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Successful implantation after reducing matrix metalloproteinase activity in the uterine cavity



Recently, the concept of recurrent implantation failure (RIF) in assisted reproductive technology has been enlarged. Chronic uterine inflammation is a known cause of implantation failure and is associated with high matrix metalloproteinase (MMP) activity in uterine cavity flushing. MMP activity of women with RIF has been reported to be higher than that of fertile women. In the present retrospective study we evaluated the efficacy of treatment for high MMP activity in the uterine cavity of patients with RIF.


Of the 597 patients recruited to the study, 360 patients underwent MMP measurements and 237 patients did not (control group). All patients had failed to become pregnant, despite at least two transfers of good-quality embryos. Gelatinase MMP-2 and MMP-9 activity in uterine flushing fluid was detected by enzymology (MMP test). All samples were classified into two groups (positive or negative) based on the intensity of the bands on the enzyme zymogram, which represents the degree of MMP activity. Patients who tested positive on the initial test were treated for 2 weeks with a quinolone antibiotic and a corticosteroid, and subsequently underwent a second MMP test. Negative results on the second MMP tests after treatment and subsequent rates of pregnancy and miscarriage were used to evaluate the efficacy of treatment. Data were analyzed by the Mann–Whitney U-test and the chi-square test.


Of the patients who underwent the MMP test, 15.6% had positive results (high MMP activity). After treatment, 89.3% of patients had negative results on the second MMP test. These patients had a significantly better pregnancy rate (42.0%) than the control group (26.6%), as well as a lower miscarriage rate (28.5% vs 36.5%, respectively).


A 2-week course of antibiotics and corticosteroids effectively improves the uterine environment underlying RIF by reducing MMP activity.


In recent decades, many infertile couples, who otherwise would not have been able to have children, have benefited considerably from assisted reproductive technology (ART). However, despite the selection of morphologically good embryos for transfer, there are still some women who fail to become pregnant. Recently, the concept of recurrent implantation failure (RIF) has emerged because the implantation process remains the least understood step in ART. It is known that the success of embryo implantation depends primarily on the quality of the embryos transferred. Nonetheless, embryo quality alone cannot fully explain all cases of RIF, particularly in young women, whose embryos should be of good quality [1, 2].

Uterine receptivity is another factor crucial for successful implantation. Numerous studies have sought to identify clinically useful markers to indicate a receptive uterine state. However, it is difficult to select useful molecular biomarkers associated with reproductive failure because endometrial receptivity is governed by the expression of a complex network of mediators, including cell adhesion molecules (e.g. integrins and cadherins), prostaglandins, and cytokines (e.g. leukemia inhibitory factor [LIF] and epithelial growth factor [EGF]).

Chronic endometrial inflammation is a known cause of implantation failure. Indeed, chronic and mild inflammations are often seen in unfavorable uterine conditions other than infectious diseases. For example, the number of macrophages and T cells, which mainly secrete inflammatory cytokines, is increased in the endometria of women with an implanted intrauterine device (IUD) [3], and the contraceptive activity of the IUD is brought about by the maintenance of this environment, which is unfavorable for implantation. As another example, implantation rates following IVF-ET are lower in patients with hydrosalpinx compared with rates in those with unexplained or male sterility because of the leakage of hydrosalpinx fluid (HF), which contains leukocytes and inflammatory cytokines such as interleukin (IL)-8, IL-12, IL-α, and tumor necrosis factor (TNF)-α, contributes to the deterioration of the intrauterine environment, leading to implantation failure [46]. Thus, chronic and mild uterine inflammation induces inflammatory cells and alters the expression and subtle balance of various molecules, without any overt clinical symptoms, contributing to implantation failure.

