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| Content Provider | PubMed Central |
|---|---|
| Author | Theaker, Sarah M. Rius, Cristina Alexander, Greenshields-watson Lloyd, Angharad Andrew, Trimby Fuller, Anna Miles, John J. Cole, David K. Mark, Peakman Sewell, Andrew K. Dolton, Garry |
| Copyright Year | 2016 |
| Abstract | Isolation of peptide-specific T-cell clones is highly desirable for determining the role of T-cells in human disease, as well as for the development of therapies and diagnostics. However, generation of monoclonal T-cells with the required specificity is challenging and time-consuming. Here we describe a library-based strategy for the simple parallel detection and isolation of multiple peptide-specific human T-cell clones from CD8+ or CD4+ polyclonal T-cell populations. T-cells were first amplified by CD3/CD28 microbeads in a 96U-well library format, prior to screening for desired peptide recognition. T-cells from peptide-reactive wells were then subjected to cytokine-mediated enrichment followed by single-cell cloning, with the entire process from sample to validated clone taking as little as 6 weeks. Overall, T-cell libraries represent an efficient and relatively rapid tool for the generation of peptide-specific T-cell clones, with applications shown here in infectious disease (Epstein–Barr virus, influenza A, and Ebola virus), autoimmunity (type 1 diabetes) and cancer. |
| Related Links | http://dx.doi.org/10.1016/j.jim.2016.01.014 |
| Ending Page | 50 |
| Page Count | 8 |
| Starting Page | 43 |
| File Format | |
| ISSN | 00221759 |
| e-ISSN | 18727905 |
| Journal | Journal of Immunological Methods |
| Volume Number | 430 |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2016-03-01 |
| Access Restriction | Open |
| Rights Holder | Elsevier |
| Subject Keyword | Immunology Immunology and Allergy Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Immunology and Allergy Immunology |
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