Abstract

BackgroundDespite 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.MethodsBreastmilk 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.ResultsThe 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.Discussion and conclusionWhole 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.

Highlights

  • Rotavirus vaccines have contributed substantially to mitigate the morbidity and mortality from rotavirus associated diarrhoea [1, 2]

  • The mean 50% inhibitory dilution titer when whole breastmilk was added to virus infected MA104 cells was 14.3

  • There are several reasons postulated to explain the reduced rotavirus vaccine efficacy in low and middle-income countries (LMIC). Among these are maternal immune and non-immune factors; some of which include the antibodies immunoglobulins A (IgA) and G (IgG), human milk olygosaccharides and glycans, mucins and innate components, Lactoferrin (LF), Lactadherin (LA) and Tenascin C (TNC) respectively that are present in breastmilk and acquired by the infant through breastfeeding [6,7,8,9,10]

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Summary

Introduction

Rotavirus vaccines have contributed substantially to mitigate the morbidity and mortality from rotavirus associated diarrhoea [1, 2]. Rotavirus vaccines have been able to avert approximately 28,000 deaths in under-five children; despite these great improvements the reduction in diarrhoea incidence in sub-Saharan Africa and Asia have not been as marked as in other regions [1] This has been attributed to the reduced rotavirus vaccine efficacy in low and middle-income countries (LMIC) compared to the high-income counterparts [3,4,5]. There are several reasons postulated to explain the reduced rotavirus vaccine efficacy in LMIC Among these are maternal immune and non-immune factors; some of which include the antibodies immunoglobulins A (IgA) and G (IgG), human milk olygosaccharides and glycans, mucins and innate components, Lactoferrin (LF), Lactadherin (LA) and Tenascin C (TNC) respectively that are present in breastmilk and acquired by the infant through breastfeeding [6,7,8,9,10]. 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

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