Receptors, CCR6

"Receptors, CCR6" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

CCR receptors with specificity for CHEMOKINE CCL20. They are expressed at high levels in T-LYMPHOCYTES; B-LYMPHOCYTES; and DENDRITIC CELLS.

Descriptor ID

D054399

MeSH Number(s)

D12.776.543.750.100.160.150.600

D12.776.543.750.705.852.125.150.600

D23.050.301.264.035.605.150.600

D23.101.100.110.605.150.600

Concept/Terms

Receptors, CCR6

Below are MeSH descriptors whose meaning is more general than "Receptors, CCR6".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Proteins [D12.776]
Membrane Proteins [D12.776.543]
Receptors, Cell Surface [D12.776.543.750]
Receptors, G-Protein-Coupled [D12.776.543.750.100]
Receptors, Chemokine [D12.776.543.750.100.160]
Receptors, CCR [D12.776.543.750.100.160.150]
Receptors, CCR6 [D12.776.543.750.100.160.150.600]
Receptors, Immunologic [D12.776.543.750.705]
Receptors, Cytokine [D12.776.543.750.705.852]
Receptors, Chemokine [D12.776.543.750.705.852.125]
Receptors, CCR [D12.776.543.750.705.852.125.150]
Receptors, CCR6 [D12.776.543.750.705.852.125.150.600]
Biological Factors [D23]
Antigens [D23.050]
Antigens, Surface [D23.050.301]
Antigens, Differentiation [D23.050.301.264]
Antigens, CD [D23.050.301.264.035]
Receptors, Chemokine [D23.050.301.264.035.605]
Receptors, CCR [D23.050.301.264.035.605.150]
Receptors, CCR6 [D23.050.301.264.035.605.150.600]
Biological Markers [D23.101]
Antigens, Differentiation [D23.101.100]
Antigens, CD [D23.101.100.110]
Receptors, Chemokine [D23.101.100.110.605]
Receptors, CCR [D23.101.100.110.605.150]
Receptors, CCR6 [D23.101.100.110.605.150.600]

Below are MeSH descriptors whose meaning is related to "Receptors, CCR6".

Below are MeSH descriptors whose meaning is more specific than "Receptors, CCR6".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Receptors, CCR6" by people in Harvard Catalyst Profiles by year, and whether "Receptors, CCR6" was a major or minor topic of these publication.

Bar chart showing 42 publications over 18 distinct years, with a maximum of 4 publications in 2002 and 2016 and 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2002	0	4	4
2003	0	2	2
2005	0	1	1
2006	0	3	3
2007	0	2	2
2008	0	1	1
2009	1	1	2
2011	1	1	2
2012	1	1	2
2013	1	0	1
2014	1	2	3
2015	1	2	3
2016	2	2	4
2017	1	1	2
2019	0	3	3
2020	0	1	1
2021	3	1	4
2022	1	1	2

Below are the most recent publications written about "Receptors, CCR6" by people in Profiles.

Peripheral blood CD4+CCR6+ compartment differentiates HIV-1 infected or seropositive elite controllers from long-term successfully treated individuals. Commun Biol. 2022 04 13; 5(1):357.

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CCR6 and CXCR6 Identify the Th17 Cells With Cytotoxicity in Experimental Autoimmune Encephalomyelitis. Front Immunol. 2022; 13:819224.

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Glycogen synthase kinase 3ß/CCR6-positive bone marrow cells correlate with disease activity in multicentric Castleman disease-TAFRO. Br J Haematol. 2022 03; 196(5):1194-1204.

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Endothelial CCR6 expression due to FLI1 deficiency contributes to vasculopathy associated with systemic sclerosis. Arthritis Res Ther. 2021 11 13; 23(1):283.

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Human prostate cancer bone metastases have an actionable immunosuppressive microenvironment. Cancer Cell. 2021 11 08; 39(11):1464-1478.e8.

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Antigen dominance hierarchies shape TCF1+ progenitor CD8 T cell phenotypes in tumors. Cell. 2021 09 16; 184(19):4996-5014.e26.

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Aberrant expression of USF2 in refractory rheumatoid arthritis and its regulation of proinflammatory cytokines in Th17 cells. Proc Natl Acad Sci U S A. 2020 12 01; 117(48):30639-30648.

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Reduction in Human Epidermal Langerhans Cells with Age Is Associated with Decline in CXCL14-Mediated Recruitment of CD14+ Monocytes. J Invest Dermatol. 2020 07; 140(7):1327-1334.

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Loss of Circulating CD8+ CD161high T Cells in Primary Progressive Multiple Sclerosis. Front Immunol. 2019; 10:1922.

View in: PubMed
Pathogenic function of bystander-activated memory-like CD4+ T cells in autoimmune encephalomyelitis. Nat Commun. 2019 02 12; 10(1):709.

View in: PubMed

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