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LIVE POLIO IRUS VACCINES

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Live Virus Vaccine Studies in Southern Africa<br />

479<br />

were immune to Type 1, as they are also immune<br />

after vaccination.<br />

It will be noted that there was a slight change<br />

in immunity status of the Type 2. Some became<br />

immune who were not previously immune. There<br />

was a more marked change with Type 3.<br />

Observations of some interest, and of possible<br />

significance in view of the other findings<br />

reported at this Conference, were that after the<br />

Salk vaccine given in 1958, before the epidemic,<br />

the immunity of 50 children was tested, and of<br />

the 50 only one had antibodies against Type 1,<br />

34 had antibodies against Type 2, and 20 against<br />

Type 3. The immunity given by the Salk-type<br />

vaccine against Type 1 was extremely inadequate.<br />

DISCUSSION<br />

It was apparent from the clinical findings that<br />

the wave of infection had swept through most of<br />

the population of both Mauritius and Rodrigues<br />

by the time the vaccination campaign was begun.<br />

This conclusion was confirmed by the laboratory<br />

studies. Of interest was the high incidence of<br />

positive findings in the pre-vaccination specimens<br />

of feces, 33 per cent. The very high proportion<br />

of the tested children who had antibodies against<br />

Type 1 virus before the administration of the live<br />

virus vaccine, was also significant, indicating that<br />

natural infection spreads very much more rapidly<br />

than the virus vaccine infection. In view of these<br />

findings, no conclusion can be drawn in regard to<br />

the value of the vaccine in bringing the epidemic<br />

to an end. However, it is noteworthy that no ill<br />

effects were reported from either Mauritius or<br />

Rodrigues following vaccination, and in the latter<br />

island, most children who were lacking antibody<br />

developed it to Type 3, and a lesser number to<br />

Type 2 after the administration of the vaccine.<br />

Kenya. In the last decade the epidemiology of<br />

poliomyelitis in Kenya has changed from a<br />

disease of high endemicity with sporadic infantile<br />

cases to one of epidemicity. There has been a<br />

steadily rising number of cases reported each<br />

year from 1945, with two major epidemics, one in<br />

1954 and one in 1957. Both were studied in<br />

detail and it was noted that Europeans, particularly<br />

young children and recent immigrants,<br />

were at great risk, with an attack rate of 244<br />

(1954) and 80 (1957) per 100,000. Asians were<br />

next with attack rates of 40 and 14 per 100,000.<br />

Africans had the lowest rates, of 4.6 and 7.2 per<br />

100,000. In 1957 Koprowski's attenuated Type 1<br />

strain was offered for trial, but after consideration<br />

was not used.<br />

In 1959 a slight increase in the number of<br />

poliomyelitis cases was noted in Mombasa. This<br />

was followed by a sudden occurrence of cases in<br />

the Kerugoya and Embu districts of Central<br />

Kenya, which had been relatively severely affected<br />

in 1957. Nearly all cases were in the<br />

under three year olds. Type 1 poliovirus was<br />

proved to be responsible.<br />

It was decided to undertake a mass immunization<br />

campaign with the attenuated Type 1 poliovirus.<br />

After consultation with Dr. Winter, 60,000 children<br />

were given Sabin's Type 1 strain during<br />

the week ending 12 December. During the seven<br />

weeks preceding this, there had been 25 cases.<br />

In the subsequent seven weeks, there were 16<br />

further cases, five of which were in non-vaccinated<br />

children, and 11 of which occurred within<br />

three weeks of vaccination. Studies since then<br />

have shown that Coxsackie A virus infections<br />

were common among the vaccinated group of<br />

children. This may have had an interference<br />

effect on the infection with the vaccine virus.<br />

The campaign has since been extended and about<br />

1,500,000 children in the Central Province and<br />

in Nairobi have been vaccinated.<br />

The study of the effects is still in progress.<br />

ACKNOWLEDGMENTS<br />

In preparing this paper, I had the help of the<br />

reports of Dr. Loconsci of Mauritius and Dr.<br />

Fendall of Kenya, to both of whom I am grateful.

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