Literature DB >> 23994245

Gastrointestinal acute graft-versus-host disease in children: histology for diagnosis, mesenchymal stromal cells for treatment, and biomarkers for prediction of response.

Friso G J Calkoen1, Cornelia M Jol-van der Zijde, M Luisa Mearin, Joachim J Schweizer, Anja M Jansen-Hoogendijk, Helene Roelofs, Astrid G S van Halteren, R Maarten Egeler, Maarten J D van Tol, Lynne M Ball.   

Abstract

Steroid-nonresponsive acute graft-versus-host disease (aGVHD) after hematopoietic stem cell transplantation carries a poor prognosis. Various groups have reported beneficial effects of mesenchymal stromal cell (MSC) infusion as salvage treatment. Response to treatment is typically evaluated using the diagnostic clinical criteria for aGVHD. In this study, we evaluated the usefulness of additional gastrointestinal biopsy specimens paired with serum biomarkers. In a cohort of 22 pediatric patients, persistent or recurrent diarrhea was seen in 18 children treated with MSC infusion for steroid-refractory aGVHD. To exclude other causes of gastrointestinal pathology, patients were biopsied for histological analysis. Eight of 12 patients exhibited residual tissue damage and villous atrophy, but no active aGVHD. Serum biomarkers have been identified as an alternative tool for monitoring the response to aGVHD treatment. The value of biomarkers for inflammation, tissue, and endothelial cell damage was evaluated in our cohort. Although predictive of response to treatment and survival, these markers lack the necessary specificity and sensitivity to predict response to MSC therapy. Objective endpoints for clinical trials on the treatment of steroid-refractory aGVHD remain to be defined. Thus, we recommend including biopsies and biomarkers to discriminate between ongoing aGVHD and postinflammatory malabsorption.
Copyright © 2013 American Society for Blood and Marrow Transplantation. All rights reserved.

Entities:  

Keywords:  Acute graft-versus-host disease; Biomarkers; Children; Gastrointestinal; Histology; Mesenchymal stromal cells

Mesh:

Substances:

Year:  2013        PMID: 23994245     DOI: 10.1016/j.bbmt.2013.08.006

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  4 in total

1.  Mesenchymal stromal cell therapy is associated with increased adenovirus-associated but not cytomegalovirus-associated mortality in children with severe acute graft-versus-host disease.

Authors:  Friso G J Calkoen; Carly Vervat; Astrid G S van Halteren; Marij J P Welters; Louise A Veltrop-Duits; Arjan C Lankester; R Maarten Egeler; Lynne M Ball; Maarten J D van Tol
Journal:  Stem Cells Transl Med       Date:  2014-06-05       Impact factor: 6.940

2.  The Use of Human Mesenchymal Stem Cells as Therapeutic Agents for the in vivo Treatment of Immune-Related Diseases: A Systematic Review.

Authors:  Alessander Leyendecker; Carla Cristina Gomes Pinheiro; Mariane Tami Amano; Daniela Franco Bueno
Journal:  Front Immunol       Date:  2018-09-11       Impact factor: 7.561

Review 3.  Immunomodulatory oligonucleotide IMT504: Effects on mesenchymal stem cells as a first-in-class immunoprotective/immunoregenerative therapy.

Authors:  Jorge Zorzopulos; Steven M Opal; Andrés Hernando-Insúa; Juan M Rodriguez; Fernanda Elías; Juan Fló; Ricardo A López; Norma A Chasseing; Victoria A Lux-Lantos; Maria F Coronel; Raul Franco; Alejandro D Montaner; David L Horn
Journal:  World J Stem Cells       Date:  2017-03-26       Impact factor: 5.326

Review 4.  Mesenchymal Stromal Cells for Graft Versus Host Disease: Mechanism-Based Biomarkers.

Authors:  Tik Shing Cheung; Giuliana Minani Bertolino; Chiara Giacomini; Martin Bornhäuser; Francesco Dazzi; Antonio Galleu
Journal:  Front Immunol       Date:  2020-06-25       Impact factor: 7.561

  4 in total

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