| pubmed-article:8810254 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8810254 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
| pubmed-article:8810254 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:8810254 | pubmed:issue | 5284 | lld:pubmed |
| pubmed-article:8810254 | pubmed:dateCreated | 1996-10-24 | lld:pubmed |
| pubmed-article:8810254 | pubmed:abstractText | Identification and characterization of antigen-specific T lymphocytes during the course of an immune response is tedious and indirect. To address this problem, the peptide-major histocompatability complex (MHC) ligand for a given population of T cells was multimerized to make soluble peptide-MHC tetramers. Tetramers of human lymphocyte antigen A2 that were complexed with two different human immunodeficiency virus (HIV)-derived peptides or with a peptide derived from influenza A matrix protein bound to peptide-specific cytotoxic T cells in vitro and to T cells from the blood of HIV-infected individuals. In general, tetramer binding correlated well with cytotoxicity assays. This approach should be useful in the analysis of T cells specific for infectious agents, tumors, and autoantigens. | lld:pubmed |
| pubmed-article:8810254 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8810254 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8810254 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:8810254 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8810254 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8810254 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:8810254 | pubmed:issn | 0036-8075 | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:McMichaelA... | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:CONER ARA | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:DavisM MMM | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:MossP APA | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:McHeyzer-Will... | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:AltmanJ DJD | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:BarouchD HDH | lld:pubmed |
| pubmed-article:8810254 | pubmed:author | pubmed-author:GoulderP JPJ | lld:pubmed |
| pubmed-article:8810254 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8810254 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:8810254 | pubmed:volume | 274 | lld:pubmed |
| pubmed-article:8810254 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8810254 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8810254 | pubmed:pagination | 94-6 | lld:pubmed |
| pubmed-article:8810254 | pubmed:dateRevised | 2009-9-29 | lld:pubmed |
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| pubmed-article:8810254 | pubmed:year | 1996 | lld:pubmed |
| pubmed-article:8810254 | pubmed:articleTitle | Phenotypic analysis of antigen-specific T lymphocytes. | lld:pubmed |
| pubmed-article:8810254 | pubmed:affiliation | Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305-5428, USA. | lld:pubmed |
| pubmed-article:8810254 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8810254 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8810254 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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