PMID- 17012867 OWN - NLM STAT- MEDLINE DCOM- 20070112 LR - 20220310 IS - 1554-8600 (Print) IS - 1554-8600 (Linking) VI - 1 IP - 5 DP - 2005 Sep-Oct TI - Yellow fever 17D vaccine safety and immunogenicity in the elderly. PG - 207-14 AB - The incidence of serious and severe multisystem adverse events (AEs) following yellow fever (YF) 17D vaccine is higher in persons of advanced age. One hypothesis for the occurrence of these AEs in the elderly is immunological senescence and a reduced ability to clear the vaccine virus infection. We determined age-specific rates of serious and nonserious AEs in two large clinical trials of two YF 17D vaccines from different manufacturers. In addition, we analyzed AEs reported in a large general practice data base in the United Kingdom. Neutralizing antibody responses were compared in young and elderly subjects. In the clinical trials, involving a total of 4,532 subjects, there were no neurological and viscerotropic AEs; interestingly, the incidence of common injection site and systemic AEs was significantly lower in elderly than in younger subjects. The neutralizing antibody categorical and quantitative responses were equivalent across younger and elderly subjects. In contrast, the larger retrospective analysis of 43,555 persons receiving YF 17D in the UK general practice database revealed a higher incidence of significant neurologic and multisystem AEs with advancing age. The age-specific reporting rate ratio (RRR) was approximately twice that in the 25-44 year-old reference group for subjects in the 45-64 year age group (RRR 1.82; 95% CI 0.88,3.77) and 3-fold higher for the 65-74 year-old age group (RRR 2.82; 95% CI 0.81, 9.81). These results are consistent with previous reports on YF vaccine safety in the US (Martin M, et al. Emerg Infect Dis 2001;6:945-51; Khromova et al., Vaccine 2005;23:3256-63). In elderly persons, YF 17D vaccine is associated with a higher frequency of significant AEs in the elderly but a lower incidence of common nonserious side-effects. The neutralizing antibody response, which is the mediator of protective immunity to YF, is not diminished in healthy, elderly persons. FAU - Monath, Thomas P AU - Monath TP AD - Acambis, Cambridge, Massachusetts 02139, USA. tom.monath@acambis.com FAU - Cetron, Martin S AU - Cetron MS FAU - McCarthy, Karen AU - McCarthy K FAU - Nichols, Richard AU - Nichols R FAU - Archambault, W Tad AU - Archambault WT FAU - Weld, Leisa AU - Weld L FAU - Bedford, Philip AU - Bedford P LA - eng PT - Journal Article PT - Randomized Controlled Trial DEP - 20050902 PL - United States TA - Hum Vaccin JT - Human vaccines JID - 101265291 RN - 0 (Antibodies, Viral) RN - 0 (Antigens, Viral) RN - 0 (Yellow Fever Vaccine) SB - IM MH - Adaptation, Physiological/immunology MH - Adolescent MH - Adult MH - Adverse Drug Reaction Reporting Systems/statistics & numerical data MH - Age Factors MH - Aged MH - Aging/*immunology MH - Antibodies, Viral/biosynthesis/blood MH - Antigens, Viral/biosynthesis/blood MH - Double-Blind Method MH - Drug Hypersensitivity/etiology/immunology MH - Humans MH - Immunocompetence/*immunology MH - Immunologic Memory/immunology MH - Middle Aged MH - Neutralization Tests/methods/statistics & numerical data MH - Retrospective Studies MH - United Kingdom MH - Yellow Fever Vaccine/administration & dosage/adverse effects/*immunology EDAT- 2006/10/03 09:00 MHDA- 2007/01/16 09:00 CRDT- 2006/10/03 09:00 PHST- 2006/10/03 09:00 [pubmed] PHST- 2007/01/16 09:00 [medline] PHST- 2006/10/03 09:00 [entrez] AID - 2221 [pii] AID - 10.4161/hv.1.5.2221 [doi] PST - ppublish SO - Hum Vaccin. 2005 Sep-Oct;1(5):207-14. doi: 10.4161/hv.1.5.2221. Epub 2005 Sep 2.