Laparoscopic uterine graft procurement and surgical autotransplantation in ovine model

Currently, uterus transplantation (UTx) is a clinical option for infertile women. Over the past three decades, treating benign or malignant gynecological diseases with minimally invasive gynecological surgery has improved, providing significant advantages over conventional open surgery. This study addresses the method used for laparoscopic live-donor ovariohysterectomy and graft harvest from a sheep model. Using a microsurgical practice, ten grafts were autotransplanted after uterine perfusion. End-to-end anastomosis techniques were used to approximate veins and arteries. Follow-ups were carried out 2-months after surgery and postoperative studies included ultrasound scan, diagnostic hysteroscopy, vascular angiography, and exploratory laparoscopy. All transplants were completed without complications. After vascular anastomosis, total reperfusion of the tissue was accomplished in all animals without confirmation of arterial or venous thrombosis. Angiographic explorations did not show any statistically significant dissimilarity in the arterial diameters between the different examination times. 3-months after uterine transplantation all animals underwent assisted reproduction techniques. Patent uterine arteries were observed 4, 8 and 12 months after the transplant. 6-months after transplantation, six sheep (60%) became pregnant with assisted reproduction practices. We noticed an increase in the degree of fibrosis of the cervix samples in non-pregnant animals of the transplant group. Laparoscopic surgery can be an advantageous approach for the uterus retrieval procedure during uterine transplantation. However, larger sample sized reports are needed in order to accomplish validation, standardization and wider use of this route.


Methods
Animals and experimental design. The Animal Welfare Ethics Committee of the Minimally Invasive Surgery Centre, endorsed all the preliminary protocols, which totally adhered the recommendations defined by the local government (Junta de Extremadura) and the EU Directive (2010/63/EU), concerning the utilization of laboratory animals for scientific purposes as well as Spanish laws (RD 53/2013), ARRIVE rules and the Guide for Care and Use 17 .
A total of 15 fertile female domestic merine sheep (Ovis orientalis aries) weighing 40-50 kg were used for this study. All ewes aged 2-3 years old and were pregnant at least once in their life. Sheep were housed in groups of five, and they were given water ad libitum and a standard eating regimen once every day. A basic physical and hematological examination (complete blood count, biochemical analysis) was carried out preoperatively, reporting the animals to be in sound condition before experiencing medical procedure. It was forced overnight fasting for 24 h, yet free admission of water was permitted up to 4-6 h before the procedure.
The animals were arbitrarily splitted into two groups; a control group (CG) of five non-transplanted ewes and an autotransplantation group (AG) of ten individuals.
Anesthesia and monitoring. The animals received intravenous (IV) induction with propofol 6 mg/kg (Propofol Sandoz 10 mg/ml; Sandoz Farmacéutica S.A., Madrid, Spain) after preoxygenation during 5 minutes, the day the surgeries took place. A cuffed endotracheal tube I.D. no. 9 mm was used to intubate the trachea, and the lungs were kept up in normocapnia by mechanical ventilation by a closed circle anesthetic breathing system (Maquet Flow-i, Maquet Critical Care AB, Solna, Sweden), that lead to a 14 breaths/minute respiratory rate. For anesthetic maintenance, all animals received sevoflurane (Sevorane; Abbott Laboratories, Madrid, Spain) at 1.4 minimum alveolar concentration (MAC) (EtSEV = 3.7%) in oxygen (fresh gas flow 1 litre/minute, FiO2 = 0.5).
Baseline angiography. The animals underwent a selective basal angiography of the uterine arteries the same day of surgery. Under general anesthesia, the ewes were secured in recumbent position on the angiography table, limbs extended cranially and caudally. The abdomen and crotch region were prepared and covered in a sterile manner. The femoral arterial access on either side was established using a modified Seldinger method. The femoral artery (right or left) was perforated with a puncture needle (Entry Needle 18 g × 2-3/4, AngioDynamics, New York, United States) further to the incision made with a scalpel blade (No. 11) at approximately 1 cm caudal to the inguinal ligament. Immediately after the arterial blood return from the needle was seen, a guide wire of a 5Fr introducer sheath set (Check-flo; William Cook Europe, Bjaeverskov, Denmark) was inserted into the femoral artery. The needle was removed whereas the guide wire was maintained in the femoral artery. The 5Fr sheath with dilator was placed in the artery over the guide wire, and then the dilator and guide wire were pulled out, leaving the sheath in place.
