Nature Reviews Clinical Oncology, Journal Year: 2018, Volume and Issue: 16(2), P. 123 - 135
Published: Nov. 6, 2018
Language: Английский
Nature Reviews Clinical Oncology, Journal Year: 2018, Volume and Issue: 16(2), P. 123 - 135
Published: Nov. 6, 2018
Language: Английский
Nature reviews. Immunology, Journal Year: 2020, Volume and Issue: 20(11), P. 651 - 668
Published: May 20, 2020
Language: Английский
Citations
3217Cell, Journal Year: 2019, Volume and Issue: 177(2), P. 414 - 427.e13
Published: April 1, 2019
PD-L1 on the surface of tumor cells binds its receptor PD-1 effector T cells, thereby suppressing their activity. Antibody blockade can activate an anti-tumor immune response leading to durable remissions in a subset cancer patients. Here, we describe alternative mechanism activity involving secretion tumor-derived exosomes. Removal exosomal inhibits growth, even models resistant anti-PD-L1 antibodies. Exosomal from suppresses cell activation draining lymph node. Systemically introduced rescues growth tumors unable secrete own. Exposure PD-L1-deficient wild-type injected at distant site, simultaneously or months later. Anti-PD-L1 antibodies work additively, not redundantly, with suppress growth. Together, these findings show that represents unexplored therapeutic target, which could overcome resistance current antibody approaches.
Language: Английский
Citations
1098Nature Nanotechnology, Journal Year: 2019, Volume and Issue: 14(11), P. 1007 - 1017
Published: Nov. 1, 2019
Language: Английский
Citations
1026Journal of Hematology & Oncology, Journal Year: 2020, Volume and Issue: 13(1)
Published: Aug. 10, 2020
Abstract In recent years, cancer immunotherapy based on immune checkpoint inhibitors (ICIs) has achieved considerable success in the clinic. However, ICIs are significantly limited by fact that only one third of patients with most types respond to these agents. The induction cell death mechanisms other than apoptosis gradually emerged as a new treatment strategy because tumors harbor innate resistance apoptosis. date, possibility combining two modalities not been discussed systematically. Recently, few studies revealed crosstalk between distinct and antitumor immunity. pyroptosis, ferroptosis, necroptosis combined showed synergistically enhanced activity, even ICI-resistant tumors. Immunotherapy-activated CD8+ T cells traditionally believed induce tumor via following main pathways: (i) perforin-granzyme (ii) Fas-FasL. identified mechanism which suppress growth inducing ferroptosis provoked review relationship system activation. Hence, this review, we summarize knowledge reciprocal interaction immunity mechanisms, particularly necroptosis, three potentially novel immunogenic death. Because evidence is derived from using animal models, also reviewed related bioinformatics data available for human tissues public databases, partially confirmed presence interactions activation
Language: Английский
Citations
976Nature reviews. Cancer, Journal Year: 2018, Volume and Issue: 19(1), P. 9 - 31
Published: Dec. 10, 2018
Language: Английский
Citations
908Journal for ImmunoTherapy of Cancer, Journal Year: 2020, Volume and Issue: 8(1), P. e000337 - e000337
Published: March 1, 2020
Cells succumbing to stress via regulated cell death (RCD) can initiate an adaptive immune response associated with immunological memory, provided they display sufficient antigenicity and adjuvanticity. Moreover, multiple intracellular microenvironmental features determine the propensity of RCD drive immunity. Here, we provide updated operational definition immunogenic (ICD), discuss key factors that dictate ability dying cells response, summarize experimental assays are currently available for assessment ICD in vitro vivo, formulate guidelines their interpretation.
Language: Английский
Citations
849Nature Immunology, Journal Year: 2022, Volume and Issue: 23(4), P. 487 - 500
Published: Feb. 10, 2022
Language: Английский
Citations
844Nature Reviews Materials, Journal Year: 2019, Volume and Issue: 4(6), P. 398 - 414
Published: April 26, 2019
Language: Английский
Citations
817Cell Death and Disease, Journal Year: 2020, Volume and Issue: 11(11)
Published: Nov. 26, 2020
Abstract Chemotherapy, radiation therapy, as well targeted anticancer agents can induce clinically relevant tumor-targeting immune responses, which critically rely on the antigenicity of malignant cells and their capacity to generate adjuvant signals. In particular, immunogenic cell death (ICD) is accompanied by exposure release numerous damage-associated molecular patterns (DAMPs), altogether confer a robust adjuvanticity dying cancer cells, they favor recruitment activation antigen-presenting cells. ICD-associated DAMPs include surface-exposed calreticulin (CALR) secreted ATP, annexin A1 (ANXA1), type I interferon, high-mobility group box 1 (HMGB1). Additional hallmarks ICD encompass phosphorylation eukaryotic translation initiation factor 2 subunit-α (EIF2S1, better known eIF2α), autophagy, global arrest in transcription translation. Here, we outline methodological approaches for measuring markers vitro ex vivo discovery next-generation antineoplastic agents, development personalized regimens, identification optimal therapeutic combinations clinical management cancer.
Language: Английский
Citations
747Nature Reviews Disease Primers, Journal Year: 2019, Volume and Issue: 5(1)
Published: Feb. 21, 2019
Language: Английский
Citations
652