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炎症性肠病患者接受免疫抑制治疗时的淋巴增殖性疾病:来自其他炎症性疾病的经验教训。

Lymphoproliferative disorders in inflammatory bowel disease patients on immunosuppression: Lessons from other inflammatory disorders.

作者信息

Lam Grace Y, Halloran Brendan P, Peters Anthea C, Fedorak Richard N

机构信息

Grace Y Lam, Department of Medicine, Division of Internal Medicine, University of Alberta, 8440 112 St NW Edmonton, Alberta, Canada.

出版信息

World J Gastrointest Pathophysiol. 2015 Nov 15;6(4):181-92. doi: 10.4291/wjgp.v6.i4.181.

Abstract

Immunosuppressive agents, such as thiopurines, methotrexate, and biologics, have revolutionized the treatment of inflammatory bowel disease (IBD). However, a number of case reports, case control studies and retrospective studies over the last decade have identified a concerning link between immunosuppression and lymphoproliferative disorders (LPDs), the oncological phenomenon whereby lymphocytes divide uncontrollably. These LPDs have been associated with Epstein-Barr virus (EBV) infection in which the virus provides the impetus for malignant transformation while immunosuppression hampers the immune system's ability to detect and clear these malignant cells. As such, the use of immunosuppressive agents may come at the cost of increased risk of developing LPD. While little is known about the LPD risk in IBD, more is known about immunosuppression in the post-transplantation setting and the development of EBV associated post-transplantation lymphoproliferative disorders (PTLD). In review of the PTLD literature, evidence is available to demonstrate that certain immune suppressants such as cyclosporine and T-lymphocyte modulators in particular are associated with an increased risk of PTLD development. As well, high doses of immunosuppressive agents and multiple immunosuppressive agent use are also linked to increased PTLD development. Here, we discuss these findings in context of IBD and what future studies can be taken to understand and reduce the risk of EBV-associated LPD development from immunosuppression use in IBD.

摘要

免疫抑制剂,如硫唑嘌呤、甲氨蝶呤和生物制剂,彻底改变了炎症性肠病(IBD)的治疗方法。然而,在过去十年中,一些病例报告、病例对照研究和回顾性研究发现,免疫抑制与淋巴增殖性疾病(LPD)之间存在令人担忧的联系,LPD是一种淋巴细胞不受控制地分裂的肿瘤学现象。这些LPD与爱泼斯坦-巴尔病毒(EBV)感染有关,在这种感染中,病毒为恶性转化提供动力,而免疫抑制则阻碍免疫系统检测和清除这些恶性细胞的能力。因此,使用免疫抑制剂可能会增加患LPD的风险。虽然对IBD中LPD的风险了解甚少,但对移植后环境中的免疫抑制以及EBV相关的移植后淋巴增殖性疾病(PTLD)的发展了解更多。在回顾PTLD文献时,有证据表明某些免疫抑制剂,特别是环孢素和T淋巴细胞调节剂,与PTLD发展风险增加有关。此外,高剂量的免疫抑制剂和多种免疫抑制剂的使用也与PTLD发展增加有关。在此,我们结合IBD讨论这些发现,以及未来可以进行哪些研究来了解和降低IBD中使用免疫抑制剂导致EBV相关LPD发展的风险。

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