In the present study, we focused on matrix metalloproteinases (MMPs) as candidate biomarkers of chronic and mild uterine inflammation. The MMPs are a family of zinc-dependent proteolytic enzymes that play a major role in the degradation and rebuilding of the extracellular matrix (ECM), as well as in cell migration. Abnormal MMP expression is involved in the pathogenesis of autoimmune diseases, cancer, endometriosis, and other inflammatory diseases [7], although MMPs are also crucial for the normal physiology of the reproductive system [810]. Of the >20 types of MMPs, MMP-2 and MMP-9 are representative gelatinases that are present in human uterine endometrial stroma [11, 12]. Both MMP-2 and MMP-9 play an integral role in human embryo implantation and are the main rate-limiting enzymes in ECM remodeling during implantation. However, MMP-2 and MMP-9 hyperactivity is associated with an unfavorable uterine environment, similar to that seen with endometrial inflammation, because successful implantation depends on a tight balance between the activation and inhibition of MMPs [13, 14]. Inagaki et al. reported significantly higher intrauterine MMP-2 and MMP-9 activity, as well as IL-β levels, in women with RIF compared with fertile women [15]. These observations suggest that MMP activity is a sensitive biomarker of an unfavorable uterine environment for implantation, such as chronic endometritis.

Accordingly, we hypothesized that treatment of the chronic intra-uterine inflammation underlying excessive MMP activity may improve uterine receptivity for transferred embryos. Therefore, in the present retrospective study, we evaluated the efficacy of anti-inflammatory treatment, comprising of corticosteroids and antibiotics, in reducing high MMP activity in women with RIF and improving ART outcomes.



The present study was performed between July 2006 and June 2011 on 597 RIF patients (see Figure 1). All patients had undergone at least two transfers of good-quality cleavage or blastocyst-stage embryos, but had failed to become pregnant. The definition of RIF varies among different infertility clinics [16]. For example, the 2005 ESHRE PGD Consortium proposed that RIF be defined as “>3 embryo transfers with high-quality embryos or the transfer of ≥10 embryos in multiple transfers; exact numbers to be determined by each centre” [17]. In our clinic, almost 80% of embryos transferred in recent years have been blastocysts (Table 1), which has resulted in better pregnancy outcomes. In 2005, the clinical pregnancy rate at first embryo transfer in our clinic was 39.7% following the transfer of at least one good-quality embryo; the clinical pregnancy rate following a second embryo transfer (after failure of the first) was also good at 37.1%. Based on these data, in our clinic most patients whose embryos are of good quality are likely get pregnant after two embryo transfers. Therefore, in the present study we defined RIF as “≥2 embryo transfers with high-quality embryos” and recommended patients undergo an MMP test after two failed embryo transfers. In the present study, “good-quality” embryos were defined as those that were higher than Grade BB according to Gardner’s criteria [18] or higher than Grade G2 according to Veeck’s criteria [19]. In each case, one or two embryos were selected for transfer. Both fresh and vitrified–thawed embryo transfer cycles were included in the present study. A clinical pregnancy was confirmed by transvaginal ultrasound observation of a gestational sac.

Figure 1
figure 1

Flow chart of the study design. In all, 597 patients with RIF were recruited and divided into two groups based on whether or not they agreed to undergo the matrix metalloproteinase (MMP) test. Patients with MMP scores ≥5 were deemed to have a positive response (Group P) and were treated with a corticosteroid and an antibiotic for 2 weeks. Patients with low MMP scores (<5) were determined as negative (Group N). Patients in Group P were given a second MMP test after the treatment and were divided into two subgroups: Group Pr (patients who had again positive results and were considered as resistant to the treatment) and Group Pe (patients in whom the treatment was effective). Patients who did not undergo an MMP test comprised the control group (Group C). Patients in all groups underwent another embryo transfer procedure and the outcomes were compared among the four groups.

