Functional heterogeneity of cytotoxic T cells and tumor resistance to cytotoxic hits limit anti‐tumor activity in vivo

Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters t...

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Published inThe EMBO journal Vol. 40; no. 11; pp. e106658 - n/a
Main Authors Khazen, Roxana, Cazaux, Marine, Lemaître, Fabrice, Corre, Beatrice, Garcia, Zacarias, Bousso, Philippe
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.06.2021
Springer Nature B.V
EMBO Press
John Wiley and Sons Inc
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Abstract Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B‐cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL–tumor contacts in vivo . In the therapeutic settings of anti‐CD19 CAR T cells, the majority of CAR T cell–tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti‐tumor responses in vivo . SYNOPSIS The efficiency of CTL or CAR T cell lethal hit delivery in the tumor microenvironment is unclear. Here, intravital imaging and functional reporters were used to quantify the various outcomes of T cell‐tumor contacts, revealing that a minority of interactions resulted in target cell killing. Most CTL‐tumor cell contacts are non‐lethal. Tumor cells often recover from CTL‐induced membrane damage. CTLs or CAR T cells exhibit extensive variability in killing capacities in vivo . Graphical Abstract Intravital imaging of T cell‐tumor contacts reveals variability in the ability of cytotoxic T cells to kill tumor cells and that the majority of interactions are non‐lethal.
AbstractList Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B-cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL-tumor contacts in vivo. In the therapeutic settings of anti-CD19 CAR T cells, the majority of CAR T cell-tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for antitumor responses in vivo.
Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B-cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL-tumor contacts in vivo. In the therapeutic settings of anti-CD19 CAR T cells, the majority of CAR T cell-tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti-tumor responses in vivo.Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B-cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL-tumor contacts in vivo. In the therapeutic settings of anti-CD19 CAR T cells, the majority of CAR T cell-tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti-tumor responses in vivo.
Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B‐cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL–tumor contacts in vivo . In the therapeutic settings of anti‐CD19 CAR T cells, the majority of CAR T cell–tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti‐tumor responses in vivo . SYNOPSIS The efficiency of CTL or CAR T cell lethal hit delivery in the tumor microenvironment is unclear. Here, intravital imaging and functional reporters were used to quantify the various outcomes of T cell‐tumor contacts, revealing that a minority of interactions resulted in target cell killing. Most CTL‐tumor cell contacts are non‐lethal. Tumor cells often recover from CTL‐induced membrane damage. CTLs or CAR T cells exhibit extensive variability in killing capacities in vivo . Graphical Abstract Intravital imaging of T cell‐tumor contacts reveals variability in the ability of cytotoxic T cells to kill tumor cells and that the majority of interactions are non‐lethal.
Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B-cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL-tumor contacts in vivo. In the therapeutic settings of anti-CD19 CAR T cells, the majority of CAR T cell-tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti-tumor responses in vivo.
Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B‐cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL–tumor contacts in vivo. In the therapeutic settings of anti‐CD19 CAR T cells, the majority of CAR T cell–tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti‐tumor responses in vivo. SYNOPSIS The efficiency of CTL or CAR T cell lethal hit delivery in the tumor microenvironment is unclear. Here, intravital imaging and functional reporters were used to quantify the various outcomes of T cell‐tumor contacts, revealing that a minority of interactions resulted in target cell killing. Most CTL‐tumor cell contacts are non‐lethal. Tumor cells often recover from CTL‐induced membrane damage. CTLs or CAR T cells exhibit extensive variability in killing capacities in vivo. Intravital imaging of T cell‐tumor contacts reveals variability in the ability of cytotoxic T cells to kill tumor cells and that the majority of interactions are non‐lethal.
Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment is unclear. Here, we visualized the capacity of single CTLs to attack tumor cells in vitro and in vivo using genetically encoded reporters that monitor cell damage and apoptosis. Using two distinct malignant B‐cell lines, we found that the majority of cytotoxic hits delivered by CTLs in vitro were sublethal despite proper immunological synapse formation, and associated with reversible calcium elevation and membrane damage in the targets. Through intravital imaging in the bone marrow, we established that the majority of CTL interactions with lymphoma B cells were either unproductive or sublethal. Functional heterogeneity of CTLs contributed to diverse outcomes during CTL–tumor contacts in vivo . In the therapeutic settings of anti‐CD19 CAR T cells, the majority of CAR T cell–tumor interactions were also not associated with lethal hit delivery. Thus, differences in CTL lytic potential together with tumor cell resistance to cytotoxic hits represent two important bottlenecks for anti‐tumor responses in vivo . Intravital imaging of T cell‐tumor contacts reveals variability in the ability of cytotoxic T cells to kill tumor cells and that the majority of interactions are non‐lethal.
Author Corre, Beatrice
Khazen, Roxana
Bousso, Philippe
Lemaître, Fabrice
Cazaux, Marine
Garcia, Zacarias
AuthorAffiliation 1 Dynamics of Immune Responses Unit Institut Pasteur, Equipe Labellisée Ligue Contre le Cancer INSERM U1223 Paris France
2 Université de Paris Paris France
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Keywords CTL
CAR T cells
intravital imaging
sublethal hit
lethal hit
Immunology
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2015; 35
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2017; 27
2016; 129
1987; 6
2015; 11
2020; 16
1988; 167
2020; 11
2019; 568
2013; 121
2017; 451
2007; 96
2012; 12
2005; 23
2016; 7
2018; 3
2016; 1
2006; 108
2010; 235
2006; 25
2003; 9
2008; 118
2013; 251
2013; 110
2019; 216
1996; 4
1994; 4
2014; 11
2011; 121
2006; 103
2016; 44
2001; 98
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SSID ssj0005871
Score 2.4647684
Snippet Cytotoxic T cells (CTLs) can eliminate tumor cells through the delivery of lethal hits, but the actual efficiency of this process in the tumor microenvironment...
SourceID pubmedcentral
hal
proquest
pubmed
crossref
wiley
springer
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage e106658
SubjectTerms Animals
Antigens, CD19 - immunology
Apoptosis
B-Lymphocytes - immunology
Bone imaging
Bone marrow
Calcium
Calcium - metabolism
CAR T cells
CD19 antigen
Cell Membrane - metabolism
Cells, Cultured
CTL
Cytotoxicity
Damage
EMBO03
EMBO19
Genetic code
Heterogeneity
Immunological synapses
Immunological Synapses - immunology
Immunology
Immunotherapy, Adoptive
intravital imaging
lethal hit
Life Sciences
Lymphocytes
Lymphocytes B
Lymphocytes T
Lymphoma
Lymphoma - immunology
Lymphoma - therapy
Membranes
Mice
Mice, Inbred C57BL
Receptors, Chimeric Antigen - immunology
sublethal hit
Synapses
T-Lymphocytes, Cytotoxic - immunology
Target recognition
Tumor cells
Tumor microenvironment
Tumors
Title Functional heterogeneity of cytotoxic T cells and tumor resistance to cytotoxic hits limit anti‐tumor activity in vivo
URI https://link.springer.com/article/10.15252/embj.2020106658
https://onlinelibrary.wiley.com/doi/abs/10.15252%2Fembj.2020106658
https://www.ncbi.nlm.nih.gov/pubmed/33855732
https://www.proquest.com/docview/2534895742
https://www.proquest.com/docview/2513243359
https://pasteur.hal.science/pasteur-03261457
https://pubmed.ncbi.nlm.nih.gov/PMC8167356
Volume 40
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