Frontiers in Immunology (Jul 2022)

SARS-CoV2 Infection During Pregnancy Causes Persistent Immune Abnormalities in Women Without Affecting the Newborns

  • Elena Vazquez-Alejo,
  • Laura Tarancon-Diez,
  • Itzíar Carrasco,
  • Itzíar Carrasco,
  • Sara Vigil-Vázquez,
  • Mar Muñoz-Chapuli,
  • Elena Rincón-López,
  • Elena Rincón-López,
  • Elena Rincón-López,
  • Jesús Saavedra-Lozano,
  • Jesús Saavedra-Lozano,
  • Jesús Saavedra-Lozano,
  • Jesús Saavedra-Lozano,
  • Mar Santos-Sebastián,
  • Mar Santos-Sebastián,
  • Mar Santos-Sebastián,
  • David Aguilera-Alonso,
  • David Aguilera-Alonso,
  • David Aguilera-Alonso,
  • Alicia Hernanz-Lobo,
  • Alicia Hernanz-Lobo,
  • Alicia Hernanz-Lobo,
  • Begoña Santiago-García,
  • Begoña Santiago-García,
  • Begoña Santiago-García,
  • Juan Antonio de León-Luis,
  • Juan Antonio de León-Luis,
  • Patricia Muñoz,
  • Manuel Sánchez-Luna,
  • Manuel Sánchez-Luna,
  • María Luisa Navarro,
  • María Luisa Navarro,
  • María Luisa Navarro,
  • María Luisa Navarro,
  • Mª Ángeles Muñoz-Fernández

DOI
https://doi.org/10.3389/fimmu.2022.947549
Journal volume & issue
Vol. 13

Abstract

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SARS-CoV2 infection in pregnancy and exposed newborns is poorly known. We performed a longitudinal analysis of immune system and determined soluble cytokine levels in pregnant women infected with SARS-CoV2 and in their newborns. Women with confirmed SARS-CoV2 infection and their exposed uninfected newborns were recruited from Hospital General Universitario Gregorio Marañón. Peripheral blood mononuclear cells (PBMCs), cord cells and plasma were collected at birth and 6 months later. Immunophenotyping of natural killer (NK), monocytes and CD4/CD8 T-cells were studied in cryopreserved PBMCs and cord cells by multiparametric flow cytometry. Up to 4 soluble pro/anti-inflammatory cytokines were assessed in plasma/cord plasma by ELISA assay. SARS-CoV2-infected mothers and their newborns were compared to matched healthy non-SARS-CoV2-infected mothers and their newborns. The TNFα and IL-10 levels of infected mothers were higher at baseline than those of healthy controls. Infected mothers showed increased NK cells activation and reduced expression of maturation markers that reverted after 6 months. They also had high levels of Central Memory and low Effector Memory CD4-T cell subsets. Additionally, the increased CD4- and CD8-T cell activation (CD154 and CD38) and exhaustion (TIM3/TIGIT) levels at baseline compared to controls remained elevated after 6 months. Regarding Treg cells, the levels were lower at infected mothers at baseline but reverted after 6 months. No newborn was infected at birth. The lower levels of monocytes, NK and CD4-T cells observed at SARS-CoV2-exposed newborns compared to unexposed controls significantly increased 6 months later. In conclusion, SARS-CoV2 infection during pregnancy shows differences in immunological components that could lead newborns to future clinical implications after birth. However, SARS-CoV2 exposed 6-months-old newborns showed no immune misbalance, whereas the infected mothers maintain increased activation and exhaustion levels in T-cells after 6 months.

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