4.2 Article

Combined blockade of IL-17A and IL-17F may prevent the development of experimental colitis

Journal

IMMUNOTHERAPY
Volume 5, Issue 9, Pages 923-925

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/imt.13.87

Keywords

Crohn's disease; IL-17A; IL-17F; secukinumab; Th17; ulcerative colitis

Categories

Funding

  1. NIH [R01 A1/DK-042316, T32 DK-067872]
  2. AHRQ [R01 HS-018975]
  3. AGENCY FOR HEALTHCARE RESEARCH AND QUALITY [R01HS018975] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI049316] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [T32DK067872, R01DK042316] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Evaluation of: Wedebye Schmidt EG, Larsen HL, Kristensen N et al. Th17 cell induction and effects of IL-17A and IL-17F blockade in experimental colitis. Inflamm. Bowel Dis. 19(8), 1567-1576 (2013). The contribution of Th17 cells to the development of colitis is well described. The effector cytokines IL-17A and IL-17F have been proposed as potential therapeutic targets for the treatment of patients with inflammatory bowel disease. In a proof-of-concept study for the treatment of patients with Crohn's disease, secukinumab, a monoclonal antibody directed against IL-17A, was ineffective and associated with more adverse events than placebo. Wedebye Schmidt et al. propose that blockade of both IL-17A and IL-17F, rather than either cytokine alone, attenuates the development of colitis in a T-cell transfer model of experimental colitis. These findings suggest that combined blockade of IL-17A and IL-17F may be an effective strategy for the treatment of patients with inflammatory bowel disease.

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