key: cord-0693880-obxjuyh4 authors: Zhang, Xiaochen; Ishikawa, Dai; Nomura, Kei; Fukuda, Naoyuki; Haraikawa, Mayuko; Haga, Keiichi; Shibuya, Tomoyoshi; Mita, Toshihiro; Nagahara, Akihito title: Donor Screening Revisions of Fecal Microbiota Transplantation in Patients with Ulcerative Colitis date: 2022-02-17 journal: J Clin Med DOI: 10.3390/jcm11041055 sha: f2eff4cb01a3b6d90bec16774f89e4965c05b3fb doc_id: 693880 cord_uid: obxjuyh4 Fecal microbiota transplantation (FMT) has been recognized as a promising treatment for dysbiosis-related diseases. Since 2014, FMT has been utilized to treat ulcerative colitis (UC) in our clinical studies and has shown efficacy and safety. As donor screening (DS) is the primary step to ensure the safety of FMT, we report our experience with DS and present the screening results to improve the prospective DS criteria and provide references for future studies. The donor candidates were screened according to the DS criteria. The first DS criteria were proposed in June 2014 and revised substantially in May 2018. We further sorted the screening results and costs of laboratory tests. From June 2014 to April 2018, the DS eligibility rate was 50%. The total laboratory testing cost for each candidate was JPY 17,580/USD 160.21. From May 2018 to September 2021, the DS eligibility rate was 25.6%. The total laboratory testing cost for each candidate was JPY 40,740/USD 371.36. The reduction in donor eligibility rates due to more stringent criteria should be considered for cost and safety. Studies must consider the latest updates and make timely modifications in the DS criteria to ensure patient safety. Fecal microbiota transplantation (FMT), a therapeutic regimen for transplanting healthy donor feces to reprogram the recipient's gut microbiota, has been proposed as a promising treatment for a wide range of dysbiosis-related diseases [1] [2] [3] [4] [5] . Moreover, FMT has a well-established role in the treatment of recurrent Clostridioides difficile infection (CDI) in the West [6] [7] [8] , with an overall cure rate of approximately 90% [2, 9, 10] . Ulcerative colitis (UC) is a refractory chronic inflammatory bowel disease (IBD), and standard drugs are not always effective for its treatment [11] . Although the pathogenesis of UC is not yet fully understood, previous reports have shown that dysbiosis caused by a decline in the diversity and abundance of intestinal microbiota in patients with UC is related to the development of the aberrant immunological response observed in IBD cases [12] [13] [14] . In a meta-analysis of four randomized controlled trials, the clinical remission rate of patients with UC who had undergone FMT was 42.1%, which was significantly higher than that of the control group, which was 22.6% [15] . Therefore, because of its efficacy, FMT has been studied extensively as a promising treatment for UC. With the continuous in-depth research and establishment of FMT as a reliable therapeutic outlet, a great demand for fecal donors has been generated. However, it is well-known 2 of 12 that pathogenic organisms can be transmitted through fecal transplantation. In fact, it has been reported that FMT may transmit cytomegalovirus (CMV) through urine-stained feces from an unscreened donor [16] . Moreover, in November 2019, the United States reported two cases of insufficient screening of Escherichia coli where one of the patients died because of bacteremia caused by drug-resistant E. coli transmission [17] . Therefore, a safe source of feces as a transplant material is the primary checkpoint for FMT. However, the screening criteria for potential infectious pathogens have always been inconsistent. Institutions in different countries have proposed their donor screening (DS) criteria for FMT. OpenBiome, the longest-standing international stool bank, has released the latest DS criteria in 2021 [18] , but the European Consensus Conference [19] , as well as other countries including Australia and Canada, have also proposed their own DS criteria [20] [21] [22] . This is because the required standards of DS vary between national health regulatory agencies. Therefore, the DS criteria should be adjusted according to the national socio-cultural context. The Chinese FMT working group reported that after two revisions to strengthen DS, the incidence of adverse events dropped from 30.7% to 20.1% [23] ; thus, strict DS security control could prevent harmful consequences. Since 2014, we have been studying the implementation of FMT in the treatment of UC and have reported the efficacy and safety [24] [25] [26] . Furthermore, we have constantly improved our DS criteria to ensure patient safety. Our first DS criteria (2014 version), which were formulated according to the Amsterdam protocol, were employed from June 2014 to April 2018 with some minor modifications [27] [28] [29] . Based on these criteria, we completed three clinical studies [24] [25] [26] . From May 2018, tremendous changes have been made to enhance safety, and these revised