Rare hyper inflammatory syndrome in children with COVID-19

Print

Rare hyper inflammatory syndrome 
in children with COVID-19

Researchers at Karolinska Institute and Science for Life Laboratory in Sweden and Tor Vergata University of Rome in Italy have mapped the immune response in children affected by a rare but life-threatening inflammatory syndrome associated with COVID-19. The study, which is published in the scientific journal Cell, reveals that the inflammatory response differs from that in Kawasaki disease and severe acute COVID-19.

In the current SARS-CoV-2 pandemic, with very few exceptions, children have presented with mild symptoms. However, pediatricians have discovered a new, life-threatening hyper inflammatory syndrome resembling Kawasaki disease and named Multisystem Inflammatory Syndrome in Children associated with COVID-19, MIS-C (see box).

In a new collaborative study, researchers have worked out the immunological aspects of this rare condition. They compared blood samples from 13 MIS-C-patients treated at Karolinska University Hospital in Stockholm, Sweden and Bambino Gesù Children’s Hospital in Rome, Italy, with samples from 28 Kawasaki disease patients collected from 2017 to 2018, prior to COVID-19. The analyses also included samples from children with mild COVID-19.

“Our results show that MIS-C is truly a distinct inflammatory condition from Kawasaki disease, despite having some shared features,” says Petter Brodin, paediatrician and researcher at the Department of Women’s and Children’s Health, Karolinska Institute, and one lead author of the study. “The hyper inflammation and cytokine storm detected in children with MIS-C is also different from that seen in adult patients with severe, acute COVID-19, which we recently described in another publication.”

When comparing MIS-C to these other inflammatory states, the study observed differential frequency of specific immune cell populations, inflammatory cytokines and chemokines in the blood. Unlike children with Kawasaki disease and children with mild COVID-19, children who developed MIS-C were lacking IgG-antibodies to common cold coronaviruses. The researchers also found several autoantibodies that target the body’s own proteins and that may contribute to the pathogenesis of MIS-C. They are now also looking into genetic risk factors for developing MIS-C after SARS-CoV-2 infection.

“There is an urgent need to better understand why a small minority of children infected with SARS-CoV-2 develop MIS-C, and we are adding a piece to the puzzle,” says Dr Brodin. “Better knowledge of the pathogenesis is important for development of optimal treatments that can dampen the cytokine storm and hopefully save lives, as well as for vaccine development to avoid MIS-C caused by vaccination.”

The study was a collaborative effort led by Petter Brodin and his team at Science for Life Laboratory and Karolinska Institutet, together with Nils Landegren’s group at KI and Paolo Palma’s lab at Tor Vergata University of Rome. It was financed by the Knut and Alice Wallenberg Foundation (KAW), Bure Equity AB, Jonas and Christina af Jochnick Foundation, the SciLifeLab/KAW national COVID-19 research program project grant, the Bambino Gesù Children’s Hospital, 5 X mille 2019, and Ricerca Corrente 2020. The authors declare that there is no conflict of interest.

Ref: “The Immunology of Multisystem Inflammatory Syndrome in Children with COVID-19”. Camila Rosat Consiglio, Nicola Cotugno, Fabian Sardh, Christian Pou, Donato Amodio, Lucie Rodriguez, Ziyang Tan, Sonia Zicari, Alessandra Ruggiero, Giuseppe Rubens Pascucci, Veronica Santilli, Tessa Campbell, Yenan Bryceson, Daniel Eriksson, Jun Wang, Alessandra Marchesi, Tadepally Lakshmikanth, Andrea Campana, Alberto Villani, Paolo Rossi, the CACTUS study team, Nils Landegren, Paolo Palma, Petter Brodin. Cell, online 6 September 2020, doi: 10.1016/j.cell.2020.09.016.

© Professional Medical Publications. All rights reserved.