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对人类体外受精胚胎进行种系基因组编辑需要严格的标准。

Stringent criteria needed for germline genome editing of human IVF embryos.

机构信息

Singapore Fertility and IVF Consultancy Pvt Ltd, 531A Upper Cross Street, #04-95, Hong Lim Complex, Chinatown, 051531, Singapore.

Department of Obstetrics and Gynecology, Kisangani University Hospital, Kisangani, Democratic Republic of the Congo.

出版信息

J Assist Reprod Genet. 2024 Jul;41(7):1727-1731. doi: 10.1007/s10815-024-03125-6. Epub 2024 May 2.

DOI:10.1007/s10815-024-03125-6
PMID:38695986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11263300/
Abstract

Germline genome editing of IVF embryos is controversial because it is not directly health or lifesaving but is intended to prevent genetic diseases in yet-unborn future offspring. The following criteria are thus proposed for future clinical trials: (i) Due to medical risks, there should be cautious and judicious application while avoiding any non-essential usage, with rigorous patient counseling. (ii) Genome editing should only be performed on the entire batch of IVF embryos without initial PGT screening if all of them are expected to be affected by genetic disease. (iii) When there is a fair chance that some IVF embryos will not be affected by genetic diseases, initial PGT screening must be performed to identify unaffected embryos for transfer. (iv) IVF embryos with carrier status should not undergo germline genome editing. (v) If patients fail to conceive after the transfer of unaffected embryos, they should undergo another fresh IVF cycle rather than opt for genome editing of their remaining affected embryos. (vi) Only if the patient is unable to produce any more unaffected embryos in a fresh IVF cycle due to advanced maternal age or diminished ovarian reserves, can the genome editing of remaining affected embryos be permitted as a last resort.

摘要

体外受精胚胎的种系基因组编辑存在争议,因为它不是直接针对健康或挽救生命的,而是旨在预防尚未出生的未来后代的遗传疾病。因此,提出了以下未来临床试验的标准:(i) 由于存在医疗风险,应谨慎、明智地应用,避免任何非必要的用途,并进行严格的患者咨询。(ii) 如果所有的体外受精胚胎都预计会受到遗传疾病的影响,那么基因组编辑应该仅在没有初始 PGT 筛选的情况下对整个胚胎批次进行。(iii) 如果有一定的机会一些体外受精胚胎不会受到遗传疾病的影响,那么必须进行初始 PGT 筛选,以识别未受影响的胚胎进行转移。(iv) 携带状态的体外受精胚胎不应进行种系基因组编辑。(v) 如果患者在转移未受影响的胚胎后未能怀孕,他们应该进行另一个新鲜的体外受精周期,而不是选择对剩余受影响的胚胎进行基因组编辑。(vi) 只有在由于母亲年龄较大或卵巢储备减少,患者在新鲜的体外受精周期中无法产生更多的未受影响的胚胎的情况下,才允许对剩余受影响的胚胎进行基因组编辑作为最后的手段。

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J Assist Reprod Genet. 2024 Jul;41(7):1733-1737. doi: 10.1007/s10815-024-03174-x. Epub 2024 Jul 5.

本文引用的文献

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Nat Med. 2024 Jan;30(1):30-32. doi: 10.1038/s41591-023-02681-1.
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Intrinsic deletion at 10q23.31, including the gene locus, is aggravated upon CRISPR-Cas9-mediated genome engineering in HAP1 cells mimicking cancer profiles.在模拟癌症特征的 HAP1 细胞中,经 CRISPR-Cas9 介导的基因组工程处理后,10q23.31 处的内在缺失(包括 基因座)加剧。
Life Sci Alliance. 2023 Nov 20;7(2). doi: 10.26508/lsa.202302128. Print 2024 Feb.
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Don't Ask Too Much: Non-maleficence as the Guiding Principle in IRB Decision-Making.别要求太多:不伤害原则作为机构审查委员会决策的指导原则。
Am J Bioeth. 2023 Jun;23(6):124-126. doi: 10.1080/15265161.2023.2201221.
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