Response of Steroid-Refractory Acute GVHD to α1-Antitrypsin

A. Mario Marcondes, David M. Hockenbery, Marina Lesnikova, Charles A. Dinarello, Ann E. Woolfrey, Terry Gernsheimer, Mahmoud Loghman‐Adham, David Gelmont, Barry E. Storer, John A. Hansen,

Biology of Blood and Marrow Transplantation · 2016 · 63 citations · 25 references

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Abstract

α1-Antitrypsin (AAT) is a serine protease inhibitor with anti-inflammatory, antiapoptotic, and immunomodulatory properties. It has therapeutic efficacy in animal models of autoimmune diseases, inflammatory disorders, and transplantation. In a phase I/II open-label single-center study, we administered AAT (Glassia; Baxalta/Kamada, New Ziona, Israel) as salvage therapy to 12 patients with steroid-refractory acute graft-versus-host disease (GVHD). AAT was given i.v. at 2 dose levels over a 15-day course. All patients had grades III or IV GVHD with stage 4 gut involvement. After treatment, plasma AAT levels increased in both cohorts and remained within 2 to 4 mg/mL for the duration of treatment. No clinically relevant toxicities attributable to AAT were observed. GVHD manifestations improved in 8 of 12 patients, and 4 responses were complete. Six patients (50%) were alive at last follow-up (>104 to >820 days). These findings show that AAT is well tolerated and has efficacy in the treatment of steroid-refractory severe acute GVHD. Further studies are warranted.

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