Naturally acquired antibodies against 4 Streptococcus pneumoniae serotypes in Pakistani adults with type 2 diabetes mellitus

Immune response elicited during pneumococcal carriage has been shown to protect against subsequent colonization and infection by Streptococcus pneumoniae. The study was designed to measure the baseline serotype-specific anti-capsular IgG concentration and opsonic titers elicited in response to asymp...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2024-08, Vol.19 (8), p.e0306921
Hauptverfasser: Ahmad, Izaz, Burton, Robert, Nahm, Moon, Ejaz, Hafiz Gohar, Arshad, Rozina, Younis, Bilal Bin, Mirza, Shaper
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 8
container_start_page e0306921
container_title PloS one
container_volume 19
creator Ahmad, Izaz
Burton, Robert
Nahm, Moon
Ejaz, Hafiz Gohar
Arshad, Rozina
Younis, Bilal Bin
Mirza, Shaper
description Immune response elicited during pneumococcal carriage has been shown to protect against subsequent colonization and infection by Streptococcus pneumoniae. The study was designed to measure the baseline serotype-specific anti-capsular IgG concentration and opsonic titers elicited in response to asymptomatic carriage in adults with and without type 2-diabetes. Level of IgG to capsular polysaccharide was measured in a total of 176 samples (124 with type 2 diabetes and 52 without type 2 diabetes) against serotype 1, 19F, 9V, and 18C. From within 176 samples, a nested cohort of 39 samples was selected for measuring the functional capacity of antibodies by measuring opsonic titer to serotypes 19F, 9V, and 18C. Next, we measured levels of IgG to PspA in 90 samples from individuals with and without diabetes (22 non-diabetes and 68 diabetes). Our results demonstrated comparable IgG titers against all serotypes between those with and without type 2-diabetes. Overall, we observed higher opsonic titers in those without diabetes as compared to individuals with diabetes for serotypes 19F and 9V. The opsonic titers for 19F and 9V significantly negatively correlated with HbA1c. For 19F, 41.66% (n = 10) showed opsonic titers ≥ 1:8 in the diabetes group as compared to 66.66% (n = 10) in the non-diabetes group. The percentage was 29.6% (n = 7) vs 66.66% (n = 10) for 9V and 70.83% (n = 17) vs 80% (n = 12) for 18C in diabetes and non-diabetes groups respectively. A comparable anti-PspA IgG (p = 0.409) was observed in those with and without diabetes, indicating that response to protein antigen is likely to remain intact in those with diabetes. In conclusion, we demonstrated comparable IgG titers to both capsular polysaccharide and protein antigens in those with and without diabetes, however, the protective capacity of antibodies differed between the two groups.
doi_str_mv 10.1371/journal.pone.0306921
format Article
fullrecord <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_3091107579</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A804372956</galeid><doaj_id>oai_doaj_org_article_6d44df5572e74e8db6abbbb6d71b9e42</doaj_id><sourcerecordid>A804372956</sourcerecordid><originalsourceid>FETCH-LOGICAL-c540t-aea012eff141a0a36520db2700913077694afdc1cc5c188393858892bc065e893</originalsourceid><addsrcrecordid>eNqNkltrFDEYhgdRbK3-A9FAQfRi1xwmc7gsxcNCsWLV2_BNktnNOjOZ5oAu-OPNuNPSlV6YXCQkz_t9ycubZc8JXhJWkrdbG90A3XK0g15ihouakgfZMakZXRQUs4d39kfZE--3GHNWFcXj7IjVhBJc8ePs9ycI0UHX7RDI62icVgiGYBqrjPYI1mAGH1COroLTY7DSShk9GgcdezsY0MhrZ8NuTLAZ0Gf4YXyAwSBQsQse_TRhg6ZrRJEy0OiQwF53nQnRP80etdB5_WxeT7Jv7999Pf-4uLj8sDo_u1hInuOwAA2YUN22JCeAgRWcYtXQEuOaMFyWRZ1DqySRkktSVaxmFa-qmjYSF1xXNTvJXu7rjp31YjbOC5b0BJe8nIjVnlAWtmJ0pge3ExaM-Htg3VqAC0Z2WhQqz1XLeUl1metKNQU0aRSqJE2tc5pqvZ67OXsdtQ-iN16mL8OgbZzbclyVE3r6D3r_42ZqDam_GVobHMipqDircM5KWvMiUct7qDSV7o1MIWlNOj8QvDkQJCboX2EN0Xuxuvry_-zl90P21R12o6ELG2-7GIwd_CGY70HprPdOt7fGEyymjN-4IaaMiznjSfZiNi02vVa3optQsz8gZfay</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3091107579</pqid></control><display><type>article</type><title>Naturally