Author: Mahyuddin, AP; Kanneganti, A; Wong, JLJ; Dimri, P Sharma; Su, LL; Biswas, A; Illanes, SE; Mattar, CNZ; Huang, RYâ€J; Choolani, M
Title: Mechanisms and evidence of vertical transmission of infections in pregnancy including SARSâ€CoVâ€2 Cord-id: mq6qjs2s Document date: 2020_6_12
ID: mq6qjs2s
Snippet: There remain unanswered questions concerning motherâ€toâ€childâ€transmission (MTCT) of SARSâ€CoVâ€2. Despite reports of neonatal COVIDâ€19, SARSâ€CoVâ€2 has not been consistently isolated in perinatal samples thus, definitive proof of transplacental infection is still lacking. To address these questions, we assessed investigative tools used to confirm maternalâ€fetal infection and known protective mechanisms of the placental barrier that prevent transplacental pathogen migration. Forty
Document: There remain unanswered questions concerning motherâ€toâ€childâ€transmission (MTCT) of SARSâ€CoVâ€2. Despite reports of neonatal COVIDâ€19, SARSâ€CoVâ€2 has not been consistently isolated in perinatal samples thus, definitive proof of transplacental infection is still lacking. To address these questions, we assessed investigative tools used to confirm maternalâ€fetal infection and known protective mechanisms of the placental barrier that prevent transplacental pathogen migration. Forty studies of COVIDâ€19 pregnancies reviewed suggest a lack of consensus on diagnostic strategy for congenital infection. While RTâ€PCR of neonatal swabs was universally performed, a wide range of clinical samples was screened including vaginal secretions (22.5%), amniotic fluid (35%), breast milk (22.5%) and umbilical cord blood. Neonatal COVIDâ€19 was reported in eight studies, two of which were based on the detection of SARSâ€CoVâ€2 IgM in neonatal blood. Histological examination demonstrated sparse viral particles, vascular malperfusion and inflammation in the placenta from pregnant women with COVIDâ€19. The paucity of placental coâ€expression of ACEâ€2 and TMPRSS2, two receptors involved in cytoplasmic entry of SARSâ€CoVâ€2, may explain its relative insensitivity to transplacental infection. Viral interactions may utilise membrane receptors other than ACEâ€2 thus, tissue susceptibility may be broader than currently known. Further spatialâ€temporal studies are needed to determine the true potential for transplacental migration. This article is protected by copyright. All rights reserved.
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