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B-cell dynamics during experimental endotoxemia in humans.

Authors :
Brinkhoff A
Zeng Y
Sieberichs A
Dolff S
Shilei X
Sun M
Engler H
Benson S
Korth J
Schedlowski M
Kribben A
Witzke O
Wilde B
Source :
Bioscience reports [Biosci Rep] 2019 May 17; Vol. 39 (5). Date of Electronic Publication: 2019 May 17 (Print Publication: 2019).
Publication Year :
2019

Abstract

Recently, B cells with regulatory functions suppressing T-cell immunity were identified. Inflammation in the context of sepsis is characterized by a profound immune dysfunction increasing the patient's risk for additional infections. The impact of endotoxemia on B-cell dynamics, regulatory B cells (Breg) and its contribution to immune dysfunction is unknown. It is the aim of the present study to characterize the dynamics of the B-cell compartment and Breg in an experimental human endotoxemia model.In this randomized placebo-controlled cross-over study, 20 healthy males received an intravenous injection of endotoxin ( Escherichia coli lipopolysaccharide, LPS, 0.8 ng/kg body weight) or placebo (saline 0.9%) on two otherwise identical study days. B cells were analyzed by flow cytometry at baseline and repeatedly up to 72 h after endotoxin/placebo injection.Absolute CD19 <superscript>+</superscript> B cells counts showed a significant decrease 3 h after endotoxin injection. Memory B cells were partially depleted from the circulation; the total number of Breg was significantly diminished 3 h after LPS challenge. Production of anti-inflammatory interleukin (IL)-10 (IL-10) by Breg was unaltered after LPS challenge. Systemic B-cell activating factor (BAFF) levels were significantly increased with a maximum after 24 h and remained increased up to 72 h post-injection.Endotoxemia causes a transient depletion of memory B cells and Breg from the circulation. However, the functional capacity of B cells to produce IL-10 is not impaired.<br /> (© 2019 The Author(s).)

Details

Language :
English
ISSN :
1573-4935
Volume :
39
Issue :
5
Database :
MEDLINE
Journal :
Bioscience reports
Publication Type :
Academic Journal
Accession number :
30962268
Full Text :
https://doi.org/10.1042/BSR20182347