Figures
Abstract
Background
Measures of bacillary load in patients with tuberculosis (TB) may be useful for predicting and monitoring response to treatment. The relationship between quantitative T-cell responses and mycobacterial load remains unclear. We hypothesised that, in a HIV-prevalent high burden setting, the magnitude of mycobacterial antigen-specific and non-specific T-cell IFN-γ responses would correlate with (a) bacterial load and (b) culture conversion in patients undergoing treatment.
Methods
We compared baseline (n = 147), 2 (n = 35) and 6 month (n = 13) purified-protein-derivative (PPD) and RD1-specific (TSPOT.TB and QFT-GIT) blood RD1-specific (TSPOT.TB; QFT-GIT) responses with associates of sputum bacillary load in patients with culture-confirmed TB in Cape Town, South Africa.
Results
IFN-γ responses were not associated with liquid culture time-to-positivity, smear-grade, Xpert MTB/RIF-generated cycle threshold values or the presence of cavities on the chest radiograph in patients with culture-confirmed TB and irrespective of HIV-status. 2-month IGRA conversion rates (positive-to-negative) were negligible [<11% for TSPOT.TB (3/28) and QFT-GIT (1/29)] and lower compared to culture [60% (21/35); p<0.01].
Citation: Theron G, Peter J, Lenders L, van Zyl-Smit R, Meldau R, Govender U, et al. (2012) Correlation of Mycobacterium Tuberculosis Specific and Non-Specific Quantitative Th1 T-Cell Responses with Bacillary Load in a High Burden Setting. PLoS ONE 7(5): e37436. https://doi.org/10.1371/journal.pone.0037436
Editor: Delia Goletti, National Institute for Infectious Diseases (L. Spallanzani), Italy
Received: February 29, 2012; Accepted: April 23, 2012; Published: May 22, 2012
Copyright: © 2012 Theron et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by an EU-FP7 award (TBSusgent). GT and UG are supported by the EDCTP (TB-NEAT), the South African National Research Foundation (GT) and the Claude Leon Foundation (GT). RVZS and JP are supported by a Discovery Foundation Fellowship, the Fogarty International Clinical Research Scholars/Fellows Support Centre National Institutes of Health grant R24TW007988, SATBAT (JP) and the EDCTP (TB-NEAT). KD is supported by the EDCTP (TB-NEAT, TESA), the SA DST and the SA NRF (SARChI). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The Xpert MTB/RIF cartridges were donated by the Foundation for Innovative and New Diagnostics (FIND). FIND had no role in the study or decision to publish. Keertan Dheda is a PLoS ONE Editor. This does not alter the authors’ adherence to all the PLoS ONE policies on sharing data and materials.
Introduction
Measures of bacillary load at diagnosis or after the intensive phase of anti-TB treatment are crudely associated with relapse and treatment failure in tuberculosis (TB) patients, yet better and more accurate prognostic and treatment monitoring tools are needed [1]. Such tools may identify high risk patients and facilitate the more rapid evaluation of new therapeutic interventions for TB. It has been suggested that immunodiagnostic biomarkers such as interferon-γ (IFN-γ) release assays (IGRAs) may serve as surrogate markers of bacillary load and treatment response [2]. Although the diagnostic accuracy of standardised IGRAs [TSPOT.TB (Oxford Immunotec, UK) and QuantiFERON TB Gold-in-tube (QFT-GIT; Cellestis, Australia)] for latent and active TB have been extensively studied [3]–[9], there are hardly any data about their relationship with bacterial load [10]. The relationship between bacillary burden and the magnitude of IFN-γ in response to RD-1 specific antigens thus remains uncertain [11]. Their role as tools of prognostication and disease monitoring have also been little studied, particularly in high burden settings.
A previous study performed in a small number of HIV-infected TB patients demonstrated a crude relationship between antigen-specific T-cell responses and sputum bacillary load [10]. This finding is supported by the longitudinal increase in quantitative IFN-γ responses in TB contacts prior to diagnosis with active TB [12], [13], as well as declining IFN-γ responses seen in TB patients in low burden settings undergoing treatment [14]–[16]. This latter aspect remains inconsistent, however, as several studies have reported persistently increased positive responses during and after treatment [17]–[25]. Thus, the role of IGRAs as tools of prognostication and disease monitoring continues to remain unclear, especially with regard to their utility in high burden settings. Evaluating the relationship between quantitative T-cell responses using both standardised IGRAs (TSPOT.TB and QFT-GIT) and bacillary load at diagnosis or during treatment has hitherto not been undertaken. These aspects are also largely unexplored with regard to non-specific antigens such as M. tuberculosis-derived purified protein derivative (PPD) and newer measures of bacillary load [such as the World Health Organisation-recommended Xpert MTB/RIF assay [26]].
