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dc.contributor.authorAit-Tahar, Kamel-
dc.contributor.authorC.N. Barnardo, Martin-
dc.contributor.authorPulford, Karen-
dc.date.accessioned2020-12-01T08:40:16Z-
dc.date.available2020-12-01T08:40:16Z-
dc.date.issued2007-03-
dc.identifier.urihttp://dspace.univ-bouira.dz:8080/jspui/handle/123456789/10617-
dc.description.abstractWe have previously shown both humoral and CTL responses to anaplastic lymphoma kinase (ALK) in patients with ALKpositive anaplastic large-cell lymphoma (ALCL). However, because CD4+ T-helper (Th) cells also play a vital role in developing and maintaining tumor immunity, we investigated the presence of a CD4+ Th response in ALK-positive ALCL. Using an IFN-; ELISPOT assay, we identified two ALK-derived DRB1-restricted 24-mer promiscuous peptides, ALK1278–301 and ALK2233–256, as being immunogenic in six ALK-positive ALCL patients but not in two ALK-negative ALCL patients or five normal subjects. A significant interleukin-4 response to the ALK peptides was detected in only one ALK-positive patient. CD4+ Th cell lines lysed ALK-positive ALCL cell lines in a MHC class II–restricted manner. This first report of a CD4+ Th response to ALK provides valuable information for developing future immunotherapeutic options for ALK-positive ALCL patients who fail to respond well to conventional therapies.en_US
dc.language.isoenen_US
dc.publisherUniversité Akli Mouhand Oulhadj-Bouiraen_US
dc.titleCD4 T-Helper Responses to the Anaplastic Lymphoma Kinase (ALK) Protein in Patients with ALK-Positive Anaplastic Large-Cell Lymphomaen_US
dc.typeArticleen_US
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