"Receptors, CCR8" 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.
CCR receptors with specificity for CHEMOKINE CCL1. They are expressed at high levels in T-LYMPHOCYTES; B-LYMPHOCYTES; and MACROPHAGES.
| Descriptor ID |
D054401
|
| MeSH Number(s) |
D12.776.543.750.695.160.150.800 D12.776.543.750.705.852.125.150.800
|
| Concept/Terms |
Receptors, CCR8- Receptors, CCR8
- CCR8 Receptors
- Antigens, CDw198
- CC Chemokine Receptor 8
- CDw198 Antigens
|
Below are MeSH descriptors whose meaning is more general than "Receptors, CCR8".
- 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 [D12.776.543.750.695]
- Receptors, Chemokine [D12.776.543.750.695.160]
- Receptors, CCR [D12.776.543.750.695.160.150]
- Receptors, CCR8 [D12.776.543.750.695.160.150.800]
- 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, CCR8 [D12.776.543.750.705.852.125.150.800]
Below are MeSH descriptors whose meaning is more specific than "Receptors, CCR8".
This graph shows the total number of publications written about "Receptors, CCR8" by people in this website by year, and whether "Receptors, CCR8" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2026 | 1 | 0 | 1 |
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Below are the most recent publications written about "Receptors, CCR8" by people in Profiles.
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Wang X, Kapoor VN, Chin DJ, Klakamp SL, Baruffaldi F, Mohan JF, Haines R, Dulak A, Panduro M, Ren Y, Masia R, Hill JA, LaVallee TM, Rajasekaran N. CHS-114: An Afucosylated Anti-CCR8 Monoclonal Antibody that Selectively Depletes Intratumoral Treg Cells and Induces Antitumor Immune Responses. Mol Cancer Ther. 2026 May 04; 25(5):685-700.