CD4 T-Helper Responses to the Anaplastic Lymphoma Kinase (ALK) Protein in Patients with ALK-Positive Anaplastic Large-Cell Lymphoma

Author:

Ait-Tahar Kamel1,Barnardo Martin C.N.2,Pulford Karen1

Affiliation:

1. 1Nuffield Department of Clinical Laboratory Sciences, Leukemia Research Fund Immunodiagnostics Unit, John Radcliffe Hospital, and

2. 2Transplant Immunology, Oxford Transplant Center, Churchill Hospital, Oxford, United Kingdom

Abstract

AbstractWe 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-γ 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. [Cancer Res 2007;67(5):1898–901]

Publisher

American Association for Cancer Research (AACR)

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