{"id":39783,"date":"2026-07-28T16:58:46","date_gmt":"2026-07-28T20:58:46","guid":{"rendered":"https:\/\/www.cancerresearch.org\/?post_type=cri_scientists&#038;p=39783"},"modified":"2026-07-28T16:58:47","modified_gmt":"2026-07-28T20:58:47","slug":"hind-rafei-md","status":"publish","type":"cri_scientists","link":"https:\/\/www.cancerresearch.org\/es\/cri-funded-scientists\/hind-rafei-md","title":{"rendered":"Hind Rafei, MD"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">CAR T-cell therapy, which engineers a patient\u2019s own immune cells to recognize and attack cancer, has produced extraordinary results in some blood cancers. However, this approach has been far less successful against solid tumors. One major reason is that solid tumors create a harsh environment that gradually weakens the engineered T cells, causing them to become \u201cexhausted\u201d and lose their ability to multiply, survive, and continue fighting the cancer.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Dr. Rafei\u2019s research focuses on a key molecular control system inside T cells called CREM, which helps determine whether T cells remain active or become exhausted. CREM exists in many different forms, known as isoforms, and these forms can have very different effects on immune function. Current gene-editing approaches typically remove CREM broadly, which risks eliminating forms that may help T cells function properly.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Dr. Rafei aims to develop a much more precise strategy by selectively blocking only the harmful CREM isoforms while preserving beneficial ones. To do this, she will use an advanced gene-targeting technology called Cas13, which can precisely target specific RNA molecules inside cells. Her team will first identify which CREM isoforms drive T-cell exhaustion under conditions that mimic solid tumors. They will then engineer CAR T cells with selective Cas13 programs and test whether these enhanced cells survive longer, remain more active, and control tumors more effectively in advanced preclinical models. If successful, this work could lead to a new generation of CAR T-cell therapies capable of treating solid tumors more effectively and establish a broadly applicable strategy for improving immune cell therapies through highly precise genetic control.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Projects and Grants<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">Splicing isoform-directed Cas13 reprogramming of CAR-T cells for solid tumor immunotherapy<\/p>\n","protected":false},"excerpt":{"rendered":"<p>CAR T-cell therapy, which engineers a patient\u2019s own immune cells to recognize and attack cancer, has produced extraordinary results in some blood cancers. However, this approach has been far less successful against [&hellip;]<\/p>\n","protected":false},"featured_media":39780,"template":"","tax_cancer_type":[894],"tax_grant_type":[485],"tax_award_year":[881],"tax_institutions":[527],"tax_location_states":[523],"class_list":["post-39783","cri_scientists","type-cri_scientists","status-publish","has-post-thumbnail","hentry"],"acf":{"scientist_subhead":"CRI CLIP Investigator","quote":"","scientist_last_name":"Rafei","show_on_landing":false,"scientist_publish_until":"20290728"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Hind Rafei, MD - Cancer Research Institute<\/title>\n<meta name=\"description\" content=\"This new clinical trial will evaluate two different FGFR3-targeted treatment strategies for patients with intermediate-risk NMIBC: 1) a vaccine targeting FGFR3 mutations and 2) a novel slow-release bladder-inserted device (TAR-210) that delivers an FGFR3 inhibitor directly to the tumor. 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