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Updated: Sep 12, 2026

Particle Agglutination Method for Poliovirus Identification
Published on: April 20, 2011
A controlled trial with inactivated poliovaccine
Insights
Early vaccination with inactivated polio vaccine (IPV) in infants demonstrated high efficacy. Two doses of IPV achieved a 100% antibody response to poliovirus type 1, offering promising protection.
Area of Science:
- Pediatrics
- Immunology
- Vaccinology
Background:
- Poliovirus type 1 is highly prevalent in rural environments.
- Early infant vaccination is crucial to prevent poliovirus exposure.
- Inactivated polio vaccine (IPV) offers a potential strategy for early immunization.
Purpose of the Study:
- To evaluate the immunogenicity of an early inactivated polio vaccine (IPV) schedule in infants.
- To compare the immune response to IPV with the traditional oral poliovirus vaccine (TOPV).
- To assess the feasibility of early IPV administration in rural settings.
Main Methods:
- A field trial involving 115 infants primed with DPT-polio at 2 and 3.5 months.
- Infants received a booster at 10 months with either DPT-polio (IPV) or DTP-TOPV.
- A control group of 53 infants received TOPV at 2, 4, 6, and 12 months.
Main Results:
- One dose of IPV induced type 1 polio antibodies in 83% of infants.
- Two doses of IPV resulted in a 100% antibody response.
- A significant anamnestic response was observed after a booster dose.
- IPV immunogenicity compared favorably with TOPV response.
Conclusions:
- Early IPV vaccination is effective in inducing robust antibody responses in infants.
- IPV provides a viable alternative to TOPV for early poliovirus protection.
- The findings support the implementation of IPV for early infant immunization programs.
Abstract:
A trail with inactivated polio vaccine (IPV) was carried out, aiming at the earliest possible vaccination of young infants from rural settlements, before their exposure to type 1 wild poliovirus, highly prevalent in the environment. One hundred and fifteen infants were primed at the age of 2 and 3 1/2 months with the quadruple antigen DPT-polio. When 10 months old, 61 were boosted with the same antigen, and 54 with TOPV associated with DTP. Another 53 babies fed with TOPV at 2, 4, 6 and 12 months were used as a control. One dose of IPV produced antibody to polio type 1 in 83% of babies. With two doses of IPV a 100% response was obtained. Six months after the second dose, a small decrease in the percentage of infants wih detectable antibody to type 1 was observed, but at one month after the booster a highly significant anamnestic response was achieved. The results with IPV compared favorably with the immune response of infants given TOPV. Details on the results of the field trial will be presented, and field implementations of IPV will be discussed.
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