Immune response to the ALK oncogenic tyrosine kinase in patients with anaplastic large-cell lymphoma

Author:

Pulford Karen1,Falini Brunangelo1,Banham Alison H.1,Codrington Diana1,Roberton Helen1,Hatton Christopher1,Mason David Y.1

Affiliation:

1. From the Nuffield Department of Clinical Laboratory Sciences and the Department of Haematology, John Radcliffe Hospital, Oxford, UK; Institute of Hematology, Perugia University, Perugia, Italy.

Abstract

Abstract Oncogenic anaplastic lymphoma kinase (ALK) fusion proteins (nucleophosmin–ALK [NPM-ALK] and other variants) are expressed in many cases of anaplastic large-cell lymphoma (ALCL) but are absent from normal tissues. The possibility that ALK proteins are immunogenic was investigated with the use of an immunocytochemical technique to screen plasma from ALK-positive ALCL on transfectants expressing ALK proteins and by an in vitro kinase assay. Circulating antibodies against NPM-ALK protein were present in all ALK-positive ALCL patients (11 out of 11 cases) studied while 10 patients also had antibodies recognizing normal ALK protein. Weak antibodies reactive with NPM-ALK (which may represent anti-NPM autoantibodies) were detected by the in vitro kinase assay in 3 of the 10 control samples (but not by immunocytochemistry). The presence of anti-ALK antibodies may be relevant to the relatively good prognosis of ALK-positive ALCL. The immunocytochemical technique for detecting anti-ALK activity is simple and semiquantative and may provide a means of detecting B-cell responses to other tumor-associated molecules.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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