| Literature DB >> 25135829 |
Philip J Cooper1,2,3, Monika Esser4, Arnaud Marchant5,6, Kinga K Smolen7, Bing Cai8, Edgardo S Fortuno8, Laura Gelinas7, Martin Larsen9,10, David P Speert8, Mustapha Chamekh5, Tobias R Kollmann7,8.
Abstract
Innate immunity instructs adaptive immunity, and suppression of innate immunity is associated with an increased risk for infection. We showed previously that whole-blood cellular components from a cohort of South African children secreted significantly lower levels of most cytokines following stimulation of pattern recognition receptors compared with whole blood from cohorts of Ecuadorian, Belgian, or Canadian children. To begin dissecting the responsible molecular mechanisms, we set out to identify the relevant cellular source of these differences. Across the four cohorts represented in our study, we identified significant variation in the cellular composition of whole blood; however, a significant reduction in the intracellular cytokine production on the single-cell level was only detected in South African children's monocytes, conventional dendritic cells, and plasmacytoid dendritic cells. We also uncovered a marked reduction in polyfunctionality for each of these cellular compartments in South African children compared with children from the other continents. Together, our data identify differences in cell composition, as well as profoundly lower functional responses of innate cells, in our cohort of South African children. A possible link between altered innate immunity and increased risk for infection or lower response to vaccines in South African infants needs to be explored.Entities:
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Year: 2014 PMID: 25135829 PMCID: PMC4157060 DOI: 10.4049/jimmunol.1400895
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422