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Clinical evaluation of QuantiFERON TB-2G test for immunocompromised patients

Division of Respiratory Diseases, Dept of Medicine, Kawasaki Medical School, Kurashiki, Japan.

CORRESPONDENCE: Y. Kobashi, Division of Respiratory Diseases, Dept of Medicine, Kawasaki Medical School, 577 Matsushima, Kurashiki, 701-0192, Japan. Fax: 81 864641041. E-mail: yoshihiro{at}med.kawasaki-m.ac.jp

Keywords: Immunocompromised patient, QuantiFERON TB-2G, tuberculin skin test

Received: April 4, 2007
Accepted July 16, 2007

	ABSTRACT

TOP ABSTRACT METHODS RESULTS DISCUSSION ACKNOWLEDGEMENTS REFERENCES

 
The usefulness of the tuberculin skin test (TST) and the QuantiFERON TB-2G (QFT-TB) test were compared in immunocompromised patients.

The subjects consisted of 252 immunocompromised patients who were clinically suspected of tuberculosis (TB) infection between April 2005 and December 2006.

Regarding the underlying diseases, 74 subjects had malignant diseases, 72 were undergoing immunosuppressive treatment, 52 had diabetes mellitus, 50 had chronic renal failure and four had HIV infection. While the positive rate of the QFT-TB test for the diagnosis of TB infection (TB disease or latent TB infection) was 78.1%, that of TST for TB infection was 50.0%. The QFT-TB test was significantly better than TST. However, 32 (13%) patients had an indeterminate QFT-TB result. Indeterminate findings were significantly more frequent in patients receiving immunosuppressive treatment (28%), especially with lymphocytopaenia in the peripheral blood, than in those who had other underlying diseases. While TST-positive and QFT-TB test-negative results were recognised in immunocompromised patients with bacille Calmette–Guérin vaccination or nontuberculous mycobacterial disease, TST-negative and QFT-TB test-positive results were recognised in immunocompromised patients with a past history of TB infection.

It was concluded that the QuantiFERON TB-2G test is a more useful diagnostic method for tuberculosis infection than tuberculin skin test for immunocompromised patients suspected of tuberculosis disease. However, because the results of the QuantiFERON TB-2G test show an indeterminate response for patients receiving immunosuppressive treatment, especially for those with lymphocytopaenia due to severe underlying diseases, care must be taken in the interpretation of the QuantiFERON TB-2G test for these patients.

In Japan, the incidence of tuberculosis (TB) is intermediate (35 cases per 100,000 population) and has recently been decreasing. However, aging of the population and the increased use of immunosuppressive treatments (e.g. cancer chemotherapy and immunomodulatory agents) highlight the need for additional strategies to maintain and improve TB control 1. Early diagnosis of infectious cases and treatment of these immunocompromised patients infected with Mycobacterium tuberculosis (MTB) are important strategies for reducing the incidence of TB in industrialised countries 1, 2. The specificity of the tuberculin skin test (TST) is limited by cross-reactivity of the purified protein derivative (PPD) with bacille Calmette–Guérin (BCG) vaccine and with most nontuberculous mycobacteria (NTM) 3. Its sensitivity is also low in immunocompromised patients, in whom the risk of progression to TB is high 2. Despite these limitations, TST is routinely used in hospital clinical practice to screen for latent TB infection 4.