With fluoroscopic guidance (BV Pulsera, Philips Healthcare, Best, Netherlands), a 5Fr selective catheter (Sos Omni-I, AngioDynamics, New York, United States) together with a 0.035″ guide wire (Glidewire ® , Terumo Medical, Tokio, Japon) was inserted through the percutaneous vascular access to the contralateral external iliac artery. After the guide wire removal, the angiographic catheter was turned and pushed into the abdominal aorta, where the distal end of the catheter was restored to its original configuration. A global angiography was done in the pelvis by manual infusion of 10 ml of contrast agent (76%, Urografin ® , Bayer Pharma AG, Berlin, Germany) in www.nature.com/scientificreports www.nature.com/scientificreports/ the standard back-front position, so as to demonstrate the vascular system of the respective bilateral external and internal iliac arteries and their branches. The angiographic catheter was specifically placed into the internal iliac arteries on both sides, respectively, with the tip of the catheter immediately cranial to the segment where the uterine artery originates. Selective angiography was performed with 5 ml manual injection of the contrast medium, by using the ipsilateral anterior oblique projection of 25°-30°. The catheter and sheath were removed after angiography and hemostasis was obtained by hand compression at the puncture site for 10 minutes. Immediately after, the animals were ready to undergo the transplantation surgery. surgical technique. Uterine graft laparoscopic procurement. Carbon dioxide (pneumoperitoneum) was insufflated in the abdomen by a Veress needle. An automatic insufflator maintained intraabdominal pressure at 12 mmHg (Electronic Endoflator, Karl Storz GmbH, Tüttlingen, Germany). At the left and right hemiabdomen, approximately 9 cm from the camera port, a 10-mm and a 5-mm trocar were placed bilaterally under direct visualization. There was another 5-mm trocar in the left iliac fossae before the animals were placed in the Trendelenburg position.
After an abdominal and reproductive tract general examination, a laparoscopic total hysterectomy with a bilateral oophorosalpingectomy was carried out. First, the uterine arteries and the utero-ovarian veins were dissected gently and exposed, using maneuvers of blunt dissection and electrocautery (Fig. 1). Secondly, all three suspensory, broad, and round ligaments were transected with a sealing device (Ligasure TM , Medtronic, Minnesota, United States). Then, the vessels were clamped with titanium clips and were cut with a laparoscopic scissor. However, five minutes prior to the vessels' occlusion, heparin was intravenously administered every hour (100UI in the first dose, and a half of the amount in the following) until the autotransplant was completed. Finally, the cervix was transected using the laparoscopic sealing device.
When the whole specimen was isolated, the optic trocar's incision was elongated in order to remove the graft.
Graft preparation. The uterus was brought immediately to a back-table, it was stored in a sterile tray and chilled with ice at 4 °C. The organ was manually flushed with chilled heparinized saline solution through each uterine artery, using a 20 G I.V. catheter until the organ was blanched and clear fluid drained from the utero-ovarian veins (Fig. 2). www.nature.com/scientificreports www.nature.com/scientificreports/ Autotransplantation surgery. To avoid a long cold ischemia period, preparatory surgery of the edges of the vessels in the patient was initiated. A surgical microscopy (OPMI ® PENTERO ® 800 de ZEISS, Oberkochen, Germany) and 8/0 non-absorbable monofilament sutures (Dafilon ® , Braun, Aschaffenburg, Germany) were required for vascular anastomosis. An end-to-end bilateral anastomosis technique with two continuous hemisutures was used to align the veins (Fig. 3), while an end-to-end bilateral anastomosis was used non-continuously to approximate the arteries (Fig. 4). Once the vascular anastomosis was completed, patency was assessed by the strip test (empty and refill test) and the color shift of the uterus, from white to reddish. The cervix was approximated to the vagina with 2/0 (Novosyn ® , Braun, Aschaffenburg, Germany) suture in a non-continuous pattern and the uterine ligaments were fixed by simple stiches to the pelvic cavity in order to avoid rotation. Finally, the incision sites for the abdominal wall and trocar were closed.
