HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype
To protect against HIV infection, passively transferred and/or vaccine-elicited neutralizing antibodies (NAbs) need to effectively target diverse subtypes that are transmitted globally. These variants are a limited subset of those present during chronic infection and display some unique features. In...
Gespeichert in:
Veröffentlicht in: | AIDS (London) 2013-06, Vol.27 (10), p.1535-1544 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1544 |
---|---|
container_issue | 10 |
container_start_page | 1535 |
container_title | AIDS (London) |
container_volume | 27 |
creator | MABUKA, Jennifer GOO, Leslie OMENDA, Maxwel M NDUATI, Ruth OVERBAUGH, Julie |
description | To protect against HIV infection, passively transferred and/or vaccine-elicited neutralizing antibodies (NAbs) need to effectively target diverse subtypes that are transmitted globally. These variants are a limited subset of those present during chronic infection and display some unique features. In the case of mother-to-child transmission (MTCT), transmitted variants tend to be resistant to neutralization by maternal autologous NAbs.
To investigate whether variants transmitted during MTCT are generally resistant to HIV-1-specific NAbs, 107 maternal or infant variants representing the dominant HIV-1 subtypes were tested against six recently identified HIV-1-specific broadly neutralizing monoclonal antibodies (bNAbs), NIH45-46W, VRC01, PGT128, PGT121, PG9 and PGT145.
Infant and maternal variants did not differ in their neutralization sensitivity to individual bNAbs, nor did viruses from transmitting versus nontransmitting mothers, although there was a trend for viruses from transmitting mothers to be less sensitive overall. No single bNAb neutralized all viruses, but a combination of bNAbs that target distinct epitopes covered 100% of the variants tested. Compared with heterosexually transmitted variants, vertically transmitted variants were significantly more sensitive to neutralization by PGT128 and PGT121 (P=0.03 in both cases), but there were no differences for the other bNAbs. Overall, subtype A variants were significantly more sensitive to NIH45-46 (P=0.04), VRC01 (P=0.002) and PGT145 (P=0.03) compared with the nonsubtype A and less sensitive to PGT121 than subtype Cs (P=0.0001).
A combination of bNAbs against distinct epitopes may be needed to provide maximum coverage against viruses in different modes of transmission and diverse subtypes. |
doi_str_mv | 10.1097/QAD.0b013e32835faba5 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4080909</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1765970042</sourcerecordid><originalsourceid>FETCH-LOGICAL-c471t-5280ff822ce31c80c755f8c2b5328d5f48e900da15af622fa847ffddaf8b5933</originalsourceid><addsrcrecordid>eNqFkU9rFTEUxYMo9ln9BiLZCC6cepNMJpmNUOqfFgoiFLfhZiZpIzOZZ5J5Mu785s6jz2rduDqL-zuHeziEPGdwwqBVbz6fvjsBC0w4wbWQHi3KB2TDaiUqKRV7SDbAm7ZqhYIj8iTnrwAgQevH5IgLLZuG1xvy8_ziS8XoiMWliAPF2NMQPcZCd5jCqpnmm-k7zWEMAyaaXcyhhF0oCy0TtWnCflhodHNJOIQfIV6vISXYqQ8uv6Z2Lvc8-1SXqV1onm1Ztu4peeRxyO7ZQY_J1Yf3V2fn1eWnjxdnp5dVVytWKsk1eK8575xgnYZOSel1x61c6_fS19q1AD0yib7h3KOulfd9j15b2QpxTN7exm5nO7q-c3H_r9mmMGJazITB3L_EcGOup52pQUML7Rrw6hCQpm-zy8WMIXduGDC6ac6GqUa2CqDm_0drgIYLKdiK1rdol6ack_N3HzEw-53NurP5d-fV9uLvNnem38OuwMsDgLnDwSeMXch_OCUFNGurX4qttks</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1400623531</pqid></control><display><type>article</type><title>HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>MABUKA, Jennifer ; GOO, Leslie ; OMENDA, Maxwel M ; NDUATI, Ruth ; OVERBAUGH, Julie</creator><creatorcontrib>MABUKA, Jennifer ; GOO, Leslie ; OMENDA, Maxwel M ; NDUATI, Ruth ; OVERBAUGH, Julie</creatorcontrib><description>To protect against HIV infection, passively transferred and/or vaccine-elicited neutralizing antibodies (NAbs) need to effectively target diverse subtypes that are transmitted globally. These variants are a limited subset of those present during chronic infection and display some unique features. In the case of mother-to-child transmission (MTCT), transmitted variants tend to be resistant to neutralization by maternal autologous NAbs.
