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[Poliovirus (Sabin strain) multiplication in human intestinal tract after oral polio vaccination]

N Morimoto1, S Abe, S Hashizume

  • 1Japan Poliomyelitis Research Institute.

Insights

Poliovirus shedding in infants varied by type after primary vaccination, with type 3 showing increased intestinal multiplication. Antibody titers after secondary vaccination were comparable to those in 2-year-old Japanese infants.

Area of Science:

  • Virology and Immunology
  • Vaccine Research

Context:

  • Poliovirus shedding dynamics in infants following vaccination are crucial for understanding transmission and vaccine efficacy.
  • Assessing viral replication and host immune response provides insights into vaccine performance in a young population.

Purpose:

  • To investigate the duration and characteristics of poliovirus shedding in infants after primary and secondary vaccinations.
  • To evaluate the temperature-dependent plaque-forming ability of poliovirus isolates from infant feces.
  • To determine neutralizing antibody titers in infants one year after secondary poliovirus vaccination.

Summary:

  • Polioviruses were isolated from infant feces for extended periods post-primary vaccination (Type 1: 28 days, Type 2: 39 days, Type 3: 36 days).
  • Type 3 poliovirus showed increased intestinal multiplication, while Type 1 and Type 2 showed diminished multiplication after primary vaccination.
  • Plaque formation varied by poliovirus type and temperature; Type 1 isolates did not form plaques at 39.0°C or 39.5°C post-primary vaccination.
  • Type 2 isolates showed increasing plaque formation at 39.5°C over time, while Type 3 isolates formed plaques readily at both tested temperatures.
  • Secondary vaccination primarily yielded Type 1 isolates within 7 days.
  • Neutralizing antibody titers one year post-secondary vaccination were Type 1: 320, Type 2: 110, and Type 3: 60, similar to 2-year-old infants in Japan.

Impact:

  • This study elucidates differential poliovirus shedding patterns and temperature-dependent replication capacities in infants, informing vaccine development and public health strategies.
  • The findings contribute to understanding the immunological response to poliovirus vaccines in infants and provide reference antibody titers for vaccine efficacy assessment.

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