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  • Abelius, Martina SLinköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten (author)

The Placental Immune Milieu is Characterized by a Th2- and Anti-Inflammatory Transcription Profile, Regardless of Maternal Allergy, and Associates with Neonatal Immunity

  • Article/chapterEnglish2015

Publisher, publication year, extent ...

  • 2014-12-10
  • Wiley-Blackwell,2015
  • electronicrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:liu-114069
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-114069URI
  • https://doi.org/10.1111/aji.12350DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • PROBLEM: How maternal allergy affects the systemic and local immunological environment during pregnancy and the immune development of the offspring is unclear.METHOD OF STUDY: Expression of 40 genes was quantified by PCR arrays in placenta, peripheral blood mononuclear cells (PBMC), and cord blood mononuclear cells (CBMC) from 7 allergic and 12 non-allergic women and their offspring.RESULTS: Placental gene expression was dominated by a Th2-/anti-inflammatory profile, irrespectively of maternal allergy, as compared to gene expression in PBMC. p35 expression in placenta correlated with fetal Tbx21 (ρ = -0.88, P < 0.001) and IL-5 expression in PBMC with fetal galectin1 (ρ = 0.91, P < 0.001). Increased expression of Th2-associated CCL22 in CBMC preceded allergy development.CONCLUSIONS: Gene expression locally and systemically during pregnancy was partly associated with the offspring's gene expression, possibly indicating that the immunological milieu is important for fetal immune development. Maternal allergy was not associated with an enhanced Th2 immunity in placenta or PBMC, while a marked prenatal Th2 skewing, shown as increased CCL22 mRNA expression, might contribute to postnatal allergy development.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Janefjord, CamillaLinköpings universitet,Avdelningen för cellbiologi,Medicinska fakulteten(Swepub:liu)camja19 (author)
  • Ernerudh, JanLinköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten,Region Östergötland, Klinisk immunologi och transfusionsmedicin(Swepub:liu)janer15 (author)
  • Berg, GöranLinköpings universitet,Avdelningen för kliniska vetenskaper,Medicinska fakulteten,Region Östergötland, Kvinnokliniken US(Swepub:liu)gorbe09 (author)
  • Matthiesen, LeifLinköpings universitet,Avdelningen för kliniska vetenskaper,Medicinska fakulteten,Region Östergötland, Kvinnokliniken US,Helsingborg Hospital, Helsingborg(Swepub:liu)leima96 (author)
  • Duchén, KarelLinköpings universitet,Avdelningen för kliniska vetenskaper,Medicinska fakulteten,Region Östergötland, Barn- och ungdomskliniken i Linköping(Swepub:liu)kardu59 (author)
  • Nilsson, Lennart JLinköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten,Region Östergötland, Allergicentrum US(Swepub:liu)lenni67 (author)
  • Jenmalm, MariaLinköpings universitet,Avdelningen för neuro- och inflammationsvetenskap,Medicinska fakulteten(Swepub:liu)marje18 (author)
  • Linköpings universitetAvdelningen för neuro- och inflammationsvetenskap (creator_code:org_t)

Related titles

  • In:American Journal of Reproductive Immunology: Wiley-Blackwell73:5, s. 445-4591046-74081600-0897

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