Cladribine and Fludarabine Nucleoside Change the Levels of CD Antigens on B-Lymphoproliferative Disorders
The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 μM, 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...
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Published in | International Journal of Proteomics Vol. 2010; no. 2010; pp. 86 - 94 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Cairo, Egypt
Hindawi Limiteds
01.01.2010
Hindawi Puplishing Corporation Hindawi Publishing Corporation |
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Abstract | The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 μM, 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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AbstractList | 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. The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 μM, 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. The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 kM, 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. |
Author | Christopherson, Richard I. Cassano, Carlos Mactier, Swetlana Belov, Larissa Mulligan, Stephen P. Huang, Pauline |
AuthorAffiliation | 1 School of Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW 2006, Australia 2 Department of Haematology and Transfusion Medicine, Royal North Shore Hospital, St. Leonards, NSW 2065, Australia |
AuthorAffiliation_xml | – name: 1 School of Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW 2006, Australia – name: 2 Department of Haematology and Transfusion Medicine, Royal North Shore Hospital, St. Leonards, NSW 2065, Australia |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22084681$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_jprot_2017_01_001 crossref_primary_10_1038_cddis_2013_155 crossref_primary_10_1586_14737140_2013_818294 crossref_primary_10_1158_1541_7786_MCR_14_0124 crossref_primary_10_1021_pr300079c crossref_primary_10_1080_15257770_2011_603716 crossref_primary_10_1038_leu_2014_199 |
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Snippet | The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 μM, 24 hours), significantly changed the levels of some surface antigens on the human... The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 μ M, 24 hours), significantly changed the levels of some surface antigens on the... The purine analogs, fludarabine nucleoside (FdA), and cladribine (CdA) (1 kM, 24 hours), significantly changed the levels of some surface antigens on the human... |
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Title | Cladribine and Fludarabine Nucleoside Change the Levels of CD Antigens on B-Lymphoproliferative Disorders |
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