To address these gaps in our knowledge we comparatively evaluated the magnitude of Th1-based M. tuberculosis-specific and non-specific quantitative T cell responses with measures of sputum bacillary load, some of which are known to be associated with treatment outcomes, prior to and during treatment in TB patients from Cape Town, South Africa.
Materials and Methods
Study Population
Sputa and blood were collected at the time of diagnosis from 513 consecutively recruited ambulatory patients with suspected TB (≥18 years of age) between February 2007 and April 2010 at two primary care clinics in Cape Town, South Africa (Figure 1). Informed written consent was obtained from all participants and the study was approved by the University of Cape Town, Faculty of Health Sciences Research Ethics Committee. Detailed patient and laboratory-specific information were recorded on a standardized case record form and captured using double data entry.
*128 patients had no chest X-ray data. †To be eligible for the study, patients needed to provide at least 2 sputum samples (spot or morning), both of which were used for concentrated fluorescent smear microscopy and liquid culture. When available, a paired second spot sputum sample was collected and archived. This was later used for Xpert MTB/RIF testing (n = 389). ‡The TSOT.TB, QFT.GIT and the PPD ELISPOT tests were not all concurrently available throughout the duration of study and thus not all patients necessarily received a combination of all 3 IGRAs. The number of valid results for TSPOT.TB, QFT-GIT and PPD respectively were 457, 457, and 462, respectively. 9 TSPOT.TB indeterminate results and 52 indeterminate QFT-GIT results occurred and are excluded. Only patients with culture-confirmed TB were included in the main analysis for the comparison of IGRA-response with bacterial load.
Patient Flow and Diagnostic Tests
All patients had at least one concentrated fluorescent smear and one BACTEC MGIT 960 (BD Diagnostics, USA) liquid culture performed on spot or morning sputum (Figure 1). Culture positivity for M. tuberculosis served as a reference standard for definite TB. An HIV test was performed after appropriate counselling. When available, a sputum sample was archived and later used for Xpert MTB/RIF (Cepheid, Sunnyvale, USA) testing [27]. Blood was collected at recruitment and used for the TSPOT.TB, QFT-GIT and PPD enzyme-linked immunosorbent spot (ELISPOT) assays. Where possible, a chest X-ray [CXR; read by 2 readers blinded to clinical information using the validated CXR scoring and recording system (CRRS) [28], [29]] was performed at recruitment. 35 randomly selected TB patients received, in addition to routine follow-up smear microscopy and culture, a TSPOT.TB, QFT-GIT and PPD ELISPOT test at 2 months post-treatment initiation. 13 of these patients received these tests again at 6 months. The accuracy of TSPOT.TB, QFT-GIT, Xpert MTB/RIF and CRRS for the diagnosis of TB in this cohort has previously been published [8], [27], [30], [31].
Interferon-γ Release Assays
All tests were performed according to the manufacturers’ instructions on blood by laboratory technicians blinded to patient information. PBMCs were isolated from the blood and each IGRA performed within 8 hours of venepuncture. TSPOT.TB, QFT-GIT and PPD ELISPOT results were reported and interpreted as described previously [8], [32].
Data Analysis
Culture positivity for M. tuberculosis from at least a single sample served as a reference standard for definite TB. Statistical analyses were performed using Graphpad Prism (version 5.0; GraphPad Software, San Diego, USA, www.graphpad.com) and OpenEpi (version 2.3.1) [33]. Statistical tests on longitudinal changes in IFN-γ levels were done on a per patient basis. TSPOT.TB and QFT-GIT results defined as indeterminate according to the manufacturers’ definitions were excluded. All data was also analysed stratified by HIV status.
