Artikel ; Online: Select sequencing of clonally expanded CD8
Proceedings of the National Academy of Sciences of the United States of America
2019 Band 116, Heft 18, Seite(n) 8995–9001
Abstract: To permit the recognition of antigens, T cells generate a vast diversity of T cell receptor (TCR) sequences. Upon binding of the TCR to an antigen-MHC complex, T cells clonally expand to establish an immune response. To study antigen-specific T cell ... ...
Abstract | To permit the recognition of antigens, T cells generate a vast diversity of T cell receptor (TCR) sequences. Upon binding of the TCR to an antigen-MHC complex, T cells clonally expand to establish an immune response. To study antigen-specific T cell clonality, we have developed a method that allows selection of rare cells, based on RNA expression, before in-depth scRNA-seq (named SELECT-seq). We applied SELECT-seq to collect both TCR sequences and then transcriptomes from single cells of peripheral blood lymphocytes activated by a |
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Mesh-Begriff(e) | Antigens/metabolism ; Base Sequence/genetics ; CD8-Positive T-Lymphocytes/immunology ; Cells, Cultured ; Clonal Selection, Antigen-Mediated/physiology ; Cytokines/metabolism ; Humans ; Lymphocyte Activation/genetics ; Lymphocyte Activation/physiology ; Mucosal-Associated Invariant T Cells/immunology ; Natural Killer T-Cells/immunology ; Receptors, Antigen, T-Cell/genetics ; Receptors, Antigen, T-Cell/immunology ; Receptors, Antigen, T-Cell/isolation & purification ; Sequence Analysis ; Sequence Analysis, RNA/methods |
Chemische Substanzen | Antigens ; Cytokines ; Receptors, Antigen, T-Cell |
Sprache | Englisch |
Erscheinungsdatum | 2019-04-16 |
Erscheinungsland | United States |
Dokumenttyp | Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't |
ZDB-ID | 209104-5 |
ISSN | 1091-6490 ; 0027-8424 |
ISSN (online) | 1091-6490 |
ISSN | 0027-8424 |
DOI | 10.1073/pnas.1902649116 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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