acquired antibodies against 4 Streptococcus pneumoniae serotypes in Pakistani adults with type 2 diabetes mellitus</title><source>Public Library of Science (PLoS) Journals Open Access</source><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Ahmad, Izaz ; Burton, Robert ; Nahm, Moon ; Ejaz, Hafiz Gohar ; Arshad, Rozina ; Younis, Bilal Bin ; Mirza, Shaper</creator><creatorcontrib>Ahmad, Izaz ; Burton, Robert ; Nahm, Moon ; Ejaz, Hafiz Gohar ; Arshad, Rozina ; Younis, Bilal Bin ; Mirza, Shaper</creatorcontrib><description>Immune response elicited during pneumococcal carriage has been shown to protect against subsequent colonization and infection by Streptococcus pneumoniae. The study was designed to measure the baseline serotype-specific anti-capsular IgG concentration and opsonic titers elicited in response to asymptomatic carriage in adults with and without type 2-diabetes. Level of IgG to capsular polysaccharide was measured in a total of 176 samples (124 with type 2 diabetes and 52 without type 2 diabetes) against serotype 1, 19F, 9V, and 18C. From within 176 samples, a nested cohort of 39 samples was selected for measuring the functional capacity of antibodies by measuring opsonic titer to serotypes 19F, 9V, and 18C. Next, we measured levels of IgG to PspA in 90 samples from individuals with and without diabetes (22 non-diabetes and 68 diabetes). Our results demonstrated comparable IgG titers against all serotypes between those with and without type 2-diabetes. Overall, we observed higher opsonic titers in those without diabetes as compared to individuals with diabetes for serotypes 19F and 9V. The opsonic titers for 19F and 9V significantly negatively correlated with HbA1c. For 19F, 41.66% (n = 10) showed opsonic titers ≥ 1:8 in the diabetes group as compared to 66.66% (n = 10) in the non-diabetes group. The percentage was 29.6% (n = 7) vs 66.66% (n = 10) for 9V and 70.83% (n = 17) vs 80% (n = 12) for 18C in diabetes and non-diabetes groups respectively. A comparable anti-PspA IgG (p = 0.409) was observed in those with and without diabetes, indicating that response to protein antigen is likely to remain intact in those with diabetes. In conclusion, we demonstrated comparable IgG titers to both capsular polysaccharide and protein antigens in those with and without diabetes, however, the protective capacity of antibodies differed between the two groups.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0306921</identifier><identifier>PMID: 39121085</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Adults ; Aged ; Antibiotics ; Antibodies ; Antibodies, Bacterial - blood ; Antibodies, Bacterial - immunology ; Antigens ; Asymptomatic ; Bacteria ; Capsular polysaccharides ; Diabetes ; Diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - immunology ; Diabetes Mellitus, Type 2 - microbiology ; Female ; Glycosylated hemoglobin ; Heat ; Humans ; Immune response ; Immunization ; Immunoglobulin G ; Immunoglobulin G - blood ; Immunoglobulin G - immunology ; Male ; Medical research ; Medicine, Experimental ; Middle Aged ; Pakistan - epidemiology ; Pneumococcal Infections - immunology ; Pneumococcal Infections - microbiology ; Pneumonia ; Polysaccharides ; Proteins ; PspA protein ; Serogroup ; Serotypes ; Streptococcus infections ; Streptococcus pneumoniae ; Streptococcus pneumoniae - immunology ; Vaccines ; Virulence</subject><ispartof>PloS one, 2024-08, Vol.19 (8), p.e0306921</ispartof><rights>Copyright: © 2024 Ahmad et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2024 Public Library of Science</rights><rights>2024 Ahmad 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>2024 Ahmad 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c540t-aea012eff141a0a36520db2700913077694afdc1cc5c188393858892bc065e893</cites><orcidid>0000-0002-6651-6101 ; 