Evidence map›Paper›PMID 32446964›Full record

Trial reportThe Journal of allergy and clinical immunology2020

Autoantibody-positive healthy individuals with lower lupus risk display a unique immune endotype.

Samantha Slight-Webb, Miles Smith, Aleksandra Bylinska, Susan Macwana, Carla Guthridge, Rufei Lu, Joan T Merrill, Eliza Chakravarty, Cristina Arriens, Melissa E Munroe and 4 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

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  11. Pathogenesis of autoimmune disease.Nature reviews. Nephrology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Samantha Slight-WebbDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Miles SmithDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Aleksandra BylinskaDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Susan MacwanaDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Carla GuthridgeDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Rufei LuDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Okla.
Joan T MerrillDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Eliza ChakravartyDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Cristina ArriensDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla; Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, Okla; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Okla.
Melissa E MunroeDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla.
Holden T MaeckerInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, Calif.
Paul J UtzDivision of Immunology and Rheumatology, Stanford University School of Medicine, Stanford, Calif.
Joel M GuthridgeDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Okla.
Judith A JamesDepartment of Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, Okla; Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, Okla; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, Okla. Electronic address: Judith-James@omrf.org.
Oklahoma Medical Research Foundation · USUniversity of Oklahoma Health Sciences Center · USStanford University · US

Funding

Tracking and Evaluation CoreU54GM104938 · NIGMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI TIMOTHY M VANWAGONER · 2013 to 2026
$68.2M
Oklahoma Rheumatic Disease Research Cores Center (Overall Application)P30AR073750 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JUDITH A JAMES · 2018 to 2026
$8.5M
Pre-Clinical Studies to Identify SLE Therapeutic TargetsU19AI082714 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JAMES, JUDITH A · 2009 to 2018
$6.2M
Molecular Basis of Immunity - Kirschtein-NRSAT32AI007633 · NIAID · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CUNNINGHAM, MADELEINE W. · 2001 to 2022
$4.0M
Th17 lymphocytes in human autoimmune diseasesU19AI082719 · NIAID · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 2009 to 2013
$3.4M
Oklahoma ACE: Molecular Destruction of Autoimmune Disease to Aid Clinical Trail SuccessUM1AI144292 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JUDITH A JAMES · 2019 to 2026
$3.3M
Understanding early events in lupus autoimmunity to aid preventionU01AI101934 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JAMES, JUDITH A · 2012 to 2016
$2.3M
Mechanisms of Lupus Disease Transition and Hydroxychloroquine Immune ModulationR01AR072401 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JAMES, JUDITH A · 2017 to 2020
$1.8M
Hypoplastic Left Heart Syndrome: Expression of RHD in the Fetus?R01HL098634 · NHLBI · WASHINGTON UNIVERSITY · PI EGHTESADY, PIROOZ · 2010 to 2014
$1.8M
Developing an animal model of HLHS: role of immune mediated injuryR21HL104391 · NHLBI · WASHINGTON UNIVERSITY · PI EGHTESADY, PIROOZ · 2011 to 2012
$416k
Oklahoma High-Throughput Serum Analyte SystemS10RR026735 · NCRR · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI JAMES, JUDITH A · 2010 to 2010
$311k
NCRR NIH HHS S10 RR026735NHLBI NIH HHS R01 HL098634NHLBI NIH HHS R21 HL104391NIAID NIH HHS T32 AI007633NIAID NIH HHS U01 AI101934NIAID NIH HHS U19 AI082714NIAID NIH HHS U19 AI082719NIAID NIH HHS UM1 AI144292NIAMS NIH HHS P30 AR073750NIAMS NIH HHS R01 AR072401NIGMS NIH HHS U54 GM104938
6 · The paper itself

Abstract

backgroundAutoimmune diseases comprise a spectrum of illnesses and are on the rise worldwide. Although antinuclear antibodies (ANAs) are detected in many autoimmune diseases, up to 20% of healthy women are ANA-positive (ANA+) and most will never develop clinical symptoms. Furthermore, disease transition is higher among ANA+ African Americans compared with ANA+ European Americans.

objectiveWe sought to determine the immune features that might define and prevent transition to clinical autoimmunity in ANA+ healthy individuals.

methodsWe comprehensively phenotyped immune profiles of African Americans and European Americans who are ANA-negative (ANA-) healthy, ANA+ healthy, or have SLE using single cell mass cytometry, next-generation RNA-sequencing, multiplex cytokine profiling, and phospho-signaling analyses.

resultsWe found that, compared with both ANA- and ANA+ healthy individuals, patients with SLE of both races displayed T-cell expansion and elevated expression of type I and II interferon pathways. We discovered a unique immune signature that suggests a suppressive immune phenotype and reduced CD11C

conclusionsWe propose that this novel immune signature identified in ANA+ healthy European Americans may protect them from T-cell expansion, heightened activation of interferon pathways, and disease transition.

Indexed as

Black or African AmericanLymphocyte ActivationWhite PeopleAdultAntibodies, AntinuclearFemaleHumansLupus Erythematosus, SystemicMaleSignal TransductionT-LymphocytesAntibodies, AntinuclearANA+ healthyAutoantibodiescytokinesimmune suppressionraceSLET cells

Identifiers

PMID32446964
PMCPMC7680268
OpenAlexW3027295473

What OpenQuestion holds

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Registered trials

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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.