golimumab

戈利木单抗
  • 文章类型: Case Reports
    葡萄膜炎,作为关节外的表现,在23%的强直性脊柱炎(AS)患者中发现,是一种具有挑战性的疾病。
    作者向医院外介绍了一名32岁的男性,抱怨8年前左眼复发性前葡萄膜炎,患有炎症性腰痛2年。因此,在许多治疗策略失败后诊断为AS,50mg/月皮下Golimumab开始治疗AS和葡萄膜炎的临床缓解。
    美国风湿病学会建议使用依那西普和阿达木单抗治疗AS患者复发性葡萄膜炎。同样,欧洲抗风湿病联盟建议使用英夫利昔单抗,阿达木单抗,或Certolizumab预防葡萄膜炎复发复发。到现在为止,发表了一例关于使用Golimumab治疗AS患者难治性葡萄膜炎的病例.
    发现戈利木单抗在治疗与脊柱关节炎相关的葡萄膜炎中至少有一种免疫抑制药物是有效的。
    UNASSIGNED: Uveitis, as an extra-articular presentation, is found in 23% of patients with ankylosing spondylitis (AS) and is a challenging disease to treat.
    UNASSIGNED: The authors presented a 32-year-old male to the out-hospital, complaining of recurrent anterior uveitis 8 years earlier in his left eye, and suffered from inflammatory lumber pain for 2 years. So a diagnosis of AS after the failure of many therapeutic strategies, 50 mg /month subcutaneous Golimumab was started with clinical remission of AS and uveitis.
    UNASSIGNED: The American College of Rheumatology recommends the use of etanercept and adalimumab in the treatment of recurrent uveitis in AS patients. Similarly, the European League Against Rheumatism recommended using Infliximab, Adalimumab, or Certolizumab to prevent the recurrence of uveitis recurrence. Till now, a case about treating refractory uveitis with Golimumab in AS patients was published.
    UNASSIGNED: Golimumab was found to be effective in the treatment of uveitis associated with spondyloarthritis refractory at least one immunosuppressive drug.
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  • 文章类型: Case Reports
    继发于荚膜组织胞浆的噬血细胞淋巴组织细胞增多症(HLH)很少见,全球影响<1%,死亡率高达31%。在这里,我们提出了一个罕见的HLH继发于H囊膜,影响一名57岁女性类风湿关节炎患者.广泛的调查没有揭示,尽管广谱抗生素,她的病情恶化了,导致呼吸衰竭,需要体外膜氧合(ECMO)支持,需要多种血管加压药的休克,和需要血液透析的急性肾损伤(AKI)。诊断证实播散性组织胞浆菌病(DHP),提示两性霉素B和甲基强的松龙治疗,导致泊沙康唑治疗的显着改善和出院。继发性HLH,主要由DHP等严重感染引起,正在讨论。在人类免疫缺陷病毒(HIV)血清阴性个体中,对这种情况的研究有限。诊断涉及HLH-2004和HScore标准。由于多器官衰竭风险和治疗复杂性,管理组织胞浆菌病相关的HLH仍然具有挑战性,需要进一步研究。
    Hemophagocytic lymphohistiocytosis (HLH) secondary to Histoplasma capsulatum is rare, impacting <1% globally, with a mortality rate of up to 31%. Herein, we present a rare case of HLH secondary to H capsulatum, affecting a 57-year-old female with rheumatoid arthritis. Extensive investigations were unrevealing and despite broad-spectrum antibiotics, her condition worsened, leading to respiratory failure requiring extracorporeal membrane oxygenation (ECMO) support, shock requiring multiple vasopressors, and acute kidney injury (AKI) requiring hemodialysis. Diagnosis confirmed disseminated histoplasmosis (DHP), prompting Amphotericin B and methylprednisolone treatment, resulting in significant improvement and discharge with posaconazole therapy. Secondary HLH, primarily arising from severe infections like DHP, is discussed. Limited research exists on this condition in human immunodeficiency virus (HIV)-seronegative individuals. Diagnosis involves HLH-2004 and HScore criteria. Managing histoplasmosis-associated HLH remains challenging due to multiorgan failure risks and treatment complexities and needs further research.
