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June 1, 1959PEDIATRICS71 citations

Clinical Trials in Infants of Orally Administered Attenuated Poliomyelitis Viruses

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SPStanley A. PlotkinHKHilary KoprowskiJSJoseph Stokes

Structured PICO

Does orally administered attenuated poliomyelitis virus safely induce an immune response in infants?

P
Population
46 infants, ranging from less than 1 day to 6 months of age
I
Intervention
Orally administered attenuated poliomyelitis viruses (CHAT type 1, Wistar type 1, Jackson type 2, P-712 type 2, Fox type 3)
O
Outcome
Antigenicity (antibody levels significantly in excess of transplacentally acquired antibodies and fecal excretion of poliomyelitis virus) and safety (occurrence of major or minor illness)surrogate

Orally administered attenuated poliomyelitis viruses are safe and antigenic in infants, though those under 2 months of age are more difficult to immunize.

Abstract

Forty-six infants, ranging from less than 1 day to 6 months of age, were given more than 100 feedings of living, attenuated poliomyelitis viruses without the occurrence of major or minor illness. The strains used were CHAT (type 1), Wistar (type 1), Jackson (type 2), P-712 (type 2) and Fox (type 3). All strains except the Jackson strain were found to be antigenic on oral administration. Response to vaccination was demonstrated in these infants by the presence after vaccination of antibody levels significantly in excess of those attributable to transplacentally acquired antibodies, and by the detection of fecal excretion of poliomyelitis virus. Infants less than 2 months old were more difficult to immunize than older infants. The evidence suggests that biologic immaturity rather than transplacental antibodies caused the difference. When the three types of poliomyelitis virus were fed at 3-week intervals, responses occurred to all types. No interference between types was observed when they were fed in all possible sequences. Three infants given a second feeding of homotypic, attenuated poliomyelitis virus 3 to 5 months after a successful vaccination showed resistance to intestinal reinfection.

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Plotkin et al. (1959) studied this question.

synapsesocial.com/papers/6a907566f009383eee84285bhttps://doi.org/10.1542/peds.23.6.1041
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