criteria (2018 version) are being utilized to perform a clinical study. Therefore, we report our experience and propose the DS criteria used in our hospital for improving the prospective DS criteria and providing a reference for future studies. The DS process ( Figure 1 ) consisted of three steps: (1) pre-screening, (2) formal screening, and (3) final screening. Pre-screening included donor candidate recruitment, preliminary assessment, and a questionnaire survey. Formal screening refers to laboratory testing. Final screening included reassessment of health conditions and enrollment of the eligible donor. With the continuous in-depth research and establishment of FMT as a reliable therapeutic outlet, a great demand for fecal donors has been generated. However, it is wellknown that pathogenic organisms can be transmitted through fecal transplantation. In fact, it has been reported that FMT may transmit cytomegalovirus (CMV) through urinestained feces from an unscreened donor [16] . Moreover, in November 2019, the United States reported two cases of insufficient screening of Escherichia coli where one of the patients died because of bacteremia caused by drug-resistant E. coli transmission [17] . Therefore, a safe source of feces as a transplant material is the primary checkpoint for FMT. However, the screening criteria for potential infectious pathogens have always been inconsistent. Institutions in different countries have proposed their donor screening (DS) criteria for FMT. OpenBiome, the longest-standing international stool bank, has released the latest DS criteria in 2021 [18] , but the European Consensus Conference [19] , as well as other countries including Australia and Canada, have also proposed their own DS criteria [20] [21] [22] . This is because the required standards of DS vary between national health regulatory agencies. Therefore, the DS criteria should be adjusted according to the national socio-cultural context. The Chinese FMT working group reported that after two revisions to strengthen DS, the incidence of adverse events dropped from 30.7% to 20.1% [23] ; thus, strict DS security control could prevent harmful consequences. Since 2014, we have been studying the implementation of FMT in the treatment of UC and have reported the efficacy and safety [24] [25] [26] . Furthermore, we have constantly improved our DS criteria to ensure patient safety. Our first DS criteria (2014 version), which were formulated according to the Amsterdam protocol, were employed from June 2014 to April 2018 with some minor modifications [27] [28] [29] . Based on these criteria, we completed three clinical studies [24] [25] [26] . From May 2018, tremendous changes have been made to enhance safety, and these revised criteria (2018 version) are being utilized to perform a clinical study. Therefore, we report our experience and propose the DS criteria used in our hospital for improving the prospective DS criteria and providing a reference for future studies. The DS process ( Figure 1 ) consisted of three steps: (1) pre-screening, (2) formal screening, and (3) final screening. Pre-screening included donor candidate recruitment, preliminary assessment, and a questionnaire survey. Formal screening refers to laboratory testing. Final screening included reassessment of health conditions and enrollment of the eligible donor. Those donor candidates, recommended to the study by patients or college student volunteers from the Juntendo University School of Medicine, took the initiative to participate after learning about the study and were then recruited. The recruitment of candidates was not restricted by sex. The preliminary candidate assessment was conducted without fixed criteria at the Juntendo University Hospital from June 2014 to September 2021, and it was mainly comprised of inquiries regarding general health conditions, such as any discomfort or illnesses the candidates recently had. Candidates who were deemed to have no abnormalities by a physician were then eligible to participate in the questionnaire survey. Concerning the demographic information in the questionnaire survey, the age [30] and body mass index (BMI) of the donor candidates are now required by the 2018 revised questionnaire. In addition, compared with the medical history checked in the 2014 version, the 2018 version further clarified which intestinal microbiota-related diseases should be excluded [31, 32] . Furthermore, a family history of colorectal carcinoma or active gastrointestinal infection has to be disclosed by the donor candidates. Additional non-infectious-related clinical information, including the use of antimicrobials or protein pump inhibitors (PPI), and the presence of psychiatric symptoms [33] [34] [35] are now required under the 2018 revision. Finally, the risk investigation of infectious diseases is also more detailed than in the 2014 version. The specific list of questionnaires employed as donor exclusion criteria can be found in Table 1 . Candidates who met any of these