0000-0003-3371-3501</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0306921&amp;type=printable$$EPDF$$P50$$Gplos$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0306921$$EHTML$$P50$$Gplos$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,860,2096,2915,23845,27901,27902,79569,79570</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39121085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahmad, Izaz</creatorcontrib><creatorcontrib>Burton, Robert</creatorcontrib><creatorcontrib>Nahm, Moon</creatorcontrib><creatorcontrib>Ejaz, Hafiz Gohar</creatorcontrib><creatorcontrib>Arshad, Rozina</creatorcontrib><creatorcontrib>Younis, Bilal Bin</creatorcontrib><creatorcontrib>Mirza, Shaper</creatorcontrib><title>Naturally acquired antibodies against 4 Streptococcus pneumoniae serotypes in Pakistani adults with type 2 diabetes mellitus</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Immune response elicited during pneumococcal carriage has been shown to protect against subsequent colonization and infection by Streptococcus pneumoniae. The study was designed to measure the baseline serotype-specific anti-capsular IgG concentration and opsonic titers elicited in response to asymptomatic carriage in adults with and without type 2-diabetes. Level of IgG to capsular polysaccharide was measured in a total of 176 samples (124 with type 2 diabetes and 52 without type 2 diabetes) against serotype 1, 19F, 9V, and 18C. From within 176 samples, a nested cohort of 39 samples was selected for measuring the functional capacity of antibodies by measuring opsonic titer to serotypes 19F, 9V, and 18C. Next, we measured levels of IgG to PspA in 90 samples from individuals with and without diabetes (22 non-diabetes and 68 diabetes). Our results demonstrated comparable IgG titers against all serotypes between those with and without type 2-diabetes. Overall, we observed higher opsonic titers in those without diabetes as compared to individuals with diabetes for serotypes 19F and 9V. The opsonic titers for 19F and 9V significantly negatively correlated with HbA1c. For 19F, 41.66% (n = 10) showed opsonic titers ≥ 1:8 in the diabetes group as compared to 66.66% (n = 10) in the non-diabetes group. The percentage was 29.6% (n = 7) vs 66.66% (n = 10) for 9V and 70.83% (n = 17) vs 80% (n = 12) for 18C in diabetes and non-diabetes groups respectively. A comparable anti-PspA IgG (p = 0.409) was observed in those with and without diabetes, indicating that response to protein antigen is likely to remain intact in those with diabetes. In conclusion, we demonstrated comparable IgG titers to both capsular polysaccharide and protein antigens in those with and without diabetes, however, the protective capacity of antibodies differed between the two groups.</description><subject>Adult</subject><subject>Adults</subject><subject>Aged</subject><subject>Antibiotics</subject><subject>Antibodies</subject><subject>Antibodies, Bacterial - blood</subject><subject>Antibodies, Bacterial - immunology</subject><subject>Antigens</subject><subject>Asymptomatic</subject><subject>Bacteria</subject><subject>Capsular polysaccharides</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - immunology</subject><subject>Diabetes Mellitus, Type 2 - microbiology</subject><subject>Female</subject><subject>Glycosylated hemoglobin</subject><subject>Heat</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunization</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin G - immunology</subject><subject>Male</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Middle Aged</subject><subject>Pakistan - epidemiology</subject><subject>Pneumococcal Infections - immunology</subject><subject>Pneumococcal Infections - microbiology</subject><subject>Pneumonia</subject><subject>Polysaccharides</subject><subject>Proteins</subject><subject>PspA protein</subject><subject>Serogroup</subject><subject>Serotypes</subject><subject>Streptococcus infections</subject><subject>Streptococcus pneumoniae</subject><subject>Streptococcus pneumoniae - immunology</subject><subject>Vaccines</subject><subject>Virulence</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNkltrFDEYhgdRbK3-A9FAQfRi1xwmc7gsxcNCsWLV2_BNktnNOjOZ5oAu-OPNuNPSlV6YXCQkz_t9ycubZc8JXhJWkrdbG90A3XK0g15ihouakgfZMakZXRQUs4d39kfZE--3GHNWFcXj7IjVhBJc8ePs9ycI0UHX7RDI62icVgiGYBqrjPYI1mAGH1COroLTY7DSShk9GgcdezsY0MhrZ8NuTLAZ0Gf4YXyAwSBQsQse_TRhg6ZrRJEy0OiQwF53nQnRP80etdB5_WxeT7Jv7999Pf-4uLj8sDo_u1hInuOwAA2YUN22JCeAgRWcYtXQEuOaMFyWRZ1DqySRkktSVaxmFa-qmjYSF1xXNTvJXu7rjp31YjbOC5b0BJe8nIjVnlAWtmJ0pge3ExaM-Htg3VqAC0Z2WhQqz1XLeUl1metKNQU0aRSqJE2tc5pqvZ67OXsdtQ-iN16mL8OgbZzbclyVE3r6D3r_42ZqDam_GVobHMipqDircM5KWvMiUct7qDSV7o1MIWlNOj8QvDkQJCboX2EN0Xuxuvry_-zl90P21R12o6ELG2-7GIwd_CGY70HprPdOt7fGEyymjN-4IaaMiznjSfZiNi02vVa3optQsz8gZfay</recordid><startdate>20240809</startdate><enddate>20240809</enddate><creator>Ahmad, Izaz</creator><creator>Burton, Robert</creator><creator>Nahm, Moon</creator><creator>Ejaz, Hafiz Gohar</creator><creator>Arshad, Rozina</creator><creator>Younis, Bilal Bin</creator><creator>Mirza, Shaper</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>COVID</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6651-6101</orcidid><orcidid>https://orcid.org/0000-0003-3371-3501</orcidid></search><sort><creationdate>20240809</creationdate><title>Naturally acquired antibodies against 4 Streptococcus pneumoniae serotypes in Pakistani adults with type 2 diabetes mellitus</title><author>Ahmad, Izaz ; Burton, Robert ; Nahm, Moon ; Ejaz, Hafiz Gohar ; Arshad, Rozina ; Younis, Bilal Bin ; Mirza, Shaper</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-aea012eff141a0a36520db2700913077694afdc1cc5c188393858892bc065e893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Adults</topic><topic>Aged</topic><topic>Antibiotics</topic><topic>Antibodies</topic><topic>Antibodies, Bacterial - blood</topic><topic>Antibodies, Bacterial - immunology</topic><topic>Antigens</topic><topic>Asymptomatic</topic><topic>Bacteria</topic><topic>Capsular polysaccharides</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - immunology</topic><topic>Diabetes Mellitus, Type 2 - microbiology</topic><topic>Female</topic><topic>Glycosylated hemoglobin</topic><topic>Heat</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunization</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin G - immunology</topic><topic>Male</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Middle Aged</topic><topic>Pakistan - epidemiology</topic><topic>Pneumococcal Infections - immunology</topic><topic>Pneumococcal Infections - microbiology</topic><topic>Pneumonia</topic><topic>Polysaccharides</topic><topic>Proteins</topic><topic>PspA protein</topic><topic>Serogroup</topic><topic>Serotypes</topic><topic>Streptococcus infections</topic><topic>Streptococcus pneumoniae</topic><topic>Streptococcus pneumoniae - immunology</topic><topic>Vaccines</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmad, Izaz</creatorcontrib><creatorcontrib>Burton, Robert</creatorcontrib><creatorcontrib>Nahm, Moon</creatorcontrib><creatorcontrib>Ejaz, Hafiz Gohar</creatorcontrib><creatorcontrib>Arshad, Rozina</creatorcontrib><creatorcontrib>Younis, Bilal Bin</creatorcontrib><creatorcontrib>Mirza, Shaper</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health &amp; Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</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>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmad, Izaz</au><au>Burton, Robert</au><au>Nahm, Moon</au><au>Ejaz, Hafiz Gohar</au><au>Arshad, Rozina</au><au>Younis, Bilal Bin</au><au>Mirza, Shaper</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Naturally acquired antibodies against 4 Streptococcus pneumoniae serotypes in Pakistani adults with type 2 diabetes mellitus</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2024-08-09</date><risdate>2024</risdate><volume>19</volume><issue>8</issue><spage>e0306921</spage><pages>e0306921-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Immune