Distinct baseline immune characteristics associated with responses to conjugated and unconjugated pneumococcal polysaccharide vaccines in older adults.

TitleDistinct baseline immune characteristics associated with responses to conjugated and unconjugated pneumococcal polysaccharide vaccines in older adults.
Publication TypeJournal Article
Year of Publication2024
AuthorsRavichandran S, Erra-Diaz F, Karakaslar OE, Marches R, Kenyon-Pesce L, Rossi R, Chaussabel D, Nehar-Belaid D, LaFon DC, Pascual V, Palucka K, Paust S, Nahm MH, Kuchel GA, Banchereau J, Ucar D
JournalNat Immunol
Volume25
Issue2
Pagination316-329
Date Published2024 Feb
ISSN1529-2916
KeywordsAged, Antibodies, Bacterial, Double-Blind Method, Female, Humans, Male, Pneumococcal Vaccines, Polysaccharides, Streptococcus pneumoniae, Vaccination, Vaccines, Conjugate
Abstract

Pneumococcal infections cause serious illness and death among older adults. The capsular polysaccharide vaccine PPSV23 and conjugated alternative PCV13 can prevent these infections; yet, underlying immunological responses and baseline predictors remain unknown. We vaccinated 39 older adults (>60 years) with PPSV23 or PCV13 and observed comparable antibody responses (day 28) and plasmablast transcriptional responses (day 10); however, the baseline predictors were distinct. Analyses of baseline flow cytometry and bulk and single-cell RNA-sequencing data revealed a baseline phenotype specifically associated with weaker PCV13 responses, which was characterized by increased expression of cytotoxicity-associated genes, increased frequencies of CD16+ natural killer cells and interleukin-17-producing helper T cells and a decreased frequency of type 1 helper T cells. Men displayed this phenotype more robustly and mounted weaker PCV13 responses than women. Baseline expression levels of a distinct gene set predicted PPSV23 responses. This pneumococcal precision vaccinology study in older adults uncovered distinct baseline predictors that might transform vaccination strategies and initiate novel interventions.

DOI10.1038/s41590-023-01717-5
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https://www.ncbi.nlm.nih.gov/pubmed/38182669?dopt=Abstract

Alternate JournalNat Immunol
PubMed ID38182669
PubMed Central IDPMC10834365
Grant ListR01 AI142086 / AI / NIAID NIH HHS / United States
P30 CA034196 / CA / NCI NIH HHS / United States
R01 AG052608 / AG / NIA NIH HHS / United States
U01 AI165452 / AI / NIAID NIH HHS / United States
P30 AG067988 / AG / NIA NIH HHS / United States

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