{"id":275614,"date":"2026-08-31T06:42:10","date_gmt":"2026-08-31T06:42:10","guid":{"rendered":"https:\/\/www.newsbeep.com\/us-pa\/275614\/"},"modified":"2026-08-31T06:42:10","modified_gmt":"2026-08-31T06:42:10","slug":"the-journey-of-car-t-cell-cancer-research-at-penn","status":"publish","type":"post","link":"https:\/\/www.newsbeep.com\/us-pa\/275614\/","title":{"rendered":"The journey of CAR T-cell cancer research at Penn"},"content":{"rendered":"<p>When immunotherapy professor Carl June started working with CAR T cells, he was not focused on treating cancer.<\/p>\n<p>At the Fred Hutchinson Cancer Center, June studied bone marrow transplantations for patients with radiation exposure during the Cold War, thinking about how to expand T cells \u2014 cells that attack foreign invaders in the body as part of an immune response \u2014 outside of the body. Later, during the AIDS epidemic, he began using those cells to treat HIV-1 in his lab at the Naval Medical Research Institute.<\/p>\n<p>June\u2019s idea was that a patient\u2019s T cells could be removed from their body, grown in the lab using certain proteins, and returned to the body to continue fighting against HIV-1. Bruce Levine \u2014 who now serves as the Barbara and Edward Netter Professor in Cancer Gene Therapy \u2014 later joined June in his lab.<\/p>\n<p>But when the pair came to Penn in 1999, they pivoted to looking at CAR T-cell applications in cancer research \u2014 specifically, leukemia.<\/p>\n<p>\u201cThe Department of Defense does infectious disease work, but they don\u2019t do cancer research,\u201d Levine explained. \u201cWe move up to Penn \u2014 now we can start clinical trials in cancer.\u201d\u00a0<\/p>\n<p class=\"font-serif\">Get the DP delivered straight to your inbox.<\/p>\n<p>  <a href=\"https:\/\/thedp.us2.list-manage.com\/subscribe?u=a96885e3aa3f8131c872ee329&amp;id=370b4800ba\" class=\"newsletter-btn font-sans no-underline\" target=\"_blank\" rel=\"noopener noreferrer nofollow\"> Sign Up<\/a><\/p>\n<p>\u201cWe used the lessons from HIV, but just changed the CAR design and then changed its targeting so that it would target leukemia-associated molecules,\u201d June added. He now <a href=\"https:\/\/www.med.upenn.edu\/cci\/junelab\" target=\"_blank\" rel=\"nofollow noopener\">serves<\/a> as the director of Penn Medicine\u2019s Center for Cellular Immunotherapies.\u00a0<\/p>\n<p>In 2010, the two treated their first patient suffering from chronic lymphocytic leukemia with CAR T-cell therapy. Two subsequent patients in the clinical trial also showed promising results.\u00a0<\/p>\n<p>\u201cWe had treated three patients,\u201d June said. \u201cAll three responded, but we had no more money.\u201d\u00a0<\/p>\n<p>The field of cancer immunotherapy had, for over a decade, been in what Levine described as \u201cthe dark ages of gene therapy,\u201d where skepticism ran rampant, and funding was hard to acquire. The team, with dwindling funds, went ahead and published the results in the New England Journal of Medicine in 2011.\u00a0<\/p>\n<p>\u201cIt\u2019s very unusual in an end-stage cancer trial to have three out of three patients respond,\u201d June added. \u201cWe had smoking-gun good evidence that the CAR T cells did it.\u201d<\/p>\n<p>Their work, including the subsequent treatment of pediatric patients, paved the way for the United States Food and Drug Administration\u2019s approval of the first CAR T-cell therapy in 2017.<\/p>\n<p>Now, researchers at Penn are looking at strengthening the effect of CAR T cells \u2014 known as \u201carmored\u201d CAR T cells \u2014 in blood cancers.<\/p>\n<p>Last year, June helped publish a study that <a href=\"https:\/\/www.pennmedicine.org\/news\/enhanced-car-t-cell-therapy-offers-new-strategy-for-lymphoma\" target=\"_blank\" rel=\"nofollow noopener\">found<\/a> promising results in using a next-generation \u201carmored\u201d CAR T-cell therapy in patients who continued to resist multiple rounds of other cancer treatments, including commercially available CAR T-cell therapies.\u00a0<\/p>\n<p>\u201cCAR T-cell therapy has transformed lymphoma treatment, but about half of patients still won\u2019t have a long-term remission,\u201d professor of Medicine at the Hospital of the University of Pennsylvania Jakub Svoboda \u2014 who pioneered the 2025 study alongside June \u2014 wrote.\u00a0<\/p>\n<p>\u201cThese armored CAR T cells are designed to produce IL-18, which may help them work better in the tumor environment and improve their ability to kill cancer cells,\u201d he explained. \u201cIn our first-in-human study, we saw response rates above 80% in patients whose disease had already progressed after standard CAR T-cell therapy, which was very encouraging.\u201d<\/p>\n<p>The 21 patients in the first phase of the clinical trial in the 2025 study had received a median of seven other therapies before enrolling, and all but one had already tried a traditional CAR T-cell therapy approved for their cancer type.\u00a0<\/p>\n<p>To combat these challenges, a team led by June developed the \u201carmored\u201d CAR T-cell product. This version was modified to secrete a small protein that is capable of enhancing the immune system \u2014 which further protects the CAR T cells and promotes their ability to attack cancerous cells.\u00a0<\/p>\n<p>The research team found strong evidence indicating that adding the protein \u2014 interleukin-18 \u2014 to CAR T cells contributed to the robust response rates.<\/p>\n<p>But leukemia, a blood cancer, is in the minority when it comes to types of cancer: it is a liquid tumor as opposed to a solid one. With solid tumors, a host of challenges arise.\u00a0<\/p>\n<p>Now, Penn researchers are devising ways to use CAR T cells to break through barriers \u2014 maybe even lowering costs and making the treatment easier on patients\u2019 bodies.\u00a0<\/p>\n<p>\u201cIt\u2019s an incredibly exciting time in the field,\u201d Svoboda wrote when asked to consider the future of CAR T-cell research. \u201cWe\u2019re studying newer generations of armored CAR T cells and developing therapies against new targets. What\u2019s especially exciting are approaches like in vivo CAR T cells and allogeneic CAR T cells, which could make these treatments faster, simpler, and more accessible for patients.\u201d<\/p>\n<p>This story is the first part in a two-part series about CAR T-cell research at Penn.\u00a0<\/p>\n","protected":false},"excerpt":{"rendered":"When immunotherapy professor Carl June started working with CAR T cells, he was not focused on treating cancer.&hellip;\n","protected":false},"author":2,"featured_media":275615,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[8],"tags":[69,71,70],"class_list":["post-275614","post","type-post","status-publish","format-standard","has-post-thumbnail","category-philadelphia","tag-philadelphia","tag-philadelphia-headlines","tag-philadelphia-news"],"_links":{"self":[{"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/posts\/275614","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/comments?post=275614"}],"version-history":[{"count":0,"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/posts\/275614\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/media\/275615"}],"wp:attachment":[{"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/media?parent=275614"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/categories?post=275614"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.newsbeep.com\/us-pa\/wp-json\/wp\/v2\/tags?post=275614"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}