| Literature DB >> 26492560 |
Geothy Chakupurakal1, María Alejandra García-Márquez1, Alexander Shimabukuro-Vornhagen1, Sebastian Theurich2, Udo Holtick1, Michael Hallek1, Christof Scheid1, Michael von Bergwelt-Baildon1.
Abstract
Steroid-refractory graft-versus-host disease (GvHD) is a complication following an allogeneic stem cell transplantation with limited therapeutic options. Studies have shown a response in up to 80% of patients with this condition after treatment with the CD25 monoclonal antibody, basiliximab. Despite the good responses to treatment, around 50% of the patients experience recurrence of their GvHD symptoms 4-6 wk following cessation of therapy. The in vivo changes in the following treatment with this antibody have not been elucidated so far. We treated 14 patients with severe steroid-refractory GvHD with basiliximab weekly for 4 wk and monitored the changes in the T-, B-, NK- and dendritic cell subsets over this time period. The overall response to treatment was 92% (13/14) with 50% (7/14) achieving a complete response. Fifty four percentage (7/13) of the patients who responded showed recurrence of their GvHD symptoms. Contrary to expectations, our observations showed a significant depletion of the regulatory T-cell subset following treatment. Our findings suggest that the undesirable depletion of the regulatory T cells along with the CD25(+) acute inflammatory cells might be responsible for the high incidence of GvHD recurrence in this cohort of patients.Entities:
Keywords: CD25 monoclonal antibody; allogeneic stem cell transplantation; basiliximab; steroid-refractory graft-versus-host disease
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Year: 2015 PMID: 26492560 DOI: 10.1111/ejh.12691
Source DB: PubMed Journal: Eur J Haematol ISSN: 0902-4441 Impact factor: 2.997