%0 Journal Article
%T Therapy of acute graft-versus-host disease
%A Malte von Bonin
%A Martin Wermke
%A Uwe Platzbecker
%A J£¿rgen Radke
%J Cellular Therapy and Transplantation
%D 2010
%I 
%X Primary therapy of acute GvHD grade II¨CIV is still based on the systemic application of corticosteroids at doses of 1¨C2 mg/kg (e.g. prednisolone). Typically, investigators combine this approach with therapeutic doses of calcineurin inhibitors, which are used as prophylactic regimens. Patients not responding to steroids within 5¨C7 days or those with progressive disease within 72 hours represent a high-risk population that requires further immunosuppressive escalation. Pharmacological second-line therapy is mainly based on centre policies and individual decisions since no strategy has been associated with an improvement in survival within a controlled prospective trial. Compounds with efficacy in phase II trials are mycophenolate mofetil, methotrexate, pentostatin, mTOR inhibitors, antibodies targeting TNFalpha or IL-2 pathways, and monoclonal or polyclonal anti-T cell antibodies. Non-pharmacological options include extracorporeal photopheresis and the infusion of allogeneic mesenchymal stromal cells. For most interventions, earlier treatment (e.g., within two weeks) is associated with a better outcome. However, the overall efficacy and toxicity of most approaches are unsatisfactory. Future developments include the use of regulatory T cells and more targeted approaches using small molecules interacting with specific signalling pathways of antigen-presenting and effector cells.
%K acute graft-versus-host disease
%K refractory
%K salvage therapy
%K toxicity
%K tolerance
%U http://www.ctt-journal.com/index.php?id=440