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How type-2 dendritic cells induce Th2 differentiation: Instruction, repression, or fostering T cell-T cell communication? | LitMetric

AI Article Synopsis

  • Allergic diseases are triggered by allergen-specific CD4+ T follicular helper cells (Tfh2) and T helper 2 (Th2) cells, which release cytokines that lead to IgE production and inflammation.
  • The study focuses on how type 2 dendritic cells (DC2s) present allergens and influence the differentiation of naïve CD4+ T cells into Th2 cells, although the specific signals involved are not yet fully understood.
  • Recent research highlights the development and variety of DC2s, mechanisms of allergen detection, and the interactions between DC2s and T cells in lymph nodes that are crucial for initiating the allergic immune response.

Article Abstract

Allergic disease is caused by the activation of allergen-specific CD4+ type-2 T follicular helper cells (Tfh2) and T helper 2 (Th2) effector cells that secrete the cytokines IL-4, IL-5, IL-9, and IL-13 upon allergen encounter, thereby inducing IgE production by B cells and tissue inflammation. While it is accepted that the priming and differentiation of naïve CD4+ T cells into Th2 requires allergen presentation by type 2 dendritic cells (DC2s), the underlying signals remain unidentified. In this review we focus on the interaction between allergen-presenting DC2s and naïve CD4+ T cells in lymph node (LN), and the potential mechanisms by which DC2s might instruct Th2 differentiation. We outline recent advances in characterizing DC2 development and heterogeneity. We review mechanisms of allergen sensing and current proposed mechanisms of Th2 differentiation, with specific consideration of the role of DC2s and how they might contribute to each mechanism. Finally, we assess recent publications reporting a detailed analysis of DC-T cell interactions in LNs and how they support Th2 differentiation. Together, these studies are starting to shape our understanding of this key initial step of the allergic immune response.

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Source
http://dx.doi.org/10.1111/all.16337DOI Listing

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