Ontology highlight
ABSTRACT: Purpose
Tumor cells from approximately 40% of patients with Hodgkin or non-Hodgkin lymphoma express the type II latency Epstein-Barr virus (EBV) antigens latent membrane protein 1 (LMP1) and LMP2, which represent attractive targets for immunotherapy. Because T cells specific for these antigens are present with low frequency and may be rendered anergic by the tumors that express them, we expanded LMP-cytotoxic T lymphocytes (CTLs) from patients with lymphoma using autologous dendritic cells and EBV-transformed B-lymphoblastoid cell lines transduced with an adenoviral vector expressing either LMP2 alone (n = 17) or both LMP2 and ΔLMP1 (n = 33).Patients and methods
These genetically modified antigen-presenting cells expanded CTLs that were enriched for specificity against type
SUBMITTER: Bollard CM
PROVIDER: S-EPMC3940538 | biostudies-literature | 2014 Mar
REPOSITORIES: biostudies-literature