• 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

巨细胞病毒免疫球蛋白预防先天性巨细胞病毒病。

Hyperimmunoglobulin for prevention of congenital cytomegalovirus disease.

机构信息

Pediatric Unit, Department of Life, Health and Environmental Sciences, University of L'Aquila, Italy.

出版信息

Clin Infect Dis. 2013 Dec;57 Suppl 4:S193-5. doi: 10.1093/cid/cit586.

DOI:10.1093/cid/cit586
PMID:24257426
Abstract

Primary cytomegalovirus (CMV) infection during the first half of pregnancy is responsible for the majority of symptomatic congenital infections. Between one-third and one-half of fetuses become infected, and up to one-half of infected fetuses will have neurologic or sensorineural sequelae at birth or later in life. Following favorable results obtained in animal experiments, observational studies have shown beneficial effects after administration of high-titer CMV hyperimmunoglobulin to pregnant women with fetal infection or disease subsequent to primary CMV infection. The mechanisms of action of hyperimmunoglobulin are multiple and not yet fully understood. However, they could reside in 2 major properties: (1) antiviral activities due to high-avidity neutralizing antibodies and (2) immunomodulating activities mostly including downregulation of cytokine-mediated cellular immune responses. A decreased viral pathogenicity occurs as an immediate consequence, whereas reduced placental inflammation and restored function are the long-term effects.

摘要

原发性巨细胞病毒(CMV)感染在妊娠前半期是导致大多数有症状先天性感染的主要原因。三分之一到一半的胎儿会受到感染,而感染的胎儿中有一半会在出生时或以后出现神经或感觉神经后遗症。在动物实验中取得良好结果后,观察性研究表明,在原发性 CMV 感染后胎儿感染或疾病的孕妇中,给予高滴度 CMV 免疫球蛋白有治疗效果。免疫球蛋白的作用机制是多方面的,目前尚未完全了解。然而,它们可能存在于 2 个主要特性中:(1)由于高亲和力中和抗体而具有抗病毒活性,以及(2)免疫调节活性,主要包括下调细胞因子介导的细胞免疫反应。作为直接后果,病毒致病性降低,而胎盘炎症减少和功能恢复是长期影响。

相似文献

1
Hyperimmunoglobulin for prevention of congenital cytomegalovirus disease.巨细胞病毒免疫球蛋白预防先天性巨细胞病毒病。
Clin Infect Dis. 2013 Dec;57 Suppl 4:S193-5. doi: 10.1093/cid/cit586.
2
The importance of cytomegalovirus-specific antibodies for the prevention of fetal cytomegalovirus infection or disease.巨细胞病毒特异性抗体对预防胎儿巨细胞病毒感染或疾病的重要性。
Herpes. 2008 Nov;15(2):24-7.
3
Findings and conclusions from CMV hyperimmune globulin treatment trials.CMV 高免疫球蛋白治疗试验的结果和结论。
J Clin Virol. 2009 Dec;46 Suppl 4:S54-7. doi: 10.1016/j.jcv.2009.08.017. Epub 2009 Sep 24.
4
Use of cytomegalovirus hyperimmunoglobulin for prevention of congenital cytomegalovirus disease: a retrospective analysis.使用巨细胞病毒高免疫球蛋白预防先天性巨细胞病毒病:回顾性分析。
J Perinat Med. 2012 Mar 27;40(4):439-46. doi: 10.1515/jpm-2011-0257.
5
Screening, diagnosis, and management of cytomegalovirus infection in pregnancy.妊娠期巨细胞病毒感染的筛查、诊断和处理。
Obstet Gynecol Surv. 2010 Nov;65(11):736-43. doi: 10.1097/OGX.0b013e31821102b4.
6
Intraperitoneal administration of cytomegalovirus hyperimmunoglobulin to the cytomegalovirus-infected fetus.向巨细胞病毒感染的胎儿腹腔内注射巨细胞病毒高免疫球蛋白。
J Perinatol. 1998 Nov-Dec;18(6 Pt 1):466-9.
7
Fetal and maternal outcome after hyperimmunoglobulin administration for prevention of maternal-fetal transmission of cytomegalovirus during pregnancy: retrospective cohort analysis.孕期应用免疫球蛋白预防巨细胞病毒母婴传播的母婴结局:回顾性队列分析。
Arch Gynecol Obstet. 2020 Dec;302(6):1353-1359. doi: 10.1007/s00404-020-05728-7. Epub 2020 Aug 4.
8
Prevention of maternal-fetal transmission of cytomegalovirus after primary maternal infection in the first trimester by biweekly hyperimmunoglobulin administration.通过每两周一次的高免疫球蛋白给药来预防原发性母体感染后第一孕期母婴传播巨细胞病毒。
Ultrasound Obstet Gynecol. 2019 Mar;53(3):383-389. doi: 10.1002/uog.19164. Epub 2019 Feb 8.
9
Twin pregnancy and congenital cytomegalovirus: case report and review.双胎妊娠与先天性巨细胞病毒感染:病例报告及文献复习
J Matern Fetal Neonatal Med. 2013 Apr;26(6):622-4. doi: 10.3109/14767058.2012.745503. Epub 2012 Nov 28.
10
[Therapy or prevention of fetal infection by cytomegalovirus with immunoglobulin infusion in pregnant women with primary infection].[通过对初次感染的孕妇输注免疫球蛋白治疗或预防巨细胞病毒胎儿感染]
Acta Biomed Ateneo Parmense. 2000;71 Suppl 1:547-51.

