| Literature DB >> 26405582 |
Claire Germain1, Thierry Guillaudeux2, Elisabeth D Galsgaard3, Catherine Hervouet4, Nedra Tekaya4, Anne-Sophie Gallouet2, Julien Fassy4, Franck Bihl4, Gwenola Poupon4, Anne Lazzari4, Pieter Spee3, Fabienne Anjuère4, Céline Pangault5, Karin Tarte5, Patrick Tas5, Luc Xerri6, Veronique M Braud4.
Abstract
Non-Hodgkin's lymphomas (NHLs) are malignant neoplasms which are clinically and biologically diverse. Their incidence is constantly increasing and despite treatment advances, there is a need for novel targeted therapies. Here, we identified Lectin-like transcript 1 (LLT1) as a biomarker of germinal center (GC)-derived B-cell NHLs. LLT1 identifies GC B cells in reactive tonsils and lymph nodes and its expression is maintained in B-cell NHLs which derive from GC, including Burkitt lymphoma (BL), follicular lymphoma (FL), and GC-derived diffuse large B-cell lymphoma (DLBCL). We further show that LLT1 expression by tumors dampens natural killer (NK) cell functions following interaction with its receptor CD161, uncovering a potential immune escape mechanism. Our results pinpoint LLT1 as a novel biomarker of GC-derived B-cell NHLs and as a candidate target for innovative immunotherapies.Entities:
Keywords: CD161; LLT1; germinal center; natural killer cells; non-Hodgkin's B-cell lymphoma
Year: 2015 PMID: 26405582 PMCID: PMC4570132 DOI: 10.1080/2162402X.2015.1026503
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110