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Updated: Oct 17, 2025

An Improved and High Throughput Respiratory Syncytial Virus RSV Micro-neutralization Assay
Published on: January 26, 2019
Transplacental transfer of RSV antibody in Australian First Nations infants
Nusrat Homaira1,2, Michael Binks3, Gregory Walker4
1Discipline of Paediatrics, School of Women's and Children's Health, Faculty of Medicine and Health, UNSW, Sydney, New South Wales, Australia.
Insights
Maternal antibodies protect infants from respiratory syncytial virus (RSV). In Australian First Nations infants, antibody transfer efficiency varied, with some experiencing impaired protection against RSV disease.
Area of Science:
- Immunology
- Public Health
- Pediatrics
Background:
- Respiratory syncytial virus (RSV) is a major cause of infant hospitalizations.
- Maternal antibodies are crucial for infant protection against severe RSV disease.
- The efficiency of transplacental transfer of RSV antibodies in Aboriginal infants is not well understood.
Purpose of the Study:
- To characterize respiratory syncytial virus (RSV) antibody levels in Australian First Nations mother-infant pairs.
- To investigate factors influencing the transplacental transfer of maternal anti-RSV antibodies.
- To assess the implications for infant protection against RSV disease.
Main Methods:
- Studied 78 Australian First Nations mother-infant pairs.
- Measured RSV antibody (Ab) titers in maternal and cord serum.
- Used multivariable logistic regression to analyze the cord-to-maternal antibody titer ratio (CMTR) and associated covariates.
Main Results:
- The mean cord-to-maternal antibody titer ratio (CMTR) was 1.02, indicating generally efficient transfer.
- One-third of pairs exhibited a CMTR below 1, suggesting impaired antibody transfer.
- Nearly 9% of term infants had low cord RSV antibody levels (
- No significant impact of covariates like birth weight, gestational age, or maternal factors on CMTR was observed.
Conclusions:
- While overall transplacental transfer of RSV antibodies is efficient in this cohort, a significant proportion of First Nations infants may have suboptimal antibody levels.
- Impaired transfer warrants further investigation into its impact on RSV disease severity in First Nations children.
- Mechanistic research is needed to understand and potentially improve infant protection against RSV.
Abstract:
Respiratory syncytial virus (RSV) is the leading cause of acute lower respiratory infection hospitalisations in Aboriginal infants specifically those aged <6 months. Maternally derived RSV antibody (Ab) can protect against severe RSV disease in infancy. However, the efficiency of transplacental transfer of maternal anti-RSV Ab remains unknown in Aboriginal infants. We characterised RSV Ab in Australian First Nations mother-infant pairs (n = 78). We investigated impact of covariates including low birthweight, gestational age (GA), sex of the baby, maternal age and multiparity of the mother on cord to maternal anti-RSV Ab titre ratio (CMTR) using multivariable logistic regression model. All (n = 78) but one infant was born full term (median GA: 39 weeks, interquartile range: 38-40 weeks) and 56% were males. The mean log2 RSV Ab titre was 10.7 (SD± 1.3) in maternal serum and 11.0 (SD ± 1.3) in cord serum at birth; a ratio of 1.02 (SD ± 0.06). One-third of the pairs had a CMTR of <1 indicating impaired transfer. Almost 9% (7/78) of the term infants had cord RSV Ab levels below
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