Abstract
Infectious diseases are a major cause for morbidity and mortality in the older population. Demographic changes will lead to increasing numbers of older persons over the next decades. Prevention of infections becomes increasingly important to ensure healthy aging for the individual, and to alleviate the socio-economic burden for societies. Undoubtedly, vaccines are the most efficient health care measure to prevent infections. Age-associated changes of the immune system are responsible for decreased immunogenicity and clinical efficacy of most currently used vaccines in older age. Efficacy of standard influenza vaccines is only 30–50% in the older population. Several approaches, such as higher antigen dose, use of MF59 as adjuvant and intradermal administration have been implemented in order to specifically target the aged immune system. The use of a 23-valent polysaccharide vaccine against Streptococcus pneumoniae has been amended by a 13-valent conjugated pneumococcal vaccine originally developed for young children several years ago to overcome at least some of the limitations of the T cell-independent polysaccharide antigens, but still is only approximately 50% protective against pneumonia. A live-attenuated vaccine against herpes zoster, which has been available for several years, demonstrated efficacy of 51% against herpes zoster and 67% against post-herpetic neuralgia. Protection was lower in the very old and decreased several years after vaccination. Recently, a recombinant vaccine containing the viral glycoprotein gE and the novel adjuvant AS01B has been licensed. Phase III studies demonstrated efficacy against herpes zoster of approx. 90% even in the oldest age groups after administration of two doses and many countries now recommend the preferential use of this vaccine. There are still many infectious diseases causing substantial morbidity in the older population, for which no vaccines are available so far. Extensive research is ongoing to develop vaccines against novel targets with several vaccine candidates already being clinically tested, which have the potential to substantially reduce health care costs and to save many lives. In addition to the development of novel and improved vaccines, which specifically target the aged immune system, it is also important to improve uptake of the existing vaccines in order to protect the vulnerable, older population.
Highlights
Reviewed by: Manish Sadarangani, The University of British Columbia, Canada Paulo Bettencourt, University of Oxford, United Kingdom
Post hoc analysis of the CAPiTA study, which investigated the efficacy of the 13-valent conjugated pneumococcal vaccine, showed that 80% of the pneumonia cases, which occurred in the unvaccinated placebo arm of the study population, affected persons with one or more co-morbidities
Since the dermis is rich in antigen-presenting cells (APC) such as dendritic cells (DC) and Langerhans cells (LC) intradermal (i.d.) application of vaccines is performed in order to facilitate antigen uptake by these APC and downstream adaptive immune responses following antigen processing and presentation [60]
Summary
Demographic changes lead to global aging of the population and the percentage of persons older than 65 years is projected to increase from 9% in 2019 to 16% in 2050 worldwide and from 18 to 25% in Europe and Northern America. Contact with drifted virus strains may rather boost immune responses to epitopes shared with the previously encountered strain(s) than inducing antibody responses toward the new antigenic determinants thereby resulting in a lower vaccine efficacy [42]. Related to this theory there is data showing that vaccine efficacy was reduced in individuals that had been vaccinated in preceding seasons compared to those vaccinated only in the current season, though this effect was neither seen consistently for all strains nor for different seasons in different study populations [43]. Evaluation of antibody specificity could benefit from further testing for functionality such as neutralization and ADCC (antibody-dependent cytotoxicity) [51]
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