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The Australian Immunisation Handbook 10th Edition 2013

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Pregnancy and breastfeeding below). Data to evaluate the effectiveness of indirect<br />

protection to infants from the cocoon approach are lacking. 28 However, this<br />

approach is expected to reduce infection risk to infants from family members,<br />

known to be an important source of pertussis infection, 13,14 especially for the<br />

youngest infants. 11,12<br />

4.12.4 Vaccines<br />

Pertussis vaccine is available in Australia only in combination with diphtheria,<br />

tetanus and other antigens.<br />

<strong>The</strong> acronym DTPa, using capital letters, signifies child formulations of<br />

diphtheria, tetanus and acellular pertussis-containing vaccines. <strong>The</strong> acronym<br />

dTpa is used for formulations that contain substantially lesser amounts<br />

of diphtheria toxoid and pertussis antigens than child (DTPa-containing)<br />

formulations; dTpa vaccines are usually used in adolescents and adults.<br />

Acellular pertussis-containing vaccines have been used for both primary and<br />

booster vaccination of children in Australia since 1999. Whole-cell pertussiscontaining<br />

vaccines were used exclusively before 1997. Between 1997 and 1999<br />

acellular vaccines were used for booster doses. <strong>The</strong>re are a number of acellular<br />

pertussis-containing vaccines that contain three or more purified components<br />

of B. pertussis. In the 3-component vaccines, these components are pertussis<br />

toxin (PT), filamentous haemagglutinin (FHA) and pertactin (PRN). In the<br />

5-component vaccines, fimbrial (FIM) antigens are also included.<br />

Pertussis vaccines provide good protection against severe and typical pertussis,<br />

but substantially less against milder coughing illness. 29,30 Vaccine efficacy of<br />

DTPa vaccines with three or more antigens has been reported as 71 to 78%<br />

for preventing milder symptoms of pertussis and 84% for preventing typical<br />

disease. 30 Epidemiological data suggest that receipt of the 1st dose of the<br />

primary DTPa course significantly reduces the incidence of severe pertussis<br />

disease in young infants, as measured by hospitalisation rates. 31-33 Data on the<br />

duration of immunity following DTPa vaccine indicate that waning occurs 5 to<br />

6 years after the last dose of vaccine. 2,34 However, these studies could not control<br />

for levels of circulating pertussis in the population, which may boost the level<br />

of immunity and lead to over-estimation of the duration of protection against<br />

symptomatic disease. 29,30<br />

Reduced antigen content formulation, dTpa, vaccines are immunogenic. 35-38<br />

A randomised trial in adults reported a point estimate of 92% efficacy against<br />

culture/nucleic acid test-positive disease within 2.5 years of vaccination<br />

with a 3-component monovalent pertussis vaccine. 4 Data on the duration of<br />

immunity to pertussis following a single booster dose of dTpa are limited. Longterm<br />

follow-up of adults vaccinated with dTpa has shown a rapid decline in<br />

levels of pertussis antibodies within the first 2 years after vaccination, with a<br />

continued steady decline out to 10 years after vaccination, although antibody<br />

levels remained above baseline. 39 A similar long-term follow-up of adolescents<br />

304 <strong>The</strong> <strong>Australian</strong> <strong>Immunisation</strong> <strong>Handbook</strong> <strong>10th</strong> edition

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