criteria were excluded. To minimize the risk of infection transmission, only candidates who passed the prescreening step underwent laboratory tests, including fecal and blood testing. The feces and blood samples of the donor candidates were sent to the laboratory of the SRL Company (Tokyo, Japan) that specializes in clinical laboratory testing, and comprehensive testing was performed in accordance with our fecal and blood screening criteria. The fecal test in the 2014 version (Table 2 ) included an examination of parasitic ova and cysts, while in the test of the 2018 revision ( Table 2 ) the parasite bodies, cryptosporidium, giardia, and Entamoeba histolytica were added. In particular, Entamoeba histolytica, combined with a clinical evaluation, was used for the diagnosis of Entamoeba histolytica in the 2018 version. As the use of A and B toxins of C. difficile alone may be unreliable for CDI diagnosis in a proportion of patients [36] , dual testing of the toxin and the glutamate dehydrogenase (GDH) protein is now employed to improve diagnostic accuracy. In addition, E. coli verotoxin testing has been performed since June 2019, and further screening of all E. coli strains has been performed promptly from August 2020 because of safety alerts (12 March 2020) issued by The U.S. Food and Drug Administration (FDA) [37] . Screening for norovirus and rotavirus, which are transmitted through the fecal-oral route and can easily cause diarrhea, as well as fecal occult blood testing, which is often used to evaluate intestinal health and to screen for colorectal cancer, have been included [38] . The blood test items of the 2014 version (Table 3 ) mainly included basic infectious diseases. In 2018 (Table 3) , testing for the hepatitis E virus and immunoglobulin M antibodies against the Epstein-Barr virus has been included. Initially, parasite positivity was solely determined through microscopic examination of stools. However, this method depends on the inspector's subjective judgment, which can potentially result in a misdiagnosis. Therefore, a parasite-specific serum antibody screening kit [39] is now additionally employed to determine positivity to the following parasites: Dirofilaria immitis; Ascaris suum; Anisakis; Gnathostoma spinigerum; Cysticercus cellulosae; Strongyloides stercoralis; Paragonimus westermanii; Clonorchis sinensis; Sparganum mansoni; Toxocara canis; Paragonimus miyazakki; and Fasciola hepatica. Furthermore, polymerase chain reaction (PCR) testing was performed [40, 41] for the reconfirmation of positive S. stercoralis results. The risk of CMV reactivation in patients with severe UC ranges from 21% to 34% [42, 43] . Since May 2018, the parameters for testing of CMV have been revised twice, continuously strengthening the specificity and accuracy of virus detection to reduce the possibility of re-exacerbation. Further, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing has been implemented from July 2020. Finally, complete blood count tests, as well as liver and kidney function examinations were conducted to assess health conditions. The complete list of clinical infectious information employed as donor exclusion criteria can be found in Tables 2 and 3 . Candidates meeting any of these criteria were excluded. The absence of any health conditions, such as diarrhea and fever, was ascertained during the days prior to stool submission. The health conditions of the cohabiting family members were also assessed [44] . The candidates could voluntarily donate feces multiple times for three months, and the donations were processed and cryopreserved at -80 • C for up to six months [45] . A total of 138 candidates came to our hospital from June 2014 to April 2018 for preliminary assessment, and 61 were excluded at this stage. Most of the remaining 77 candidates were blood relatives (n = 44) or spouses (n = 26) recommended by patients, and a small number of candidates were volunteers (n = 7). The ratio of volunteers to candidates who passed the preliminary assessment was 9.1% (7/77). This cohort comprised 30 men and 47 women, with an average age of 42.2 years (range, 20-68 years). After questionnaire completion, three candidates were excluded because of their medical history, while one patient was also excluded of acute diarrhea that had been present for the previous three months. Laboratory testing was performed on 73 candidates. Of these, one individual was ruled out due to C. difficile toxin-positive feces, and three candidates were rejected because of CMV-positive blood testing. The remaining 69 candidates and their cohabitants were all reconfirmed to be in healthy condition. Therefore, 50.0% of the initial volunteers passed the DS process. The final cohort included 27 men and 42 women, with an average age of 41.9 years (range, 20-68 years) (Figure 2 ). Among the 117 candidates who visited our hospital between May 2018 and September 2021, 43 were excluded after preliminary assessment. The remaining 74 candidates comprised volunteers (n = 43) and