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Prefusion F, Postfusion F, G Antibodies, and Disease Severity in Infants and Young Children With Acute Respiratory Syncytial Virus Infection.

Authors :
Capella, Cristina
Chaiwatpongsakorn, Supranee
Gorrell, Erin
Risch, Zachary A.
Fang Ye
Mertz, Sara E.
Johnson, Sara M.
Moore-Clingenpeel, Melissa
Ramilo, Octavio
Mejias, Asuncion
Peeples, Mark E.
Ye, Fang
Source :
Journal of Infectious Diseases; Dec2017, Vol. 216 Issue 11, p1398-1406, 9p
Publication Year :
2017

Abstract

<bold>Background: </bold>Respiratory syncytial virus (RSV) is the most frequent cause of lower respiratory tract infection in infants. Maternally derived RSV-specific antibodies play a role in protection against RSV infection in early life, but data regarding the concentration and specificity of those antibodies are incomplete.<bold>Methods: </bold>We prospectively enrolled a cohort of previously healthy infants and young children hospitalized (n = 45) or evaluated as outpatients (n = 20) for RSV infection, and healthy noninfected age-matched controls (n = 18). Serum samples were obtained at enrollment to quantify the concentrations and neutralizing activity of serum immunoglobulin G antibodies to the RSV prefusion (pre-F), postfusion (post-F), and G glycoproteins. We also assessed the associations between antibody concentrations and clinical disease severity.<bold>Results: </bold>Concentrations of pre-F antibodies were ≥3-fold higher than post-F antibodies and >30-fold higher than G antibodies in serum from infants with acute RSV infection. Antibody concentrations and neutralizing activity inversely correlated with age. The pre-F antibodies displayed the greatest neutralizing activity (55%-100%), followed by G (0%-45%), and post-F (0%-29%) antibodies. Higher concentrations of pre-F and G antibodies, but not post-F antibodies, were associated with lower clinical disease severity scores.<bold>Conclusions: </bold>Maternal antibodies directed to pre-F, followed by antibodies directed to G, can modulate RSV disease severity in young infants. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
216
Issue :
11
Database :
Complementary Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
126784382
Full Text :
https://doi.org/10.1093/infdis/jix489