- Research article
- Open Access
T-SPOT.TBresponses during treatment of pulmonary tuberculosis
BMC Infectious Diseases volume 9, Article number: 23 (2009)
Immune responses to Mycobacterium tuberculosis antigens could serve as surrogate markers of treatment response.
Using the T-SPOT.TB assay and frozen peripheral blood mononuclear cells, we enumerated ESAT-6- and CFP-10-specific IFN-γ-producing T cells over time in pulmonary TB patients receiving directly observed treatment. T cell responses (measured as "spot forming cells" or "SFCs") were assessed prior to treatment and at 16 and 24 weeks of treatment.
58 patients were evaluated, of whom 57 were HIV seronegative. Mean (SD) ESAT-6, CFP-10, and summed RD1 specific SFCs declined from 42.7 (72.7), 41.2 (66.4), and 83.8 (105.7) at baseline to 23.3 (39.4, p = 0.01), 23.2 (29.4, p = 0.18), and 46.5 (59.5, p = 0.02) at completion of 24 weeks of treatment, respectively. Only 10% of individuals with a baseline reactive test reverted to negative at treatment week 24. For the group that was culture positive at completion of 8 weeks of treatment compared to the culture negative group, the incidence rate ratio (IRR) of ESAT-6, CFP-10, and summed RD1 specific SFC counts were, respectively, 2.23 (p = 0.048), 1.51 (p = 0.20), and 1.83 (p = 0.047). Patients with cavitary disease had mean ESAT-6 specific SFC counts that were higher than those without cavitary disease (IRR 2.08, p = 0.034).
IFN-γ-producing RD1-specific T cells, as measured in the T-SPOT.TB assay, may be directly related to bacterial load in patients undergoing treatment for pulmonary TB. However, high inter-subject variability in quantitative results coupled with failure of reversion to negative of qualitative results in most subjects at treatment completion may limit the utility of this assay as a surrogate marker for treatment efficacy.
Progress in understanding the genome of Mycobacterium tuberculosis and human host responses has led to the rational development of diagnostic tests for tuberculosis (TB). Early secretory antigenic target-6 (ESAT-6) and culture filtrate protein 10 (CFP-10) are secreted antigens encoded by region of difference-1 (RD1) of M. tuberculosis. These antigens elicit IFN-γ secretion by peptide-specific T cells.[1, 2] Diagnostic tests have been developed to measure response T cell responses to these antigens. T-SPOT.TB (Oxford Immunotec Ltd, Abingdon, Oxon, UK) is an ex vivo enzyme-linked immunospot (ELISPOT) assay that uses overlapping peptide panels to stimulate IFN-γ secretion by ESAT-6 and CFP-10-specific T cells.
Among individuals with active TB, the T-SPOT.TB test and similar ELISPOT tests have reported sensitivities of 83–97%. [1, 4–10] In addition, compared with the tuberculin skin test, the T-SPOT.TB and similar ELISPOT tests have been shown to correlate more closely with extent of M. tuberculosis exposure in contacts of TB patients. [11–13]
However, the role of T-SPOT.TB in monitoring response to TB treatment is less well-established. A blood test that correlated well with severity of disease or treatment response might be useful as a surrogate marker in clinical trials of new TB treatments, to predict TB treatment failure and/or relapse, and to monitor treatment response in conditions such as extrapulmonary TB or childhood TB in which sputum is uninformative or not readily obtainable. In order to assess the potential utility of T-SPOT.TB for monitoring treatment efficacy, we evaluated the relationship between frequency of antigen-specific IFNγ-secreting T cells and treatment response in patients with pulmonary TB receiving directly observed therapy (DOT) in the context of a phase II TB treatment study. We also evaluated the relationship between SFC counts and markers of TB disease severity at baseline.
Setting and design
We performed a longitudinal cohort study of a diagnostic test, nested in a Phase II, single-center, double-blind TB treatment trial in Rio de Janeiro, Brazil . The aims of the treatment trial were to evaluate and compare the antimicrobial activity of two daily TB treatment regimens administered during the first 8 weeks of treatment in patients with pulmonary TB. The control treatment arm was comprised of isoniazid, rifampin, pyrazinamide, and ethambutol (HRZE), and the experimental arm was comprised of isoniazid, rifampin, pyrazinamide, and moxifloxacin (HRZM). All drugs were given by directly observed therapy (DOT) five days per week. For the treatment trial, the primary endpoint was sputum culture status (positive or negative for M. tuberculosis) at completion of 8 weeks of treatment. All participants in the treatment trial were eligible for participation in the T-SPOT.TB diagnostic study. Blood for the T-SPOT.TB assay was collected just prior to initiation of TB therapy (week 0, baseline) and at 16 and 24 weeks of treatment. The treatment and diagnostic studies were approved by the ethics review boards of the Johns Hopkins University School of Medicine and the Hospital Universitario Clementino Fraga Filho in Rio de Janeiro, Brazil.
