University Maternal Hospital, Research Group for Reproductive Medicine and IVF-Laboratory, Department of Obstetrics and Genecology, Cologne University, Cologne, Germany.
University Maternal Hospital, Research Group for Reproductive Medicine and IVF-Laboratory, Department of Obstetrics and Genecology, Cologne University, Cologne, Germany.
Cryobiology. 2020 Apr;93:115-120. doi: 10.1016/j.cryobiol.2020.01.022. Epub 2020 Jan 31.
Cancer is the second major cause of death in the world. The problem of post-cancer infertility plays a significant role, because chemotherapy can be gonadotoxic. Cryopreservation of ovarian tissue before cancer therapy with re-implantation after convalescence is the potential key solution to this problem. The aim of this study was to test the viability of cryopreserved human ovarian cortex after long-term cooling in culture medium composed of permeable cryoprotectants. Ovarian fragments from sixteen patients were randomly divided into two groups. After the operation, tissue pieces assigned to both groups were cooled to 5 °C for 22-24 h, frozen and thawed. Group 1 pieces (n = 32) were cooled before cryopreservation in the standard culture medium, and Group 2 pieces (n = 32) were cooled in the freezing medium (culture medium+6% ethylene glycol+6% dimethyl sulfoxide+0.15 M sucrose). Freezing was performed in standard 5 ml cryo-vials with ice formation at -9 °C, cooling from -9 to -34 °C at a rate of -0.3 °C/min and plunging at -34 °C into liquid nitrogen. After thawing in a 100 °C (boiling) water bath, the removal of cryoprotectants was performed in 0.5 M sucrose with 20 min exposure in sucrose and 30 min stepping rehydration. The effectiveness of the pre-freezing cooling of tissue was evaluated by the development of follicles (histology). Six months after the autotransplantation, oocytes from the twenty-seven-year old, hormonally stimulated patient were retrieved and fertilized with her partner sperm through the intracytoplasmic spermatozoa injection (ICSI). For groups 1 and 2, 93.5 ± 1.9% and 96.4 ± 2.0% of the preantral follicles, respectively, were morphologically normal (P > 0.1) (with a tendency toward increasing in quality in Group 2). Six months after the auto-transplantation, two ICSI cycles resulted in the gathering and transplantation of high quality embryos, but no pregnancy had been established. Thirteen months after the auto-transplantation, the patient became spontaneously pregnant and delivered a healthy baby girl at term. Long-term (24 h) cooling of ovarian tissue to 5 °C before cryopreservation in the presence of permeable cryoprotectants simplifies the protocol of cryopreservation and has a tendency of increasing of the cells viability after thawing.
癌症是世界上第二大死亡原因。癌症后不孕的问题起着重要作用,因为化疗可能具有性腺毒性。在癌症治疗前冷冻保存卵巢组织,在康复后再进行再植入,这是解决这个问题的潜在关键方法。本研究的目的是测试在由可渗透的冷冻保护剂组成的培养基中长时间冷却后冷冻保存的人类卵巢皮质的活力。将来自 16 名患者的卵巢组织片段随机分为两组。手术后,两组的组织切片分别在 5°C 下冷却 22-24 小时,然后冷冻和解冻。第 1 组(n=32)的组织在冷冻保存前在标准培养基中冷却,第 2 组(n=32)的组织在冷冻培养基(培养基+6%乙二醇+6%二甲基亚砜+0.15M 蔗糖)中冷却。使用标准的 5ml 冷冻小瓶进行冷冻,在-9°C 时形成冰晶,以 0.3°C/min 的速度从-9°C 冷却至-34°C,然后在-34°C 时浸入液氮中。在 100°C(沸水)水浴中解冻后,在 0.5M 蔗糖中去除冷冻保护剂,在蔗糖中暴露 20 分钟,然后进行 30 分钟的逐渐复水。通过评估卵泡的发育(组织学)来评估组织的预冷冻冷却效果。在 27 岁的接受激素刺激的患者的自体移植后 6 个月,从卵巢中取出卵母细胞,并通过胞浆内精子注射(ICSI)与她的伴侣精子受精。对于第 1 组和第 2 组,分别有 93.5±1.9%和 96.4±2.0%的原始卵泡形态正常(P>0.1)(第 2 组的质量有增加的趋势)。在自体移植后 6 个月,两次 ICSI 周期收集和移植了高质量的胚胎,但未建立妊娠。在自体移植后 13 个月,患者自然怀孕并足月分娩一名健康女婴。在存在可渗透的冷冻保护剂的情况下,将卵巢组织在 5°C 下长时间(24 小时)冷却,然后再进行冷冻保存,简化了冷冻保存方案,并在解冻后具有增加细胞活力的趋势。