引用本文的文献

1
Maternal Fc-mediated non-neutralizing antibody responses correlate with protection against congenital human cytomegalovirus infection.母体 Fc 介导的非中和抗体反应与预防先天性人巨细胞病毒感染相关。
J Clin Invest. 2022 Aug 15;132(16). doi: 10.1172/JCI156827.
2
Lessons from Acquired Natural Immunity and Clinical Trials to Inform Next-Generation Human Cytomegalovirus Vaccine Development.从获得性天然免疫和临床试验中汲取经验教训,为下一代人巨细胞病毒疫苗的开发提供信息。
Annu Rev Virol. 2022 Sep 29;9(1):491-520. doi: 10.1146/annurev-virology-100220-010653. Epub 2022 Jun 15.
3
Congenital Human Cytomegalovirus Infection Is Associated With Decreased Transplacental IgG Transfer Efficiency Due to Maternal Hypergammaglobulinemia.
先天性人巨细胞病毒感染与母体高丙种球蛋白血症导致的胎盘 IgG 转移效率降低有关。
Clin Infect Dis. 2022 Apr 9;74(7):1131-1140. doi: 10.1093/cid/ciab627.
4
Bright and Early: Inhibiting Human Cytomegalovirus by Targeting Major Immediate-Early Gene Expression or Protein Function.早期研究:通过靶向主要即刻早期基因表达或蛋白功能抑制人巨细胞病毒。
Viruses. 2020 Jan 16;12(1):110. doi: 10.3390/v12010110.
5
Vaccine Vectors Harnessing the Power of Cytomegaloviruses.利用巨细胞病毒力量的疫苗载体
Vaccines (Basel). 2019 Oct 17;7(4):152. doi: 10.3390/vaccines7040152.
6
Congenital Cytomegalovirus Infection.先天性巨细胞病毒感染
Ochsner J. 2019 Summer;19(2):123-130. doi: 10.31486/toj.18.0095.
7
Cytomegalovirus: Shape-Shifting the Immune System.巨细胞病毒:改变免疫系统形态。
J Immunol. 2018 Jun 15;200(12):3881-3889. doi: 10.4049/jimmunol.1800171.
8
Vaccination against the human cytomegalovirus.人巨细胞病毒疫苗接种。
Vaccine. 2019 Nov 28;37(50):7437-7442. doi: 10.1016/j.vaccine.2018.02.089. Epub 2018 Apr 3.
9
Comparison of the Cytomegalovirus (CMV) Enzyme-Linked Immunosorbent Spot and CMV QuantiFERON Cell-Mediated Immune Assays in CMV-Seropositive and -Seronegative Pregnant and Nonpregnant Women.巨细胞病毒(CMV)酶联免疫斑点试验与CMV全血γ干扰素释放试验在CMV血清阳性和血清阴性孕妇及非孕妇中的比较
J Clin Microbiol. 2016 May;54(5):1352-6. doi: 10.1128/JCM.03128-15. Epub 2016 Mar 9.