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Inflammatory cytokine-mediated evasion of virus-induced tumors from NK cell control.

ABSTRACT: Infections with DNA tumor viruses, including members of the polyomavirus family, often result in tumor formation in immune-deficient hosts. The complex control involved in antiviral and antitumor immune responses during these infections can be studied in murine polyomavirus (PyV)-infected mice as a model. We found that NK cells efficiently kill cells derived from PyV-induced salivary gland tumors in vitro in an NKG2D (effector cell)-RAE-1 (target cell)-dependent manner; but in T cell-deficient mice, NK cells only delay but do not prevent the development of PyV-induced tumors. In this article, we show that the PyV-induced tumors have infiltrating functional NK cells. The freshly removed tumors, however, lack surface RAE-1 expression, and the tumor tissues produce soluble factors that downregulate RAE-1. These factors include the proinflammatory cytokines IL-1?, IL-1?, IL-33, and TNF. Each of these cytokines downregulates RAE-1 expression and susceptibility to NK cell-mediated cytotoxicity. CD11b(+)F4/80(+) macrophages infiltrating the PyV-induced tumors produce high amounts of IL-1? and TNF. Thus, our data suggest a new mechanism whereby inflammatory cytokines generated in the tumor environment lead to evasion of NK cell-mediated control of virus-induced tumors.

SUBMITTER: Mishra R

PROVIDER: S-EPMC3711091 | biostudies-literature | 2013 Jul

REPOSITORIES: biostudies-literature

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Inflammatory cytokine-mediated evasion of virus-induced tumors from NK cell control.

Mishra Rabinarayan R Polic Bojan B Welsh Raymond M RM Szomolanyi-Tsuda Eva E

Journal of immunology (Baltimore, Md. : 1950) 20130614 2

Infections with DNA tumor viruses, including members of the polyomavirus family, often result in tumor formation in immune-deficient hosts. The complex control involved in antiviral and antitumor immune responses during these infections can be studied in murine polyomavirus (PyV)-infected mice as a model. We found that NK cells efficiently kill cells derived from PyV-induced salivary gland tumors in vitro in an NKG2D (effector cell)-RAE-1 (target cell)-dependent manner; but in T cell-deficient m ...[more]

PMID: 23772039

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Inflammatory cytokine-mediated evasion of virus-induced tumors from NK cell control.

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Inflammatory cytokine-mediated evasion of virus-induced tumors from NK cell control.

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