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胞葬作用:自身免疫性疾病治疗的现状与未来前景

Efferocytosis: Current status and future prospects in the treatment of autoimmune diseases.

作者信息

Li Qianwei, Liu Huan, Yin Geng, Xie Qibing

机构信息

Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.

Department of General Practice, General Practice Medical Center, West China Hospital, Sichuan University, Chengdu, Sichuan, 610041, China.

出版信息

Heliyon. 2024 Mar 31;10(7):e28399. doi: 10.1016/j.heliyon.2024.e28399. eCollection 2024 Apr 15.


DOI:10.1016/j.heliyon.2024.e28399
PMID:38596091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11002059/
Abstract

Billions of apoptotic cells are swiftly removed from the human body daily. This clearance process is regulated by efferocytosis, an active anti-inflammatory process during which phagocytes engulf and remove apoptotic cells. However, impaired clearance of apoptotic cells is associated with the development of various autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus, and inflammatory bowel disease. In this review, we conducted a comprehensive search of relevant studies published from January 1, 2000, to the present, focusing on efferocytosis, autoimmune disease pathogenesis, regulatory mechanisms governing efferocytosis, and potential treatments targeting this process. Our review highlights the key molecules involved in different stages of efferocytosis-namely, the "find me," "eat me," and "engulf and digest" phases-while elucidating their relevance to autoimmune disease pathology. Furthermore, we explore the therapeutic potential of modulating efferocytosis to restore immune homeostasis and mitigate autoimmune responses. By providing theoretical underpinnings for the targeting of efferocytosis in the treatment of autoimmune diseases, this review contributes to the advancement of therapeutic strategies in this field.

摘要

人体每天会迅速清除数十亿的凋亡细胞。这一清除过程由胞葬作用调节,胞葬作用是一个活跃的抗炎过程,在此过程中吞噬细胞吞噬并清除凋亡细胞。然而,凋亡细胞清除受损与多种自身免疫性疾病的发生发展有关,如类风湿性关节炎、系统性红斑狼疮和炎症性肠病。在本综述中,我们全面检索了2000年1月1日至今发表的相关研究,重点关注胞葬作用、自身免疫性疾病发病机制、胞葬作用的调控机制以及针对这一过程的潜在治疗方法。我们的综述强调了参与胞葬作用不同阶段的关键分子,即“找到我”“吃掉我”以及“吞噬并消化”阶段,同时阐明了它们与自身免疫性疾病病理学的相关性。此外,我们探讨了调节胞葬作用以恢复免疫稳态和减轻自身免疫反应的治疗潜力。通过为在自身免疫性疾病治疗中靶向胞葬作用提供理论基础,本综述有助于推动该领域治疗策略的进步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/159c/11002059/058a0e4d0d86/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/159c/11002059/058a0e4d0d86/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/159c/11002059/058a0e4d0d86/gr1.jpg

相似文献

[1]
Efferocytosis: Current status and future prospects in the treatment of autoimmune diseases.

Heliyon. 2024-3-31

[2]
Efferocytosis: Unveiling its potential in autoimmune disease and treatment strategies.

Autoimmun Rev. 2024-6

[3]
The Role of Efferocytosis in Autoimmune Diseases.

Front Immunol. 2018-7-20

[4]
Efferocytosis and autoimmune disease.

Int Immunol. 2018-11-14

[5]
Drugging the efferocytosis process: concepts and opportunities.

Nat Rev Drug Discov. 2022-8

[6]
The role of secreted proteins in efferocytosis.

Front Cell Dev Biol. 2024-1-8

[7]
The role of nuclear factors as "Find-Me"/alarmin signals and immunostimulation in defective efferocytosis and related disorders.

Int Immunopharmacol. 2020-3

[8]
First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis.

Cell Metab. 2021-11-2

[9]
Efferocytosis of vascular cells in cardiovascular disease.

Pharmacol Ther. 2022-1

[10]
Apoptotic cell clearance components in inflammatory arthritis.

Immunol Rev. 2023-10

引用本文的文献

[1]
Mapping the evolving trend of research on efferocytosis: a comprehensive data-mining-based study.

BioData Min. 2025-8-25

[2]
Therapeutic potential of five frequently prescribed herbs in obesity-associated Hashimoto's thyroiditis: insights from efferocytosis regulation.

Front Med (Lausanne). 2025-5-19

[3]
Nanoimmunotherapy: the smart trooper for cancer therapy.

Explor Target Antitumor Ther. 2025-4-10

[4]
Emerging Mechanisms and Biomarkers Associated with T-Cells and B-Cells in Autoimmune Disorders.

Clin Rev Allergy Immunol. 2025-2-11

[5]
12/15-Lipoxygenase-Derived Electrophilic Lipid Modifications in Phagocytic Macrophages.

ACS Chem Biol. 2025-2-21

[6]
Phytochemical-mediated efferocytosis and autophagy in inflammation control.

Cell Death Discov. 2024-12-18

[7]
Efferocytosis dysfunction in CXCL4-induced M4 macrophages: phenotypic insights in systemic sclerosis and .

Front Immunol. 2024

[8]
Consequence of alcohol intoxication-mediated efferocytosis impairment.

Front Immunol. 2024

本文引用的文献

[1]
Proteinase 3 promotes formation of multinucleated giant cells and granuloma-like structures in patients with granulomatosis with polyangiitis.

Ann Rheum Dis. 2023-6

[2]
PFKFB2-mediated glycolysis promotes lactate-driven continual efferocytosis by macrophages.

Nat Metab. 2023-3

[3]
Effects of Ruxolitinib on fibrosis in preclinical models of systemic sclerosis.

Int Immunopharmacol. 2023-3

[4]
Chimeric efferocytic receptors improve apoptotic cell clearance and alleviate inflammation.

Cell. 2022-12-22

[5]
Eosinophil-derived IL-4 is necessary to establish the inflammatory structure in innate inflammation.

EMBO Mol Med. 2023-2-8

[6]
Pro-resolving and anti-arthritic properties of the MC selective agonist PL8177.

Front Immunol. 2022

[7]
Impaired Efferocytosis by Synovial Macrophages in Patients With Knee Osteoarthritis.

Arthritis Rheumatol. 2023-5

[8]
Deletion of macrophage Gpr101 disrupts their phenotype and function dysregulating host immune responses in sterile and infectious inflammation.

Biochem Pharmacol. 2023-1

[9]
Immunogenic cell death as driver of autoimmunity in granulomatosis with polyangiitis.

Front Immunol. 2022

[10]
Mesenchymal stem cell-derived exosome-educated macrophages alleviate systemic lupus erythematosus by promoting efferocytosis and recruitment of IL-17 regulatory T cell.

Stem Cell Res Ther. 2022-9-24

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