[HTML][HTML] A mycolic acid–specific CD1-restricted T cell population contributes to acute and memory immune responses in human tuberculosis infection

DJ Montamat-Sicotte, KA Millington… - The Journal of …, 2011 - Am Soc Clin Investig
DJ Montamat-Sicotte, KA Millington, CR Willcox, S Hingley-Wilson, S Hackforth, J Innes…
The Journal of clinical investigation, 2011Am Soc Clin Investig
Current tuberculosis (TB) vaccine strategies are largely aimed at activating conventional T
cell responses to mycobacterial protein antigens. However, the lipid-rich cell wall of
Mycobacterium tuberculosis (M. tuberculosis) is essential for pathogenicity and provides
targets for unconventional T cell recognition. Group 1 CD1–restricted T cells recognize
mycobacterial lipids, but their function in human TB is unclear and their ability to establish
memory is unknown. Here, we characterized T cells specific for mycolic acid (MA), the …
Current tuberculosis (TB) vaccine strategies are largely aimed at activating conventional T cell responses to mycobacterial protein antigens. However, the lipid-rich cell wall of Mycobacterium tuberculosis (M. tuberculosis) is essential for pathogenicity and provides targets for unconventional T cell recognition. Group 1 CD1–restricted T cells recognize mycobacterial lipids, but their function in human TB is unclear and their ability to establish memory is unknown. Here, we characterized T cells specific for mycolic acid (MA), the predominant mycobacterial cell wall lipid and key virulence factor, in patients with active TB infection. MA-specific T cells were predominant in TB patients at diagnosis, but were absent in uninfected bacillus Calmette-Guérin–vaccinated (BCG-vaccinated) controls. These T cells were CD1b restricted, detectable in blood and disease sites, produced both IFN-γ and IL-2, and exhibited effector and central memory phenotypes. MA-specific responses contracted markedly with declining pathogen burden and, in patients followed longitudinally, exhibited recall expansion upon antigen reencounter in vitro long after successful treatment, indicative of lipid-specific immunological memory. T cell recognition of MA is therefore a significant component of the acute adaptive and memory immune response in TB, suggesting that mycobacterial lipids may be promising targets for improved TB vaccines.
The Journal of Clinical Investigation