Cholera toxin and O-specific polysaccharide immune responses after oral cholera vaccination with Dukoral in different age groups of Bangladeshi participants
Vaccination is important to prevent cholera. There are limited data comparing anti-O-specific polysaccharide (OSP) and anti-cholera toxin-specific immune responses following oral whole-cell with cholera toxin B-subunit (WC-rBS) vaccine (Dukoral, Valneva) administration in different age groups. An understanding of the differences is relevant because young children are less well protected by oral cholera vaccines than older children and adults. We compared responses in 50 adults and 49 children (ages 2 to <18) who were administered two doses of WC-rBS at a standard 14-day interval. All age groups had significant IgA and IgG plasma-blast responses to the OSP and cholera toxin B-subunit (CtxB) antigens that peaked 7 days after vaccination. However, in adults and older children (ages 5 to <18), antibody responses directed at the OSP antigen were largely IgA and IgG, with a minimal IgM response, while younger children (ages 2 to <5) mounted significant increases in IgM with minimal increases in IgA and IgG antibody responses 30 days after vaccination. In adults, anti-OSP and CtxB memory B-cell responses were detected after completion of the vaccination series, while children only mounted CtxB-specific IgG memory B-cell responses and no OSP-memory B-cell responses. In summary, children and adults living in a cholera endemic area mounted different responses to the WC-rBS vaccine, which may be a result of more prior exposure to Vibrio cholerae in older participants. The absence of class-switched antibody responses and memory B-cell responses to OSP may explain why protection wanes more rapidly after vaccination in young children compared to older vaccinees.IMPORTANCEVaccination is an important strategy to prevent cholera. Though immune responses targeting the OSP of V. cholerae are believed to mediate protection against cholera, there are limited data on anti-OSP responses after vaccination in different age groups, which is important as young children are not well protected by current oral cholera vaccines. In this study, we found that adults mounted memory B-cell responses to OSP, which were not seen in children. Adults and older children mounted class-switched (IgG and IgA) serum antibody responses to OSP, which were not seen in young children who had only IgM responses to OSP. The lack of class-switched antibody responses and memory B-cell responses to OSP in younger participants may be due to lack of prior exposure to V. cholerae and could explain why protection wanes more rapidly after vaccination in young children.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:9 |
|---|---|
| Enthalten in: |
mSphere - 9(2024), 3 vom: 26. März, Seite e0056523 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Dash, Pinki [VerfasserIn] |
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| Links: |
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| Anmerkungen: |
Date Completed 27.03.2024 Date Revised 06.04.2024 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1128/msphere.00565-23 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM368812146 |
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| 245 | 1 | 0 | |a Cholera toxin and O-specific polysaccharide immune responses after oral cholera vaccination with Dukoral in different age groups of Bangladeshi participants |
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| 500 | |a Date Revised 06.04.2024 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Vaccination is important to prevent cholera. There are limited data comparing anti-O-specific polysaccharide (OSP) and anti-cholera toxin-specific immune responses following oral whole-cell with cholera toxin B-subunit (WC-rBS) vaccine (Dukoral, Valneva) administration in different age groups. An understanding of the differences is relevant because young children are less well protected by oral cholera vaccines than older children and adults. We compared responses in 50 adults and 49 children (ages 2 to <18) who were administered two doses of WC-rBS at a standard 14-day interval. All age groups had significant IgA and IgG plasma-blast responses to the OSP and cholera toxin B-subunit (CtxB) antigens that peaked 7 days after vaccination. However, in adults and older children (ages 5 to <18), antibody responses directed at the OSP antigen were largely IgA and IgG, with a minimal IgM response, while younger children (ages 2 to <5) mounted significant increases in IgM with minimal increases in IgA and IgG antibody responses 30 days after vaccination. In adults, anti-OSP and CtxB memory B-cell responses were detected after completion of the vaccination series, while children only mounted CtxB-specific IgG memory B-cell responses and no OSP-memory B-cell responses. In summary, children and adults living in a cholera endemic area mounted different responses to the WC-rBS vaccine, which may be a result of more prior exposure to Vibrio cholerae in older participants. The absence of class-switched antibody responses and memory B-cell responses to OSP may explain why protection wanes more rapidly after vaccination in young children compared to older vaccinees.IMPORTANCEVaccination is an important strategy to prevent cholera. Though immune responses targeting the OSP of V. cholerae are believed to mediate protection against cholera, there are limited data on anti-OSP responses after vaccination in different age groups, which is important as young children are not well protected by current oral cholera vaccines. In this study, we found that adults mounted memory B-cell responses to OSP, which were not seen in children. Adults and older children mounted class-switched (IgG and IgA) serum antibody responses to OSP, which were not seen in young children who had only IgM responses to OSP. The lack of class-switched antibody responses and memory B-cell responses to OSP in younger participants may be due to lack of prior exposure to V. cholerae and could explain why protection wanes more rapidly after vaccination in young children | ||
| 650 | 4 | |a Journal Article | |
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| 650 | 4 | |a O-specific polysaccharide | |
| 650 | 4 | |a antibody secreting cells | |
| 650 | 4 | |a vibriocidal assay | |
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| 650 | 7 | |a Cholera Vaccines |2 NLM | |
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| 650 | 7 | |a 9012-63-9 |2 NLM | |
| 650 | 7 | |a O Antigens |2 NLM | |
| 650 | 7 | |a Immunoglobulin M |2 NLM | |
| 650 | 7 | |a Antibodies, Bacterial |2 NLM | |
| 650 | 7 | |a Immunoglobulin A |2 NLM | |
| 650 | 7 | |a Immunoglobulin G |2 NLM | |
| 700 | 1 | |a Hakim, Al |e verfasserin |4 aut | |
| 700 | 1 | |a Akter, Aklima |e verfasserin |4 aut | |
| 700 | 1 | |a Banna, Hasan Al |e verfasserin |4 aut | |
| 700 | 1 | |a Kaisar, M Hasanul |e verfasserin |4 aut | |
| 700 | 1 | |a Aktar, Amena |e verfasserin |4 aut | |
| 700 | 1 | |a Jahan, Sultana Rownok |e verfasserin |4 aut | |
| 700 | 1 | |a Ferdous, Jannatul |e verfasserin |4 aut | |
| 700 | 1 | |a Basher, Salima Raiyan |e verfasserin |4 aut | |
| 700 | 1 | |a Kamruzzaman, Mohammad |e verfasserin |4 aut | |
| 700 | 1 | |a Chowdhury, Fahima |e verfasserin |4 aut | |
| 700 | 1 | |a Akter, Afroza |e verfasserin |4 aut | |
| 700 | 1 | |a Tauheed, Imam |e verfasserin |4 aut | |
| 700 | 1 | |a Weil, Ana A |e verfasserin |4 aut | |
| 700 | 1 | |a Charles, Richelle C |e verfasserin |4 aut | |
| 700 | 1 | |a Calderwood, Stephen B |e verfasserin |4 aut | |
| 700 | 1 | |a Ryan, Edward T |e verfasserin |4 aut | |
| 700 | 1 | |a LaRocque, Regina C |e verfasserin |4 aut | |
| 700 | 1 | |a Harris, Jason B |e verfasserin |4 aut | |
| 700 | 1 | |a Bhuiyan, Taufiqur Rahman |e verfasserin |4 aut | |
| 700 | 1 | |a Qadri, Firdausi |e verfasserin |4 aut | |
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