"T-Lymphocyte Subsets" 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.
A classification of T-lymphocytes, especially into helper/inducer, suppressor/effector, and cytotoxic subsets, based on structurally or functionally different populations of cells.
| Descriptor ID |
D016176
|
| MeSH Number(s) |
A11.118.637.555.567.550.500 A11.118.637.555.567.569.500 A15.145.229.637.555.567.550.500 A15.145.229.637.555.567.569.500 A15.382.490.555.567.550.500 A15.382.490.555.567.569.500
|
| Concept/Terms |
T-Lymphocyte Subsets- T-Lymphocyte Subsets
- Subset, T-Lymphocyte
- Subsets, T-Lymphocyte
- T Lymphocyte Subsets
- T-Lymphocyte Subset
- T-Cell Subsets
- Subset, T-Cell
- Subsets, T-Cell
- T Cell Subsets
- T-Cell Subset
|
Below are MeSH descriptors whose meaning is more general than "T-Lymphocyte Subsets".
Below are MeSH descriptors whose meaning is more specific than "T-Lymphocyte Subsets".
This graph shows the total number of publications written about "T-Lymphocyte Subsets" by people in this website by year, and whether "T-Lymphocyte Subsets" 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 |
|---|
| 1994 | 0 | 1 | 1 |
| 1995 | 1 | 0 | 1 |
| 1996 | 1 | 0 | 1 |
| 1997 | 0 | 1 | 1 |
| 2000 | 1 | 1 | 2 |
| 2001 | 1 | 1 | 2 |
| 2004 | 2 | 3 | 5 |
| 2005 | 0 | 2 | 2 |
| 2006 | 3 | 0 | 3 |
| 2008 | 2 | 0 | 2 |
| 2009 | 2 | 1 | 3 |
| 2010 | 1 | 1 | 2 |
| 2011 | 3 | 1 | 4 |
| 2012 | 5 | 1 | 6 |
| 2013 | 1 | 3 | 4 |
| 2014 | 1 | 2 | 3 |
| 2015 | 2 | 0 | 2 |
| 2016 | 3 | 1 | 4 |
| 2017 | 30 | 30 | 60 |
| 2018 | 33 | 36 | 69 |
| 2019 | 10 | 7 | 17 |
| 2020 | 3 | 11 | 14 |
| 2021 | 6 | 11 | 17 |
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Below are the most recent publications written about "T-Lymphocyte Subsets" by people in Profiles.
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Recurrent assessment of lymphocyte subsets in 32 patients with multisystem inflammatory syndrome in children (MIS-C). Pediatr Allergy Immunol. 2021 11; 32(8):1857-1865.
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Integrated longitudinal immunophenotypic, transcriptional and repertoire analyses delineate immune responses in COVID-19 patients. Sci Immunol. 2021 08 10; 6(62).
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The Immunological Factors Predisposing to Severe Covid-19 Are Already Present in Healthy Elderly and Men. Front Immunol. 2021; 12:720090.
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COVID-19 vaccine mRNA-1273 elicits a protective immune profile in mice that is not associated with vaccine-enhanced disease upon SARS-CoV-2 challenge. Immunity. 2021 08 10; 54(8):1869-1882.e6.
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Differential T-Cell Reactivity to Endemic Coronaviruses and SARS-CoV-2 in Community and Health Care Workers. J Infect Dis. 2021 07 02; 224(1):70-80.
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Longitudinal Analysis of Human Memory T-Cell Response According to the Severity of Illness up to 8 Months After Severe Acute Respiratory Syndrome Coronavirus 2 Infection. J Infect Dis. 2021 07 02; 224(1):39-48.
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IFN-?+ cell response and IFN-? release concordance after in vitro SARS-CoV-2 stimulation. Eur J Clin Invest. 2021 Dec; 51(12):e13636.
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Baseline T-lymphocyte subset absolute counts can predict both outcome and severity in SARS-CoV-2 infected patients: a single center study. Sci Rep. 2021 06 17; 11(1):12762.
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Deep spatial profiling of human COVID-19 brains reveals neuroinflammation with distinct microanatomical microglia-T-cell interactions. Immunity. 2021 07 13; 54(7):1594-1610.e11.
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Different T cell related immunological profiles in COVID-19 patients compared to healthy controls. Int Immunopharmacol. 2021 Aug; 97:107828.