| Literature DB >> 24731748 |
Willemijn van den Ancker1, Marvin M van Luijn1, Martine E D Chamuleau1, Angèle Kelder1, Nicole Feller1, Monique Terwijn1, Adri Zevenbergen1, Gerrit-Jan Schuurhuis1, S Marieke van Ham2, Theresia M Westers1, Gert J Ossenkoppele1, Arjan A van de Loosdrecht3.
Abstract
The presence of class II-associated invariant chain (CLIP) on leukemic cells is negatively associated with clinical outcome in untreated acute myeloid leukemia (AML). CLIP plays a role in the immune escape of leukemic cells, suggesting that it impairs the immunogenicity of minimal residual disease (MRD) cells causing a relapse. Here, we demonstrate that CLIP expression on leukemia-associated phenotype (LAP)-positive cells during follow-up is significantly correlated with a shortened relapse-free survival, even in those patients who are generally considered as MRD(low) (0.01-0.1% LAP(+) cells). Consequently, CLIP evaluation could be of additional value in the evaluation of MRD to predict a relapse of AML.Entities:
Keywords: CD4(+) T cells; HLA; Immune escape; Leukemia-associated phenotype; Minimal residual disease
Mesh:
Substances:
Year: 2014 PMID: 24731748 DOI: 10.1016/j.leukres.2014.03.014
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156