Intraoperative blood loss, complications and operative times (total dissection), laparoscopic total procurement, time of cold ischemia, of the first period of warm ischemia (I), of the second period of warm ischemia (II), total warm ischemia (I + II), and the total surgery time) were also recorded.
post-operative care and follow-up. The animals were fed the night after surgery with hay and the following days with a regular diet. All animals received analgesics as postoperative treatment: buprenorphine (0.02 mg/kg/8 h, during 2 days) and meloxicam (0.2 mg/kg/12 h, during 5 days); antibiotics: enrofloxacin (5-7,5 mg/kg/24 h, during 7 days); a stomach protector: sucralfate (1 g per day, every day) and an anticoagulant: acetylsalicylic acid (1 g per day, every day). Daily physical exams were performed during this follow -up period to detect symptoms of pain or infection. Biochemical and hematological analyses, angiography (as described previously), transvaginal ultrasound, abdominal color Doppler ultrasound, and vaginoscopy were carried out at predetermined time points (15 days, 1 month and 2 months after surgery) in order to assess the general health condition of the animal, the  www.nature.com/scientificreports www.nature.com/scientificreports/ vascular patency and viability of the graft. In addition, an exploratory laparoscopy was also performed one month after surgery.
Artificial insemination and pregnancy determination. All animals were included in this phase of the study, namely, the autotransplant group animals and the control group animals.
Three months after the surgery, the ewes were stimulated during 14 days using progesterone intravaginal sponges (Sincropart ® , Ceva Salud Animal, Barcelona, Spain). The day of sponge removal, each animal was administered with pregnant mare´s serum gonadotropin (PMSG) (Foligon ® , MSD, New Jersey, United States) to trigger ovulation. Cervical insemination with fresh semen was accomplished 55 hours after PMSG injection. The presence of pregnancy was confirmed via abdominal ultrasonography on day 40 after the artificial insemination. If the sheep was not pregnant, estrus induction and insemination were repeated once more, with a maximum of three attempts.
pregnancy follow-up and Caesarean section delivery. Daily physical exams were performed to detect any abnormalities. Fetal biparietal diameter (BPD) and renal length (RL) were measured by abdominal ultrasound at day 40, 65, 90, 115 and 140 after insemination, to monitor fetal growth and verify that it was in accordance with its gestational age. In addition, fetal heartbeat was also assessed to determine fetal viability. On estimated pregnancy day 142, under general anesthesia, both transplanted and controlled animals underwent a planned caesarean section (as described before). Vital signs were checked in the newborns, weighed and handled using standard practices of neonatal care.

post-mortem analyses and histology.
At the end of the study (2 months after delivery), all animals except for the lambs, were euthanized. Postmortem analyses were done immediately after, to look for evidence of abdominal adhesion or any lesion or abnormal tissue in the uterus. For their histological study, the uterine samples were sent to an anatomical pathology laboratory and stained with light green hematoxyline, eosin and Masson's trichrome. statistical analysis. Values are shown as single values and means ± standard deviation. Statistical analysis was conducted using SPSS 15.0 for Windows (SPSS Inc., Chicago, Illinois) statistics software. To determine the normal distribution of the samples, a Kolmogorov-Smirnov test was performed. With this condition verified, a Student's t-test was applied with a statistical significance of p ≤ 0.05 to perform a comparison between groups.
Results outcome of surgery. In all ten cases, laparoscopic procurement surgery was performed without complications. The average transplant procurement duration was 112 ± 22.79 min. The median duration of the whole operation incision to closure was 373.44 ± 47.65 min. The median cold ischaemic period was 59.11 ± 10.62 min. The median of the first phase of warm ischemia and the second phase of warm ischemia were 16.78 ± 2.05 min and 105.56 ± 19.29 min, respectively. The median time of the phase of total warm ischemia was 122.22 ± 20.22 min (Table 1).
