Employing CRISPR-Cas9 to Enhance T Cell Effector Function
Methods in Molecular Biology, ISSN: 1940-6029, Vol: 2782, Page: 195-208
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Book Chapter Description
As part of the adaptive immune system, T cells are critical to maintain immune homeostasis. T cells provide protective immunity by killing infected cells and combatting cancerous cells. To do so, T cells produce and secrete effector molecules, such as granzymes, perforin, and cytokines such as tumor necrosis factor α and interferon γ. However, in immune suppressive environments, such as tumors, T cells gradually lose the capacity to perform their effector function. One way T cell effector function can be enhanced is through genetic engineering with tools such as clustered regularly interspaced short palindromic repeat (CRISPR)Clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 (Cas9). This protocol explains in a step-by-step fashion how to perform a controlled electroporation-based CRISPR experiment to enhance human T cell effector function. Of note, these steps are suitable for CRISPR-mediated genome editing in T cells in general and can thus also be used to study proteins of interest that do not influence T cell effector function.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85190785081&origin=inward; http://dx.doi.org/10.1007/978-1-0716-3754-8_16; http://www.ncbi.nlm.nih.gov/pubmed/38622404; https://link.springer.com/10.1007/978-1-0716-3754-8_16; https://dx.doi.org/10.1007/978-1-0716-3754-8_16; https://link.springer.com/protocol/10.1007/978-1-0716-3754-8_16
Springer Science and Business Media LLC
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