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  • 文章类型: Case Reports
    这里,我们报告了一例87岁女性类风湿关节炎(RA)患者,接受甲氨蝶呤(MTX)和戈利木单抗治疗,出现了严重的肺囊虫肺炎(PCP),也被称为肺孢子虫肺炎。患者主要表现为劳累时呼吸困难,干咳,和疲劳。高分辨率胸部CT扫描显示弥漫性,在整个两肺中分布不均匀的毛玻璃混浊。根据临床设置,患者被临床诊断为PCP,成像,和高水平的血清β-D-葡聚糖.病人需要高流量氧气治疗,低剂量甲氧苄啶/磺胺甲恶唑和皮质类固醇治疗改善了她的病情,患者在第25天出院。尽管据我们所知,尚未发表有关使用戈利木单抗治疗的RA患者的PCP的病例报告,该病例强调了在接受免疫抑制治疗的老年患者中注意机会性感染的重要性.MTX与肿瘤坏死因子抑制剂如戈利木单抗一起使用可能会增加严重感染如PCP的风险。该案例强调了对PCP采取预防措施和早期干预的必要性,强调RA管理中免疫抑制益处和感染风险之间的微妙平衡。
    Here, we report a case of an 87-year-old female patient with rheumatoid arthritis (RA) treated with methotrexate (MTX) and golimumab who developed severe pneumocystis pneumonia (PCP), also known as Pneumocystis jirovecii pneumonia. The patient presented with chief complaints of dyspnea on exertion, dry cough, and fatigue. A high-resolution chest CT scan revealed diffuse, unevenly distributed ground-glass opacities throughout both lungs. The patient was clinically diagnosed with PCP based on the clinical settings, imaging, and a high level of serum β-D-glucan. While the patient required high-flow oxygen therapy, low-dose trimethoprim/sulfamethoxazole and corticosteroid therapy improved her condition, and the patient was discharged on day 25. Although to our knowledge no case report has been published regarding PCP in patients with RA treated with golimumab, this case emphasizes the importance of attention to opportunistic infections in elderly patients receiving immunosuppressive therapy. MTX use alongside tumor necrosis factor inhibitors like golimumab may increase the risk of serious infections such as PCP. The case underscores the necessity of prophylactic measures and early intervention for PCP, highlighting the delicate balance between immunosuppression benefits and infection risks in RA management.
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  • 文章类型: Case Reports
    一名51岁的日本男子在41岁时被诊断出患有左侧溃疡性结肠炎(UC)。他接受了美沙拉嗪和硫唑嘌呤治疗,并保持缓解。51岁时,患者出现血便,腹痛,巩膜炎,关节炎,咳嗽,血痰,和心包积液.考虑到心包积液是UC的非典型肠外并发症,患者符合复发性多软骨炎(RP)的诊断标准,诊断为RP合并UC复发.进行类固醇治疗,两种疾病都有所改善。Golimumab,抗肿瘤坏死因子-α抑制剂,被引入作为UC的维持治疗。所有症状,包括心包积液,改进。随后,未观察到UC或RP复发。由于仅报道了少数RP与UC重叠的病例,并且尚未建立治疗方案,我们认为这个案子很有价值,值得出版。
    A 51-year-old Japanese man was diagnosed with left-sided ulcerative colitis (UC) at age 41. He was treated with mesalazine and azathioprine and maintained remission. At age 51, the patient developed bloody stools, abdominal pain, scleritis, arthritis, cough, bloody sputum, and pericardial effusion. Considering that pericardial effusion is an atypical extraintestinal complication of UC, and the patient met the diagnostic criteria for relapsing polychondritis (RP), a diagnosis of RP complicating a relapse of UC was made. Steroid therapy was administered, and both diseases improved. Golimumab, an anti-tumor necrosis factor-α inhibitor, was introduced as maintenance therapy for UC. All symptoms, including pericardial effusion, improved. Subsequently, no relapse of UC or RP was observed. As only a few cases of RP overlapping with UC have been reported and no treatment protocol has been established, we considered this case valuable and worthy of publication.
