Human Complement Bactericidal Responses to a Group A Meningococcal Conjugate Vaccine in Africans and Comparison to Responses Measured by 2 Other Group A Immunoassays

Background. PsA-TT (MenAfriVac) is a conjugated polysaccharide vaccine developed to eliminate group A meningococcal disease in Africa. Vaccination of African study participants with 1 dose of PsA-TT led to the production of anti-A polysaccharide antibodies and increased serum bactericidal activity m...

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Veröffentlicht in:Clinical infectious diseases 2015-11, Vol.61 (suppl_5), p.S554-S562
Hauptverfasser: Price, Gregory A., Hollander, Aimee M., Plikaytis, Brian D., Mocca, Brian T., Carlone, George, Findlow, Helen, Borrow, Ray, Sow, Samba O., Diallo, Aldiouma, Idoko, Olubukola T., Enwere, Godwin C., Elie, Cheryl, Preziosi, Marie-Pierre, Kulkarni, Prasad S., Bash, Margaret C.
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container_end_page S562
container_issue suppl_5
container_start_page S554
container_title Clinical infectious diseases
container_volume 61
creator Price, Gregory A.
Hollander, Aimee M.
Plikaytis, Brian D.
Mocca, Brian T.
Carlone, George
Findlow, Helen
Borrow, Ray
Sow, Samba O.
Diallo, Aldiouma
Idoko, Olubukola T.
Enwere, Godwin C.
Elie, Cheryl
Preziosi, Marie-Pierre
Kulkarni, Prasad S.
Bash, Margaret C.
description Background. PsA-TT (MenAfriVac) is a conjugated polysaccharide vaccine developed to eliminate group A meningococcal disease in Africa. Vaccination of African study participants with 1 dose of PsA-TT led to the production of anti-A polysaccharide antibodies and increased serum bactericidal activity measured using rabbit complement (rSBA). Bactericidal responses measured with human complement (hSBA) are presented here. Methods. Sera collected before and at 28 days and 1 year after vaccination with either PsA-TT or quadrivalent polysaccharide vaccine (PsACWY) from a random, age-distributed 360-subject subset of the Meningitis Vaccine Project study of PsA-TT in Africans aged 2–29 years were tested for hSBA. Geometric mean titer, fold-rise, and threshold analyses were compared between vaccine groups and age groups. hSBA, rSBA, and immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) results were compared and assay correlation and agreement determined. Results. hSBA responses to PsA-TT were substantially higher than those to PsACWY at 28 days and 1 year following immunization, similar to previously reported rSBA and IgG results. The hSBA and IgG ELISA results identified differences between age groups that were not evident by rSBA. The rSBA data indicated sustained high titers 1 year after immunization, whereas hSBA GMTs at 1 year approached 4 in young children. Conclusions. The high level of protection following PsA-TT immunization campaigns is consistent with the strong hSBA immune responses observed here. Future implementation decisions will likely depend on immunologic data and their long-term correlation with disease and carriage prevention. Expanded immunologic and epidemiologic surveillance may improve the interpretation of differences between these immunoassays.
doi_str_mv 10.1093/cid/civ504
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PsA-TT (MenAfriVac) is a conjugated polysaccharide vaccine developed to eliminate group A meningococcal disease in Africa. Vaccination of African study participants with 1 dose of PsA-TT led to the production of anti-A polysaccharide antibodies and increased serum bactericidal activity measured using rabbit complement (rSBA). Bactericidal responses measured with human complement (hSBA) are presented here. Methods. Sera collected before and at 28 days and 1 year after vaccination with either PsA-TT or quadrivalent polysaccharide vaccine (PsACWY) from a random, age-distributed 360-subject subset of the Meningitis Vaccine Project study of PsA-TT in Africans aged 2–29 years were tested for hSBA. Geometric mean titer, fold-rise, and threshold analyses were compared between vaccine groups and age groups. hSBA, rSBA, and immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) results were compared and assay correlation and agreement determined. Results. hSBA responses to PsA-TT were substantially higher than those to PsACWY at 28 days and 1 year following immunization, similar to previously reported rSBA and IgG results. The hSBA and IgG ELISA results identified differences between age groups that were not evident by rSBA. The rSBA data indicated sustained high titers 1 year after immunization, whereas hSBA GMTs at 1 year approached 4 in young children. Conclusions. The high level of protection following PsA-TT immunization campaigns is consistent with the strong hSBA immune responses observed here. Future implementation decisions will likely depend on immunologic data and their long-term correlation with disease and carriage prevention. Expanded immunologic and epidemiologic surveillance may improve the interpretation of differences between these immunoassays.