In vivo immune signatures of healthy human pregnancy: Inherently inflammatory or anti-inflammatory?

Autor: Piush J. Mandhane, Stuart E. Turvey, Malcolm R. Sears, Rishma Chooniedass, Kent T. HayGlass, Caroline Graham, William P. Stefura, Allan B. Becker, Child Study Investigators, Padmaja Subbarao
Rok vydání: 2017
Předmět:
0301 basic medicine
Physiology
Maternal Health
Anti-Inflammatory Agents
lcsh:Medicine
Pathology and Laboratory Medicine
Biochemistry
Monocytes
White Blood Cells
0302 clinical medicine
Pregnancy
Animal Cells
Immune Physiology
Medicine and Health Sciences
Longitudinal Studies
lcsh:Science
Immune Response
Innate Immune System
Multidisciplinary
T Cells
Obstetrics and Gynecology
Gestational age
Body Fluids
3. Good health
Blood
Cytokines
Biomarker (medicine)
Female
Inflammation Mediators
Cellular Types
Anatomy
medicine.symptom
Research Article
Adult
Canada
Adolescent
Immune Cells
Immunology
Gestational Age
Inflammation
Biology
Blood Plasma
Young Adult
03 medical and health sciences
Signs and Symptoms
Immune system
Diagnostic Medicine
Immunity
medicine
Humans
Fetus
Blood Cells
Innate immune system
Macrophages
lcsh:R
Biology and Life Sciences
Cell Biology
Molecular Development
medicine.disease
Immunity
Innate

Kinetics
030104 developmental biology
Immune System
Women's Health
lcsh:Q
Biomarkers
Developmental Biology
030215 immunology
Zdroj: PLoS ONE
PLoS ONE, Vol 12, Iss 6, p e0177813 (2017)
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0177813
Popis: Changes in maternal innate immunity during healthy human pregnancy are not well understood. Whether basal immune status in vivo is largely unaffected by pregnancy, is constitutively biased towards an inflammatory phenotype (transiently enhancing host defense) or exhibits anti-inflammatory bias (reducing potential responsiveness to the fetus) is unclear. Here, in a longitudinal study of healthy women who gave birth to healthy infants following uncomplicated pregnancies within the Canadian Healthy Infant Longitudinal Development (CHILD) cohort, we test the hypothesis that a progressively altered bias in resting innate immune status develops. Women were examined during pregnancy and again, one and/or three years postpartum. Most pro-inflammatory cytokine expression, including CCL2, CXCL10, IL-18 and TNFα, was reduced in vivo during pregnancy (20-57%, p
Databáze: OpenAIRE