Subjects were adults with smear positive, culture-confirmed pulmonary TB that was susceptible to all of the treatment drugs. Additional inclusion criteria were documented HIV status (positive or negative), no history of prior TB treatment, and Karnofsky performance status score 70 or greater. Subjects were excluded if they had only extrapulmonary TB, were being treated with HIV-1 protease inhibitors, were pregnant or breastfeeding, had AST > 3 times normal, total bilirubin > 2.5 times normal, creatinine > 2 times normal, hemoglobin < 7.0 g/dL, potassium < 3.5 mEq/L, or platelet count < 50,000/mm3. Upon initiation of the T-SPOT.TB substudy, all subjects enrolled into the parent treatment trial were co-enrolled in the TSPOT-TB study until completion of the treatment trial.
Enumeration of RD1-specific T cells
Whole venous blood was drawn into 8 ml CPT tubes (Becton Dickinson, Franklin Lakes, NJ) at weeks 0, 16, and 24 of TB treatment. Peripheral blood mononuclear cells (PBMC) were isolated by centrifugation, washed twice, resuspended in Recovery™ cell culture freezing media (Gibco, Invitrogen Corp., Carlsbad, CA), and frozen in liquid nitrogen until T-SPOT.TB testing. Just prior to testing, samples were thawed; twice, AIM V medium (Gibco, Invitrogen) was added and the samples were centrifuged. The PBMC pellet was resuspended in AIM V medium, and T-SPOT.TB assays using 8-well strips were performed according to the manufacturer's instructions. For an individual study subject, all frozen samples were thawed and tested at one time, such that the final specimen (the 24 week specimen) was frozen for a minimum of 30 days. The assay included nil control, ESAT-6-derived peptide (Panel A), CFP-10-derived peptide (Panel B), and positive control wells. SFCs were enumerated on-site using a hand-held magnifying glass. As per the manufacturer's instructions, for ESAT-6 and for CFP-10, a test was scored as qualitatively reactive if either: (1) for nil control of 0–5 SFCs, the antigen well SFC count minus the nil control SFC count was ≥ 6; or (2) for nil control of > 5 SFCs, the antigen SFC count was ≥ 2 times the nil control SFC count. Overall, a T-SPOT.TB test was considered reactive if either ESAT-6 or CFP-10 was reactive, or considered nonreactive if both ESAT-6 and CFP-10 were nonreactive. The number of ESAT-6-specific SFCs was calculated by subtracting the nil control SFC count from the Panel A SFC count; the number of CFP-10-specific SFCs was calculated by subtracting the nil control SFC count from the Panel B SFC count. The resulting ESAT-6 and CFP-10 values were summated to give the total RD1 SFC count. Those wells with too-numerous-to-count SFCs were assigned a value of 400 which approximates the upper limit of quantification. The technologist performing the TSPOT-TB assays was not aware of patients' clinical or microbiological status.
For each subject, sputa were collected weekly through week 8, then monthly. Specimens were digested and decontaminated using the Nalc-NaOH method, and resuspended in 2.0 mL of phosphate buffer. Two 0.2 ml portions of resuspended sediment were plated onto Löwenstein-Jensen medium and incubated at 37°C for up to 8 weeks. For positive cultures, species identification was performed using conventional biochemical methods.
To determine whether or not overall SFC counts changed over time with TB treatment, we compiled T-SPOT.TB results from baseline, 16 weeks of treatment, and 24 weeks of treatment. To compare SFC counts between those with positive and negative sputum cultures at treatment week 8 and to compare SFC counts between those with and without cavitary disease, we performed a longitudinal data analysis. To model the dependency resulting from repeated measures, and given that SFC counts represented overdispersed count data, the data were analyzed using a marginal model with negative binomial approach with generalized estimating equation methods (GEE). We chose an independent correlation structure with robust standard errors for the GEE models, as quantitative statistical comparisons of fit showed that this correlation structure provided the best fit. Negative binomial regression models were used to analyze differences in SFC counts between groups at treatment week 24. Signrank tests were used to compare SFC counts before and after treatment. Two-sided alpha levels of 0.05 were used to determine statistical significance in all analyses. Statistical analyses were performed using STATA statistical software (StataCorp, College Station, Texas).
