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LIVE POLIO IRUS VACCINES

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Capacity of Live Attenuated Polioviruses to Cause Human Infection 181<br />

as the response to Type 1 attenuated poliovirus<br />

was concerned, an interfering role on the part of<br />

non-poliovirus enteroviruses was appreciable. If<br />

any particular enterovirus could be incriminated,<br />

it may have been ECHO 12. With Type 3, however,<br />

there was no evidence of interference. Actually,<br />

the opposite may have occurred (see Fig.<br />

10).<br />

Figure 10 shows the rates at which potential<br />

vaccinees excreted Type 1 poliovirus as compared<br />

with rates at which members of the same group<br />

were excreting non-poliovirus enteroviruses.<br />

Prior to the administration of the triple vaccine<br />

and two months later, the incidence of non-polioviruses<br />

was about 20 per cent, but during the<br />

period of greatest infection with polioviruses this<br />

level was reduced to about 10 per cent.<br />

Thus, the impression we have derived from this<br />

study is that, if any virus can be regarded as an<br />

"interfering agent," it was the Type 3 attenuated<br />

poliovirus used in the vaccine. This "took" so<br />

well and was so efficient in producing lasting infection<br />

that it dominated the scene and appeared<br />

to crowd out the other competing attenuated<br />

polioviruses, and perhaps, the "competing" nonpoliovirus<br />

enteroviruses as well. The ultimate<br />

extent to which this dominant effect of Type 3<br />

poliovirus actually excluded or merely postponed<br />

ultimate infection in the vaccinees by the two<br />

other attenuated polioviruses is not known, for<br />

our observations on antibody determinations cover<br />

only 11 weeks in these index children.<br />

Spread within Households. The findings on<br />

intra-familial spread reflect fairly closely the infectivity<br />

rates which resulted from feeding these<br />

three attenuated strains to the index children in<br />

the form of a trivalent vaccine given on two occasions<br />

a month apart. The strain which "took"<br />

the best spread the best. Infectivity and spreading<br />

capacity seem to be closely related properties.<br />

I cannot say that they are identical. Thus, during<br />

the ll-week-period of observation, Type 3<br />

poliovirus, given at a dose of 105 ' 5, which had the<br />

capacity to infect at a rate of about 91 per cent<br />

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