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/civ504</identifier><identifier>PMID: 26553688</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adolescent ; Adult ; Africa ; Animals ; Antibodies, Bacterial - blood ; Bacteria ; Blood Bactericidal Activity ; Carbohydrates ; Child ; Child, Preschool ; Complement System Proteins ; Epidemiology ; Humans ; Immunization ; Immunoassay ; Immunoassay - methods ; Immunoglobulin G - blood ; Immunoglobulins ; Meningitis ; Meningococcal Vaccines - administration &amp; dosage ; Meningococcal Vaccines - immunology ; Neisseria meningitidis ; Neisseria meningitidis, Serogroup A - immunology ; Rabbits ; SEROLOGIC AND SAFETY STUDIES OF A GROUP A MENINGOCOCCAL CONJUGATE VACCINE ; Vaccines ; Young Adult</subject><ispartof>Clinical infectious diseases, 2015-11, Vol.61 (suppl_5), p.S554-S562</ispartof><rights>Published by Oxford University Press for the Infectious Diseases Society of America 2015. This work is written by (a) US Government employee(s) and is in the public domain in the US.</rights><rights>Copyright Oxford University Press, UK Nov 15, 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-1fa1119b5cd199309f8fab7031620d6740a2bf4b519da38cd828e917095576a83</citedby><cites>FETCH-LOGICAL-c406t-1fa1119b5cd199309f8fab7031620d6740a2bf4b519da38cd828e917095576a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26369158$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26369158$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26553688$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Price, Gregory A.</creatorcontrib><creatorcontrib>Hollander, Aimee M.</creatorcontrib><creatorcontrib>Plikaytis, Brian D.</creatorcontrib><creatorcontrib>Mocca, Brian T.</creatorcontrib><creatorcontrib>Carlone, George</creatorcontrib><creatorcontrib>Findlow, Helen</creatorcontrib><creatorcontrib>Borrow, Ray</creatorcontrib><creatorcontrib>Sow, Samba O.</creatorcontrib><creatorcontrib>Diallo, Aldiouma</creatorcontrib><creatorcontrib>Idoko, Olubukola T.</creatorcontrib><creatorcontrib>Enwere, Godwin C.</creatorcontrib><creatorcontrib>Elie, Cheryl</creatorcontrib><creatorcontrib>Preziosi, Marie-Pierre</creatorcontrib><creatorcontrib>Kulkarni, Prasad S.</creatorcontrib><creatorcontrib>Bash, Margaret C.</creatorcontrib><title>Human Complement Bactericidal Responses to a Group A Meningococcal Conjugate Vaccine in Africans and Comparison to Responses Measured by 2 Other Group A Immunoassays</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Background. PsA-TT (MenAfriVac) is a conjugated polysaccharide vaccine developed to eliminate group A meningococcal disease in Africa. Vaccination of African study participants with 1 dose of PsA-TT led to the production of anti-A polysaccharide antibodies and increased serum bactericidal activity measured using rabbit complement (rSBA). Bactericidal responses measured with human complement (hSBA) are presented here. Methods. Sera collected before and at 28 days and 1 year after vaccination with either PsA-TT or quadrivalent polysaccharide vaccine (PsACWY) from a random, age-distributed 360-subject subset of the Meningitis Vaccine Project study of PsA-TT in Africans aged 2–29 years were tested for hSBA. Geometric mean titer, fold-rise, and threshold analyses were compared between vaccine groups and age groups. hSBA, rSBA, and immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) results were compared and assay correlation and agreement determined. Results. hSBA responses to PsA-TT were substantially higher than those to PsACWY at 28 days and 1 year following immunization, similar to previously reported rSBA and IgG results. The hSBA and IgG ELISA results identified differences between age groups that were not evident by rSBA. The rSBA data indicated sustained high titers 1 year after immunization, whereas hSBA GMTs at 1 year approached 4 in young children. Conclusions. The high level of protection following PsA-TT immunization campaigns is consistent with the strong hSBA immune responses observed here. Future implementation decisions will likely depend on immunologic data and their long-term correlation with disease and carriage prevention. 