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The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya
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 po...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779853/ https://www.ncbi.nlm.nih.gov/pubmed/19956576 http://dx.doi.org/10.1371/journal.pone.0008088 |
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author | Ochola, Rachel Sande, Charles Fegan, Gregory Scott, Paul D. Medley, Graham F. Cane, Patricia A. Nokes, D. James |
author_facet | Ochola, Rachel Sande, Charles Fegan, Gregory Scott, Paul D. Medley, Graham F. Cane, Patricia A. Nokes, D. James |
author_sort | Ochola, Rachel |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2779853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27798532009-12-03 The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya Ochola, Rachel Sande, Charles Fegan, Gregory Scott, Paul D. Medley, Graham F. Cane, Patricia A. Nokes, D. James PLoS One Research Article 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. Public Library of Science 2009-12-02 /pmc/articles/PMC2779853/ /pubmed/19956576 http://dx.doi.org/10.1371/journal.pone.0008088 Text en Ochola et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ochola, Rachel Sande, Charles Fegan, Gregory Scott, Paul D. Medley, Graham F. Cane, Patricia A. Nokes, D. James The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya |
title | The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya |
title_full | The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya |
title_fullStr | The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya |
title_full_unstemmed | The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya |
title_short | The Level and Duration of RSV-Specific Maternal IgG in Infants in Kilifi Kenya |
title_sort | level and duration of rsv-specific maternal igg in infants in kilifi kenya |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779853/ https://www.ncbi.nlm.nih.gov/pubmed/19956576 http://dx.doi.org/10.1371/journal.pone.0008088 |
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