Results
Baselines Characteristics of Study Population
Table 1 and Figure 1 show the baseline characteristics of the cohort. Of the 513 participants, 63% (354/513) were male and 26% (133/445) were HIV-infected. 29% (147/513) of participants had definite TB, 67% (98/147) of whom were smear-positive. TB patients were significantly more likely to be younger (p<0.01), of black (p<0.01) or mixed ancestry (p<0.01), have a history of previous TB (p = 0.02), HIV-infected (p<0.05) and TSPOT.TB- (p<0.01) or QFT-GIT-positive (p<0.01).
Correlation of Interferon-γ Responses with Liquid Culture
Median IFN-γ responses differed significantly in culture-positive vs. -negative individuals when measured using TSPOT.TB [111 (IQR: 500-194) vs. 32 (10–104) SFC⋅10−6 PBMCs; p<0.01] and QFT-GIT [2.2 (0.6, 5.2) vs. 0.7 (0.1, 3.1) international units (IU)⋅ml−1; p<0.01], but not in response to PPD [100 (36, 161) vs. 86 (16, 157) SFC⋅10−6 PBMCs; p = 0.28]. On average, the magnitude of IFN-γ response decreased with increasing TTP in individuals with definite TB, however, this did not reach significance [p-value; Spearman’s rank correlation coefficient (rS)] for TSPOT.TB (0.11; −0.14), QFT-GIT (0.07; −0.16) or PPD ELISPOT (0.09; −0.15) (Figure 2).
Culture, smear-microscopy and the Xpert MTB/RIF assay were performed on a paired sputum sample collected at diagnosis. P-values and Spearman’s rank correlation coefficient (rS) are shown where appropriate. Abbreviations: SFC, spot-forming colonies; IFN-γ, interferon–γ; QFT-GIT, QuantiFERON TB Gold-in-tube; ELISPOT, enzyme-linked immunosorbent spot; PBMCs, peripheral blood mononuclear cells; IU, international units; TTP, time-to-positivity; CT, cycle threshold.
Correlation of Interferon-γ Responses with Smear Status and Grade
Median IFN-γ responses did not differ significantly in individuals with smear-positive vs. -negative definite TB [114 (IQR: 63-208) vs. 92 (30, 172) SFC•10−6 PBMCs for TSPOT.TB (p = 0.12); 2.3 (0.7–5.5) vs. 1.6 (0.4–4.8) IU⋅ml−1 for QFT-GIT (p = 0.14); 100 (51–158) vs. 99 (18–151) SFC⋅10−6 PBMCs for PPD (p = 0.39)]. IFN-γ responses did not significantly correlate with increasing smear grade for either assay (p-values for T.SPOT.TB, QFT-GIT and PPD of 0.42, 0.09, and 0.85, respectively) (Figure 2).
Correlation of Interferon-γ Responses with Xpert MTB/RIF Performance
Median IFN-γ responses differed significantly in Xpert MTB/RIF-positive (130/480) vs. Xpert MTB/RIF-negative (350/480) individuals when measured using the TSPOT.TB [109 (IQR: 49–206) vs. 40 (10–115) SFC⋅10−6 PBMCs; p<0.01] and QFT-GIT assays [2.2 (0.6–5.4) vs. 0.7 (0.1–3.1) IU⋅ml−1; p<0.01], but not in response to PPD [100 (45–160) vs. 91 (17–185) SFC⋅10−6 PBMCs; p = 0.21]. On average, IFN-γ responses decreased with increasing Xpert MTB/RIF-generated cycle threshold (CT) values in Xpert MTB/RIF-positive individuals with definite TB, however, this relationship was not significant (p-value; rS) for TSPOT.TB (0.70; −0.04), QFT-GIT (0.91; 0.01) or PPD ELISPOT (0.49; −0.07) (Figure 2).
Correlation of Interferon-γ Responses with Chest Radiography Data
IFN-γ responses differed significantly in individuals who had CXR suspicious of active TB (344/416) vs. those who had a normal CXR (72/416), when measured using TSPOT.TB [58 (IQR: 15–153) vs. 31 (8–101) SFC⋅10−6 PBMCs; p<0.01] and QFT-GIT assays [1.1 (0.2–4.6) vs. 0.3 (0.0–2.3) IU⋅ml−1; p<0.01], but not in response to PPD [96 (28–180) vs. 92 (20–142) SFC⋅10−6 PBMCs; p = 0.37]. In patients with definite TB who had a CXR compatible with active disease, median IFN-γ responses did not differ significantly between those who had cavities (52/124) and those who did not (72/124) when measured using TSPOT.TB [140 (80–208) vs. 112 (33–190) SFC⋅10−6 PBMCs; p = 0.12], QFT-GIT [3.0 (1.0–5.8) vs. 1.6 (0.4–4.6) IU⋅ml−1; p>0.05] or PPD ELISPOT [106 (28–194) vs. 117 (34–159) SFC⋅10−6 PBMCs; p = 0.88].
