Molecular characterization of respiratory syncytial viruses infecting children reported to have received palivizumab immunoprophylaxis

J Clin Virol. 2015 Apr:65:26-31. doi: 10.1016/j.jcv.2015.01.016. Epub 2015 Jan 24.

Abstract

Background: Respiratory syncytial virus (RSV) is a major cause of respiratory infections in children. Palivizumab (PZ) is the only RSV-specific immunoprophylaxis approved by the U.S. Food and Drug Administration. Mutations leading to amino acid substitutions in the PZ binding site of the RSV F protein have been associated with breakthrough RSV infections in patients receiving PZ.

Objective: To detect PZ resistance conferring mutations in RSV strains from children who received PZ.

Study design: Children aged ≤ 24 months on October 31 who were hospitalized or had outpatient visits for respiratory illness and/or fever during October-May 2001-2008 in 3 US counties were included. PZ receipt was obtained from parent interviews and medical records among children subsequently infected with RSV. Archived nasal/throat swab specimens were tested for RSV by real-time RT-PCR. The coding region of the PZ binding site of the RSV F protein was sequenced using both Sanger and pyrosequencing methods.

Results: Of 8762 enrolled children, 375 (4.3%) were tested for RSV and had a history of PZ receipt, of which 56 (14.9%) were RSV-positive and 45 of these had available archived specimens. Molecular typing identified 42 partial F gene sequences in specimens from 39 children: 19 single RSV subgroup A, 17 subgroup B and 3 mixed infections. Nucleotide substitutions were identified in 12/42 (28.6%) RSV strains. PZ resistance mutations were identified in 4 (10.2%) of the 39 children, of which one had documented PZ receipt.

Conclusions: Although RSV PZ resistance mutations were infrequent, most RSV-associated illnesses in children with a history of PZ receipt were not due to strain resistance.

Keywords: Palivizumab resistance; Pyrosequencing; Respiratory syncytial virus.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use*
  • Child
  • Child, Preschool
  • Drug Resistance, Viral / genetics
  • Female
  • Humans
  • Male
  • Mutation
  • Palivizumab / pharmacology
  • Palivizumab / therapeutic use*
  • Respiratory Syncytial Virus Infections / prevention & control*
  • Respiratory Syncytial Virus Infections / virology*
  • Respiratory Syncytial Viruses / drug effects*
  • Respiratory Syncytial Viruses / genetics*
  • Sequence Analysis, DNA
  • Time Factors
  • United States

Substances

  • Antiviral Agents
  • Palivizumab