• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肝移植受者中肿瘤坏死因子拮抗剂治疗炎症性肠病。

Anti-tumour necrosis factor treatment of inflammatory bowel disease in liver transplant recipients.

机构信息

Department of Internal Medicine, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

出版信息

Aliment Pharmacol Ther. 2012 Sep;36(6):569-74. doi: 10.1111/j.1365-2036.2012.05217.x. Epub 2012 Jul 10.

DOI:10.1111/j.1365-2036.2012.05217.x
PMID:22779779
Abstract

BACKGROUND

Ulcerative colitis (UC) and Crohn's disease can sometimes relapse and be refractory to standard treatment following orthotopic liver transplantation (OLT) despite post-transplantation immunosuppressive therapy.

AIM

To evaluate the efficacy and safety of anti-tumour necrosis factor (anti-TNF) agents for the management of IBD following OLT.

METHODS

We reviewed the records of patients with a diagnosis of IBD who underwent OLT at Mayo Clinic Rochester between 1985 and 2009. Patients were included if they had received anti-TNF therapy post-OLT. Clinical response was defined as a physician's assessment of improvement after 12 weeks of anti-TNF usage, and mucosal healing was defined as the absence of ulcerations on follow-up endoscopy.

RESULTS

The median age of the eight study patients was 42.0 years and 37.5% were female patients. All had been diagnosed with IBD prior to OLT (UC in three and Crohn's disease in five). Indication for OLT was cirrhotic stage primary sclerosing cholangitis (PSC), and three concomitantly had cholangiocarcinoma. Clinical response was demonstrated in seven of eight patients (87.5%) and mucosal healing was demonstrated in three of seven (42.9%). Four infections (oral candidiasis, Clostridium difficile colitis, bacterial pneumonia and cryptosporidiosis) in three patients were reported. One patient developed an Epstein-Barr virus-positive post-transplant lympho-proliferative disorder. One death occurred due to complications from recurrent PSC.

CONCLUSIONS

Starting Anti-TNF therapy following orthotopic liver transplantation appears to be a potential option for inflammatory bowel disease management. Additional studies are needed, however, to confirm these findings and to further assess risks associated with this treatment strategy.

摘要

背景

溃疡性结肠炎(UC)和克罗恩病在接受原位肝移植(OLT)后,尽管接受了移植后免疫抑制治疗,但有时仍会复发且对标准治疗无效。

目的

评估抗肿瘤坏死因子(anti-TNF)药物在OLT 后治疗 IBD 的疗效和安全性。

方法

我们回顾了 1985 年至 2009 年在梅奥诊所罗切斯特分校接受 OLT 的 IBD 诊断患者的病历。如果患者在 OLT 后接受了抗 TNF 治疗,则将其纳入研究。临床反应定义为医生在使用抗 TNF 药物 12 周后评估的改善,黏膜愈合定义为随访内镜检查无溃疡。

结果

八名研究患者的中位年龄为 42.0 岁,女性占 37.5%。所有患者在 OLT 前均被诊断为 IBD(UC 患者 3 例,克罗恩病患者 5 例)。OLT 的适应证为肝硬化期原发性硬化性胆管炎(PSC),同时有 3 例患者合并胆管癌。八名患者中有七名(87.5%)显示出临床反应,七名中有三名(42.9%)显示出黏膜愈合。三名患者出现了四种感染(口腔念珠菌病、艰难梭菌结肠炎、细菌性肺炎和隐孢子虫病)。一名患者发生了 EBV 阳性移植后淋巴组织增生性疾病。一名患者因复发性 PSC 并发症而死亡。

