# The immunogenicity and safety of an inactivated quadrivalent influenza vaccine and a 23-valent pneumococcal polysaccharide vaccine in individuals with chronic diseases

**Authors:** Wanqin Tang, Xi Lu, Zhongkui Zhu, Dan Yu, Huaxian Liu, Yufei Song, Lu Shen, Yang Yu, Yanwei Zhao, Yan Xie

PMC · DOI: 10.3389/fimmu.2025.1624095 · 2025-08-01

## TL;DR

This study shows that giving two vaccines together is safe and effective for older adults with chronic diseases, similar to healthy individuals.

## Contribution

The study provides new clinical evidence on the safety and immunogenicity of simultaneous administration of IIV4 and PPSV23 in individuals with chronic diseases.

## Key findings

- Antibody responses in the chronic disease group were non-inferior to those in the healthy group for both vaccines.
- Adverse events were rare and mostly mild in both groups, with no serious events observed.
- Simultaneous administration of the vaccines was as safe and effective as separate administration.

## Abstract

The inactivated quadrivalent influenza vaccine (IIV4) and the 23-valent pneumococcal polysaccharide vaccine (PPSV23) are widely administered. However, there was limited clinical evidence on the immunogenicity and safety of administration of the two vaccines in individuals with chronic diseases, especially concerning simultaneous administration.

A total of 480 participants aged ≥60 years were randomly assigned to receive simultaneous or separate administration of IIV4 and PPSV23 and categorized into the Chronic Disease group or Healthy group based on their baseline health status. Blood samples were drawn before and 28 days after each vaccination to test the antibodies against all four influenza virus strains and 23 pneumococcus serotypes.

The geometric mean titer ratios (Chronic Disease group/Healthy group) of influenza antibodies ranged from 1.04 to 1.37 in the whole population and from 1.02 to 1.39 in the simultaneous administration population. The geometric mean concentration ratios of pneumococcal antibodies ranged from 0.87 to 1.12 in the whole population and from 0.97 to 1.33 in the simultaneous administration population. All ratios met the criteria for non-inferiority. The rate of adverse events was 0.96% in the Chronic Disease group and 1.47% in the Healthy group, with most events being mild (grade 1). No serious adverse events were observed.

The immunogenicity and safety profiles of IIV4 and PPSV23, particularly when administered simultaneously, in individuals with chronic diseases were comparable to those in healthy individuals, supporting the vaccination strategy of IIV4 and PPSV23 in chronic disease population.

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** heart disease (MESH:D006331), HL (MESH:C538324), Chronic Disease (MESH:D002908), fever (MESH:D005334), Influenza (MESH:D007251), asthma (MESH:D001249), cardiovascular disorder (MESH:D002318), pneumococcal diseases (MESH:D011008), disease (MESH:D004194), epilepsy (MESH:D004827), neurological condition (MESH:D019636), allergic reactions (MESH:D004342), infectious diseases (MESH:D003141), death (MESH:D003643), infected (MESH:D007239), COPD (MESH:D029424), weakness (MESH:D018908), diabetes (MESH:D003920), CKD (MESH:D051436), obesity (MESH:D009765), pneumonia (MESH:D011014), compromised immunity (MESH:D007154), Hypertension (MESH:D006973), pain (MESH:D010146), cough (MESH:D003371)
- **Chemicals:** polysaccharides (MESH:D011134), GMC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], H1N1 subtype (serotype) [taxon 114727], Streptococcus pneumoniae (species) [taxon 1313], H3N2 subtype (serotype) [taxon 119210]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12355927/full.md

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Source: https://tomesphere.com/paper/PMC12355927