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  • 文章类型: Case Reports
    后部可逆性脑病综合征(PRES)是一种以癫痫发作为特征的神经毒性状态,头痛,视觉障碍,麻痹,和改变精神状态。Golimumab是抗肿瘤坏死因子-α抑制剂(抗TNF-α),可用于治疗风湿性疾病。这里,我们介绍了一名在戈利木单抗治疗强直性脊柱炎(AS)后出现PRES的患者.一名四十五岁女病人因新发作的严重头痛而入住急诊服务,双眼视力丧失,和两次持续3至4分钟的全身性强直阵挛性癫痫发作。患者诊断为AS12年,高血压3年,并接受戈利木单抗和卡维地洛治疗。根据当前的临床和扩散颅磁共振成像(MRI)发现,患者被诊断为PRES。怀疑是这种情况的导火索,戈利木单抗停止了。在开始抗惊厥治疗和控制血压后,神经系统检查结果迅速恢复,未见癫痫发作.控制MRI图像,在第一个月的访问,是正常的。虽然化疗药物是众所周知的PRES的原因,文献中很少报道使用抗TNF-α药物的病例。据我们所知,这是戈利木单抗后出现PRES的首例病例.脱髓鞘疾病是抗TNF-α治疗最可怕的神经系统并发症;然而,出现神经系统症状的患者应该想到PRES。
    Posterior reversible encephalopathy syndrome (PRES) is a neurotoxic state which is characterized by seizures, headache, visual disturbances, paresis, and altered mental status. Golimumab is anti-tumor necrosis factor-α inhibitor (anti-TNF-α) that can be used in the treatment of rheumatologic diseases. Here, we present a patient who had developed PRES after golimumab treatment for ankylosing spondylitis (AS). A 45-year-old female patient was admitted to the emergency service with a newly onset severe headache, loss of vision in both eyes, and two generalized tonic-clonic seizures that lasted for 3 to 4 min. The patient had the diagnoses of AS for 12 years and hypertension for 3 years and receiving golimumab and carvedilol. The patient was diagnosed with PRES based on the current clinical and diffusion cranial magnetic resonance imaging (MRI) findings. On suspicion of being the trigger of this situation, golimumab was stopped. After starting anti-convulsant therapy and controlling blood pressure, the neurological findings recovered rapidly and no seizures were seen. Control MRI images, in the first month\'s visit, were normal. Although chemotherapeutic agents are well-known causes of PRES, there are few reported cases with anti-TNF-α agents in the literature. To our knowledge, this is the first case that developed PRES after golimumab. Demyelinating diseases are the most frightening neurologic complication of anti-TNF-α treatment; however, PRES should come to mind in patients presenting with neurological symptoms.
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  • 文章类型: Case Reports
    结节性红斑(EN)是一种表现为发热的自限性间隔脂膜炎,关节痛,和关节炎。已发现肿瘤坏死因子α(TNF-α)抑制剂如戈利木单抗治疗炎症性肠病(IBD)中的EN。我们在此报告戈利木单抗治疗强直性脊柱炎后EN的反常发生。
    一名34岁女性于2022年6月就诊,她的脚上出现了“疮”,间歇性出现了大约5个月,但在最后24小时内急剧恶化。该患者有8年的强直性脊柱炎病史,持续7年。每4周给予皮下戈利木单抗,因为她对其他治疗没有反应。第五次皮下注射24小时后,痛苦,出现红斑结节,组织学上与EN兼容。尽管有这种副作用,我们继续治疗,由于良好的反应和疗效。
    皮肤反应与戈利木单抗治疗有关,包括注射部位周围温暖柔软的皮肤,喷发,瘙痒,有时全身出现皮疹.Golimumab已成功用于治疗克罗恩病的EN。因为我们的病人继续服用戈利木单抗,EN耀斑与治疗性注射的时间相关性以及缺乏任何病因支持EN和戈利木单抗治疗之间的直接因果关系.
    TNF-α抑制剂可用于治疗克罗恩病患者的EN,尽管它可能是这种治疗的不良反应。需要进一步的工作。
    UNASSIGNED: Erythema nodosum (EN) is a self-limited septal panniculitis that presents with fever, arthralgia, and arthritis. Tumor necrosis factor alpha (TNF-α) inhibitor such as golimumab has been found to treat EN in inflammatory bowel diseases (IBD). We herein report the paradoxical occurrence of EN following golimumab for ankylosing spondylitis.