Minimal bleeding occurred during the procedures, and the estimated loss of blood in all animals was 40 ml. All vaginal and vascular anastomosis were completed in all ten autotransplanted sheep. Recirculation of the grafts was satisfactory according to the pulsation observed through the anastomosed vessels and the colour change from pale to reddish (Fig. 5). This colour change occurred immediately, within 30 seconds to 1 min after the removal of the vascular clamps. The autotransplantation procedure was considered successful in all animals at the end of surgery. 3 after surgery the animals were in good health conditions. The median rectal temperature during the study was 39.1 ± 0.4 °C (no fever) and the same amount of food and water was consumed before and after transplantation.
In order to evaluate uterine structures, sequential transvaginal ultrasonography was performed at 2 weeks, 1 month and 2 months after surgery. In all transplanted ewes, the uterus with both horns and ovaries was identified, and the intensity of the myometrial and endometrial signals was normal, except for one animal at T2. Doppler Ultrasonography revealed no stasis in any of the vascular anastomoses, indicating that the graft had satisfactory recirculation, in nine out of ten ewes. The angiographies showed patency of all arterial anastomosis in all animals except for one at T2, which revealed a completely total lack of blood flow in the uterine arteries. In addition, one of the animals developed an aneurysm in the right uterine artery, which was observed for the first time at T2 angiography.
Vaginal examination with a hysteroscope showed a pinkish cervix and vagina and no lesion in the vaginal mucosa. As expected, it was impossible to assess the vaginal anastomosis site due to the morphologic characteristics of the ovine cervix, which does not allow a hysteroscope to pass through it. In three out of ten animals of the study, the uterine cervix was completely closed.
An exploratory laparoscopy was also performed one month after the transplant procedure. Eight animals encountered abdominal adhesions; however, in three of them the extent of adhesions was remarkable. In order to avoid damaging adjacent organs, these cases were approached with meticulous sharp dissections. The sites of vaginal and vascular anastomosis appeared to be healed completely with a filled utero-ovarian vein and a pulsating uterine artery. In addition, gross morphology, colour, texture and size of the grafts were normal in all animals except for one. The uterus of that ewe had a pale yellowish colouring, hard consistency and a fibrous appearance and belonged to the same animal that showed the abnormalities in the angiographic and ultrasound examinations. This individual was not excluded from the study but was euthanized for postmortem analysis. In the postmortem examination that followed, it was reported the arterial vasculature thrombi of this uterus.
Fertility and offspring. The nine remaining transplanted ewes and the 5 ewes of the control group underwent artificial insemination after hormonal induction.
Examinations were carried out to determine pregnancies at day 40 after insemination. In all control animals and in six out of nine transplanted ewes, the abdominal ultrasound indicated pregnancies. The values of serial fetal biparietal diameter and renal length measurements were in accordance with the fetuses' gestational age displaying no major differences between groups. Two ewes of the control group gave birth to healthful female lambs (on day 140 and 141 of pregnancy) before the planned date for caesarean section. On day 141 of pregnancy, one transplanted ewe showed signs of labour initiation with unrest behavior, regular abdominal contractions and vaginal dilation. After 8 hours, abdominal contractions stopped and a caesarean section was carried out. The fetus was dead and showed no signs of maceration or congenital malformations. The remaining pregnant animals (control and transplanted) had a cesarean section on the 142 day of gestation, all delivering a singleton pregnancy. The lambs were appropriately developed according to their estimated gestational age, sibling number (one in all  www.nature.com/scientificreports www.nature.com/scientificreports/ cases) and sex, showing vital signs. Heart rate, fetal body weight and crown-rump length were found to be similar in the newborn lambs of the control and transplanted groups, with no significant differences.

Macroscopic inspection and Histology.
There was a good correlation between the laparoscopic images obtained at one-month follow-up and the macroscopic inspection findings in the transplanted animals, with the exception that in the gross inspection we found more abdominal adhesions. In the transplanted group, including the non-pregnant ewes, macroscopically, both uterine and ovarian morphology, colour and consistency were similar to those of the control animals, and patent vascular anastomoses were found. However statistically significant differences regarding abdominal adhesions were found between the two groups, being the abdominal adhesions more remarkable in the transplanted group. All the transplanted uteri revealed minor stenosis at the vaginal anastomosis, that did not show the control group.
