Effect on diphtheria immunity of combined tetanus and diphtheria booster vaccination in adults

Citation
S. Marlovits et al., Effect on diphtheria immunity of combined tetanus and diphtheria booster vaccination in adults, EUR J CL M, 19(7), 2000, pp. 506-513
Citations number
36
Categorie Soggetti
Microbiology
Journal title
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES
ISSN journal
09349723 → ACNP
Volume
19
Issue
7
Year of publication
2000
Pages
506 - 513
Database
ISI
SICI code
0934-9723(200007)19:7<506:EODIOC>2.0.ZU;2-A
Abstract
The effect of a single booster injection of an adult formulation of a combi ned diphtheria-tetanus vaccine (Td) on diphtheria-specific immunity was eva luated. The booster injection, containing 2 IU diphtheria toroid per dose, was given as part of the surgical wound management for adults with open sof t tissue injuries. Diphtheria antitoxin concentrations were determined in s erum samples from 534 patients (199 women and 335 men, aged 18-70 years) us ing an enzyme immunoassay and a tissue culture toxin neutralization assay. Seroimmunity against diphtheria toxin was classified at three levels: susce ptibility, basic protection, and full protection against the toxic manifest ations of the disease. Before vaccination, 27.1% of the subjects were susce ptible to diphtheria, 26.5% had basic protection, and 46.4% were fully prot ected. Six weeks (minimum 25 days, maximum 98 days) after a single booster injection, 89.7% of the subjects achieved full protection against diphtheri a, and only 3.9% had antitoxin levels below the protective level. The media n increase from the prevaccination to postvaccination antitoxin concentrati on was found to be 14-fold (4.4-47; quartiles Q25 to Q75). The change in an titoxin levels after revaccination was higher in older age groups (P < 0.00 1), whereas neither sex (P = 0.86) nor the country of previous immunization with a different national immunization schedule (P = 0.61) had a significa nt influence on the revaccination effect. Systemic adverse reactions were r are, and local reactions of clinical significance were reported in only 1.9 % of subjects.