Ovarian tissue cryopreservation and transplantation: scientific implications
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After fresh or frozen ovary transplantation, FSH levels return to normal, and menstrual cycles resume by 150 days, coincident with anti-Müllerian hormone rising to higher than normal levels. AMH then returns to well below normal levels by 240 days, remaining as such for many years with nonetheless normal ovulation and fertility. To date, 20 babies have been born in our program from 11 fresh and 13 cryopreserved ovary transplant recipients with a live baby rate of over 70 % (11 babies from fresh and 9 from frozen). Globally, over 70 live births have been reported for both fresh and frozen ovary transplants with an approximate 30 % live birth rate. Given the rapid rise of AMH after the fall of FSH, with a subsequent AMH decrease with retention of ovarian function, it is tempting to speculate the existence of a shared mechanism controlling primordial follicle recruitment, fetal oocyte meiotic arrest, and recruitment in the adult ovary. With the massive recruitment of primordial follicles observed after human ovarian cortical tissue transplantation, which subsides to an extremely low recruitment rate, we will discuss how this phenomenon suggests a unifying theory implicating ovarian cortical tissue rigidity in the regulation of both fetal oocyte arrest and recruitment of follicles in the adult ovary. As the paper by Winkler-Crepaz et al. in this issue demonstrates, our in vivo results are consistent with the in vitro demonstration that primordial follicles in the fetal cortex are “locked” in development, resulting in meiotic arrest, which spares the oocytes from being rapidly lost all at once (Winkler-Crepaz et al., J Assist Reprod Genet, 1). Winkler-Crepaz et al. demonstrate that follicle loss after ovarian cortex transplantation is unlikely due to ischemic apoptosis, but rather from a “burst” of primordial follicle recruitment. In vivo, primordial follicles are normally resistant to further development or activation to prevent oocyte depletion. The dense fibrous ovarian cortex, through as yet unresolved mechanisms, arrests the further continuation of meiosis and also prevents a sudden depletion of all resting follicles in the adult ovary. Intrinsic tissue pressure is released after cortical tissue transplantation, temporarily resulting in a rapid follicle depletion. These results are consistent with the observation that once the ovarian reserve is reduced in the graft, the rate of recruitment diminishes and the ovarian tissue exhibits a relatively long duration of function.
KeywordsPrimordial follicle Oocyte recruitment Oocyte arrest Ovary transplant Cryopreservation Fertility preservation In vitro oogenesis
The developed world is in the midst of a widespread infertility epidemic. Economies in Japan, the USA, southern Europe, and even China are threatened by a decreasing population of young people having to support an increasing population of elderly and retirees . Infertility clinics are popping up throughout the world in huge numbers because of a worldwide decline in fertility as women age and become less fertile . In her teen years, a woman has a 0.2 % chance of being infertile, and by her early twenties, it is up to 2 %. By her early thirties, it is up to 20 % [2, 3]. Many modern women today do not consider having children until their mid-thirties, by which time nearly 20 % are infertile, simply due to the age-related decline in the number and quality of their oocytes. This is clearly demonstrated by the high pregnancy rate using donor oocytes from young women placed into the uterus of older women [2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12].
As important for reproductive medicine as is aging of the population and the subsequent worldwide epidemic of infertility, is the high incidence of cancer in girls and young women, curable in the majority of cases at the cost of rendering them sterile. Almost 6 % of women of reproductive age are cancer survivors. They will eventually have been sterilized by their chemotherapy or radiation [13, 14, 15, 16, 17, 18, 19, 20, 21].
Until recently, oocyte freezing had very poor to no success, and thus ovary tissue slow freezing was the only cryopreservation method we could rely upon [22, 23, 24]. More commonly now, vitrification is used instead of slow freeze for oocyte cryopreservation [25, 26, 27, 28, 29, 30, 31, 32, 33, 34]. However, many programs do not have follow-up results with oocyte freezing especially in cancer patients undergoing sterilizing chemotherapy and radiation. Furthermore, it may require several cycles of ovarian stimulation to obtain enough oocytes to give women some level of comfort, because even with fresh oocytes, there is only a 5 % pregnancy rate per egg .