patients' blood relatives (n = 28) and spouses (n = 3). The ratio of volunteers to candidates who passed the preliminary assessment was 58.1% (43/74). This cohort included 43 men and 31 women, with an average age of 33.2 years (range, 19-70 years). After questionnaire completion, one, two, one, one, three, and two candidates were excluded because of a family history of colorectal carcinoma, BMI > 25 kg/m 2 , received antimicrobial therapy within the previous three months, received probiotics or PPI therapy within the previous three months, vaccinations received in the previous three months, and high-risk sex performed in the previous three months, respectively. Laboratory testing was performed on the remaining 64 candidates. A total of eight candidates showed abnormal fecal test results, twenty-one had abnormal blood test results, and another eight showed abnormalities in both blood and fecal tests. The details of the abnormal testing results are described in Supplemental Table S1 . A total of 20 (31.3%) candidates were excluded due to positive results on parasite antibody testing, more prominent than other laboratory testing items ( Table 4 ). The most common parasite detected was S. stercoralis (55.0%, n = 11; Table 5 ), but PCR testing confirmed that all the participants were negative. Of these, the stools of three candidates (Patients 2, 5, and 7) who showed negative results with laboratory tests, except for S. stercoralis, were nonetheless utilized for FMT (Supplemental Table S2 ). Among the 117 candidates who visited our hospital between May 2018 and September 2021, 43 were excluded after preliminary assessment. The remaining 74 candidates comprised volunteers (n = 43) and patients' blood relatives (n = 28) and spouses (n = 3). The ratio of volunteers to candidates who passed the preliminary assessment was 58.1% (43/74). This cohort included 43 men and 31 women, with an average age of 33.2 years (range, 19-70 years). After questionnaire completion, one, two, one, one, three, and two candidates were excluded because of a family history of colorectal carcinoma, BMI > 25 kg/m 2 , received antimicrobial therapy within the previous three months, received probiotics or PPI therapy within the previous three months, vaccinations received in the previous three months, and high-risk sex performed in the previous three months, respectively. Laboratory testing was performed on the remaining 64 candidates. A total of eight candidates showed abnormal fecal test results, twenty-one had abnormal blood test results, and another eight showed abnormalities in both blood and fecal tests. The details of the abnormal testing results are described in Supplemental Table S1 . A total of 20 (31.3%) candidates were excluded due to positive results on parasite antibody testing, more prominent than other laboratory testing items ( Table 4 ). The most common parasite detected was S. stercoralis (55.0%, n = 11; Table 5 ), but PCR testing confirmed that all the participants were negative. Of these, the stools of three candidates (Patients 2, 5, and 7) who showed negative results with laboratory tests, except for S. stercoralis, were nonetheless utilized for FMT (Supplemental Table S2 ). After reconfirming the health status of the candidates and their cohabitants, 30 candidates were included in the final cohort. Therefore, 25.6% of the initial candidates passed the screening, including 18 men and 12 women, with an average age of 36.0 years (range, 20-69 years) (Figure 3) . The total cost of laboratory testing for performing fecal (JPY 14,260/USD 129.99) and blood testing (JPY 26,480/USD 241.37) was JPY 40,740/USD 371.36. After reconfirming the health status of the candidates and their cohabitants, 30 candidates were included in the final cohort. Therefore, 25.6% of the initial candidates passed the screening, including 18 men and 12 women, with an average age of 36.0 years (range, 20-69 years) ( Figure 3) . Since 2014, no serious adverse events have been noted in patients admitted to our studies, regardless of the use of either the 2014 or the 2018 version of the DS criteria. However, other institutions have reported serious adverse events due to insufficient DS [16, 17] . Therefore, it is necessary to continuously strengthen the screening of infectious diseases and minimize the occurrence of adverse events. To the best of our knowledge, this is the first report in Japan that describes the screening items, costs, and results to provide reference for future studies. It has been shown that the microbial diversity of the donor is the main factor affecting the efficacy of FMT for patients with UC [46, 47] . In addition, feces donated by siblings provide a greater long-term remission rate than those obtained from a parent or an offspring [26] . However, the current evidence concerning the features of optimal donors for UC treatment remains limited. In addition, in our study, although patients were more receptive to transplanting feces from donors recommended by the patients