The Gut Microbiota and Autoimmune Disease

A special issue of Microorganisms (ISSN 2076-2607). This special issue belongs to the section "Gut Microbiota".

Deadline for manuscript submissions: 31 July 2025 | Viewed by 1898

Special Issue Editors


E-Mail Website
Guest Editor
Department of Microbiology and Immunology, University of Louisville, 505 South Hancock St, Rm 611, Louisville, KY 40202, USA
Interests: autoimmune disease; gut microbiota; immunoregulation; immunity

E-Mail Website
Guest Editor
Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202, USA
Interests: immunoregulation; tolerance; autoimmunity and microbiota

Special Issue Information

Dear Colleagues,

The intestinal microbiota is an important component of the body that exists in symbiosis with the host and helps with various functions, e.g., digesting insoluble fibers. More importantly, the intestinal microbiota is necessary for the proper development of the immune response and a dysbiotic intestinal microbiota has been associated with development of autoimmune diseases. Furthermore, intestinal microbiota is not only associated with induction of autoimmunity but also its prevention. High-throughput human multi-omics data, including metagenomics and metabolomics data, have shed some light on potential mechanisms by which autoimmune diseases can be induced or prevented. Through this issue, we will discuss the current knowledge of how the intestinal microbiota and derived microbial compounds may be associated with pathogenesis or prevention of autoimmunity.

The aim of this Special Issue of Microorganisms is to present a collection of articles that provide a snapshot of current research into the effects of the gut microbiota on autoimmunity and inflammatory disease such as colitis. Manuscripts covering all aspects of research relating to this area are welcome.

Dr. Pascale Alard
Dr. Michele M. Kosiewicz
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Microorganisms is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • intestinal microbiota
  • autoimmune diseases
  • inflammatory disease
  • immune regulation

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

Jump to: Review

22 pages, 4320 KiB  
Article
Characterization of Sex-Based Differences in Gut Microbiota That Correlate with Suppression of Lupus in Female BWF1 Mice
by James W. Harder, Jing Ma, James Collins, Pascale Alard, Venkatakrishna R. Jala, Haribabu Bodduluri and Michele M. Kosiewicz
Microorganisms 2025, 13(5), 1023; https://doi.org/10.3390/microorganisms13051023 - 29 Apr 2025
Abstract
Systemic lupus erythematosus (SLE) is more prevalent in female mice and humans and is associated with microbiota dysbiosis. We analyzed the fecal microbiota composition in female and male NZBxNZWF1 (BWF1) mice, a model of SLE, using 16S RNA gene sequencing. Composition of gut [...] Read more.
Systemic lupus erythematosus (SLE) is more prevalent in female mice and humans and is associated with microbiota dysbiosis. We analyzed the fecal microbiota composition in female and male NZBxNZWF1 (BWF1) mice, a model of SLE, using 16S RNA gene sequencing. Composition of gut microbiota differed between adult disease-prone female (pre-disease) and disease-resistant male mice. Transfer of male cecal contents by gavage into female mice suppressed kidney disease (decreased proteinuria) and improved survival. After our mouse colony was moved to a new barrier facility with similar housing, male cecal transplants failed to suppress disease in female recipients. After two years, the protective phenotype reemerged: male cecal transplants once again suppressed disease in female mice. We compared the gut microbiota composition in female and male BWF1 mice for the three different periods, during which the male microbiota either protected or failed to protect female recipients. In female vs. male mice and in female mice receiving male cecal transplants, we found Bacteroides was high, Clostridium was low (high Bacteroides/Clostridium ratio), and Alistipes was present during periods when male cecal transplants suppressed disease. These data suggest that specific bacterial populations may have opposing effects on disease suppression in a model of microbiota transplantation. Full article
(This article belongs to the Special Issue The Gut Microbiota and Autoimmune Disease)
Show Figures

Figure 1

Review

Jump to: Research

26 pages, 1070 KiB  
Review
Dysregulated Intestinal Host–Microbe Interactions in Systemic Lupus Erythematosus: Insights from Patients and Mouse Models
by Miki Kume, Jin Din and Daniel F. Zegarra-Ruiz
Microorganisms 2025, 13(3), 556; https://doi.org/10.3390/microorganisms13030556 - 1 Mar 2025
Viewed by 1605
Abstract
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by chronic inflammation that affects multiple organs, with its prevalence varying by ethnicity. Intestinal dysbiosis has been observed in both SLE patients and murine models. Additionally, intestinal barrier impairment is thought to contribute to [...] Read more.
Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by chronic inflammation that affects multiple organs, with its prevalence varying by ethnicity. Intestinal dysbiosis has been observed in both SLE patients and murine models. Additionally, intestinal barrier impairment is thought to contribute to the ability of pathobionts to evade and breach immune defenses, resulting in antigen cross-reactivity, microbial translocation, subsequent immune activation, and, ultimately, multiple organ failure. Since the detailed mechanisms underlying these processes are difficult to examine using human samples, murine models are crucial. Various SLE murine models, including genetically modified spontaneous and inducible murine models, offer insights into pathobionts and how they dysregulate systemic immune systems. Furthermore, since microbial metabolites modulate systemic immune responses, bacteria and their metabolites can be targeted for treatment. Based on human and mouse research insights, this review examines how lupus pathobionts trigger intestinal and systemic immune dysregulation. Therapeutic approaches, such as fecal microbiota transplantation and dietary adjustments, show potential as cost-effective and safe methods for preventing and treating SLE. Understanding the complex interactions between the microbiota, host factors, and immune dysregulation is essential for developing novel, personalized therapies to tackle this multifaceted disease. Full article
(This article belongs to the Special Issue The Gut Microbiota and Autoimmune Disease)
Show Figures

Figure 1

Back to TopTop