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The role of tolerogenic dendritic cells in systematic lupus erythematosus progression and remission

•Systematic lupus erythematosus (SLE) is an autoimmune disease reflecting an imbalance between effector and regulatory immune responses.•Inflammatory DCs (inflDC) can initiate and trigger lymphocyte responses in SLE with over-expression of surface molecules and pro-inflammatory cytokine.•Tolerogenic...

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Published in:International immunopharmacology 2023-02, Vol.115, p.109601-109601, Article 109601
Main Authors: mohammadi, Bita, saghafi, Mohammadreza, Abdulsattar Faraj, Tola, Kamal Kheder, Ramiar, Sajid Abdulabbas, Hadi, Esmaeili, Seyed-Alireza
Format: Article
Language:English
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Summary:•Systematic lupus erythematosus (SLE) is an autoimmune disease reflecting an imbalance between effector and regulatory immune responses.•Inflammatory DCs (inflDC) can initiate and trigger lymphocyte responses in SLE with over-expression of surface molecules and pro-inflammatory cytokine.•Tolerogenic DCs (tolDC) express inhibitory interacting surface molecules and repressive mediators.•tolDCs can be a therapeutic candidate for patients with SLE to suppress their systematic inflammation.•Recent pre-clinical and clinical studies showed the efficacy of tolDCs therapy in autoimmune diseases, particularly SLE. Systematic lupus erythematosus (SLE) is an autoimmune disease reflecting an imbalance between effector and regulatory immune responses. Dendritic cells (DC) are a link between innate and adaptive immunity. Inflammatory DCs (inflDC) can initiate and trigger lymphocyte responses in SLE with over-expression of surface molecules and pro-inflammatory cytokine, including Interferon (IFN) α, Interleukin (IL) 1α, IL-1β, and IL-6, resulting in the overreaction of T helper cells (Th), and B cells immune responses. On the opposite side, tolerogenic DCs (tolDC) express inhibitory interacting surface molecules and repressive mediators, such as IL-10, Transforming growth factor beta (TGF-β), and Indoleamine 2, 3-dioxygenase (IDO), which can maintain self-tolerance in SLE by induction of regulatory T cells (Treg), T cells deletion and anergy. Hence, tolDCs can be a therapeutic candidate for patients with SLE to suppress their systematic inflammation. Recent pre-clinical and clinical studies showed the efficacy of tolDCs therapy in autoimmune diseases. In this review, we provide a wide perspective on the effect of inflDCs in promoting inflammation and the role of tolDC in the suppression of immune cells’ overreaction in SLE. Furthermore, we reviewed the finding of clinical trials and experimental studies related to autoimmune diseases, particularly SLE.
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2022.109601