CD20 expression in normal canine B cells and in canine non-Hodgkin lymphoma

  • C. M. Jubala
  • , J. W. Wojcieszyn
  • , V. E O Valli
  • , D. M. Getzy
  • , S. P. Fosmire
  • , D. Coffey
  • , D. Bellgrau
  • , J. F. Modiano

Research output: Contribution to journalArticlepeer-review

78 Scopus citations

Abstract

We examined the expression of CD20 in normal canine peripheral blood mononuclear cells, normal canine spleen, and canine non-Hodgkin lymphoma (NHL) to determine the feasibility of using this antigen as a diagnostic aid and as a possible target for therapy. An antibody generated against a C-terminal (intracytoplasmic) epitope of human CD20 recognized proteins of 32-36 kd in normal and malignant canine lymphocytes. This antibody showed restricted membrane binding in a subset of lymphocytes in peripheral blood, in the B-cell regions from a normal canine spleen and lymph node, and in malignant cells from 19 dogs with B-cell NHL, but not from 15 dogs with T-cell NHL. The patterns of CD20 reactivity in these samples overlapped those seen using an antibody that recognizes canine CD79a. This anti-CD20 antibody is therefore suitable as an aid to phenotype canine NHL. In contrast, normal canine B cells were not recognized by any of 28 antibodies directed against the extracellular domains of human CD20 (including the chimeric mouse-human antibody Rituximab) or by any of 12 antibodies directed against the extracellular domains of mouse CD20. Thus, the use of CD20 as a therapeutic target will require the generation of specific antibodies against the extracellular domains of canine CD20.

Original languageEnglish (US)
Pages (from-to)468-476
Number of pages9
JournalVeterinary pathology
Volume42
Issue number4
DOIs
StatePublished - Jul 2005

Keywords

  • B cells
  • CD20
  • Canine
  • Flow cytometry
  • Immunoblotting
  • Immunohistology
  • Non-Hodgkin lymphoma

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