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Élément Dublin Core | Valeur | Langue |
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dc.contributor.author | Ait-Taha, Kamel | - |
dc.contributor.author | C.N.Barnardo, Martin | - |
dc.contributor.author | Pulford, Karen | - |
dc.date.accessioned | 2020-12-01T08:30:10Z | - |
dc.date.available | 2020-12-01T08:30:10Z | - |
dc.date.issued | 2007-03 | - |
dc.identifier.uri | http://dspace.univ-bouira.dz:8080/jspui/handle/123456789/10615 | - |
dc.description.abstract | We have previously shown both humoral and CTL responses to anaplastic lymphoma kinase (ALK) in patients with ALK- positive 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, ALK1 278–301 and ALK2 233–256 , 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 devel- oping future immunotherapeutic options for ALK-positive ALCL patients who fail to respond well to conventional therapies. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Université Akli Mouhand Oulhadj-Bouira | en_US |
dc.title | CD4 T-Helper Responses to the Anaplastic Lymphoma Kinase (ALK) Protein in Patients with ALK-Positive Anaplastic Large-Cell Lymphoma | en_US |
dc.type | Article | en_US |
Collection(s) : | Articles |
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