尿中脱落的巨细胞病毒粒子对上皮细胞进入具有可逆性阻断,并且对抗体中和具有高度抗性。

Q2 Biochemistry, Genetics and Molecular Biology Clinical and Vaccine Immunology Pub Date : 2017-06-05 Print Date: 2017-06-01 DOI:10.1128/CVI.00024-17
Xiaohong Cui, Stuart P Adler, Mark R Schleiss, Ravit Arav-Boger, Gail J Demmler Harrison, Michael A McVoy
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引用次数: 6

摘要

巨细胞病毒(CMV)在子宫内感染可引起新生儿感音神经性听力损失和发育障碍。孕妇可通过口腔接触幼儿尿液或唾液中的巨细胞病毒感染巨细胞病毒。母体唾液中的中和抗体有可能预防母体感染,进而预防胎儿感染。由于巨细胞病毒使用不同的病毒糖蛋白复合物进入不同的细胞类型,因此在口腔中第一批被感染的细胞可以确定破坏口腔传播所需的抗体类型。针对五聚体复合体(PC)的抗体应该阻止巨细胞病毒进入上皮细胞,但不能进入成纤维细胞或朗格汉斯细胞(不需要PC进入),而针对糖蛋白复合体gB或gH/gL的抗体则需要阻止进入成纤维细胞、朗格汉斯细胞或其他细胞类型。为了评估抗体破坏口腔获取的可能性,研究人员使用培养阳性尿液样本(uCMV)中的巨细胞病毒(CMV)来研究细胞的趋向性和对抗体中和的敏感性。与进入成纤维细胞相比,uCMV进入上皮细胞的能力较差。cmv高免疫球蛋白或靶向gB、gH/gL或PC的单克隆抗体不能阻断uCMV进入成纤维细胞或上皮细胞。在培养成纤维细胞中,两种表型在一次传代后都消失了,这提示了非遗传机制。这些结果表明,uCMV病毒粒子对上皮细胞的进入具有可逆的阻断作用。抗体在预防母体口服巨细胞病毒获得方面可能无效,但可能限制病毒在血液或组织中的传播,从而减少或预防胎儿感染和疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Cytomegalovirus Virions Shed in Urine Have a Reversible Block to Epithelial Cell Entry and Are Highly Resistant to Antibody Neutralization.

Cytomegalovirus (CMV) causes sensorineural hearing loss and developmental disabilities in newborns when infections are acquired in utero Pregnant women may acquire CMV from oral exposure to CMV in urine or saliva from young children. Neutralizing antibodies in maternal saliva have the potential to prevent maternal infection and, in turn, fetal infection. As CMV uses different viral glycoprotein complexes to enter different cell types, the first cells to be infected in the oral cavity could determine the type of antibodies needed to disrupt oral transmission. Antibodies targeting the pentameric complex (PC) should block CMV entry into epithelial cells but not into fibroblasts or Langerhans cells (which do not require the PC for entry), while antibodies targeting glycoprotein complexes gB or gH/gL would be needed to block entry into fibroblasts, Langerhans cells, or other cell types. To assess the potential for antibodies to disrupt oral acquisition, CMV from culture-positive urine samples (uCMV) was used to study cell tropisms and sensitivity to antibody neutralization. uCMV entered epithelial cells poorly compared with the entry into fibroblasts. CMV-hyperimmune globulin or monoclonal antibodies targeting gB, gH/gL, or the PC were incapable of blocking the entry of uCMV into either fibroblasts or epithelial cells. Both phenotypes were lost after one passage in cultured fibroblasts, suggestive of a nongenetic mechanism. These results suggest that uCMV virions have a reversible block to epithelial cell entry. Antibodies may be ineffective in preventing maternal oral CMV acquisition but may limit viral spread in blood or tissues, thereby reducing or preventing fetal infection and disease.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
期刊最新文献
Correction for Nishimori et al., “Identification of an Atypical Enzootic Bovine Leukosis in Japan by Using a Novel Classification of Bovine Leukemia Based on Immunophenotypic Analysis” GI-19007, a Novel Saccharomyces cerevisiae-Based Therapeutic Vaccine against Tuberculosis. High-Definition Mapping of Four Spatially Distinct Neutralizing Epitope Clusters on RiVax, a Candidate Ricin Toxin Subunit Vaccine. Progress toward Development of a Vaccine against Congenital Cytomegalovirus Infection. Stable Chromosomal Expression of Shigella flexneri 2a and 3a O-Antigens in the Live Salmonella Oral Vaccine Vector Ty21a.
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