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Similar severity of influenza primary and re-infections in pre-school children requiring outpatient treatment due to febrile acute respiratory illness: prospective, multicentre surveillance study (2013-2015).
Streng, Andrea; Prifert, Christiane; Weissbrich, Benedikt; Sauerbrei, Andreas; Krumbholz, Andi; Schmidt-Ott, Ruprecht; Liese, Johannes G.
Afiliación
  • Streng A; Department of Pediatrics, University Hospital of Würzburg, Josef-Schneider-Str. 2, 97080, Würzburg, Germany. Streng_A@ukw.de.
  • Prifert C; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Weissbrich B; Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
  • Sauerbrei A; Section Experimental Virology, Institute of Medical Microbiology, Jena University Hospital, Jena, Germany.
  • Krumbholz A; Institute for Infection Medicine, Christian Albrecht University of Kiel and University Medical Centre of Schleswig Holstein, Kiel, Germany.
  • Schmidt-Ott R; GSK, Wavre, Belgium.
  • Liese JG; Department of Pediatrics, University Hospital of Würzburg, Josef-Schneider-Str. 2, 97080, Würzburg, Germany.
BMC Infect Dis ; 22(1): 12, 2022 Jan 04.
Article en En | MEDLINE | ID: mdl-34983428
BACKGROUND: Influenza virus infections in immunologically naïve children (primary infection) may be more severe than in children with re-infections who are already immunologically primed. We compared frequency and severity of influenza virus primary and re-infections in pre-school children requiring outpatient treatment. METHODS: Influenza-unvaccinated children 1-5 years of age presenting at pediatric practices with febrile acute respiratory infection < 48 h after symptom onset were enrolled in a prospective, cross-sectional, multicenter surveillance study (2013-2015). Influenza types/subtypes were PCR-confirmed from oropharyngeal swabs. Influenza type/subtype-specific IgG antibodies serving as surrogate markers for immunological priming were determined using ELISA/hemagglutination inhibition assays. The acute influenza disease was defined as primary infection/re-infection by the absence/presence of influenza type-specific immunoglobulin G (IgG) and, in a second approach, by the absence/presence of subtype-specific IgG. Socio-demographic and clinical data were also recorded. RESULTS: Of 217 influenza infections, 178 were due to influenza A (87 [49%] primary infections, 91 [51%] re-infections) and 39 were due to influenza B (38 [97%] primary infections, one [3%] re-infection). Children with "influenza A primary infections" showed fever with respiratory symptoms for a shorter period than children with "influenza A re-infections" (median 3 vs. 4 days; age-adjusted p = 0.03); other disease characteristics were similar. If primary infections and re-infections were defined based on influenza A subtypes, 122 (87%) primary infections (78 "A(H3N2) primary infections", 44 "A(H1N1)pdm09 primary infections") and 18 (13%) re-infections could be classified (14 "A(H3N2) re-infections" and 4 "A(H1N1)pdm09 re-infections"). Per subtype, primary infections and re-infections were of similar disease severity. Children with re-infections defined on the subtype level usually had non-protective IgG titers against the subtype of their acute infection (16 of 18; 89%). Some patients infected by one of the influenza A subtypes showed protective IgG titers (≥ 1:40) against the other influenza A subtype (32/140; 23%). CONCLUSIONS: Pre-school children with acute influenza A primary infections and re-infections presented with similar frequency in pediatric practices. Contrary to expectation, severity of acute "influenza A primary infections" and "influenza A re-infections" were similar. Most "influenza A re-infections" defined on the type level turned out to be primary infections when defined based on the subtype. On the subtype level, re-infections were rare and of similar disease severity as primary infections of the same subtype. Subtype level re-infections were usually associated with low IgG levels for the specific subtype of the acute infection, suggesting only short-time humoral immunity induced by previous infection by this subtype. Overall, the results indicated recurring influenza virus infections in this age group and no or only limited heterosubtypic antibody-mediated cross-protection.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Gripe Humana / Subtipo H1N1 del Virus de la Influenza A Tipo de estudio: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies / Screening_studies Límite: Child / Child, preschool / Humans Idioma: En Revista: BMC Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Gripe Humana / Subtipo H1N1 del Virus de la Influenza A Tipo de estudio: Clinical_trials / Observational_studies / Prevalence_studies / Risk_factors_studies / Screening_studies Límite: Child / Child, preschool / Humans Idioma: En Revista: BMC Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2022 Tipo del documento: Article País de afiliación: Alemania