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Cardiac myosin-Th17 responses promote heart failure in human myocarditis
Open accessAbstract
In human myocarditis and its sequela dilated cardiomyopathy (DCM), the mechanisms and immune phenotype governing disease and subsequent heart failure are not known. Here, we identified a Th17 cell immunophenotype of human myocarditis/DCM with elevated CD4 + IL17 + T cells and Th17-promoting cytokines IL-6, TGF-β, and IL-23 as well as GM-CSF–secreting CD4 + T cells. The Th17 phenotype was linked with the effects of cardiac myosin on CD14 + monocytes, TLR2, and heart failure. Persistent heart failure was associated with high percentages of IL-17–producing T cells and IL-17–promoting cytokines, and the myocarditis/DCM phenotype included significantly low percentages of FOXP3 + Tregs, which may contribute to disease severity. We demonstrate a potentially novel mechanism in human myocarditis/DCM in which TLR2 peptide ligands from human cardiac myosin stimulated exaggerated Th17-related cytokines including TGF-β, IL-6, and IL-23 from myocarditic CD14 + monocytes in vitro, and an anti-TLR2 antibody abrogated the cytokine response. Our translational study explains how an immune phenotype may be initiated by cardiac myosin TLR ligand stimulation of monocytes to generate Th17-promoting cytokines and development of pathogenic Th17 cells in human myocarditis and heart failure, and provides a rationale for targeting IL-17A as a therapeutic option.
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“IL-1 β also increases serum and cardiac IL-6 levels that are needed to drive Th17 responses, which also promote fibrosis and progression to DCM and heart failure in patients with myocarditis and in animal models. 36,165,172-174”
From COVID-19, Myocarditis and Pericarditis (2023) · cites this paper as [36]
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“Following infection, viruses and heart antigens resulting from cardiac damage trigger innate immune responses by engaging TLRs, potentially leading to the activation of antiviral adaptive immunity and B cells and T cells targeting cardiac autoantigens”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [64]
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“Recent studies implemented pathogenic T cells as potential diagnostic or therapeutic targets for autoimmune myocarditis including ICI myocarditis, demonstrating promising outcomes at both clinical and preclinical levels. 51,64,238,254,260,311,312”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [64]
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“Subsequent investigations revealed the presence of these autoreactive T cells in the peripheral blood mononuclear cells of patients with myocarditis”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [64]
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“in patients with myocarditis, the number of Th17 cells was increased in the PBMC and myocardial tissue, and Th17-type cytokine levels were associated with heart failure and nonrecovery conditions”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [64]
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“a decreased number of circulating regulatory T cells were found in patients with myocarditis, and adoptive transfer of CD4 + T cells with regulatory T-cell depletion induced fatal myocarditis in mice”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [64]
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“In patients with myocarditis or idiopathic DCM who tested negative for specific viruses, the presence of circulating Th17 cells specific for cardiac myosin in the blood has been reported, along with a reduced number of regulatory T cells. 64,238,311”
From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [64]
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Research works printed but not linked: 2
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- 10.1161/CIRCRESAHA.109.213157 · DOI · Paper page
Cited by
Sorted by citations
Guzik, T. J., MOHIDDIN, S. A., Dimarco, A. D., Patel, V., Savvatis, K., Marelli‐Berg, F. M., Madhur, M. S., Tomaszewski, M., Maffia, P., D’Acquisto, F., et al. (2020) · Cardiovascular Research · doi:10.1093/cvr/cvaa106 · Cited by 1,484
Myocarditis and inflammatory cardiomyopathy: current evidence and future directions
Tschöpe, C., Ammirati, E., Bozkurt, B., Caforio, A. L. P., Cooper, L. T., Felix, S. B., Hare, J. M., Heidecker, B., Heymans, S., Hübner, N., et al. (2021) · Nature Reviews Cardiology · doi:10.1038/s41569-020-00435-x · Cited by 1,217
Self-citationSchultheiss, H.-P., Fairweather, D., Caforio, A. L. P., Escher, F., Hershberger, R. E., Lipshultz, S. E., Liu, P. P., Matsumori, A., Mazzanti, A., McMurray, J., et al. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0084-1 · Cited by 720
Self-citationMultifunctional nanoparticle-mediated combining therapy for human diseases
Li, X., Peng, X., Zoulikha, M., Boafo, G. F., Magar, K. T., Ju, Y., & He, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01668-1 · Cited by 573
Pathogenesis, epidemiology and control of Group A Streptococcus infection
Brouwer, S., Rivera-Hernández, T., Curren, B. F., Harbison-Price, N., Oliveira, D. M. P. D., Jespersen, M. G., Davies, M. R., & Walker, M. J. (2023) · Nature Reviews Microbiology · doi:10.1038/s41579-023-00865-7 · Cited by 381
Metadata
- Authors
- Myers, J. M., Cooper, L. T., Kem, D. C., Stavrakis, S., Kosanke, S. D., Shevach, E. M., Fairweather, D., Stoner, J. A., Cox, C. J., & Cunningham, M. W.
- Affiliations
- University of Oklahoma Health Sciences Center (US)
- Mayo Clinic in Florida (US)
- Department of Medicine/Endocrinology,
- Medicine/Cardiology, and
- National Institutes of Health (US)
- Johns Hopkins University (US)
- Corresponding author
- Cox, Carol J.
- Cunningham, Madeleine W.
- ORCID
- Venue
- JCI Insight
- Published
- 2016-06-16
- Volume
- 1
- Issue
- 9
- ISSN
- 2379-3708 (ISSN-L)
- PMC
- PMC4924810
- OpenAlex
- W2434470226
- Cited by
- 230
- References
- 88
- Citations by year
- 2026: 22 · 2025: 26 · 2024: 33 · 2023: 34 · 2022: 24 · 2021: 29 · 2020: 24 · 2019: 16 · 2018: 12 · 2017: 9 · 2016: 1
- FWCI
- 10.43
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- JCI Insight (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Heart Association (U54GM104938)
- University of Oklahoma
- University of Oklahoma Health Sciences Center
- National Heart, Lung, and Blood Institute (R01HL135165, R56HL056267, R01HL111938, R01HL056267, R37HL035280)
- National Institute of General Medical Sciences (U54GM104938)
- National Institute of Allergy and Infectious Diseases (T32AI007633)
- National Institute of Environmental Health Sciences (R21ES024414)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Viral Infections and Immunology Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
- Health Sciences › Medicine › Ophthalmology › Ocular Diseases and Behçet’s Syndrome
- Keywords
- myocarditis, dilated cardiomyopathy, heart failure, Th17 cells, cardiac myosin, TLR2, CD14+ monocytes, IL-17, interleukin-6, TGF-beta, IL-23, GM-CSF, regulatory T cells, Foxp3, autoimmunity
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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