1887

Abstract

The emergence of drug-resistant strains and the widespread occurrence of AIDS demand newer and more efficient control of tuberculosis. The protective efficacy of the current bacille Calmette–Guérin (BCG) vaccine is highly variable. Therefore, development of an effective new vaccine has gained momentum in recent years. Recently, several mutants were tested as potential vaccine candidates in the mouse model of tuberculosis. However, only some of these mutants were able to generate protection equivalent to that of BCG in mice. This study reports the vaccine potential of an attenuated 5′-adenosine phosphosulfate reductase mutant (Δ) of . Immunization of mice with either BCG or Δ followed by infection with the virulent Erdman strain demonstrated that Δ can generate protection equivalent to that of the BCG vaccine.

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2007-04-01
2024-04-20
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