4.7 Article

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

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 216, 期 11, 页码 1398-1406

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jix489

关键词

antibodies; infant; severity; prefusion; RSV

资金

  1. National Institutes of Health [P01 AI112524 2524, R01 AI093848, R01 AI095684]
  2. Nationwide Children's Hospital intramural grants
  3. Janssen
  4. Medimmune
  5. Trimeris
  6. ReViral
  7. HuMabs
  8. Regeneron
  9. Novartis
  10. Gilead
  11. Pfizer

向作者/读者索取更多资源

Background. 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. Methods. 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. Results. 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. Conclusions. Maternal antibodies directed to pre-F, followed by antibodies directed to G, can modulate RSV disease severity in young infants.

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