To investigate whether variants transmitted during MTCT are generally resistant to HIV-1-specific NAbs, 107 maternal or infant variants representing the dominant HIV-1 subtypes were tested against six recently identified HIV-1-specific broadly neutralizing monoclonal antibodies (bNAbs), NIH45-46W, VRC01, PGT128, PGT121, PG9 and PGT145.
Infant and maternal variants did not differ in their neutralization sensitivity to individual bNAbs, nor did viruses from transmitting versus nontransmitting mothers, although there was a trend for viruses from transmitting mothers to be less sensitive overall. No single bNAb neutralized all viruses, but a combination of bNAbs that target distinct epitopes covered 100% of the variants tested. Compared with heterosexually transmitted variants, vertically transmitted variants were significantly more sensitive to neutralization by PGT128 and PGT121 (P=0.03 in both cases), but there were no differences for the other bNAbs. Overall, subtype A variants were significantly more sensitive to NIH45-46 (P=0.04), VRC01 (P=0.002) and PGT145 (P=0.03) compared with the nonsubtype A and less sensitive to PGT121 than subtype Cs (P=0.0001).
A combination of bNAbs against distinct epitopes may be needed to provide maximum coverage against viruses in different modes of transmission and diverse subtypes.</description><identifier>ISSN: 0269-9370</identifier><identifier>EISSN: 1473-5571</identifier><identifier>DOI: 10.1097/QAD.0b013e32835faba5</identifier><identifier>PMID: 23856624</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Antibodies, Monoclonal - immunology ; Antibodies, Neutralizing - immunology ; Biological and medical sciences ; Female ; HIV Antibodies - immunology ; HIV Infections - immunology ; HIV Infections - transmission ; HIV-1 - immunology ; Human immunodeficiency virus 1 ; Human viral diseases ; Humans ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; Immunopathology ; Infant ; Infectious Disease Transmission, Vertical ; Infectious diseases ; Lentivirus ; Medical sciences ; Neutralization Tests ; Retroviridae ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids</subject><ispartof>AIDS (London), 2013-06, Vol.27 (10), p.1535-1544</ispartof><rights>2014 INIST-CNRS</rights><rights>2013 Wolters Kluwer Health | Lippincott Williams & Wilkins</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-5280ff822ce31c80c755f8c2b5328d5f48e900da15af622fa847ffddaf8b5933</citedby><cites>FETCH-LOGICAL-c471t-5280ff822ce31c80c755f8c2b5328d5f48e900da15af622fa847ffddaf8b5933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27530609$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23856624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MABUKA, Jennifer</creatorcontrib><creatorcontrib>GOO, Leslie</creatorcontrib><creatorcontrib>OMENDA, Maxwel M</creatorcontrib><creatorcontrib>NDUATI, Ruth</creatorcontrib><creatorcontrib>OVERBAUGH, Julie</creatorcontrib><title>HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype</title><title>AIDS (London)</title><addtitle>AIDS</addtitle><description>To protect against HIV infection, passively transferred and/or vaccine-elicited neutralizing antibodies (NAbs) need to effectively target diverse subtypes that are transmitted globally. These variants are a limited subset of those present during chronic infection and display some unique features. In the case of mother-to-child transmission (MTCT), transmitted variants tend to be resistant to neutralization by maternal autologous NAbs.
To investigate whether variants transmitted during MTCT are generally resistant to HIV-1-specific NAbs, 107 maternal or infant variants representing the dominant HIV-1 subtypes were tested against six recently identified HIV-1-specific broadly neutralizing monoclonal antibodies (bNAbs), NIH45-46W, VRC01, PGT128, PGT121, PG9 and PGT145.
