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Children and Adults in a Household Cohort Study Have Robust Longitudinal Immune Responses Following SARS-CoV-2 Infection or Exposure.
Neeland, Melanie R; Bannister, Samantha; Clifford, Vanessa; Nguyen, Jill; Dohle, Kate; Overmars, Isabella; Toh, Zheng Quan; Anderson, Jeremy; Donato, Celeste M; Sarkar, Sohinee; Do, Lien Anh Ha; McCafferty, Conor; Licciardi, Paul V; Ignjatovic, Vera; Monagle, Paul; Bines, Julie E; Mulholland, Kim; Curtis, Nigel; McNab, Sarah; Steer, Andrew C; Burgner, David P; Saffery, Richard; Tosif, Shidan; Crawford, Nigel W.
  • Neeland MR; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Bannister S; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Clifford V; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Nguyen J; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Dohle K; Infectious Diseases Unit, The Royal Children's Hospital, Parkville, VIC, Australia.
  • Overmars I; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Toh ZQ; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Anderson J; Infectious Diseases Unit, The Royal Children's Hospital, Parkville, VIC, Australia.
  • Donato CM; Laboratory Services, The Royal Children's Hospital, Parkville, VIC, Australia.
  • Sarkar S; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Do LAH; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • McCafferty C; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Licciardi PV; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Ignjatovic V; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Monagle P; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Bines JE; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Mulholland K; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Curtis N; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • McNab S; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Steer AC; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Burgner DP; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Saffery R; Department of Paediatrics, The University of Melbourne, Parkville, VIC, Australia.
  • Tosif S; Clinical Sciences Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Crawford NW; Infection and Immunity Theme, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Front Immunol ; 12: 741639, 2021.
Article in English | MEDLINE | ID: covidwho-1497078
ABSTRACT
Children have reduced severity of COVID-19 compared to adults and typically have mild or asymptomatic disease. The immunological mechanisms underlying these age-related differences in clinical outcomes remain unexplained. Here, we quantify 23 immune cell populations in 141 samples from children and adults with mild COVID-19 and their PCR-negative close household contacts at acute and convalescent time points. Children with COVID-19 displayed marked reductions in myeloid cells during infection, most prominent in children under the age of five. Recovery from infection in both children and adults was characterised by the generation of CD8 TCM and CD4 TCM up to 9 weeks post infection. SARS-CoV-2-exposed close contacts also had immunological changes over time despite no evidence of confirmed SARS-CoV-2 infection on PCR testing. This included an increase in low-density neutrophils during convalescence in both exposed children and adults, as well as increases in CD8 TCM and CD4 TCM in exposed adults. In comparison to children with other common respiratory viral infections, those with COVID-19 had a greater change in innate and T cell-mediated immune responses over time. These findings provide new mechanistic insights into the immune response during and after recovery from COVID-19 in both children and adults.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: CD4-Positive T-Lymphocytes / CD8-Positive T-Lymphocytes / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Young adult Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.741639

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Full text: Available Collection: International databases Database: MEDLINE Main subject: CD4-Positive T-Lymphocytes / CD8-Positive T-Lymphocytes / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Young adult Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.741639