The histological report described a normal architecture of the uterus and cervix in the samples of both groups. No apoptosis in cell fragments, necrosis, vascular stasis, edema or arteritis were observed in any of the samples, except for one in which we observed some areas of necrosis in the endometrium (Fig. 6) and numerous macrophages full of hemosiderin (Fig. 7). This sample belonged to the pregnant transplanted animal that went into labour and finally suffered a miscarriage. Transplanted uteri revealed patchy areas of fibrosis along the uterine wall, unlike the control group.

Discussion
Recent advances in assisted reproductive technology, such as in vitro fertilization (IVF), hormone stimulation, and intracytoplasmic sperm inoculation (ICSI) have improved infertility treatments in both males and females, but women with absolute uterine factor infertility (AUFI) still remain untreated. Women suffering from AUFI either have an absence of the uterus or a malformation (acquired congenitally or surgically) that interferes with the implantation of the embryo or the ability to carry a pregnancy to term 13,18 . An estimated 1 in 500 women of  www.nature.com/scientificreports www.nature.com/scientificreports/ reproductive age experience AUFI 12 , which affects almost 1.5 million women of the world population 15,19 . The only way women with AUFI could have children until recently, was through adoption or gestational surrogacy 15 .
While many patients may be satisfied with these alternatives, adoption and gestational surrogacy might be inaccessible or unacceptable to others, due to restrictive adoption or surrogacy laws, cultural norms, personal values, or other ethical and financial reasons 20 . Thus, uterus transplantation has become a brand new potential treatment for these females with AUFI, and furthermore, the eleven live births after human uterus transplantation that have been reported [2][3][4] , are a proof of concept based on facts, for women with this kind of infertility.
After the first successful kidney transplantation 21 more than half a century ago, transplantation surgery developed extensively. In addition, the introduction of cyclosporine in the 1980s resulted in significantly improved organ transplant survival 22 . Constant progress has been made in organ transplantation, microvascular anastomosis and immunosuppressive drugs over the last decade, making it possible for organ transplantation surgery to be no longer restricted to those who depend on these vital organs to stay alive. Transplantation surgery has also extended to include other organs or tissues which will improve patients quality of life 23 such as face 24 , hand 25,26 , abdominal wall 27 , and larynx 28 transplantation. Uterus transplantation is now included within this new quality-of-life group improving transplants 19,29,30 as its main objective is to treat infertility, which is in turn linked to a deterioration of quality-of-life 31 . This case is also considered as a potentially life-giving transplantation. In addition, uterus transplantation is the first temporary organ transplantation, since the allograft would just be maintained during a given period of time, i.e., until the recipient had achieved the desired family size. So, this reduced graft time exposure would minimize the side effects of immunosuppressive medications in the long term.
Just like as other organs, transplantation of the uterus can be done with live or deceased donors, although so far the birth of a child has occurred only subsequent to living-donor transplants. A living donor is advantageous because it enables surgery to be scheduled according to optimal health conditions of both the ideal donor and the recipient. Furthermore, the operating rooms of donors and recipients can be nearby, which is relevant to substantially minimize cold ischemia time, thereby reducing the risk of graft complications after transplantation and increasing the graft survival rate. However, because a live donor's uterine procurement involves anaesthetics risks and operational complications 5,6,20,32 , we believe that uterine recovery with a minimally invasive approach would be a more appropriate ethical and safe method.
Minimally invasive surgery is often used in various medical fields, including gynaecological and transplant surgery. Several authors have proved that minimally invasive surgical techniques used for the retrieval of grafts obtained from living donors realize similar results as open surgery, while providing the donor with the additional advantages 8 . In fact, laparoscopic surgery has been commonly used in the organ procurement procedure for liver, renal, and pancreas live-donor transplantations, resulting in a safe and useful method for the donor, with a reduced hospital stay and morbidity 8 . Almost all uterus transplantation studies conducted so far, either in animal models or humans, were carried out by open surgery except for a recent single case of uteri retrieval, using robotic or laparoscopic assistance 11,33 .
