Evidence map›Paper›PMID 32341806›Full record

ArticleImmunometabolism2020

Metabolic Targets for Treatment of Autoimmune Diseases.

Paramarjan Piranavan, Manjeet Bhamra, Andras Perl

Open access · diamondAbstract read
In one paragraph

Article in Immunometabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 9% 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.

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

36 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Semaphorin3A Rewires CD4International journal of molecular sciences · 2025
    Article
  3. Technologies for Decoding Cancer Metabolism with Spatial Resolution.Cold Spring Harbor perspectives in medicine · 2025
    Review
  4. Review
  5. Review
  6. Metabolomics in systemic sclerosis.Rheumatology international · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Targeted saliva metabolomics in Sjögren's syndrome.Clinics (Sao Paulo, Brazil) · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Glucose Requirement of Antigen-Specific Autoreactive B Cells and CD4+ T Cells.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  15. Review
  16. Review
  17. Article
  18. Endogenous drivers of altered immune cell metabolism.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  19. Principles behind SLE treatment withImmunometabolism (Cobham, Surrey) · 2022
    Review
  20. 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

3 authors at 1 institution in 1 country.

Paramarjan PiranavanDepartment of Medicine, College of Medicine, State University of New York, Syracuse, NY 13210, USA.
Manjeet BhamraDepartment of Medicine, College of Medicine, State University of New York, Syracuse, NY 13210, USA.
Andras PerlDepartment of Medicine, College of Medicine, State University of New York, Syracuse, NY 13210, USA.
State University of New York · US

Funding

SLE Treatment with N-acetylcysteineU01AR076092 · NIAMS · UPSTATE MEDICAL UNIVERSITY · PI Michael P McDermott, Andras Perl · 2020 to 2026
$7.9M
Metabolic Control of T-cell Lineage Specification in SLER01AI072648 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI PERL, ANDRAS · 2008 to 2024
$6.1M
Endocytic Control of Autophagosome Formation in Lupus T cellsR01AI122176 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI PERL, ANDRAS · 2016 to 2020
$2.0M
Treatment of Systemic Lupus Erythematosus (SLE) with N-acetylcysteine (NAC)R34AR068052 · NIAMS · UPSTATE MEDICAL UNIVERSITY · PI MCDERMOTT, MICHAEL P, PERL, ANDRAS · 2016 to 2017
$405k
Treatment of SLE with sirolimusR34AI141304 · NIAID · UPSTATE MEDICAL UNIVERSITY · PI PERL, ANDRAS · 2019 to 2019
$243k
NIAID NIH HHS R01 AI072648NIAID NIH HHS R01 AI122176NIAID NIH HHS R34 AI141304NIAMS NIH HHS R34 AR068052NIAMS NIH HHS U01 AR076092
6 · The paper itself

Abstract

There is a considerable unmet demand for safe and efficacious medications in the realm of autoimmune and inflammatory diseases. The fate of the immune cells is precisely governed by control of various metabolic processes such as mitochondrial oxidative phosphorylation, glycolysis, fatty acid synthesis, beta-oxidation, amino acid metabolism, and several others including the pentose phosphate pathway, which is a unique source of metabolites for cell proliferation and maintenance of a reducing environment. These pathways are tightly regulated by the cytokines, growth factors, availability of the nutrients and host-microbe interaction. Exploring the immunometabolic pathways that govern the fate of cells of the innate and adaptive immune system, during various stages of activation, proliferation, differentiation and effector response, is crucial for new development of new treatment targets. Identifying the pathway connections and key enzymes will help us to target the dysregulated inflammation in autoimmune diseases. The mechanistic target of rapamycin (mTOR) pathway is increasingly recognized as one of the key drivers of proinflammatory responses in autoimmune diseases. In this review, we provide an update on the current understanding of the metabolic signatures noted within different immune cells of many different autoimmune diseases with a focus on selecting pathways and specific metabolites as targets for treatment.

Indexed as

acetylcysteineglycolysisimmune metabolic pathwayskynureninemechanistic target of rapamycinoxidative phosphorylationoxidative stresspentose phosphate pathwaypsoriasisrheumatoid arthritissclerodermasystemic lupus erythematosustryptophan

Identifiers

PMID32341806
PMCPMC7184931
OpenAlexW3014499862

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.