"Receptors, CXCR5" 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.
CXCR receptors isolated initially from BURKITT LYMPHOMA cells. CXCR5 receptors are expressed on mature, recirculating B-LYMPHOCYTES and are specific for CHEMOKINE CXCL13.
Descriptor ID |
D054380
|
MeSH Number(s) |
D12.776.543.750.695.160.500.500 D12.776.543.750.705.852.125.500.500
|
Concept/Terms |
Receptors, CXCR5- Receptors, CXCR5
- CXC Chemokine Receptor 5
- CD185 Antigens
- Antigens, CD185
- CXCR5 Receptors
- Burkitt Lymphoma Receptor 1
|
Below are MeSH descriptors whose meaning is more general than "Receptors, CXCR5".
- 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, CXCR [D12.776.543.750.695.160.500]
- Receptors, CXCR5 [D12.776.543.750.695.160.500.500]
- 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, CXCR [D12.776.543.750.705.852.125.500]
- Receptors, CXCR5 [D12.776.543.750.705.852.125.500.500]
Below are MeSH descriptors whose meaning is more specific than "Receptors, CXCR5".
This graph shows the total number of publications written about "Receptors, CXCR5" by people in this website by year, and whether "Receptors, CXCR5" 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 |
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2014 | 0 | 1 | 1 |
2015 | 0 | 1 | 1 |
2017 | 0 | 6 | 6 |
2018 | 2 | 3 | 5 |
2019 | 1 | 1 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Receptors, CXCR5" by people in Profiles.
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Naturally activated adaptive immunity in COVID-19 patients. J Cell Mol Med. 2020 11; 24(21):12457-12463.
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Fate of CD8+: Cytotoxic or Suppressor T Cells in Antibody-mediated Rejection in Solid Organ Transplantation? Transplantation. 2019 09; 103(9):1756-1757.
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Circulating CXCR3-CCR6-CXCR5+CD4+ T cells are associated with acute allograft rejection in liver transplantation. Immunol Lett. 2019 09; 213:55-61.
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The exhausted CD4+CXCR5+ T cells involve the pathogenesis of human tuberculosis disease. Int J Infect Dis. 2018 Sep; 74:1-9.
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Differentiation and Function of Follicular CD8 T Cells During Human Immunodeficiency Virus Infection. Front Immunol. 2018; 9:1095.
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Spatial distribution and function of T follicular regulatory cells in human lymph nodes. J Exp Med. 2018 06 04; 215(6):1531-1542.
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Circulating follicular helper T cells (CD4+CXCR5+ICOS+) decrease in patients with rheumatoid arthritis treated with abatacept. Clin Exp Rheumatol. 2018 Jul-Aug; 36(4):685.
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A pilot study on the characteristics of circulating T follicular helper cells in liver transplant recipients. Transpl Immunol. 2018 04; 47:32-36.
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IL-21 Is Increased in Nasal Polyposis and after Stimulation with Staphylococcus aureus Enterotoxin B. Int Arch Allergy Immunol. 2017; 174(3-4):161-169.
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Generation of T follicular helper cells in vitro: requirement for B-cell receptor cross-linking and cognate B- and T-cell interaction. Immunology. 2018 02; 153(2):214-224.