The ovine model has been used by other authors in the field of uterus transplantation 42,[44][45][46][47][48][49][50][51][52][53][54] . This model is one of the most commonly developed in translational gynaecological and paediatric research and surgical education, and It is becoming a progressively reliable alternative to models of canine and non-human primates and other smaller models, such as rodents. The ovine model is not only very suitable for its reproductive functional and physiological similarities with humans 62,63 , but also for its availability, reduced cost and ethical restrictions on other species. In our case and in addition to the above, we developed an ovine model for uterus transplantation since the foetal growth in this domestic animal is well-known. This fact would allow us to evaluate the foetal development during the gestational follow-up period. It is worth noting that all these previously mentioned characteristics to describe the sheep animal model can also be attributed to the porcine model, except for the anatomy of the reproductive system. The Swedish uterus transplantation research team used a porcine model in their first efforts to achieve a large animal uterine transplant model, and the success rate was below 20% 55 . This low rates of success in pig transplants were probably due to the very small caliber of the anastomosed uterine arteries and veins, and the higher thrombosis rate associated with these sites 46,64 .
An important issue in experimental transplantation research is to prevent as many harmful events as possible resulting in failed transplantation. These potential risky events mainly concern the surgeries at organ procurement and transplantation, ischaemia-reperfusion, rejection and effects of immunosuppressive drugs. Like other authors [46][47][48][49]51,53,54 , we performed an autotransplantation to prevent the potential detrimental effects of rejection and immunosuppression, but we also assessed the feasibility of laparoscopic organ retrieval the surgical technique. The present study is the first trial performed in animal, resulting in successful orthotopic transplantation of uterine vascular anastomosis after laparoscopic graft retrieval. Several animal studies have described orthotopic autotransplantation of the uterus by either vascular anastomosis [47][48][49]51,53,54,61,65 or omentopexy 66-68 with good results. We agree, though with Dahm-Kähler et al. 46 and Wei et al. 52 who questioned whether adequate uterine blood flow would be restored in an organ of this size before major necrosis occurred, using other techniques than vascular anastomosis. Thus, omental wrapping neovascularization does not provide the conditions necessary for the normal function of the transplanted uterus. This opinion is also supported by a dog study, that showed that the autotransplanted uterus could not be saved with neovascularization through omentopexy 69 . In our study we performed an end-to-end pattern to accomplish the vascular anastomosis of the uterine vessels 44,45,52,55,56 , but this method is limited to the small number of human cases where hysterectomy is performed simultaneously to the recipient 30 . www.nature.com/scientificreports www.nature.com/scientificreports/ Another important issue in organ transplantation is the ischaemia-reperfusion damage. Transplanted organs can occur to be injured both during the ischaemic phase, when the organ is free of circulation, and when it is exposed to blood flow following prolonged ischaemia. Two warm ischaemic episodes (organ recovery and vascular anastomosis) and one cold ischaemic period (organ storage) are present. Due to the partial protection provided by the preservation solution remaining in the graft and the gradual increase in organ temperature 70 , the second warm ischaemic period is considered less harmful. Ischaemia-reperfusion injury affects transplantation success, which correlates with reduced post-transplant perfusion 71 , delayed graft function 72 , augmented rejection frequency 73 and increased chronic rejection 74 . Therefore, any possible steps should be taken to reduce the severity of this injury. During organ storage, lower temperature is used to minimize ischaemic damage and therefore reperfusion injury. In addition, the blood of the donor is flushed out and it is restored by a protecting buffer to decrease the presence of an inflammatory reaction and to provide antioxidants, metabolic precursors and colloids 75 .
