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Developing T-cell therapies for lymphoma without receptor engineering
Author(s) -
Melanie Grant,
Catherine M. Bollard
Publication year - 2017
Publication title -
hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.321
H-Index - 91
eISSN - 1520-4391
pISSN - 1520-4383
DOI - 10.1182/asheducation-2017.1.622
Subject(s) - chimeric antigen receptor , lymphoma , medicine , antigen , t cell , immunotherapy , immunology , immune system , cell therapy , receptor , cancer research , t cell receptor , cell , biology , genetics
T-cell therapy has emerged from the bench for the treatment of patients with lymphoma. Responses to T-cell therapeutics are regulated by multiple factors, including the patient’s immune system status and disease stage. Outside of engineering of chimeric antigen receptors and artificial T-cell receptors, T-cell therapy can be mediated by ex vivo expansion of antigen-specific T cells targeting viral and/or nonviral tumor-associated antigens. These approaches are contributing to enhanced clinical responses and overall survival. In this review, we summarize the available T-cell therapeutics beyond receptor engineering for the treatment of patients with lymphoma.

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