Chen Hu (physician) explained

Chen Hu (; 17 February 1962 – 24 July 2019) was a Chinese military physician and stem cell researcher. He served as Director of the PLA Institute of Hematopoietic Stem Cell Research and the Beijing Hematopoietic Stem Cell Therapy Laboratory. Known for his research on hematopoietic stem cell therapy for leukemia, he was awarded the State Science and Technology Progress Award (First Class) in 2015 and the Ho Leung Ho Lee Prize in 2016. In 2017, he and Deng Hongkui engineered resistance to HIV in mice using CRISPR gene editing, and for the first time used the technique on an AIDS patient. He died of a sudden heart attack before their findings were published.

Biography

Chen Hu was born 17 February 1962 in Chongqing, China, with his ancestral home in Luoyang, Henan. He enlisted in the People's Liberation Army (PLA) in September 1979 and enrolled at the Third Military Medical University (now Army Medical University).[1] [2] He earned both a Ph.D. and an M.D.

After graduation, Chen became a physician at the Affiliated Hospital of the Academy of Military Medical Sciences. He later served as Director of the Beijing Hematopoietic Stem Cell Therapy Laboratory and Director of the PLA Institute of Hematopoietic Stem Cell Research at the Fifth Medical Center (formerly the 307 Hospital) of the People's Liberation Army General Hospital in Beijing.

Chen spent more than 30 years researching treatment for leukemia, with a focus on hematopoietic stem cell (HSC) therapy. He treated more than 40,000 patients and performed over 3,200 HSC transplants, improving the survival rate from nearly 0% at the beginning to 65%. In 2015, his research on the treatment of radiation damage using adult stem cells won the State Science and Technology Progress Award (First Class). A year later, he won the Ho Leung Ho Lee Prize for Science and Technology Progress.

In 2017, Chen and his collaborator, Deng Hongkui of Peking University, used CRISPR gene editing to transplant human HSCs with the edited CCR5 gene to mice, and conferred HIV resistance to the animals.[3] 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.[4] [5] 19 months later, the patient's ALL was in complete remission. 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%.[6] Their research was published in The New England Journal of Medicine in September 2019, after Chen had died.[7]

On 24 July 2019, Chen Hu died from a sudden heart attack in Beijing, aged 57. At the time of his death he was a candidate for election to the Chinese Academy of Sciences.[8]

Notes and References

  1. Web site: 痛惜!全军造血干细胞研究所所长陈虎离世,仅57岁. 26 July 2019. Jiankang Shibao (Health Times). live. https://web.archive.org/web/20190922084236/http://www.jksb.com.cn/html/news/headlines/2019/0726/138881.html . 22 September 2019 . 22 September 2019.
  2. Web site: 解放军总医院第五医学中心教授陈虎逝世,享年57岁. Yue. Huairang. 26 July 2019. The Paper. live. https://web.archive.org/web/20190922084236/https://www.thepaper.cn/newsDetail_forward_4011979 . 22 September 2019 . 22 September 2019.
  3. Web site: Resistance to HIV Engineered Via CRISPR. Azvolinsky. Anna. 3 August 2017. The Scientist Magazine. live. https://web.archive.org/web/20180908181219/https://www.the-scientist.com/daily-news/resistance-to-hiv-engineered-via-crispr-31137 . 8 September 2018 . 22 September 2019.
  4. Web site: Chinese scientists use CRISPR tool on HIV patient for the first time. Julie Zaugg and Serenitie Wang. 13 September 2019. CNN. live. https://web.archive.org/web/20190913100049/https://www.cnn.com/2019/09/13/health/china-crispr-hiv-intl-hnk/index.html . 13 September 2019 . 22 September 2019.
  5. Web site: CRISPR编辑干细胞治疗HIV和急性淋巴细胞白血病患者. 12 September 2019. Sciencenet. live. https://web.archive.org/web/20190922090948/http://news.sciencenet.cn/htmlpaper/2019/9/20199121694142952412.shtm . 22 September 2019 . 22 September 2019.
  6. Web site: In a CRISPR first, therapy aiming to cure HIV patient appears safe. Begley. Sharon. 11 September 2019. STAT. live. https://web.archive.org/web/20190913003657/https://www.statnews.com/2019/09/11/in-a-crispr-first-therapy-intended-to-cure-hiv-patient-appears-safe-though-ineffective/ . 13 September 2019 . 22 September 2019.
  7. Xu. Lei. Wang. Jun. Liu. Yulin. Xie. Liangfu. Su. Bin. Mou. Danlei. Wang. Longteng. Liu. Tingting. Wang. Xiaobao. 11 September 2019. CRISPR-Edited Stem Cells in a Patient with HIV and Acute Lymphocytic Leukemia . New England Journal of Medicine . 381. 13. 1240–1247. 10.1056/NEJMoa1817426. 31509667. free.
  8. Web site: 院士候选人陈虎去世!生前正研究基因编辑治疗艾滋病. Zhang Wenkang 张文康. 28 July 2019. Sina. live. https://web.archive.org/web/20190922084235/https://med.sina.com/article_detail_103_2_69154.html . 22 September 2019 .