Inhibition of Vascular Adhesion Protein‐1 for Treatment of Graft‐Versus‐Host Disease in Mice. Issue 8 (28th February 2018)

• Record Type: Journal Article
• Authors: Mukai, Shin; Ogawa, Yoko; Kawakami, Yutaka; Mashima, Yukihiko; Tsubota, Kazuo
• Is Part Of: FASEB journal. Volume 32:Issue 8(2018)
• Page Start: 4085
• Page End: 4095
• Publication Date: 2018-02-28
• Subjects: age‐associated disease -- refractory disease -- inhibitor -- inflammation -- fibrosis; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201700176R
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : Graft‐versus‐host disease (GVHD) is a potentially lethal complication of hematopoietic stem cell trans‐plantation (HSCT). GVHD comprises acute and chronic forms. To date, several approaches to treat acute GVHD or chronic GVHD have been reported. However, there is no literature precedent regarding all‐in‐one methods to address the 2 GVHD types. Severe inflammation in organs affected by GVHD is highly problematic, and vascular adhesion protein‐1 (VAP‐1) is known to be detrimentally involved in various inflammatory diseases. Based on the previous reports, we envisaged that there would be a link between GVHD and VAP‐1, and we strived to create effective therapies for the 2 types of GVHD using a mouse model of GVHD. Our investigation indicated that expression of VAP‐1 was elevated in organs disordered by GVHD. Hence, we subsequently attempted to block VAP‐1 by using a novel inhibitor. Our results indicate that systemic injection of the inhibitor prevented aberrant influx of inflammatory cells into tissues and thereby mitigate GVHD‐elicited inflammation and fibrosis. Collectively, our study suggests that the increased expression of VAP‐1 is detrimentally associated with the development of GVHD and that the blockade of VAP‐1 could be a promising medical modality to combat the acute and chronic variants.—Mukai, S., Ogawa, Y., Kawakami, Y., Mashima, Y., Tsubota, K. Inhibition of vascular adhesion protein‐1 for treatment of graft‐versus‐host disease in mice. FASEB J . 32, 4085–4095 (2018). www.fasebj.org