The two commercialised ex vivo interferon (IFN)- assays, QuantiFERON TB-2G (QFT-TB; Cellestis Ltd, Carnegie, Victoria, Australia) and T-SPOT.TB (Oxford Immunotec, Oxford, UK), use early secretory antigenic target (ESAT)-6 and culture filtrate protein (CFP)-10 as MTB-specific stimulants on ELISA and enzyme-linked immunospot assay (ELISPOT), respectively 5–8. The US Food and Drug Administration has approved the QFT-TB test and is evaluating the T-SPOT.TB test, which has been approved for use in Europe. These tests demonstrate a positive result for most individuals with a high likelihood of TB infection (TB disease or latent TB infection) and a negative result for BCG-vaccinated individuals with a low likelihood of TB infection. Of these tests, the QFT-TB was first used commercially in Japan in April 2005 for the diagnosis of TB infection. Although there have been several reports investigating whether QFT-TB test and T-SPOT.TB test would be useful in immunocompromised patients 9–11, there has been only one report investigating the usefulness of the new test separately in individual important underlying disease 11. Therefore, the present authors prospectively report on the results of an analysis in which the QFT-TB test was routinely performed on many consecutive immunocompromised patients separated according to individual underlying disease in several community hospitals. The present study evaluated the feasibility and performance of the QFT-TB test compared with those of TST for immunocompromised patients in a hospital-based population, and included the interpretation of concordant and discordant results of both tests.

	METHODS

TOP ABSTRACT METHODS RESULTS DISCUSSION ACKNOWLEDGEMENTS REFERENCES

 
Study population
The study was approved by the Ethics Committee of Kawasaki Medical School (Kurashiki, Japan). In total, 264 immunocompromised patients (>16 yrs old) with underlying diseases who were clinically suspected of TB disease were prospectively enrolled in the present study between April 2005 and December 2006. The patients suspected of TB disease demonstrated the appearance of new lesions in the lung field, pleural effusion, or lymphadenopathy on chest radiograph or chest computed tomography (CT) during follow-up of the underlying disease. Of these, 12 patients were excluded because there were no obvious findings suggesting TB disease on chest CT. The remaining 252 immunocompromised patients (204 in-patients and 48 outpatients) were analysed in the present study. Most of these patients had the underlying disease on admission for which they consulted the following hospitals: Kawasaki Medical School Hospital, Kawasaki Medical School Kawasaki Hospital, Kurashiki Central Hospital, Kurashiki Daiichi Hospital (all Kurashiki, Japan), and Asahigaoka Hospital (Okayama, Japan). Written, informed consent was obtained from all participants in the present study. All patients except for the four with HIV infection had negative results on serological tests for HIV or had no obvious risk factors for HIV infection. Demographic, clinical, radiological and microbiological data were collected for all patients. Collected data included any history of previous TB disease and risk factors for TB (i.e. malignant diseases, including leukaemia; immunosuppressive treatments, such as systemic immunosuppressive drugs or anti-tumour necrosis factor (TNF)- agents within the past 3 months; diabetes mellitus; chronic renal failure with haemodialysis; and HIV infection with anti-HIV treatment). The diagnosis of TB disease was definitively confirmed by culture of sputum, bronchoalveolar lavage fluid (BALF) or pleural fluid samples found to be positive for MTB microbiologically. In Japan, inoculation with the BCG vaccination is first administered during infancy. Thereafter, if the response to TST is negative at the time of entrance of junior high school, BCG vaccination is administered again until conversion of the TST to positive. Information regarding any previous Mantoux TST results and BCG vaccination, as well as information about clinical and laboratory findings, was collected from each patient at the time of enrolment. Sputum or other appropriate respiratory samples were collected from all patients, and culture samples were obtained for the detection of MTB.

Sample collection and TST
A heparinised blood sample was collected from individual patients by vein puncture for whole-blood IFN- assay. Blood samples were collected before administration of the Mantoux TST. For the TST, 0.1 mL of tuberculin PPD (Nippon BCG, Tokyo, Japan; equivalent to three tuberculin units of PPD-saline) was injected intradermally into the volar aspect of the forearm, and the transverse induration diameter was measured 48 h later. The TST results were interpreted according to the level of risk, as reported in current guidelines 12.

