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

被引:14
作者
Gomez-Melero, Sara [1 ]
Caballero-Villarraso, Javier [1 ,2 ]
机构
[1] Maimonides Biomed Res Inst Cordoba, Avda Menendez Pidal S-N, Cordoba 14004, Spain
[2] Univ Cordoba, Fac Med & Nursing, Dept Biochem & Mol Biol, Avda Menendez Pidal S-N, Cordoba 14004, Spain
关键词
CCR6; antibody; therapy; GPCRs; inflammation; immune system; Th17; cells; CHEMOKINE RECEPTOR CCR6; CCR6-EXPRESSING TH17 CELLS; PROTEIN-COUPLED RECEPTORS; REGULATORY T-CELLS; RHEUMATOID-ARTHRITIS; CCL20; AXIS; EXPRESSION; ASSOCIATION; CCR6/CCL20;
D O I
10.3390/antib12020030
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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页数:16
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共 117 条
  • [1] Chemokine Receptor Ccr6 Deficiency Alters Hepatic Inflammatory Cell Recruitment and Promotes Liver Inflammation and Fibrosis
    Affo, Silvia
    Rodrigo-Torres, Daniel
    Blaya, Delia
    Morales-Ibanez, Oriol
    Coll, Mar
    Millan, Cristina
    Altamirano, Jose
    Arroyo, Vicente
    Caballeria, Joan
    Bataller, Ramon
    Gines, Pere
    Sancho-Bru, Pau
    [J]. PLOS ONE, 2015, 10 (12):
  • [2] Association study of CCR6 rs3093024 with Rheumatoid Arthritis in a Pakistani cohort
    Akhtar, Mehran
    Khan, Suleman
    Ali, Yasir
    Haider, Shohra
    Din, Jalal Ud
    Zia-ul Islam
    Jalil, Fazal
    [J]. SAUDI JOURNAL OF BIOLOGICAL SCIENCES, 2020, 27 (12) : 3354 - 3358
  • [3] [Anonymous], SINGLE CELL TYPE CCR
  • [4] [Anonymous], CCL20 TRANSCRIPTOMIC
  • [5] [Anonymous], AMGEN ACQUIRE CHEMOC
  • [6] [Anonymous], PARTNERED PROGRAMS S
  • [7] Identification of CCR6, the specific receptor for a novel lymphocyte-directed CC chemokine LARC
    Baba, M
    Imai, T
    Nishimura, M
    Kakizaki, M
    Takagi, S
    Hieshima, K
    Nomiyama, H
    Yoshie, O
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (23) : 14893 - 14898
  • [8] International Union of Pharmacology. LXXXIX. Update on the Extended Family of Chemokine Receptors and Introducing a New Nomenclature for Atypical Chemokine Receptors
    Bachelerie, Francoise
    Ben-Baruch, Adit
    Burkhardt, Amanda M.
    Combadiere, Christophe
    Farber, Joshua M.
    Graham, Gerard J.
    Horuk, Richard
    Sparre-Ulrich, Alexander Hovard
    Locati, Massimo
    Luster, Andrew D.
    Mantovani, Alberto
    Matsushima, Kouji
    Murphy, Philip M.
    Nibbs, Robert
    Nomiyama, Hisayuki
    Power, Christine A.
    Proudfoot, Amanda E. I.
    Rosenkilde, Mette M.
    Rot, Antal
    Sozzani, Silvano
    Thelen, Marcus
    Yoshie, Osamu
    Zlotnik, Albert
    [J]. PHARMACOLOGICAL REVIEWS, 2014, 66 (01) : 1 - 79
  • [9] Antibodies Targeting Chemokine Receptors CXCR4 and ACKR3
    Bobkov, Vladimir
    Arimont, Marta
    Zarca, Aurelien
    De Groof, Timo W. M.
    van der Woning, Bas
    de Haard, Hans
    Smit, Martine J.
    [J]. MOLECULAR PHARMACOLOGY, 2019, 96 (06) : 753 - 764
  • [10] The chemokine receptor CCR6 facilitates the onset of mammary neoplasia in the MMTV-PyMT mouse model via recruitment of tumor-promoting macrophages
    Boyle, Sarah T.
    Faulkner, Jessica W.
    McColl, Shaun R.
    Kochetkova, Marina
    [J]. MOLECULAR CANCER, 2015, 14