Impact of HIV-status on Interferon-γ Response
HIV-infected patients with definite TB had a similar IFN-γ response compared to those without HIV-infection when measured using the TSPOT.TB assay [86 (IQR: 31–158) vs. 115 (56–200); p = 0.22], but when measured using QFT-GIT [2.2 (0.4–3.8) vs. 3.7 (0.9–6.1); p = 0.02] or the PPD ELISPOT [62 (20–118) vs. 122 (62–196); p<0.01] the magnitude of response was significantly lower in the HIV-infected group. When the definite TB group was stratified by HIV-status, the correlation between IFN-γ response and bacterial load proxy [for each marker (including cavitation) and for each IGRA] was non-significant, irrespective of HIV-status (data not shown).
Smear- and Culture-status of Patients Undergoing Treatment
The status of the 35 culture-positive patients who were available for IGRA-based follow-up is shown in Table 2. After 2 months of anti-TB therapy, 60% (21/35) of these individuals had culture-converted and were identified as responders to therapy.
Longitudinal Changes in Interferon-γ Release Assay Status
11% (3/28) of individuals who were TSPOT.TB-positive at 0 months were negative at 2 months and 5% (1/29) of individuals with TB who were QFT-GIT-positive at 0 months were negative at 2 months (Table 2). In contrast, 63% (15/24) of smear-positive individuals at 0 months were negative at 2 months (p-values of <0.01 and <0.01 compared to TSPOT.TB and QFT-GIT, respectively). 60% (21/35) of culture-positive individuals at 0 months were negative at 2 months (p-values of <0.01 and <0.01 compared to TSPOT.TB and QFT-GIT, respectively). At 6 months, the proportions of patients who had converted were 8% (1/13) and 30% (3/11) for TSPOT.TB and QFT-GIT respectively.
Longitudinal Changes in Quantitative Interferon-γ Responses
Quantitative IFN-γ responses to RD-1 specific antigens or PPD did not change on a per patient basis between 0 vs. 2 months (p-values of 0.51, 0.88 and 0.26 for TSPOT.TB, QFT-GIT and PPD, respectively) or between 0 vs. 6 months (p-values of 0.83, 0.32, and 0.11 for each test) in individuals with definite TB (Figure 3). There was also no significant longitudinal change in per patient IFN-γ levels across all 3 time points (p-values of 0.69, 0.06 and 0.13 for each test respectively). Furthermore, no longitudinal changes in IFN-γ response were detected in individuals who culture converted at 2 months, irrespective of the type of IGRA used (p-values of 0.27, 0.60, and 0.22 respectively for individuals culture-negative at 2 months; p-values of 0.08, 0.24 and 1.00 for TSPOT.TB, QFT-GIT and PPD respectively for individuals still culture-positive at 2 months) (Table 3). IFN-γ responses also did not differ in culture-negative vs. –positive individuals at this time point [96 (IQR: 24-164) vs. 136 (77 vs. 210) SFC⋅10−6 PBMCs for TSPOT.TB (p = 0.21), 3.2 (0.0–8.9) vs. 1.3 (0.3–4.4) for QFT-GIT (p = 0.78), and 93 (50–125) vs. 96 (51–166) for PPD (p = 0.67)] nor were there any differences in baseline IFN-γ response between 2 month culture converters and non-converters [110 (34–207) vs. 76 (4 vs. 98) SFC⋅10−6 PBMCs for TSPOT.TB (p = 0.10), 2.2 (0.4–4.9) vs. 4.2 (0.5–5.3) for QFT-GIT (p = 0.63), and 122 (27–161) vs. 81 (27–157) for PPD (p = 0.57)].
Capped horizontal bars represent the median IFN-γ response at each time-point.
