Anti-TNF immunotherapy reduces CD8( ) T cell-mediated antimicrobial activity against Mycobacterium tuberculosis in humans

作者：Bruns Heiko; Meinken Christoph; Schauenberg Philipp; Haerter Georg; Kern Peter; Modlin Robert L; Antoni Christian; Stenger Steffen^*

来源：Journal of Clinical Investigation, 2009, 119(5): 1167-1177.

DOI：10.1172/JCI38482

The incidence of tuberculosis is increased during treatment of autoimmune diseases with anti-TNF antibodies. This is a significant clinical complication, but also provides a unique model to study immune mechanisms in human tuberculosis. Given the key role for cell-mediated immunity in host defense against Mycobacterium tuberculosis, we hypothesized that anti-TNF treatment impairs T cell-directed antimicrobial activity. Anti-TNF therapy reduced the expression in lymphocytes of perforin and granulysin, 2 components of the T cell-mediated antimicrobial response to intracellular pathogens. Specifically, M. tuberculosis-reactive CD8( )CCR7(-)CD45RA( ) effector memory T cells (T-EMRA cells) expressed the highest levels of granulysin, lysed M. tuberculosis, and infected macrophages and mediated an antimicrobial activity against intracellular M. tuberculosis. Furthermore, T-EMRA cells expressed cell surface TNF and bound the anti-TNF therapeutic infliximab in vitro, making them susceptible to complement-mediated lysis. Immune therapy with anti-TNF was associated with reduced numbers of CD8( ) T-EMRA cells and decreased antimicrobial activity against M. tuberculosis, which could be rescued by the addition of CD8( ) T-EMRA cells. These results suggest that anti-TNF therapy triggers a reduction of CD8( ) T-EMRA cells with antimicrobial activity against M. tuberculosis, providing insight into the mechanism whereby key effector T cell subsets contribute to host defense against tuberculosis.

• 出版日期2009-5
• 单位河北医科大学