{"id":178912,"date":"2023-12-23T13:27:03","date_gmt":"2023-12-23T19:27:03","guid":{"rendered":"https:\/\/lifeboat.com\/blog\/2023\/12\/this-first-crispr-gene-editing-treatment-is-just-the-beginning-heres-whats-coming-next"},"modified":"2023-12-28T05:11:26","modified_gmt":"2023-12-28T11:11:26","slug":"this-first-crispr-gene-editing-treatment-is-just-the-beginning-heres-whats-coming-next","status":"publish","type":"post","link":"https:\/\/lifeboat.com\/blog\/2023\/12\/this-first-crispr-gene-editing-treatment-is-just-the-beginning-heres-whats-coming-next","title":{"rendered":"This first CRISPR gene-editing treatment is just the beginning. Here\u2019s what\u2019s coming next"},"content":{"rendered":"<p><a class=\"aligncenter blog-photo\" href=\"https:\/\/lifeboat.com\/blog.images\/this-first-crispr-gene-editing-treatment-is-just-the-beginning-heres-whats-coming-next2.jpg\"><\/a><\/p>\n<p>2023 was the year that CRISPR gene-editing sliced its way out of the lab and into the public consciousness\u2014and American medical system. The Food and Drug Administration recently approved the <a rel=\"\u201cnoopener noopener\" href=\"https:\/\/www.fastcompany.com\/90994486\/fda-approved-first-crispr-gene-editing-drug-what-to-know\" target=\"\u201d_blank\u201d\">first gene-editing CRISPR therapy<\/a>, Casgevy (or exa-cel), a treatment from CRISPR Therapeutics and partner Vertex for patients with sickle cell disease. This comes on the heels of a similar green light by U.K. regulators in a historic moment for a gene-editing technology <a rel=\"\u201d noopener noopener\" href=\"https:\/\/www.fastcompany.com\/90825719\/5-most-promising-uses-crispr-gene-editing-technology\" target=\"\u201d_blank\u201d\">whose foundations were laid back in the 1980s<\/a>, eventually resulting in a 2020 Nobel Prize in Chemistry for pioneering CRISPR scientists Jennifer Doudna and Emmanuelle Charpentier.<\/p>\n<p>That decades-long gap between initial scientific spark, widespread academic recognition, and now the market entry of a potential cure for blood disorders like sickle cell disease that afflict hundreds of thousands of people around the world is telling. If past is prologue, even <a rel=\"noopener noopener\" href=\"https:\/\/www.nature.com\/articles\/d41586-023-03797-7\" target=\"_blank\">newer CRISPR gene-editing approaches being studied today<\/a> have the <a rel=\"noopener noopener\" href=\"https:\/\/innovativegenomics.org\/news\/crispr-clinical-trials-2023\/\" target=\"_blank\">potential to treat diseases ranging from cancer and muscular dystrophy to heart disease<\/a>, birth more resilient livestock and plants <a rel=\"noopener noopener\" href=\"https:\/\/www.fastcompany.com\/90965691\/crispr-chickens-whats-next-gmo-gene-modified-food-chain\" target=\"_blank\">that can grapple with climate change and new strains of deadly viruses<\/a>, and even upend the energy industry by <a rel=\"noopener noopener\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/26874259\/\" target=\"_blank\">tweaking bacterial DNA to create more efficient biofuels<\/a> in future decades. And novel uses of CRISPR, with assists from other technologies like artificial intelligence, might fuel even more precise, targeted gene-editing\u2014in turn accelerating future discovery with implications for just about any industry that relies on biological material, from medicine to agriculture to energy.<\/p>\n<p>With new CRISPR discoveries guided by AI, specifically, we can expand the toolbox available for gene editing, which is crucial for therapeutic, diagnostic, and research applications\u2026 but also a great way to better understand the vast diversity of microbial defense mechanisms, said Feng Zhang, another CRISPR pioneer, molecular biologist, and core member at the <a rel=\"noopener noopener\" href=\"https:\/\/www.broadinstitute.org\/bios\/feng-zhang\" target=\"_blank\">Broad Institute of MIT and Harvard<\/a> in an emailed statement to <em>Fast Company<\/em>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>2023 was the year that CRISPR gene-editing sliced its way out of the lab and into the public consciousness\u2014and American medical system. The Food and Drug Administration recently approved the first gene-editing CRISPR therapy, Casgevy (or exa-cel), a treatment from CRISPR Therapeutics and partner Vertex for patients with sickle cell disease. This comes on the [\u2026]<\/p>\n","protected":false},"author":661,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1902,11,19,1506,412,6],"tags":[],"class_list":["post-178912","post","type-post","status-publish","format-standard","hentry","category-bioengineering","category-biotech-medical","category-chemistry","category-food","category-genetics","category-robotics-ai"],"_links":{"self":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/178912","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/users\/661"}],"replies":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/comments?post=178912"}],"version-history":[{"count":1,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/178912\/revisions"}],"predecessor-version":[{"id":179352,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/178912\/revisions\/179352"}],"wp:attachment":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/media?parent=178912"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/categories?post=178912"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/tags?post=178912"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}