结论

OLT 后开始使用抗 TNF 治疗似乎是治疗 IBD 的一种潜在选择。然而,需要进一步的研究来证实这些发现,并进一步评估这种治疗策略相关的风险。

相似文献

1
Anti-tumour necrosis factor treatment of inflammatory bowel disease in liver transplant recipients.肝移植受者中肿瘤坏死因子拮抗剂治疗炎症性肠病。
Aliment Pharmacol Ther. 2012 Sep;36(6):569-74. doi: 10.1111/j.1365-2036.2012.05217.x. Epub 2012 Jul 10.
2
The safety and efficacy of antitumour necrosis factor-alpha therapy for inflammatory bowel disease in patients post liver transplantation: a case series.肿瘤坏死因子-α 拮抗剂治疗肝移植后炎症性肠病患者的安全性和疗效:病例系列研究。
Aliment Pharmacol Ther. 2012 Jul;36(2):159-65. doi: 10.1111/j.1365-2036.2012.05141.x. Epub 2012 May 23.
3
Serious infections in patients with inflammatory bowel disease receiving anti-tumor-necrosis-factor-alpha therapy: an Australian and New Zealand experience.抗肿瘤坏死因子-α治疗的炎症性肠病患者的严重感染:澳大利亚和新西兰的经验。
J Gastroenterol Hepatol. 2010 Nov;25(11):1732-8. doi: 10.1111/j.1440-1746.2010.06407.x.
4
Efficacy of adalimumab for the management of inflammatory bowel disease in the clinical setting.阿达木单抗在临床环境中治疗炎症性肠病的疗效。
J Gastroenterol Hepatol. 2009 Jul;24(7):1252-7. doi: 10.1111/j.1440-1746.2009.05786.x. Epub 2009 Feb 12.
5
Anti-TNF therapy in inflammatory bowel diseases: a huge review.炎症性肠病中的抗 TNF 治疗:一篇全面综述。
Minerva Gastroenterol Dietol. 2010 Jun;56(2):233-43.
6
Mucosal healing in pediatric Crohn's disease after anti-TNF therapy: a long-term experience at a single center.儿童克罗恩病抗 TNF 治疗后的黏膜愈合:单中心长期经验。
Eur J Gastroenterol Hepatol. 2014 Apr;26(4):458-65. doi: 10.1097/MEG.0000000000000045.
7
Pre-operative use of anti-TNF-α agents and the risk of post-operative complications in patients with ulcerative colitis - a nationwide cohort study.术前使用抗 TNF-α 药物与溃疡性结肠炎患者术后并发症风险的关系:一项全国性队列研究。
Aliment Pharmacol Ther. 2012 Jun;35(11):1301-9. doi: 10.1111/j.1365-2036.2012.05099.x. Epub 2012 Apr 16.
8
Safety aspects of infliximab in inflammatory bowel disease patients. A retrospective cohort study in 100 patients of a German University Hospital.英夫利昔单抗在炎症性肠病患者中的安全性。对德国一家大学医院100例患者的回顾性队列研究。
Digestion. 2004;70(1):3-9. doi: 10.1159/000080075. Epub 2004 Aug 3.
9
Concomitant therapy with methotrexate and anti-TNF-α in pediatric patients with refractory crohn's colitis: a case series.在难治性克罗恩病患儿中联合使用甲氨蝶呤和抗 TNF-α 治疗:病例系列研究。
Inflamm Bowel Dis. 2012 Aug;18(8):1488-92. doi: 10.1002/ibd.21885. Epub 2011 Aug 31.
10
Methotrexate for psoriasiform lesions associated with anti-tumour necrosis factor therapy in inflammatory bowel disease.甲氨蝶呤治疗与抗肿瘤坏死因子治疗相关的炎症性肠病的银屑病样病变。
Aliment Pharmacol Ther. 2012 May;35(10):1175-80. doi: 10.1111/j.1365-2036.2012.05082.x. Epub 2012 Apr 2.

引用本文的文献

1
Liver Transplantation for Primary Sclerosing Cholangitis (PSC) With or Without Inflammatory Bowel Disease (IBD)-A European Society of Organ Transplantation (ESOT) Consensus Statement.原发性硬化性胆管炎(PSC)伴或不伴炎症性肠病(IBD)的肝移植-欧洲器官移植学会(ESOT)共识声明。
Transpl Int. 2023 Sep 29;36:11729. doi: 10.3389/ti.2023.11729. eCollection 2023.
2
Concurrent inflammatory bowel disease and primary sclerosing cholangitis: a review of pre- and post-transplant outcomes and treatment options.炎症性肠病与原发性硬化性胆管炎并存:移植前后结局及治疗选择综述
Gastroenterol Hepatol Bed Bench. 2023;16(3):259-269. doi: 10.22037/ghfbb.v16i2.2589.
3
Unique Phenotypic Characteristics and Clinical Course in Patients With Ulcerative Colitis and Primary Sclerosing Cholangitis: A Multicenter US Experience.
溃疡性结肠炎和原发性硬化性胆管炎患者的独特表型特征和临床病程:一项多中心美国经验。
Inflamm Bowel Dis. 2020 Apr 11;26(5):774-779. doi: 10.1093/ibd/izz209.
4
Specific Features of Patients With Inflammatory Bowel Disease and Primary Sclerosing Cholangitis.炎症性肠病合并原发性硬化性胆管炎患者的特征
J Clin Med Res. 2019 Feb;11(2):81-88. doi: 10.14740/jocmr3680. Epub 2019 Jan 5.
5
Harmful Effects and Potential Benefits of Anti-Tumor Necrosis Factor (TNF)-α on the Liver.抗肿瘤坏死因子-α(TNF-α)对肝脏的有害影响和潜在益处。
Int J Mol Sci. 2018 Jul 27;19(8):2199. doi: 10.3390/ijms19082199.
6
Tumor Necrosis Factor Alpha Inhibition for Inflammatory Bowel Disease after Liver Transplant for Primary Sclerosing Cholangitis.肝移植治疗原发性硬化性胆管炎后肿瘤坏死因子α抑制治疗炎症性肠病
Case Rep Gastrointest Med. 2018 May 15;2018:1015408. doi: 10.1155/2018/1015408. eCollection 2018.
7
Natural History of Established and De Novo Inflammatory Bowel Disease After Liver Transplantation for Primary Sclerosing Cholangitis.原发性硬化性胆管炎行肝移植术后新发和已确立的炎症性肠病的自然病程。
Inflamm Bowel Dis. 2018 Apr 23;24(5):1074-1081. doi: 10.1093/ibd/izx096.
8
Evolving strategies to reduce colectomy rates in primary sclerosing cholangitis-inflammatory bowel disease: clinical remission of corticosteroid refractory colitis post-liver transplant with vedolizumab.降低原发性硬化性胆管炎合并炎症性肠病结肠切除率的不断演变策略:维得利珠单抗治疗肝移植后皮质类固醇难治性结肠炎的临床缓解
Frontline Gastroenterol. 2016 Oct;7(4):271-274. doi: 10.1136/flgastro-2016-100711. Epub 2016 Aug 5.
9
Inflammatory bowel disease in liver transplanted patients.肝移植患者中的炎症性肠病
World J Gastroenterol. 2017 May 14;23(18):3214-3227. doi: 10.3748/wjg.v23.i18.3214.
10
Vedolizumab is safe and effective in moderate-to-severe inflammatory bowel disease following liver transplantation.维多珠单抗在肝移植术后中重度炎症性肠病中安全有效。
Liver Transpl. 2017 Jul;23(7):968-971. doi: 10.1002/lt.24757.