Author
Listed:
- Rachel Ochola
- Charles Sande
- Gregory Fegan
- Paul D Scott
- Graham F Medley
- Patricia A Cane
- D James Nokes
Abstract
Background: Respiratory syncytial virus (RSV) is the major cause of lower respiratory tract infection in infants. The rate of decay of RSV-specific maternal antibodies (RSV-matAb), the factors affecting cord blood levels, and the relationship between these levels and protection from infection are poorly defined. Methods: A birth cohort (n = 635) in rural Kenya, was studied intensively to monitor infections and describe age-related serological characteristics. RSV specific IgG antibody (Ab) in serum was measured by the enzyme linked immunosorbent assay (ELISA) in cord blood, consecutive samples taken 3 monthly, and in paired acute and convalescent samples. A linear regression model was used to calculate the rate of RSV-matAb decline. The effect of risk factors on cord blood titres was investigated. Results: The half-life of matAb in the Kenyan cohort was calculated to be 79 days (95% confidence limits (CL): 76–81 days). Ninety seven percent of infants were born with RSV-matAb. Infants who subsequently experienced an infection in early life had significantly lower cord titres of anti-RSV Ab in comparison to infants who did not have any incident infection in the first 6 months (P = 0.011). RSV infections were shown to have no effect on the rate of decay of RSV-matAb. Conclusion: Maternal-specific RSV Ab decline rapidly following birth. However, we provide evidence of protection against severe disease by RSV-matAb during the first 6–7 months. This suggests that boosting maternal-specific Ab by RSV vaccination may be a useful strategy to consider.
Suggested Citation
Rachel Ochola & Charles Sande & Gregory Fegan & Paul D Scott & Graham F Medley & Patricia A Cane & D James Nokes, 2009.
"The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya,"
PLOS ONE, Public Library of Science, vol. 4(12), pages 1-6, December.
Handle:
RePEc:plo:pone00:0008088
DOI: 10.1371/journal.pone.0008088
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