Streptococcus pyogenes pharyngitis elicits diverse antibody responses to key vaccine antigens influenced by the imprint of past infections

Knowledge gaps regarding human immunity to Streptococcus pyogenes have impeded vaccine development. To address these gaps and evaluate vaccine candidates, we established a human challenge model of S. pyogenes pharyngitis. Here, we analyse antibody responses in serum and saliva against 19 antigens to identify characteristics distinguishing 19 participants who developed pharyngitis and 6 who did not. We show that pharyngitis elicits serum IgG responses to key vaccine antigens and a muted mucosal IgA response, whereas IgG responses are minimal and IgA responses more pronounced in participants without pharyngitis. Serum IgG responses to pharyngitis in adult participants resemble those in children and are inversely correlated with the magnitude of pre-existing responses. While a straightforward correlate of protection is not evident, baseline antibody signatures distinguish clinical and immunological outcomes following experimental challenge. This highlights the influence of a complex humoral imprint from previous exposure, relevant for interpreting immunogenicity in forthcoming vaccine trials.

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Publication Details

Journal
Nature Communications
Published
2024-12-03
DOI
https://doi.org/10.1038/s41467-024-54665-5
Citations
10
Primary Topic
Streptococcal Infections and Treatments
Type
article
Field-Weighted Citation Impact
5.43

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article

Streptococcus pyogenes pharyngitis elicits diverse antibody responses to key vaccine antigens influenced by the imprint of past infections

Lauren H. Carlton, Pierre R. Smeesters, Mark J. Walker, Paul V. Licciardi et al.
10 citations
Nature Communications
Streptococcal Infections and Treatments
5.43
article

Streptococcus pyogenes pharyngitis elicits diverse antibody responses to key vaccine antigens influenced by the imprint of past infections

Lauren H. Carlton, Pierre R. Smeesters, Mark J. Walker, Paul V. Licciardi, Danika L. Hill, Jonathan Rhys Carapetis, Hannah R. Frost, Michael F. Good, Ciara Baker, Joshua Osowicki, Alana L. Whitcombe, Kristy Azzopardi, Manisha Pandey, Nicole J. Moreland, Andrew C. Steer, Loraine Fabri, Reuben McGregor
article en
10 citations

Abstract

Knowledge gaps regarding human immunity to Streptococcus pyogenes have impeded vaccine development. To address these gaps and evaluate vaccine candidates, we established a human challenge model of S. pyogenes pharyngitis. Here, we analyse antibody responses in serum and saliva against 19 antigens to identify characteristics distinguishing 19 participants who developed pharyngitis and 6 who did not. We show that pharyngitis elicits serum IgG responses to key vaccine antigens and a muted mucosal IgA response, whereas IgG responses are minimal and IgA responses more pronounced in participants without pharyngitis. Serum IgG responses to pharyngitis in adult participants resemble those in children and are inversely correlated with the magnitude of pre-existing responses. While a straightforward correlate of protection is not evident, baseline antibody signatures distinguish clinical and immunological outcomes following experimental challenge. This highlights the influence of a complex humoral imprint from previous exposure, relevant for interpreting immunogenicity in forthcoming vaccine trials.

Nature CommunicationsVol. 15(1)
Griffith University (AU), Royal Children's Hospital (AU), University of Auckland (NZ), The University of Queensland (AU), The University of Melbourne (AU), The University of Western Australia (AU), Princess Margaret Hospital for Children (AU), Queen Fabiola Children's University Hospital (BE), Maurice Wilkins Centre (NZ), Murdoch Children's Research Institute (AU), Perth Children's Hospital, Monash University (AU)
GlaxoSmithKline, Michelson Prize and Grants, University of Otago, Maurice Wilkins Centre for Molecular Biodiscovery, Medical Research Council, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 4%
Streptococcal Infections and Treatments
5.43
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