Histopathology and immunophenotype of the spleen during acute antibody-mediated rejection

Am J Transplant. 2010 May;10(5):1316-20. doi: 10.1111/j.1600-6143.2010.03067.x. Epub 2010 Mar 19.

Abstract

Splenectomy has been reported to have a beneficial effect in treating Acute antibody-mediated rejection (ABMR). This reason for this often rapid and profound beneficial effect is not readily apparent from what is known about normal splenic immunoarchitecture. While the spleen is rich in mature B cells, it has not been noted to be a repository for direct antibody-secreting cells. We present a case of a Native American female who received a renal transplant and developed a severe episode of ABMR. The patient was initially refractory to both plasmapheresis and IVIG. The patient underwent an emergent splenectomy with almost immediate improvement in her renal function and a rapid drop in her DR51 antibodies. Immunohistochemical stains of the spleen demonstrated abundant clusters of CD138+ plasma cells (>10% CD138 cells as opposed to 1% CD138 cells as seen in traumatic controls). Though this is a single case, these findings offer a rationale for the rapid ameliorative effect of splenectomy in cases of antibody rejection. It is possible that the spleen during times of excessive antigenic stress may rapidly turn over B cells to active antibody-secreting cells or serve as a reservoir for these cells produced at other sites.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antibodies / immunology
  • Antibody-Producing Cells / immunology
  • Female
  • Humans
  • Immunoglobulins / immunology
  • Immunoglobulins, Intravenous / immunology
  • Immunophenotyping
  • Indians, North American
  • Kidney Transplantation / immunology
  • Kidney Transplantation / pathology
  • Plasma Cells / immunology
  • Plasma Cells / pathology
  • Plasmapheresis
  • Spleen / immunology*
  • Spleen / pathology*
  • Splenectomy
  • Syndecan-1 / immunology

Substances

  • Antibodies
  • Immunoglobulins
  • Immunoglobulins, Intravenous
  • Syndecan-1