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LIVE POLIO IRUS VACCINES

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384<br />

Effieacy-Laboratory Evidence<br />

384 Efficacy-Laboratory Evidence<br />

At this point, the remaining negative children<br />

in the group that were being followed serologically,<br />

were fed another dose of trivalent vaccine<br />

and they then exhibited a further marked immunogenic<br />

effect. The total conversion rate after<br />

the two doses of vaccine was 96 per cent for<br />

Types 1 and 2, and 72 per cent for Type 3-<br />

despite the interfering effects resulting from the<br />

massive infection with other enteric viruses<br />

(which was still 55 per cent in January 1960),<br />

and the simultaneous administration of all three<br />

types of poliovirus. The lower final conversion<br />

rate for Type 3 may also be related to the fact<br />

that we did not use the pH test for low-avidity<br />

antibody, which occurs more commonly after<br />

infection with the Type 3 virus. It should also be<br />

noted that the second feeding was not a mass<br />

feeding but involved only 44 children under four<br />

years of age, who were distributed among a<br />

large number of families throughout the city.<br />

The results might have been even better if nature<br />

had been given another chance at dissemination<br />

of the polioviruses in the community by feeding<br />

all the children under four years of age another<br />

dose of the vaccine.<br />

Fig. 5 shows that with these two feedings of vaccine<br />

it was possible to achieve an immunogenic<br />

effect within a few months and without any cost in<br />

paralysis, comparable to that achieved by nature<br />

only after four years and at a price of about 56<br />

cases of paralytic poliomyelitis.<br />

The comparable serologic effectiveness of the<br />

same lots and doses of vaccine used in trivalent<br />

or monovalent form under different conditions in<br />

children in northern climates is shown in Table<br />

7. It is evident that when the interval between<br />

the separate, sequential feedings of the three<br />

types was not less than four weeks, the antibody<br />

conversion rates were 100 per cent or close to it,<br />

while the mixture of all three types yielded conversion<br />

rates of only 82, 80, and 71 per cent,<br />

respectively, for the three types in a mixed<br />

group of single-negative, double-negative, and<br />

triple-negative children, living under conditions<br />

TABLE 7. EFFECTIVENESS OF ALIQUOTS OF SAME LOTS AND SAME DOSES OF VACCINE USED IN TOLUCA,<br />

MEXICO WHEN GIVEN TO CHILDREN OF COMPARABLE AGE DURING WINTER AND SPRING MONTHS IN<br />

NORTHERN CLIMATES<br />

Trivalent Versus Monovalent (1-3-2)<br />

INVESTIGATOR<br />

PER CENT DEVELOPED<br />

PLACE METHOD No. OF CHILDREN ANTIBODY FOR<br />

AGE OF CHILDREN OF WITHOUT ANTIBODY INDICATED TYPE<br />

TIME OF YEAR ADMINISTRATION FOR INDICATED TYPE 1 2 3<br />

Smorodintsev Trivalent 29 neg. for 1 82<br />

Leningrad, USSR<br />

Children's Homes Tested 4 months 54 neg. for 2 80<br />

Up to 7 years<br />

later<br />

May, 1958 All together in 38 neg. for 3 71<br />

camp during<br />

summer<br />

Smorodintsev<br />

Leningrad, USSR<br />

Children's Homes<br />

Up to 3 years<br />

Feb., March, Apr. 1958<br />

Monovalent<br />

4 week interval<br />

Tested one month<br />

after each type<br />

147 neg. for 1<br />

68 neg. for 2<br />

67 neg. for 3<br />

97<br />

100<br />

96<br />

Verlinde Monovalent 20 neg. for 1 100<br />

Leiden, Holland<br />

Individual Families 3 week interval 18 neg. for 2 90<br />

Up to 14 years<br />

May or Dec. 1957 28 neg. for 3 100

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