In our study, following the usual guidelines for organ transplantation, we maintained the uterus at 4 °C during the back-table surgery. A number of preservation solutions are commercially available and are all designed to reduce loss of cellular homeostasis, to provide antioxidant reperfusion defence and allow for rapid rescue from ischaemic energy stores depletion 75 53 , and heparinized saline 54 have been described to be used. We used heparinized saline solution to flush the uterus and preserve it during the back-table surgery and our mean duration of the cold ischaemia and warm ischaemia were similar to those described by other authors 50,51 who performed their studies in an ovine model too. As the Swedish team did [46][47][48]50,51 we sutured the vaginal anastomosis after removing the vascular clamps in order to reduce the duration of the second warm period. Although the main processes of cellular response to hypothermia, ischemia and reperfusion are similar for all cell types 76,77 , there is a large variety of ischaemic tolerability among different organs. For instance, it has been shown in clinical practice that the kidney can endure cold ischaemia time up to 36 hours, whereas the heart is under 6 hours 30 . This difference in ischaemic tolerance and reperfusion can be attributed to a variation of organ characteristics, such as energy requirement, parenchymal cell activity and resident populations of immune-cells 47 . Recommended ischaemia times in uterus transplantation are not known yet, however, studies of uterine transplantation ischaemia-reperfusion damage show that this organ is quite resistant to ischaemia 37,47,78 .
Regarding the graft procurement total surgical time, our results showed lower values compared to those reported in a series of conventional open surgery graft retrieval in ovine model 47,51,52 . Moreover, our execution times were shorter even though our graft procurement total surgical time included specific laparoscopic surgery manoeuvres such as pneumoperitoneum creation and trocar insertion. This could indicate that laparoscopic removal of the organ in uterus transplantation reduces the total time invested in surgical graft procurement, just as Johannensson et al. 1 suggested. However, when we contrasted our results with past reports of uterus transplantation in ewes using an aortocava patch 50 , our times were higher. This may have been due to the fact that these authors harvested the whole internal reproductive organs 'en bloc' (involving the abdominal aortocava vessels, the internal iliac artery and vein, both uterine and ovarian arteries as well as utero-ovarian veins) and to the use of an endostapler to transect the sigmoid colon in order to save time for the exposure and removal of the entire intact vascular bifurcation. On the other hand, mean total surgery time (retrieval plus transplant) was lower in our study when compared with the mean total surgery times reported by Wranning et al. 47 44 and Gauthier et al. 50 who also performed the whole surgery with the open technique, our mean total surgery time is higher. This is basically because they carried out allotransplantations instead of autotransplantations. In general, performing an autotransplant takes longer time of surgery, mainly because both organ recovery and organ transplantation are performed by the same surgeon 16 .
During the surgery and the immediate postoperative period, there were no complications, a fact that highlights the surgical safety of combining the microsurgical transplantation with the laparoscopic approach.
We used angiography, transvaginal ultrasound, abdominal colour Doppler ultrasound, vaginoscopy, and exploratory laparoscopy to assess the vascular patency and graft viability. Other authors have used the ultrasound 52 , the vaginoscopy 48,50 , and the exploratory laparoscopy 52 for graft assessment; however, we are the first ones to introduce the angiography for that purpose. On the other hand, magnetic resonance imaging 50 and indocyanine green fluorescence imaging 60,79,80 have been also described to evaluate the transplanted uteri.
It is essential to mention that the expression 'successful uterus transplantation' should include restarted uterine cycle and also the complete capability for terminating the pregnancy and giving birth to live offsprings 16 . For this reason, one of the aims of our study is to determine fertility after uterus transplantation. There are only two previous reports of graft fertility after transplantation in the ovine model 44,48 . One study tested the fertility of the transplanted uteri after natural mating and pregnancy occurred in 60% of the transplanted mated ewes. These pregnancies ended up in one miscarriage and two healthy lambs 48 . In the second study, five transplanted ewes were subjected to embryo transfer. Among these, three pregnancies occurred with the outcome of one ectopic pregnancy, one miscarriage and one live birth 44 . Our fertility results were similar, but slightly better than the previously described. In our study, six of the transplanted ewes became pregnant after artificial insemination and resulted in one miscarriage and five live births. The lambs were similar in size to those of the ewes control group.
Regarding the histopathological findings, in all the samples there was an absence of necrosis, oedema, apoptotic cell fragments, vascular stasis and arteritis, which are all acute markers of cellular damage, we would like to indicate that there was no acute ischaemic and reperfusion damage in the uterus when the samples were taken. Nevertheless, the transplanted uteri showed patchy areas of fibrosis along the uterine wall when compared to the controls. This could be explained by the fact that there was an ischaemic and reperfusion injury after the transplantation surgery, as fibrosis is a chronic marker of tissue damage.