Clinical quantitation of immune signature in follicular lymphoma by RT-PCR-based gene expression profiling.

2.50
Hdl Handle:
http://hdl.handle.net/10541/67953
Title:
Clinical quantitation of immune signature in follicular lymphoma by RT-PCR-based gene expression profiling.
Authors:
Byers, Richard J; Sakhinia, Ebrahim; Joseph, Preethi; Glennie, Caroline; Hoyland, Judith A; Menasce, Lia P; Radford, John A ( 0000-0001-7898-2786 ) ; Illidge, Timothy M ( 0000-0003-3191-7324 )
Abstract:
Microarray gene expression profiling studies have demonstrated immune response gene signatures that appear predictive of outcome in follicular lymphoma (FL). However, measurement of these marker genes in routine practice remains difficult. We have therefore investigated the immune response in FL using real-time polymerase chain reaction (PCR) to measure expression levels of 35 candidate Indicator genes, selected from microarray studies, to polyA cDNAs prepared from 60 archived human frozen lymph nodes, in parallel with immunohistochemical analysis for CD3, CD4, CD7, CD8, CD10, CD20, CD21, and CD68. High levels of CCR1, a marker of monocyte activation, were associated with a shorter survival interval, and high levels of CD3 with better survival, while immunohistochemistry demonstrated association of high numbers of CD68(+) macrophages with a shorter survival interval and of high numbers of CD7(+) T cells with a longer survival interval. The results confirm the role of the host immune response in outcome in FL and identify CCR1 as a prognostic indicator and marker of an immune switch between macrophages and a T cell-dominant response. They demonstrate the utility of polyA DNA and real-time PCR for measurement of gene signatures and the applicability of using this type of "molecular block" in clinical practice.
Affiliation:
Department of Histopathology and Manchester Molecular Diagnostic Center, Manchester Royal Infirmary, Central Manchester, UK. r.byers@manchester.ac.uk
Citation:
Clinical quantitation of immune signature in follicular lymphoma by RT-PCR-based gene expression profiling. 2008, 111 (9):4764-70 Blood
Journal:
Blood
Issue Date:
1-May-2008
URI:
http://hdl.handle.net/10541/67953
DOI:
10.1182/blood-2007-10-115915
PubMed ID:
18174380
Type:
Article
Language:
en
ISSN:
1528-0020
Appears in Collections:
All Paterson Institute for Cancer Research; Medical Oncology; Pathology ; School of Cancer and Imaging Sciences

Full metadata record

DC FieldValue Language
dc.contributor.authorByers, Richard J-
dc.contributor.authorSakhinia, Ebrahim-
dc.contributor.authorJoseph, Preethi-
dc.contributor.authorGlennie, Caroline-
dc.contributor.authorHoyland, Judith A-
dc.contributor.authorMenasce, Lia P-
dc.contributor.authorRadford, John A-
dc.contributor.authorIllidge, Timothy M-
dc.date.accessioned2009-05-12T16:04:13Z-
dc.date.available2009-05-12T16:04:13Z-
dc.date.issued2008-05-01-
dc.identifier.citationClinical quantitation of immune signature in follicular lymphoma by RT-PCR-based gene expression profiling. 2008, 111 (9):4764-70 Blooden
dc.identifier.issn1528-0020-
dc.identifier.pmid18174380-
dc.identifier.doi10.1182/blood-2007-10-115915-
dc.identifier.urihttp://hdl.handle.net/10541/67953-
dc.description.abstractMicroarray gene expression profiling studies have demonstrated immune response gene signatures that appear predictive of outcome in follicular lymphoma (FL). However, measurement of these marker genes in routine practice remains difficult. We have therefore investigated the immune response in FL using real-time polymerase chain reaction (PCR) to measure expression levels of 35 candidate Indicator genes, selected from microarray studies, to polyA cDNAs prepared from 60 archived human frozen lymph nodes, in parallel with immunohistochemical analysis for CD3, CD4, CD7, CD8, CD10, CD20, CD21, and CD68. High levels of CCR1, a marker of monocyte activation, were associated with a shorter survival interval, and high levels of CD3 with better survival, while immunohistochemistry demonstrated association of high numbers of CD68(+) macrophages with a shorter survival interval and of high numbers of CD7(+) T cells with a longer survival interval. The results confirm the role of the host immune response in outcome in FL and identify CCR1 as a prognostic indicator and marker of an immune switch between macrophages and a T cell-dominant response. They demonstrate the utility of polyA DNA and real-time PCR for measurement of gene signatures and the applicability of using this type of "molecular block" in clinical practice.en
dc.language.isoenen
dc.subjectMicroarrayen
dc.subject.meshAntigens, CD-
dc.subject.meshGene Expression Profiling-
dc.subject.meshHumans-
dc.subject.meshImmunity-
dc.subject.meshImmunohistochemistry-
dc.subject.meshLymphoma, Follicular-
dc.subject.meshMacrophages-
dc.subject.meshPoly A-
dc.subject.meshPrognosis-
dc.subject.meshReceptors, CCR1-
dc.subject.meshReverse Transcriptase Polymerase Chain Reaction-
dc.subject.meshT-Lymphocytes-
dc.titleClinical quantitation of immune signature in follicular lymphoma by RT-PCR-based gene expression profiling.en
dc.typeArticleen
dc.contributor.departmentDepartment of Histopathology and Manchester Molecular Diagnostic Center, Manchester Royal Infirmary, Central Manchester, UK. r.byers@manchester.ac.uken
dc.identifier.journalBlooden

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