Recognition of stage-specific mycobacterial antigens differentiates between acute and latent infections with Mycobacterium tuberculosis

Abebech Demissie, Eliane M S Leyten, Markos Abebe, Liya Wassie, Abraham Aseffa, Getahun Abate, Helen Fletcher, Patrick Owiafe, Philip C Hill, Roger Brookes, Graham Rook, Alimuddin Zumla, Sandra M Arend, Michel Klein, Tom H M Ottenhoff, Peter Andersen, T Mark Doherty
Clinical and Vaccine Immunology: CVI 2006, 13 (2): 179-86
Mycobacterium tuberculosis is estimated to infect 80 to 100 million people annually, the majority of whom do not develop clinical tuberculosis (TB) but instead maintain the infection in a latent state. These individuals generally become positive in response to a tuberculin skin test and may develop clinical TB at a later date, particularly if their immune systems are compromised. Latently infected individuals are interesting for two reasons. First, they are an important reservoir of M. tuberculosis, which needs to be considered for TB control. Second, if detected prior to recrudescence of the disease, they represent a human population that is making a protective immune response to M. tuberculosis, which is very important for defining correlates of protective immunity. In this study, we show that while responsiveness to early secretory antigenic target 6 is a good marker for M. tuberculosis infection, a strong response to the 16-kDa Rv2031c antigen (HspX or alpha-crystallin) is largely restricted to latently infected individuals, offering the possibility of differential immunodiagnosis of, or therapeutic vaccination against, TB.

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