Evidence map›Paper›PMID 25481648›Full record

ReviewCytokine2015

Interleukin-10 paradox: A potent immunoregulatory cytokine that has been difficult to harness for immunotherapy.

Ankit Saxena, Sam Khosraviani, Sanjeev Noel, Divya Mohan, Thomas Donner, Abdel Rahim A Hamad

Registry-linked trialAbstract readReview
In one paragraph

Review in Cytokine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07728877 (A Culture-tailored Plant-based Dietary Intervention in Taiwan), which is not on this map. Cited by 163 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed, 7 pooled it
6.1field-weighted citation impact, top 3% of its field
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.

NCT07728877 nacompletednot on this mapstarted 2023, after this paper: background citation

A Culture-tailored Plant-based Dietary Intervention in Taiwan: A Pilot Randomized Crossover Feasibility Trial With Preliminary Inflammatory and Metabolic Outcomes

TypeinterventionalSponsorTzu Chi UniversityRan2023 to 2023Enrolled30ConditionsHealthy, Dietary HabitsArmsPlant-Based Diet, General Diet
3 · Its place in the literature

Who cites it

163 citing papers in PubMed, 7 syntheses or guidelines pooled it, 298 citations in OpenAlex.

  1. Pooled it
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  11. Elevated IL-10 is Linked With the Expansion of T-betJournal of clinical immunology · 2026
    Article
  12. Review
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  20. Armored human CAR TScience advances · 2025
    Article

103 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Ankit SaxenaDepartment of Pathology, Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA.
Sam KhosravianiDepartment of Pathology, Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA.
Sanjeev NoelDepartment of Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD 21287, USA.
Divya MohanDepartment of Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD 21287, USA.
Thomas DonnerDepartment of Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD 21287, USA.
Abdel Rahim A HamadDepartment of Pathology, Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA; Department of Medicine, Johns Hopkins University, School of Medicine, Baltimore, MD 21287, USA. Electronic address: ahamad@jhmi.edu.
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

Mechanisms of Fas Ligand Control of Insulitis in Autoimmune DiabetesR01AI099027 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HAMAD, ABDEL RAHIM · 2013 to 2017
$2.0M
Mechanisms of Fas Ligand Control of Insulitis Initiation in Autoimmune DiabetesR56AI099027 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HAMAD, ABDEL RAHIM · 2012 to 2012
$411k
NIAID NIH HHS 1R01AI099027-01A1NIAID NIH HHS R01 AI099027NIAID NIH HHS R56 AI099027
6 · The paper itself

Abstract

Interleukin-10 (IL-10) is arguably the most potent anti-inflammatory cytokine. It is produced by almost all the innate and adaptive immune cells. These cells also serve as its targets, indicating that IL-10 secretion and action is highly regulated and perhaps compartmentalized. Consistent with this notion, various efforts directed at systemic administration of IL-10 to modulate autoimmune diseases (type 1 diabetes, multiple sclerosis, rheumatoid arthritis, psoriasis) have produced conflicting and largely inconsequential effects. On the other hand, IL-10 can promote humoral immune responses, enhancing class II expression on B cells and inducing immunoglobulin (Ig) production. Consequently, the high IL-10 level in systemic lupus erythematosus (SLE) patients is considered pathogenic and its blockade ameliorates the disease. In this perspective, we review preclinical findings and results of recent clinical studies using exogenous IL-10 to treat the aforementioned autoimmune diseases. In addition, given the limited success of IL-10 supplementation, we suggest that future studies should be expanded beyond modulating the delivery modes to include developing new strategies to protect and replenish the endogenous sources of IL-10. As an example, we provide evidence that aberrant Fas-mediated deletion of IL-10-producing B cells subverts the immunoregulatory role of IL-10 in autoimmune diabetes and that modulation of the Fas pathway preserves the IL-10-producing B cells and completely protects NOD mice from developing the disease.

Indexed as

ImmunotherapyAnimalsAutoimmune DiseasesB-LymphocytesClinical Trials as TopicFemaleHumansInterleukin-10Mice, Inbred NODMultiple SclerosisIL10 protein, humanIL10 protein, mouseInterleukin-10AutoimmunityB-cellsFas pathwaygldInterleukin-10

Identifiers

PMID25481648
PMCPMC4454631
OpenAlexW2047543986

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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 OpenQuestion graph.