QuantiFERON TB-2G test
The QFT-TB test was performed according to the recommendations of the manufacturer (Cellestis Ltd). Briefly, the test consisted of a negative control (a "nil" well, i.e. whole blood without antigens or mitogen), a positive control (a "mitogen" well, i.e. whole blood stimulated with the mitogen phytohaemaggulutinin) and two "sample" wells (i.e. whole blood stimulated with either ESAT-6 or CFP-10). Whole-blood specimens were incubated for 18 h (overnight) at 37°C in a humidified atmosphere. The IFN- level of the nil well was considered to be the background value and was subtracted from the values for the mitogen well and the antigen-stimulated wells. The test result was considered positive and suspected of TB infection if the IFN- level in the sample well after stimulation with ESAT-6 and/or CFP-10 was >0.35 IU·mL^–1 (after subtraction of the value for the nil well), irrespective of the result for the positive control well. The test result was considered negative and it was difficult to diagnose TB infection if the IFN- level was <0.35 IU·mL^–1 and if the IFN- level of the positive control well (after subtraction of the value for the nil well) was >0.5 IU·mL^–1. The test result was considered indeterminate and it was impossible to interpret the result if the IFN- level was <0.35 IU·mL^–1 in both antigen wells and <0.5 IU·mL^–1 in the positive control well, or if the IFN- level was below half of the negative control well in both antigen wells and >0.7 IU·mL^–1 in the negative control well. This judgment was performed according to the guidelines proposed by the Centers for Disease Control and Prevention for using the QFT-TB test 13.

Statistical analysis
Information from the questionnaires, TST results and whole-blood IFN- assay results were subjected to statistical analyses. Statistical analyses were performed to assess the following: 1) the feasibility and performance of the QFT-TB test compared with those of TST; 2) the proportion of QFT-TB tests with an indeterminate result and the associated risk factors; 3) the concordance and discordance between the QFT-TB and TST results; and 4) the positive rate of the QFT-TB and TST results in patients with a final diagnosis of active TB disease. The analysis of concordance between the QFT-TB and TST results was calculated using the -value. Both the QFT-TB and TST results were compared using the Chi-squared test. The Wilson score method was used to calculate 95% confidence intervals for the positive rate of both tests 14.

	RESULTS

TOP ABSTRACT METHODS RESULTS DISCUSSION ACKNOWLEDGEMENTS REFERENCES

 
In total, 252 patients who were clinically suspected of TB disease were tested with the TST and the QFT-TB test between April 2005 and December 2006. Their demographic and clinical characteristics are shown in table 1. Regarding the underlying diseases among these patients, 74 patients had malignant diseases (all of these patients had advanced cancer without surgical treatment), including leukaemia (12 patients during the follow-up period including patients receiving anti-cancer therapy); 72 were undergoing immunosuppressive treatment for underlying diseases (52 were receiving the systemic steroid prednisone, 10 were receiving anti-TNF- agents and 10 were receiving the systemic steroid prednisone plus other immunosuppressive agents); 52 had diabetes mellitus (all patients were receiving oral hypoglycaemic agents or insulin); 50 had chronic renal failure (all patients were receiving haemodialysis); and four had HIV infection (all patients were receiving anti-HIV treatment). The mean age of all immunocompromised patients was 62.0 yrs and there were 156 males and 96 females. A past history of BCG vaccination was present in 152 (60.3%) patients and 24 (9.5%) had a past history of healed pulmonary TB. The incidence of TB disease was 12.7% in the overall patient group. On separation of patients by underlying immunocompromised diseases, there were no significant differences, but in laboratory findings, the peripheral lymphocyte count and CD4 lymphocyte count were significantly lower in patients with immunosuppressive treatment than in those with other underlying diseases. There were 31 (12.3%) patients with bed-ridden status and there were no significant differences between individual groups with any underlying disease.

Five (15.6%) out of 32 patients with a QFT-TB indeterminate response appeared to have TB disease; 25 (69.4%) out of 36 patients with a QFT-TB-positive response appeared to have TB disease. Two patients out of 184 with a QFT-TB-negative response appeared to have TB disease. While 16 (15.7%) patients appeared to have TB disease out of 102 with a TST-positive response, 16 (10.7%) patients among 150 with a TST-negative response also appeared to have TB disease. The incidence of TB disease was significantly higher in the QFT-TB-positive response group than in TST-positive response group (p<0.05).

