Therapeutic Potential of Targeting the Th17/Treg Axis in Autoimmune Disorders.
Open accessAbstract
A disruption of the crucial balance between regulatory T-cells (Tregs) and Th17-cells was recently implicated in various autoimmune disorders. Tregs are responsible for the maintenance of self-tolerance, thus inhibiting autoimmunity, whereas pro-inflammatory Th17-cells contribute to the induction and propagation of inflammation. Distortion of the Th17/Treg balance favoring the pro-inflammatory Th17 side is hence suspected to contribute to exacerbation of autoimmune disorders. This review aims to summarize recent data and advances in targeted therapeutic modification of the Th17/Treg-balance, as well as information on the efficacy of candidate therapeutics with respect to the treatment of autoimmune diseases.
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Th17 and Treg are connected in differentiation and function and are frequently in a state of dynamic equilibrium; if their proportion is no longer balanced, it results in aberrant immunological responses such as inflammatory, tumor and autoimmune reactions.
“Furthermore, Th17 and Treg are connected in differentiation and function, and they are frequently in a state of dynamic equilibrium. If the proportion of them is no longer balanced, it will result in aberrant immunological responses such as inflammatory, tumor and autoimmune reactions [54].”
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The role of HIF in immunity and inflammation
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- Authors
- Fasching, P., Stradner, M., Graninger, W., Dejaco, C., & Fessler, J.
- Affiliations
- Medical University of Graz (AT)
- Corresponding author
- Dejaco, Christian
- Venue
- Molecules
- Publisher
- MDPI AG
- Published
- 2017-01-14
- Volume
- 22
- Issue
- 1
- Pages
- 134
- ISSN
- 1420-3049 (ISSN-L)
- PMC
- PMC6155880
- OpenAlex
- W2576351276
- Cited by
- 254
- References
- 202
- Citations by year
- 2026: 13 · 2025: 19 · 2024: 32 · 2023: 29 · 2022: 31 · 2021: 44 · 2020: 37 · 2019: 25 · 2018: 16 · 2017: 6 · 2015: 1
- FWCI
- 2.36
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecules (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Rheumatology › Rheumatoid Arthritis Research and Therapies
- Keywords
- Th17/Treg balance, regulatory T cells, Th17 cells, autoimmune disease, self-tolerance, inflammation, therapeutic targeting
- MeSH terms
- Ustekinumab, Animals, Antibodies, Monoclonal, Autoimmune Diseases, Gene Expression Regulation, Humans, Immunologic Factors, Inflammation, Piperidines, Pyrimidines, Pyrroles, Signal Transduction, Interleukin-17, T-Lymphocytes, Regulatory, Forkhead Transcription Factors, Nuclear Receptor Subfamily 1, Group F, Member 3, Th17 Cells, Antibodies, Monoclonal, Humanized
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.
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