Frontiers in Immunology (Jul 2013)

Unique versus redundant functions of IL-1α and IL-1β in the tumor microenvironment

  • Elena eVoronov,
  • Shahar eDotan,
  • Yakov eKrelin,
  • Xiaoping eSong,
  • Moshe eElkabets,
  • Yaron eCarmi,
  • Peleg eRider,
  • Idan eCohen,
  • Marianna eRomzova,
  • Irena eKaplanov,
  • Ron Nathan Apte

DOI
https://doi.org/10.3389/fimmu.2013.00177
Journal volume & issue
Vol. 4

Abstract

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Interleukin-1 (IL-1) is a major alarm upstream pro-inflammatory cytokine that also affects immunity and hematopoiesis by inducing cytokine cascades. In the tumor arena, IL-1 is produced by malignant or microenvironment cells. As a pleiotropic cytokine, IL-1 is involved in tumorigenesis and tumor invasiveness, but also in the control of anti-tumor immunity. IL-1α and IL-1β are the major agonists of IL-1, while IL-1Ra is a physiological inhibitor of pre-formed IL-1. In their secreted form, IL-1α and IL-1β bind to the same receptors and induce the same biological functions, but IL-1α and IL-1β differ in their compartmentalization within the producing cell or the microenvironment. IL-1β is only active in its processed secreted form and mediates inflammation, which promotes carcinogenesis, tumor invasiveness and immunosuppression, whereas IL-1α is mainly cell-associated and in the tumor contest, when expressed on the cell membrane, it stimulates anti-tumor cell immunity manifested by tumor regression. It the tumor milieu, extracellular level of IL-1α is usually low and do not stimulate broad inflammation that promotes progression. Immunosuppression induced by IL-1β in the tumor microenvironment, mainly through MDSC induction, usually inhibits or masks anti-tumor cell immunity induced by cell-associated IL-1α. However, in different tumor systems, redundant or unique patterns of IL-1α and IL-1β expression and function have been observed. Recent breakthroughs in inflammasome biology and IL-1β processing/secretion have spurred the development of novel anti-IL-1 agents, which are being used in clinical trials in patients with diverse inflammatory diseases. Better understanding of the integrative role of IL-1α and IL-1β in distinct malignancies, will enable the application of novel IL-1 modulation approaches at the bedside, in cancer patients with minimal residual disease (MRD), as an adjunct to conventional approaches to reduce the tumor burden.

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