themselves, this caused some inconveniences. For example, as the screening process is quite time-consuming, the patient's therapeutic opportunity may be delayed; there is also a risk of revealing the donor's personal medical history. A previous report showed that there is no significant difference in the remission rate of CDI between patients who have undergone FMT with feces from a patient-recommended donor and those who have been transplanted with undirected donor materials [48] . Therefore, many institutions have adopted the method of recruiting volunteers as donor candidates [18, 20, 49, 50] . We have also strengthened the recruitment of undirected donor volunteers after revising the DS criteria in 2018. The ratio of volunteers to candidates who passed the preliminary assessment increased from 9.1% (7/77) to 58.1% (43/74) . In this study, most of the recruited volunteers were medical students who had medical knowledge and, thus, could better understand our recruitment requirements. Overall, although the questionnaire has become more rigorous from May 2018, the pre-screening pass rates did not decrease (Figures 2 and 3) . The main reason for this may be related to the change in the target population from which the recruited candidates are selected. In 2015, the infection rate following parasite testing in Tokyo using the feces of school students as samples was <10% and showed a downward trend [51] . However, the parasitespecific antibody screening method employed in this study produced unexpectedly high positive results (31.3%). All the positive patients had the lowest evaluation of +1 on a 4-point positive scale, which is normally considered a false positive. We hypothesized that non-specific reactions would be the cause of this, although it has not been confirmed because only testing for S. stercoralis was conducted. In fact, the PCR test revealed that all 11 candidates were negative for S. stercoralis. Three candidates who had originally tested positive for S. stercoralis were nonetheless selected based on their epidemiological information and background [52] . Although several PCR inaccuracies for the diagnosis of S. stercoralis have been reported, PCR may have a confirmatory test effect [53] . In our study, the unnecessary exclusion due to S. stercoralis was also reduced by PCR. In addition, some of the parasites included in the screening method, such as Gnathostoma spinigerum and Anisakis, are unlikely to infect the recipient through FMT. Taken together, the current screening methods of parasites may cause the unnecessary exclusion of some donor candidates, and detection technology for parasites still needs to be further optimized. There were limitations to this study. First, we did not record the reasons why candidates were excluded at the preliminary assessment stage. Second, this was a single-center clinical study, and volunteers were recruited non-randomly. Third, the current parasite screening guidelines may cause unnecessary exclusion of candidates; thus, pass rates may not be representative. In the ongoing clinical study, we have begun to evaluate the enteric pathogens in the fecal solution immediately after the donor submits the feces by using the FilmArray gastrointestinal panel (BioFire Diagnostics, Salt Lake City, UT, USA), which distinguishes possible causes of gastroenteritis (seven bacteria, four parasites, five viruses, and three diarrheagenic E. coli and Shigella) to strengthen the response to the safety alert from the FDA (12 March 2020). We also aim to use a highly sensitive intestinal inflammatory marker, calprotectin, in the next study [54] . We hope to always propose the most optimized DS criteria to support future FMT studies in different emerging fields. Screening stool donors for successful FMT in patients with UC is challenging. Researchers in this field should always consider the latest microbiota studies and global epidemic status to allow for timely revisions of the DS criteria to minimize the occurrence of adverse events. In addition, the reduction in the donor eligibility rates due to more stringent criteria should be considered in light of the balance between cost and safety. Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/jcm11041055/s1, Table S1 : Reasons for failed laboratory testing (5/2018-9/2021). Table S2 : Result of parasite-specific antibody screening testing. Fecal microbiota transplantation: Review and update Transfer of intestinal microbiota from lean donors increases insulin sensitivity in individuals with metabolic syndrome Faecal microbiota transplantation alters gut microbiota in patients with irritable bowel syndrome: Results from a randomised, double-blind placebo-controlled study Long-term benefit of microbiota transfer therapy on autism symptoms and gut microbiota Guidelines for diagnosis, treatment, and prevention of Clostridium difficile infections Clinical practice guidelines for clostridium difficile infection in adults and children: 2017 update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA) European