    UNASSIGNED: A 34-year-old female presented in June 2022 with a complaint of \'sores\' on her feet that intermittently presented for approximately 5 months but that had worsened dramatically in the last 24 h. The patient had an 8-year history of ankylosing spondylitis for 7 years. Subcutaneous golimumab was administered every 4 weeks as she had not responded to other treatments. Twenty-four hours after the fifth subcutaneous injection, painful, erythematous nodules appeared, histologically compatible with EN. Despite this side effect, we continue therapy due to the good response and efficacy.
    UNASSIGNED: Skin reactions were associated with the treatment with golimumab, including warm tender skin around the injection site, eruptions, itchiness, and sometimes a full-body rash. Golimumab was successfully used in treating EN in Crohn\'s disease. Because our patient continued on golimumab, the temporal association of EN flares with therapeutic injection and the lack of any etiology support a direct causal relationship between EN and golimumab treatment.
    UNASSIGNED: TNF-α inhibitors are useful in treating Crohn\'s disease patients with EN, although it may present as an adverse effect of this treatment. Further work is needed.
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  • 文章类型: Case Reports
    虽然中枢神经系统脱髓鞘病变作为肿瘤坏死因子(TNF)-α抑制剂的副作用已被报道,这种疗法仍用于一些自身免疫性疾病。
    一名34岁的叙利亚男性表现出行走困难和刺痛,在接下来的4天里,他的身体左侧麻木,在戈利木单抗治疗期间。在过去的两个月里,疲劳,反复的小腿痉挛,发现四肢麻木。神经系统检查发现下肢感觉障碍和反射过度。MRI显示变异型脱髓鞘病变。开始类固醇治疗,戈利木单抗被停用,随着症状消失,结果良好。
    抗TNF治疗后脱髓鞘的发生率并不常见。大多数研究报道,抗TNFα抑制剂治疗和脱髓鞘病变存在之间的平均时间为5个月至4年,即使在停止抗TNFα抑制剂后,这些病变也可能出现;同时,在我们的病例中,治疗停止后症状完全治愈,这表明了因果关系,虽然是一种时间关系,在这种情况下,不能建立。作者认为戈利木单抗在脱髓鞘病变的发展中起作用,尽管它可能是Behcet病过程中的临床表现。
    应注意戈利木单抗治疗的副作用,如脱髓鞘病变,需要对Bechet病患者进行长期监测。
    Although central nervous system demyelinating lesions as a side effect of tumor necrosis factor (TNF)-alpha inhibitors have been reported, this treatment is still used in some autoimmune diseases.
    UNASSIGNED: A 34-year-old Syrian male presented with difficulty walking and tingling, and numbness on the left side of his body over the next 4 days, during golimumab treatment. Over the past 2 months, fatigue, recurrent calf spasms, and extremity numbness were found. Sense disturbance and hyper-reflexes of the lower extremities were found on neurological examination. MRI demonstrated variant demyelinating lesions. Steroid therapy was initiated, and golimumab was discontinued, with good outcomes as the symptoms have disappeared.
    UNASSIGNED: The incidence of demyelination following anti-TNF therapy is uncommon. Most studies have reported that the average time between the anti-TNFα inhibitor treatment and the demyelinating lesion presence is from 5 months to 4 years, and these lesions may appear even after the cessation of the anti-TNFα inhibitor; meanwhile, a total cure of the symptoms after treatment cessation happened in our case, which suggests a causal relation, although a temporal relationship, in this case, cannot be established. The authors believe that golimumab plays a role in the demyelinating lesions development, although it may be a clinical manifestation during the course of Behcet\'s disease.
    UNASSIGNED: Caution should be taken for the side effects of Golimumab treatment, such as demyelinating lesions, and long-term monitoring of patients with Bechet disease is required.
