Abstract

Rabbit anti-thymocyte globulin (rATG) is currently the treatment of choice for glucocorticoid-resistant, recurrent, or severe acute allograft rejection (AR). However, rATG is associated with severe infusion-related side effects. Alemtuzumab is incidentally given to kidney transplant recipients as treatment for AR. In the current study, the outcomes of patients treated with alemtuzumab for AR were compared with that of patients treated with rATG for AR. The patient-, allograft-, and infection-free survival and adverse events of 116 alemtuzumab-treated patients were compared with those of 108 patients treated with rATG for AR. Propensity scores were used to control for differences between the two groups. Patient- and allograft survival of patients treated with either alemtuzumab or rATG were not different [hazard ratio (HR) 1.14, 95%-confidence interval (CI) 0.48-2.69, p = 0.77, and HR 0.82, 95%-CI 0.45-1.5, p = 0.52, respectively). Infection-free survival after alemtuzumab treatment was superior compared with that of rATG-treated patients (HR 0.41, 95%-CI 0.25-0.68, p < 0.002). Infusion-related adverse events occurred less frequently after alemtuzumab treatment. Alemtuzumab therapy may therefore be an alternative therapy for glucocorticoid-resistant, recurrent, or severe acute kidney transplant rejection.

Highlights

  • Alemtuzumab is incidentally used to treat acute kidney allograft rejection (AR) [1,2,3,4,5]

  • The outcomes were compared to those of a cohort of patients treated with Rabbit anti-thymocyte globulin (rATG)

  • The results of this study suggest that alemtuzumab could be an alternative to rATG for the treatment of glucocorticoid-resistant, severe or recurrent AR

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Summary

Introduction

Alemtuzumab is incidentally used to treat acute kidney allograft rejection (AR) [1,2,3,4,5]. Alemtuzumab is a humanized monoclonal rat antibody directed against the cell surface glycoprotein CD52 [6]. Treatment with alemtuzumab causes a long-lasting depletion of various cells of the adaptive (T- and B cells) and innate immune system (NK cells, dendritic cells, monocytes, and granulocytes) [6]. The drug is registered for the treatment of relapsing-remitting multiple sclerosis [7]. The Campath R Distribution Program offers off-label treatment with alemtuzumab for other indications, including therapy for kidney transplant recipients and patients with chronic lymphocytic leukemia [8]. Frontiers in Immunology | www.frontiersin.org van der Zwan et al

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