Characteristics and impact of infiltration of B-cells from systemic sclerosis patients in a 3D healthy skin model

Front Immunol. 2024 Aug 9:15:1373464. doi: 10.3389/fimmu.2024.1373464. eCollection 2024.

Abstract

Introduction: In systemic sclerosis (SSc), B-cells are activated and present in the skin and lung of patients where they can interact with fibroblasts. The precise impact and mechanisms of the interaction of B-cells and fibroblasts at the tissular level are poorly studied.

Objective: We investigated the impact and mechanisms of B-cell/fibroblast interactions in cocultures between B-cells from patients with SSc and 3-dimensional reconstituted healthy skin model including fibroblasts, keratinocytes and extracellular matrix.

Methods: The quantification and description of the B-cell infiltration in 3D cocultures were performed using cells imagery strategy and cytometry. The effect of coculture on the transcriptome of B-cells and fibroblasts was studied with bulk and single-cell RNA sequencing approaches. The mechanisms of this interaction were studied by blocking key cytokines like IL-6 and TNF.

Results: We showed a significant infiltration of B-cells in the 3D healthy skin model. The amount but not the depth of infiltration was higher with B-cells from SSc patients and with activated B-cells. B-cell infiltrates were mainly composed of naïve and memory cells, whose frequencies differed depending on B-cells origin and activation state: infiltrated B-cells from patients with SSc showed an activated profile and an overexpression of immunoglobulin genes compared to circulating B-cells before infiltration. Our study has shown for the first time that activated B-cells modified the transcriptomic profile of both healthy and SSc fibroblasts, toward a pro-inflammatory (TNF and IL-17 signaling) and interferon profile, with a key role of the TNF pathway.

Conclusion: B-cells and 3D skin cocultures allowed the modelization of B-cells infiltration in tissues observed in SSc, uncovering an influence of the underlying disease and the activation state of B-cells. We showed a pro-inflammatory effect on skin fibroblasts and pro-activation effect on infiltrating B-cells during coculture. This reinforces the role of B-cells in SSc and provide potential targets for future therapeutic approach in this disease.

Keywords: 3D coculture; B-cell; fibroblast; fibrosis; skin; systemic sclerosis.

MeSH terms

  • Adult
  • B-Lymphocytes* / immunology
  • B-Lymphocytes* / metabolism
  • Cell Communication / immunology
  • Cells, Cultured
  • Coculture Techniques*
  • Cytokines / metabolism
  • Female
  • Fibroblasts* / immunology
  • Fibroblasts* / metabolism
  • Humans
  • Keratinocytes / immunology
  • Keratinocytes / metabolism
  • Lymphocyte Activation / immunology
  • Male
  • Middle Aged
  • Scleroderma, Systemic* / immunology
  • Scleroderma, Systemic* / metabolism
  • Scleroderma, Systemic* / pathology
  • Skin* / immunology
  • Skin* / metabolism
  • Skin* / pathology
  • Transcriptome

Substances

  • Cytokines

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work received a grant from the French Society for Dermatology (SFD) and the French Patient association (ASF).