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Flow cytometric analysis of peripheral blood dendritic cells in patients with severe sepsis
Author(s) -
Riccardi Francesca,
Della Porta Matteo G.,
Rovati Bianca,
Casazza Alberto,
Radolovich Danila,
De Amici Mara,
Danova Marco,
Langer Martin
Publication year - 2011
Publication title -
cytometry part b: clinical cytometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.646
H-Index - 61
eISSN - 1552-4957
pISSN - 1552-4949
DOI - 10.1002/cyto.b.20540
Subject(s) - cd11c , sepsis , medicine , chemokine , compartment (ship) , septic shock , myeloid , cxcr4 , prospective cohort study , resuscitation , chemokine receptor , receptor , gastroenterology , immunology , surgery , biology , gene , biochemistry , oceanography , phenotype , geology
Abstract Background: Dendritic cells (DC) play a key role in cell‐mediated immunity. We aimed to analyse the number and function of peripheral blood (PB) myeloid and plasmacytoid DC (mDC/pDC) in patients with severe sepsis. Methods: Twenty‐six septic patients, 20 surgical patients (abdominal aortic aneurysm) and 20 healthy controls were enrolled in this prospective study. Results: At day 1 (enrollment in the study), septic patients showed in comparison with healthy controls, decreased mDC ( P < 0.001) and increased pDC ( P = 0.03), resulting in a reduction of the mDC/pDC ratio ( P < 0.001). Surgery induced a decrease in both mDCs and pDCs level, without modification of mDC/pDC ratio. Septic patients included 15 survivors and 11 nonsurvivors. At day 1 no significant difference was found in mDC between the two groups, while pDCs were significantly higher in nonsurvivors ( P = 0.03). At the outcome, mDC were selectively increased with respect to day 1 in survivors ( P = 0.001), while no significant differences were observed as far as pDC count is concerned in both groups. Sorted DC from septic patients showed in comparison with healthy controls, reduced levels of HLA DR ( P < 0.001), CD11c ( P < 0.001), CD83 ( P = 0.006) and of costimulatory molecule CD86 ( P = 0.003); an up‐regulation of chemokine receptor CXCR4 ( P = 0.031) and increased apoptosis ( P < 0.001). Conclusions: Sepsis has a profound effect on PB DC compartment. These alterations appear to be sepsis‐specific. Increased apoptosis and alteration of migration and trafficking mechanism may be involved in DC compartment modification. DC alterations could contribute to sepsis‐mediated immunoparalysis. © 2010 International Clinical Cytometry Society