At 6 months post-treatment initiation IFN-γ levels did not change significantly from diagnosis in individuals who had culture-converted (p-values of 1.00, 0.08 and 0.46 for TSPOT.TB, QFT-GIT and PPD respectively). Due to the small number of culture-positive TB cases after 6 months of treatment (n = 3), we were unable to conclusively compare differences in IFN-γ responses between converters and non-converters at this time point, however, all 3 6 month non-converters were TSPOT.TB- and QFT-GIT-positive.
Discussion
It has been suggested that IFN-γ responses to RD1-specific and non-specific antigens may be useful as prognostic tools, and for monitoring bacterial load and treatment response [2]. However, there is limited information from high-burden settings. Our main aim was to evaluate, at diagnosis, the relationship between IGRAs and measures of bacterial load, which is a prognostic tool associated with treatment failure [1], in patients with TB. We further comparatively evaluated one in-house and two standardised IGRAs longitudinally in relation to 2-month culture conversion, a measure known to be associated with treatment-related outcome [1].
The key findings of our study were: (i) T-cell IFN-γ responses do not correlate with measures of bacterial load in TB patients at diagnosis including culture TTP, smear status and grade, Xpert MTB/RIF CT values, or the presence of cavities on the CXR and this occurred irrespective of HIV status; (ii) IFN-γ levels (whether in response to the RD1-specific antigens or PPD) do not change significantly after 2 or 6 months of anti-TB treatment, irrespective of culture conversion status.
We did not detect any relationship between quantitative IFN-γ responses and bacillary load at diagnosis irrespective of HIV status. By contrast, a smaller study in HIV-infected TB patients in similar setting found a significant but weak correlation between quantitative TSPOT.TB responses and smear grade (a relatively crude measure of bacterial load) but none with culture TTP [10]. Cavitation on the radiograph, previously shown to be associated with either significantly elevated sputum bacillary load or RD1-specific responses in low burden settings [21], [34], was not associated with elevated IFN-γ responses in our study. There is, to the best of our knowledge, no published literature on the correlation of IFN-γ responses with Xpert MTB/RIF CT values. The poor relationship between IFN-γ response and bacillary load may be a function of T cell compartmentalisation and immunosuppressive mediators including IL-10, TGF-β and regulatory T cells [35], [36]. Thus, TB-specific T cells are concentrated in the lung and not in the sampled compartment, and those with the most extensive disease may have the greatest attenuation of RD-1-specific Th1 immunity. Whether other antigens such as HBHA behave differently remains unclear [37]–[40].
Are serial IFN-γ responses useful for monitoring patient-related outcomes in TB patients undergoing treatment? A comparative analysis of the different IGRA formats for treatment monitoring (or correlation of initial bacillary load) has not previously been undertaken. The majority of studies that have examined longitudinal IGRA responses have been performed in a low burden setting [17], [19], [23], [24]. In our study, and similar to findings in The Gambia where an in-house assay was used [25], standardised IFN-γ responses to both RD1-specific antigens and PPD did not appreciably change longitudinally. Although the sensitivity of the T-SPOT and QFT-GIT assays are known to differ [6] we found no differences in the longitudinal readouts. In contrast to a previous study which found that RD-1, but not PPD responses, selectively diminished during the course of treatment [16] we found that responses to both antigens remained persistently elevated. Of note, however, is that this earlier study used an in-house experimental assay which, in contrast to the commercially available TSPOT.TB or QFT-GIT tests, utilised two ESAT-6-derived peptides. This, rather than setting-specific differences with our study, might account for these discordant results, especially given that the findings of the original study have since been confirmed in India, where a similar assay was used [41].
Given the poor correlation we found between IFN-γ responses and culture TTP and cavitation at diagnosis, both of which are known associates of 2-month culture conversion [34], [42]–[45]; it is unsurprising that we also detected no association between IFN-γ responses and this outcome. This high proportion of persistent T-cell responses may be due to several factors including: a history of repeated or on-going TB exposure in a high burden environment, the slow decay kinetics of T cells [24], [46], or greater T cell stimulation with antigen release during the course of treatment. Indeed, history of past-exposure is likely to cause an initially high IFN-γ response which, in patients with latent TB, has shown to remain largely unchanged throughout chemotherapy [46].
