US approves CRISPR gene-editing to treat sickle cell disease | Health - Hindustan Times
close_game
close_game

US approves CRISPR gene-editing to treat sickle cell disease

By | Posted by Krishna Priya Pallavi
Dec 10, 2023 12:35 PM IST

The treatment for sickle cell disease uses the revolutionary gene-editing tool CRISPR to permanently change DNA in the patient's blood cells.

The United States Food and Drug Administration (FDA) Friday approved a landmark gene-editing treatment for sickle cell disease. The US drug regulator "approved two milestone treatments, Casgevy and Lyfgenia, representing the first cell-based gene therapies for the treatment of sickle cell disease," it said in a statement.

A genetic mutation causes cells to become sickle or crescent-shaped, which can block blood flow. (DW/NCATS/AP/picture alliance)
A genetic mutation causes cells to become sickle or crescent-shaped, which can block blood flow. (DW/NCATS/AP/picture alliance)

As DW reported last month, Exa-cel, using the brand name Casgevz, is based on CRISPR, a Nobel Prize-winning gene editing tool, used to snip patients' DNA.

Hindustan Times - your fastest source for breaking news! Read now.

Casgevy was also approved by Britain's Medicines and Healthcare Products Regulatory Agency last month.

What is sickle cell disease?

"Sickle cell disease is a rare, debilitating and life-threatening blood disorder with significant unmet need," the FDA's Dr. Nicole Verdun said in a statement announcing the approvals.

"We are excited to advance the field especially for individuals whose lives have been severely disrupted by the disease."

In the US, an estimated 100,000 people have the disease, and globally, it affects more than 7.7 million people, primarily people of African or Caribbean descent.

(Also Read | Sleep deprivation and vertigo: Here's how lack of sleep can impact balance)

Sickle cell patients have elongated blood cells resembling sickles rather than normal blood cells' typical donut shape. These misshaped cells can get stuck in the blood vessels and block the oxygen supply, causing patients to experience excruciating pain, strokes, and organ damage.

How does the Casgevy gene editing tool work?

The new medication, Casgevy, targets the problematic gene in a patient's bone marrow stem cells. It results in the production of properly functioning hemoglobin, the protein in red blood cells that carries oxygen, in the body.

Patients first receive a course of chemotherapy before doctors take stem cells from the patient's bone marrow, and then those cells are treated with the medication in a lab, which, using the CRISPR gene editing tool, essentially cuts out the sections of DNA that cause the sickle shape.

The treated stem cells are reintroduced into the body.

Gene therapy treatments can cost millions of dollars and experts have raised concerns that they could remain out of reach for the people who would benefit most.

The other treatment approved by the FDA, Lyfgenia, utilizes a harmless virus to insert a gene into patients' stem cells.

Before Casgevy and Lyfgenia were approved treatments included medications and blood transfusions.

The only permanent solution was a bone marrow transplant, which must come from a closely matched donor without the disease and brings a risk of rejection.

Catch your daily dose of Fashion, Health, Festivals, Travel, Relationship, Recipe and all the other Latest Lifestyle News on Hindustan Times Website and APPs
SHARE THIS ARTICLE ON
Share this article
SHARE
Story Saved
Live Score
OPEN APP
Saved Articles
Following
My Reads
Sign out
New Delhi 0C
Wednesday, February 28, 2024
Start 14 Days Free Trial Subscribe Now
Follow Us On