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预防先天性巨细胞病毒感染的免疫接种。

Immunization to prevent congenital cytomegalovirus infection.

机构信息

Department of Microbiology, Medical College of Virginia Campus/Virginia Commonwealth University, PO Box 163, Richmond, VA 23298, USA.

出版信息

Br Med Bull. 2013;107:57-68. doi: 10.1093/bmb/ldt023. Epub 2013 Aug 16.

Abstract

INTRODUCTION

A primary maternal cytomegalovirus (CMV) during pregnancy causes newborn disease that includes hearing deficit and/or mental retardation.

SOURCES OF DATA

Relevant published literature.

AREAS OF AGREEMENT

There are no biologic obstacles to immunization against fetal/placental infection with CMV.

AREAS OF UNCERTAINTY

CMV vaccine trials may be difficult due to a lack of public awareness of CMV. Vaccine trials that use fetal infection as an endpoint will be prolonged, since vaccination will need to occur preconception.

AREAS TIMELY FOR DEVELOPING RESEARCH

Vaccines in preclinical development include antigens of the CMV gB glycoprotein and the gH/gL UL128, 130 and 131 pentameric complex. These antigens induce antibodies that block viral entry into fibroblasts and endothelial/epithelial cells. Vaccines immunogenic in animals include an inactivated virus with a wild-type UL131 gene, a DNA vaccine using a wild-type UL130 gene and peptide vaccines using peptides from UL130 and 131.

CONCLUSIONS

In spite of these potential obstacles, successful evaluation of CMV vaccines is possible.

摘要

简介

妊娠期间原发性巨细胞病毒 (CMV) 会导致新生儿疾病,包括听力缺陷和/或智力迟钝。

资料来源

相关已发表文献。

共识领域

针对 CMV 引起的胎儿/胎盘感染进行免疫接种不存在生物学障碍。

不确定领域

由于公众对 CMV 认识不足,CMV 疫苗试验可能很困难。使用胎儿感染作为终点的疫苗试验将延长,因为疫苗接种需要在受孕前进行。

研究的及时领域

临床前开发的疫苗包括 CMV gB 糖蛋白和 gH/gL UL128、130 和 131 五聚体复合物的抗原。这些抗原诱导的抗体可阻止病毒进入成纤维细胞和内皮/上皮细胞。在动物中具有免疫原性的疫苗包括具有野生型 UL131 基因的灭活病毒、使用野生型 UL130 基因的 DNA 疫苗和使用 UL130 和 131 肽的肽疫苗。

结论

尽管存在这些潜在障碍,但 CMV 疫苗的成功评估是可能的。

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