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Autoimmune Disease

Autoimmune disease occurs when the immune system mistakenly attacks the body's own tissues, causing inflammation in places like the joints, thyroid, gut or nerves. Vitamin D and omega-3 fatty acids have the strongest evidence among supplements for calming immune activity, while a review found thunder god vine strongly suppressed immune function in autoimmune conditions. That effect carried serious side-effect risks, and options like idebenone and punarnava rest mostly on animal or lab work.

Sources: PMID 23957087

Supplements studied
3
Graded outcomes
3

Evidence by supplement

  • Strong
  • Moderate
  • Limited
  • Very limited

3 supplements

Thunder god vine: outcomes studied for Autoimmune Disease
GradeOutcomeEffectSizeStudiesPeopleStudies list
Immune Function Suppression

A review of clinical and laboratory findings confirmed Lei Gong Teng's potent immunosuppressive properties, with mechanisms including T-cell suppression and NF-κB inhibition. Multiple human studies in autoimmune conditions demonstrate clinically significant immunosuppression, which underlies both therapeutic effects and serious adverse event risk.

Changes; see studiesLarge effect2 studies

Studies that measured immune function suppression

Idebenone: outcomes studied for Autoimmune Disease
GradeOutcomeEffectSizeStudiesPeopleStudies list
Autoimmune Inflammation in Lupus

In a murine lupus model, idebenone improved mitochondrial metabolism and reduced inflammation (PMID:31566908). A review of CoQ10 analogs discussed immunomodulatory potential in systemic autoimmune diseases (PMID:33924642). No human clinical trial data for autoimmune indications.

Improves (the measure goes down)Moderate effect3 studies

Studies that measured autoimmune inflammation in lupus

Punarnava: outcomes studied for Autoimmune Disease
GradeOutcomeEffectSizeStudiesPeopleStudies list
Immunosuppression

In animal and in vitro studies, Boerhaavia diffusa suppresses T-cell proliferation and immune cell activity. This immunosuppressive effect could theoretically benefit autoimmune conditions but poses risk during infections. No human trials exist.

Changes; see studiesModerate effect1 study

Studies that measured immunosuppression

Key findings

  • Immune Function SuppressionThunder god vineChanges; see studies
  • Autoimmune Inflammation in LupusIdebenoneImproves (the measure goes down)
  • ImmunosuppressionPunarnavaChanges; see studies

Safety notes in the studies

  • Multiple human studies in autoimmune conditions demonstrate clinically significant immunosuppression, which underlies both therapeutic effects and serious adverse event risk.
  • This immunosuppressive effect could theoretically benefit autoimmune conditions but poses risk during infections.

The Autoimmune Disease General Support protocol

2 primary supplements · 6 supporting supplements

See the full protocol

Shop the evidence-backed picks

Support alongside medical care. These supplements are not a treatment for Autoimmune Disease. If you are being treated for it, talk to your clinician before adding one: supplements can interact with medicines.

Fullscript collectionImmune support: evidence-graded picksOpen on Fullscript

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Studies cited

6 studies from PubMed

  1. A novel SPE-LC-MRM strategy for serum demethylzeylasteral quantitation developed with an 18O-labeled internal standardAnalytical and Bioanalytical Chemistry, 2024 · PMID 37993551
  2. Ethnomedicinal values of Boerhaavia diffusa L. as a panacea against multiple human ailments: a state of art review.Frontiers in Chemistry, 2023 · PMID 38033469
  3. Therapeutic Potential and Immunomodulatory Role of Coenzyme Q(10) and Its Analogues in Systemic Autoimmune Diseases.Antioxidants (Basel, Switzerland), 2021 · PMID 33924642
  4. Traditional immunosuppression--Lei Gong Teng in modern medicineHarefuah, 2013 · PMID 23957087
  5. Pharmacokinetic evaluation of idebenone.Expert Opinion on Drug Metabolism & Toxicology, 2010 · PMID 20955109
  6. Pharmacokinetics and metabolism of idebenone in healthy male subjects.European Journal of Clinical Pharmacology, 2009 · PMID 19125241