B and CTL responses to the ALK protein in patients with ALK-positive ALCL

Kamel Ait-Tahar, Vincenzo Cerundolo, Alison H. Banham, Christian Hatton, Tom Blanchard, Rajko Kusec, Marion Becker, Geoffrey L. Smith, Karen Pulford

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Anaplastic lymphoma kinase (ALK)-positive anaplastic large cell lymphoma (ALCL) has a good prognosis compared to ALK-negative ALCL, possibly as a result of the immune recognition of the ALK proteins. The aim of our study was to investigate the presence of both a B and cytotoxic T cell (CTL) response to ALK in ALK-positive ALCL. We confirmed the presence of an antibody response to ALK in all 9 ALK-positive ALCL patients investigated. An ELISpot assay was used to detect a γ-interferon (IFN) T cell response after short term culture of mononuclear blood cells with 2 ALK-derived HLA-A*0201 restricted peptides: ALKa and ALKb. A significant γ-IFN response was identified in all 7 HLA-A*0201-positive ALK-positive ALCL patients but not in ALK-negative ALCL patients (n = 2) or normal subjects (n = 6). CTL lines (>95% CD8-positive) raised from 2 ALK-positive ALCL patients lysed ALK-positive ALCL derived cell lines in a MHC-Class I restricted manner. This is the first report of both a B cell and CTL response to ALK in patients with ALK-positive ALCL. This response persisted during long-term remission. The use of modified vaccinia virus Ankara (MVA) to express ALK is also described. Our findings are of potential prognostic value and open up therapeutic options for those ALK-positive patients who do not respond to conventional treatment. © 2005 Wiley-Liss, Inc.
    Original languageEnglish
    Pages (from-to)688-695
    Number of pages7
    JournalInternational Journal of Cancer
    Volume118
    Issue number3
    DOIs
    Publication statusPublished - 1 Mar 2006

    Keywords

    • ALCL
    • ALK
    • CTL responses
    • ELISpot
    • Tumour-associated antigens

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