FIRST SICKEL CELL PATIENT CURED

For the first time, a 13-year-old patient has been ‘cured’ of sickle cell anaemia after gene therapy allowed complete remission of clinical symptoms of disease and correction of biological signs.

Gene therapy is the introduction of normal genes into cells in place of missing or defective ones in order to correct genetic disorders. The result of the study published yesterday in the New England Journal of Medicine is quite significant since Nigeria has the highest prevalence of sickle cell disease in the world with over 40 million Nigerians carrying the genes.

It is believed that when the gene therapy is fully deployed, the patients would no longer have to battle recurrent pain and complications caused by the disease, which could interfere with many aspects of the patient’s life, including education, employment and psychosocial development.

A team led by Pr. Marina Cavazzana conducted at Necker Children’s Hospital, AP-HP and the Imagine Institute (AP-HP / Inserm / Université Paris Descartes) in October 2014 gene therapy in the context of a phase I clinical trial / II in a 13-year old patient with severe sickle cell disease.

Conducted in collaboration with Pr. Philippe Leboulch (CEA / University Faculties of Medicine of Paris-Sud and Harvard University) who developed the innovative treatment, vector used and directed the preclinical studies.

Scientists had in September 2016 reported that gene therapy for sickle cell disease passed key preclinical test. Researchers from Dana-Farber/Boston Children’s Cancer and Blood Disorders Centre, United States (U.S.), had reported in the Journal of Clinical Investigation that a precision-engineered gene therapy virus, inserted into blood stem cells that are then transplanted, markedly reduced sickle-induced red-cell damage in mice with sickle cell disease.

Sickle-cell disease (SCD) is a genetic blood disorder that affects the haemoglobin within the red blood cells. This disease causes episodes of very severe pain caused by vaso-occlusive crisis. It also causes lesions of all vital organs, sensitivity to infections, as well as iron overload and endocrine disorders.

According to the World Health Organisation (WHO), in countries such as Cameroon, Republic of Congo, Gabon, Ghana and Nigeria, the prevalence is between 20 per cent and 30 per cent while in some parts of Uganda it is as high as 45 per cent.