Paediatrics (RCH) - Research Publications

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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, MR ; Bannister, S ; Clifford, V ; Nguyen, J ; Dohle, K ; Overmars, I ; Toh, ZQ ; Anderson, J ; Donato, CM ; Sarkar, S ; Do, LAH ; McCafferty, C ; Licciardi, PV ; Ignjatovic, V ; Monagle, P ; Bines, JE ; Mulholland, K ; Curtis, N ; McNab, S ; Steer, AC ; Burgner, DP ; Saffery, R ; Tosif, S ; Crawford, NW (FRONTIERS MEDIA SA, 2021-10-13)
    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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    Persistence of SARS-CoV-2-Specific IgG in Children 6 Months After Infection, Australia
    Toh, ZQ ; Higgins, RA ; Do, LAH ; Rautenbacher, K ; Mordant, FL ; Subbarao, K ; Dohle, K ; Nguyen, J ; Steer, AC ; Tosif, S ; Crawford, NW ; Mulholland, K ; Licciardi, PV (CENTERS DISEASE CONTROL & PREVENTION, 2021-08)
    The duration of the humoral immune response in children infected with severe acute respiratory syndrome coronavirus 2 is unknown. We detected specific IgG 6 months after infection in children who were asymptomatic or had mild symptoms of coronavirus disease. These findings will inform vaccination strategies and other prevention measures.
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    Innate cell profiles during the acute and convalescent phase of SARS-CoV-2 infection in children
    Neeland, MR ; Bannister, S ; Clifford, V ; Dohle, K ; Mulholland, K ; Sutton, P ; Curtis, N ; Steer, AC ; Burgner, DP ; Crawford, NW ; Tosif, S ; Saffery, R (NATURE PORTFOLIO, 2021-02-17)
    Children have mild severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) confirmed disease (COVID-19) compared to adults and the immunological mechanisms underlying this difference remain unclear. Here, we report acute and convalescent innate immune responses in 48 children and 70 adults infected with, or exposed to, SARS-CoV-2. We find clinically mild SARS-CoV-2 infection in children is characterised by reduced circulating subsets of monocytes (classical, intermediate, non-classical), dendritic cells and natural killer cells during the acute phase. In contrast, SARS-CoV-2-infected adults show reduced proportions of non-classical monocytes only. We also observe increased proportions of CD63+ activated neutrophils during the acute phase to SARS-CoV-2 in infected children. Children and adults exposed to SARS-CoV-2 but negative on PCR testing display increased proportions of low-density neutrophils that we observe up to 7 weeks post exposure. This study characterises the innate immune response during SARS-CoV-2 infection and household exposure in children.
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    Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
    Tosif, S ; Neeland, MR ; Sutton, P ; Licciardi, PV ; Sarkar, S ; Selva, KJ ; Lien, AHD ; Donato, C ; Toh, ZQ ; 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 (NATURE PORTFOLIO, 2020-11-11)
    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.