M1-like monocytes are a major immunological determinant of severity in previously healthy adults with life-threatening influenza
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Suzanne L Cole Jake Dunning Wai Ling Kok Kambez Hajipouran Benam Adel Benlahrech Emmanouela Repapi Fernando O Martinez Lydia Drumright Timothy J Powell Michael Bennett Ruth Elderfield Catherine Thomas MOSAIC investigators Tao Dong John Mccauley Foo Y Liew Stephen Taylor Maria Zambon Wendy Barclay Vincenzo Cerundolo Peter J Openshaw Andrew J McMichael Ling-Pei HoAbstract
In each influenza season, a distinct group of young, otherwise healthy individuals with no risk factors succumbs to life-threatening infection. To better understand the cause for this, we analyzed a broad range of immune responses in bloodfrom a unique cohort of patients, comprising previously healthy individuals hospitalized with and without respiratory failureduring one influenza season, and infected with one specific influenza A strain. This analysis was compared with similarlyhospitalized influenza patients with known risk factors (total of n = 60 patients recruited). We found a sustained increase ina specific subset of proinflammatory monocytes, with high TNF-α expression and an M1-like phenotype (independent ofviral titers), in these previously healthy patients with severe disease. The relationship between M1-like monocytes andimmunopathology was strengthened using murine models of influenza, in which severe infection generated using differentmodels (including the high-pathogenicity H5N1 strain) was also accompanied by high levels of circulating M1-likemonocytes. Additionally, a raised M1/M2 macrophage ratio in the lungs was observed. These studies identify a specificsubtype of monocytes as a modifiable immunological determinant of disease severity in this subgroup of severely ill,previously healthy patients, offering potential novel therapeutic avenues
Journal details
Journal JCI insight
Volume 2
Issue number 7
Pages e91868
Available online
Publication date
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Publisher website (DOI) 10.1172/jci.insight.91868
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Europe PubMed Central 28405622
Pubmed 28405622