Mixed Leukocyte Reaction Using Human Plasmacytoid Dendritic Cells and CD4+ T Cells
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Assessing the Innate Sensing of HIV-1 Infected CD4+ T Cells by Plasmacytoid Dendritic Cells Using an Ex vivo Co-culture System.
Published on: September 1, 2015
Sorely Adelina Sosa-Luis1, Alexia Almaraz-Arreortua1, Honorio Torres-Aguilar1
1Clinical and Basic Immunology Research Department of Biochemical Sciences Faculty, Universidad Autónoma "Benito Juárez" de Oaxaca, Oaxaca, Mexico.
Plasmacytoid dendritic cells (pDCs) are critical in antiviral immune responses and play a significant role in developing autoimmune diseases and transplant rejection. Despite their scarcity in peripheral blood, the accessibility of blood peripheral pDCs makes them a promising source for evaluating T-cell antigen-specific responses in viral infections and autoimmune diseases, as well as alloreactive stimulation in transplantation, including graft-versus-host disease. T-cell priming assays with pDCs have presented a significant challenge due to the low proliferation of T cells. This underscores the critical need for meticulous standardization of suitable conditions for cell purification and coculture in peripheral blood pDC-based mixed leukocyte reactions (MLRs) to ensure productive and quantitative results. This chapter presents a thorough methodology for isolating peripheral blood human pDCs and their application in an MLR assay to evaluate alloreactive T-cell responses using flow cytometry and the adjustments to analyze antigen-specific reactions.
Plasmacytoid dendritic cells (pDCs) are critical in antiviral immune responses and play a significant role in developing autoimmune diseases and transplant rejection. Despite their scarcity in peripheral blood, the accessibility of blood peripheral pDCs makes them a promising source for evaluating T-cell antigen-specific responses in viral infections and autoimmune diseases, as well as alloreactive stimulation in transplantation, including graft-versus-host disease. T-cell priming assays with pDCs have presented a significant challenge due to the low proliferation of T cells. This underscores the critical need for meticulous standardization of suitable conditions for cell purification and coculture in peripheral blood pDC-based mixed leukocyte reactions (MLRs) to ensure productive and quantitative results. This chapter presents a thorough methodology for isolating peripheral blood human pDCs and their application in an MLR assay to evaluate alloreactive T-cell responses using flow cytometry and the adjustments to analyze antigen-specific reactions.

