Evidence map›Paper›PMID 33870241›Full record

ArticleMed (New York, N.Y.)2021

Mucosal-associated invariant T cell responses differ by sex in COVID-19.

Chen Yu, Sejiro Littleton, Nicholas S Giroux, Rose Mathew, Shengli Ding, Joan Kalnitsky, Yuchen Yang, Elizabeth Petzold, Hong A Chung, Grecia O Rivera and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Med (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

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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

21 authors at 3 institutions in 1 country.

Chen YuDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
Sejiro LittletonDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
Nicholas S GirouxDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Rose MathewDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
Shengli DingDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Joan KalnitskyDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
Yuchen YangDepartment of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Elizabeth PetzoldCenter for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
Hong A ChungDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Grecia O RiveraDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Tomer RotsteinDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Rui XiDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Emily R KoCenter for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
Ephraim L TsalikCenter for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
Gregory D SempowskiDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA.
Thomas N DennyDuke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA.
Thomas W BurkeCenter for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
Micah T McClainCenter for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
Christopher W WoodsCenter for Applied Genomics and Precision Medicine, Duke University, Durham, NC 27710, USA.
Xiling ShenDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27710, USA.
Daniel R SabanDepartment of Ophthalmology, Duke University School of Medicine, Durham, NC 27710, USA.
Duke University · USDuke Medical Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Antibacterial Resistance Leadership Group (ARLG)UM1AI104681 · NIAID · DUKE UNIVERSITY · PI Vance G. Fowler, Henry F HENRY CHAMBERS · 2013 to 2026
$180.8M
NIAID VIROLOGY QUALITY ASSURANCE (VQA) COVID-1975N93019C00015 · NIAID · DUKE UNIVERSITY · PI DENNY, THOMAS · 2019 to 2025
$24.4M
VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
Robust Control of the Stem Cell NicheR35GM122465 · NIGMS · TERASAKI INSTITUTE FOR BIOMEDICAL INNOVATION · PI Xiling Shen · 2017 to 2026
$5.6M
Defining the Immune Cell Roles in Meibomian Gland Dysfunction in the Context of Ocular Surface Immune DiseasesR01EY021798 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI SABAN, DANIEL RAPHAEL · 2012 to 2025
$5.3M
Cellular and Molecular Dynamics of Retinal Microglial in the Context of Photoreceptor DegenerationR01EY030906 · NEI · DUKE UNIVERSITY · PI Daniel Raphael Saban · 2020 to 2026
$3.5M
Epigenomic Reprogramming in Patient Derived Models of Colorectal CancerU01CA217514 · NCI · DUKE UNIVERSITY · PI HSU, SHIAOWEN DAVID · 2018 to 2022
$3.1M
Plasma Protein Biomarker-Based Diagnostics Of Outcome In Sepsis and CAPU01AI066569 · NIAID · NATIONAL CENTER FOR GENOME RESOURCES · PI KINGSMORE, STEPHEN FRANCIS · 2005 to 2010
$2.9M
NCI NIH HHS U01 CA217514NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY030906NIAID NIH HHS 75N93019C00015NIAID NIH HHS U01 AI066569NIAID NIH HHS UC6 AI058607NIAID NIH HHS UM1 AI104681NIGMS NIH HHS R35 GM122465
6 · The paper itself

Abstract

backgroundSexual dimorphisms in immune responses contribute to coronavirus disease 2019 (COVID-19) outcomes, but the mechanisms governing this disparity remain incompletely understood.

methodsWe carried out sex-balanced sampling of peripheral blood mononuclear cells from hospitalized and non-hospitalized individuals with confirmed COVID-19, uninfected close contacts, and healthy control individuals for 36-color flow cytometry and single-cell RNA sequencing.

findingsOur results revealed a pronounced reduction of circulating mucosal-associated invariant T (MAIT) cells in infected females. Integration of published COVID-19 airway tissue datasets suggests that this reduction represented a major wave of MAIT cell extravasation during early infection in females. Moreover, MAIT cells from females possessed an immunologically active gene signature, whereas cells from males were pro-apoptotic.

conclusionsOur findings uncover a female-specific protective MAIT cell profile, potentially shedding light on reduced COVID-19 susceptibility in females.

fundingThis work was supported by NIH/NIAID (U01AI066569 and UM1AI104681), the Defense Advanced Projects Agency (DARPA; N66001-09-C-2082 and HR0011-17-2-0069), the Veterans Affairs Health System, and Virology Quality Assurance (VQA; 75N93019C00015). The content is solely the responsibility of the authors and does not necessarily represent the official view of the National Institutes of Health. COVID-19 samples were processed under Biosafety level 2 (BSL-2) with aerosol management enhancement or BSL-3 in the Duke Regional Biocontainment Laboratory, which received partial support for construction from NIH/NIAID (UC6AI058607).

Indexed as

COVID-19Mucosal-Associated Invariant T CellsFemaleFlow CytometryHumansLeukocytes, MononuclearLymphocyte ActivationMaleUnited StatesapoptosisIL-7innate immunitymonocyteSARS-CoV-2

Identifiers

PMID33870241
PMCPMC8043578
OpenAlexW3156501804

What OpenQuestion holds

Textmetadata
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.