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In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity
According to in vitro assays, T cells are thought to kill rapidly and efficiently, but the efficacy and dynamics of cytotoxic T lymphocyte (CTL)-mediated killing of virus-infected cells in vivo remains elusive. We used two-photon microscopy to quantify CTL-mediated killing in mice infected with herp...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846978/ https://www.ncbi.nlm.nih.gov/pubmed/26872694 http://dx.doi.org/10.1016/j.immuni.2016.01.010 |
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author | Halle, Stephan Keyser, Kirsten Anja Stahl, Felix Rolf Busche, Andreas Marquardt, Anja Zheng, Xiang Galla, Melanie Heissmeyer, Vigo Heller, Katrin Boelter, Jasmin Wagner, Karen Bischoff, Yvonne Martens, Rieke Braun, Asolina Werth, Kathrin Uvarovskii, Alexey Kempf, Harald Meyer-Hermann, Michael Arens, Ramon Kremer, Melanie Sutter, Gerd Messerle, Martin Förster, Reinhold |
author_facet | Halle, Stephan Keyser, Kirsten Anja Stahl, Felix Rolf Busche, Andreas Marquardt, Anja Zheng, Xiang Galla, Melanie Heissmeyer, Vigo Heller, Katrin Boelter, Jasmin Wagner, Karen Bischoff, Yvonne Martens, Rieke Braun, Asolina Werth, Kathrin Uvarovskii, Alexey Kempf, Harald Meyer-Hermann, Michael Arens, Ramon Kremer, Melanie Sutter, Gerd Messerle, Martin Förster, Reinhold |
author_sort | Halle, Stephan |
collection | PubMed |
description | According to in vitro assays, T cells are thought to kill rapidly and efficiently, but the efficacy and dynamics of cytotoxic T lymphocyte (CTL)-mediated killing of virus-infected cells in vivo remains elusive. We used two-photon microscopy to quantify CTL-mediated killing in mice infected with herpesviruses or poxviruses. On average, one CTL killed 2–16 virus-infected cells per day as determined by real-time imaging and by mathematical modeling. In contrast, upon virus-induced MHC class I downmodulation, CTLs failed to destroy their targets. During killing, CTLs remained migratory and formed motile kinapses rather than static synapses with targets. Viruses encoding the calcium sensor GCaMP6s revealed strong heterogeneity in individual CTL functional capacity. Furthermore, the probability of death of infected cells increased for those contacted by more than two CTLs, indicative of CTL cooperation. Thus, direct visualization of CTLs during killing of virus-infected cells reveals crucial parameters of CD8(+) T cell immunity. |
format | Online Article Text |
id | pubmed-4846978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-48469782016-05-06 In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity Halle, Stephan Keyser, Kirsten Anja Stahl, Felix Rolf Busche, Andreas Marquardt, Anja Zheng, Xiang Galla, Melanie Heissmeyer, Vigo Heller, Katrin Boelter, Jasmin Wagner, Karen Bischoff, Yvonne Martens, Rieke Braun, Asolina Werth, Kathrin Uvarovskii, Alexey Kempf, Harald Meyer-Hermann, Michael Arens, Ramon Kremer, Melanie Sutter, Gerd Messerle, Martin Förster, Reinhold Immunity Article According to in vitro assays, T cells are thought to kill rapidly and efficiently, but the efficacy and dynamics of cytotoxic T lymphocyte (CTL)-mediated killing of virus-infected cells in vivo remains elusive. We used two-photon microscopy to quantify CTL-mediated killing in mice infected with herpesviruses or poxviruses. On average, one CTL killed 2–16 virus-infected cells per day as determined by real-time imaging and by mathematical modeling. In contrast, upon virus-induced MHC class I downmodulation, CTLs failed to destroy their targets. During killing, CTLs remained migratory and formed motile kinapses rather than static synapses with targets. Viruses encoding the calcium sensor GCaMP6s revealed strong heterogeneity in individual CTL functional capacity. Furthermore, the probability of death of infected cells increased for those contacted by more than two CTLs, indicative of CTL cooperation. Thus, direct visualization of CTLs during killing of virus-infected cells reveals crucial parameters of CD8(+) T cell immunity. Cell Press 2016-02-16 /pmc/articles/PMC4846978/ /pubmed/26872694 http://dx.doi.org/10.1016/j.immuni.2016.01.010 Text en © 2016 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Halle, Stephan Keyser, Kirsten Anja Stahl, Felix Rolf Busche, Andreas Marquardt, Anja Zheng, Xiang Galla, Melanie Heissmeyer, Vigo Heller, Katrin Boelter, Jasmin Wagner, Karen Bischoff, Yvonne Martens, Rieke Braun, Asolina Werth, Kathrin Uvarovskii, Alexey Kempf, Harald Meyer-Hermann, Michael Arens, Ramon Kremer, Melanie Sutter, Gerd Messerle, Martin Förster, Reinhold In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity |
title | In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity |
title_full | In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity |
title_fullStr | In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity |
title_full_unstemmed | In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity |
title_short | In Vivo Killing Capacity of Cytotoxic T Cells Is Limited and Involves Dynamic Interactions and T Cell Cooperativity |
title_sort | in vivo killing capacity of cytotoxic t cells is limited and involves dynamic interactions and t cell cooperativity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846978/ https://www.ncbi.nlm.nih.gov/pubmed/26872694 http://dx.doi.org/10.1016/j.immuni.2016.01.010 |
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