Demographic and clinical characteristics of study participants
During the T-SPOT.TB study period, 73 individuals were enrolled in the TB treatment trial. Among these 73 subjects, 11 had no baseline T-SPOT.TB result and 4 had only a baseline T-SPOT.TB result; these 15 subjects were excluded from the analysis. The remaining 58 patients had at least two blood samples collected, including a baseline sample, and were included in the analysis.
Table 1 shows the baseline characteristics of the study population. Only one subject was HIV-infected (CD4 426 cells/mm3); ESAT-6 and CFP-10 spot forming counts for this patient were 14 and 99 at week 0, 4 and 77 at week 16, and 8 and 63 at week 24, resulting in a qualitatively reactive test at all time-points. Sensitivity of the T-SPOT.TB test, as measured by baseline reactivity of frozen samples, was 72.4% (95% CI 59–83%).
Association between SFC counts and severity of TB disease at baseline
To determine whether or not SFC counts were higher among those with more severe TB, we evaluated the association between SFC counts and two markers of disease severity at baseline – cavitary lung disease and low body mass index (BMI). For ESAT-6, those with cavitary disease had, on average, 2.08 times higher SFC counts than those without cavitary disease (95% confidence interval for the incidence rate ratio [IRR] 1.06 to 4.10, p = 0.034), but CFP-10 SFC counts did not differ between the two groups (p = 0.64). There was no association between baseline BMI and either ESAT-6 or CFP-10 SFC counts (p = 0.48 and 0.48, respectively).
SFC counts over time during TB treatment
As shown in Figure 1, mean SFC counts declined over 24 weeks for ESAT-6, CFP-10, and summed RD1. Mean (SD) ESAT-6 SFC declined by 22.2 (62.9) over 24 weeks (p = 0.01 by signrank test), but CFP-10 SFC declined, on average, by only 8.9 (41.2) over 24 weeks (p = 0.18).
Table 2 shows the percent of study subjects having a reactive qualitative result for ESAT-6, CFP-10, and RD1 at the three time-points. Using qualitative results, there were no significant trends over time, and no differences between percentages of subjects positive by ESAT-6 versus by CFP-10 at any of the time-points. Of 42 individuals who had a reactive baseline test, 40 were retested at week 24; of these 40, 4 (10%) had a non-reactive T-SPOT.TB test at week 24.
SFC counts among patients who were sputum culture positive versus negative at completion of 8 weeks of TB treatment
Next, we compared SFC counts between individuals who remained sputum culture positive at completion of 8 weeks of treatment and individuals who were sputum culture negative at completion of 8 weeks of treatment. Forty-eight (82.8%) of 58 individuals were culture negative at 8 weeks, and 10 (17.2%) of 58 remained culture positive. As shown in Figure 2, individual participant RD1 SFC response profiles demonstrated large intersubject and intrasubject variability. Mean SFC counts are shown in Figure 3. Compared with subjects having negative culture results, culture positive subjects had higher mean SFC counts at all time points and for both ESAT-6 and CFP-10. Mean ESAT-6 SFC count was on average 2.23 times higher for the group that was culture positive at completion of 8 weeks of treatment than for the group that was culture negative (IRR 95% CI 1.01 to 4.93, p = 0.048). The mean CFP-10 SFC count was on average 1.51 times higher for the culture positive group compared to the culture negative group, but this difference did not reach statistical significance (IRR 95% CI 0.80 to 2.85, p = 0.20). The mean RD1 SFC count was on average 1.83 times higher for the culture positive group compared to the culture negative group (IRR 95% CI 1.01 to 3.33, p = 0.047); the rate of decline did not differ between the two groups (p = 0.54). At completion of 24 weeks of therapy, the culture positive group had ESAT-6 and CFP-10 counts that were 2.27 (IRR 95% CI 0.82 to 6.31) and 2.36 (IRR 95% CI 0.92 to 6.04) times higher than the culture negative group, but neither of these differences reached statistical significance.
Using qualitative results (Table 2), compared with culture negative subjects, slightly higher percentages of culture positive subjects had ESAT-6 or CFP-10 results classified as reactive at weeks 0, 16, and 24, but differences were not statistically significant.
