Staphylococcal-enterotoxin-dependent cell-mediated cytotoxicity |
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Authors: | M Dohlsten G Hedlund T Kalland |
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Affiliation: | 1. Department of Physical, Earth and Environmental Sciences, University of Siena, via Mattioli, 4-53100 Siena, Italy;2. Department of Environment and Toxicology, DHI, Agern Allé 5, 2970 Hoersholm, Denmark;3. Department of Environment, Land and Infrastructure Engineering (DIATI), Politecnico di Torino, Italy;4. Department of Chemistry, Materials, and Chemical Engineering “G. Natta”, Politecnico di Milano and RU INSTM, Via Mancinelli 7, 20131 Milano, Italy;5. Department of Bioscience, University of Milano, via Celoria 26, 20133 Milano, Italy;6. Department of Biology, University of Naples Federico II, via Cinthia ed. 7, 80126 Naples, Italy;7. Department of Chemical and Biology “A. Zambelli”, University of Salerno, via Giovanni Paolo II 132, 84084 Fisciano, SA, Italy;8. Regional Technological District for Advanced Materials, c/o ASEV SpA (management entity), via delle Fiascaie 12, 50053 Empoli, FI, Italy;9. Acque Industriali SRL, Via Molise, 1, 56025 Pontedera, PI, Italy;10. LABROMARE SRL, Via dell''Artigianato 69, 57121 Livorno, Italy;11. Department of Chemistry & RU INSTM at the University of Firenze, Via della Lastruccia 3, 50019 Sesto Fiorentino, Italy;12. Institute for Environmental Protection and Research (ISPRA), Piazzale dei marmi 12, 57013 Livorno, Italy |
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Abstract: | ![]() T cells equipped with sophisticated TCR and MHC recognition structures, an efficient cytokine communication network and lethal cytotoxic effector functions constitute one of the bulwarks of the mammalian immune system. However, infective agents have developed strategies to undermine T-cell immunity; for example, certain bacterial toxins serve as 'superantigens' by binding to preserved determinants on MHC class-II-encoded proteins and activating T cells expressing particular sequences of TCR V beta gene products. In this paper, Mikael Dohlsten and colleagues present evidence suggesting that these bacterial superantigens direct T cells to eradicate MHC class-II-expressing antigen-presenting cells, thus counteracting specific T-cell functions. |
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