Infant and maternal variants did not differ in their neutralization sensitivity to individual bNAbs, nor did viruses from transmitting versus nontransmitting mothers, although there was a trend for viruses from transmitting mothers to be less sensitive overall. No single bNAb neutralized all viruses, but a combination of bNAbs that target distinct epitopes covered 100% of the variants tested. Compared with heterosexually transmitted variants, vertically transmitted variants were significantly more sensitive to neutralization by PGT128 and PGT121 (P=0.03 in both cases), but there were no differences for the other bNAbs. Overall, subtype A variants were significantly more sensitive to NIH45-46 (P=0.04), VRC01 (P=0.002) and PGT145 (P=0.03) compared with the nonsubtype A and less sensitive to PGT121 than subtype Cs (P=0.0001).
A combination of bNAbs against distinct epitopes may be needed to provide maximum coverage against viruses in different modes of transmission and diverse subtypes.</description><subject>Antibodies, Monoclonal - immunology</subject><subject>Antibodies, Neutralizing - immunology</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>HIV Antibodies - immunology</subject><subject>HIV Infections - immunology</subject><subject>HIV Infections - transmission</subject><subject>HIV-1 - immunology</subject><subject>Human immunodeficiency virus 1</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Infant</subject><subject>Infectious Disease Transmission, Vertical</subject><subject>Infectious diseases</subject><subject>Lentivirus</subject><subject>Medical sciences</subject><subject>Neutralization Tests</subject><subject>Retroviridae</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><issn>0269-9370</issn><issn>1473-5571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9rFTEUxYMo9ln9BiLZCC6cepNMJpmNUOqfFgoiFLfhZiZpIzOZZ5J5Mu785s6jz2rduDqL-zuHeziEPGdwwqBVbz6fvjsBC0w4wbWQHi3KB2TDaiUqKRV7SDbAm7ZqhYIj8iTnrwAgQevH5IgLLZuG1xvy8_ziS8XoiMWliAPF2NMQPcZCd5jCqpnmm-k7zWEMAyaaXcyhhF0oCy0TtWnCflhodHNJOIQfIV6vISXYqQ8uv6Z2Lvc8-1SXqV1onm1Ztu4peeRxyO7ZQY_J1Yf3V2fn1eWnjxdnp5dVVytWKsk1eK8575xgnYZOSel1x61c6_fS19q1AD0yib7h3KOulfd9j15b2QpxTN7exm5nO7q-c3H_r9mmMGJazITB3L_EcGOup52pQUML7Rrw6hCQpm-zy8WMIXduGDC6ac6GqUa2CqDm_0drgIYLKdiK1rdol6ack_N3HzEw-53NurP5d-fV9uLvNnem38OuwMsDgLnDwSeMXch_OCUFNGurX4qttks</recordid><startdate>20130619</startdate><enddate>20130619</enddate><creator>MABUKA, Jennifer</creator><creator>GOO, Leslie</creator><creator>OMENDA, Maxwel M</creator><creator>NDUATI, Ruth</creator><creator>OVERBAUGH, Julie</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T2</scope><scope>7T5</scope><scope>7U2</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20130619</creationdate><title>HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype</title><author>MABUKA, Jennifer ; GOO, Leslie ; OMENDA, Maxwel M ; NDUATI, Ruth ; OVERBAUGH, Julie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-5280ff822ce31c80c755f8c2b5328d5f48e900da15af622fa847ffddaf8b5933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antibodies, Monoclonal - immunology</topic><topic>Antibodies, Neutralizing - immunology</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>HIV Antibodies - immunology</topic><topic>HIV Infections - immunology</topic><topic>HIV Infections - transmission</topic><topic>HIV-1 - immunology</topic><topic>Human immunodeficiency virus 1</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Infant</topic><topic>Infectious Disease Transmission, Vertical</topic><topic>Infectious diseases</topic><topic>Lentivirus</topic><topic>Medical sciences</topic><topic>Neutralization Tests</topic><topic>Retroviridae</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MABUKA, Jennifer</creatorcontrib><creatorcontrib>GOO, Leslie</creatorcontrib><creatorcontrib>OMENDA, Maxwel M</creatorcontrib><creatorcontrib>NDUATI, Ruth</creatorcontrib><creatorcontrib>OVERBAUGH, Julie</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Safety Science and