Haematologica (Aug 2016)

Mesenchymal stromal cells from pooled mononuclear cells of multiple bone marrow donors as rescue therapy in pediatric severe steroid-refractory graft-versus-host disease: a multicenter survey

  • Zyrafete Kuçi,
  • Halvard Bönig,
  • Hermann Kreyenberg,
  • Milica Bunos,
  • Anna Jauch,
  • Johannes W.G. Janssen,
  • Marijana Škifić,
  • Kristina Michel,
  • Ben Eising,
  • Giovanna Lucchini,
  • Shahrzad Bakhtiar,
  • Johann Greil,
  • Peter Lang,
  • Oliver Basu,
  • Irene von Luettichau,
  • Ansgar Schulz,
  • Karl-Walter Sykora,
  • Andrea Jarisch,
  • Jan Soerensen,
  • Emilia Salzmann-Manrique,
  • Erhard Seifried,
  • Thomas Klingebiel,
  • Peter Bader,
  • Selim Kuçi

DOI
https://doi.org/10.3324/haematol.2015.140368
Journal volume & issue
Vol. 101, no. 8

Abstract

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To circumvent donor-to-donor heterogeneity which may lead to inconsistent results after treatment of acute graft-versus-host disease with mesenchymal stromal cells generated from single donors we developed a novel approach by generating these cells from pooled bone marrow mononuclear cells of 8 healthy “3rd-party” donors. Generated cells were frozen in 209 vials and designated as mesenchymal stromal cell bank. These vials served as a source for generation of clinical grade mesenchymal stromal cell end-products, which exhibited typical mesenchymal stromal cell phenotype, trilineage differentiation potential and at later passages expressed replicative senescence-related markers (p21 and p16). Genetic analysis demonstrated their genomic stability (normal karyotype and a diploid pattern). Importantly, clinical end-products exerted a significantly higher allosuppressive potential than the mean allosuppressive potential of mesenchymal stromal cells generated from the same donors individually. Administration of 81 mesenchymal stromal cell end-products to 26 patients with severe steroid-resistant acute graft-versus-host disease in 7 stem cell transplant centers who were refractory to many lines of treatment, induced a 77% overall response at the primary end point (day 28). Remarkably, although the cohort of patients was highly challenging (96% grade III/IV and only 4% grade II graft-versus-host disease), after treatment with mesenchymal stromal cell end-products the overall survival rate at two years follow up was 71±11% for the entire patient cohort, compared to 51.4±9.0% in graft-versus-host disease clinical studies, in which mesenchymal stromal cells were derived from single donors. Mesenchymal stromal cell end-products may, therefore, provide a novel therapeutic tool for the effective treatment of severe acute graft-versus-host disease.