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10.1038/s41467-020-19545-8

http://scihub22266oqcxt.onion/10.1038/s41467-020-19545-8
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33177504!7658256!33177504
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suck abstract from ncbi


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pmid33177504      Nat+Commun 2020 ; 11 (1): 5703
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  • Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19 #MMPMID33177504
  • Tosif S; Neeland MR; Sutton P; Licciardi PV; Sarkar S; Selva KJ; Do LAH; Donato C; Quan Toh Z; Higgins R; Van de Sandt C; Lemke MM; Lee CY; Shoffner SK; Flanagan KL; Arnold KB; Mordant FL; Mulholland K; Bines J; Dohle K; Pellicci DG; Curtis N; McNab S; Steer A; Saffery R; Subbarao K; Chung AW; Kedzierska K; Burgner DP; Crawford NW
  • Nat Commun 2020[Nov]; 11 (1): 5703 PMID33177504show ga
  • Compared to adults, children with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have predominantly mild or asymptomatic infections, but the underlying immunological differences remain unclear. Here, we describe clinical features, virology, longitudinal cellular, and cytokine immune profile, SARS-CoV-2-specific serology and salivary antibody responses in a family of two parents with PCR-confirmed symptomatic SARS-CoV-2 infection and their three children, who tested repeatedly SARS-CoV-2 PCR negative. Cellular immune profiles and cytokine responses of all children are similar to their parents at all timepoints. All family members have salivary anti-SARS-CoV-2 antibodies detected, predominantly IgA, that coincide with symptom resolution in 3 of 4 symptomatic members. Plasma from both parents and one child have IgG antibody against the S1 protein and virus-neutralizing activity detected. Using a systems serology approach, we demonstrate higher levels of SARS-CoV-2-specific antibody features of these family members compared to healthy controls. These data indicate that children can mount an immune response to SARS-CoV-2 without virological confirmation of infection, raising the possibility that immunity in children can prevent the establishment of SARS-CoV-2 infection. Relying on routine virological and serological testing may not identify exposed children, with implications for epidemiological and clinical studies across the life-span.
  • |Adult[MESH]
  • |Antibodies, Viral/*blood/immunology[MESH]
  • |Australia[MESH]
  • |Betacoronavirus/*immunology[MESH]
  • |CD4-Positive T-Lymphocytes/immunology[MESH]
  • |CD8-Positive T-Lymphocytes/immunology[MESH]
  • |COVID-19[MESH]
  • |Child[MESH]
  • |Child, Preschool[MESH]
  • |Coronavirus Infections/immunology/*transmission[MESH]
  • |Cytokines/*blood[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunoglobulin A/blood/immunology[MESH]
  • |Immunoglobulin G/blood/immunology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Monocytes/immunology[MESH]
  • |Pandemics[MESH]
  • |Parents[MESH]
  • |Pneumonia, Viral/immunology/*transmission[MESH]
  • |SARS-CoV-2[MESH]
  • |Saliva/*immunology[MESH]
  • |Serologic Tests[MESH]


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