ],
      "name": "Gishnu Harikumar Parvathy",
      "orcid": "0009-0004-3524-9102"
    },
    {
      "affs": [
        0
      ],
      "name": "Pia Jäger"
    },
    {
      "affs": [
        1
      ],
      "name": "Christina Götz"
    },
    {
      "affs": [
        1
      ],
      "name": "Georg Damm"
    },
    {
      "affs": [
        1
      ],
      "name": "Daniel Seehofer"
    },
    {
      "affs": [
        2
      ],
      "name": "Christian Bayerl"
    },
    {
      "affs": [
        3
      ],
      "name": "Hermann Herbst"
    },
    {
      "affs": [
        4
      ],
      "name": "Alexander Macke"
    },
    {
      "affs": [
        4
      ],
      "name": "Verena Frese"
    },
    {
      "affs": [
        4
      ],
      "name": "Akio Sakaki"
    },
    {
      "affs": [
        4
      ],
      "name": "Marlene Hanisch-Hernandez"
    },
    {
      "affs": [
        5
      ],
      "name": "Friederike Rosseck"
    },
    {
      "affs": [
        6
      ],
      "name": "Sascha Treskatsch"
    },
    {
      "affs": [
        7
      ],
      "name": "Frank Friedersdorff"
    },
    {
      "affs": [
        8
      ],
      "name": "Christoph Treese"
    },
    {
      "affs": [
        8
      ],
      "name": "Severin Daum"
    },
    {
      "affs": [
        9
      ],
      "name": "Dominik Laue"
    },
    {
      "affs": [
        10
      ],
      "name": "Benjamin Ruf"
    },
    {
      "affs": [
        11
      ],
      "name": "Sören Lukassen"
    },
    {
      "affs": [
        0
      ],
      "name": "Katja Kotsch"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/929z824tdytwf.bib",
  "cited_by": 0,
  "doi": "10.3389/fimmu.2026.1924000",
  "fulltext_url": "https://europepmc.org/articles/PMC13677909",
  "id": "929z824tdytwf",
  "issns": [
    "1664-3224"
  ],
  "landing_url": "https://www.frontiersin.org/articles/10.3389/fimmu.2026.1924000/full",
  "language": "eng",
  "licence": "CC-BY-4.0",
  "licence_label": "CC BY 4.0",
  "licence_source": "article",
  "licence_url": "https://creativecommons.org/licenses/by/4.0/",
  "metadata_licence": null,
  "native_subjects": [
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      "2403|Immune Cell Function and Interaction"
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  "openalex": "W7220451621",
  "pdf_url": "https://europepmc.org/articles/PMC13677909?pdf=render",
  "pmcid": "PMC13677909",
  "pmid": "42898377",
  "published": "2026-10-05",
  "publisher": "Frontiers Media SA",
  "ris": "https://research.draconitic.com/paper/929z824tdytwf.ris",
  "sources": [
    {
      "first_seen": "2026-10-30T12:19:15Z",
      "native_id": "10.3389/fimmu.2026.1924000",
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      "url": "https://www.frontiersin.org/articles/10.3389/fimmu.2026.1924000/full"
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  "subjects": [
    {
      "field": "biology",
      "origin": "openalex:2403|Immune Cell Function and Interaction",
      "subfield": "immunology"
    }
  ],
  "title": "Comparative profiling of MAIT cells across gastrointestinal cancers identifies conserved NK receptor dysregulation and HCC-specific defects in cytotoxicity and XBP1s signaling",
  "title_text": "Comparative profiling of MAIT cells across gastrointestinal cancers identifies conserved NK receptor dysregulation and HCC-specific defects in cytotoxicity and XBP1s signaling",
  "type": "peer-reviewed",
  "updated_at": "2026-10-30T12:19:37Z",
  "url": "https://research.draconitic.com/paper/929z824tdytwf",
  "venue": "Frontiers in Immunology",
  "versions": []
}