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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
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.
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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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