As an alternative strategy for cancer patients, ovarian tissue freezing has benefits over egg freezing. In some patients, freezing ovarian tissue obviates the need to delay treatment for a stimulation cycle. Furthermore, transplanting ovarian tissue not only restores fertility but also restores endocrine function.
As important as these clinical benefits afforded by ovary cryopreservation and transplantation are, there may be even more important basic science implications to be learned about the ovary, as is evident in the current paper by Winkler et al., as well as recent papers by Silber et al. and by Hayashi et al. [36, 37, 38, 39, 40, 41, 42]. The purposes of this review are to explain the clinical employment of ovary freezing and transplantation and to delineate what we have learned about primordial follicle arrest and recruitment.
Ovarian cortex cryopreservation and transplantation
The question was raised of what effect ovary donation might have on the donors’ reproductive lifespan. This question is not just an ethical one. It impacts the whole scientific issue of primordial follicle recruitment rate related to a decrease in ovarian reserve. The potential effect of unilateral oophorectomy on both fertility and age of onset of menopause is crucial for understanding how these ovarian grafts can last so long despite a very low AMH. Gosden and colleagues in 1989 described a compensatory mechanism of follicle rescue in mice that prevented any major effect on fertility . A later study in 1992 noted that long-term ovarian function is not substantially affected by reduction of ovarian mass . Other more clinical papers also support a lack of major effect on fertility of unilateral oophorectomy in human beings, with menopause occurring only 1 or 2 years earlier than in controls. Only one study has disputed this view in rats and suggested an earlier onset of menopause after unilateral oophorectomy than in controls [55, 56, 57, 58, 59, 60, 61, 62, 63]. However, if the traditional view is correct, in which unilateral oophorectomy does not negatively affect fertility and does not hasten the onset of menopause, this would support partial or complete oophorectomy and ovarian tissue cryopreservation to expand the reproductive lifespan of normal women who wish to delay childbearing but do not want to lose their current reproductive potential. Thus, we felt comfortable in undertaking a series of fresh ovary transplants, which led the way toward improving our ovarian freezing transplantation methods [64, 65, 66]. Also, we feel confident that removing an ovary will not harm long-term fertility. Contrarily, it follows that transplanting the removed ovary could extend a woman’s reproductive lifespan.
Several techniques have been described for transplantation of the ovarian cortex [37, 43, 48, 49, 50]. In mice, Parrot used sliced little pieces of ovarian cortex. Others prepared peritoneum near the ovary but then switched to a technique similar to that described for fresh ovarian tissue . Ovarian cortical slices can also be transplanted under the surface of the cortex in the nonfunctional ovary . All these techniques have resulted in babies and there is no consensus on which is best.
Initially, there were only a few case reports, some very recently, of successful cryopreserved ovary transplantation but no unified single series [68, 69, 70, 71, 72, 73, 74, 75, 76]. However, it appears now that there is a worldwide live birth rate of over 30 to 70 %, with more than 70 babies, and long-term function of the transplant has been observed despite very low AMH. Robust results are seen in series from St. Louis, Brussels, Paris, Spain, Denmark, Israel, Japan, Italy, Germany, Australia, and Russia [77, 78]. Cryopreserved ovarian tissue grafts with the slow-freezing method as well as with vitrification are functional for more than 5 years, and many spontaneous pregnancies have been reported with no need for in vitro fertilization or other ancillary treatment. Most pregnancies were achieved without the need for in vitro fertilization and resulted instead from regular intercourse with no other treatment.
With this in mind, the remarkable long-term hormonal and ovulatory function of these cortical grafts despite extremely low AMH after the initial primordial follicle over-recruitment emphasizes the compensatory relationship of a low remaining ovarian reserve to a slower recruitment rate of primordial follicles .
