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Volumn 7, Issue 2, 1995, Pages 188-195

Positive selection of T cells

Author keywords

[No Author keywords available]

Indexed keywords

CD4 ANTIGEN; CD8 ANTIGEN; T LYMPHOCYTE RECEPTOR;

EID: 0029038175     PISSN: 09527915     EISSN: None     Source Type: Journal    
DOI: 10.1016/0952-7915(95)80003-4     Document Type: Article
Times cited : (76)

References (54)
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    • of special interest, Using a recently developed polymerase chain reaction-restriction fragment length polymorphism technique to calculate the in-frame/out-of-frame ratios of TCRβ rearrangement in sorted populations, the authors speculate that the primary function of TCRβ at the double negative (CD4-CD8-) CD25+→CD25- transition is to induce clonal expansion.
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    • of outstanding interest, Using reaggregated organ cultures (see [10,12]) the authors present evidence that the cortical thymic epithelium is unique in providing the necessary signal(s) for positive selection.
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    • Evidence for a differential avidity model of T cell selection in the thymus
    • -/- fetal thymic organ cultures from TCR-transgenic mice, the authors elegantly show that changing the TCR occupancy from low to high converts positive selection into deletion.
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    • T cell receptor antagonist peptides induce positive selection
    • -/- mice are used to show the specificity and sensitivity of positive selection to agonist and antagonist peptide ligands.
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    • of special interest, See annotation [31].
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    • of special interest, See annotation [31].
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    • Robey1    Itano2    Fanslow3    Fowlkes4
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    • of special interest, See annotation [31].
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    • Chan1    Waltzinger2    Baron3    Benoist4    Mathis5
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    • Thymic development in human CD4 transgenic mice — positive selection occurs after commitment to the CD8 lineage
    • of special interest, Along with [27–30], this paper reports that constitutively expressed co-receptor transgenes are able to show that some T cells choose the CD4 or CD8 lineage independent of MHC class specificity. Also, the choice of T-cell effector function correlated with co-receptor expression rather than with MHC recognition [28-30].
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    • Another view of the selective model of thymocyte selection
    • of outstanding interest, These experiments demonstrate the existence of a transitional subset of thymocytes in class II MHC deficient mice that may be committed to the CD4 lineage and that these cells require MHC engagement for their generation, and provide evidence that positive selection is a multistep event.
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  • 33
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    • Regulation of RAG-1 and CD69 expression in the thymus during positive and negative selection
    • of special interest, This study provides further evidence that positive selection requires multiple hits or sustained MHC engagement.
    • (1994) European Journal of Immunology , vol.24 , pp. 145-151
    • Brandle1    Muller2    Muller3    Hengartner4    Pircher5
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    • Small cortical thymocytes are subject to positive selection
    • +) cells can give rise to mature T cells with kinetics that suggests a three to four day window for positive selection. (See also [42]).
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    • CD4 or CD8 down-regulation occurs at different stages of thymocyte differentiation
    • of special interest, Generation of mature T cell populations in the thymus, Careful phenotypic and repertoire analysis suggests that CD4 and CD8 lineage development is not entirely symmetrical. (See also [39]).
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    • A lineage-specific transcriptional silencer regulates CD4 gene expression during T lymphocyte development
    • of special interest, See annotation [44].
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    • A transcriptional silencer controls the developmental expression of the CD4 gene
    • of special interest, Along with [43], this paper analyzes transgenic mice carrying different portions of the murine CD4 gene (coupled to reporter cDNA) and locates a transcriptional silencer in the first intron of the gene. This sequence appears to be involved in regulating CD4 expression during thymocyte development.
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    • + thymic selection in humans lacking ZAP-70 kinase
    • of special interest, See annotation [48].
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    • A role for the cytoplasmic tail of the β-chain of CD8 in thymic selection
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.