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Expression of interleukin-22 in decidua of patients with early pregnancy and unexplained recurrent pregnancy loss

  • Candice O’Hern Perfetto
  • , Xiujun Fan
  • , Sabita Dahl
  • , Sacha Krieg
  • , Lynn Marie Westphal
  • , Ruth Bunker Lathi
  • , Nihar R. Nayak

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose Researchers have hypothesized that an imbalance of immune cells in the uterine decidua and a dysfunction in cytokines they produce may contribute to recurrent pregnancy loss (RPL). The objective of this study was to determine if IL- 22, IL-23 and IL-17 are expressed abnormally in the decidua of patients with RPL compared to those women with a normal pregnancy. We also sought to confirm that uterine natural killer (uNK) cells are lower in the decidua of patients with RPL, as well as identify IL-22 expression by uNK cells. Methods After meeting strict inclusion criteria, maternal decidua of nine patients with unexplained RPL and a confirmed euploid fetal loss, and 11 gestational age-matched patients undergoing elective pregnancy termination were included in our analysis. Quantitative real time-polymerase chain reaction (qRT-PCR) was performed to quantify RNA expression, Western blot was performed to quantify protein expression and immunohistochemistry (IHC) was performed to identify IL-22 and uNK cells. Results We found that women with unexplained RPL and a euploid fetal loss had significantly less gene and protein expression of IL-22 in the decidua. Additionally, we found that IL-22 is primarily expressed by uNK cells in the decidua. Conclusions In conclusion, our results suggest that lower levels of IL-22 in the uterine decidua in patients with unexplained RPL may contribute to a disruption of decidual homeostasis and ultimately lead to early pregnancy loss.

Original languageEnglish (US)
Article numberA012
Pages (from-to)977-984
Number of pages8
JournalJournal of Assisted Reproduction and Genetics
Volume32
Issue number6
DOIs
StatePublished - Jun 1 2015
Externally publishedYes

Funding

This research was made possible through the support of the Ernest and Amelia Gallo Endowed Postdoctoral fellowship, the Child Health Research Institute, Lucile Packard Foundation for Children’s Health, as well as the Stanford CTSA (grant number UL1 TR000093).

FundersFunder number
Lucile Packard Foundation for Children’s Health
Stanford NIH-NCATS-CTSAUL1 TR000093
Author National Institutes of Health National Institutes of Health National Institutes of Health National Institutes of Health The Bev Hartig Huntington's Disease Foundation National Institutes of Health
National Center for Advancing Translational SciencesUL1TR000093
Women's & Children's Health Research Institute

    Keywords

    • Interleukin-17
    • Interleukin-22
    • Interleukin-23
    • Recurrent pregnancy loss
    • Uterine deciduas

    ASJC Scopus subject areas

    • Reproductive Medicine
    • Genetics
    • Obstetrics and Gynecology
    • Developmental Biology
    • Genetics(clinical)

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