Shared TCR Vβ21.3+ T cell immunological signature between MIS-A and MIS-C

Multisystem inflammatory syndrome (MIS) is a severe and potentially life-threatening complication of SARS-CoV-2 infection that affects both children (MIS-C) and adults (MIS-A). While the inflammatory response in MIS-C has been studied in detail, the immune dysregulation underlying MIS-A remains poorly understood, mainly due to the rarity of its condition. Using flow cytometry, we analyzed the T cell response in two, Danish and French, MIS-A cohorts, encompassing a total of 16 cases. We observed an expansion of Vβ21.3+ T cells in at least one of the major T cell subsets (CD3+, CD4+, or CD8+) in 9 out of 16 MIS-A patients. Vβ21.3+ T cells showed increased expression of activation and exhaustion markers along with a higher abundance of effector memory T cells compared to their Vβ21.3-negative counterparts in patients with or without Vβ21.3 expansion. These findings demonstrate that MIS-A shares the same Vβ21.3+ T cell signature previously reported in MIS-C, suggesting a shared pathological immune-related mechanism between the two conditions.

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Publication Details

Journal
Journal of Human Immunity
Published
2025-12-12
DOI
https://doi.org/10.70962/jhi.20250050
Primary Topic
Kawasaki Disease and Coronary Complications
Type
article
Field-Weighted Citation Impact
0.00
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article

Shared TCR Vβ21.3+ T cell immunological signature between MIS-A and MIS-C

Andreas Ronit, Liliane Khoryati, Sarah Benezech, A. Belot et al.
Journal of Human Immunity
Kawasaki Disease and Coronary Complications
article

Shared TCR Vβ21.3+ T cell immunological signature between MIS-A and MIS-C

Andreas Ronit, Liliane Khoryati, Sarah Benezech, A. Belot, Christophe Parizot, Casper Roed, Sofie E. Jørgensen, Samira Khaldi-Plassart, Raphaëlle Lautraite, Signe Bech Sørensen, Guillaume Hekimian, Trine Mogensen, Guy Gorochov, Merete Storgaard, MIS-A & COVID-19 Taskforce, Marc Pineton de Chambrun, Ann-Britt Eg Hansen
article en

Abstract

Multisystem inflammatory syndrome (MIS) is a severe and potentially life-threatening complication of SARS-CoV-2 infection that affects both children (MIS-C) and adults (MIS-A). While the inflammatory response in MIS-C has been studied in detail, the immune dysregulation underlying MIS-A remains poorly understood, mainly due to the rarity of its condition. Using flow cytometry, we analyzed the T cell response in two, Danish and French, MIS-A cohorts, encompassing a total of 16 cases. We observed an expansion of Vβ21.3+ T cells in at least one of the major T cell subsets (CD3+, CD4+, or CD8+) in 9 out of 16 MIS-A patients. Vβ21.3+ T cells showed increased expression of activation and exhaustion markers along with a higher abundance of effector memory T cells compared to their Vβ21.3-negative counterparts in patients with or without Vβ21.3 expansion. These findings demonstrate that MIS-A shares the same Vβ21.3+ T cell signature previously reported in MIS-C, suggesting a shared pathological immune-related mechanism between the two conditions.

Journal of Human ImmunityVol. 2(2)
Université Claude Bernard Lyon 1 (FR), École Normale Supérieure de Lyon (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Aarhus University (DK), Aarhus University Hospital (DK), Sorbonne Université (FR), Assistance Publique – Hôpitaux de Paris (FR), Laboratoire National de Référence (MA), Pitié-Salpêtrière Hospital (FR), Centre d'Immunologie et des Maladies Infectieuses (FR), Centre International de Recherche en Infectiologie (FR), Imation (United States) (US)
Openalex Percentile: Top 24%
Kawasaki Disease and Coronary Complications
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