Maternal and neonatal lipopolysaccharide and Fas responses are altered by antenatal risk factors for sepsis.

Abstract:

:The diagnosis of neonatal sepsis is difficult, resulting in unnecessary treatment to minimize morbidity and mortality. We hypothesized that exposure to antenatal risk factors for sepsis alters the perinatal neutrophil phenotype. The study setting was a tertiary referral university-affiliated maternity and neonatal hospital. Neutrophils from adults, normal neonates, neonates with antenatal sepsis risk factors and their respective maternal samples were incubated alone, with agonistic Fas antibody or with lipopolysaccharide (LPS). Surface receptor CD11b expression and the percentage apoptosis (persistent inflammatory response) were assessed using flow cytometry. Both mothers and asymptomatic neonates exposed to maternal sepsis risk factors had increased spontaneous neutrophil apoptosis compared to their respective controls. Infants with sepsis were LPS and Fas hyporesponsive. Maternal neutrophils had a delay in apoptosis in all groups with enhanced LPS and Fas responses associated with neonatal sepsis. CD11b expression was not altered significantly between groups. Maternal neutrophil function is altered in neonatal sepsis and may have a diagnostic role. Neonatal sepsis was associated with LPS hyporesponsiveness, potentially increasing susceptibility to infection.

journal_name

Clin Exp Immunol

authors

Molloy EJ,O'Neill AJ,Grantham-Sloan JJ,Webb DW,Watson RW

doi

10.1111/j.1365-2249.2007.03540.x

subject

Has Abstract

pub_date

2008-02-01 00:00:00

pages

244-50

issue

2

eissn

0009-9104

issn

1365-2249

pii

CEI3540

journal_volume

151

pub_type

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