	DISCUSSION

TOP ABSTRACT METHODS RESULTS DISCUSSION ACKNOWLEDGEMENTS REFERENCES

 
In Japan, most patients receiving immunosuppressive treatment for systemic underlying diseases have a past history of BCG vaccination. However, it has been noted that the sensitivity of TST is not high in immunosuppressed patients, in whom the risk of progression to TB is high 3. In place of the TST test in vivo, the QFT-TB test in vitro was first used commercially for patients with TB infection in Japan in April 2005 because the QFT-TB test demonstrated a negative result for BCG-vaccinated individuals and a negative result for most NTM 2, 15. Therefore, the present authors prospectively investigated the results of QFT-TB test being routinely performed on consecutive immunocompromised patients in several community hospitals. Although the patients were separated according to individual systemic underlying diseases (malignant diseases including leukaemia, those receiving immunosuppressive treatment, diabetes mellitus, chronic renal failure and HIV infection) that induce immunosuppression, there were no significant differences among the clinical characteristics (table 1). However, while no significant differences could be detected between other immunosuppressive patients in the laboratory findings, except for those in several patients with HIV infection, patients receiving immunosuppressive treatment showed significantly lower lymphocyte and CD4 lymphocyte counts than other immunocompromised patients.

Regarding the specificity and sensitivity of the QFT-TB test, Mori et al. 6 reported a sensitivity of 89% in a selected population of patients with clinical signs suggestive of TB infection. They also reported a specificity of 98% in low-risk subjects who had been vaccinated with BCG and who were assumed to be truly free of TB. However, in the present study, the positive response rate for the QFT-TB test was relatively low at 78.1% (25 out of 32 patients with TB disease). An indeterminate result for the QFT-TB test was recognised in 12.7% (32 out of 252 immunocompromised patients) and it appeared most frequently in patients receiving immunosuppressive treatments who presented with lymphocytopaenia (especially CD4 lymphocytopaenia). In previous reports, Ferrara et al. 9 noted that the QFT-TB-positive control failed in 21% of tests performed in routine clinical diagnostic microbiology laboratories and community-based contact tracing protocols, and that these indeterminate results were significantly overrepresented among patients receiving immunosuppressive treatments. A similar result (indeterminate rate: 11%) has been confirmed in a prospective study of 393 individuals 16; however, there was no speculation concerning the reason. In the present study, a similar result was obtained and all patients showed QFT-TB-positive control failure (IFN- <0.5 IU·mL^–1), although the indeterminate result of the QFT-TB test was 12.7%, similar to the data reported by Ferrara et al. 9. One reason was that lymphocytopaenia, especially CD4 lymphocytopaenia, predominantly appeared in patients with immunosuppressive treatment (table 1) 17. The QFT-TB test depends on the elaboration of inflammatory cytokines by T-cells previously sensitised to MTB-specific antigens. In the blood, mononuclear cells from peripheral blood are stimulated in vitro, and the production of IFN- from sensitised T-lymphocytes by MTB-specific antigen is measured by ELISA in the QFT-TB test 18. Therefore, it was first speculated that lymphocytopaenia caused decreased production of IFN- and lower mitogen, ESAT-6 or CFP-10 QFT-TB levels. Secondly, immunosuppressive drugs, such as corticosteroid drugs, directly reduce the production of inflammatory cytokines, such as IFN-, interleukin-1 and TNF- from T-lymphocytes 13, 19, 20. Finally, the decrease of IFN- induced indeterminate results of the QFT-TB test because of the lower mitogen, ESAT-6 or CFP-10 QFT-TB levels. For these reasons, indeterminate results due to positive control failure seem to be less frequent with the T-SPOT.TB test, which detects individual T-cells producing IFN- using an ELISPOT method, than the QFT-TB test 10, 16, 21. This also applies to the use of the T-SPOT.TB in subgroups with impaired cellular immunity, with a recent report that HIV-infected subjects tested with the T-SPOT.TB showed only one (3%) indeterminate result, and that positive control responses were not adversely affected by CD4 counts 22. Otherwise, a new IFN- release assay including MTB-specific antigen (TB 7.7; QuantiFERON TB-Gold In-Tube; Cellestis Ltd) 23 has recently been developed and will replace the QFT-TB-2G test in Japan as soon as possible. Immunocompromised patients suspected of TB infection had to be examined using the QFT-TB test in the present study because only this test is currently commercially available in Japan. Hereafter, although Liebeschuetz et al. 24 had reported the results of ELISPOT test for immunosuppressed populations with HIV and suspected TB disease, the present authors would like to carry out a prospective, large-scale study of immunocompromised patients with various severe underlying diseases other than HIV infection in a community hospital-based population with suspected TB infection using the T-SPOT.TB test instead of the QFT-TB test.

