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A 12-week supplementation with quercetin does not affect natural killer cell activity, granulocyte oxidative burst activity or granulocyte phagocytosis in female human subjects

Serena A Heinz, Dru A Henson, David C Nieman, Melanie D Austin, Fuxia Jin
The British journal of nutrition 2010 104(6):849

Bibliography

PubMed
PMID 20500927
Funding
Funding was not specified in the indexed record or the disclosure metadata available for this entry.
Competing interests
A competing-interest declaration was not available in the indexed record or the disclosure metadata used for this entry.

Study snapshot

DesignRandomized double-blind placebo-controlled immune-function analysis
ModelHuman intervention research
Sample120 women; smaller subsets underwent individual immune assays
InterventionQuercetin 500 or 1,000 mg/day or placebo
Duration12 weeks
EndpointsInflammatory measures

What the study showed, in plain terms

Published in 2010, this source examined immunity and respiratory health. Design: Randomized double-blind placebo-controlled immune-function analysis. Sample/model: 120 women; smaller subsets underwent individual immune assays. The exposure or intervention was Quercetin 500 or 1,000 mg/day or placebo. Follow-up or treatment period: 12 weeks.

Natural killer-cell activity, granulocyte function, leukocyte subsets, and measured cytokines did not improve.

Subset analyses from a larger community supplementation program. Higher plasma exposure did not demonstrate enhanced innate immunity.

Continue with Quercetin Data Center

For topic-level interpretation, read Quercetin for Immune Health, Colds and COVID-19. This is a related guide; the citation panel separately identifies articles that directly cite this paper.

Key findings

  • Natural killer-cell activity, granulocyte function, leukocyte subsets, and measured cytokines did not improve.
  • The recorded outcome domains were Inflammatory measures.
  • The result applies to the tested exposure: Quercetin 500 or 1,000 mg/day or placebo; 12 weeks.

What this study can and cannot tell us

  • Subset analyses from a larger community supplementation program. Higher plasma exposure did not demonstrate enhanced innate immunity.
  • An individual controlled trial must be interpreted alongside its comparator, sample size, endpoint selection and independent replication. It does not validate a different commercial formulation or a general longevity claim.
  • Companion or correction records are linked below. They should not be counted automatically as independent replications; see the individual source notes for the relationship.
  • Source basis: Source check: PubMed abstract and indexed metadata; full methods were not independently confirmed for this entry. Missing method details, funding information or participant denominators are not inferred.

Citation network

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