In-vitro inhibitory effect of maternal breastmilk components on rotavirus vaccine replication and association with infant seroconversion to live oral rotavirus vaccine

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 impl...

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Veröffentlicht in:PloS one 2020-11, Vol.15 (11), p.e0240714-e0240714
Hauptverfasser: Kazimbaya, Katayi Mwila, Chisenga, Caroline C, Simuyandi, Michelo, Phiri, Cynthia Mubanga, Laban, Natasha Makabilo, Bosomprah, Samuel, Permar, Sallie R, Munsaka, Sody, Chilengi, Roma
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container_issue 11
container_start_page e0240714
container_title PloS one
container_volume 15
creator Kazimbaya, Katayi Mwila
Chisenga, Caroline C
Simuyandi, Michelo
Phiri, Cynthia Mubanga
Laban, Natasha Makabilo
Bosomprah, Samuel
Permar, Sallie R
Munsaka, Sody
Chilengi, Roma
description 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 inf
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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0240714</identifier><identifier>PMID: 33170860</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Administration, Oral ; Antibodies ; Babies ; Biology and life sciences ; Breast milk ; Breastfeeding &amp; lactation ; Cell culture ; Cell Line ; Depletion ; Developed countries ; Diarrhea ; Dilution ; Exposure ; Female ; Health aspects ; Health sciences ; HIV ; Human immunodeficiency virus ; Humans ; Immunogenicity ; Immunoglobulin A ; Immunoglobulin A - pharmacology ; Immunoglobulin G ; Immunoglobulin G - pharmacology ; In Vitro Techniques ; Incubation ; Infant ; Infants ; Infectious diseases ; Lactoferrin ; Medical research ; Medicine and health sciences ; Milk ; Milk, Human - immunology ; Mothers ; Multiplication ; People and Places ; Physiological aspects ; Proteins ; Rotavirus ; Rotavirus - drug effects ; Rotavirus - immunology ; Rotavirus - physiology ; Rotavirus Vaccines - immunology ; Rotaviruses ; Seroconversion ; Tenascin ; Tenascin C ; Vaccine efficacy ; Vaccines ; Vaccines, Attenuated - immunology ; Viral vaccines ; Virus Replication ; Viruses</subject><ispartof>PloS one, 2020-11, Vol.15 (11), p.e0240714-e0240714</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Kazimbaya et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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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.</description><subject>Administration, Oral</subject><subject>Antibodies</subject><subject>Babies</subject><subject>Biology and life sciences</subject><subject>Breast milk</subject><subject>Breastfeeding &amp; lactation</subject><subject>Cell culture</subject><subject>Cell Line</subject><subject>Depletion</subject><subject>Developed countries</subject><subject>Diarrhea</subject><subject>Dilution</subject><subject>Exposure</subject><subject>Female</subject><subject>Health aspects</subject><subject>Health sciences</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immunogenicity</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin A - pharmacology</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin G - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Incubation</subject><subject>Infant</subject><subject>Infants</subject><subject>Infectious diseases</subject><subject>Lactoferrin</subject><subject>Medical research</subject><subject>Medicine and health sciences</subject><subject>Milk</subject><subject>Milk, Human - immunology</subject><subject>Mothers</subject><subject>Multiplication</subject><subject>People and Places</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Rotavirus</subject><subject>Rotavirus - drug effects</subject><subject>Rotavirus - immunology</subject><subject>Rotavirus - physiology</subject><subject>Rotavirus Vaccines - immunology</subject><subject>Rotaviruses</subject><subject>Seroconversion</subject><subject>Tenascin</subject><subject>Tenascin C</subject><subject>Vaccine efficacy</subject><subject>Vaccines</subject><subject>Vaccines, Attenuated - immunology</subject><subject>Viral vaccines</subject><subject>Virus 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inhibitory effect of maternal breastmilk components on rotavirus vaccine replication and association with infant seroconversion to live oral rotavirus vaccine</title><author>Kazimbaya, Katayi Mwila ; Chisenga, Caroline C ; Simuyandi, Michelo ; Phiri, Cynthia Mubanga ; Laban, Natasha Makabilo ; Bosomprah, Samuel ; Permar, Sallie R ; Munsaka, Sody ; Chilengi, Roma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-9243f20c121a09ebf5280589c360c6899fe8ff6280b5215a1be45f5de470c5a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Administration, Oral</topic><topic>Antibodies</topic><topic>Babies</topic><topic>Biology and life sciences</topic><topic>Breast milk</topic><topic>Breastfeeding &amp; lactation</topic><topic>Cell culture</topic><topic>Cell Line</topic><topic>Depletion</topic><topic>Developed 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Database</collection><collection>Materials science collection</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazimbaya, Katayi Mwila</au><au>Chisenga, Caroline C</au><au>Simuyandi, Michelo</au><au>Phiri, Cynthia Mubanga</au><au>Laban, Natasha Makabilo</au><au>Bosomprah, Samuel</au><au>Permar, Sallie R</au><au>Munsaka, Sody</au><au>Chilengi, Roma</au><au>Yeruva, Laxmi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In-vitro inhibitory effect of maternal breastmilk components on rotavirus vaccine replication and association with infant seroconversion to live oral rotavirus vaccine</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2020-11-10</date><risdate>2020</risdate><volume>15</volume><issue>11</issue><spage>e0240714</spage><epage>e0240714</epage><pages>e0240714-e0240714</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>33170860</pmid><doi>10.1371/journal.pone.0240714</doi><tpages>e0240714</tpages><orcidid>https://orcid.org/0000-0002-8482-4693</orcidid><orcidid>https://orcid.org/0000-0003-0221-9527</orcidid><oa>free_for_read</oa></addata></record>
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1932-6203
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source MEDLINE; PMC (PubMed Central); Directory of Open Access Journals; Public Library of Science; Free Full-Text Journals in Chemistry; EZB Electronic Journals Library
subjects Administration, Oral
Antibodies
Babies
Biology and life sciences
Breast milk
Breastfeeding & lactation
Cell culture
Cell Line
Depletion
Developed countries
Diarrhea
Dilution
Exposure
Female
Health aspects
Health sciences
HIV
Human immunodeficiency virus
Humans
Immunogenicity
Immunoglobulin A
Immunoglobulin A - pharmacology
Immunoglobulin G
Immunoglobulin G - pharmacology
In Vitro Techniques
Incubation
Infant
Infants
Infectious diseases
Lactoferrin
Medical research
Medicine and health sciences
Milk
Milk, Human - immunology
Mothers
Multiplication
People and Places
Physiological aspects
Proteins
Rotavirus
Rotavirus - drug effects
Rotavirus - immunology
Rotavirus - physiology
Rotavirus Vaccines - immunology
Rotaviruses
Seroconversion
Tenascin
Tenascin C
Vaccine efficacy
Vaccines
Vaccines, Attenuated - immunology
Viral vaccines
Virus Replication
Viruses
title In-vitro inhibitory effect of maternal breastmilk components on rotavirus vaccine replication and association with infant seroconversion to live oral rotavirus vaccine
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