Table 1 Clinical characteristics of two patients groups, MMP test group and control group

The 597 patients included in the present study were divided into two groups based on whether they had undergone the MMP test, which measured MMP-2 and MMP-9 activity in uterine flushing fluid: 360 patients underwent the MMP test after repeated unsuccessful transfers, whereas the remaining 237 did not (Group C; control group). Of the patients who underwent the MMP test (see below), those with higher MMP activity (score ≥5; Group P) were treated for 2 weeks with an oral corticosteroid plus an antibiotic. After treatment, the patients underwent a second MMP test to evaluate the efficacy of treatment (see Figure 2). Based on the results of the second MMP test, Group P patients were further subdivided into those who were medication resistant (Group Pr) and those in whom the treatment was effective (Group Pe). All patients then underwent the next round of embryo transfers, with the outcomes evaluated in terms of the clinical pregnancy and miscarriage rates.

Figure 2
figure 2

A schedule of the MMP tests, the medication and the next embryo transfer. According to the results of the first MMP test, all the patients were divided into two groups, Group N (Panel a) and Group P (Panel b). Group P patients who had shown a positive result had a two-week treatment composed of antibiotics and corticosteroids at the next proliferative phase (panel b). After the treatment, Group P patients had the 2nd MMP test at the mid luteal phase of the same cycle, whereas Group N patients did not have the 2nd test (Panel a). In the subsequent cycle (the next cycle after the completion of the treatment), Group P patients had the next embryo transfers.

Patients ≥43 years of age were excluded from this study even if a good-quality embryo was obtained. All patients underwent transvaginal ultrasound scanning and hysterosalpingography, and those with findings suggestive of macropolyps, submucosal myomas, or anomalies of the uterine cavity were examined further by hysteroscopy. To confirm diagnoses of leiomyoma, adenomyosis, or other organic dysfunctions, magnetic resonance imaging (MRI) was often used. Endometrial biopsies were performed only in those women with abnormal genital bleeding or with findings of uterine endometrial thickening (≥15 mm). Patients diagnosed as having uterine complications, such as endometrial hyperplasia, leiomyoma, adenomyosis, or endometrial polyps, were excluded from the present study, because a previous report has already demonstrated that uterine flushing samples from women with uterine complications have higher MMP activity than samples from women without complications [20]. Patients with uterine cavity anomalies were also excluded from the study.

The present study was approved by the Ethics Committees of the Japanese Institution for Standardizing Assisted Reproductive Technology. Samples were collected only from those patients who provided informed consent.

Uterine flushing fluid

Samples were collected at the mid luteal phase, the fifth to seventh day post-ovulation, which is considered as an implantation window. The method used to irrigate the uterine cavity was as described previously [15, 2022], using an 8 Fr Foley catheter and a syringe filled with 5 mL saline solution. The catheter was first inserted into the uterine cavity through the cervix and then connected to the syringe. Subsequently, ≤5 mL saline solution was injected into the cavity and aspirated immediately without contamination by the vaginal and cervical fluids. The samples collected were centrifuged at 1000g for 10 min to remove blood corpuscles, large-sized protein molecules, and other impurities. The supernatant was collected and stored at −80°C until use.

Gelatin zymography for MMP-2 and MMP-9 activity

Gelatin zymography was performed according to methods of Fridman et al.[23], with the slight modifications of Kleiner and Stetler-Stevenson [21]. Gelatin (final concentration 1 mg/mL) was incorporated into the running polyacrylamide gel containing 10% acrylamide (Bio-Rad, CA,USA), 25% Tris buffer (1.5 mol/L, pH 8.8), 0.4% sodium dodecyl sulfate (SDS; Sigma-Aldrich Japan, Tokyo, Japan), 0.3% ammonium peroxodisulfate (APS; Sigma-Aldrich Japan, Tokyo, Japan), and 0.1% N,N,N,N-tetramethylethylendiamine (TEMED; Sigma-Aldrich Japan, Tokyo, Japan). The stacking gel contained 2% acrylamide, 25% Tris buffer (0.5 M Tris, pH 6.5), 0.4% SDS, 0.4% APS, and 0.1% TEMED, and was put on the top of the running gel. The same volume of sample buffer, consisting of 17.5% SDS, 7% sucrose, and bromophenol blue, was added to each sample. Then, 10 μL of each sample was loaded into individual wells and proteins were electrophoresed for approximately 1 h at 200 V. After electrophoresis, the gels were washed five times for 5 min each time in a Tris-based solution consisting of 3% Triton X-100 (Wako, Osaka, Japan). The gels were then washed three times and incubated for 48 h at 37°C in a solution containing 5.8% Tris–HCl, 1.7% Tris base, 0.1% NaN3, 0.7% CaCl22H2O, and 5% of 100 μM ZnCl2. After incubation, the gels were stained for 6 h with 0.1% Coomassie brilliant blue.

