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Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment

Dendritic cells (DCs) and monocytes are critical regulators and effectors of innate and adaptive immune responses. Monocyte expansion has been described in many pathological states while monocyte and DC deficiency syndromes are relatively recent additions to the catalog of human primary immunodefici...

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Autores principales: Jardine, Laura, Barge, Dawn, Ames-Draycott, Ashley, Pagan, Sarah, Cookson, Sharon, Spickett, Gavin, Haniffa, Muzlifah, Collin, Matthew, Bigley, Venetia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873601/
https://www.ncbi.nlm.nih.gov/pubmed/24416034
http://dx.doi.org/10.3389/fimmu.2013.00495
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author Jardine, Laura
Barge, Dawn
Ames-Draycott, Ashley
Pagan, Sarah
Cookson, Sharon
Spickett, Gavin
Haniffa, Muzlifah
Collin, Matthew
Bigley, Venetia
author_facet Jardine, Laura
Barge, Dawn
Ames-Draycott, Ashley
Pagan, Sarah
Cookson, Sharon
Spickett, Gavin
Haniffa, Muzlifah
Collin, Matthew
Bigley, Venetia
author_sort Jardine, Laura
collection PubMed
description Dendritic cells (DCs) and monocytes are critical regulators and effectors of innate and adaptive immune responses. Monocyte expansion has been described in many pathological states while monocyte and DC deficiency syndromes are relatively recent additions to the catalog of human primary immunodeficiency disorders. Clinically applicable screening tests to diagnose and monitor these conditions are lacking. Conventional strategies for identifying human DCs and monocytes have been based on the use of a lineage gate to exclude lymphocytes, thus preventing simultaneous detection of DCs, monocytes, and lymphocyte subsets. Here we demonstrate that CD4 is a reliable lineage marker for the human peripheral blood antigen-presenting cell compartment that can be used to identify DCs and monocytes in parallel with lymphocytes. Based on this principle, simple modification of a standard lymphocyte phenotyping assay permits simultaneous enumeration of four lymphocyte and five DC/monocyte populations from a single sample. This approach is applicable to clinical samples and facilitates the diagnosis of DC and monocyte disorders in a wide range of clinical settings, including genetic deficiency, neoplasia, and inflammation.
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spelling pubmed-38736012014-01-11 Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment Jardine, Laura Barge, Dawn Ames-Draycott, Ashley Pagan, Sarah Cookson, Sharon Spickett, Gavin Haniffa, Muzlifah Collin, Matthew Bigley, Venetia Front Immunol Immunology Dendritic cells (DCs) and monocytes are critical regulators and effectors of innate and adaptive immune responses. Monocyte expansion has been described in many pathological states while monocyte and DC deficiency syndromes are relatively recent additions to the catalog of human primary immunodeficiency disorders. Clinically applicable screening tests to diagnose and monitor these conditions are lacking. Conventional strategies for identifying human DCs and monocytes have been based on the use of a lineage gate to exclude lymphocytes, thus preventing simultaneous detection of DCs, monocytes, and lymphocyte subsets. Here we demonstrate that CD4 is a reliable lineage marker for the human peripheral blood antigen-presenting cell compartment that can be used to identify DCs and monocytes in parallel with lymphocytes. Based on this principle, simple modification of a standard lymphocyte phenotyping assay permits simultaneous enumeration of four lymphocyte and five DC/monocyte populations from a single sample. This approach is applicable to clinical samples and facilitates the diagnosis of DC and monocyte disorders in a wide range of clinical settings, including genetic deficiency, neoplasia, and inflammation. Frontiers Media S.A. 2013-12-27 /pmc/articles/PMC3873601/ /pubmed/24416034 http://dx.doi.org/10.3389/fimmu.2013.00495 Text en Copyright © 2013 Jardine, Barge, Ames-Draycott, Pagan, Cookson, Spickett, Haniffa, Collin and Bigley. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Jardine, Laura
Barge, Dawn
Ames-Draycott, Ashley
Pagan, Sarah
Cookson, Sharon
Spickett, Gavin
Haniffa, Muzlifah
Collin, Matthew
Bigley, Venetia
Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment
title Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment
title_full Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment
title_fullStr Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment
title_full_unstemmed Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment
title_short Rapid Detection of Dendritic Cell and Monocyte Disorders Using CD4 as a Lineage Marker of the Human Peripheral Blood Antigen-Presenting Cell Compartment
title_sort rapid detection of dendritic cell and monocyte disorders using cd4 as a lineage marker of the human peripheral blood antigen-presenting cell compartment
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873601/
https://www.ncbi.nlm.nih.gov/pubmed/24416034
http://dx.doi.org/10.3389/fimmu.2013.00495
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