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 in | The EMBO journal Vol. 40; no. 11; pp. e106658 - n/a |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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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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... |
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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 |
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