Abstract

Inhalational anthrax caused by Bacillus anthracis, a spore-forming Gram-positive bacterium, is a highly lethal infection. Antibodies targeting the protective antigen (PA) binding component of the toxins have recently been authorized as an adjunct to antibiotics, although no conclusive evidence demonstrates that anthrax antitoxin therapy has any significant benefit. We discuss here the rational basis of anti-PA development regarding the pathogenesis of the disease. We argue that inductive reasoning may induce therapeutic bias. We identified anthrax animal model analysis as another bias. Further studies are needed to assess the benefit of anti-PA antibodies in the treatment of inhalational anthrax, while a clearer consensus should be established around what evidence should be proven in an anthrax model.

Highlights

  • Inhalational anthrax caused by Bacillus anthracis, a spore-forming Grampositive bacterium, is a highly lethal infection

  • The 2001 inhalational anthrax patient cohort had the best historical survival rate, no specific therapeutic was available at that time besides antibiotics [2]

  • Three anthrax antitoxins have been approved by the U.S Food and Drug Administration (FDA): two of them are monoclonal antibodies, and the third is human polyclonal purified IgG from vaccinated humans, intravenous anthrax immune globulin (AIG-IV)

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Summary

Introduction

Inhalational anthrax caused by Bacillus anthracis, a spore-forming Grampositive bacterium, is a highly lethal infection. The 2001 inhalational anthrax patient cohort had the best historical survival rate, no specific therapeutic was available at that time besides antibiotics [2]. As a matter of fact, it should be kept in mind that anthrax is a toxi-infection (i.e., a combination of toxin and bacterial-sepsis components).

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Conclusion

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