Receptors, CXCR3

"Receptors, CXCR3" 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

CXCR receptors that are expressed on the surface of a number of cell types, including T-LYMPHOCYTES; NK CELLS; DENDRITIC CELLS; and a subset of B-LYMPHOCYTES. The receptors are activated by CHEMOKINE CXCL9; CHEMOKINE CXCL10; and CHEMOKINE CXCL11.

Descriptor ID

D054367

MeSH Number(s)

D12.776.543.750.100.160.500.300

D12.776.543.750.705.852.125.500.300

D23.050.301.264.035.605.500.300

D23.101.100.110.605.500.300

Concept/Terms

Receptors, CXCR3

Below are MeSH descriptors whose meaning is more general than "Receptors, CXCR3".

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, CXCR [D12.776.543.750.100.160.500]
Receptors, CXCR3 [D12.776.543.750.100.160.500.300]
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, CXCR3 [D12.776.543.750.705.852.125.500.300]
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, CXCR [D23.050.301.264.035.605.500]
Receptors, CXCR3 [D23.050.301.264.035.605.500.300]
Biological Markers [D23.101]
Antigens, Differentiation [D23.101.100]
Antigens, CD [D23.101.100.110]
Receptors, Chemokine [D23.101.100.110.605]
Receptors, CXCR [D23.101.100.110.605.500]
Receptors, CXCR3 [D23.101.100.110.605.500.300]

Below are MeSH descriptors whose meaning is related to "Receptors, CXCR3".

Below are MeSH descriptors whose meaning is more specific than "Receptors, CXCR3".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Receptors, CXCR3" by people in Harvard Catalyst Profiles by year, and whether "Receptors, CXCR3" was a major or minor topic of these publication.

Bar chart showing 142 publications over 26 distinct years, with a maximum of 12 publications in 2008

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

Year	Major Topic	Minor Topic	Total
1998	0	4	4
1999	0	3	3
2000	0	6	6
2001	0	8	8
2002	0	6	6
2003	0	7	7
2004	0	6	6
2005	0	4	4
2006	0	11	11
2007	1	5	6
2008	10	2	12
2009	2	2	4
2010	4	2	6
2011	6	1	7
2012	4	6	10
2013	2	3	5
2014	2	3	5
2015	2	0	2
2016	2	2	4
2017	1	1	2
2018	1	3	4
2019	2	3	5
2020	1	4	5
2021	3	4	7
2022	1	0	1
2023	0	2	2

Below are the most recent publications written about "Receptors, CXCR3" by people in Profiles.

Inhibition of cellular activation induced by platelet factor 4 via the CXCR3 pathway ameliorates Japanese encephalitis and dengue viral infections. J Thromb Haemost. 2024 Mar; 22(3):818-833.

View in: PubMed
PD-1highCXCR5-CD4+ peripheral helper T cells promote CXCR3+ plasmablasts in human acute viral infection. Cell Rep. 2023 01 31; 42(1):111895.

View in: PubMed
Location bias contributes to functionally selective responses of biased CXCR3 agonists. Nat Commun. 2022 10 04; 13(1):5846.

View in: PubMed
Transcriptome and TCR Repertoire Measurements of CXCR3+ T Follicular Helper Cells Within HIV-Infected Human Lymph Nodes. Front Immunol. 2022; 13:859070.

View in: PubMed
CXCL10 chemokine regulates heterogeneity of the CD8+ T cell response and viral set point during chronic infection. Immunity. 2022 01 11; 55(1):82-97.e8.

View in: PubMed
Pathological role of activated mTOR in CXCR3+ memory B cells of rheumatoid arthritis. Rheumatology (Oxford). 2021 11 03; 60(11):5452-5462.

View in: PubMed
Smoking and Human Immunodeficiency Virus 1 Infection Promote Retention of CD8+ T Cells in the Airway Mucosa. Am J Respir Cell Mol Biol. 2021 11; 65(5):513-520.

View in: PubMed
Natural killer cell immunosuppressive function requires CXCR3-dependent redistribution within lymphoid tissues. J Clin Invest. 2021 09 15; 131(18).

View in: PubMed
CXCL10+ peripheral activation niches couple preferred sites of Th1 entry with optimal APC encounter. Cell Rep. 2021 08 10; 36(6):109523.

View in: PubMed
Complete response in a patient with advanced melanoma following anti-PD-1 therapy is associated with a high frequency of melanoma-infiltrating CXCR3+ resident memory CD8+ T cells and multiple chemokine pathways. Br J Dermatol. 2021 09; 185(3):663-666.

View in: PubMed

Related Networks

People

Explore

Similar Concepts

Top Journals

J Immunol
Immunity
Eur J Immunol
Blood
Cancer Immunol Res
Transplantation
J Virol
J Biol Chem
J Invest Dermatol
J Am Soc Nephrol