Perforin and granzymes: function, dysfunction and human pathology
By I. Voskoboinik, James C. Whisstock, J. Trapani. Nature reviews. Immunology, 2015
1,126 citations recorded by the source corpus.
Subfields: Hematology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health
View Paper: https://www.semanticscholar.org/paper/9da5de3c65dda564b5ca944b946d1341eaebed06
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Citations in the corpus
- CD8+ T cells and fatty acids orchestrate tumor ferroptosis and immunity via ACSL4 (2022, background): “It is well known that CTLs kill targets via the perforin-granzyme-caspase-mediated apoptosis (Voskoboinik et al., 2015).”
- How Do Cytotoxic Lymphocytes Kill Cancer Cells? (2015, background): “However, additional GZMs with possible functional significance (in total 5 in humans and 10 in mice) and other cytoplasmic granuleassociated molecules like the human-specific protein granulysin (17) have been described, though their biologic functions during cancer immunity and immunotherapy have no”
- MetaCell: analysis of single-cell RNA-seq data using K-nn graph partitions (2019, background): “Activation of the T cell effector program ultimately depends on expression of units of the cytotoxic granule (granzymes, cathepsins, granulysin) and of the machinery required for perforating target cells (e.g., perforin) [45].”
- Role of pyroptosis in inflammation and cancer (2022, background): “Furthermore, cytotoxic lymphocyte-mediated immunity is dependent on granzymes, which can enhance antitumor immunity and may be a potential candidate targeted site for tumor treatments [121, 123] (Fig.”