Prevalence of IgG and Neutralizing Antibodies Against Staphylococcus aureus Alpha Toxin in Healthy Human Subjects and Diverse Patient Populations

causes an array of serious infections resulting in high morbidity and mortality worldwide. This study evaluated naturally occurring serum anti-alpha toxin (AT) antibody levels in human subjects from various age groups, individuals with dialysis and surgical-site infections, and colonized versus nonc...

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Veröffentlicht in:Infection and immunity 2018-03, Vol.86 (3)
Hauptverfasser: Wu, Yuling, Liu, Xu, Akhgar, Ahmad, Li, Jia J, Mok, Hoyin, Sellman, Bret R, Yu, Li, Roskos, Lorin K, Esser, Mark T, Ruzin, Alexey
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container_issue 3
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container_title Infection and immunity
container_volume 86
creator Wu, Yuling
Liu, Xu
Akhgar, Ahmad
Li, Jia J
Mok, Hoyin
Sellman, Bret R
Yu, Li
Roskos, Lorin K
Esser, Mark T
Ruzin, Alexey
description causes an array of serious infections resulting in high morbidity and mortality worldwide. This study evaluated naturally occurring serum anti-alpha toxin (AT) antibody levels in human subjects from various age groups, individuals with dialysis and surgical-site infections, and colonized versus noncolonized subjects. Anti-AT immunoglobulin G (IgG) and neutralizing antibody (NAb) levels in infants (aged ≤1 year) were significantly lower than those in other populations. Young children (aged 2-10 years) had equivalent anti-AT IgG levels but significantly lower anti-AT NAb levels compared with the corresponding levels in adolescent, adult, and elderly populations. Therefore, the development of anti-AT NAbs appears to occur later than AT-specific IgG, suggesting a maturation of the immune response to AT. Anti-AT IgG levels were slightly higher in colonized than in noncolonized subjects. Methicillin susceptibility status of colonizing isolates had no effect on anti-AT antibody levels in -colonized subjects. The highest anti-AT IgG and NAb levels were observed in dialysis patients with acute infection. Anti-AT IgG and NAb levels were well correlated in subjects aged >10 years, regardless of colonization or infection status. These data demonstrate that AT elicits a robust IgG humoral response in infants and young children that becomes stable prior to adolescence, matures into higher levels of NAbs in healthy adolescents, and becomes elevated during infection. These findings may assist in identifying subjects and patient populations that could benefit from vaccination or immunoprophylaxis with anti-AT monoclonal antibodies.
doi_str_mv 10.1128/IAI.00671-17
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This study evaluated naturally occurring serum anti-alpha toxin (AT) antibody levels in human subjects from various age groups, individuals with dialysis and surgical-site infections, and colonized versus noncolonized subjects. Anti-AT immunoglobulin G (IgG) and neutralizing antibody (NAb) levels in infants (aged ≤1 year) were significantly lower than those in other populations. Young children (aged 2-10 years) had equivalent anti-AT IgG levels but significantly lower anti-AT NAb levels compared with the corresponding levels in adolescent, adult, and elderly populations. Therefore, the development of anti-AT NAbs appears to occur later than AT-specific IgG, suggesting a maturation of the immune response to AT. Anti-AT IgG levels were slightly higher in colonized than in noncolonized subjects. Methicillin susceptibility status of colonizing isolates had no effect on anti-AT antibody levels in -colonized subjects. The highest anti-AT IgG and NAb levels were observed in dialysis patients with acute infection. Anti-AT IgG and NAb levels were well correlated in subjects aged &gt;10 years, regardless of colonization or infection status. These data demonstrate that AT elicits a robust IgG humoral response in infants and young children that becomes stable prior to adolescence, matures into higher levels of NAbs in healthy adolescents, and becomes elevated during infection. These findings may assist in identifying subjects and patient populations that could benefit from vaccination or immunoprophylaxis with anti-AT monoclonal antibodies.