In 2017, Deng and his collaborator, Chen Hu of the 307 Hospital, used CRISPR gene editing to transplant human hematopoietic stem cells with the edited CCR5 gene to mice, and conferred HIV resistance to the animals.[7] They subsequently used the technique to treat an AIDS patient who suffered from acute lymphoblastic leukemia (ALL). It was the first time CRISPR was used on a human HIV patient.[8][6] 19 months later, the patient's ALL was in complete remission.[8] Their research demonstrated the safety of CRISPR for humans, although the therapy was not effective for curing AIDS as only 5% to 8% of the patient's bone marrow cells carried the edited CCR5 gene, much lower than the ideal 100%.[4] Their findings were published in The New England Journal of Medicine in September 2019.[9]
References
^ abc"Hongkui Deng". Peking University. Archived from the original on 16 December 2017. Retrieved 23 September 2019.
^ ab"邓宏魁". Peking University School of Life Sciences. Archived from the original on 28 April 2019. Retrieved 23 September 2019.
^Cong Lanlan 丛兰兰 (24 June 2003). "北大生命科学院教授邓宏魁:北大加紧抗非研究". People's Daily. Archived from the original on 23 September 2019. Retrieved 23 September 2019.