Immunohistochemistry of affected tissue may guide cGVHD treatment decisions

Bone Marrow Transplant. 2012 May;47(5):731-3. doi: 10.1038/bmt.2011.164. Epub 2011 Sep 19.

Abstract

Chronic graft-vs-host disease (cGVHD) myositis is a rare complication of hematopoietic SCT, for which the pathogenesis and optimal therapy are unclear. We performed immunohistochemistry on muscle biopsies from pediatric cGVHD myositis and typical cases of autoimmune dermatomyositis and polymyositis. The immunostaining pattern of cGVHD myositis was distinct from that of typical cases of autoimmunity. There was a high proportion of CD20+ and CD68+ cells, and the best therapeutic response was achieved with rituximab (anti-CD20). These results suggest that cGVHD myositis may be mediated by different leukocytes than similar autoimmune diseases and that treatment may be optimized by targeting the specific cellular infiltrates identified in affected tissue.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal, Murine-Derived / therapeutic use
  • Antigens, CD / immunology
  • Antigens, CD20 / immunology
  • Antigens, Differentiation, Myelomonocytic / immunology
  • Autoimmune Diseases / immunology
  • B-Lymphocytes / immunology
  • Child
  • Dermatomyositis / pathology
  • Dermatomyositis / therapy
  • Graft vs Host Disease / drug therapy*
  • Graft vs Host Disease / immunology
  • Graft vs Host Disease / pathology*
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Immunohistochemistry
  • Polymyositis / pathology
  • Polymyositis / therapy
  • Rituximab

Substances

  • Antibodies, Monoclonal, Murine-Derived
  • Antigens, CD
  • Antigens, CD20
  • Antigens, Differentiation, Myelomonocytic
  • CD68 antigen, human
  • Rituximab