There has been considerable debate about the immune response to M. tuberculosis and correlates of bacterial containment in the human host. It has been postulated that active TB infection is immunosuppressive and that treatment of TB would lead to improved immune function and an increase in antigen-specific IFN-γ production by T cells. Our data support an alternate hypothesis that treatment leads to decreased antigen burden and, in turn, diminished frequency of circulating antigen-specific T cells. In this regard, our findings are consistent with those of several prior studies using precommercial RD1-based interferon gamma release ELISPOT assays. [1, 4, 18, 19] Specifically, Pathan et al. used an RD1-specific ELISPOT assay to evaluate kinetics of T cell responses in 12 active TB patients undergoing treatment. They observed an average 38% decrease in SFCs over a mean follow-up period of 18.6 weeks. Aiken et al. showed that 55% of treated pulmonary TB patients had negative ESAT-6/CFP-10 ELISPOT tests one year after treatment initiation. Some studies using precommercial assays, however, have demonstrated persistently high or positive RD1-specific ELISPOT test results even after treatment; multiple technical or environmental factors may affect assay performance characteristics.[20, 21] One study using the commercially-available T-SPOT.TB comparing patients early in their TB treatment to patients late in their TB treatment showed significantly higher positive T-SPOT.TB proportions in the early-treatment group (83% vs. 17%).
Our findings add strength to the hypothesis that SFC counts directly reflect bacillary burden and, importantly, used the commercially available T-SPOT.TB assay. Mean ESAT-6 and summed RD1 SFC counts were statistically significantly higher in the group with positive sputum cultures at week 8 compared with the group having negative sputum cultures at week 8. These differences were apparent at baseline (time 0), and overall rates of decline in RD1 SFC counts did not differ between groups. These data suggest that higher SFC counts in those with positive sputum culture results at week 8 resulted from higher pre-treatment bacillary burdens of M. tuberculosis rather than from a slower decline in SFC counts during treatment. In addition, there was an association between ESAT-6 SFC count and presence of lung cavitation – a manifestation of TB disease usually characterized by high bacillary burden.
Additional studies of M. tuberculosis exposure, progression from latent to active TB, and treatment of latent TB also support the hypothesis that quantitative ELISPOT readout reflects mycobacterial burden. Specifically, Hill et al. found that, in individuals with positive ELISPOT responses to ESAT-6 and CFP-10, quantitative ELISPOT responses to PPD reflected the infectious load of M. tuberculosis as a result of recent exposure. Richeldi et al. reported a newborn child exposed to TB – ELISPOT results turned positive at age 6 months, and were approximately 10-fold higher at age 24 months when the child developed overt TB disease. In another case report, a rising ELISPOT count heralded progression to active TB in a patient with known latent TB. With respect to treatment of latent TB, Ewer et al. used an RD1-specific ELISPOT assay to evaluate kinetics of T cell responses in individuals presumably recently infected with M. tuberculosis in the context of a point-source school-associated TB outbreak. Tuberculin skin test-positive students treated with a three-month course of isoniazid and rifampin had an average 68% decline per year in frequencies of RD1 specific SFCs, but no change in frequencies of these cells was observed in untreated individuals. Chee et al. recently demonstrated that among individuals undergoing treatment for latent TB infection, treatment had a significant effect on response to CFP-10 but not on response to ESAT-6 as measured by the T-SPOT.TB assay.
While our results and those of others indicate that immunologic responsiveness as measured by RD1-based interferon gamma release ELISPOT assays is dynamic during the course of M. tuberculosis disease and its treatment, our results indicate that the test's utility in evaluating or predicting treatment response in individual patients appears poor. Our results do not support this test's use as an early surrogate marker for treatment response in clinical trials. While overall SFC counts declined over the course of treatment, individual patient response profiles (mapping SFC counts over time) were highly variable in our study. Furthermore, the proportion of patients with positive qualitative test results was not different between groups and did not decline over time during treatment. Further studies evaluating this test in subgroups, such as HIV-seropositive patients or patients with solely extrapulmonary disease, may help determine the utility of this test in these special populations. The utility of an RD1-based interferon gamma release ELISPOT assay in combination with other immunologic tests to evaluate treatment response also remains to be studied.