The presence of gelatinases (MMP-2 and MMP-9) was confirmed by their inhibition using EDTA and o-phenanthroline. Other MMPs that can be detected by casein rather than gelatin zymography (e.g. MMP-1, MMP-3, and MMP-7) were not detected in diluted fluid from the uterine cavity.

Quantitation of MMPs on zymograms

All samples were diluted 20-fold before being run on the gels. When clear bands were seen against the blue gel background, gelatinase activity was determined on the basis of the intensity of those bands. Individual bands were identified on the gels for proMMP-2, active MMP-2, proMMP-9, active MMP-9, and dimeric MMP-9. Zymograms can be quantitated by densitometric analysis, but this is accurate only at picogram levels of MMPs when the bands on the zymograms are very faint. Because of the high gelatinase activity in uterine flushing fluid, an alternative semiquantitative technique was used to assess gelatinase activity in this study, rather than densitometric measurement which can underestimate the intensity of strong bands [24]. Two independent observers scored the intensity of each band by visual inspection from 0 (no band) to 5 (very strong). A total MMP score for each sample was achieved by adding the scores for each band in that sample. To confirm the reliability of the method of evaluation, we performed preliminary studies in which three observers independently scored the intensity of bands in >100 samples. The results indicated a concordance rate of total scores ≥95%. In addition, the incidence of a ≥2 difference in total scores among the three observers was ≤2%; the incidence of a ≥3 difference in total scores was 0%. As a standard, we used the supernatant of BHK9 breast carcinoma cell culture in the present study.

MMP scoring system

A total MMP score was represented from 0 to 25 [24]. Since mean total MMP score of RIF patients was demonstrated as 5.0 ± 3.1 [15], samples with a score >4 were defined as having high MMP activity and as a positive result on the MMP test. Samples with scores of 0–4 were deemed negative. All women who tested positive were recommended to start treatment with an oral corticosteroid (prednisolone 10 mg/day; Predonisolone®; TAKEDA, Osaka, Japan) and a quinolone antibiotic (ofloxacin 300 mg/day; Tarivid®; DAIICHI SANKYO, Tokyo, Japan). Treatment lasted for 2 weeks. After the treatment period, samples of uterine flushing fluid were collected at the next luteal phase and the MMP test repeated.

Statistical analyses

The outcomes of transfers in the different groups were evaluated by comparing the clinical pregnancy and miscarriage rates. Data were analyzed by the Mann–Whitney U-test and the χ2 test. All analyses were performed using SPSS version 19 (IBM Japan, Tokyo, Japan). P < 0.05 was considered to be statistically significantly different.


The 597 RIF patients in the present study were divided into two groups depending on whether they agreed to undergo an MMP test after receiving a comprehensive explanation of the procedure. The characteristics of patients in both groups are summarized in Table 1. There were no significant differences in age, Day 3 serum FSH levels, total number of transfers, the number of embryos transferred, or the percentage of blastocysts (not cleavage-stage embryos) that developed from the transferred embryos between the two groups before the treatment intervention.