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  • 文章类型: Case Reports
    未经证实:溃疡性结肠炎是一种免疫介导的疾病,在儿科中面临挑战,因为它经常严重和广泛。当前的小儿溃疡性结肠炎指南对低体重儿童戈利木单抗的用法和剂量提供了较弱的建议。我们提出了一个标签外的案例,不推荐剂量的皮下戈利木单抗治疗低体重慢性活动性溃疡性结肠炎儿童。
    未经授权:一个10岁的叙利亚女孩,抗TNF幼稚,慢性活动性溃疡性结肠炎体重25公斤,身高142厘米,体表面积(BSA)0.993m2,过去的药物包括口服泼尼松和美沙拉嗪,没有事先手术。我们用戈利木单抗200毫克,在第0、2周100毫克作为诱导,然后每四周50毫克,持续大约两年。
    UNASSIGNED:关于在儿科中使用皮下golimumab的建议很弱,因为这是基于开放标签的药代动力学队列。它在100毫克/1毫升可用,50mg/0.5ml作为智能SmartJect,或在VarioJect中以45mg/0.45ml提供10mg至45mg的戈利木单抗,增量为5mg/0.05ml。GolimumabVarioject供不应求,在包括叙利亚在内的几个地区都不可用。推荐的戈利木单抗维持剂量总是需要两个注射器,这增加了另一个负担。
    UNASSIGNED:该病例证明戈利木单抗200毫克,在第0周,第2周100mg作为诱导,然后每四周50mg在<45kg儿童中是有效和安全的,在2年的治疗期间没有出现副作用或不良事件.
    UNASSIGNED: Ulcerative colitis is an immune-mediated disease that carries challenges in pediatrics since it\'s frequently severe and extensive. Current pediatric ulcerative colitis guidelines offer a weak recommendation regarding the usage and the dosage of golimumab in low-weight children. We present a case of an off-label, unrecommended dose of subcutaneous golimumab to treat low-weight chronic active ulcerative colitis child.
    UNASSIGNED: A 10-year-old Syrian girl, anti-TNF naïve, chronically active ulcerative colitis was weighs 25 kg, standing 142 cm tall, body surface area (BSA) of 0.993 m2, past medications included oral prednisone and mesalamine, no prior surgery. We used golimumab 200 mg, 100 mg at weeks 0, 2 as induction, then 50 mg every four weeks for about two years.
    UNASSIGNED: The recommendation regarding the use of subcutaneous golimumab in pediatrics is weak since is based on an open-label pharmacokinetics cohort. It is available in 100 mg/1 ml, 50 mg/0.5 ml as a smart SmartJect, or in 45 mg/0.45 ml in VarioJect which provides golimumab from 10 mg to 45 mg in increments of 5 mg/0.05 ml. Golimumab Varioject is in short supply, and unavailable in several regions including Syria. The recommended golimumab maintenance dose always requires two injectors, which adds another burden.
    UNASSIGNED: This case demonstrated that golimumab 200 mg, 100 mg at week 0, 2 as an induction then 50 mg every four weeks was efficacious and safe in<45 kg children, there were no side effects or adverse events during two years therapy period.
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  • 文章类型: Case Reports
    背景和目的:强直性脊柱炎(AS)是一种影响成年人口0.1%至0.5%的疾病。本病例报告的目的是通过进行非常详细的分析,研究用于治疗AS的药物以及COVID-19的mRNA疫苗接种对精液质量的可能影响。材料和方法:通过光学显微镜检查精子特征,通过流式细胞术分析DNA片段(DFI),并通过透射电子显微镜(TEM)评估形态。结果:(1)塞来昔布和柳氮磺吡啶治疗下的精液分析显示:浓度为47百万/mL,53%的渐进性运动,7%正常形态和9.6%DFI,(2)戈利木单抗和mRNA疫苗接种前显示:浓度为1.08亿/mL,82%的渐进性运动,1%正常形态和7.6%DFI,和(3)戈利木单抗和3剂量的mRNA疫苗接种后显示:浓度为142百万/mL,85%的渐进性运动,1%正常形态和6.8%DFI。透射电镜显示头部,颈部和尾部异常,以及在接受塞来昔布和柳氮磺吡啶治疗的样品中存在精子生成不完全的白细胞和吞噬细胞。戈利木单抗治疗导致延长头部的发生率增加,但通常减少炎症,因为在TEM中没有明显的白细胞。结论:抗炎药物塞来昔布和柳氮磺胺吡啶对精子质量无不良影响,因为所有参数均在正常范围内,患者在自然受孕后获得2次妊娠,分别导致健康男孩和女孩出生。使用Golimumab的抗TNFa治疗对形态学有负面影响,但对浓度没有影响。运动性和DFI。3剂mRNA疫苗接种后,精子浓度增加而运动,形态学和DFI与疫苗接种前的值相似,表明COVID-19mRNA疫苗对精子质量没有负面影响。
