Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2020 Nov 1;11(6):1758-1773.
doi: 10.1080/19490976.2020.1768644. Epub 2020 Jun 7.

Alteration in gut microbiota is associated with dysregulation of cytokines and glucocorticoid therapy in systemic lupus erythematosus

Affiliations
Comparative Study

Alteration in gut microbiota is associated with dysregulation of cytokines and glucocorticoid therapy in systemic lupus erythematosus

Mengchen Guo et al. Gut Microbes. .

Abstract

A growing corpus of evidence implicates the involvement of the commensal microbiota and immune cytokines in the initiation and progression of systemic lupus erythematosus (SLE). Glucocorticoids have been widely used in the treatment of SLE patients, however, glucocorticoid treatment carries a higher risk of other diseases. Using the 16S rRNA technique, we investigated the differences between the gut microbiota associated with the immune cytokines of SLE and relevant glucocorticoid treatment in a female cohort of 20 healthy control subjects (HC), 17 subjects with SLE (SLE-G), and 20 SLE patients having undergone glucocorticoid treatment (SLE+G). We observed that the diversity and structure of the microbial community in SLE+G patients were significantly changed compared to that of SLE-G patients, whereas the gut microbial community of the SLE+G group showed a similarity with the HC group, which implicate that the shift in the gut microbiome could represent a return to homeostasis. Furthermore, the up-regulations of immune cytokines in SLE-G were identified as closely related to gut dysbiosis, which indicates that the overrepresented genera in SLE patients may play roles in regulating expression level of these immune cytokines. This associated analysis of gut microbiota, glucocorticoid therapy, and immune factors might provide novel and insightful clues revealing the pathogenesis of SLE patients.

Keywords: Systemic lupus erythematosus (SLE); autoimmune disease; cytokines; glucocorticoid; gut microbiota.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
SLE patients displayed alternation of gut microbiota and glucocorticoid treatment changed gut microbiota composition of SLE patients.
Figure 2.
Figure 2.
Co-occurrence network of microbiota in HC (a), SLE-G patients (b) and SLE+G patients (c).
Figure 3.
Figure 3.
Analysis of twelve immune cytokines in HC, SLE-G and SLE+G groups.
Figure 4.
Figure 4.
Correlation analysis of these differential genera and cytokines between any two groups.
Figure 5.
Figure 5.
Microbial functions annotation in HC, SLE-G and SLE+G patients.
Figure 6.
Figure 6.
The summary for the analysis of gut microbiota and cytokines in SLE patients with/without Glucocorticoid treatment.

Similar articles

Cited by

References

    1. Stojan G, Petri M.. Epidemiology of systemic lupus erythematosus: an update. Curr Opin Rheumatol. 2018;30:144–150. - PMC - PubMed
    1. Raj P, Rai E, Song R, Khan S, Wakeland BE, Viswanathan K, Arana C, Liang C, Zhang B, Dozmorov I, et al. Regulatory polymorphisms modulate the expression of HLA class II molecules and promote autoimmunity. Elife. 2016;5. doi:10.7554/eLife.12089. - DOI - PMC - PubMed
    1. Wu HJ, Wu E. The role of gut microbiota in immune homeostasis and autoimmunity. Gut Microbes. 2012;3:4–14. doi:10.4161/gmic.19320. - DOI - PMC - PubMed
    1. Anaya JM, Ramirez-Santana C, Alzate MA, Molano-Gonzalez N, Rojas-Villarraga A. The autoimmune ecology. Front Immunol. 2016;7:139. doi:10.3389/fimmu.2016.00139. - DOI - PMC - PubMed
    1. McLean MH, Dieguez D Jr., Miller LM, Young HA. Does the microbiota play a role in the pathogenesis of autoimmune diseases? Gut. 2015;64(2):332–341. doi:10.1136/gutjnl-2014-308514. - DOI - PMC - PubMed

Publication types

MeSH terms