Evidence map›Paper›PMID 39195859›Full record

ArticleNature cardiovascular research2024

An engineered human cardiac tissue model reveals contributions of systemic lupus erythematosus autoantibodies to myocardial injury.

Sharon Fleischer, Trevor R Nash, Manuel A Tamargo, Roberta I Lock, Gabriela Venturini, Margaretha Morsink, Pamela L Graney, Vanessa Li, Morgan J Lamberti, Martin Liberman and 11 more

Abstract read
In one paragraph

Article in Nature cardiovascular research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. A practical toolbox for modelling fibrosis in vitro.Nature biomedical engineering · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Sharon Fleischer *Department of Biomedical Engineering, Columbia University, New York, NY, USA.
Trevor R Nash *Department of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0003-4555-7577
Manuel A TamargoDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Roberta I LockDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Gabriela VenturiniDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Margaretha MorsinkDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Pamela L GraneyDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0003-0428-2634
Vanessa LiDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Morgan J LambertiDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Martin LibermanDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Youngbin KimDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.ORCID http://orcid.org/0000-0003-1919-1575
Daniel N TavakolDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Richard Z ZhuangDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Jaron WhiteheadDepartment of Biomedical Engineering, Columbia University, New York, NY, USA.
Richard A FriedmanBiomedical Informatics Shared Resource, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, USA.
Rajesh K SoniProteomics and Macromolecular Crystallography Shared Resource, Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, USA.
Jonathan G SeidmanDepartment of Genetics, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-9082-3566
Christine E SeidmanDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Laura Geraldino-PardillaDepartment of Medicine, Columbia University, New York, NY, USA.
Robert WinchesterDepartment of Medicine, Columbia University, New York, NY, USA.
Gordana Vunjak-NovakovicDepartment of Biomedical Engineering, Columbia University, New York, NY, USA. gv2131@columbia.edu.ORCID http://orcid.org/0000-0002-9382-1574

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Tissue Engineering Resource Center: TTDP41EB027062 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Gordana Vunjak-Novakovic · 2019 to 2026
$12.6M
Engineering Vascularized Cardiac MuscleR01HL076485 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Gordana Vunjak-Novakovic · 2005 to 2026
$9.2M
American Heart Association (American Heart Association, Inc.) 19TPA34910217NCI NIH HHS P30 CA013696NHLBI NIH HHS R01 HL076485NIBIB NIH HHS P41 EB027062U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 3R01HL076485U.S. Department of Health & Human Services | NIH | National Institute of Biomedical Imaging and Bioengineering (NIBIB) P41EB027062
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) is a heterogenous autoimmune disease that affects multiple organs, including the heart. The mechanisms of myocardial injury in SLE remain poorly understood. In this study, we engineered human cardiac tissues and cultured them with IgG from patients with SLE, with and without myocardial involvement. IgG from patients with elevated myocardial inflammation exhibited increased binding to apoptotic cells within cardiac tissues subjected to stress, whereas IgG from patients with systolic dysfunction exhibited enhanced binding to the surface of live cardiomyocytes. Functional assays and RNA sequencing revealed that, in the absence of immune cells, IgG from patients with systolic dysfunction altered cellular composition, respiration and calcium handling. Phage immunoprecipitation sequencing (PhIP-seq) confirmed distinctive IgG profiles between patient subgroups. Coupling IgG profiling with cell surfaceome analysis identified four potential pathogenic autoantibodies that may directly affect the myocardium. Overall, these insights may improve patient risk stratification and inform the development of new therapeutic strategies.

Indexed as

AutoantibodiesLupus Erythematosus, SystemicMyocytes, CardiacTissue EngineeringAdultApoptosisCase-Control StudiesCells, CulturedFemaleHumansImmunoglobulin GMaleMiddle AgedMyocarditisMyocardiumAutoantibodiesImmunoglobulin G

Identifiers

PMID39195859
PMCPMC11399098

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.