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  Vol. 281 No. 22, June 9, 1999 TABLE OF CONTENTS
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Preemies and Pertussis Vaccine

Rebecca Voelker

JAMA. 1999;281:2078.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Despite concerns about safety and immunogenicity, German researchers have reported that efficacy is high and adverse reactions low with a two-component acellular pertussis vaccine used in preterm infants.

The researchers compared antibody responses and adverse reactions in 46 preterm infants and a control group of 50 term infants at Children's University Hospital in Frankfurt. The infants initially were vaccinated in the second month of life. A second dose was given within the next 8 weeks, and a third within the following 8 weeks. The two-component vaccine contained pertussis toxin (PT) and filamentous hemagglutinin (FHA).

Even though antibody titers were about 50% higher in the term infants, the researchers reported that the preterm infants experienced a 14-fold increase in antibodies to PT and FHA after the third dose of vaccine. They said that an efficient immune response can be assumed after a greater than four-fold increase in antibodies. Adverse . . . [Full Text of this Article]







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