Society of Clinical Microbiology and Infectious Diseases: Update of the treatment guidance document for Clostridium difficile infection Systematic review with meta-analysis: The efficacy of faecal microbiota transplantation for the treatment of recurrent and refractory Clostridium difficile infection Efficacy of different faecal microbiota transplantation protocols for Clostridium difficile infection: A systematic review and meta-analysis. United Eur Reduced diversity and imbalance of fecal microbiota in patients with ulcerative colitis The microbiome in inflammatory bowel disease: Current status and the future ahead The involvement of gut microbiota in inflammatory bowel disease pathogenesis: Potential for therapy Systematic Review and Meta-analysis: Fecal Microbiota Transplantation for Treatment of Active Ulcerative Colitis Case Records of the Massachusetts General Hospital. Case 25-2014. A 37-year-old man with ulcerative colitis and bloody diarrhea Drug-resistant E. coli bacteremia transmitted by fecal microbiota transplant European consensus conference on faecal microbiota transplantation in clinical practice Establishing a Fecal Microbiota Transplant Service for the Treatment of Clostridium difficile Infection Multidonor intensive faecal microbiota transplantation for active ulcerative colitis: A randomised placebo-controlled trial Fecal Microbiota Therapy Used in the Treatment of Clostridium difficile Infection not Responsive to Conventional Therapies Shanghai Tongji FMT Working Group. Donor screening for fecal microbiota transplantation in China: Evaluation of 8483 candidates Changes in intestinal microbiota following combination therapy with fecal microbial transplantation and antibiotics for ulcerative colitis The microbial composition of bacteroidetes species in ulcerative colitis is effectively improved by combination therapy with fecal microbiota transplantation and antibiotics Matching between donors and ulcerative colitis patients is important for long-term maintenance after fecal microbiota transplantation Fecal microbiota transplantation and donor standardization Fecal microbiota transplantation as novel therapy in gastroenterology: A systematic review Investigating deep phylogenetic relationships among cyanobacteria and plastids by small subunit rRNA sequence analysis Age-related changes in gut microbiota composition from newborn to centenarian: A cross-sectional study Journal of Gastroenterology Lecture: Intestinal microbiota and the role of fecal microbiota transplant (FMT) in treatment of C. difficile infection Gut microbiota: A source of novel tools to reduce the risk of human disease? Pediatric Res Gut microbiota and major depressive disorder: A systematic review and meta-analysis The role of the gut microbiota in development, function and disorders of the central nervous system and the enteric nervous system The brain-gut-microbiome axis Laboratory diagnosis of clostridium difficile infection. An evaluation of tests for faecal toxin, glutamate dehydrogenase, lactoferrin and toxigenic culture in the diagnostic laboratory Food & Drug. Safety Alert Regarding Use of Fecal Microbiota for Transplantation and Risk of Serious Adverse Events Likely Due to Transmission of Pathogenic Organisms Fecal occult blood test in colorectal cancer screening Serological and molecular detection of Strongyloides stercoralis infection among an Orang Asli community in Malaysia A PCR-based molecular detection of strongyloides stercoralisin human stool samples from Tabriz city Antiviral treatment for colonic cytomegalovirus infection in ulcerative colitis patients significantly improved their surgery free survival The prevalence and efficacy of ganciclovir on steroid-refractory ulcerative colitis with cytomegalovirus infection: A prospective multicenter study Cohabiting family members share microbiota with one another and with their dogs Faecal microbiota transplant for recurrent Clostridium difficile infection using long-term frozen stool is effective: Clinical efficacy and bacterial viability data Donor species richness determines faecal microbiota transplantation success in inflammatory bowel disease The taxonomic composition of the donor intestinal microbiota is a major factor influencing the efficacy of faecal microbiota transplantation in therapy refractory ulcerative colitis Fecal microbiota transplantation for Clostridium difficile infection: Systematic review and meta-analysis Donor recruitment for fecal microbiota transplantation Extended screening costs associated with selecting donors for fecal microbiota transplantation for treatment of metabolic syndrome-associated diseases Status of strongyloidiasis in Japan Accuracy of molecular biology techniques for the diagnosis of Strongyloides stercoralis infection-A systematic review and meta-analysis We are also grateful to Maya Kobayashi, Yoko Sugiura, Tsubasa Nagaoka, and Yoko Otani for providing general support. The authors declare no conflict of interest.