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REVIEW article

Front. Immunol.

Sec. Immunological Tolerance and Regulation

This article is part of the Research TopicImmunomodulation of the immune system by phytochemicals: Exploring the therapeutic potential of natural compoundsView all 6 articles

Phytochemicals as modulators of dendritic cell functions: implications for tolerogenic cell-based therapy

Provisionally accepted
  • Department of Immunology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary

The final, formatted version of the article will be published soon.

Dendritic cells (DCs) constitute a heterogeneous population of immune cells that acting as antigen presenting cells link innate and adaptive immune responses. Their functions are mainly dictated by microenvironmental cues, enabling them to either maintain immune tolerance or initiate robust humoral and cellular immune responses. While DCs are important for orchestrating immune responses, accumulating evidence suggests that aberrant DC activation contributes to the pathogenesis of autoimmune and chronic inflammatory diseases, making them promising targets for therapeutic modulation. Modulating DC functionality therefore represents a potent strategy to attenuate excessive inflammation in such conditions. Plant-derived bioactive compounds, or phytochemicals, are structurally diverse secondary metabolites with established anti-inflammatory and immunomodulatory properties. This review consolidates current in vitro, in vivo, and in silico findings on ten well-characterized phytochemicals including curcumin, 6-gingerol, 6-shogaol, resveratrol, epigallocatechin-3-gallate, quercetin, apigenin, capsaicin, berberine and ginsenosides, which have the capacity to modulate DC phenotype and function. Notably, these phytochemicals can skew DCs toward a tolerogenic phenotype, characterized by reduced expression of antigen presenting and co-stimulatory molecules, diminished pro-inflammatory cytokine secretion, and enhanced regulatory T cell induction. Mechanistic insights reveal convergence on key signaling pathways such as nuclear factor-kappa B (NF-κB), mitogen activated protein kinase (MAPK) and mammalian target of rapamycin (mTOR) in DCs. In silico studies further predict interactions of these compounds with various molecular targets, providing a structural basis for their immunoregulatory effects. Furthermore, studies using preclinical models of autoimmune and inflammatory diseases have demonstrated that these phytochemicals can attenuate disease severity, likely through DC modulation. Given their multifaceted immunomodulatory capacity, phytochemicals hold promise both as adjuvant therapies in DC-mediated autoimmune diseases and as agents for generating tolerogenic DCs for cell-based immunotherapies.

Keywords: phytochemicals1, dendritic cells3, bioactive compounds2, inflammation4, Autoimmune disease5, therapy6, tolerogenic7

Received: 25 Jun 2025; Accepted: 29 Oct 2025.

Copyright: © 2025 Fekete and Pázmándi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Tünde Fekete, fekete.tunde@med.unideb.hu

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