Our study has important limitations. First, we used frozen cells for cost reasons. Freeze-thaw processes may have diminished T cell reactivity, and this could account for the lower-than-expected baseline sensitivity of the T-SPOT.TB assay. We cannot exclude the possibility that frozen samples that were stored longest before testing (i.e., baseline samples) could have been most affected by storage and might have given spuriously low results; this could have diminished our ability to detect a decrease in assay responses with treatment. The effects of prolonged freezing could be studied by dividing samples into two aliquots, with one aliquot tested immediately and the other frozen for later testing. Second, we compared T-SPOT.TB to a surrogate marker–sputum culture status at completion of eight weeks of treatment–and not to the accepted gold standard of durable TB cure without relapse after treatment. This was done for efficiency and convenience in our study but highlights the need and provides rationale for additional studies of T-SPOT.TB responses during long-term follow-up after completion of TB treatment. In our study, only 10% of subjects with a reactive T-SPOT.TB test at baseline had a nonreactive test at completion of 24 weeks of treatment. Aiken et al. showed that 55% of treated pulmonary TB patients had negative ESAT-6/CFP-10 ELISPOT tests one year after treatment initiation. It remains to be seen whether, after successful TB treatment, SFC counts return to zero in a substantial majority of patients at time points beyond one year. If this were the case, the test might have utility in predicting or diagnosing relapsed or recurrent TB disease. In our study, there were no subjects with recognized TB treatment failure, and therefore we were not able to evaluate T-SPOT.TB responses in this important clinical scenario. We were also unable to assess the kinetics of T cell responses early in treatment, as funding limitations precluded the performance of an 8-week TSPOT-TB test. Of note, current manufacturer instructions in the U.S. FDA-approved T-SPOT.TB assay classify those with spot counts of 5, 6, or 7 as borderline and recommend retesting. Retesting was not done for three individuals in our study who had spot counts of 5 at baseline, as manufacturer instructions at the time of our study classified them as negative. Using the current classification system, two of the three had positive results upon completion of treatment while one had a negative result, resulting in no substantive change in our overall results or conclusions.
On the other hand, our study has several strengths. First, the lab study was undertaken in a setting in which TB treatment (under direct observation), sputum monitoring, and subject follow-up were standardized and rigorous. In addition, the T-SPOT.TB laboratory technologist was not aware of patient status, thereby reducing potential bias. Finally, for each study subject, all T-SPOT.TB specimens were thawed and tested at the same time, thereby reducing the impact of potential unrecognized time-related differences in study procedures.
In conclusion, the correlation between ESAT-6 SFC counts and cavitation on baseline chest radiograph, the decline in SFC counts during treatment, and the observed differences in SFC counts between the group having positive 8-week cultures versus the group having negative 8-week cultures indicate that IFN-γ-producing RD1-specific T cells, as measured by the T-SPOT.TB assay, may be directly related to bacterial load in individuals undergoing treatment for pulmonary TB. However, high inter-patient variability in quantitative results as well as lack of reversion to negative of qualitative results in patients at the time of treatment completion, may limit the utility of this test as an early surrogate marker for treatment response. Longitudinal studies with long-term patient follow-up are warranted in order to determine the utility of the T-SPOT.TB test for detecting relapse after TB treatment.
Pathan AA, Wilkinson KA, Klenerman P, McShane H, Davidson RN, Pasvol G, Hill AV, Lalvani A: Direct ex vivo analysis of antigen-specific IFN-gamma-secreting CD4 T cells in Mycobacterium tuberculosis-infected individuals: associations with clinical disease state and effect of treatment. J Immunol. 2001, 167 (9): 5217-5225.
Mantegani P, Piana F, Codecasa L, Galli L, Scarpellini P, Lazzarin A, Cirillo D, Fortis C: Comparison of an in-house and a commercial RD1-based ELISPOT-IFN-gamma assay for the diagnosis of Mycobacterium tuberculosis infection. Clin Med Res. 2006, 4 (4): 266-272.
Goletti D, Butera O, Bizzoni F, Casetti R, Girardi E, Poccia F: Region of difference 1 antigen-specific CD4+ memory T cells correlate with a favorable outcome of tuberculosis. J Infect Dis. 2006, 194 (7): 984-992. 10.1086/507427.
Lalvani A, Pathan AA, McShane H, Wilkinson RJ, Latif M, Conlon CP, Pasvol G, Hill AV: Rapid detection of Mycobacterium tuberculosis infection by enumeration of antigen-specific T cells. Am J Respir Crit Care Med. 2001, 163 (4): 824-828.
