Title | Distinct baseline immune characteristics associated with responses to conjugated and unconjugated pneumococcal polysaccharide vaccines in older adults. |
Publication Type | Journal Article |
Year of Publication | 2024 |
Authors | Ravichandran 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 |
Journal | Nat Immunol |
Volume | 25 |
Issue | 2 |
Pagination | 316-329 |
Date Published | 2024 Feb |
ISSN | 1529-2916 |
Keywords | Aged, 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. |
DOI | 10.1038/s41590-023-01717-5 |
Custom 1 | |
Alternate Journal | Nat Immunol |
PubMed ID | 38182669 |
PubMed Central ID | PMC10834365 |
Grant List | R01 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 |