response elicited during pneumococcal carriage has been shown to protect against subsequent colonization and infection by Streptococcus pneumoniae. The study was designed to measure the baseline serotype-specific anti-capsular IgG concentration and opsonic titers elicited in response to asymptomatic carriage in adults with and without type 2-diabetes. Level of IgG to capsular polysaccharide was measured in a total of 176 samples (124 with type 2 diabetes and 52 without type 2 diabetes) against serotype 1, 19F, 9V, and 18C. From within 176 samples, a nested cohort of 39 samples was selected for measuring the functional capacity of antibodies by measuring opsonic titer to serotypes 19F, 9V, and 18C. Next, we measured levels of IgG to PspA in 90 samples from individuals with and without diabetes (22 non-diabetes and 68 diabetes). Our results demonstrated comparable IgG titers against all serotypes between those with and without type 2-diabetes. Overall, we observed higher opsonic titers in those without diabetes as compared to individuals with diabetes for serotypes 19F and 9V. The opsonic titers for 19F and 9V significantly negatively correlated with HbA1c. For 19F, 41.66% (n = 10) showed opsonic titers ≥ 1:8 in the diabetes group as compared to 66.66% (n = 10) in the non-diabetes group. The percentage was 29.6% (n = 7) vs 66.66% (n = 10) for 9V and 70.83% (n = 17) vs 80% (n = 12) for 18C in diabetes and non-diabetes groups respectively. A comparable anti-PspA IgG (p = 0.409) was observed in those with and without diabetes, indicating that response to protein antigen is likely to remain intact in those with diabetes. In conclusion, we demonstrated comparable IgG titers to both capsular polysaccharide and protein antigens in those with and without diabetes, however, the protective capacity of antibodies differed between the two groups.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>39121085</pmid><doi>10.1371/journal.pone.0306921</doi><tpages>e0306921</tpages><orcidid>https://orcid.org/0000-0002-6651-6101</orcidid><orcidid>https://orcid.org/0000-0003-3371-3501</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1932-6203
ispartof PloS one, 2024-08, Vol.19 (8), p.e0306921
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_3091107579
source Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry
subjects Adult
Adults
Aged
Antibiotics
Antibodies
Antibodies, Bacterial - blood
Antibodies, Bacterial - immunology
Antigens
Asymptomatic
Bacteria
Capsular polysaccharides
Diabetes
Diabetes mellitus
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - immunology
Diabetes Mellitus, Type 2 - microbiology
Female
Glycosylated hemoglobin
Heat
Humans
Immune response
Immunization
Immunoglobulin G
Immunoglobulin G - blood
Immunoglobulin G - immunology
Male
Medical research
Medicine, Experimental
Middle Aged
Pakistan - epidemiology
Pneumococcal Infections - immunology
Pneumococcal Infections - microbiology
Pneumonia
Polysaccharides
Proteins
PspA protein
Serogroup
Serotypes
Streptococcus infections
Streptococcus pneumoniae
Streptococcus pneumoniae - immunology
Vaccines
Virulence
title Naturally acquired antibodies against 4 Streptococcus pneumoniae serotypes in Pakistani adults with type 2 diabetes mellitus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T20%3A58%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Naturally%20acquired%20antibodies%20against%204%20Streptococcus%20pneumoniae%20serotypes%20in%20Pakistani%20adults%20with%20type%202%20diabetes%20mellitus&rft.jtitle=PloS%20one&rft.au=Ahmad,%20Izaz&rft.date=2024-08-09&rft.volume=19&rft.issue=8&rft.spage=e0306921&rft.pages=e0306921-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0306921&rft_dat=%3Cgale_plos_%3EA804372956%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3091107579&rft_id=info:pmid/39121085&rft_galeid=A804372956&rft_doaj_id=oai_doaj_org_article_6d44df5572e74e8db6abbbb6d71b9e42&rfr_iscdi=true