The most common benefit of ovarian transplantation was previously thought to be the preservation of fertility and future endocrine function in young women undergoing cancer treatment. However, in the absence of pelvic irradiation for cancer treatment, why not use ovarian tissue cryopreservation in otherwise healthy women who wish to preserve their fertility for nonmedical reasons? With vitrification methods, there is no difference in the viability or integrity of cryopreserved ovarian tissue compared with fresh ovarian tissue . Furthermore, with cryopreserved ovarian tissue transplantation, hormonal function is restored in addition to fertility [73, 74, 75, 76, 77].
Ovarian cryopreservation techniques
In the past, all of the frozen ovary cases transplanted back to the patient have utilized the slow freeze approach [22, 23, 24, 79]. However, we now use vitrification exclusively for cryopreservation in humans because of the results of in vitro viability analysis in humans, as well as in vivo transplant studies in the bovine and human [65, 66]. Three of our successful eight pregnancies were from vitrified ovarian tissue. Five were from ovarian tissue that was frozen long ago (as early as 1996) with slow freeze.
For thaw, the protective cover is removed and the Cryotissue metal strip is immersed directly into 40 ml of 37 °C HM solution supplemented with 1.0 mol/1 sucrose for 1 min. Then, ovary tissues are transferred into 40 ml of 0.5 mol/1 sucrose HM solution for 5 min at room temperature and washed twice in HM solution for 10 min before viability analysis or transplantation. No ice crystal formation occurs during any of these vitrification procedures [65, 66].
Clinical benefit of ovarian tissue freezing: cancer, ovarian reserve, and long-term function
The most common benefit of ovarian transplant is not the unusual case of fresh grafting in identical twins but rather to protect the fertility and future endocrine function of young women undergoing treatment for cancer or other diseases that result in ovotoxicity. Since 1996, we have frozen ovary tissue for over 100 young women with cancer, or at risk for POF, of whom 16 had spare frozen tissue subjected to detailed viability testing before cryopreservation and after thaw.
The return of FSH to normal at 4 to 5 months indicates that this is the period of time required for primordial follicles, once recruited, to develop on to the antral and ovulatory stage. The concomitant rise of AMH to well over normal levels followed by a drop to very low levels indicates a massive over-recruitment of follicles and subsequent depletion. This is substantiated by the current report of Winkler-Crepaz et al. transplanting human ovarian tissue into SCID mice, demonstrating no ischemic apoptosis of follicles, but rather a massive over-recruitment . However, these transplanted slices of ovarian cortex continue to function normally for many years because of a decreased rate of primordial follicle recruitment that occurs when there is decreased ovarian reserve .
After ovarian transplantation, all patients were able to attempt natural conception every month without medical assistance. In fact, the commonly held view that egg freezing is a proven technique and ovary tissue transplantation is “experimental” is belied by the fact that most of the successful pregnancies resulting from fertility preservation in cancer patients thus far have been from frozen ovary tissue, and few at the date of this writing have come from frozen oocytes [77, 78].
At the time of this submission, we are aware of numerous other births after implanting ovarian tissue for a total of over 70 live births thus far . To date, no reports of transmission of cancer from ovarian transplants have appeared (Fig. 9). One reason for the lack of transmission may be because the dense ovarian cortical fibrous tissue, like the tunica albuginea of the testis, is an inappropriate location for cancer cells to lodge.
Another plausible clinical benefit of the massive over-recruitment occurring after ovarian cortex transplantation is the recruitment of “trapped” follicles in menopausal ovaries [83, 84]. As we have shown, a reduced ovarian reserve results in a reduced rate of primordial follicle recruitment. The point at which the ovarian reserve is so low as to preclude recruitment, a state of POF is obtained (or ovarian POI), i.e., premature ovarian failure. We speculate that autotransplanting this tissue can result in recruitment and ovulation of these few remaining follicles.
