Treg cell Notch receptors drive SARS-CoV-2-induced MIS-C

By Neha MathurReviewed by Aimee MolineuxApr 12 2022

In a recent study under consideration at Nature Portfolio Journal and posted to the Research Square* preprint server, researchers demonstrated the evolution of multi-system inflammatory syndrome in children (MIS-C) following acute severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.

MIS-C is a rare hyperinflammatory immune response to acute SARS-CoV-2 infection observed in children. MIS-C patients exhibit features such as intense cytokine production, particularly interferon-gamma (IFN-γ), and lymphocyte activation, associated with fever and organ dysfunction.

Recent studies have outlined a prominent role for the Notch receptor (Notch) signaling pathways, particularly the Notch4 locus, in association with acute coronavirus disease 2019 (COVID-19) and related respiratory illnesses. It is upregulated on lung tissue regulatory T (T _reg) cells in an interleukin (IL)-6-dependent manner and helps subvert tissue repair function in favor of an inflammatory response.

In addition, the Notch family, composed of five ligands (Delta-like 1, 3, 4, Jagged1, and 2), and four Notch receptors (Notch1 to 4) influence conventional T (T_conv) cell responses. However, the underlying immune dysregulation mechanisms governing post-acute COVID-19 syndromes, including MIS-C, remain unknown.

Study: Notch1-CD22-Dependent Immune Dysregulation in the SARS-CoV2-Associated Multisystem Inflammatory Syndrome in Children. Image Credit: NIAID

This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. Links to the preliminary and peer-reviewed reports are available in the Sources section at the bottom of this article. View Sources

About the study

In the current study, researchers examined a cohort of 45 children with MIS-C and 50 children with COVID-19 from centers in the United States, Turkey, and Italy. As controls, they evaluated 12 adults with COVID-19, five children with Kawasaki disease (KD), and 18 healthy children.

The team collected the peripheral blood of three MIS-C patients before treatment, another five after treatment, and four healthy controls for single-cell ribonucleic acid (RNA) sequencing (scRNA-seq) analysis to examine the cluster of differentiation 4 (CD4⁺⁾ T cell dynamics. Further, they used whole-genome sequence (WGS) analysis using Fischer testing and Monte-Carlo simulation for gene enrichment analysis.

All the MIS-C patients met the Centers For Disease Prevention (CDC) case definition and had one or more of the following symptoms- rash, conjunctivitis, and gastrointestinal (GI) symptoms. Moreover, they were highly inflamed, lymphopenic, and coagulopathic. Additionally, over 90% of MIS-C patients showed SARS-CoV-2 seropositivity.

Study findings

The scRNA-seq analysis outlined six subsets of CD4⁺ T cells; however, performing a graph-based clustering analysis using Seurat revealed 16 more CD4⁺ T cell clusters.

The authors observed that eight of the 16 clusters (Clusters 1 to 8) were enriched in cells annotated as CD4⁺ naïve and expressed C-C motif chemokine receptor 7 (CCR7) and selectin L (SELL) genes. Clusters 10 to 14 were enriched in activated CD4⁺ T cells, such as CD69, with Cluster 10 displaying high nuclear factor kappa B (NF-kB) signaling.

The remaining three clusters encompassed both naïve and activated cells, including one cluster, Cluster 9 defined by viral sensing gene transcripts interferon-Induced Protein With Tetratricopeptide Repeats (IFIT) 2 and IFIT3. Other clusters, Clusters 15 and 16 were enriched in T_reg cell transcripts Forkhead Box P3 (FOXP3) and with Mitotic Cells T Cell Receptor Beta Constant 1 (TRBC1).

In mouse models, an immunostimulant, polyinosinic: polycytidylic acid (poly I: C) recapitulated the MIS-C phenotype, especially those actively expressing Notch1 in T_reg cells.

Notch1 induction induced the B cell inhibitory receptor siglec 2 (CD22), which destabilized T_reg cells and impaired their suppressive function. Finally, the treatment of mice with an anti-CD22 monoclonal antibody (mAb) suppressed the development of systemic inflammation and restored the T _reg cells' suppressive function.

These findings indicated how different Notch receptors governing the MIS-C phenotype mobilized T _reg cell-specific tissue inflammatory licensing modules. Therefore, interventions targeting the Notch1-CD22 alignment could serve as a therapeutic strategy in MIS-C. Consequently, in patients resistant to standard anti-inflammatory therapies, therapies targeting cytokines involved in Notch1 induction, including anti-CD22 antibodies, might prove effective

Furthermore, the authors found variants in several Notch pathway genes in patients with MIS-C. Importantly, functional mutations in phosphotyrosine binding (PTB) domains of NUMB and NUMBL genes resulted in increased Notch1 expression and signaling. The results of the Monte Carlo simulation and Fischer test validated the role of Notch pathway-related mutations in MIS-C. Exceptionally, MIS-C patients demonstrated an increased CD22 expression on T_reg but not T_conv cells, =in mice.

Conclusions

Taken together, the study results could help in the development of a model that traces the evolutionary trajectory of MIS-C. It demonstrated how SARS-CoV-2 infection resulted in an immune dysregulation process that aggravated the systemic inflammation and disrupted tissue-resident T _reg cell function.

However, the findings pointed to the reversible nature of this process and ways to reverse it using anti-inflammatory therapies targeting cytokines involved in Notch1 induction, such as CD22.

This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. Links to the preliminary and peer-reviewed reports are available in the Sources section at the bottom of this article. View Sources