Immunogenicity and Reactogenicity in Q Fever Vaccine Development

Abstract

Coxiella burnetiiis an obligate intracellular bacterium which, in humans, causes the disease Q fever. Although Q fever is most often a mild, self-limiting respiratory disease, it can cause a range of severe syndromes including hepatitis, myocarditis, spontaneous abortion, chronic valvular endocarditis, and Q fever fatigue syndrome. This agent is endemic worldwide, except for New Zealand and Antarctica, transmittedviaaerosols, persists in the environment for long periods, and is maintained through persistent infections in domestic livestock. Because of this, elimination of this bacterium is extremely challenging and vaccination is considered the best strategy for prevention of infection in humans. Many vaccines againstC. burnetiihave been developed, however, only a formalin-inactivated, whole cell vaccine derived from virulentC. burnetiiis currently licensed for use in humans. Unfortunately, widespread use of this whole cell vaccine is impaired due to the severity of reactogenic responses associated with it. This reactogenicity continues to be a major barrier to access to preventative vaccines againstC. burnetiiand the pathogenesis of this remains only partially understood. This review provides an overview of past and current research onC. burnetiivaccines, our knowledge of immunogenicity and reactogenicity inC. burnetiivaccines, and future strategies to improve the safety of vaccines againstC. burnetii.