There are several limitations to this study. Firstly, all patients did not receive the same combination of tests due to the study design. Although this restricted our sample size, our study nonetheless remains the largest that has specifically looked at the issue of IFN-γ responses and bacillary load. Second, only a subset of patients underwent 6 month follow-up and, as a result, the conclusiveness of our findings limited. Third, given the relatively high prevalence of TB and HIV co-infection in South Africa, these findings may not be generalizable to other settings. Fourth, the Xpert MTB/RIF assay in this cohort was performed on archived sputum samples, which may influence the CT values generated by the assay, however, this effect has previously not shown to be significant [27], [47]. Finally, it is worth noting that culture conversion itself correlates only crudely with unfavourable treatment outcomes [1] but nevertheless remains the best surrogate biomarker of treatment outcome.
In conclusion, our data suggest that T-cell IFN-γ responses to either RD1-specific or non-specific antigens do not correlate with bacillary burden or treatment outcome amongst TB patients in a high burden setting. They are hence unlikely to have utility as prognostic tools at initial evaluation or to monitor either disease severity or treatment response.
Author Contributions
Conceived and designed the experiments: GT JP KD. Performed the experiments: LL RM. Analyzed the data: GT JP RVZS KD UG. Contributed reagents/materials/analysis tools: GT KD. Wrote the paper: GT KD.
References
- 1. Horne DJ, Royce SE, Gooze L, Narita M, Hopewell PC, et al. (2010) Sputum monitoring during tuberculosis treatment for predicting outcome: systematic review and meta-analysis. The Lancet infectious diseases 10: 387–394.
- 2. Lalvani A (2004) Counting antigen-specific T cells: a new approach for monitoring response to tuberculosis treatment? Clinical Infectious Diseases 38: 757.
- 3.
Rangaka MX, Wilkinson KA, Glynn JR, Ling D, Menzies D, et al. (2011) Predictive value of interferon-[gamma] release assays for incident active tuberculosis: a systematic review and meta-analysis. The Lancet Infectious Diseases.
- 4.
WHO (2011) Commercial Serodiagnostic Tests for Diagnosis of Tuberculosis. Publication number WHO/HTM/TB/2011. World Health Organization, Geneva, Switzerland.
- 5. Cattamanchi A, Smith R, Steingart KR, Metcalfe JZ, Date A, et al. (2011) Interferon-gamma release assays for the diagnosis of latent tuberculosis infection in HIV-infected individuals: a systematic review and meta-analysis. JAIDS Journal of Acquired Immune Deficiency Syndromes 56: 230.
- 6. Pai M, Zwerling A, Menzies D (2008) Systematic review: T-cell–based assays for the diagnosis of latent tuberculosis infection: an update. Annals of Internal Medicine 149: 177.
- 7. Pai M, Riley LW, Colford JM (2004) Interferon-[gamma] assays in the immunodiagnosis of tuberculosis: a systematic review. The Lancet infectious diseases 4: 761–776.
- 8.
Ling DI, Pai M, Davids V, Brunet L, Lenders L, et al. (2011) Are interferon- release assays useful for active tuberculosis in a high-burden setting? European Respiratory Journal.
- 9. Diel R, Goletti D, Ferrara G, Bothamley G, Cirillo D, et al. (2011) Interferon-γ release assays for the diagnosis of latent Mycobacterium tuberculosis infection: a systematic review and meta-analysis. European Respiratory Journal 37: 88.
- 10. Oni T, Patel J, Gideon HP, Seldon R, Wood K, et al. (2010) Enhanced diagnosis of HIV-1-associated tuberculosis by relating T-SPOT. TB and CD4 counts. European Respiratory Journal 36: 594–600.
- 11. Daniel TM, Oxtoby M, Pinto E, Moreno E (1981) The immune spectrum in patients with pulmonary tuberculosis. The American review of respiratory disease 123: 556.
- 12. Hill PC, Fox A, Jeffries DJ, Jackson-Sillah D, Lugos MD, et al. (2005) Quantitative T cell assay reflects infectious load of Mycobacterium tuberculosis in an endemic case contact model. Clinical Infectious Diseases 40: 273.
- 13. Doherty TM, Demissie A, Olobo J, Wolday D, Britton S, et al. (2002) Immune responses to the Mycobacterium tuberculosis-specific antigen ESAT-6 signal subclinical infection among contacts of tuberculosis patients. Journal of Clinical Microbiology 40: 704.
- 14. Sauzullo I, Mengoni F, Lichtner M, Massetti AP, Rossi R, et al. (2009) In vivo and in vitro effects of antituberculosis treatment on mycobacterial interferon-γ T cell response. PloS one 4: e5187.
