Frontiers in Immunology (Jun 2021)

The Immune Atlas of Human Deciduas With Unexplained Recurrent Pregnancy Loss

  • Pengfei Chen,
  • Pengfei Chen,
  • Liying Zhou,
  • Jiying Chen,
  • Ying Lu,
  • Chaoxia Cao,
  • Shuangli Lv,
  • Zhihong Wei,
  • Zhihong Wei,
  • Liping Wang,
  • Jiao Chen,
  • Xinglin Hu,
  • Zijing Wu,
  • Xiaohua Zhou,
  • Danna Su,
  • Xuefeng Deng,
  • Changchun Zeng,
  • Huiyun Wang,
  • Zuhui Pu,
  • Ruiying Diao,
  • Lisha Mou

DOI
https://doi.org/10.3389/fimmu.2021.689019
Journal volume & issue
Vol. 12

Abstract

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Recurrent pregnancy loss (RPL) is a common fertility problem that affects 1%-2% of couples all over the world. Despite exciting discoveries regarding the important roles of the decidual natural killer cell (dNK) and regulatory T cell in pregnancy, the immune heterogeneity in patients with unexplained recurrent pregnancy loss (URPL) remains elusive. Here, we profiled the transcriptomes of 13,953 CD45+ cells from three normal and three URPL deciduas. Based on our data, the cellular composition revealed three major populations of immune cells including dNK cell, T cell, and macrophage, and four minor populations including monocytes, dendritic cell (DC), mast cell, and B cell. Especially, we identified a subpopulation of CSF1+ CD59+ KIRs-expressing dNK cells in normal deciduas, while the proportion of this subpopulation was decreased in URPL deciduas. We also identified a small subpopulation of activated dDCs that were accumulated mainly in URPL deciduas. Furthermore, our data revealed that in decidua at early pregnancy, CD8+ T cells exhibited cytotoxic properties. The decidual macrophages expressed high levels of both M1 and M2 feature genes, which made them unique to the conventional M1/M2 classification. Our single-cell data revealed the immune heterogeneity in decidua and the potentially pathogenic immune variations in URPL.

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