Centre for Infectious Disease Research in Zambia, Lusaka, Zambia.
Department of Biomedical Sciences, School of Health Sciences, University of Zambia, Lusaka, Zambia.
PLoS One. 2020 Nov 10;15(11):e0240714. doi: 10.1371/journal.pone.0240714. eCollection 2020.
Despite contributing to a significant reduction in rotavirus associated diarrhoea in highly burdened low- and middle-income countries, live attenuated, oral rotavirus vaccines have lower immunogenicity and efficacy in these settings in comparison to more developed countries. Breastmilk has been implicated among factors contributing to this lowered oral vaccine efficacy. We conducted in-vitro experiments to investigate the inhibitory effects of maternal antibody and other non-antibody components in breastmilk on rotavirus vaccine strain (Rotarix) multiplication in MA104 cell culture system and assessed associations with in-vivo vaccine seroconversion in vaccinated infants.
Breastmilk samples were collected from mothers before routine rotavirus vaccination of their infant at 6 weeks of age. For each sample, whole breastmilk, purified IgA, purified IgG and IgG and IgA depleted breastmilk samples were prepared as exposure preparations. A 96 well microtitre plate was set up for each sample including a control in which only MA104 cells were grown as well as a virus control with MA104 cells and virus only. The outcome of interest was 50% inhibition dilution of each of the exposure preparations calculated as the titer at which 50% of virus dilution was achieved. Samples from 30 women were tested and correlated to vaccine seroconversion status of the infant. HIV status was also correlated to antiviral breastmilk proteins.
The mean 50% inhibitory dilution titer when whole breastmilk was added to virus infected MA104 cells was 14.3 (95% CI: 7.1, 22.7). Incubation with purified IgG resulted in a mean 50% inhibitory dilution of 5 (95%CI -1.6, 11.6). Incubating with purified IgA resulted in a mean 50% inhibitory dilution of 6.5 (95% CI -0.7, 13.7) and IgG and IgA depleted breastmilk did not yield any inhibition with a titer of 1.06 (95%CI 0.9, 1.2). Higher milk IgA levels contributed to a failure of infants to seroconvert. HIV was also not associated with any antiviral breastmilk proteins.
Whole breastmilk and breastmilk purified IgG and IgA fractions showed inhibitory activity against the rotavirus vaccine Rotarix™ whilst IgA and IgG depleted breastmilk with non-antibody breastmilk fraction failed to show any inhibition activity in-vitro. These findings suggest that IgA and IgG may have functional inhibitory properties and indicates a possible mechanism of how mothers in rotavirus endemic areas with high titres of IgA and IgG may inhibit viral multiplication in the infant gut and would potentially contribute to the failure of their infants to serocovert. There was not association of HIV with either lactoferrin, lactadherin or tenascin-C concentrations.
尽管减毒活口服轮状病毒疫苗在高负担的低收入和中等收入国家显著降低了轮状病毒相关性腹泻的发病率,但与更发达的国家相比,该疫苗在这些环境中的免疫原性和效果较低。母乳是导致口服疫苗效力降低的因素之一。我们进行了体外实验,以研究母乳中的母体抗体和其他非抗体成分对 MA104 细胞培养系统中轮状病毒疫苗株(Rotarix)繁殖的抑制作用,并评估了其与接种婴儿体内疫苗血清转化率的相关性。
在婴儿 6 周龄时常规接种轮状病毒疫苗前,从母亲那里采集母乳样本。对于每个样本,制备全母乳、纯化 IgA、纯化 IgG 和 IgG 和 IgA 耗尽的母乳样本作为暴露制剂。为每个样本设置了 96 孔微量滴定板,包括仅生长 MA104 细胞的对照以及仅含有 MA104 细胞和病毒的病毒对照。感兴趣的结果是计算出每个暴露制剂 50%抑制稀释度的 50%抑制稀释度,即达到 50%病毒稀释度时的滴度。测试了 30 名女性的样本,并将其与婴儿的疫苗血清转化率相关联。还将 HIV 状态与抗病毒母乳蛋白相关联。
当全母乳加入感染病毒的 MA104 细胞中时,病毒 50%抑制稀释度的平均值为 14.3(95%CI:7.1,22.7)。孵育纯化 IgG 导致 50%抑制稀释度的平均值为 5(95%CI-1.6,11.6)。孵育纯化 IgA 导致 50%抑制稀释度的平均值为 6.5(95%CI-0.7,13.7),而 IgG 和 IgA 耗尽的母乳则没有产生任何抑制作用,其滴度为 1.06(95%CI0.9,1.2)。母乳中较高的 IgA 水平导致婴儿无法血清转化。HIV 也与任何抗病毒母乳蛋白无关。
全母乳以及母乳纯化的 IgG 和 IgA 部分显示出对轮状病毒疫苗 Rotarix™的抑制活性,而 IgA 和 IgG 耗尽的母乳以及不含抗体的母乳部分在体外未能显示出任何抑制活性。这些发现表明,IgA 和 IgG 可能具有功能抑制特性,并表明在轮状病毒流行地区,高 IgA 和 IgG 水平的母亲如何可能抑制婴儿肠道中的病毒繁殖,并可能导致其婴儿无法血清转化。HIV 与乳铁蛋白、乳白蛋白或 tenascin-C 浓度之间没有关联。