PT  - JOURNAL ARTICLE
AU  - Andreas Fløe
AU  - Liselotte Brix
AU  - Christian Wejse
AU  - Ole Hilberg
TI  - Tuberculosis-specific CD8 cells in HLA A*02-positive TB and LTBI patients
AID  - 10.1183/13993003.congress-2016.PA2694
DP  - 2016 Sep 01
TA  - European Respiratory Journal
PG  - PA2694
VI  - 48
IP  - suppl 60
4099  - http://erj.ersjournals.com/content/48/suppl_60/PA2694.short
4100  - http://erj.ersjournals.com/content/48/suppl_60/PA2694.full
SO  - Eur Respir J2016 Sep 01; 48
AB  - Background: Understanding the CD8+ response against Mycobacterium tuberculosis (MTB) may be a key to improved TB diagnostics and vaccine development.Aims and Objectives: To detect a CD8+ T-cell response against Mycobacterium tuberculosis (MTB) in active tuberculosis (TB) and latent TB (LTBI), in HLA A*02 positive patients.Methods: We identified possible epitopes (antigen fragments) from 9 MTB antigens (Ag85B, ESAT-6, EsxH, Hsp65, EsxJ, rv1490, rv1614, rv2626c and 16 kDa antigen) by searching the literature, and by computer prediction of likely binding to MHC-1. We selected 24 epitope candidates, from which we constructed MHC multimers (Dextramers). Peripheral blood mononuclear cells (PBMC) from 7 TB-patients, 16 LTBI patients and 8 MTB-exposed, IGRA-negative, healthy subjects (HE), all HLA A*02 positive, were stained with the Dextramers and with anti-CD8 and anti-CD3, and analyzed on a flow cytometer. The MTB epitopes were analyzed in 5 pools (3-7 epitopes each). Positive responses included >0.001 % of CD8+, CD3+ cells, supported by inspection of flow cytometry plots.Results: MTB-specific CD8+ T-cells were detected more often in TB patients (57%) than in LTBI patients (41%) and in HE (25%), though differences were insignificant. CD8+ responses were seen against a broad spectrum of antigens, including not previously described Rv2626c epitopes. Reactivity against multiple antigens was observed in 3 of 7 LTBI patients and in 2 of 4 TB patients with detectable CD8+ responses.Conclusion: Broad diversity in epitope-specificity was seen among MTB-specific CD8+ T-cells in HLA A*02, consistent with previous reports. A trend of more common detection of MTB-specific CD8+ cells in TB than in LTBI and HE was found.