Figure 3 shows representative results of gelatin zymography using the supernatant from uterine flushing fluid. The previous report had implied that there was no correlation between MMP score and protein concentration in the flushing fluid of RIF [15]. Therefore all neat samples were diluted 20-folds before being run on the gels and the MMP score was defined by the intensity of each band. In this example, only lane 4 is deemed positive with totally scored 8 (≥5). Of the patients who agreed to undergo the MMP test, 15.6% (n=56) were deemed to have a positive response (Group P); the remaining 84.4% (n=304) of patients had low (≤4) MMP scores (Figure 4). After 2 weeks treatment of patients in Group P with an antibiotic and corticosteroid, 89.3% (n=50) had a negative response to the second MMP test (Group Pe). The MMP score remained high in 10.7% (n=6) of patients (Group Pr).

Figure 3
figure 3

A representative image of a gelatin zymogram used for MMP scoring in a MMP test. The lanes represent uterine fluid samples from individual patients with recurrent implantation failure (RIF). Lanes 1, 2, 3, 4 and 6 were scored 4, 2, 4, 8 and 0, respectively. Lane 5 shows a result from the standard used in the present study (supernatant of BHK9 breast carcinoma cell culture). Details of the scoring system are described in the Methods section.

Figure 4
figure 4

The MMP test results before and after the treatment of patients with RIF. Prior to the treatment, 15.6% of patients showed a positive test result (Group P). These patients were then treated with a corticosteroid and an antibiotic for 2 weeks and subjected to another MMP test. Most patients (89.3%) became negative (Group Pe) after the treatment, whereas 10.7% of patients remained positive (Group Pr).

As indicated in Figure 5, patients in Group Pe had a higher clinical pregnancy rate than patients in Group C (21/50 [42.0%] vs 63/237 [26.6%], respectively; P < 0.05). In addition, patients in Group Pe tended to have a higher clinical pregnancy rate than patients who tested negative to the first MMP test (Group N), although the difference did not reach statistical significance. The miscarriage rates in Groups Pe, Pr, N, and C were 6/21 (28.6%), 1/1 (100%), 29/92 (31.5%), and 23/63 (36.5%), respectively. Although there was a tendency for a lower miscarriage rate in Group Pe compared with Group C patients, the difference did not reach statistical significance.

Figure 5
figure 5

Clinical pregnancy rate after the next embryo transfer for the four groups of RIF patients. Group Pe, a positive initial MMP test, but a negative second MMP test after the treatment; Group Pr, a positive initial MMP test, and a positive second MMP test despite the treatment; Group N, a negative response to the MMP test; Group C, the control group who did not undergo the MMP test. Patients in Group Pe had a significantly greater pregnancy rate than patients in Groups N and C (*P < 0.05).


Numerous studies have reported on the roles of various molecules in ensuring a receptive endometrium and uterine milieu [2529]. Some studies have used uterine flushing as a simple and minimally invasive technique to assess the cytokine concentration of uterine secretions around the time of implantation in vivo[15, 20, 24, 30, 31]. Lopata et al. used zymography to measure MMP-2 and MMP-9 activity in uterine flushing fluid and reported the band intensity of the MMPs using an “MMP score” [24]. Using this MMP scoring system, another study showed that overexpression of MMP-2 and MMP-9 is associated with increased IL-1β levels in RIF patients [15]. This previous study suggests that chronic uterine inflammation contributes to implantation failure because IL-1β is a representative inflammatory cytokine and an inducer of MMPs. In other words, chronic uterine inflammation is considered to be a major cause of RIF and high MMP activity.

The present study investigated whether treatment of an unfavorable uterine environment in women with high MMP scores could normalize MMP activity and improve rates of successful implantation. We hypothesized that antibiotic and corticosteroid treatment for the chronic inflammation responsible for MMP overactivity would reduce MMP scores in uterine flushings, improve the uterine environment for implantation, and consequently improve clinical pregnancy outcomes in patients with RIF. The results of the present study strongly support our hypothesis. After treatment, most patients in Group P (i.e. those with RIF and a positive result on the first MMP test) had a negative response to the second MMP test. Moreover, there were better clinical pregnancy rates and a tendency for a decrease in miscarriage rates in this group compared with Groups C and N.