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/IAI.00671-17</identifier><identifier>PMID: 29263109</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Microbial Immunity and Vaccines</subject><ispartof>Infection and immunity, 2018-03, Vol.86 (3)</ispartof><rights>Copyright © 2017 American Society for Microbiology.</rights><rights>Copyright © 2018 American Society for Microbiology. 2018 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c314t-e0ac58087aec88d6f799a8368e190e0ff840397fdd9e628188fbff9b0d1b00ec3</citedby><cites>FETCH-LOGICAL-c314t-e0ac58087aec88d6f799a8368e190e0ff840397fdd9e628188fbff9b0d1b00ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820940/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820940/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3174,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29263109$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Torres, Victor J.</contributor><creatorcontrib>Wu, Yuling</creatorcontrib><creatorcontrib>Liu, Xu</creatorcontrib><creatorcontrib>Akhgar, Ahmad</creatorcontrib><creatorcontrib>Li, Jia J</creatorcontrib><creatorcontrib>Mok, Hoyin</creatorcontrib><creatorcontrib>Sellman, Bret R</creatorcontrib><creatorcontrib>Yu, Li</creatorcontrib><creatorcontrib>Roskos, Lorin K</creatorcontrib><creatorcontrib>Esser, Mark T</creatorcontrib><creatorcontrib>Ruzin, Alexey</creatorcontrib><title>Prevalence of IgG and Neutralizing Antibodies Against Staphylococcus aureus Alpha Toxin in Healthy Human Subjects and Diverse Patient Populations</title><title>Infection and immunity</title><addtitle>Infect Immun</addtitle><description>causes an array of serious infections resulting in high morbidity and mortality worldwide. This study evaluated naturally occurring serum anti-alpha toxin (AT) antibody levels in human subjects from various age groups, individuals with dialysis and surgical-site infections, and colonized versus noncolonized subjects. Anti-AT immunoglobulin G (IgG) and neutralizing antibody (NAb) levels in infants (aged ≤1 year) were significantly lower than those in other populations. Young children (aged 2-10 years) had equivalent anti-AT IgG levels but significantly lower anti-AT NAb levels compared with the corresponding levels in adolescent, adult, and elderly populations. Therefore, the development of anti-AT NAbs appears to occur later than AT-specific IgG, suggesting a maturation of the immune response to AT. Anti-AT IgG levels were slightly higher in colonized than in noncolonized subjects. Methicillin susceptibility status of colonizing isolates had no effect on anti-AT antibody levels in -colonized subjects. The highest anti-AT IgG and NAb levels were observed in dialysis patients with acute infection. Anti-AT IgG and NAb levels were well correlated in subjects aged &gt;10 years, regardless of colonization or infection status. These data demonstrate that AT elicits a robust IgG humoral response in infants and young children that becomes stable prior to adolescence, matures into higher levels of NAbs in healthy adolescents, and becomes elevated during infection. 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This study evaluated naturally occurring serum anti-alpha toxin (AT) antibody levels in human subjects from various age groups, individuals with dialysis and surgical-site infections, and colonized versus noncolonized subjects. Anti-AT immunoglobulin G (IgG) and neutralizing antibody (NAb) levels in infants (aged ≤1 year) were significantly lower than those in other populations. Young children (aged 2-10 years) had equivalent anti-AT IgG levels but significantly lower anti-AT NAb levels compared with the corresponding levels in adolescent, adult, and elderly populations. Therefore, the development of anti-AT NAbs appears to occur later than AT-specific IgG, suggesting a maturation of the immune response to AT. Anti-AT IgG levels were slightly higher in colonized than in noncolonized subjects. Methicillin susceptibility status of colonizing isolates had no effect on anti-AT antibody levels in -colonized subjects. 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title Prevalence of IgG and Neutralizing Antibodies Against Staphylococcus aureus Alpha Toxin in Healthy Human Subjects and Diverse Patient Populations
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