"Epitopes, T-Lymphocyte" 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.
Antigenic determinants recognized and bound by the T-cell receptor. Epitopes recognized by the T-cell receptor are often located in the inner, unexposed side of the antigen, and become accessible to the T-cell receptors after proteolytic processing of the antigen.
Descriptor ID |
D018984
|
MeSH Number(s) |
D23.050.550.402
|
Concept/Terms |
Epitopes, T-Lymphocyte- Epitopes, T-Lymphocyte
- Epitopes, T Lymphocyte
- T-Cell Epitopes
- Epitopes, T-Cell
- T Cell Epitopes
- T-Lymphocyte Epitopes
- T Lymphocyte Epitopes
- T-Cell Epitope
- Epitope, T-Cell
- T Cell Epitope
- T-Lymphocyte Epitope
- Epitope, T-Lymphocyte
- T Lymphocyte Epitope
|
Below are MeSH descriptors whose meaning is more general than "Epitopes, T-Lymphocyte".
Below are MeSH descriptors whose meaning is more specific than "Epitopes, T-Lymphocyte".
This graph shows the total number of publications written about "Epitopes, T-Lymphocyte" by people in this website by year, and whether "Epitopes, T-Lymphocyte" 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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1995 | 1 | 1 | 2 |
1996 | 1 | 0 | 1 |
1998 | 0 | 1 | 1 |
1999 | 1 | 0 | 1 |
2000 | 0 | 1 | 1 |
2001 | 1 | 1 | 2 |
2002 | 0 | 1 | 1 |
2003 | 1 | 3 | 4 |
2004 | 1 | 3 | 4 |
2005 | 3 | 0 | 3 |
2006 | 3 | 2 | 5 |
2007 | 2 | 2 | 4 |
2008 | 1 | 1 | 2 |
2009 | 1 | 0 | 1 |
2010 | 4 | 1 | 5 |
2011 | 2 | 1 | 3 |
2012 | 1 | 0 | 1 |
2013 | 4 | 1 | 5 |
2014 | 4 | 1 | 5 |
2015 | 0 | 1 | 1 |
2016 | 2 | 2 | 4 |
2017 | 14 | 22 | 36 |
2018 | 18 | 18 | 36 |
2019 | 11 | 11 | 22 |
2020 | 12 | 16 | 28 |
2021 | 13 | 23 | 36 |
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Below are the most recent publications written about "Epitopes, T-Lymphocyte" by people in Profiles.
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T-CoV: a comprehensive portal of HLA-peptide interactions affected by SARS-CoV-2 mutations. Nucleic Acids Res. 2022 01 07; 50(D1):D883-D887.
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Tracking the pipeline: immunoinformatics and the COVID-19 vaccine design. Brief Bioinform. 2021 11 05; 22(6).
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CD8+PD-L1+CXCR3+ polyfunctional T cell abundances are associated with survival in critical SARS-CoV-2-infected patients. JCI Insight. 2021 09 22; 6(18).
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Large-Scale Identification of T-Cell Epitopes Derived From Severe Acute Respiratory Syndrome Coronavirus 2 for the Development of Peptide Vaccines Against Coronavirus Disease 2019. J Infect Dis. 2021 09 17; 224(6):956-966.
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SARS-CoV-2-reactive T-cell receptors isolated from convalescent COVID-19 patients confer potent T-cell effector function. Eur J Immunol. 2021 11; 51(11):2651-2664.
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A novel and efficient approach to high-throughput production of HLA-E/peptide monomer for T-cell epitope screening. Sci Rep. 2021 08 26; 11(1):17234.
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Peptide Platform as a Powerful Tool in the Fight against COVID-19. Viruses. 2021 08 23; 13(8).
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Optimization of antigen-specific CD8+ T cell activation conditions for infectious diseases including COVID-19. STAR Protoc. 2021 09 17; 2(3):100789.
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Structural basis of biased T cell receptor recognition of an immunodominant HLA-A2 epitope of the SARS-CoV-2 spike protein. J Biol Chem. 2021 09; 297(3):101065.
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GIANA allows computationally-efficient TCR clustering and multi-disease repertoire classification by isometric transformation. Nat Commun. 2021 08 04; 12(1):4699.