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LIVE POLIO IRUS VACCINES

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2. VIROLOGIC AND SEROLOGIC INVESTIGATIONS OF<br />

CHILDREN IMMUNIZED WITH TRIVALENT <strong>LIVE</strong><br />

VACCINE FROM A.B. SABIN'S STRAINS<br />

M. K. VOROSHILOVA, V. I. ZHEVANDROVA, E. A. TOLSKAYA,<br />

G. A. KOROLEVA, AND G. P. TARANOVA<br />

DR. VOROSHILOVA<br />

(presenting the paper):<br />

Simultaneous use of three immunologic types<br />

of attenuated strains for mass oral poliomyelitis<br />

immunization allows the vaccination of large<br />

population groups against all three types of<br />

poliovirus within a short time, with most complete<br />

coverage.<br />

It is believed, however, that serologic response<br />

to trivalent vaccine may be lower than that obtained<br />

with individual monovaccines because of<br />

interference between vaccine strains. Therefore,<br />

further accumulation and examination of serological<br />

data is necessary.<br />

The serologic survey of children vaccinated<br />

during the winter of 1959 with trivalent live vaccine<br />

from Sabin strains, in the Estonian and<br />

Lithuanian SSR (Dobrova, Yankevich, Chumakov<br />

et al., 1959), demonstrated sufficiently regular<br />

antibody response to the three poliovirus types in<br />

from 66.7 to 88.6-89.0 per cent of children without<br />

pre-vaccination antibody to one or more types<br />

of poliomyelitis virus. The results varied, however,<br />

in different observations. It would be of<br />

interest to determine factors which affect serologic<br />

response.<br />

In May, June, and July 1959, trivalent live<br />

vaccine was used for mass immunization of children<br />

in the Karaganda and Moscow regions. This<br />

paper presents the results of virologic and serologic<br />

surveys of children vaccinated in the summer<br />

in towns and settlements of the Moscow region<br />

and in three towns of the Karaganda region,<br />

and in Moscow in the winter of 1960.<br />

Surveys consisted of studying the dynamics of<br />

vaccine virus excretion by vaccinees and their contacts<br />

and in determining serological changes. A<br />

number of children was tested for the resistance<br />

of the intestinal tract on additional administration<br />

of vaccine strains one to six months after<br />

primary immunization.<br />

At the same time, we studied multiplication of<br />

vaccine strains in poliomyelitis convalescents who<br />

were treated in a Moscow regional hospital for<br />

poliomyelitis sequelae, in a sanatorium for poliomyelitis<br />

convalescents in Karaganda, and in the<br />

clinic of the Institute for Poliomyelitis Research.<br />

Materials and methods. Children aged two<br />

months to 15 years were immunized orally with<br />

a mixture of monovaccines, prepared at the Institute<br />

for Poliomyelitis Research, from Sabin<br />

attenuated strains of the three poliovirus types.<br />

The vaccine was diluted immediately before use<br />

so that two drops contained 100,000 TCD 50 of<br />

each strain. Practically, of the diluent one ml.<br />

to seven ml. of monovaccine of each type were<br />

added. The vaccine was given to children in a<br />

spoonful of water or tea, followed by the ingestion<br />

of water. The vaccine was fed once or twice<br />

with 1-11/2 month interval.<br />

Before vaccination, stool specimens (one or<br />

two) from all children were tested for enteric<br />

viruses, and blood specimens were tested for<br />

poliomyelitis antibody.<br />

In order to study the dynamics of vaccine virus<br />

excretion after oral immunization with trivalent<br />

live-poliovirus vaccine, important investigations<br />

were carried out in four children's homes: in two<br />

(L. and R.) in the summer of 1959, and in two<br />

(No. 5 and No. 10) in the winter of 1960.<br />

Table 1 presents data on the age and number<br />

of vaccinees, dates of vaccination, and vaccine lot<br />

numbers.<br />

During the first month after vaccination four<br />

to five stool specimens were tested, and during<br />

the second month two to three stool specimens<br />

from each child were tested (Table 2). Stool<br />

suspensions (10 per cent by weight) were prepared<br />

and after centrifugation were treated with<br />

antibiotics.<br />

240

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