- 15. Dheda K, Pooran A, Pai M, Miller R, Lesley K, et al. (2007) Interpretation of Mycobacterium tuberculosis antigen-specific IFN-[gamma] release assays (T-SPOT. TB) and factors that may modulate test results. Journal of Infection 55: 169–173.
- 16. Carrara S, Vincenti D, Petrosillo N, Amicosante M, Girardi E, et al. (2004) Use of a T cell–based assay for monitoring efficacy of antituberculosis therapy. Clinical Infectious Diseases 38: 754.
- 17. Pai M, Joshi R, Bandyopadhyay M, Narang P, Dogra S, et al. (2007) Sensitivity of a whole-blood interferon-gamma assay among patients with pulmonary tuberculosis and variations in T-cell responses during anti-tuberculosis treatment. Infection 35: 98–103.
- 18. Al-Attiyah R, Mustafa A, Abal A, Madi N, Andersen P (2003) Restoration of mycobacterial antigen-induced proliferation and interferon-γ responses in peripheral blood mononuclear cells of tuberculosis patients upon effective chemotherapy. FEMS Immunology and Medical Microbiology 38: 249–256.
- 19. Wu-Hsieh BA, Chen CK, Chang JH, Lai SY, Wu C, et al. (2001) Long-lived immune response to early secretory antigenic target 6 in individuals who had recovered from tuberculosis. Clinical Infectious Diseases 33: 1336.
- 20. Ferrand R, Bothamley G, Whelan A, Dockrell H (2005) Interferon-gamma responses to ESAT-6 in tuberculosis patients early into and after anti-tuberculosis treatment. The International Journal of Tuberculosis and Lung Disease 9: 1034–1039.
- 21. Ribeiro S, Dooley K, Hackman J, Loredo C, Efron A, et al. (2009) T-SPOT. TB responses during treatment of pulmonary tuberculosis. BMC infectious diseases 9: 23.
- 22. Hill PC, Brookes RH, Fox A, Jackson-Sillah D, Jeffries DJ, et al. (2007) Longitudinal assessment of an ELISPOT test for Mycobacterium tuberculosis infection. PLoS medicine 4: e192.
- 23. Bocchino M, Chairadonna P, Matarese A, Bruzzese D, Salvatores M, et al. (2010) Limited usefulness of QuantiFERON-TB Gold In-Tube® for monitoring anti-tuberculosis therapy. Respiratory Medicine 104: 1551–1556.
- 24. Lee SW, Lee CT, Yim JJ (2010) Serial interferon-gamma release assays during treatment of active tuberculosis in young adults. BMC infectious diseases 10: 300.
- 25. Adetifa IMO, Ota MOC, Walther B, Hammond AS, Lugos MD, et al. (2010) Decay kinetics of an interferon gamma release assay with anti-tuberculosis therapy in newly diagnosed tuberculosis cases. PloS one 5: e12502.
- 26.
WHO (2011) Rapid Implementation of the Xpert MTB/RIF diagnostic test. Publication number WHO/HTM/TB/2011.2. World Health Organization, Geneva, Switzerland.
- 27.
Theron G, Peter J, van Zyl-Smit R, Mishra H, Streicher E, et al. (2011) Evaluation of the Xpert (R) MTB/RIF assay for the diagnosis of pulmonary tuberculosis in a high HIV prevalence setting. American Journal of Respiratory and Critical Care Medicine. pp. 201101–200056OCv201101.
- 28. Dawson R, Masuka P, Edwards D, Bateman E, Bekker L, et al. (2010) Chest radiograph reading and recording system: evaluation for tuberculosis screening in patients with advanced HIV. Int J Tuberc Lung Dis 14: 52–58.
- 29. Den Boon S, Bateman E, Enarson D, Borgdorff M, Verver S, et al. (2005) Development and evaluation of a new chest radiograph reading and recording system for epidemiological surveys of tuberculosis and lung disease. The International Journal of Tuberculosis and Lung Disease 9: 1088–1096.
- 30.
Theron G, Pinto L, Peter J, Mishra HK, van Zyl-Smit R, et al. (2011) The Use of An Automated Quantitative Polymerase Chain Reaction (Xpert MTB/RIF) to Predict the Sputum Smear Status of Tuberculosis Patients. Clinical Infectious Diseases.
