Evidence map›Paper›PMID 32601182›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Sex differences in neutrophil biology modulate response to type I interferons and immunometabolism.

Sarthak Gupta, Shuichiro Nakabo, Luz P Blanco, Liam J O'Neil, Gustaf Wigerblad, Rishi R Goel, Pragnesh Mistry, Kan Jiang, Carmelo Carmona-Rivera, Diana W Chan and 15 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04690816 (The Natural History of Coronavirus Disease), which is not on this map. Cited by 125 papers.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed
7.2field-weighted citation impact, top 2% 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.

NCT04690816 completednot on this mapstarted 2021, after this paper: background citation

The Natural History of Coronavirus Disease (COVID-19) in Systemic Autoimmune Diseases; An Observational Prospective Study

TypeobservationalSponsorNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)Ran2021 to 2024Enrolled293ConditionsSystemic Autoimmune Diseases
3 · Its place in the literature

Who cites it

125 citing papers in PubMed, 198 citations in OpenAlex.

  1. Trial
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  8. Alzheimer's Disease Risk Factor APOE4 Exerts Dimorphic Effects on Female Bone.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  9. Article
  10. Article
  11. Article
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  13. Differential disease tolerance mediates sex-biased illness severity in sepsis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  14. Review
  15. Exploratory analysis of the impact of sex on sputum proteomic response to inhaled wood smoke in humans.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

65 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

25 authors at 3 institutions in 1 country.

Sarthak GuptaSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892; sarthak.gupta@nih.gov mariana.kaplan@nih.gov.
Shuichiro NakaboSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0002-9250-1851
Luz P BlancoSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0002-8468-6518
Liam J O'NeilSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.
Gustaf WigerbladSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.
Rishi R GoelSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0003-1715-5191
Pragnesh MistrySystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.
Kan JiangBiodata Mining and Discovery Section, NIAMS, NIH, Bethesda, MD 20892.
Carmelo Carmona-RiveraSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0002-7706-1464
Diana W ChanSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.
Xinghao WangSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.
Hege L PedersenSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0002-3768-9513
Manasi GadkariSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.
Katherine N HoweLaboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD 20892.ORCID 0000-0002-5814-2795
Faiza NazLaboratory of Muscle Stem Cells and Gene Regulation, NIAMS, NIH, Bethesda, MD 20892.
Stefania Dell'OrsoLaboratory of Muscle Stem Cells and Gene Regulation, NIAMS, NIH, Bethesda, MD 20892.
Sarfaraz A HasniSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0002-4164-8837
Caeden DempseyFood Allergy Research Unit, NIAID, NIH, Bethesda, MD 20892.
Ashley BuscettaMedical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892.
Pamela A Frischmeyer-GuerrerioFood Allergy Research Unit, NIAID, NIH, Bethesda, MD 20892.
Paul KruszkaMedical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892.ORCID 0000-0003-4949-0875
Maximilian MuenkeMedical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892.
Luis M FrancoSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892.ORCID 0000-0002-0540-5942
Hong-Wei SunBiodata Mining and Discovery Section, NIAMS, NIH, Bethesda, MD 20892.
Mariana J KaplanSystemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD 20892; sarthak.gupta@nih.gov mariana.kaplan@nih.gov.ORCID 0000-0003-2968-0815
National Institute of Arthritis and Musculoskeletal and Skin Diseases · USNational Human Genome Research Institute · USNational Institute of Allergy and Infectious Diseases · US

Funding

Systemic AutoimmunityZIAAR041199 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KAPLAN, MARIANA · 2014 to 2025
$32.5M
High Throughput Next Generation Sequencing: supports genomics and epigenomics research in muscle, skin, bone and autoimmune diseases.ZICAR041207 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI DELL'ORSO, STEFANIA · 2016 to 2025
$12.3M
Applying Bioinformatics to Research in Immune, Muscle, and Bone DiseasesZIHAR041173 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI GADINA, MASSIMO · 2009 to 2020
$11.0M
The Role of Transforming Growth Factor Beta (TGFbeta) in Promoting Allergic InflammationZIAAI001203 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FRISCHMEYER-GUERRERIO, PAMELA · 2015 to 2025
$10.6M
Integrative genomic analysis of the human response to glucocorticoidsZIAAR041213 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI FRANCO, LUIS · 2020 to 2025
$4.8M
6 · The paper itself

Abstract

Differences between female and male immunity may contribute to variations in response to infections and predisposition to autoimmunity. We previously reported that neutrophils from reproductive-age males are more immature and less activated than their female counterparts. To further characterize the mechanisms that drive differential neutrophil phenotypes, we performed RNA sequencing on circulating neutrophils from healthy adult females and males. Female neutrophils displayed significant up-regulation of type I IFN (IFN)-stimulated genes (ISGs). Single-cell RNA-sequencing analysis indicated that these differences are neutrophil specific, driven by a distinct neutrophil subset and related to maturation status. Neutrophil hyperresponsiveness to type I IFNs promoted enhanced responses to Toll-like receptor agonists. Neutrophils from young adult males had significantly increased mitochondrial metabolism compared to those from females and this was modulated by estradiol. Assessment of ISGs and neutrophil maturation genes in Klinefelter syndrome (47, XXY) males and in prepubescent children supported that differences in neutrophil phenotype between adult male and female neutrophils are hormonally driven and not explained by X chromosome gene dosage. Our results indicate that there are distinct sex differences in neutrophil biology related to responses to type I IFNs, immunometabolism, and maturation status that may have prominent functional and pathogenic implications.

Indexed as

AdultFemaleHumansImmunity, InnateInterferon Type IKlinefelter SyndromeMaleNeutrophilsSex FactorsYoung AdultInterferon Type Iinnate immunityinterferonsneutrophilssex differences

Identifiers

PMID32601182
PMCPMC7368314
OpenAlexW3039009674

What OpenQuestion holds

Textmetadata
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.