Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Ochola, Rachel, Sande, Charles, Fegan, Gregory, Scott, Paul D., Medley, Graham F., Cane, Patricia A., Nokes, D. James
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
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
_version_ 1782174439857717248
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
work_keys_str_mv AT ocholarachel thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT sandecharles thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT fegangregory thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT scottpauld thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT medleygrahamf thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT canepatriciaa thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT nokesdjames thelevelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT ocholarachel levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT sandecharles levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT fegangregory levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT scottpauld levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT medleygrahamf levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT canepatriciaa levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya
AT nokesdjames levelanddurationofrsvspecificmaternaliggininfantsinkilifikenya