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抗 CMV 药物在造血干细胞移植受者中的应用

Antiviral Agents for Preventing Cytomegalovirus Disease in Recipients of Hematopoietic Cell Transplantation.

机构信息

Division of Hematology and Oncology, Department of Pediatrics, Chang Gung Memorial Hospital, Taoyuan 33315, Taiwan.

Division of Nursing, Chang Gung Memorial Hospital, Taoyuan 33315, Taiwan.

出版信息

Viruses. 2024 Aug 8;16(8):1268. doi: 10.3390/v16081268.

DOI:10.3390/v16081268
PMID:39205242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11359103/
Abstract

This systematic review discusses the use of prophylaxis to prevent cytomegalovirus (CMV) infection in recipients who have undergone hematopoietic cell transplantation. It highlights the need for new approaches to control and prevent CMV infection. The approval of the anti-CMV drug letermovir has made antiviral prophylaxis more popular. CMV-specific T cell-mediated immunity tests are effective in identifying patients who have undergone immune reconstitution and predicting disease progression. Maribavir (MBV) has been approved for the treatment of post-transplant CMV infection/disease in adolescents. Adoptive T-cell therapy and the PepVax CMV vaccine show promise in tackling refractory and resistant CMV. However, the effectiveness of PepVax in reducing CMV viremia/disease was not demonstrated in a phase II trial. Cell-mediated immunity assays are valuable for personalized management plans, but more interventional studies are needed. MBV and adoptive T-cell therapy are promising treatments, and trials for CMV vaccines are ongoing.

摘要

这篇系统综述讨论了在接受造血细胞移植的患者中使用预防措施来预防巨细胞病毒(CMV)感染。它强调了需要新的方法来控制和预防 CMV 感染。抗 CMV 药物来特莫韦的批准使得抗病毒预防更受欢迎。CMV 特异性 T 细胞介导的免疫试验可有效识别已进行免疫重建的患者,并预测疾病进展。马拉韦罗(MBV)已获准用于治疗青少年移植后 CMV 感染/疾病。过继性 T 细胞疗法和 PepVax CMV 疫苗在解决难治性和耐药性 CMV 方面显示出希望。然而,PepVax 在 II 期试验中并未显示出降低 CMV 病毒血症/疾病的有效性。细胞介导的免疫测定对个性化管理计划很有价值,但需要更多的干预性研究。MBV 和过继性 T 细胞疗法是有前途的治疗方法,CMV 疫苗的试验正在进行中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03be/11359103/a46a9193a07d/viruses-16-01268-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03be/11359103/a46a9193a07d/viruses-16-01268-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03be/11359103/a46a9193a07d/viruses-16-01268-g001.jpg

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本文引用的文献

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Impact of cytomegalovirus (CMV) seroconversion pre-allogeneic hematopoietic cell transplantation on posttransplant outcomes.巨细胞病毒(CMV)血清转化对异基因造血细胞移植后结局的影响。
Eur J Haematol. 2024 Oct;113(4):441-453. doi: 10.1111/ejh.14251. Epub 2024 Jun 16.
2
Safety and Immunogenicity of a Messenger RNA-Based Cytomegalovirus Vaccine in Healthy Adults: Results From a Phase 1 Randomized Clinical Trial.信使 RNA 基于的巨细胞病毒疫苗在健康成年人中的安全性和免疫原性:一项 1 期随机临床试验结果。
J Infect Dis. 2024 Sep 23;230(3):e668-e678. doi: 10.1093/infdis/jiae114.
3
Cytomegalovirus Reactivations in Allogeneic Hematopoietic Stem Cell Transplantation from HLA-Matched and Haploidentical Donors with Post-Transplantation Cyclophosphamide.
移植后环磷酰胺治疗 HLA 匹配和单倍体相合异基因造血干细胞移植后巨细胞病毒再激活。
Transplant Cell Ther. 2024 May;30(5):538.e1-538.e10. doi: 10.1016/j.jtct.2024.01.082. Epub 2024 Feb 6.
4
Human Cytomegalovirus mRNA-1647 Vaccine Candidate Elicits Potent and Broad Neutralization and Higher Antibody-Dependent Cellular Cytotoxicity Responses Than the gB/MF59 Vaccine.人巨细胞病毒 mRNA-1647 疫苗候选物比 gB/MF59 疫苗诱导更强和更广泛的中和及抗体依赖性细胞细胞毒性反应。
J Infect Dis. 2024 Aug 16;230(2):455-466. doi: 10.1093/infdis/jiad593.
5
Efficacy and safety of extended duration letermovir prophylaxis in recipients of haematopoietic stem-cell transplantation at risk of cytomegalovirus infection: a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.延长疗程乐韦莫韦预防造血干细胞移植受者巨细胞病毒感染的疗效和安全性:一项多中心、随机、双盲、安慰剂对照的 3 期临床试验。
Lancet Haematol. 2024 Feb;11(2):e127-e135. doi: 10.1016/S2352-3026(23)00344-7. Epub 2023 Dec 21.
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