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CCR6 as a Potential Target for Therapeutic Antibodies for the Treatment of Inflammatory Diseases.

作者信息

Gómez-Melero Sara, Caballero-Villarraso Javier

机构信息

Maimonides Biomedical Research Institute of Cordoba, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain.

Department of Biochemistry and Molecular Biology, Faculty of Medicine and Nursing, University of Córdoba, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain.

出版信息

Antibodies (Basel). 2023 Apr 20;12(2):30. doi: 10.3390/antib12020030.


DOI:10.3390/antib12020030
PMID:37092451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10123731/
Abstract

The CC chemokine receptor 6 (CCR6) is a G protein-coupled receptor (GPCR) involved in a wide range of biological processes. When CCR6 binds to its sole ligand CCL20, a signaling network is produced. This pathway is implicated in mechanisms related to many diseases, such as cancer, psoriasis, multiple sclerosis, HIV infection or rheumatoid arthritis. The CCR6/CCL20 axis plays a fundamental role in immune homeostasis and activation. Th17 cells express the CCR6 receptor and inflammatory cytokines, including IL-17, IL-21 and IL-22, which are involved in the spread of inflammatory response. The CCL20/CCR6 mechanism plays a crucial role in the recruitment of these pro-inflammatory cells to local tissues. To date, there are no drugs against CCR6 approved, and the development of small molecules against CCR6 is complicated due to the difficulty in screenings. This review highlights the potential as a therapeutic target of the CCR6 receptor in numerous diseases and the importance of the development of antibodies against CCR6 that could be a promising alternative to small molecules in the treatment of CCR6/CCL20 axis-related pathologies.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e0/10123731/5dea7309c693/antibodies-12-00030-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e0/10123731/d66c7f30b064/antibodies-12-00030-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e0/10123731/5dea7309c693/antibodies-12-00030-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e0/10123731/d66c7f30b064/antibodies-12-00030-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e0/10123731/5dea7309c693/antibodies-12-00030-g002.jpg

相似文献

[1]
CCR6 as a Potential Target for Therapeutic Antibodies for the Treatment of Inflammatory Diseases.

Antibodies (Basel). 2023-4-20

[2]
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[3]
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[4]
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[5]
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[6]
An immune paradox: how can the same chemokine axis regulate both immune tolerance and activation?: CCR6/CCL20: a chemokine axis balancing immunological tolerance and inflammation in autoimmune disease.

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[7]
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[8]
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[9]
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[10]
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[9]
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[10]
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本文引用的文献

[1]
Discovery of small-molecules targeting the CCL20/CCR6 axis as first-in-class inhibitors for inflammatory bowel diseases.

Eur J Med Chem. 2022-12-5

[2]
CCL20/CCR6 axis mediates macrophages to promote proliferation and migration of ESCs by blocking autophagic flux in endometriosis.

Stem Cell Res Ther. 2022-7-15

[3]
Development of a High-Throughput Calcium Mobilization Assay for CCR6 Receptor Coupled to Hydrolase Activity Readout.

Biomedicines. 2022-2-10

[4]
CCR6 activation links innate immune responses to mucosa-associated lymphoid tissue lymphoma development.

Haematologica. 2022-6-1

[5]
Single-cell sequencing unveils distinct immune microenvironments with CCR6-CCL20 crosstalk in human chronic pancreatitis.

Gut. 2022-9

[6]
Reduced CCR6IL-17ATreg Cells in Blood and CCR6-Dependent Accumulation of IL-17ATreg Cells in Lungs of Patients With Allergic Asthma.

Front Immunol. 2021-8-23

[7]
Role of Th22 Cells in the Pathogenesis of Autoimmune Diseases.

Front Immunol. 2021

[8]
Amino terminal recognition by a CCR6 chemokine receptor antibody blocks CCL20 signaling and IL-17 expression via β-arrestin.

BMC Biotechnol. 2021-7-5

[9]
Targeting the CCR6/CCL20 Axis in Entheseal and Cutaneous Inflammation.

Arthritis Rheumatol. 2021-12

[10]
CCR6-CCL20 axis as a therapeutic target for autoimmune diseases.

Autoimmun Rev. 2021-7

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