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病例报告:通过高剂量 CMV 特异性免疫球蛋白、免疫抑制调节和诱导 CMV 特异性细胞免疫来治疗肾移植受者中的多重耐药 CMV 株。

Case Report: Management of a Multidrug-Resistant CMV-Strain in a Renal Transplant Recipient by High-Dose CMV-Specific Immunoglobulins, Modulation in Immunosuppression, and Induction of CMV-Specific Cellular Immunity.

机构信息

Transplant Nephrology/Department of Internal Medicine D, University Hospital Münster, Westphalian Wilhelm's University Münster, Münster, Germany.

Department of Transplant and Infection Immunology, Saarland University, Homburg, Germany.

出版信息

Front Immunol. 2021 Jan 25;11:623178. doi: 10.3389/fimmu.2020.623178. eCollection 2020.

Abstract

The management of multidrug-resistant strains of cytomegalovirus after solid organ transplantation is challenging. This case report demonstrates the successful treatment of a multidrug-resistant strain of cytomegalovirus that may represent a valuable option for problematic cases. This report illustrates the emergence of a multidrug-resistant cytomegalovirus (CMV) UL54 mutant strain in a renal transplant recipient with severe lymphopenia and thrombocytopenia. We show that the combined treatment with high-dose intravenous cytomegalovirus-specific immunoglobulins (CMV-IVIG) after the switch to a mammalian target of rapamycin (mTOR)-inhibitor and cyclosporine A was a successful treatment alternative to direct antiviral treatment with high-dose ganciclovir and foscarnet. This treatment was associated with a quantitative induction of CMV-specific CD4 and CD8 T cells that showed maturation in phenotype and functionality with decreasing viral load. Our case report illustrates that high-dose CMV-IVIG and conversion of immunosuppressive drugs to mTOR inhibitors and cyclosporine A can be a successful treatment in a situation where the use of direct antiviral drugs was considered insufficient.

摘要

器官移植后耐多药巨细胞病毒的管理具有挑战性。本病例报告展示了一种成功治疗耐多药巨细胞病毒的方法,可能为棘手病例提供了有价值的选择。本报告描述了一例肾移植受者出现严重淋巴细胞减少和血小板减少的耐多药巨细胞病毒(CMV)UL54 突变株。我们表明,在切换至雷帕霉素(mTOR)抑制剂和环孢素 A 后,联合使用高剂量静脉用巨细胞病毒特异性免疫球蛋白(CMV-IVIG)是一种成功的治疗选择,可替代高剂量更昔洛韦和膦甲酸的直接抗病毒治疗。这种治疗与 CMV 特异性 CD4 和 CD8 T 细胞的定量诱导相关,这些细胞在表型和功能上随着病毒载量的降低而成熟。本病例报告表明,在考虑使用直接抗病毒药物治疗不足的情况下,高剂量 CMV-IVIG 和将免疫抑制剂转换为 mTOR 抑制剂和环孢素 A 可作为一种成功的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9674/7868410/558ad71fd12f/fimmu-11-623178-g001.jpg

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