Volume 27, Issue 2 pp. 538-543
Article
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Sensitivity of Epstein-Barr virus-induced B cell tumor to apoptosis mediated by anti-CD95/Apo-1/fas antibody

Anne Durandy

Corresponding Author

Anne Durandy

Institut National de la Santé et de la Recherche Médicale U 429, Hǒpital Necker-Enfants Malades, Paris, France

INSERM U 429, Hǒpital Necker-Enfants Malades, 149, rue de Sèvres, F-75743 Paris Cédex 15, France Fax: +33-1-42730640Search for more papers by this author
Françoise Le Deist

Françoise Le Deist

Institut National de la Santé et de la Recherche Médicale U 429, Hǒpital Necker-Enfants Malades, Paris, France

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Jean-François Emile

Jean-François Emile

Service d'Anatomopathologie, Hǒpital Necker-Enfants Malades, Paris, France

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Klaus Debatin

Klaus Debatin

Haematology Oncology, University Children's Hospital, Heidelberg, Germany

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Alain Fischer

Alain Fischer

Institut National de la Santé et de la Recherche Médicale U 429, Hǒpital Necker-Enfants Malades, Paris, France

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First published: 05 December 2005
Citations: 18

Abstract

Epstein-Barr virus (EBV) can induce uncontrolled B lymphocyte proliferation leading to fatal lymphoma in immunocompromised patients. The sensitivity to apoptosis of B lymphoid cell lines (LCL) derived from EBV-induced lymphopro-liferative disorders was investigated. In vitro and in vivo, these B LCL strongly express CD95/Apo-1/fas antigen and undergo apoptosis upon stimulation with anti-Apo-1 monoclonal antibody. When inoculated into severe-combined immunodeficient (scid) mice, human B cells lines developed into rapidly growing tumors. Administration of an agonistic anti-Apo-1 antibody significantly delayed tumor progression. Relapses were frequent, but were not caused by selection of resistant B cells, since B cells from relapsing tumors underwent apoptosis on re-exposure. Induction of apoptosis by an anti-C95/Apo-1/fas-specific antibody could be applied for therapy of EBV-induced B cell tumors and contribute to our understanding of the mechanisms of T cell-mediated elimination of EBV lymphomas in immunodeficient patients.

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