Correlation between human cytomegalovirus quantitative p72 antigenemia and viremia

Jordi Reina, Isabel Blanco, Maria Munar
{"title":"Correlation between human cytomegalovirus quantitative p72 antigenemia and viremia","authors":"Jordi Reina,&nbsp;Isabel Blanco,&nbsp;Maria Munar","doi":"10.1016/S0928-0197(96)00249-8","DOIUrl":null,"url":null,"abstract":"<div><p><strong>Objective:</strong> We present a prospective study of the correlation between the human cytomegalovirus (HCMV) quantitative antigenemia with monoclonal antibody to p72 protein (immediate-early antigen) and the number of infected cell foci detected in the shell-vial culture. A comparative study was made of the value of quantitative antigenemia (pp65 and p72) in 14 patients.</p><p><strong>Results:</strong> The average value of the pp65 antigenemia was 195 pp65-positive PMNLs per 10<sup>5</sup> PMNLs (range 10–1000) and that of the p72, 21 p72-positive PMNLs per 10<sup>5</sup> PMNLs (range 0–120) (<em>P</em> &lt; 0.001). The p72 antigenemia value represented 10.7% of the pp65 value (range 4.4–70%). A statistical correlation was observed between the total number of infected cell foci detected in the shell-vial culture and the total number of p72-positive PMNLs (<em>P</em> &lt; 0.001), but not with the number of pp65-positive PMNLs (<em>P</em> = 0.4). A study of the number of infected cell foci detected in the shell-vial per 100 000 PMNLs inoculated showed a statistical correlation with the value of the p72 antigenemia (<em>P</em> &lt; 0.001).</p><p><strong>Conclusions:</strong> According to results, there seems to be a general population of PMNLs carrying viral particles which are detected by means of the pp65 monoclonal antibody, and a subpopulation carrying active and replicative viral particles which is detected with the p72 antibody. This last subpopulation would be responsible for the formation of infected cell foci in the shell-vial culture. However due to the technical difficulties presented by the routine performance of p72 antigenemia, we recommend the routine application of the quantitative shell-vial culture and the use of the number of infected cell foci × 100 000 PMNLs inoculated as a parameter of replicative viral load for the diagnosis of infection and disease caused by HCMV.</p></div>","PeriodicalId":79479,"journal":{"name":"Clinical and diagnostic virology","volume":"7 1","pages":"Pages 63-67"},"PeriodicalIF":0.0000,"publicationDate":"1996-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0928-0197(96)00249-8","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical and diagnostic virology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0928019796002498","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Objective: We present a prospective study of the correlation between the human cytomegalovirus (HCMV) quantitative antigenemia with monoclonal antibody to p72 protein (immediate-early antigen) and the number of infected cell foci detected in the shell-vial culture. A comparative study was made of the value of quantitative antigenemia (pp65 and p72) in 14 patients.

Results: The average value of the pp65 antigenemia was 195 pp65-positive PMNLs per 105 PMNLs (range 10–1000) and that of the p72, 21 p72-positive PMNLs per 105 PMNLs (range 0–120) (P < 0.001). The p72 antigenemia value represented 10.7% of the pp65 value (range 4.4–70%). A statistical correlation was observed between the total number of infected cell foci detected in the shell-vial culture and the total number of p72-positive PMNLs (P < 0.001), but not with the number of pp65-positive PMNLs (P = 0.4). A study of the number of infected cell foci detected in the shell-vial per 100 000 PMNLs inoculated showed a statistical correlation with the value of the p72 antigenemia (P < 0.001).

Conclusions: According to results, there seems to be a general population of PMNLs carrying viral particles which are detected by means of the pp65 monoclonal antibody, and a subpopulation carrying active and replicative viral particles which is detected with the p72 antibody. This last subpopulation would be responsible for the formation of infected cell foci in the shell-vial culture. However due to the technical difficulties presented by the routine performance of p72 antigenemia, we recommend the routine application of the quantitative shell-vial culture and the use of the number of infected cell foci × 100 000 PMNLs inoculated as a parameter of replicative viral load for the diagnosis of infection and disease caused by HCMV.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
人巨细胞病毒p72抗原血症与病毒血症的相关性研究
目的:对人巨细胞病毒(HCMV) p72蛋白(即早期抗原)单克隆抗体定量抗原血症与壳瓶培养中感染细胞灶数量的相关性进行前瞻性研究。对14例患者进行了定量抗原血症(pp65和p72)的比较研究。结果:pp65抗原血症的平均值为195 / 105(范围10-1000),p72抗原血症的平均值为21 / 105(范围0-120)(P <0.001)。p72抗原血症值占pp65值的10.7%(范围4.4-70%)。壳瓶培养中检测到的感染细胞病灶总数与p72阳性PMNLs总数(P <0.001),但与pp65阳性PMNLs的数量无关(P = 0.4)。一项对每10万接种PMNLs的贝壳瓶中检测到的感染细胞灶数量的研究表明,p72抗原血症值与p72抗原血症(P <0.001)。结论:pp65单克隆抗体可检测到PMNLs的一般群体携带病毒颗粒,p72单克隆抗体可检测到PMNLs的亚群携带活性和复制性病毒颗粒。这最后一个亚群将负责在壳瓶培养中形成感染细胞灶。然而,由于常规检测p72抗原血症存在技术上的困难,我们建议常规应用定量壳瓶培养,并使用接种的感染细胞灶数× 10万个PMNLs作为复制病毒载量的参数,以诊断HCMV引起的感染和疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Editorial Immune mediated and inherited defences against flaviviruses Maternal recognition of foetal infection with bovine virus diarrhoea virus (BVDV)—the bovine pestivirus The conformation of hepatitis C virus NS3 proteinase with and without NS4A: a structural basis for the activation of the enzyme by its cofactor Repression of the PKR protein kinase by the hepatitis C virus NS5A protein: a potential mechanism of interferon resistance
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1