Tumor-Specific T Cells Exacerbate Mortality and Immune Dysregulation during Sepsis

J Immunol. 2021 May 15;206(10):2412-2419. doi: 10.4049/jimmunol.2000865. Epub 2021 Apr 28.

Abstract

Sepsis induces significant immune dysregulation characterized by lymphocyte apoptosis and alterations in the cytokine milieu. Because cancer patients exhibit a 10-fold greater risk of developing sepsis compared with the general population, we aimed to understand how pre-existing malignancy alters sepsis-induced immune dysregulation. To address this question, we assessed the impact of tumor-specific CD8+ T cells on the immune response in a mouse model of cecal ligation and puncture (CLP)-induced sepsis. Tumor-bearing animals containing Thy1.1+ tumor-specific CD8+ T cells were subjected to CLP, and groups of animals received anti-Thy1.1 mAb to deplete tumor-specific CD8+ T cells or isotype control. Results indicated that depleting tumor-specific T cells significantly improved mortality from sepsis. The presence of tumor-specific CD8+ T cells resulted in increased expression of the 2B4 coinhibitory receptor and increased apoptosis of endogenous CD8+ T cells. Moreover, tumor-specific T cells were not reduced in number in the tumors during sepsis but did exhibit impaired IFN-γ production in the tumor, tumor draining lymph node, and spleen 24 h after CLP. Our research provides novel insight into the mechanisms by which pre-existing malignancy contributes to increased mortality during sepsis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • Cell Line, Tumor
  • Cytokines / blood
  • Immunity*
  • Interferon-gamma / metabolism
  • Lung Neoplasms / blood
  • Lung Neoplasms / complications*
  • Lung Neoplasms / immunology*
  • Lymph Nodes / immunology
  • Male
  • Melanoma, Experimental / blood
  • Melanoma, Experimental / complications*
  • Melanoma, Experimental / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Phenotype
  • Sepsis / blood
  • Sepsis / complications*
  • Sepsis / immunology*
  • Sepsis / mortality
  • Skin Neoplasms / blood
  • Skin Neoplasms / complications*
  • Skin Neoplasms / immunology*
  • Spleen / immunology
  • Thy-1 Antigens / genetics

Substances

  • Cytokines
  • IFNG protein, mouse
  • Thy-1 Antigens
  • Interferon-gamma