Primordial follicle recruitment and in vitro oogenesis
The ovarian cortex participates in the locking and the unlocking of the primordial follicle, and until the transplant is healed, we suspect this underlying mechanism to be disrupted. Intrinsic tissue pressure may be one mechanism at work to control primordial follicle status. The study by Winkler-Crepaz et al. provides evidence to suggest that the over-recruitment of follicles after ovarian cortical transplantation may be mediated by a biochemical mechanism via PTEN . FOXO 3 translocation into the nucleus is already recognized as one mediator of primordial follicle arrest possibly induced by intrinsic pressure gradients established in the fibrous ovarian cortex.
Going beyond this, why should the oocyte begin meiosis and then be locked for a lifetime, while sperm are constantly produced by spermatogenic stem cells? What is the benefit to the species of such a dichotomy? The benefit of this dichotomy between spermatogenesis and oogenesis is that most of the mutations that occur in a species over many years occur during spermatogenesis in the testis, as “xeroxing” errors. The oocyte is spared that risk by not having to undergo recurrent mitosis. But of course the oocyte unfortunately ages, causing infertility. These two mechanisms are wedded to each other evolutionarily. Without the mutations caused by spermatogenesis and thus constant germ cell error-prone duplication, there would be no evolution. However, without the locking of the oocyte and avoidance of constant duplication errors as what occurs in the sperm, the species would have no stability.
The oocyte’s problem clinically is that it ages. The sperm’s problem is that it is constantly making errors during cell cycle duplication. Thus, in this view, the oocyte genetically stabilizes the species, while the sperm allows for evolution by encouraging the acquisition of a mutational load. These two opposing mechanisms have to strike a balance with each other. Men remain fertile as they age but threaten the genetic stability of the species, whereas women become infertile as they age but genetically stabilize the species. Primordial follicles were designed to resist oocyte development, in order to save the oocyte, and stabilize the species.
Primordial follicle arrest is the key to saving the oocyte from disappearing after the fetal initiation of meiosis and the continuation all the way through meiosis with subsequent apoptosis. It is also the key to the cautious gradual release every month in the young adult of an average of 1000 oocytes (30 per day) to develop over 4 months into gonadotropin-sensitive antral and Graffian follicles, sparing the resting oocytes from sudden total depletion, such as what occurs briefly after ovarian transplantation.
After this depletion of resting follicles is halted, the ovarian transplant then proceeds to function for years quite well despite a very low AMH and a low remaining number of follicles. That is because as the ovarian reserve goes down, the rate of primordial follicle recruitment in a compensatory way also goes down. That is why unilateral oophorectomy does not cause much of an earlier menopause (perhaps 1 year earlier in the human) . The less the number of remaining oocytes, the better able primordial follicles are at maintaining their locking mechanism and, as a result, limiting the number of resting follicles allowed to activate and hence maintaining the follicle reserve [38, 39, 40, 41, 42].
- 2.Silber SJ. Are we infertile? Simpler treatments. In: How to get pregnant. Boston: Little, Brown; 2007. p. 87.Google Scholar
- 3.Mosher WD, Pratt WF. Fecundity and infertility in the United States, 1965–82. Advance Data. 1985.Google Scholar
- 11.Fretts RC. Effect of advanced age on fertility and pregnancy in women. Up To Date Online 2007. Available at: http://www.uptodate.com.
- 12.SART. Assisted reproductive technology success rates. National summary and fertility clinic reports. Atlanta, GA: Centers for Disease Control and Prevention, 2005.Google Scholar
- 14.Ries LAG. Cancer incidence and survival among children and adolescents: United States SEER program 1975–1995. 1999.Google Scholar
- 36.Winkler-Crepaz et al. Follicular growth after xenotransplantation of cryopreserved/thawed human ovarian tissue in SCID mice: dynamic and molecular aspects. J Assist Reprod Genet. 2016. 10.1007/s10815-016-0769-2.
- 76.Piver P, Amiot C, Agnani G, et al. Two pregnancies obtained after a new technique of autotransplantation of cryopreserved ovarian tissue. Hum Reprod. 2009;24(15):10–35.Google Scholar
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