Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Fasching, P; Stradner, M; Graninger, W; Dejaco, C; Fessler, J.
Therapeutic Potential of Targeting the Th17/Treg Axis in Autoimmune Disorders.
Molecules. 2017; 22(1): Doi: 10.3390/molecules22010134 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Führende Autor*innen der Med Uni Graz
Dejaco Christian
Fasching Patrizia
Co-Autor*innen der Med Uni Graz
Fessler Johannes
Graninger Winfried
Stradner Martin Helmut
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
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.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Antibodies, Monoclonal - therapeutic use
Autoimmune Diseases - drug therapy
Autoimmune Diseases - genetics
Autoimmune Diseases - immunology
Autoimmune Diseases - pathology
Forkhead Transcription Factors - antagonists & inhibitors
Forkhead Transcription Factors - genetics
Forkhead Transcription Factors - immunology
Gene Expression Regulation -
Humans -
Immunologic Factors - therapeutic use
Inflammation -
Interleukin-17 - antagonists & inhibitors
Interleukin-17 - genetics
Interleukin-17 - immunology
Nuclear Receptor Subfamily 1, Group F, Member 3 - antagonists & inhibitors
Nuclear Receptor Subfamily 1, Group F, Member 3 - genetics
Nuclear Receptor Subfamily 1, Group F, Member 3 - immunology
Piperidines - therapeutic use
Pyrimidines - therapeutic use
Pyrroles - therapeutic use
Signal Transduction -
T-Lymphocytes, Regulatory - drug effects
T-Lymphocytes, Regulatory - immunology
T-Lymphocytes, Regulatory - pathology
Th17 Cells - drug effects
Th17 Cells - immunology
Th17 Cells - pathology
Ustekinumab - therapeutic use

Find related publications in this database (Keywords)
Th17-cells
regulatory T-cells
autoimmunity
RORt
Foxp3
© Med Uni Graz Impressum