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 |
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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 |
doi_str_mv | 10.1371/journal.pone.0240714 |
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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 & 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. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Kazimbaya et al 2020 Kazimbaya et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-9243f20c121a09ebf5280589c360c6899fe8ff6280b5215a1be45f5de470c5a43</citedby><cites>FETCH-LOGICAL-c692t-9243f20c121a09ebf5280589c360c6899fe8ff6280b5215a1be45f5de470c5a43</cites><orcidid>0000-0002-8482-4693 ; 0000-0003-0221-9527</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654788/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654788/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33170860$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Yeruva, Laxmi</contributor><creatorcontrib>Kazimbaya, Katayi Mwila</creatorcontrib><creatorcontrib>Chisenga, Caroline C</creatorcontrib><creatorcontrib>Simuyandi, Michelo</creatorcontrib><creatorcontrib>Phiri, Cynthia Mubanga</creatorcontrib><creatorcontrib>Laban, Natasha Makabilo</creatorcontrib><creatorcontrib>Bosomprah, Samuel</creatorcontrib><creatorcontrib>Permar, Sallie R</creatorcontrib><creatorcontrib>Munsaka, Sody</creatorcontrib><creatorcontrib>Chilengi, Roma</creatorcontrib><title>In-vitro inhibitory effect of maternal breastmilk components on rotavirus vaccine replication and association with infant seroconversion to live oral rotavirus vaccine</title><title>PloS one</title><addtitle>PLoS One</addtitle><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 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 & 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 & lactation</topic><topic>Cell culture</topic><topic>Cell Line</topic><topic>Depletion</topic><topic>Developed countries</topic><topic>Diarrhea</topic><topic>Dilution</topic><topic>Exposure</topic><topic>Female</topic><topic>Health aspects</topic><topic>Health sciences</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immunogenicity</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulin A - pharmacology</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin G - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Incubation</topic><topic>Infant</topic><topic>Infants</topic><topic>Infectious diseases</topic><topic>Lactoferrin</topic><topic>Medical research</topic><topic>Medicine and health sciences</topic><topic>Milk</topic><topic>Milk, Human - immunology</topic><topic>Mothers</topic><topic>Multiplication</topic><topic>People and Places</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Rotavirus</topic><topic>Rotavirus - drug effects</topic><topic>Rotavirus - immunology</topic><topic>Rotavirus - 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Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science 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> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2020-11, Vol.15 (11), p.e0240714-e0240714 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2459280713 |
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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