{"id":3281,"date":"2021-10-18T16:23:36","date_gmt":"2021-10-18T16:23:36","guid":{"rendered":"https:\/\/medschool.prd.vanderbilt.edu\/vanderbilt-medicine\/?p=3281"},"modified":"2021-10-18T16:23:36","modified_gmt":"2021-10-18T16:23:36","slug":"gene-editing-used-to-treat-rare-genetic-disorder","status":"publish","type":"post","link":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/gene-editing-used-to-treat-rare-genetic-disorder\/","title":{"rendered":"Gene editing used to treat rare genetic disorder"},"content":{"rendered":"

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Patient Eddie Axelson, 9, and his mom, Tanya Axelson, play with Legos as Kim Bettis, RN, prepares to give Eddie the first-ever dose of LogicBio Therapeutics\u2019 single-administration gene editing therapy for an inborn metabolic condition called Methylmalonic Acidemia. Photo by Erin O. Smith.<\/figcaption><\/figure>\n

A 9-year-old patient of Monroe Carell Jr. Children\u2019s Hospital at Vanderbilt is the first in the world to receive an investigational gene editing therapy for Methylmalonic Acidemia (MMA), a rare genetic disorder diagnosed at birth.<\/p>\n

On May 29, Eddie Axelson, of Clarksville, Tennessee, received LogicBio Therapeutics\u2019 investigational single-administration targeted gene editing therapy, hLB-001, which seeks to correct MMA, an inborn metabolism disorder in which the body cannot properly process protein from food.<\/p>\n

Axelson received the dose of hLB-001, administered via IV infusion, as part of LogicBio\u2019s SUNRISE multicenter clinical trial. The study will assess the safety, tolerability and effectiveness of this potential gene editing therapy for MMA.<\/p>\n

The investigational gene therapy, created by LogicBio Therapeutics, also marks the first-ever such genetic therapy administered for a biochemical disorder at Children\u2019s Hospital and Vanderbilt University Medical Center.<\/p>\n

\u201cThis is a gene editing trial in which we use a harmless virus to transport the missing gene into liver cells, so that the liver cells will start producing the deficient enzyme to correct the defect in body chemistry,\u201d said Thomas Morgan, MD, associate professor of Pediatrics and Genetics and lead principal investigator for the study at Vanderbilt.<\/p>\n

People with MMA have too much methylmalonic acid in their blood because their livers can\u2019t break down certain fats and protein building blocks, specifically four amino acids known by the acronym VOMIT (valine, odd chain fatty acids, methionine, isoleucine and threonine).<\/p>\n

Currently, the only treatment is to restrict protein in a patient\u2019s diet and to provide a special formula without the four amino acids.<\/p>\n

\u201cWhile the current treatment is usually adequate, it\u2019s not good enough to keep kids from getting sick or potentially needing a liver transplant or a combined kidney and liver transplant later in life,\u201d Morgan said. \u201cIf this works, it could alter the DNA in the liver so that it fixes the problem for the rest of the patient\u2019s life, potentially sparing them the need for a transplant in the future.\u201d<\/p>\n

The hLB-001 gene editing therapy is designed to use an engineered adeno-associated virus to precisely deliver a working copy of the mutase gene to the patient\u2019s hepatocytes and integrate it right next to another gene called albumin, the most highly active gene in the liver. In this way, albumin drives the production of the mutase enzyme, with the goal of replacing enough mutase activity to improve the patient\u2019s metabolic status.<\/p>\n

MMA is diagnosed at birth through the state\u2019s newborn screening \u2014 a simple heel stick blood sample at birth used to check for numerous diseases. Tennessee currently screens for 71 conditions, including MMA. In the first few days of life, a newborn\u2019s symptoms can include vomiting, dehydration, weak muscle tone, lethargy and failure to thrive. MMA occurs in about 1 in 50,000 live births, affecting males and females from all demographics.<\/p>\n

Children can see long periods of stability where the acid levels can be controlled. But if they get a viral infection, they can become extremely sick and often need intensive care in the hospital. Long-term consequences of the disorder can include damage to all organs, including the brain, liver and kidneys.<\/p>\n

Children\u2019s Hospital is one of seven sites participating in the SUNRISE trial, which seeks to enroll eight patients over the study period.<\/p>\n

Eligible participants are children with MMA, whose MMA is caused by a mutation in the methylmalonyl-CoA mutase gene, or MMUT, and who are 6 months to 12 years of age. Initially, the trial will start with patients ages 3 to 12 years old.<\/p>\n

Patients must be in stable health for two months prior to enrolling. Following infusion, participants in the trial will have regular screening follow-ups. \u00a0\u2013\u00a0Christina Echegaray<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

  A 9-year-old patient of Monroe Carell Jr. Children\u2019s Hospital at Vanderbilt is the first in the world to receive an investigational gene editing therapy for Methylmalonic Acidemia (MMA), a rare genetic disorder diagnosed at birth. On May 29, Eddie Axelson, of Clarksville, Tennessee, received LogicBio Therapeutics\u2019 investigational single-administration targeted gene editing therapy, hLB-001, which…<\/p>\n","protected":false},"author":205,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"_links_to":"","_links_to_target":""},"categories":[43,20],"tags":[],"class_list":["post-3281","post","type-post","status-publish","format-standard","hentry","category-vm-fall-2021","category-vm-related-content"],"acf":[],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/pcDnub-QV","_links":{"self":[{"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/posts\/3281","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/users\/205"}],"replies":[{"embeddable":true,"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/comments?post=3281"}],"version-history":[{"count":1,"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/posts\/3281\/revisions"}],"predecessor-version":[{"id":3283,"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/posts\/3281\/revisions\/3283"}],"wp:attachment":[{"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/media?parent=3281"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/categories?post=3281"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/medschool.vanderbilt.edu\/vanderbilt-medicine\/wp-json\/wp\/v2\/tags?post=3281"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}