Plasma exchange eliminates residual mogamulizumab but does not warrant prompt recovery of peripheral Treg levels

Transfus Apher Sci. 2019 Aug;58(4):472-474. doi: 10.1016/j.transci.2019.05.011. Epub 2019 Jul 9.

Abstract

Mogamulizumab (Mog), a humanized anti-CCR4 antibody, provides an important treatment option for relapsed/refractory adult T cell leukemia/lymphoma. However, administration of Mog before allogenic hematopoietic stem cell transplantation has been reported to be a risk factor for severe acute graft-versus-host disease (GVHD). The etiological hypothesis is Mogamulizumab may eradicate CCR4-positive regulatory T cells (Tregs). Theoretically, Treg homeostasis and course of GVHD can be affected by plasma exchange (PE) with decreasing plasma Mog concentration. Here, we present a case of severe acute GVHD after pretransplantation Mog, in which PE was performed for liver failure. As a result, plasma Mog concentration was decreased but it did not lead to the prompt elevation of Treg levels in peripheral blood and clinical responses of GVHD were limited to partial remission. Our case suggests that recovery of donor-derived Treg in the acute phase after HSCT is multifactorial and the single procedure of PE-based Mog depletion does not necessarily warrant the quick restoration of Treg homeostasis.

Keywords: Graft-versus-host disease; Mogamulizumab; Plasma exchange; Regulatory T cells.

Publication types

  • Case Reports

MeSH terms

  • Acute Disease
  • Allografts
  • Antibodies, Monoclonal, Humanized* / administration & dosage
  • Antibodies, Monoclonal, Humanized* / adverse effects
  • Antibodies, Monoclonal, Humanized* / pharmacokinetics
  • Female
  • Graft vs Host Disease* / chemically induced
  • Graft vs Host Disease* / immunology
  • Graft vs Host Disease* / prevention & control
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Leukemia-Lymphoma, Adult T-Cell* / immunology
  • Leukemia-Lymphoma, Adult T-Cell* / pathology
  • Leukemia-Lymphoma, Adult T-Cell* / therapy
  • Liver Failure / immunology
  • Liver Failure / therapy
  • Middle Aged
  • Plasma Exchange*
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • Antibodies, Monoclonal, Humanized
  • mogamulizumab