There are some issues that require further discussion. First is the question of the effects of uterine flushings themselves on implantation. There have been some trials investigating improved pregnancy outcomes following uterine endometrial injury or uterine cavity flushing. In these studies, local injury to the endometrium, such as endometrial biopsy or curettage, is usually applied before the cycle used for embryo transfer and has been shown to improve the chances of successful implantation [32, 33]. In contrast, uterine flushing or injection of medium into the uterine cavity is usually performed during the same cycle as embryo transfer [34]. The effect of simple flushing of the uterine cavity remains contentious [35, 36]. In the present study, uterine flushing was performed once for Group N, but twice for Group P. Regardless of the number of uterine flushings, in all cases they occurred in cycles other than those used for embryo transfer. Therefore, we believe that any effect of the uterine flushing on embryo implantation is likely to be very limited. The second is regarding the broad effects of corticosteroids on the uterine environment. Although we used a corticosteroid to control uterine inflammation, including non-infectious endometritis, in the present study, the corticosteroid has a myriad of effects other than its anti-inflammatory actions. It has been reported that the high numbers of uterine natural killer cells (uNK) in the endometria of women with recurrent miscarriage were reduced following the administration of corticosteroids [37, 38]. Because uNK cells secrete not only various cytokines, such as TNF-α, IFN-γ, TGF-β1 and IL-1β, but also MMP-2 and MMP-9 [5], the reduction in MMP scores in the present study may be due, in part, to a reduction in the number of uNK cells.

The third is the choice of a control group. If Group Pe is compared with Group N, there was a tendency for a higher pregnancy rate in Group Pe after treatment. This could be due to differences between Groups Pe and N in terms of the underlying cause of RIF. For example, the likely cause of RIF in MMP-positive patients is high MMP activity related to inflammation, whereas RIF in MMP-negative patients may be due to something other than inflammation. Therefore, after elimination of the cause of RIF by medication, Group Pe patients had a better pregnancy rate than Group N, who did not undergo any treatment for the cause of RIF. In the present study, we chose Group C as the control group. Patients in Group C did not undergo any medical intervention. In contrast, patients in Group Pe were identified as having high MMP activity in the setting of RIF and subsequently underwent treatment to correct high MMP activity. By comparing these two groups, our aim was to determine whether the intervention was effective in improving pregnancy rates in RIF. Strictly speaking, the present study should have included a more appropriate control group consisting of patients matched with those in Group P and treated with placebo. However, there was a large number of patients enrolled in the present study and there was clear change in the MMP test results from positive to negative after treatment in approximately 90% of patients. Therefore, we concluded the 2-week treatment period was sufficiently effective in normalizing the receptivity of the uterus.

Recently, benign endometrial pathologies have been linked to implantation failure and infertility [3941]. Indeed, Inagaki et al.[20] have reported that MMP scores of patients with benign uterine complications, such as leiomyoma, adenomyosis, or endometrial polyps, are higher than in the control group. In the present study, those who have such uterine complications were excluded. However, we did undertake another investigation about RIF with uterine complications (see Additional file 1: Figure S1), which showed that the same treatment for 2 weeks was also effective to reduce the high MMP scores in the RIF patients with uterine complications. To date, the exact mechanisms by which these uterine disorders often limit fertility remain unclear, but changes in the endometrial immune and molecular environment have been suggested as a possible cause [41]. A marked increase in the density of macrophages and natural killer (NK) cells in endometrial stromal cells has been observed in the uteri of women with adenomyosis [42]. Both macrophages and uterine NK cells are known to be able to release inflammatory cytokines. Presumably these uterine disorders may bring about a condition similar to that of chronic inflammation in the endometrium, resulting in an induction of MMP activity and MMP production by endometrial stromal cells in response to the macrophages and other inflammatory cytokines [11, 12].

