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Serology confirms SARS-CoV-2 infection in PCR-negative children presenting with Paediatric Inflammatory Multi-System Syndrome
Marisol Perez-Toledo; Sian E. Faustini; Sian E. Jossi; Adrian Shields; Hari Krishnan Kanthimathinathan; Joel D. Allen; Yasunori Watanabe; Margaret Goodall; David C. Wraith; Tonny V. Veenith; Mark T. Drayson; Deepthi Jyothish; Eslam Al-Abadi; Ashish Chikermane; Steven Welch; Kavitha Masilamani; Scott Hackett; Max Crispin; Barnaby Scholefield; Adam F. Cunningham; Alex G. Richter.
Affiliation
  • Marisol Perez-Toledo; University of Birmingham
  • Sian E. Faustini; University of Birmingham
  • Sian E. Jossi; University of Birmingham
  • Adrian Shields; University of Birmingham
  • Hari Krishnan Kanthimathinathan; Birmingham Women and Children's NHS Foundation Trust
  • Joel D. Allen; University of Southampton
  • Yasunori Watanabe; University of Southampton
  • Margaret Goodall; University of Birmingham
  • David C. Wraith; University of Birmingham
  • Tonny V. Veenith; University Hospitals Birmingham NHS Trust
  • Mark T. Drayson; University of Birmingham
  • Deepthi Jyothish; Birmingham Women's and Children's NHS Foundation Trust
  • Eslam Al-Abadi; Birmingham Women's and Children's NHS Foundation Trust
  • Ashish Chikermane; Birmingham Women's and Children's NHS Foundation Trust
  • Steven Welch; University Hospitals Birmingham
  • Kavitha Masilamani; Birmingham Women's and Children's NHS Foundation Trust
  • Scott Hackett; University Hospitals Birmingham
  • Max Crispin; University of Southampton
  • Barnaby Scholefield; University of Birmingham
  • Adam F. Cunningham; University of Birmingham
  • Alex G. Richter; University of Birmingham
Preprint in English | medRxiv | ID: ppmedrxiv-20123117
ABSTRACT
BackgroundDuring the COVID-19 outbreak, reports have surfaced of children who present with features of a multisystem inflammatory syndrome with overlapping features of Kawasaki disease and toxic shock syndrome - Paediatric Inflammatory Multisystem Syndrome-temporally associated with SARS-CoV-2 pandemic (PIMS-TS). Initial reports find that many of the children are PCR-negative for SARS-CoV-2, so it is difficult to confirm whether this syndrome is a late complication of viral infection in an age group largely spared the worst consequences of this infection, or if this syndrome reflects enhanced surveillance. MethodsChildren hospitalised for symptoms consistent with PIMS-TS between 28 April and 8 May 2020, and who were PCR-negative for SARS-CoV-2, were tested for antibodies to viral spike glycoprotein using an ELISA test. ResultsEight patients (age range 7-14 years, 63% male) fulfilled case-definition for PIMS-TS during the study period. Six of the eight patients required admission to intensive care. All patients exhibited significant IgG and IgA responses to viral spike glycoprotein. Further assessment showed that the IgG isotypes detected in children with PIMS-TS were of the IgGl and lgG3 subclasses, a distribution similar to that observed in samples from hospitalised adult COVID-19 patients. In contrast, lgG2 and lgG4 were not detected in children or adults. IgM was not detected in children, which contrasts with adult hospitalised adult COVID-19 patients of whom all had positive IgM responses. ConclusionsStrong IgG antibody responses can be detected in PCR-negative children with PIMS-TS. The low detection rate of IgM in these patients is consistent with infection having occurred weeks previously and that the syndrome onset occurs well after the control of SARS-CoV-2 viral load. This implies that the disease is largely immune-mediated. Lastly, this indicates that serology can be an appropriate diagnostic tool in select patient groups.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Rct Language: English Year: 2020 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Rct Language: English Year: 2020 Document type: Preprint
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