Offspring born to influenza A virus infected pregnant mice have increased susceptibility to viral and bacterial infections in early life.
Henning JacobsenKerstin Walendy-GnirßNilgün Tekin-BubenheimNancy Mounogou KouassiIsabel Ben-BatallaNikolaus BerenbrokMartin WolffVinicius Pinho Dos ReisMartin ZicklerLucas SchollAnnette GriesHanna JaniaAndreas KloetgenArne DüsedauGundula Pilnitz-StolzeAicha JeridiAli Oender YildirimHelmut FuchsValérie Gailus-DurnerClaudia StoegerMartin Hrabě de AngelisTatjana ManuylovaKarin KlingelFiona J CulleyJochen BehrendsSonja LogesBianca SchneiderSusanne Krauss-EtschmannPeter J M OpenshawGülsah GabrielPublished in: Nature communications (2021)
Influenza during pregnancy can affect the health of offspring in later life, among which neurocognitive disorders are among the best described. Here, we investigate whether maternal influenza infection has adverse effects on immune responses in offspring. We establish a two-hit mouse model to study the effect of maternal influenza A virus infection (first hit) on vulnerability of offspring to heterologous infections (second hit) in later life. Offspring born to influenza A virus infected mothers are stunted in growth and more vulnerable to heterologous infections (influenza B virus and MRSA) than those born to PBS- or poly(I:C)-treated mothers. Enhanced vulnerability to infection in neonates is associated with reduced haematopoetic development and immune responses. In particular, alveolar macrophages of offspring exposed to maternal influenza have reduced capacity to clear second hit pathogens. This impaired pathogen clearance is partially reversed by adoptive transfer of alveolar macrophages from healthy offspring born to uninfected dams. These findings suggest that maternal influenza infection may impair immune ontogeny and increase susceptibility to early life infections of offspring.
Keyphrases
- high fat diet
- early life
- immune response
- birth weight
- gestational age
- low birth weight
- mouse model
- public health
- climate change
- insulin resistance
- adipose tissue
- staphylococcus aureus
- type diabetes
- pregnancy outcomes
- emergency department
- dendritic cells
- preterm infants
- bipolar disorder
- bone marrow
- mesenchymal stem cells
- cell therapy
- inflammatory response
- saccharomyces cerevisiae
- newly diagnosed
- adverse drug
- health promotion