BACKGROUND. The identification and treatment of individuals with tuberculosis (TB) is a global public health priority. Accurate diagnosis of pulmonary active TB (ATB) disease remains challenging and relies on extensive medical evaluation and detection of Mycobacterium tuberculosis (Mtb) in the patient’s sputum. Further, the response to treatment is monitored by sputum culture conversion, which takes several weeks for results. Here, we sought to identify blood-based host biomarkers associated with ATB and hypothesized that immune activation markers on Mtb-specific CD4+ T cells would be associated with Mtb load in vivo and could thus provide a gauge of Mtb infection.
METHODS. Using polychromatic flow cytometry, we evaluated the expression of immune activation markers on Mtb-specific CD4+ T cells from individuals with asymptomatic latent Mtb infection (LTBI) and ATB as well as from ATB patients undergoing anti-TB treatment.
RESULTS. Frequencies of Mtb-specific IFN-γ+CD4+ T cells that expressed immune activation markers CD38 and HLA-DR as well as intracellular proliferation marker Ki-67 were substantially higher in subjects with ATB compared with those with LTBI. These markers accurately classified ATB and LTBI status, with cutoff values of 18%, 60%, and 5% for CD38+IFN-γ+, HLA-DR+IFN-γ+, and Ki-67+IFN-γ+, respectively, with 100% specificity and greater than 96% sensitivity. These markers also distinguished individuals with untreated ATB from those who had successfully completed anti-TB treatment and correlated with decreasing mycobacterial loads during treatment.
CONCLUSION. We have identified host blood-based biomarkers on Mtb-specific CD4+ T cells that discriminate between ATB and LTBI and provide a set of tools for monitoring treatment response and cure.
TRIAL REGISTRATION. Registration is not required for observational studies.
FUNDING. This study was funded by Emory University, the NIH, and the Yerkes National Primate Center.
Toidi Adekambi, Chris C. Ibegbu, Stephanie Cagle, Ameeta S. Kalokhe, Yun F. Wang, Yijuan Hu, Cheryl L. Day, Susan M. Ray, Jyothi Rengarajan
Analysis of the frequencies of (A) CD38+IFN-γ+ T cells (B), HLA-DR+IFN-γ+ T cells, and (C) Ki-67+IFN-γ+ T cells in PBMCs from individuals with LTBI (n = 25) and treatment-naive ATB (n = 24) as well as those who received 6 months of anti-TB treatment (ATB treated 6 mo; n = 10). Mann-Whitney U test was used to compare the differences between groups. Bars represent medians. P < 0.05 was considered statistically significant. Analysis of the frequencies of (D) CD38+IFN-γ+ T cells, (E) HLA-DR+IFN-γ+ T cells, and (F) Ki-67+IFN-γ+ T cells of treatment-naive ATB (n = 10) and ATB treated individuals (6 months) (n = 10). Wilcoxon matched-paired rank test was used for comparison between paired samples. P < 0.05 was considered statistically significant.