1992年至2008年,乌干达农村普通人群中EB病毒抗体随时间变化。

IF 3.1 2区 医学 Q3 IMMUNOLOGY Infectious Agents and Cancer Pub Date : 2023-09-29 DOI:10.1186/s13027-023-00534-7
Katherine R Sabourin, Joseph Mugisha, Gershim Asiki, Angela Nalwoga, Nazzarena Labo, Wendell Miley, Rachel Beyer, Rosemary Rochford, Thomas W Johnston, Robert Newton, Denise Whitby
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引用次数: 0

摘要

背景:EB病毒(Epstein-Barr virus,EBV)感染在撒哈拉以南非洲地区普遍存在,发生在生命早期。在一个以人口为基础的非洲农村队列中,我们利用乌干达普通人群队列(GPC)的历史样本来检查艾滋病毒时代EBV感染的流行病学。方法:我们使用了1992年、2000年、2008年从GPC收集的9024份血清样本,来自7576名年龄段(0-99岁)的参与者,并使用基于多重珠粒的测定法测试针对EAd、VCA和EBNA-1的抗EBV免疫球蛋白G(IgG)抗体。通过重组蛋白酶联免疫吸附测定法检测K8.1或ORF73的抗KSHV IgG抗体,也确定了相关的γ-疱疹病毒、卡波西肉瘤相关疱疹病毒(KSHV)血清阳性。还收集了有关性别、年龄和艾滋病毒血清状态的数据。EBV血清阳性率根据年龄(不包括一岁以下的人,他们可能有母体抗体)、性别、HIV血清状态和KSHV血清状态进行建模,使用广义线性混合效应模型产生β估计值。结果:93%以上的儿童在一岁时EBV血清阳性。EBV血清阳性与KSHV血清阳性显著相关。抗-EBNA-1抗体水平随着年龄的增长而下降,在艾滋病毒感染者中平均水平较低。总的来说,抗EAd抗体水平随着年龄的增长而增加,在男性和KSHV血清阳性者中更高,但随着时间的推移而下降。抗VCA抗体水平随着年龄和日历时间的增加而增加,KSHV血清阳性者的抗体水平较高,但男性的抗体水平较低。结论:这是第一项确定撒哈拉以南非洲农村整个生命过程中与EBV抗体相关因素的研究。与其他研究一致,EBV在一岁的人群中几乎无处不在。抗体模式显示出随年龄、性别和日历时间的变化,但与艾滋病毒没有明显的关联,这表明EBV血清流行病学与乌干达人群中艾滋病毒的长期传播之间没有关系。
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Epstein-Barr virus (EBV) antibody changes over time in a general population cohort in rural Uganda, 1992-2008.

Background: Epstein-Barr virus (EBV) infection is ubiquitous and in sub-Saharan Africa, occurs early in life. In a population-based rural African cohort, we leveraged historical samples from the General Population Cohort (GPC) in Uganda to examine the epidemiology of infection with EBV over time, in the era of HIV.

Methods: We used 9024 serum samples collected from the GPC in 1992, 2000, 2008, from 7576 participants across the age range (0-99 years of age) and tested for anti-EBV immunoglobulin G (IgG) antibodies to EAd, VCA, and EBNA-1 using a multiplex bead-based assay. The related gammaherpesvirus, Kaposi's sarcoma-associated herpesvirus (KSHV) seropositivity was also determined by detection of anti-KSHV IgG antibodies to K8.1 or ORF73 measured by recombinant protein enzyme-linked immunosorbent assay. Data on sex, age, and HIV serostatus were also collected. EBV seropositivity was modeled with age (excluding those under one year, who may have had maternal antibodies), sex, HIV serostatus, and KSHV serostatus using generalized linear mixed effects models to produce beta estimates.

Results: More than 93% of children were EBV seropositive by one year of age. EBV seropositivity was significantly associated with KSHV seropositivity. Anti-EBNA-1 antibody levels decreased with increasing age and were lower on average in people living with HIV. In general, anti-EAd antibody levels increased with age, were higher in males and KSHV seropositive persons, but decreased over calendar time. Anti-VCA antibody levels increased with age and with calendar time and were higher in KSHV seropositive persons but lower in males.

Conclusions: This is the first study to identify factors associated with EBV antibodies across the entire life-course in rural sub-Saharan Africa. Consistent with other studies, EBV was near ubiquitous in the population by age one year. Patterns of antibodies show changes by age, sex and calendar time, but no association with HIV was evident, suggesting no relationship between EBV sero-epidemiology and the spread of HIV in the population over time in Uganda.

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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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