    Background and Objectives: Ankylosing spondylitis (AS) is a condition that affects 0.1% to 0.5% of the adult population. The aim of this case report was to investigate the possible effects of the drugs taken for treatment of AS as well as mRNA vaccination for COVID-19 on semen quality by performing a highly detailed analysis. Materials and Methods: Sperm characteristics were examined by light microscopy, DNA fragmentation (DFI) was analysed by flow cytometry and morphology was evaluated by transmission electron microscopy (TEM). Results: Semen analysis under therapy with (1) celecoxib and sulphasalazine showed: concentration 47 million/mL, 53% progressive motility, 7% normal morphology and 9.6% DFI, (2) Golimumab and before mRNA Vaccination showed: concentration 108 million/mL, 82% progressive motility, 1% normal morphology and 7.6% DFI, and (3) Golimumab and after 3 doses of mRNA Vaccination showed: concentration 142 million/mL, 85% progressive motility, 1% normal morphology and 6.8% DFI. TEM revealed head, neck and tail abnormalities, as well as the presence of cells with incomplete spermiogenesis white cells and phagocytes in the sample under therapy with celecoxib and sulphasalazine. Golimumab treatment lead to an increased incidence of elongated heads but in general reduced inflammation as no white cells were evident in TEM. Conclusion: The anti-inflamatory drugs celecoxib and sulphasalazine had no adverse effect on sperm quality as all parameters were within normal limits and the patient achieved under that treatment 2 pregnancies following natural conception that lead to the birth of a healthy boy and girl respectively. Anti-TNFa treatment with Golimumab exerted a negative effect on morphology but not on concentration, motility and DFI. After 3 doses of mRNA Vaccination, sperm concentration increased while motility, morphology and DFI remained similar to the values before vaccination suggesting no negative effect of the mRNA vaccine for COVID-19 on sperm quality.
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  • 文章类型: Case Reports
    背景:流行病学研究表明,幽门螺杆菌感染/暴露与炎症性肠病患病率/发病率呈负相关,然而,没有关于根除幽门螺杆菌后出现“非短暂性”溃疡性结肠炎(UC)的个别患者的报告.
    方法:我们报告了一例72岁女性患者,患有老年UC,是在根除幽门螺杆菌后发展的,并对其进展为类固醇依赖性结肠炎并发肠病性关节炎并最终使用戈利木单抗控制疾病进行了3年随访。在我们的病人身上,根除幽门螺杆菌与泛结肠炎的发展相关,内窥镜,病理组织学证实为UC。
    结论:我们患者的案例为越来越多的文献提供了独特的临床背景,这些文献表明涉及基因相互作用的分子机制,环境,微生物群在UC的病因中至关重要,因此,为该主题的临床前和流行病学研究提供了一组有价值的补充翻译信息。
    BACKGROUND: Epidemiological studies suggest an inverse association between H. pylori infection/exposure and inflammatory bowel disease prevalence/incidence, however, there are no reports of individual patients who developed a \"non-transient\" ulcerative colitis (UC) following H. pylori eradication.
    METHODS: We report a case of a 72-year-old female with an elderly-onset UC developed upon H. pylori eradication and a 3-year follow-up of the progression to steroid-dependent colitis complicated with enteropathic arthritis and final containment of the disease with golimumab. In our patient, H. pylori eradication was associated with the development of pancolitis that evolved into clinically, endoscopically, and pathohistologically confirmed UC.
    CONCLUSIONS: The case of our patient provides a unique clinical context for a growing body of literature suggesting molecular mechanisms involved in the interaction of genes, environment, and microbiota to be of critical importance in the etiopathogenesis of UC, and thus, provides a valuable set of complementary translational information for preclinical and epidemiological research on the topic.
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