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LIVE POLIO IRUS VACCINES

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NOTE: The Spanish translation of this paper was<br />

published in the Boletín OSP 50 (6): 525-<br />

549, Junio de 1961.<br />

<strong>POLIO</strong>MYELITIS VACCINE<br />

IG INFANTS<br />

'E<br />

KONALD A. PREM, JAMES W. FERGUS, JOHN E. MATHERS, AND JOHN L. MCKELVEY<br />

Department of Obstetrics and Gynecology, University of Minnesota School of<br />

Medicine, Minneapolis, Minnesota<br />

DR. PREM (presenting the paper): This report<br />

describes the work currently being done by the<br />

Department of Obstetrics and Gynecology of the<br />

University of Minnesota Medical School on certain<br />

aspects of pregnant women and young infant<br />

immunization with live attenuated oral poliomyelitis<br />

viruses. The reasons for our interest in<br />

these fields have been stated previously.1 ' 14<br />

Preliminary reports of this work were presented<br />

to this Conference one year ago. Since<br />

that Conference new ideas, observations, speculations,<br />

and conclusions have appeared for consideration.<br />

Some of the old have been modified<br />

or discarded. This report brings the results of<br />

our studies up to date. It is divided into two<br />

parts.<br />

The first part concerns a study designed to:<br />

(1) determine the immunologic response of<br />

the pregnant woman to trivalent oral poliomyelitis<br />

vaccine when administered in different dosages<br />

and at different time intervals; and<br />

(2) determine if the fetus she carries in utero<br />

is significantly affected by this vaccination.<br />

The second part concerns studies designed to:<br />

(1) observe and compare the immunologic responses<br />

of young infants to trivalent oral poliomyelitis<br />

vaccine when fed soon after birth and<br />

at age four months;<br />

(2) observe the virus excretion patterns ot<br />

the infant and its family contacts when the infant<br />

is fed this vaccine;<br />

(3) determine the relationship, if possible, of<br />

the passively transferred maternal antibody to<br />

the immunologic response and the virus excretion<br />

pattern of the young infant fed this vaccine;<br />

(4) determine the duration of antibody persistence;<br />

and the proper time for and the immunologic<br />

response to revaccination with trivalent<br />

oral vaccine;<br />

(5) determine the proper time for and the<br />

immunologic response to revaccination with<br />

trivalent oral vaccine if it becomes necessary.<br />

Part 1.<br />

Immunization of Pregnant Women with Live Attenuated Oral<br />

Poliomyeliti is Vaccine<br />

MATERIAL AND METHODS<br />

Participants. Three hundred and ten pregnant<br />

women who attended prenatal clinics under the<br />

supervision of the Department of Obstetrics and<br />

Gynecology of the University of Minnesota participated<br />

in this study. Of these, 152 received<br />

their care at Booth Memorial Hospital (BMH)<br />

and 105 at Catholic Infants' Home (CIH) in<br />

St. Paul, Minnesota. These groups of women<br />

included all patients registered for prenatal care<br />

at these institutions during the period of study.<br />

All were unwed. The remaining 53 were private<br />

207<br />

and clinic patients who received obstetrical care<br />

in the clinics of University of Minnesota Hospitals.<br />

These participants were not consecutively<br />

registered patients. Participation in the program<br />

was voluntary.<br />

Among the BMH and CIH women, the ages,<br />

previous Salk experience, and trimester of pregnancy<br />

in which the vaccine was fed, is similar to<br />

that previously reported.' Because they report<br />

earlier for prenatal care than either indigent<br />

or unwed women, the majority of the first trimester<br />

vaccinations were done in the private<br />

patient group.

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