Abstract

Pertussis and Bordetella pertussis infections since 1906 are reviewed with an attempt to address facts, myths, and misconceptions. Clinical pertussis is a noninflammatory illness which occurs without fever or productive cough, and its hallmark is the distinctive paroxysmal cough. Because of its significant mortality and morbidity, whole-cell vaccines were developed in the 1930s, and the universal use of these vaccines decreased the incidence of reported pertussis 157-fold by 1970. Because of real and perceived reactions to diphtheria and tetanus toxoids and whole cell pertussis vaccine (DTwP) vaccines, diphtheria and tetanus toxoids and acellular pertussis vaccine (DTaP) vaccines were developed and put into universal use in the USA in 1997. Pertussis has two epidemiologies; one is reported pertussis and the other is B. pertussis illness. The study of these two epidemiologies indicate that reported pertussis is just the tip of the iceberg and B. pertussis cough illnesses occur in all age groups and they are very common; also, asymptomatic infection is more common than symptomatic infection. DTaP vaccines are less reactogenic than DTwP vaccines, but their effectiveness is less. B. pertussis infection is caused by many protein antigens, but illness due to this organism is caused by just two factors, pertussis toxin (PT) and a “cough toxin” which, as yet, has not been discovered. The present “resurgence of pertussis” is mainly due to greater awareness and the use of PCR for diagnosis. There are also many other factors which have contributed to the “resurgence.” New vaccines are clearly needed; with our present vaccines (DTaP and adolescent and adult formulated tetanus and diphtheria toxoids and acellular pertussis vaccine (Tdap)), if used correctly, severe pertussis and deaths in infants can be prevented.

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