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Cladribine and Fludarabine Nucleoside Change the Levels of CD Antigens on B-Lymphoproliferative Disorders
Author(s) -
Carlos Cassano,
Swetlana Mactier,
Stephen P. Mulligan,
Larissa Belov,
Pauline Huang,
Richard I. Christopherson
Publication year - 2010
Publication title -
international journal of proteomics
Language(s) - English
Resource type - Journals
eISSN - 2090-2174
pISSN - 2090-2166
DOI - 10.1155/2010/964251
Subject(s) - cladribine , fludarabine , antigen , cd86 , microbiology and biotechnology , immunology , medicine , biology , t cell , chemotherapy , immune system , cyclophosphamide
The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1  μ M, 24 hours), significantly changed the levels of some surface antigens on the human B-cell lines MEC2 and Raji. Changes in the surface proteins were identified using a Cluster of Differentiation (CD) antibody microarray that captures live cells and confirmed by flow cytometry. For Raji cells, CdA up-regulated CD10, CD54, CD80, and CD86, with repression of CD22, while FdA up-regulated CD20, CD54, CD80, CD86 and CD95. For MEC2 cells, CdA up-regulated CD11a, CD20, CD43, CD45, CD52, CD54, CD62L, CD80, CD86, and CD95, but FdA had no effect. Up-regulation of particular CD antigens induced on a B-cell lymphoproliferative disorder by a purine analog could provide targets for therapeutic antibodies with synergistic cell killing.

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