Abstract
Virtually all of the measurable cell-mediated cytotoxicity delivered by cytotoxic T lymphocytes and natural killer cells comes from either the granule exocytosis pathway or the Fas pathway. The granule exocytosis pathway utilizes perforin to traffic the granzymes to appropriate locations in target cells, where they cleave critical substrates that initiate DNA fragmentation and apoptosis; granzymes A and B induce death via alternate, nonoverlapping pathways. The Fas/FasL system is responsible for activation-induced cell death but also plays an important role in lymphocyte-mediated killing under certain circumstances. The interplay between these two cytotoxic systems provides opportunities for therapeutic…
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Authors
2Topics & keywords
Topics
Keywords
- Granzyme
- Perforin
- Cytotoxic T cell
- Biology
- Fas ligand
- Cell biology
- Cytotoxicity
- Programmed cell death
UN Sustainable Development Goals
- Good health and well-being
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