Division of Epidemiology, School of Public Health, University of California, Berkeley, California, USA.
Division of Infectious Diseases & Vaccinology, School of Public Health, University of California, Berkeley, California, USA.
J Infect Dis. 2023 Feb 14;227(4):498-511. doi: 10.1093/infdis/jiac098.
Interactions of Streptococcus pneumoniae with viruses feature in the pathogenesis of numerous respiratory illnesses.
We undertook a case-control study among adults at Kaiser Permanente Southern California between 2015 and 2019. Case patients had diagnoses of lower respiratory tract infection (LRTI; including pneumonia or nonpneumonia LRTI diagnoses), with viral infections detected by multiplex polymerase chain reaction testing. Controls without LRTI diagnoses were matched to case patients by demographic and clinical attributes. We measured vaccine effectiveness (VE) for 13-valent (PCV13) against virus-associated LRTI by determining the adjusted odds ratio for PCV13 receipt, comparing case patients and controls.
Primary analyses included 13 856 case patients with virus-associated LRTI and 227 887 matched controls. Receipt of PCV13 was associated with a VE of 24.9% (95% confidence interval, 18.4%-30.9%) against virus-associated pneumonia and 21.5% (10.9%-30.9%) against other (nonpneumonia) virus-associated LRTIs. We estimated VEs of 26.8% (95% confidence interval, 19.9%-33.1%) and 18.6% (9.3%-27.0%) against all virus-associated LRTI episodes diagnosed in inpatient and outpatient settings, respectively. We identified statistically significant protection against LRTI episodes associated with influenza A and B viruses, endemic human coronaviruses, parainfluenza viruses, human metapneumovirus, and enteroviruses but not respiratory syncytial virus or adenoviruses.
Among adults, PCV13 conferred moderate protection against virus-associated LRTI. The impacts of pneumococcal conjugate vaccines may be mediated, in part, by effects on polymicrobial interactions between pneumococci and respiratory viruses.
肺炎链球菌与病毒的相互作用是许多呼吸道疾病发病机制的特征。
我们在 2015 年至 2019 年期间对 Kaiser Permanente 南加州的成年人进行了病例对照研究。病例患者被诊断患有下呼吸道感染(LRTI;包括肺炎或非肺炎 LRTI 诊断),并通过多重聚合酶链反应检测到病毒感染。无 LRTI 诊断的对照患者通过人口统计学和临床特征与病例患者相匹配。我们通过确定 13 价肺炎球菌结合疫苗(PCV13)接种的调整比值比,比较病例患者和对照患者,来衡量针对病毒相关 LRTI 的疫苗效力(VE)。
主要分析包括 13856 例病毒相关 LRTI 病例患者和 227887 例匹配对照患者。PCV13 的接种与病毒相关肺炎的 24.9%(95%置信区间,18.4%-30.9%)和其他(非肺炎)病毒相关 LRTI 的 21.5%(10.9%-30.9%)的 VE 相关。我们估计门诊和住院环境中诊断的所有病毒相关 LRTI 病例分别为 26.8%(95%置信区间,19.9%-33.1%)和 18.6%(9.3%-27.0%)的 VE。我们发现针对流感 A 和 B 病毒、地方性人类冠状病毒、副流感病毒、人偏肺病毒和肠道病毒的 LRTI 有统计学显著的保护作用,但对呼吸道合胞病毒或腺病毒没有保护作用。
在成年人中,PCV13 对病毒相关 LRTI 提供了适度的保护。肺炎球菌结合疫苗的影响可能部分是通过肺炎球菌和呼吸道病毒之间的多微生物相互作用来介导的。