Human spleen contains different subsets of dendritic cells and regulatory T lymphocytes

ABSTRACT: Most knowledge about dendritic cells (DCs) and regulatory T cells in humans has been gathered from circulating cells but little is known about their frequency and distribution in lymphoid organs. This report shows the frequency, phenotype and location of DCs and regulatory T cells in decea...

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Autores:
Velásquez Lopera, Margarita María
García Moreno, Luis Fernando
Correa Londoño, Luis Alfonso
Tipo de recurso:
Article of investigation
Fecha de publicación:
2008
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/41220
Acceso en línea:
https://hdl.handle.net/10495/41220
Palabra clave:
Biomarcadores
Biomarkers
Células Dendríticas
Dendritic Cells
Citometría de Flujo
Flow Cytometry
Factores de Transcripción Forkhead
Forkhead Transcription Factors
Inmunohistoquímica
Immunohistochemistry
Subunidad alfa del Receptor de Interleucina-2
Interleukin-2 Receptor alpha Subunit
Bazo
Spleen
Subgrupos de Linfocitos T
T-Lymphocyte Subsets
https://id.nlm.nih.gov/mesh/D015415
https://id.nlm.nih.gov/mesh/D003713
https://id.nlm.nih.gov/mesh/D005434
https://id.nlm.nih.gov/mesh/D051858
https://id.nlm.nih.gov/mesh/D007150
https://id.nlm.nih.gov/mesh/D053645
https://id.nlm.nih.gov/mesh/D013154
https://id.nlm.nih.gov/mesh/D016176
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
Description
Summary:ABSTRACT: Most knowledge about dendritic cells (DCs) and regulatory T cells in humans has been gathered from circulating cells but little is known about their frequency and distribution in lymphoid organs. This report shows the frequency, phenotype and location of DCs and regulatory T cells in deceased organ donors' spleens. As determined by flow cytometry, conventional/myeloid DCs (cDCs) CD11c(high)HLA-DR(+)CD123(-/low) were 2.3 +/- 0.9% and LIN(-) HLA-DR(+)CD11c(high) 2.1 +/- 0.3% of total spleen cells. Mature CD11c(high)HLA-DR(+)CD83(+) were 1.5 +/- 0.8% and 1.0 +/- 1.6% immature CD11c(high)HLA-DR(+)CD83(-) cDC. There were 0.3 +/- 0.3% plasmacytoid DCs (pDC) CD11c(-/low)HLA-DR(+)CD123(high) and 0.3 +/- 0.1% LIN(-)HLA DR(+)CD123(high). Cells expressing cDCs markers, BDCA-1 and BDCA-3, and pDCs markers BDCA-2 and BDCA-4 were observed in higher frequencies than DCs with other phenotypes evaluated. CD11c(+), CD123(+) and CD83(+) cells were located in subcapsular zone, T cells areas and B-cell follicles. CD4(+)CD25(high) Tregs were 0.2 +/- 0.2% and CD8(+)CD28(-) comprised 11.5 +/- 8.1% of spleen lymphocytes. FOXP3(+) cells were found in T- and B-cell areas. The improvement in cell separation, manipulation and expansion techniques, will facilitate the manipulation of donor spleen cells as a part of protocols for induction and maintenance of allograft tolerance or treatment of autoimmune diseases.