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Class II–Associated Invariant Chain Peptide Expression Represents a Novel Parameter for Flow Cytometric Detection of Acute Promyelocytic Leukemia

Authors :
S. Marieke van Ham
Gert J. Ossenkoppele
Arjan A. van de Loosdrecht
Martine E.D. Chamuleau
Marvin M. van Luijn
Theresia M. Westers
Hematology laboratory
Hematology
CCA - Innovative therapy
Landsteiner Laboratory
Source :
The American Journal of Pathology, 179(5), 2157-2161. Elsevier Inc., van Luijn, M M, Westers, T M, Chamuleau, M E D, van der Ham, S M, Ossenkoppele, G J & van de Loosdrecht, A A 2011, ' Class II-Associated Invariant Chain Peptide Expression Represents a Novel Parameter for Flow Cytometric Detection of Acute Promyelocytic Leukemia ', The American Journal of Pathology, vol. 179, no. 5, pp. 2157-2161 . https://doi.org/10.1016/j.ajpath.2011.07.027, American journal of pathology, 179(5), 2157-2161. Elsevier Inc.
Publication Year :
2011
Publisher :
Elsevier BV, 2011.

Abstract

Because of severe bleeding complications, patients with acute promyelocytic leukemia (APL) have to be treated with all-trans retinoic acid immediately following diagnosis. In addition to morphology, flow cytometry contributes to a rapid detection of APL according to phenotypic characteristics of leukemic cells. In some patients, these analyses are inconclusive or even contradictory to diagnosis. Previously, we showed the clinical and functional impact of class II associated invariant chain peptide (CLIP) in acute myeloid leukemia (AML). This study focuses on the analysis of CLIP expression on leukemic cells to characterize HLA-DR negative AML, including APL. We demonstrate exclusive and significant CLIP expression in all cases of typical and variant APL, as compared to other HLA-DR negative non-APL-type AML. CLIP appears to be a highly sensitive and specific flow cytometric marker, resolving discrepant identification of both genetic subgroups. Our findings show the additive value of CLIP analysis for a fast and unequivocal recognition of APL by flow cytometry in conjunction with morphology. (Am J Pathol 2011, 179:2157-2161; DOI: 10.1016/j.ajpath.2011.07.027)

Details

ISSN :
00029440
Volume :
179
Database :
OpenAIRE
Journal :
The American Journal of Pathology
Accession number :
edsair.doi.dedup.....78d0bc115e6cd9723384066610bb6edf
Full Text :
https://doi.org/10.1016/j.ajpath.2011.07.027