 Epitopes, T-Lymphocyte
"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
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| MeSH Number(s) |
D23.050.550.402
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| 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
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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 |
|---|
| 2007 | 1 | 0 | 1 |
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Below are the most recent publications written about "Epitopes, T-Lymphocyte" by people in Profiles.
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Turnquist HR, Raimondi G, Zahorchak AF, Fischer RT, Wang Z, Thomson AW. Rapamycin-conditioned dendritic cells are poor stimulators of allogeneic CD4+ T cells, but enrich for antigen-specific Foxp3+ T regulatory cells and promote organ transplant tolerance. J Immunol. 2007 Jun 01; 178(11):7018-31.
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Winer S, Gunaratnam L, Astsatourov I, Cheung RK, Kubiak V, Karges W, Hammond-McKibben D, Gaedigk R, Graziano D, Trucco M, Becker DJ, Dosch HM. Peptide dose, MHC affinity, and target self-antigen expression are critical for effective immunotherapy of nonobese diabetic mouse prediabetes. J Immunol. 2000 Oct 01; 165(7):4086-94.
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