4.5 Review

Interleukin-1β as emerging therapeutic target in hematological malignancies and potentially in their complications

Journal

BLOOD REVIEWS
Volume 31, Issue 5, Pages 306-317

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.blre.2017.05.001

Keywords

Interleukin-1 beta; Inflammation; Hematopoietic malignancies; Hematopoiesis; Preclinical models; Bone; Pain; Autoinunune diseases

Categories

Funding

  1. Northern Norway Regional Health Authority
  2. University Hospital of Northern Norway (UNN)
  3. UiT The Arctic University of Norway (UiT) [2014/5668]
  4. Young Research Talent grant from the Research Council of Norway, (Stem Cell Program) [247596]
  5. Young Research Talent grant from the Research Council of Norway (FRIPRO Program) [250901]
  6. Norwegian Cancer Society [6765150]
  7. Northern Norway Regional Health Authority [HNF1338-17]

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Interleukin-1 beta (IL-1 beta) is a pleiotropic cytokine that exerts multiple roles in both physiological and pathological conditions. It is produced by different cell subsets, and drives a wide range of inflammatory responses in numerous target cells. Enhanced IL-1 beta signaling is a common event in patients of hematological malignancies. Recent body of evidence obtained in preclinical models shows the pathogenic role of these alterations, and the promising therapeutic value of IL-1 targeting. In this review, we further highlight a potential contribution of IL-1 beta linking to complications and autoimmune disease that should be investigated in future studies. Hence, drugs that target IL-1 may be helpful to improve outcome or reduce morbidity in patients. Some of them are FDA approved, and used efficiently against autoimmune diseases, like IL-1 receptor antagonist. In the clinic, however, this agent seems to have limited properties. Current improved drugs will allow to determine the true potential of IL-1 and IL-1 beta targeting as therapy in hematological malignancies and their related complications.

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