German Esther L, Al-Hakim Bahij, Mitsi Elena, Pennington Shaun H, Gritzfeld Jenna F, Hyder-Wright Angie D, Banyard Antonia, Gordon Stephen B, Collins Andrea M, Ferreira Daniela M
1Respiratory Infection Group, Liverpool School of Tropical Medicine, Liverpool, UK.
3Present address: Aintree University Hospital, Liverpool, UK.
Pneumonia (Nathan). 2018 Jun 5;10:5. doi: 10.1186/s41479-018-0048-3. eCollection 2018.
The incidence of community-acquired pneumonia and lower respiratory tract infection rises considerably in later life. Immunoglobulin M (IgM) antibody levels to pneumococcal capsular polysaccharide are known to decrease with age; however, whether levels of IgM antibody to pneumococcal proteins are subject to the same decline has not yet been investigated.
This study measured serum levels and binding capacity of IgM antibody specific to the pneumococcal surface protein A (PspA) and an unencapsulated pneumococcal strain in serum isolated from hospital patients aged < 60 and ≥ 60, with and without lower respiratory tract infection. A group of young healthy volunteers was used as a comparator to represent adults at very low risk of pneumococcal pneumonia. IgM serum antibody levels were measured by enzyme-linked immunosorbent assay (ELISA) and flow cytometry was performed to assess IgM binding capacity. Linear regression and one-way analysis of variance (ANOVA) tests were used to analyse the results.
Levels and binding capacity of IgM antibody to PspA and the unencapsulated pneumococcal strain were unchanged with age.
These findings suggest that protein-based pneumococcal vaccines may provide protective immunity in the elderly.
The LRTI trial (LRTI and control groups) was approved by the National Health Service Research Ethics Committee in October 2013 (12/NW/0713). Recruitment opened in January 2013 and was completed in July 2013. Healthy volunteer samples were taken from the EHPC dose-ranging and reproducibility trial, approved by the same Research Ethics Committee in October 2011 (11/NW/0592). Recruitment for this study ran from October 2011 until December 2012. LRTI trial: (NCT01861184), EHPC dose-ranging and reproducibility trial: (ISRCTN85403723).
社区获得性肺炎和下呼吸道感染的发病率在晚年显著上升。已知针对肺炎球菌荚膜多糖的免疫球蛋白M(IgM)抗体水平会随年龄下降;然而,针对肺炎球菌蛋白的IgM抗体水平是否也会出现同样的下降尚未得到研究。
本研究测量了年龄<60岁和≥60岁、患有和未患有下呼吸道感染的住院患者血清中针对肺炎球菌表面蛋白A(PspA)和非包膜肺炎球菌菌株的IgM抗体的血清水平和结合能力。一组年轻健康志愿者作为对照,以代表肺炎球菌肺炎风险极低的成年人。通过酶联免疫吸附测定(ELISA)测量IgM血清抗体水平,并进行流式细胞术以评估IgM结合能力。使用线性回归和单因素方差分析(ANOVA)测试来分析结果。
针对PspA和非包膜肺炎球菌菌株的IgM抗体水平和结合能力不会随年龄变化。
这些发现表明基于蛋白的肺炎球菌疫苗可能为老年人提供保护性免疫。
LRTI试验(LRTI组和对照组)于2013年10月获得英国国家医疗服务体系研究伦理委员会批准(12/NW/0713)。招募工作于2013年1月开始,并于2013年7月完成。健康志愿者样本取自EHPC剂量范围和可重复性试验,该试验于2011年10月获得同一研究伦理委员会批准(11/NW/0592)。本研究的招募工作从2011年10月持续到2012年12月。LRTI试验:(NCT01861184),EHPC剂量范围和可重复性试验:(ISRCTN85403723)。