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Polio; Mass Vaccination Better Than Routine Vaccination Source:
Vaccine Weekly
Oral polio vaccine (OPV) is better when taken with company. Lots
of company. Comparison of OPV immunogenicity after multiple routine
childhood vaccinations and after mass vaccination campaigns in
Jordan showed that OPV is more effective when administered en masse.
The findings suggest that adding further doses of OPV to the routine
schedule is unlikely to have as great an impact on the immune state
of children as administering the same number of doses during mass
campaigns," wrote U.S. Centers for Disease Control and Prevention
(CDC) researcher Mary R. Reichler and colleagues in a special supplement
of the Journal of Infectious Diseases dedicated to the Global Poliomyelitis
Eradication Initiative ("Increased Immunogenicity of Oral Poliovirus
Vaccine Administered in Mass Vaccination Campaigns Compared with
the Routine Vaccination Program in Jordan," J Infect Dis, 1997;175(Suppl
1):S198-204).
Although they represent a crucial component of the World
Health Organization (WHO) strategy to eliminate polio from the
planet, massive vaccination campaigns are more expensive than routine
OPV administration. For this reason, several nations in which polio
is endemic have yet to implement mass vaccinations, usually given
during National Immunization Days (NIDs). Reichler et al. studied
254 Jordanian children who had received one to five OPV doses.
They obtained serum samples before and after two subnational mass
OPV vaccination campaigns (January 29 to February 19, 1994 and
March 12 to April 3, 1994). A striking finding ... is the relatively
low level of serologic immunity to poliovirus infection, especially
to type 3, among children in the Jordan Valley after as many as
five routine doses of OPV," Reichler et al. reported.
Regardless of the number of previous routine OPV doses they had
received, children had high rates of seroconversion to all three
types of poliovirus after receiving the vaccine during the mass
vaccinations. Implementing mass vaccination campaigns may be an
important means of boosting poliovirus type-specific immunity in
populations with suboptimal immunity following routine vaccination,
Reichler et al. concluded. A previous study conducted in Morocco
yielded similar data (Richardson et al., Bull World Health Org,
1995;73:769-77).
These findings are not merely of technical interest: there
have been several polio outbreaks in populations with relatively
high routine OPV coverage. The effectiveness of mass vaccination
campaigns in raising poliovirus type- specific immunity demonstrated
in the present study suggests a role for conducting these campaigns
not just in polio-endemic countries but also in tropical and subtropical
countries for a period of time following the apparent elimination
of polio, thus reducing the risk of outbreaks if reintroduction
of wild poliovirus occurs," Reichler et al. suggested. It is not
clear why the mass vaccination was so much more effective than
routine vaccination. The subjects in the Reichler et al. study
received the same vaccine during routine vaccination as they did
during the mass vaccinations. Subject age was the same for both
means of OPV administration, making it unlikely that the findings
were due to differences in maternal antibody, breast feeding, or
age-related immune responsiveness.
Maintenance of the cold chain could have been better during
the relatively brief period of the mass vaccination campaign, but
visits to 10 Jordanian vaccine-storage facilities during the investigation
of a 1991 outbreak discovered no problems. Reichler et al. noted
that secondary spread of vaccine virus to non- recipients has been
documented during mass OPV vaccinations. They suggested that the
study children may similarly have received multiple exposures to
the vaccine virus: first as a vaccinee and later as a contact.
The corresponding author for this study is Mary R. Reichler, Mailstop
E-05, NIP, CDC, 1600 Clifton Rd., Atlanta, Georgia 30333. |
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