- 31.
Theron G, Pooran A, Peter J, van Zyl-Smit R, Mishra H, et al. (2011) Do adjunct TB tests, when combined with Xpert MTB/RIF, improve accuracy and the cost of diagnosis in a resource-poor setting? European Respiratory Journal.
- 32. Dheda K, van Zyl-Smit RN, Meldau R, Meldau S, Symons G, et al. (2009) Quantitative lung T cell responses aid the rapid diagnosis of pulmonary tuberculosis. Thorax 64: 847.
- 33. Sullivan K, Dean A, Minn minn S (2009) OpenEpi: a web-based epidemiologic and statistical calculator for public health. Public Health Reports 124: 471–474.
- 34. Perrin F, Woodward N, Phillips P, McHugh T, Nunn A, et al. (2010) Radiological cavitation, sputum mycobacterial load and treatment response in pulmonary tuberculosis. The International Journal of Tuberculosis and Lung Disease 14: 1596–1602.
- 35. Schwander S, Dheda K (2011) Human lung immunity against Mycobacterium tuberculosis: insights into pathogenesis and protection. American Journal of Respiratory and Critical Care Medicine 183: 696.
- 36. Dheda K, Schwander SK, Zhu B, Van ZYL-SMIT RN, Zhang Y (2010) The immunology of tuberculosis: from bench to bedside. Respirology 15: 433–450.
- 37.
GG G, Locht C (2011) Recombinant HBHA Boosting Effect on BCG-Induced Immunity against Mycobacterium tuberculosis Infection. Clinical and Developmental Immunology 2011.
- 38. Pethe K, Alonso S, Biet F, Delogu G, Brennan MJ, et al. (2001) The heparin-binding haemagglutinin of M. tuberculosis is required for extrapulmonary dissemination. Nature 412: 190–194.
- 39. Delogu G, Chiacchio T, Vanini V, Butera O, Cuzzi G, et al. (2011) Methylated HBHA produced in M. smegmatis discriminates between active and non-active tuberculosis disease among RD1-responders. PloS one 6: e18315.
- 40. Hougardy JM, Hildebrand M, Drowart A, Debrie AS, Locht C, et al. (2007) Regulatory T cells depress immune responses to protective antigens in active tuberculosis. American Journal of Respiratory and Critical Care Medicine 176: 409–416.
- 41. Basirudeen K, Alamelu R, Balambal R, Satheesh T, Marc L, et al. (2011) IP-10 response to RD1 antigens might be a useful biomarker for monitoring tuberculosis therapy. BMC Infectious Diseases 11:
- 42. Hesseling A, Walzl G, Enarson D, Carroll N, Duncan K, et al. (2010) Baseline sputum time to detection predicts month two culture conversion and relapse in non-HIV-infected patients. The International Journal of Tuberculosis and Lung Disease 14: 560–570.
- 43. Visser ME, Stead MC, Walzl G, Warren R, Schomaker M, et al. (2012) Baseline Predictors of Sputum Culture Conversion in Pulmonary Tuberculosis: Importance of Cavities, Smoking, Time to Detection and W-Beijing Genotype. PloS one 7: e29588.
- 44.
Diacon A, Maritz J, Venter A, Van Helden P, Andries K, et al. (2010) Time to detection of the growth of Mycobacterium tuberculosis in MGIT 960 for determining the early bactericidal activity of antituberculosis agents. European Journal of Clinical Microbiology and Infectious Diseases. pp. 1–5.
- 45. Bark CM, Thiel BA, Johnson JL (2012) Pretreatment Time to Detection of Mycobacterium tuberculosis in Liquid Culture Is Associated with Relapse after Therapy. Journal of Clinical Microbiology 50: 538–538.
- 46. Franken W, Arend S, Thijsen S, Bouwman J, Koster B, et al. (2008) Interferon-gamma release assays during follow-up of tuberculin skin test-positive contacts. The International Journal of Tuberculosis and Lung Disease 12: 1286–1294.
- 47. Moure R, Munoz L, Torres M, Santin M, Martín R, et al. (2011) Rapid detection of Mycobacterium tuberculosis complex and rifampin resistance in smear-negative clinical samples by use of an integrated real-time PCR method. Journal of Clinical Microbiology 49: 1137–1139.