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LIVE POLIO IRUS VACCINES

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148<br />

Saf ety-Field Evidence of Saf ety<br />

148 Safety-Field Evidence of Safety<br />

quent in children below 6 years of age and in sulted in abortive infection.<br />

the low-titer group. Overall, spread was clearly<br />

more extensive in the more heavily seeded Franklin<br />

community (70 per cent of low and 32 per<br />

cent of high-titer children) than in Morgan City<br />

(33 and 25 per cent, respectively). All told, 28<br />

low-titer children developed alimentary infection<br />

and, of these, all but nine manifested significant<br />

antibody response. In the high-titer group, 17<br />

were observed to excrete virus, but only four<br />

evinced antibody response.<br />

Wide variations were observed in duration of<br />

fecal virus excretion. In the vaccine-fed children,<br />

the mean observed excretion was 22 and 9.7 days<br />

for the low and high-titer groups, and the range<br />

was, respectively, from 1 to 63 days and from 1<br />

to 31 days. Among the placebo-fed children, the<br />

corresponding figures were 17 and 6.8 days for<br />

the means, and from 1 to 37 days and from 1 to<br />

34 days for the ranges. For the vaccine-fed children,<br />

Fig. 3 indicates the relation of the postfeeding<br />

antibody titer to that observed prefeeding<br />

and also, on a rough qualitative basis, to the fact<br />

and duration of fecal excretion of virus. Of those<br />

actually observed to shed virus in the feces, abortive<br />

excretion for only one or two days, indicated<br />

by the circle with a central dot, was observed in<br />

5 of 53 low and 14 of 40 high-titer children. Similar<br />

data for the placebo-fed children are presented<br />

in Fig. 4 which indicates the much greater<br />

frequency with which contact transmission re-<br />

Such was observed<br />

in 7 of 28 infected low-titer children and in 9 of<br />

17 in the high-titer group. Of special importance<br />

is the fact that these abortive infections were<br />

commonly associated with failure to develop a<br />

significant increase in antibody titer. Finally,<br />

in agreement with our previous observations, well<br />

established alimentary infection also failed to<br />

elicit a significant response in children with very<br />

high initial antibody titers.<br />

The pattern of vaccine virus spread. It is difficult<br />

to generalize about the pattern of spread<br />

within the placebo-fed household units. In one<br />

Franklin and four Morgan City families, the entire<br />

household episode of P3 virus infection consisted<br />

of fecal excretion by only one child detected<br />

on only one day (2 in high and 3 in low-titer<br />

children), despite the availability of from 5 to 8<br />

other children in each family, including a total<br />

of 11 with low and 19 with high titers. At the<br />

other extreme, all or all but one child became infected<br />

in six families, three in each community.<br />

When more than one child became infected, the<br />

interval between onsets of viral excretion varied<br />

widely; several children might begin excretion<br />

within a few days with others beginning excretion<br />

two or more weeks later. In one household,<br />

in which all of six children became infected, the<br />

onsets of excretion were on days 28, 28, 29, 46,<br />

60, and 60 of observation.<br />

What might be ternied the week-by-week volume<br />

TABLE 3.<br />

FECAL EXCRETION OF TYPE 3 <strong>POLIO</strong>V<strong>IRUS</strong> AND ANTIBODY RESPONSE IN PLACEBO-FED<br />

CHILDREN, BY AGE, PRIOR HOMOLOGOUS<br />

ANTIBODY TITER AND RESIDENCE<br />

Neighborhood Age Prior titer 1 :

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