Tests for IgG and IgM antibodies for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) became available in February 2020. On March 4, 2020, the seventh edition of the New Coronavirus Pneumonia Prevention and Control Protocol for the novel coronavirus disease 2019 (COVID-19) was released by the National Health Commission of the People’s Republic of China and added serological diagnostic criteria.1 A previous study of 9 pregnant women and their infants found no maternal-infant transmission of SARS-CoV-2 based on reverse transcriptase–polymerase chain reaction (RT-PCR).2 We applied these new criteria to 6 pregnant women with confirmed COVID-19 and their infants because serologic criteria would allow more detailed investigation of infection in newborns.
Clinical records and laboratory results were retrospectively reviewed for 6 pregnant women with COVID-19 admitted to Zhongnan Hospital of Wuhan University from February 16 to March 6, 2020, confirmed based on symptoms, chest computed tomography, and positive RT-PCR results.
Blood samples were collected from the mothers at delivery and neonatal blood and throat swab samples were collected at birth. Quantitative RT-PCR for SARS-CoV-2 nucleic acid (RT-PCR Kit, BioGerm) was conducted on neonatal serum and throat swabs. Inflammatory cytokines (CBA Human Th1/Th2 Cytokine Kit II, BD Biosciences) were tested on neonatal serum. Maternal and neonatal sera samples were used to test for IgG and IgM antibodies. All tests were performed by 2 researchers (Y.T. and Q.D.), with SARS-CoV-2 IgG and IgM samples from infants double checked (CLIA assays Kit, YHLO). Sample collection, processing, and laboratory testing followed guidance from the World Health Organization.3 The sensitivity and specificity reported by the manufacturer for IgM are 88.2% and 99.0% respectively, and for IgG are 97.8% and 97.9%.4
This study was approved by the Zhongnan Hospital of Wuhan University institutional review board, which waived informed consent for this retrospective study.
All 6 mothers had mild clinical manifestations. All had cesarean deliveries in their third trimester in negative pressure isolation rooms. All mothers wore masks, and all medical staff wore protective suits and double masks. The infants were isolated from their mothers immediately after delivery.
All 6 infants had 1-minute Apgar scores of 8 to 9 and 5-minute Apgar scores of 9 to 10. Neonatal throat swabs and blood samples all had negative RT-PCR test results. All 6 infants had antibodies detected in their serum. Two infants had IgG and IgM concentrations higher than the normal level (<10 AU/mL). One infant had an IgG level of 125.5 and IgM level of 39.6 AU/mL; the second infant, had an IgG level of 113.91 AU/mL and IgM level of 16.25 AU/mL (Table 1). Their mothers also had elevated levels of IgG and IgM (Table 2). Three infants had elevated IgG levels (75.49, 73.19, 51.38 AU/mL) but normal IgM levels; all 3 mothers had elevated IgG and 2 also had elevated IgM levels. Inflammatory cytokine IL-6 was significantly increased in all infants. None of the infants presented any symptoms as of March 8, 2020.
Among 6 mothers with confirmed COVID-19, SARS-CoV-19 was not detected in the serum or throat swab by RT-PCR in any of their newborns. However, virus-specific antibodies were detected in neonatal blood sera samples. The IgG concentrations were elevated in 5 infants. IgG is passively transferred across the placenta from mother to fetus beginning at the end of the second trimester and reaches high levels at the time of birth.5 However, IgM, which was detected in 2 infants, is not usually transferred from mother to fetus because of its larger macromolecular structure. In a study6 of mothers with SARS, the placentas of 2 women who were convalescing from SARS-CoV infection in the third trimester of pregnancy had abnormal weights and pathology. Whether the placentas of women in this study were damaged and abnormal is unknown. Alternatively, IgM could have been produced by the infant if the virus crossed the placenta.
This study is limited by the small sample size, lack of cord blood, amniotic fluid, and breast milk and by incomplete information on the outcome of the infants. These findings are important for understanding the serological characteristics of infants whose mothers are infected with SARS-CoV-2 and further study is necessary.
Corresponding Authors: Xinghua Long, MD, PhD (zhoulongxinghua@qq.com) and Wei Zhang, MD, PhD (zw6676@163.com), Zhongnan Hospital of Wuhan University, 169 Donghu Rd, Wuhan, China.
Published Online: March 26, 2020. doi:10.1001/jama.2020.4861
Author Contributions: Drs Long and Zhang had full access to all the data in the study and take responsibility for the integrity of the data and accuracy of the data analysis. Dr Zeng and Ms Xu contributed equally to the study.
Concept and design: Zeng, Xu, Long.
Acquisition, analysis, or interpretation of data: Fan, Tang, Deng, Zhang.
Drafting of the manuscript: Zeng, Xu, Long.
Critical revision of the manuscript for important intellectual content: Fang, Tang, Deng, Zhang.
Statistical analysis: Zeng, Xu, Fan, Tang, Deng.
Obtained funding: Long.
Supervision: Zhang.
Conflict of Interest Disclosures: None reported.
Funding/Support: This study was supported by grants 81272372 from the National Natural Science Foundation of China and znpy2016033 from Zhongnan Hospital of Wuhan University Science, Technology, and Innovation Seed Fund.
Role of the Funder/Sponsor: The sponsors had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.