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Immunogenicity and safety of low-dose intradermal rabies vaccination given during an Expanded Programme on Immunization session in Viet Nam: results of a comparative randomized trial

✍ Scribed by Jean Lang; Duong Q. Hoa; Nguyen V. Gioi; Le Than Tho; Nguyen C. Vien; Nicolas Rouyrre; Remi Forrat


Publisher
Elsevier Science
Year
1999
Tongue
English
Weight
839 KB
Volume
93
Category
Article
ISSN
0035-9203

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✦ Synopsis


The World Health Organization recently recommended a rabies vaccine pre-exposure schedule using 3 intradermal (ID) injections of one-fifth the standard intramuscular (IM) dose of current cell culture vaccines as a cost-reducing alternative for developing countries. As a strategy to improve further the acceptability of childhood rabies immunization, we assessed, in a controlled, randomized trial performed in 240 Vietnamese infants, the possibility of associating ID administration of a one-fifth dose of purified Verocell rabies vaccine (PVRV) with routine Expanded Programme on Immunization vaccines given at 2,3 and 4 months of age (diphtheria, tetanus, whole-cell pertussis and inactivated poliomyelitis combined vaccine, DTP-IPV).

Safety and immunogenicity results were compared with a group of infants given 2 IM doses of PVRV (2, 4 months) in association with DTP-IPV (2, 3, 4 months). After ID injection, more infants experienced local reactions, particularly redness, but these reactions were generally mild and transient. The rate of systemic reactions was the same in both groups. Although the rabies antibody titres (rapid fluorescent focus inhibition test) were higher 1 month after the third vaccine dose in the IM group (30.6 IU/mL vs 12.0 IU/mL in the ID group), all infants in both groups had achieved WHO-acceptable protective antibody titres (5 0.5 IU/mL) at this time. There was no evidence for any interference between DTP-IPV and rabies vaccine, supporting the interest of a low-dose ID PVRV pre-exposure regimen in infants living in rabiesendemic developing countries.