» Articles » PMID: 38806966

The Therapeutic Effects of Probiotic on Systemic Lupus Erythematosus in Lupus Mice Models: A Systematic Review

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

Increasing evidence suggests the beneficial immunomodulatory effects of probiotics can reduce inflammation in systemic lupus erythematosus (SLE). However, there is no summary of the existing evidence available. This study aims to investigate the therapeutic effects of probiotics on SLE in a lupus mouse model by examining various markers, including inflammatory cytokines, Treg cells, disease activity, and gut microbiota. A systematic search was conducted using three databases (Web of Science, PubMed, and Scopus) to identify animal studies that reported the therapeutic benefits of probiotics against SLE. Data extracted from the selected articles were qualitatively synthesized. The SYRCLE risk of bias tool was used to evaluate the risk of bias. Out of a total of 3205 articles, 12 met the inclusion criteria. Probiotic strains, quantities, and routes of administration varied among the studies. The treatment ranged from 8 to 47 weeks. Probiotic strains such as L. fermentum CECT5716, L. casei B255, L. reuteri DSM 17509, L. plantarum LP299v, and L. acidophilus can significantly reduce pro-inflammatory cytokines (TNF-α, IL-12, IL-6, IL-1β, IL-17, and IFN-γ) levels while increasing anti-inflammatory IL-10 and Treg cells. Probiotics also delay the production of autoantibodies, thus prolonging the remission period, decreasing flare frequency, and delaying disease progression. Furthermore, probiotic administration prevents gut dysbiosis, increases intestinal stability, and prevents pathogen colonization. In conclusion, probiotics can be considered a new alternative therapeutic approach for the management of SLE. Further clinical studies are required to investigate and validate the safety and effectiveness of probiotics in humans.

Citing Articles

The Complex Role of Gut Microbiota in Systemic Lupus Erythematosus and Lupus Nephritis: From Pathogenetic Factor to Therapeutic Target.

Parodi E, Novi M, Bottino P, La Porta E, Merlotti G, Castello L Microorganisms. 2025; 13(2).

PMID: 40005809 PMC: 11858628. DOI: 10.3390/microorganisms13020445.

References
1.
Karrar S, Cunninghame Graham D . Abnormal B Cell Development in Systemic Lupus Erythematosus: What the Genetics Tell Us. Arthritis Rheumatol. 2017; 70(4):496-507. PMC: 5900717. DOI: 10.1002/art.40396. View

2.
Tian J, Zhang D, Yao X, Huang Y, Lu Q . Global epidemiology of systemic lupus erythematosus: a comprehensive systematic analysis and modelling study. Ann Rheum Dis. 2022; 82(3):351-356. PMC: 9933169. DOI: 10.1136/ard-2022-223035. View

3.
Barber M, Drenkard C, Falasinnu T, Hoi A, Mak A, Kow N . Global epidemiology of systemic lupus erythematosus. Nat Rev Rheumatol. 2021; 17(9):515-532. PMC: 8982275. DOI: 10.1038/s41584-021-00668-1. View

4.
Allen M, Rus V, Szeto G . Leveraging Heterogeneity in Systemic Lupus Erythematosus for New Therapies. Trends Mol Med. 2020; 27(2):152-171. PMC: 8667782. DOI: 10.1016/j.molmed.2020.09.009. View

5.
Dibas M, Ameer A, Atiah M, Ibrahim A, Alkhalifa O, Hossain M . Characteristics, Determinants, and Outcomes of Traumatic Vertebral and Spinal Injuries: A Retrospective Study in the Al-Qassim Region of Saudi Arabia. Cureus. 2023; 14(12):e32426. PMC: 9833627. DOI: 10.7759/cureus.32426. View