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Disease · Blood disorders

Beta Thalassemia

An inherited disorder in which the body makes too little beta-globin, leaving many patients dependent on blood transfusions for life — and the second condition with an approved CRISPR therapy.

Approved bloodapprovedHBB
Approved treatment At least one medicine using this approach has been authorised by a national regulator for this use.

Simple explanation

Haemoglobin is built from two kinds of protein chain. In beta thalassemia the beta chains are made in far too small an amount, so haemoglobin cannot be assembled properly and red blood cells fail. The severe form means a transfusion every few weeks, for life, and iron builds up from those transfusions until it damages the heart and liver. The same CRISPR therapy approved for sickle cell disease is also approved here, and it works the same way: by switching fetal haemoglobin back on.

Go deeper

Beta thalassemia results from HBB mutations reducing (β+) or abolishing (β0) beta-globin synthesis. Unpaired alpha chains precipitate, causing ineffective erythropoiesis and haemolysis. Transfusion-dependent disease requires lifelong transfusion with iron chelation. Reactivating fetal haemoglobin through BCL11A enhancer disruption restores functional haemoglobin tetramers independent of beta-globin, which is why the same intervention serves both conditions.

How common it is

Beta thalassemia is most common around the Mediterranean, in the Middle East, South and Southeast Asia. As with sickle cell disease, carrier frequency is elevated in historically malaria-endemic regions. Estimates of transfusion-dependent cases worldwide run into the hundreds of thousands, and the distribution again means most patients live where a cell-therapy infrastructure does not exist.

Gene editing status

Casgevy is approved for transfusion-dependent beta thalassemia in patients 12 and over, in the United States and several other jurisdictions. In trials, the great majority of participants became transfusion-independent. A separate approved gene-addition therapy, Zynteglo, delivers a functional beta-globin gene by lentiviral vector rather than editing — the same disease treated by two genuinely different approaches, which makes it one of the clearest illustrations of the distinction.

Gene editing status
Haemoglobin assembling from its subunits — the step that fails in this disease. Illustration generated for The CRISPR Atlas — a visual aid, not a photograph or a literal depiction of molecular structure.

Current standard of care

Regular transfusion with iron chelation, luspatercept in some patients, and allogeneic transplant where a matched donor is available. Iron overload management is the long-term determinant of outcome for most transfusion-dependent patients.

Sources

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Educational information only This page is a reference, not medical advice. Research and regulatory status change; check the last-updated date above and confirm anything important against the primary sources listed.