Regarding the comparison of TST and QFT-TB test results, the present findings support the conclusion that QFT-TB test provides more accurate results than TST in immunocompromised patients 25. The findings also suggest that the QFT-TB test might have limited clinical usefulness in patients receiving immunosuppressive treatment. However, in most patients, the QFT-TB test produced a valid result, although this IFN- blood test may raise some questions regarding the validity of a negative TST result. Specifically, because TST does not have an internal positive control the clinician cannot distinguish between a true-negative result and a false-negative result. With the QFT-TB test, a proportion of false-negative test results will be scored as indeterminate, allowing the clinician to disregard such results. Naturally, there would still be a certain proportion of false-negative test results associated with a valid positive control, as was also observed. The present authors think that the reasons for the discordances between the TST and QFT-TB tests can be predominantly explained by BCG vaccination or NTM infection causing the result of TST to be positive and that of QFT-TB test to be negative, and by a past history of TB infection causing the result of TST to be negative and that of QFT-TB test to be positive, based on the results of the present study.

In conclusion, the present study demonstrated the clinical utility of the QuantiFERON TB-2G test compared with the tuberculin skin test for immunocompromised patients with tuberculosis infection. However, because the QuantiFERON TB-2G test result showed an indeterminate response for patients receiving immunosuppressive treatment, especially with lymphocytopaenia due to severe underlying diseases, care must be taken when making a diagnosis of tuberculosis for these patients based on QuantiFERON TB-2G test results. In the future, the present authors would like to increase the diagnostic rate of tuberculosis infection (tuberculosis disease or latent tuberculosis infection) for immunocompromised patients with underlying diseases in a community hospital-based population suspected of tuberculosis infection by utilising other interferon- detecting methods (T-SPOT.TB or QuantiFERON-TB Gold In-Tube).

	ACKNOWLEDGEMENTS

TOP ABSTRACT METHODS RESULTS DISCUSSION ACKNOWLEDGEMENTS REFERENCES

 
The authors would like to thank T. Matsushima (Kurashiki Daiichi Hospital, Kurashiki, Japan; Asahigaoka Hospital, Okayama, Japan), N. Okimoto (Kawasaki Medical School Kawasaki Hospital, Kurashiki, Japan) and T. Kageoka (Kurashiki Central Hospital, Kurashiki, Japan) for helpful comments.

	REFERENCES

TOP ABSTRACT METHODS RESULTS DISCUSSION ACKNOWLEDGEMENTS REFERENCES

 

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This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Permissions Request Permissions Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via ISI Web of Science (5) Citing Articles via Google Scholar Google Scholar Articles by Kobashi, Y. Articles by Oka, M. Search for Related Content PubMed PubMed Citation Articles by Kobashi, Y. Articles by Oka, M.