| Literature DB >> 28179497 |
Jana Blazkova1, Sarthak Gupta2, Yudong Liu2, Brice Gaudilliere3, Edward A Ganio3, Christopher R Bolen4, Ron Saar-Dover4, Gabriela K Fragiadakis4, Martin S Angst3, Sarfaraz Hasni2, Nima Aghaeepour3, David Stevenson5, Nicole Baldwin6, Esperanza Anguiano7, Damien Chaussabel1, Matthew C Altman8, Mariana J Kaplan2, Mark M Davis4,9,10, David Furman11,4,9.
Abstract
Despite clear differences in immune system responses and in the prevalence of autoimmune diseases between males and females, there is little understanding of the processes involved. In this study, we identified a gene signature of immature-like neutrophils, characterized by the overexpression of genes encoding for several granule-containing proteins, which was found at higher levels (up to 3-fold) in young (20-30 y old) but not older (60 to >89 y old) males compared with females. Functional and phenotypic characterization of peripheral blood neutrophils revealed more mature and responsive neutrophils in young females, which also exhibited an elevated capacity in neutrophil extracellular trap formation at baseline and upon microbial or sterile autoimmune stimuli. The expression levels of the immature-like neutrophil signature increased linearly with pregnancy, an immune state of increased susceptibility to certain infections. Using mass cytometry, we also find increased frequencies of immature forms of neutrophils in the blood of women during late pregnancy. Thus, our findings show novel sex differences in innate immunity and identify a common neutrophil signature in males and in pregnant women.Entities:
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Year: 2017 PMID: 28179497 PMCID: PMC5337813 DOI: 10.4049/jimmunol.1601855
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422