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LIVE POLIO IRUS VACCINES

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27. LARGE-SCALE PRACTICAL TRIALS AND USE OF<br />

<strong>LIVE</strong> <strong>POLIO</strong>V<strong>IRUS</strong> VACCINE IN THE USSR<br />

PROFESSOR V. M. ZHDANOV<br />

with the participation of<br />

PROFESSOR M. P. CHUMAKOV AND PROFESSOR A. A. SMORODINTSEV<br />

USSR Academy of Medical Sciences, Moscow, USSR<br />

DR. ZHDANOV (presenting the paper): Since<br />

the text of my report* was distributed among<br />

the participants of the Conference, there is no<br />

need for me to read it. I shall therefore only<br />

try briefly to convey its content, and then mention<br />

some additional considerations on the problem.<br />

I have been encouraged to do so both by<br />

the interesting remarks made by Dr. Stuart-<br />

Harris and by Dr. Paul's profound and wellpresented<br />

report.<br />

The problem of mass immunization against<br />

poliomyelitis-a comparatively rare but severe<br />

disease-has suggested some specific requirements<br />

for the use of the vaccine, namely:<br />

1. Complete safety of the preparations;<br />

2. The practically full irreactivity of vaccination;<br />

3. Sufficiently full efficacy of the vaccine, in<br />

the sense of prevention of the disease;<br />

4. The possibility of a sharp reduction of<br />

poliovirus circulation;<br />

5. Low cost of preparation, facility of production,<br />

and availability to the population;<br />

6. A suitable and convenient method of administration.<br />

The Salk vaccine meets the first three requirements<br />

mentioned above. Therefore, once its production<br />

was organized, an intensive offensive<br />

against poliomyelitis was started. However, soon<br />

thereafter, some deficiencies in this generally<br />

good preparation became evident.<br />

Although it produces in individuals a specific<br />

defense against the paralytic disease, immunization<br />

with the Salk vaccine does not prevent the<br />

circulation of wild poliovirus strains becatse<br />

the intestinal-tract cells remain susceptible to<br />

them. Moreover, about 20 to 30 per cent of vaccinees<br />

remain unprotected against the paralytic<br />

disease, and the immunity decreases at a significant<br />

rate during subsequent years.<br />

* For complete text, see pp. 578-587.<br />

These deficiencies became dramatically known<br />

soon after the first triumphant years of the<br />

Salk vaccine, when severe epidemics of poliomyelitis<br />

appeared in Israel, Hungary, and some<br />

localities of the USA, despite the large percentage<br />

of vaccinated persons in those countries.<br />

As a result of research work done by Sabin,<br />

Koprowski, Cox, Smorodintsev, Chumakov, and<br />

others, a basis for production and field trials of<br />

live poliomyelitis vaccine derived from attenuated<br />

virus strains was established, and this vaccine<br />

appeared to satisfy the six principal requirements<br />

mentioned above. Its particularly<br />

important property is the capacity to produce<br />

in vaccinees a degree of immunity which not<br />

only ensures the individual defense of the vaccinees<br />

but also renders the intestinal-tract cells<br />

insusceptible to the virus, thus sharply reducing<br />

the circulation of wild polioviruses among the<br />

population.<br />

Other important advantages of this vaccine<br />

are its low cost, its availability to the population,<br />

and its simple method of administration,<br />

i.e., by the oral route, as compared to injections<br />

of the Salk vaccine.<br />

The various stages of research and practical<br />

use of the live poliomyelitis vaccine in the USSR<br />

are well known to you. They constitute a good<br />

example of cooperation between scientists of the<br />

USA and USSR, namely, A. Sabin, M. Chumakov,<br />

A. Smorodintsev, and their associates.<br />

These stages were:<br />

Research work done by A. Smorodintsev<br />

(1957-1958) and M. Chumakov (1958) and<br />

their associates on the safety of Sabin's attenuated<br />

strains, and carefully carried out mass<br />

experiments in children;<br />

First field trials (1958) in sorne tens of<br />

thousands of the population;<br />

Mass immunization of the population early<br />

in 1959 in the Baltic republics of Esthonia,<br />

Latvia, and Lithuania;<br />

576

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