Chronic endometritis is the most frequent inflammatory condition of the uterine endometrium that is thought to be related to infertility and spontaneous abortion [43, 44]. The prevalence of chronic endometritis in the general population is estimated to range between 0.8% and 19.0% [45]. In patients undergoing ART, the prevalence of chronic endometritis has been reported to be approximately 15%, or up to 42% of patients with RIF [46, 47]. Thus, there is considerable variation in the reported prevalence of chronic endometritis. This may be due to the fact that mild chronic endometritis is often clinically silent, as well as to difficulties in diagnosing the condition based on histopathological examination or using a hysteroscope [48, 49]. However, the MMP test used in the present study is able to detect inflammatory conditions caused by mild and chronic endometritis. The overexpression of MMPs is induced by any type of inflammatory condition, and not just infection, hyperplasia or carcinoma, whereas the appearance of many other inflammatory cells and mediators is sometimes temporary and specifically dependent on the cause of the inflammation. As such, the MMP test can be used to detect various causes of inflammation that may create an unfavorable environment for implantation.

In the present study, only approximately 16% of all patients tested positive on the first MMP test, despite the sensitivity of the test. This rate is lower than expected based on the reported frequency of chronic endometritis in RIF patients. However, we need to take into account the advanced maternal age of the patients recruited to the present study; older patients are more likely to have embryos with chromosomal abnormalities. Indeed, it has been reported [50] that the frequency of aneuploid embryos is higher in older RIF patients (mean age 39.8 years), similar to the mean patient age of 38.1 years in the present study; specifically, the rate of aneuploidy in oocytes and blastocysts was 65.5% and 45.2%, respectively. Thus, of the possible causes of RIF, embryonic factors, particularly chromosomal abnormalities, become more important with increasing maternal age. Taking this into consideration, the fact that 16% of women were positive to the first MMP test in the present study is not necessarily low and indicates that, although not a major cause of RIF, high MMP activity is likely to contribute to a considerable number of cases of RIF. The results of the present study show that an inflammatory uterine environment can be detected by the MMP test and can be treated successfully to improve uterine receptivity.


The MMP test using uterine flushing fluid and the newly designed treatment strategy of a 2-week course of antibiotics and corticosteroids is likely to be useful for women with RIF. However, further studies, including prospective studies, are needed to clarify a causal relationship between the medication and pregnancy outcomes. In addition, the routine use of a corticosteroid is not recommended before further studies have been conducted to confirm its effect against uterine non-infectious inflammation in RIF.



Matrix metalloproteinase


Recurrent implantation failure


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This work was supported, in part, by Grants-in-Aid from the Japan Society for the Promotion of Science (Kiban-C-23592413 to O.I., N.Y., and T.H.) and by a National Grant-in-Aid from the Japanese Ministry of Health, Labor, and Welfare (NCCHD24-6 to T.H.). The authors wish to thank Dr. Angus Thomson (Inter-Biotec Limited.) for the linguistic revision of the manuscript.

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Correspondence to Toshio Hamatani.

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The authors declare that they have no competing interests.

Authors’ contributions

NY and YY designed the project and experiments. NY, TH, and YO took uterine flushing samples from the patients. MMP zymography and scoring were carried out by OI, MY, RM, and NI. NY and TH wrote the paper. TH and YY organized and supervised the project. All authors read and approved the final manuscript.

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Additional file 1: Figure S1: Results of the matrix metalloproteinase (MMP) test for recurrent implantation failure (RIF) patients with mild uterine complications. (PDF 151 KB)

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Yoshii, N., Hamatani, T., Inagaki, N. et al. Successful implantation after reducing matrix metalloproteinase activity in the uterine cavity. Reprod Biol Endocrinol 11, 37 (2013).

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