Fc Gamma Receptor 3B (FCGR3B-c.233C>A-rs5030738) Polymorphism Modifies the Protective Effect of Malaria Specific Antibodies in Ghanaian Children
Immunoglobulin G (IgG) cross-linking with Fc gamma receptor IIIB (FcyRIIIB) triggers neutrophil degranulation, releasing reactive oxygen species with high levels associated with protection against malaria. The FCGR3B-c.233C>A polymorphism thought to influence the interaction between IgG and FcyRI...
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Veröffentlicht in: | The Journal of infectious diseases 2014-01, Vol.209 (2), p.285-289 |
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creator | Adu, Bright Jepsen, Micha Phill Grønholm Gerds, Thomas A. Kyei-Baafour, Eric Christiansen, Michael Dodoo, Daniel Theisen, Michael |
description | Immunoglobulin G (IgG) cross-linking with Fc gamma receptor IIIB (FcyRIIIB) triggers neutrophil degranulation, releasing reactive oxygen species with high levels associated with protection against malaria. The FCGR3B-c.233C>A polymorphism thought to influence the interaction between IgG and FcyRIIIB was recently associated with malaria. We studied the statistical interaction between glutamate rich protein antibodies and FCGR3B-c.233C>A genotypes on risk of malaria in a cohort of Ghanaian children. The absolute risk of malaria decreased more rapidly with increasing antibody levels for 233AA/AC individuals compared with 233CC children. This genotype related effect modification may significantly influence malaria sero-epidemiological and vaccine trial studies. |
doi_str_mv | 10.1093/infdis/jit422 |
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The FCGR3B-c.233C>A polymorphism thought to influence the interaction between IgG and FcyRIIIB was recently associated with malaria. We studied the statistical interaction between glutamate rich protein antibodies and FCGR3B-c.233C>A genotypes on risk of malaria in a cohort of Ghanaian children. The absolute risk of malaria decreased more rapidly with increasing antibody levels for 233AA/AC individuals compared with 233CC children. 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The FCGR3B-c.233C>A polymorphism thought to influence the interaction between IgG and FcyRIIIB was recently associated with malaria. We studied the statistical interaction between glutamate rich protein antibodies and FCGR3B-c.233C>A genotypes on risk of malaria in a cohort of Ghanaian children. The absolute risk of malaria decreased more rapidly with increasing antibody levels for 233AA/AC individuals compared with 233CC children. This genotype related effect modification may significantly influence malaria sero-epidemiological and vaccine trial studies.</description><subject>Antibodies</subject><subject>Antibodies, Protozoan - immunology</subject><subject>Antigens</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cohort Studies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Predisposition to Disease</subject><subject>Genotypes</subject><subject>Ghana</subject><subject>GPI-Linked Proteins - genetics</subject><subject>Human protozoal diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Logistic regression</subject><subject>Malaria</subject><subject>Malaria - immunology</subject><subject>Malaria vaccines</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Neutrophils</subject><subject>Parasitemia</subject><subject>PARASITES</subject><subject>Parasitic diseases</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Protective effects</subject><subject>Protozoal diseases</subject><subject>Receptors, IgG - genetics</subject><subject>Sickle cell trait</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo90UFr2zAUB3AxNtYs3XHHDV0G3cGtpGdJ1mWQmiYdtLR029nIikQUbMuVnEG_xT7yNJzmpAf6_d_h_RH6RMklJQqu_OC2Pl3t_VQy9gYtKAdZCEHhLVoQwlhBK6XO0IeU9oSQEoR8j84YKOCMkAX6uzZ4o_te4ydr7DiFiOEaX6zrzRNcF-aSAdTfV0VMnACRUH3Dj6F76UMcdz71-D5svfM24Wln8WMMkzWT_2PxjXN5wsHhe93p6DX-OVqTqcGrYfJtjuWQH_Bmpwft9YDrne-20Q7n6J3TXbIfj-8S_V7f_Kpvi7uHzY96dVeYkpOpaEtFW66cNoxZx6igggjDlVRStowaXgmoAIyCUjoDwllSOUWhIsYB1RKW6GLeO8bwfLBpanqfjO06PdhwSA0tFZGcyXzPJSpmamJIKVrXjNH3Or40lDT_S2jmEpq5hOy_HFcf2t5uT_r16hl8PQKdjO5c1IPJ8ZOrgCpR0ew-z26fcjGn_xIkkYor-AcD_pfb</recordid><startdate>20140115</startdate><enddate>20140115</enddate><creator>Adu, Bright</creator><creator>Jepsen, Micha Phill Grønholm</creator><creator>Gerds, Thomas A.