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Hollander, Aimee M. ; Plikaytis, Brian D. ; Mocca, Brian T. ; Carlone, George ; Findlow, Helen ; Borrow, Ray ; Sow, Samba O. ; Diallo, Aldiouma ; Idoko, Olubukola T. ; Enwere, Godwin C. ; Elie, Cheryl ; Preziosi, Marie-Pierre ; Kulkarni, Prasad S. ; Bash, Margaret C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-1fa1119b5cd199309f8fab7031620d6740a2bf4b519da38cd828e917095576a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Africa</topic><topic>Animals</topic><topic>Antibodies, Bacterial - blood</topic><topic>Bacteria</topic><topic>Blood Bactericidal Activity</topic><topic>Carbohydrates</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Complement System Proteins</topic><topic>Epidemiology</topic><topic>Humans</topic><topic>Immunization</topic><topic>Immunoassay</topic><topic>Immunoassay - methods</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulins</topic><topic>Meningitis</topic><topic>Meningococcal Vaccines - administration &amp; dosage</topic><topic>Meningococcal Vaccines - immunology</topic><topic>Neisseria meningitidis</topic><topic>Neisseria meningitidis, Serogroup A - immunology</topic><topic>Rabbits</topic><topic>SEROLOGIC AND SAFETY STUDIES OF A GROUP A MENINGOCOCCAL CONJUGATE VACCINE</topic><topic>Vaccines</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Price, Gregory A.</creatorcontrib><creatorcontrib>Hollander, Aimee M.</creatorcontrib><creatorcontrib>Plikaytis, Brian D.</creatorcontrib><creatorcontrib>Mocca, Brian T.</creatorcontrib><creatorcontrib>Carlone, George</creatorcontrib><creatorcontrib>Findlow, Helen</creatorcontrib><creatorcontrib>Borrow, Ray</creatorcontrib><creatorcontrib>Sow, Samba O.</creatorcontrib><creatorcontrib>Diallo, Aldiouma</creatorcontrib><creatorcontrib>Idoko, Olubukola T.</creatorcontrib><creatorcontrib>Enwere, Godwin C.</creatorcontrib><creatorcontrib>Elie, Cheryl</creatorcontrib><creatorcontrib>Preziosi, Marie-Pierre</creatorcontrib><creatorcontrib>Kulkarni, Prasad S.</creatorcontrib><creatorcontrib>Bash, Margaret C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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PsA-TT (MenAfriVac) is a conjugated polysaccharide vaccine developed to eliminate group A meningococcal disease in Africa. Vaccination of African study participants with 1 dose of PsA-TT led to the production of anti-A polysaccharide antibodies and increased serum bactericidal activity measured using rabbit complement (rSBA). Bactericidal responses measured with human complement (hSBA) are presented here. Methods. Sera collected before and at 28 days and 1 year after vaccination with either PsA-TT or quadrivalent polysaccharide vaccine (PsACWY) from a random, age-distributed 360-subject subset of the Meningitis Vaccine Project study of PsA-TT in Africans aged 2–29 years were tested for hSBA. Geometric mean titer, fold-rise, and threshold analyses were compared between vaccine groups and age groups. hSBA, rSBA, and immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) results were compared and assay correlation and agreement determined. Results. hSBA responses to PsA-TT were substantially higher than those to PsACWY at 28 days and 1 year following immunization, similar to previously reported rSBA and IgG results. The hSBA and IgG ELISA results identified differences between age groups that were not evident by rSBA. The rSBA data indicated sustained high titers 1 year after immunization, whereas hSBA GMTs at 1 year approached 4 in young children. Conclusions. The high level of protection following PsA-TT immunization campaigns is consistent with the strong hSBA immune responses observed here. Future implementation decisions will likely depend on immunologic data and their long-term correlation with disease and carriage prevention. Expanded immunologic and epidemiologic surveillance may improve the interpretation of differences between these immunoassays.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>26553688</pmid><doi>10.1093/cid/civ504</doi><oa>free_for_read</oa></addata></record>
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source MEDLINE; JSTOR Archive Collection A-Z Listing; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adolescent
Adult
Africa
Animals
Antibodies, Bacterial - blood
Bacteria
Blood Bactericidal Activity
Carbohydrates
Child
Child, Preschool
Complement System Proteins
Epidemiology
Humans
Immunization
Immunoassay
Immunoassay - methods
Immunoglobulin G - blood
Immunoglobulins
Meningitis
Meningococcal Vaccines - administration & dosage
Meningococcal Vaccines - immunology
Neisseria meningitidis
Neisseria meningitidis, Serogroup A - immunology
Rabbits
SEROLOGIC AND SAFETY STUDIES OF A GROUP A MENINGOCOCCAL CONJUGATE VACCINE
Vaccines
Young Adult
title Human Complement Bactericidal Responses to a Group A Meningococcal Conjugate Vaccine in Africans and Comparison to Responses Measured by 2 Other Group A Immunoassays
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