Goletti D, Carrara S, Vincenti D, Saltini C, Rizzi EB, Schinina V, Ippolito G, Amicosante M, Girardi E: Accuracy of an immune diagnostic assay based on RD1 selected epitopes for active tuberculosis in a clinical setting: a pilot study. Clin Microbiol Infect. 2006, 12 (6): 544-550. 10.1111/j.1469-0691.2006.01391.x.
Wang J, Chou C, Lee L, Hsu H, Jan I, Hsueh P, Yang P, Luh K: Diagnosis of tuberculosis by an enzyme-linked immunospot assay for interferon-gamma. Emerg Infec Dis. 2007, 13: 553-558.
Meier T, Eulenbruch HP, Wrighton-Smith P, Enders G, Regnath T: Sensitivity of a new commercial enzyme-linked immunospot assay (T SPOT-TB) for diagnosis of tuberculosis in clinical practice. Eur J Clin Microbiol Infect Dis. 2005, 24 (8): 529-536. 10.1007/s10096-005-1377-8.
Liebeschuetz S, Bamber S, Ewer K, Deeks J, Pathan AA, Lalvani A: Diagnosis of tuberculosis in South African children with a T-cell-based assay: a prospective cohort study. Lancet. 2004, 364 (9452): 2196-2203. 10.1016/S0140-6736(04)17592-2.
Wilkinson KA, Wilkinson RJ, Pathan A, Ewer K, Prakash M, Klenerman P, Maskell N, Davies R, Pasvol G, Lalvani A: Ex vivo characterization of early secretory antigenic target 6-specific T cells at sites of active disease in pleural tuberculosis. Clin Infect Dis. 2005, 40 (1): 184-187. 10.1086/426139.
Richeldi L, Luppi M, Losi M, Luppi F, Potenza l, Roversi P, Cerri S, Millington K, Ewer K, Fabbri L, Torelli G, Lalvani A: Diagnosis of occult tuberculosis in hematological malignancy by enumeration of antigen-specific T cells. Leukemia. 2005, 1-3.
Zellweger JP, Zellweger A, Ansermet S, de Senarclens B, Wrighton-Smith P: Contact tracing using a new T-cell-based test: better correlation with tuberculosis exposure than the tuberculin skin test. Int J Tuberc Lung Dis. 2005, 9 (11): 1242-1247.
Richeldi L, Ewer K, Losi M, Bergamini BM, Roversi P, Deeks J, Fabbri LM, Lalvani A: T cell-based tracking of multidrug resistant tuberculosis infection after brief exposure. Am J Respir Crit Care Med. 2004, 170 (3): 288-295. 10.1164/rccm.200403-307OC.
Ewer K, Deeks J, Alvarez L, Bryant G, Waller S, Andersen P, Monk P, Lalvani A: Comparison of T-cell-based assay with tuberculin skin test for diagnosis of Mycobacterium tuberculosis infection in a school tuberculosis outbreak. Lancet. 2003, 361 (9364): 1168-1173. 10.1016/S0140-6736(03)12950-9.
Conde MB, Efron AR, Loredo C, Muzy de Souza GR, Graça NP, Cezar MC, Ram M, Chaudhary MA, Bishai WR, Kritski AL, Chaisson RE: Moxifloxacin in the initial therapy of tuberculosis : a randomized, phase 2 trial. Lancet.
Anonymous: T-SPOT.TB An aid in the diagnosis of tuberculosis infection: visual procedure guide for in vitro diagnostic use, Oxford Immunotec. 2005
Zeger SL, Liang KY: Longitudinal data analysis for discrete and continuous outcomes. Biometrics. 1986, 42 (1): 121-130. 10.2307/2531248.
Hirsch CS, Toossi Z, Othieno C, Johnson JL, Schwander SK, Robertson S, Wallis RS, Edmonds K, Okwera A, Mugerwa R, Peters P, Ellner JJ: Depressed T-cell interferon-gamma responses in pulmonary tuberculosis: analysis of underlying mechanisms and modulation with therapy. J Infect Dis. 1999, 180 (6): 2069-2073. 10.1086/315114.
Carrara S, Vincenti D, Petrosillo N, Amicosante M, Girardi E, Goletti D: Use of a T cell-based assay for monitoring efficacy of antituberculosis therapy. Clin Infect Dis. 2004, 38 (5): 754-756. 10.1086/381754.