</creator><creator>Kyei-Baafour, Eric</creator><creator>Christiansen, Michael</creator><creator>Dodoo, Daniel</creator><creator>Theisen, Michael</creator><general>Oxford University Press</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></search><sort><creationdate>20140115</creationdate><title>Fc Gamma Receptor 3B (FCGR3B-c.233C>A-rs5030738) Polymorphism Modifies the Protective Effect of Malaria Specific Antibodies in Ghanaian Children</title><author>Adu, Bright ; Jepsen, Micha Phill Grønholm ; Gerds, Thomas A. ; Kyei-Baafour, Eric ; Christiansen, Michael ; Dodoo, Daniel ; Theisen, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-b491b59fac22ef2161606c597977b21c5863833c9347fc36fe08f91380cf31a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antibodies</topic><topic>Antibodies, Protozoan - immunology</topic><topic>Antigens</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cohort Studies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Predisposition to Disease</topic><topic>Genotypes</topic><topic>Ghana</topic><topic>GPI-Linked Proteins - genetics</topic><topic>Human protozoal diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Logistic regression</topic><topic>Malaria</topic><topic>Malaria - immunology</topic><topic>Malaria vaccines</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Neutrophils</topic><topic>Parasitemia</topic><topic>PARASITES</topic><topic>Parasitic diseases</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Protective effects</topic><topic>Protozoal diseases</topic><topic>Receptors, IgG - genetics</topic><topic>Sickle cell trait</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adu, Bright</creatorcontrib><creatorcontrib>Jepsen, Micha Phill Grønholm</creatorcontrib><creatorcontrib>Gerds, Thomas A.</creatorcontrib><creatorcontrib>Kyei-Baafour, Eric</creatorcontrib><creatorcontrib>Christiansen, Michael</creatorcontrib><creatorcontrib>Dodoo, Daniel</creatorcontrib><creatorcontrib>Theisen, Michael</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><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adu, Bright</au><au>Jepsen, Micha Phill Grønholm</au><au>Gerds, Thomas A.</au><au>Kyei-Baafour, Eric</au><au>Christiansen, Michael</au><au>Dodoo, Daniel</au><au>Theisen, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fc Gamma Receptor 3B (FCGR3B-c.233C>A-rs5030738) Polymorphism Modifies the Protective Effect of Malaria Specific Antibodies in Ghanaian Children</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2014-01-15</date><risdate>2014</risdate><volume>209</volume><issue>2</issue><spage>285</spage><epage>289</epage><pages>285-289</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Immunoglobulin G (IgG) cross-linking with Fc gamma receptor IIIB (FcyRIIIB) triggers neutrophil degranulation, releasing reactive oxygen species with high levels associated with protection against malaria. The FCGR3B-c.233C>A polymorphism thought to influence the interaction between IgG and FcyRIIIB was recently associated with malaria. We studied the statistical interaction between glutamate rich protein antibodies and FCGR3B-c.233C>A genotypes on risk of malaria in a cohort of Ghanaian children. The absolute risk of malaria decreased more rapidly with increasing antibody levels for 233AA/AC individuals compared with 233CC children. This genotype related effect modification may significantly influence malaria sero-epidemiological and vaccine trial studies.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>23935200</pmid><doi>10.1093/infdis/jit422</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Antibodies, Protozoan - immunology Antigens Biological and medical sciences Child Child, Preschool Cohort Studies Female Fundamental and applied biological sciences. Psychology Genetic Predisposition to Disease Genotypes Ghana GPI-Linked Proteins - genetics Human protozoal diseases Humans Infant Infectious diseases Logistic regression Malaria Malaria - immunology Malaria vaccines Male Medical sciences Microbiology Neutrophils Parasitemia PARASITES Parasitic diseases Polymorphism, Single Nucleotide Protective effects Protozoal diseases Receptors, IgG - genetics Sickle cell trait |
title | Fc Gamma Receptor 3B (FCGR3B-c.233C>A-rs5030738) Polymorphism Modifies the Protective Effect of Malaria Specific Antibodies in Ghanaian Children |
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