| Literature DB >> 28718418 |
Charlotte M de Winde1, Suraya Elfrink1, Annemiek B van Spriel2.
Abstract
Standard therapy of patients with B cell non-Hodgkin lymphoma (B-NHL) predominantly consists of chemotherapy combined with anti-CD20 (e.g., rituximab) immunotherapy. However, relapse of aggressive B-NHL occurs frequently, and this may coincide with therapy resistance. This demonstrates the urgent need for exploring new lymphoma-targeted therapies. We review here recent insights in the pathophysiology of B-NHL and discuss CD20 and three alternative membrane targets (B cell receptor, immune checkpoints PD-1/PD-L1, tetraspanin CD37) that are currently in the spotlight for B-NHL treatment. Furthermore, we present a novel concept in which the plasma membrane organization of the lymphoma B cell determines the efficacy of membrane-targeted therapies, and this has consequences for treatment application and clinical outcome in patients with B cell lymphoma.Entities:
Keywords: B cell; immunotherapy; membrane organization; membrane target; non-Hodgkin lymphoma
Mesh:
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Year: 2017 PMID: 28718418 DOI: 10.1016/j.trecan.2017.04.006
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025