# Detection of spike protein in term placentas of COVID-19 vaccinated and/or SARS-CoV-2 infected women

**Authors:** Catharina Bartmann, Vanessa Schmidt, Michael Mörz, Michael Schwab, Monika Rehn, Bettina Blau-Schneider, Achim Wöckel, Ulrike Kämmerer, Jayonta Bhattacharjee, Moises Leon Juarez, Moises Leon Juarez, Moises Leon Juarez

PMC · DOI: 10.1371/journal.pone.0344185 · 2026-03-05

## TL;DR

This study found SARS-CoV-2 spike protein in placentas of vaccinated and infected women, suggesting possible transplacental transfer.

## Contribution

Demonstrates detection of spike protein in placental cells after vaccination or infection, indicating potential transplacental transfer.

## Key findings

- Spike protein detected in 31 placentas, primarily in Hofbauer cells and trophoblasts.
- No viral RNA found, but mRNA from vaccines detected in two samples.
- No significant difference in staining patterns based on vaccination or infection status.

## Abstract

COVID-19 (Corona Virus Induced Disease-19) caused by the SARS-CoV-2 coronavirus can be a serious in pregnancy. Therefore, vaccination with modRNA vaccines was recommended depending on the immunity status for women of reproductive age and pregnant women since 2022. However, there are only preliminary data on transplacental transmission of the virus and modRNA from genetic vaccines so far.

The study population included 106 women who have given birth at the Department of Obstetrics and Gynecology, University Hospital of Würzburg during November 2020 to October 2022. In addition to medical data and vaccination history, immunohistochemical examination of the placenta was performed with antibodies against SARS-CoV-2 spike and nucleocapsid proteins. RNAscope in situ Hybridization was used to show RNA detection in positive placental tissues as a proof of concept.

Altogether, 87% of participants received at least one vaccine dose against SARS-CoV-2 and 56 women (42 vaccinated, 14 not vaccinated) contracted COVID-19. In total, 31 placentas were found positive for the spike protein. Spike positive cells were predominantly Hofbauer cells and trophoblasts. In three cases of vaccinated and then infected woman, an additional nucleocapsid staining was detected, but there was no significant difference in staining pattern in correlation to the vaccine/COVID-19 status. Interestingly, we did not find viral RNA in the investigated samples, but we could show a positive in situ Hybridization of BNT162b2 and S-encoding mRNA-1273 in two individual samples.

The spike protein of SARS-CoV-2 has been be detected in placental Hofbauer and Trophoblast cells as well as villous endothelia after infection and vaccination indicating a possible transplacental transfer or uptake. These findings may suggest a potential for transplacental transfer or cellular uptake; however, the extent, mechanisms, and clinical significance of this phenomenon remain to be fully understood.

Clinical trial registration: DRKS00022506.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, MUC1 (mucin 1, cell surface associated) [NCBI Gene 4582] {aka ADMCKD, ADMCKD1, ADTKD2, CA 15-3, CD227, Ca15-3}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, CD163 (CD163 molecule) [NCBI Gene 9332] {aka M130, MM130, SCARI1}, NRP1 (neuropilin 1) [NCBI Gene 8829] {aka BDCA4, CD304, NP1, NRP, VEGF165R}, Cd68 (CD68 antigen) [NCBI Gene 12514] {aka Lamp4, Scard1, gp110}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}
- **Diseases:** pregnancy disorders (MESH:D011254), vomiting (MESH:D014839), infectious diseases (MESH:D003141), -19 (MESH:D000094024), congenital diseases (MESH:D030342), malformations (MESH:C564254), necrosis (MESH:D009336), maternal (MESH:D000079262), Fever (MESH:D005334), allergic reactions (MESH:D004342), pneumonia (MESH:D011014), diarrhea (MESH:D003967), premature (MESH:C536271), muscle and joint pain (MESH:D063806), stillbirth (MESH:D050497), embolism (MESH:D004617), neonatal diseases (MESH:D007232), common cold (MESH:D003139), miscarriages (MESH:D000022), nausea (MESH:D009325), pre-eclampsia (MESH:D011225), cough (MESH:D003371), STB infection (MESH:D007239), shortness of breath (MESH:D004417), premature birth (MESH:D047928), nasal congestions (MESH:D009668), placental infection (MESH:D010922), endothelial damage (MESH:D014652), COVID-19 (MESH:D000086382), respiratory disease (MESH:D012140), death (MESH:D003643), sore throat (MESH:D010612), flu (MESH:D007251), congenital malformations (OMIM:163000), viral infection (MESH:D014777), headache (MESH:D006261), gastrointestinal problems (MESH:D012817), inflammatory (MESH:D007249), disease symptoms (MESH:D004194), thrombose (MESH:D013927), rhinorrhea (MESH:D012818), taste and odor disorders (MESH:D013651)
- **Chemicals:** formalin (MESH:D005557), ethanol (MESH:D000431), PBS (MESH:D007854), eosin (MESH:D004801), DAB (MESH:C000469), alcohol (MESH:D000438), lipid (MESH:D008055), water (MESH:D014867), xylene (MESH:D014992), nitrogen (MESH:D009584), FC (MESH:C095424), sodium citrate (MESH:D000077559), Hematoxylin (MESH:D006416), paraffin (MESH:D010232), AP-red (-), hydrogen peroxide (MESH:D006861), methanol (MESH:D000432)
- **Species:** Gammacoronavirus (genus) [taxon 694013], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Syntrophorhabdus sp. TB (species) [taxon 979969], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12962466/full.md

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Source: https://tomesphere.com/paper/PMC12962466