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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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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fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1751229042</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>26369158</jstor_id><sourcerecordid>26369158</sourcerecordid><originalsourceid>FETCH-LOGICAL-c406t-1fa1119b5cd199309f8fab7031620d6740a2bf4b519da38cd828e917095576a83</originalsourceid><addsrcrecordid>eNqNkU1r3DAQhkVpaT7aS-8tgl5CwK3GsmTpuFmaD0gIlLZXM5bl1IstuZJV2B_U_xltNk1LTz0MMzAPzzC8hLwB9gGY5h_N0OX6KVj1jByC4HUhhYbneWZCFZXi6oAcxbhhDEAx8ZIclFIILpU6JL8u04SOrv00j3aybqFnaBYbhizFkX62cfYu2kgXT5FeBJ9muqI31g3uzhtvTIbW3m3SHS6WfkNjBmfp4Oiqzw50kaLrHvQYhujdzvNHemMxpmA72m5pSW-X7zY83biapuQ8xojb-Iq86HGM9vVjPyZfzz99WV8W17cXV-vVdWEqJpcCegQA3QrTgdac6V712NaMgyxZJ-uKYdn2VStAd8iV6VSprIaaaSFqiYofk5O9dw7-R7JxaaYhGjuO6KxPsYFaQFlqVpX_gfJSaFWBzOj7f9CNT8HlR3aU1KC01Jk63VMm-BiD7Zs5DBOGbQOs2eXc5Eiafc4ZfveoTO1kuyf0d7AZeLsHNnHx4a_97p5Q_B7nOq3c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1736918969</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><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.</creator><creatorcontrib>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.</creatorcontrib><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.</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 & 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. Expanded immunologic and epidemiologic surveillance may improve the interpretation of differences between these immunoassays.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Africa</subject><subject>Animals</subject><subject>Antibodies, Bacterial - blood</subject><subject>Bacteria</subject><subject>Blood Bactericidal Activity</subject><subject>Carbohydrates</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Complement System Proteins</subject><subject>Epidemiology</subject><subject>Humans</subject><subject>Immunization</subject><subject>Immunoassay</subject><subject>Immunoassay - methods</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulins</subject><subject>Meningitis</subject><subject>Meningococcal Vaccines - administration & dosage</subject><subject>Meningococcal Vaccines - immunology</subject><subject>Neisseria meningitidis</subject><subject>Neisseria meningitidis, Serogroup A - immunology</subject><subject>Rabbits</subject><subject>SEROLOGIC AND SAFETY STUDIES OF A GROUP A MENINGOCOCCAL CONJUGATE VACCINE</subject><subject>Vaccines</subject><subject>Young Adult</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1r3DAQhkVpaT7aS-8tgl5CwK3GsmTpuFmaD0gIlLZXM5bl1IstuZJV2B_U_xltNk1LTz0MMzAPzzC8hLwB9gGY5h_N0OX6KVj1jByC4HUhhYbneWZCFZXi6oAcxbhhDEAx8ZIclFIILpU6JL8u04SOrv00j3aybqFnaBYbhizFkX62cfYu2kgXT5FeBJ9muqI31g3uzhtvTIbW3m3SHS6WfkNjBmfp4Oiqzw50kaLrHvQYhujdzvNHemMxpmA72m5pSW-X7zY83biapuQ8xojb-Iq86HGM9vVjPyZfzz99WV8W17cXV-vVdWEqJpcCegQA3QrTgdac6V712NaMgyxZJ-uKYdn2VStAd8iV6VSprIaaaSFqiYofk5O9dw7-R7JxaaYhGjuO6KxPsYFaQFlqVpX_gfJSaFWBzOj7f9CNT8HlR3aU1KC01Jk63VMm-BiD7Zs5DBOGbQOs2eXc5Eiafc4ZfveoTO1kuyf0d7AZeLsHNnHx4a_97p5Q_B7nOq3c</recordid><startdate>20151115</startdate><enddate>20151115</enddate><creator>Price, Gregory A.</creator><creator>Hollander, Aimee M.</creator><creator>Plikaytis, Brian D.</creator><creator>Mocca, Brian T.</creator><creator>Carlone, George</creator><creator>Findlow, Helen</creator><creator>Borrow, Ray</creator><creator>Sow, Samba O.</creator><creator>Diallo, Aldiouma</creator><creator>Idoko, Olubukola T.</creator><creator>Enwere, Godwin C.</creator><creator>Elie, Cheryl</creator><creator>Preziosi, Marie-Pierre</creator><creator>Kulkarni, Prasad S.</creator><creator>Bash, Margaret C.</creator><general>Oxford University Press</general><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>7QL</scope><scope>7T2</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20151115</creationdate><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><author>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.</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 & 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 & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Price, Gregory A.</au><au>Hollander, Aimee M.</au><au>Plikaytis, Brian D.</au><au>Mocca, Brian T.</au><au>Carlone, George</au><au>Findlow, Helen</au><au>Borrow, Ray</au><au>Sow, Samba O.</au><au>Diallo, Aldiouma</au><au>Idoko, Olubukola T.</au><au>Enwere, Godwin C.</au><au>Elie, Cheryl</au><au>Preziosi, Marie-Pierre</au><au>Kulkarni, Prasad S.</au><au>Bash, Margaret C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human Complement Bactericidal Responses to a Group A Meningococcal Conjugate Vaccine in Africans and Comparison to Responses Measured by 2 Other Group A Immunoassays</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2015-11-15</date><risdate>2015</risdate><volume>61</volume><issue>suppl_5</issue><spage>S554</spage><epage>S562</epage><pages>S554-S562</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>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.</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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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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