Risk</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>AIDS (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MABUKA, Jennifer</au><au>GOO, Leslie</au><au>OMENDA, Maxwel M</au><au>NDUATI, Ruth</au><au>OVERBAUGH, Julie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype</atitle><jtitle>AIDS (London)</jtitle><addtitle>AIDS</addtitle><date>2013-06-19</date><risdate>2013</risdate><volume>27</volume><issue>10</issue><spage>1535</spage><epage>1544</epage><pages>1535-1544</pages><issn>0269-9370</issn><eissn>1473-5571</eissn><abstract>To protect against HIV infection, passively transferred and/or vaccine-elicited neutralizing antibodies (NAbs) need to effectively target diverse subtypes that are transmitted globally. These variants are a limited subset of those present during chronic infection and display some unique features. In the case of mother-to-child transmission (MTCT), transmitted variants tend to be resistant to neutralization by maternal autologous NAbs.
To investigate whether variants transmitted during MTCT are generally resistant to HIV-1-specific NAbs, 107 maternal or infant variants representing the dominant HIV-1 subtypes were tested against six recently identified HIV-1-specific broadly neutralizing monoclonal antibodies (bNAbs), NIH45-46W, VRC01, PGT128, PGT121, PG9 and PGT145.
Infant and maternal variants did not differ in their neutralization sensitivity to individual bNAbs, nor did viruses from transmitting versus nontransmitting mothers, although there was a trend for viruses from transmitting mothers to be less sensitive overall. No single bNAb neutralized all viruses, but a combination of bNAbs that target distinct epitopes covered 100% of the variants tested. Compared with heterosexually transmitted variants, vertically transmitted variants were significantly more sensitive to neutralization by PGT128 and PGT121 (P=0.03 in both cases), but there were no differences for the other bNAbs. Overall, subtype A variants were significantly more sensitive to NIH45-46 (P=0.04), VRC01 (P=0.002) and PGT145 (P=0.03) compared with the nonsubtype A and less sensitive to PGT121 than subtype Cs (P=0.0001).
A combination of bNAbs against distinct epitopes may be needed to provide maximum coverage against viruses in different modes of transmission and diverse subtypes.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>23856624</pmid><doi>10.1097/QAD.0b013e32835faba5</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0269-9370 |
ispartof | AIDS (London), 2013-06, Vol.27 (10), p.1535-1544 |
issn | 0269-9370 1473-5571 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4080909 |
source | MEDLINE; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals |
subjects | Antibodies, Monoclonal - immunology Antibodies, Neutralizing - immunology Biological and medical sciences Female HIV Antibodies - immunology HIV Infections - immunology HIV Infections - transmission HIV-1 - immunology Human immunodeficiency virus 1 Human viral diseases Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunopathology Infant Infectious Disease Transmission, Vertical Infectious diseases Lentivirus Medical sciences Neutralization Tests Retroviridae Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids |
title | HIV-1 maternal and infant variants show similar sensitivity to broadly neutralizing antibodies, but sensitivity varies by subtype |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T19%3A45%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=HIV-1%20maternal%20and%20infant%20variants%20show%20similar%20sensitivity%20to%20broadly%20neutralizing%20antibodies,%20but%20sensitivity%20varies%20by%20subtype&rft.jtitle=AIDS%20(London)&rft.au=MABUKA,%20Jennifer&rft.date=2013-06-19&rft.volume=27&rft.issue=10&rft.spage=1535&rft.epage=1544&rft.pages=1535-1544&rft.issn=0269-9370&rft.eissn=1473-5571&rft_id=info:doi/10.1097/QAD.0b013e32835faba5&rft_dat=%3Cproquest_pubme%3E1765970042%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1400623531&rft_id=info:pmid/23856624&rfr_iscdi=true |