Evidence mapPaperPMID 40925130Full record

ReviewThe Journal of pharmacology and experimental therapeutics2025

Pharmacological insights into gut microbiota modulation in systemic lupus erythematosus: Mechanisms, treatment strategies, and clinical implications.

Kantrol Kumar Sahu, Krishna Yadav, Madhulika Pradhan, Mukesh Sharma, Akhilesh Dubey, Sucheta, J John Kirubakaran

Abstract readReview
In one paragraph

Review in The Journal of pharmacology and experimental therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Kantrol Kumar SahuInstitute of Pharmaceutical Research, GLA University, Mathura, Uttar Pradesh, India.
Krishna YadavRungta College of Pharmaceutical Sciences and Research, Bhilai, Kohka, Chhattisgarh, India; School of Pharmacy, Rungta International Skills University, Bhilai, Chhattisgarh, India.
Madhulika PradhanRungta College of Pharmaceutical Sciences and Research, Bhilai, Kohka, Chhattisgarh, India; School of Pharmacy, Rungta International Skills University, Bhilai, Chhattisgarh, India.
Mukesh SharmaRungta College of Pharmaceutical Sciences and Research, Bhilai, Kohka, Chhattisgarh, India; School of Pharmacy, Rungta International Skills University, Bhilai, Chhattisgarh, India.
Akhilesh DubeyDepartment of Pharmaceutics, Nitte (Deemed to be University), NGSM Institute of Pharmaceutical Sciences, Karnataka, India.
SuchetaSchool of Medical and Allied Sciences, K. R. Mangalam University, Gurugram, Haryana, India.
J John KirubakaranDepartment of Pharmacy Practice, Parul Institute of Pharmacy & Research, Parul University, Limda, Waghodia, Vadodara, Gujarat, India. Electronic address: john.mpharm@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by widespread inflammation and immune system dysregulation. Recent research suggests that the gut microbiota may play a role in the development of SLE by modulating immune system responses, affecting cytokine production, and altering the activity of T and B cells lymphocytes. As a result, there is a growing interest in microbiota-targeted therapies, including probiotics, dietary changes, and fecal microbiota transplantation. These methods may help restore the balance of microbes and reduce disease activity, but there are still a number of problems to solve. For example, microbiota composition varies greatly from person to person, and it is not clear how dysbiosis causes disease onset. There are also safety concerns about fecal microbiota transplantation. Experimental and clinical studies have started to shed light on the complicated ways in which microbial communities and immune function affect each other in SLE. These studies provide useful information, but their results are often inconsistent. As research continues, integrative methods like metagenomics and metabolomics may help find microbial signatures linked to disease, helping create more accurate and personalized treatments. The gut microbiome is a promising yet still developing area of research that could help us learn more about autoimmune diseases and their treatment, such as SLE. SIGNIFICANCE STATEMENT: Grasping the complex interplay between gut microbiota and systemic lupus erythematosus (SLE) has provided an avenue for therapeutic intervention. This study emphasizes the importance of gut dysbiosis in immune dysregulation, with connections between microbial translocation, molecular mimicry, and inflammatory pathways as contributing factors to the progression of SLE. This work sets the stage for novel and targeted approaches to treating SLE and improving patient outcomes by investigating microbiota-centric treatment options, such as probiotics, dietary interventions, and fecal microbiota transplantation.

Indexed as

Gastrointestinal MicrobiomeLupus Erythematosus, SystemicAnimalsDysbiosisFecal Microbiota TransplantationHumansProbioticsGut-immune axisImmune dysregulationLeaky gutMicrobial translocationMolecular mimicrySystemic lupus erythematosus

Identifiers

PMID40925130
PMCPMC12597648

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.