Aiken AM, Hill PC, Fox A, McAdam KP, Jackson-Sillah D, Lugos MD, Donkor SA, Adegbola RA, Brookes RH: Reversion of the ELISPOT test after treatment in Gambian tuberculosis cases. BMC Infect Dis. 2006, 6: 66-10.1186/1471-2334-6-66.
Ferrand RA, Bothamley GH, Whelan A, Dockrell HM: Intereron-gamma responses to ESAT-6 in tuberculosis patients early into and after anti-tuberculosis treatment. Int J Tuberc Lung Dis. 2005, 9 (9): 1034-1039.
Ulrichs T, Anding R, Kaufmann SH, Munk ME: Numbers of IFN-gamma-producing cells against ESAT-6 increase in tuberculosis patients during chemotherapy. Int J Tuberc Lung Dis. 2000, 4 (12): 1181-1183.
Dheda K, Pooran A, Pai M, Miller RF, Lesley K, Booth HL, Scott GM, Akbar AN, Zumla A, Rook GA: Interpretation of Mycobacterium tuberculosis antigen-specific IFN-gamma release assays (T-SPOT.TB) and factors that may modulate test results. J Infect. 2007, 55 (2): 169-173. 10.1016/j.jinf.2007.02.005.
Hill PC, Fox A, Jeffries DJ, Jackson-Sillah D, Lugos MD, Owiafe PK, Donkor SA, Hammond AS, Corrah T, Adegbola RA, McAdam KP, Brookes RH: Quantitative T cell assay reflects infectious load of Mycobacterium tuberculosis in an endemic case contact model. Clin Infect Dis. 2005, 40 (2): 273-278. 10.1086/427030.
Richeldi L, Ewer K, Losi M, Bergamini BM, Millington K, Fabbri LM, Lalvani A: T-cell-based diagnosis of neonatal multidrug-resistant latent tuberculosis infection. Pediatrics. 2007, 119 (1): e1-5. 10.1542/peds.2006-1057.
Adetifa IM, Brookes R, Lugos MD, de Jong BC, Antonio M, Adegbola RA, Hill PC: Rising ELISPOT count prior to the onset of symptoms of full-blown tuberculosis disease. Int J Tuberc Lung Dis. 2007, 11 (3): 350-352.
Ewer K, Millington KA, Deeks JJ, Alvarez L, Bryant G, Lalvani A: Dynamic antigen-specific T-cell responses after point-source exposure to Mycobacterium tuberculosis. Am J Respir Crit Care Med. 2006, 174 (7): 831-839. 10.1164/rccm.200511-1783OC.
Chee CB, KhinMar KW, Gan SH, Barkham TM, Pushparani M, Wang YT: Latent tuberculosis infection treatment and T-cell responses to Mycobacterium tuberculosis-specific antigens. Am J Respir Crit Care Med. 2007, 175 (3): 282-287. 10.1164/rccm.200608-1109OC.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2334/9/23/prepub
T-SPOT.TB assay kits were generously supplied by Oxford Immunotec Ltd. This study was supported by grants from the National Institutes of Health (AI51528 to S. Dorman), the United States Agency for International Development (to S. Dorman), the United States Food and Drug Administration (FD-R2135 to R. Chaisson), and Fundaçao de Amparo a Pesquisa do Estado do Rio de Janeiro (E-26/100.653/2007 to M. Conde).
The authors thank Jose R. Lapa e Silva for support and assistance with equipment and supplies, and Patricia Lago for assistance with performance of the T-SPOT.TB assays.
The authors declare that they have no competing interests.
SED conceived of and designed the study and helped to draft the manuscript. KD performed the statistical analyses and drafted the manuscript. NB, MBC, and REC assisted with study design, interpretation of results, and manuscript preparation. SR performed the TSPOT.TB laboratory assays. JH, AE, and CL coordinated the study and recruited study participants. All authors read and approved the final manuscript.
Samantha Ribeiro, Kelly Dooley, Neio Boechat and Susan E Dorman contributed equally to this work.
About this article
Cite this article
Ribeiro, S., Dooley, K., Hackman, J. et al. T-SPOT.TBresponses during treatment of pulmonary tuberculosis. BMC Infect Dis 9, 23 (2009). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2334-9-23
- Incidence Rate Ratio
- Sputum Culture
- Directly Observe Therapy
- Positive Sputum Culture
- Cavitary Disease