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Wiley InterScience

British Journal of Haematology

British Journal of Haematology

Volume 137 Issue 4, Pages 307 - 318

Published Online: 19 Apr 2007

© 2010 Blackwell Publishing Ltd



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research paper
The lymphoid cell surface receptor NTB-A: a novel monoclonal antibody target for leukaemia and lymphoma therapeutics
Wouter Korver 1 , Shweta Singh 1 , Shouchun Liu 1 , Xiaoxian Zhao 2 , Shirlee Yonkovich 1 , Allison Sweeney 1 , Kristin Anton 1 , Woodrow E. Lomas III 1 , Rachel Greenwood 1 , Ashley Smith 1 , Denise Hoang Tran 1 , Pauline Shinkawa 1 , Mark Jimenez 1 , Patricia Yeung 1 , Gerard Aguilar 1 , Servando Palencia 1 , Paolo Vatta 1 , Matthew Mueller 1 , Xiaoming Zhan 1 , Elizabeth M. Newton 1 , Yi Liu 1 , Jingsong Zhao 1 , Peter Emtage 1 , Michael D. Levy 1 , Eric D. Hsi 2 , Walter D. Funk 1 and Arie Abo 1
  1 Nuvelo, Inc., San Carlos, CA , and   2 Department of Clinical Pathology, Cleveland Clinic, Cleveland, OH, USA
Correspondence to Wouter Korver and Arie Abo, Nuvelo, Inc., 201 Industrial Rd, Suite 310, San Carlos, CA 94070, USA. E-mail: wkorver@nuvelo.com and aabo@nuvelo.com
Copyright 2007 The Authors Journal Compilation 2007 Blackwell Publishing Ltd
KEYWORDS
leukaemia • lymphoma • chronic lymphocytic leukaemia • immunotherapy • monoclonal antibody

ABSTRACT

NTB-A is a CD2-related cell surface protein expressed primarily on lymphoid cells including B-lymphocytes from chronic lymphocytic leukaemia (CLL) and lymphoma patients. We have generated a series of monoclonal antibodies (mAbs) against NTB-A and assessed their therapeutic potential for CLL. Selective mAbs to NTB-A were further tested in functional complement-dependent cytotoxicity (CDC) and antibody-dependent cellular cytotoxicty (ADCC) assays in cell lines and B lymphocytes freshly isolated from CLL patients. While lower levels of NTB-A were detected in T and natural killer (NK) cells, CDC activity was demonstrated primarily in B cells isolated from CLL patients and B lymphoma cell lines. Knockdown of NTB-A by small interfering RNA in target cells results in lower cytotoxicity, demonstrating the specificity of the mAbs. Furthermore, anti NTB-A mAbs demonstrated anti-tumour activity against CA46 human lymphoma xenografts in nude mice and against systemically disseminated Raji human lymphoma cells in severe combined immunodeficient mice. Taken together, these results demonstrate NTB-A as a potential new target for immunotherapy of leukaemia and lymphomas.


Received 3 January 2007; accepted for publication 12 February 2007

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1365-2141.2007.06569.x About DOI

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