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. 2013 Dec 5;13:1128. doi: 10.1186/1471-2458-13-1128

Prevalence of latent tuberculosis infection in Sudan: a case–control study comparing interferon-γ release assay and tuberculin skin test

Amani Osman Shakak 1, Eltahir Awad Gasim Khalil 2,7,✉, Ahmed Mudawi Musa 2, Kawthar Abd Eljalil Mohamed Salih 3, Abd Elgadir Ali Bashir 4, Ala Hassan Ahmed 5, Fath Elrahman Mohamed Idris 6, Ahmed Mohamed Elhassan 2, Tuberculosis Research Group/Sudan
PMCID: PMC4029475  PMID: 24313987

Abstract

Background

Most people exposed to M. tuberculosis show no evidence of clinical disease. Five to 10% of individuals with latent infection progress to develop overt disease during their life time. Identification of people with latent TB infection will increase case detection rates and may dictate new treatment policies to control tuberculosis. This study aimed to determine LTBI point prevalence in a population from Sudan using two different diagnostic methods: the tuberculin skin test (TST) and the IFN-γ release assay (IGRA).

Methods

This was a prospective, community-based and case-controlled study. Following informed consent, household contacts (HHCs; n = 98) of smear-positive index cases and Community controls (CCs; 186), were enrolled. Tuberculin skin test (TST), whole blood stimulation with ESAT-6/CFP-10 ± TB7.7 antigens or purified protein derivative (PPD) and IFN-γ levels determination with ELISA were performed. The levels of IFN-γ and TST induration between the CCs and the HHCs were compared using student t-test, Chi-square and Kappa coefficient. Pearson correlation test was used to compare TST and IFN-γ. P levels of <0.05 were considered significant.

Results

TST induration of ≥ 10 mm gave an LTBI point prevalence of 327 cases/1000 individuals among HHCs compared to 126 cases/1000 individuals among CCs (p = 0.000). PPD-induced IFN-γ release assay gave an LTBI point prevalence of 418 cases/1000 individuals among HHCs compared to 301 cases/1000 individuals among CCs (p =0.06). On the other hand ESAT-6/CFP-10 ± TB7.7-induced IFN-γ gave an LTBI point prevalence of 429 cases/1000 individuals among HHCs compared to 268 cases/1000 individuals among CCs (p = 0.01). IFN-γ productions levels induced by ESAT-6/CPF-10 ± TB7.7 antigens in HHCS and CCs were not significantly different from those induced by PPD (p = 0.7).

Conclusion

IFN-γ release assay (IGRA) gave higher LTBI point prevalence compared to TST in HHCs and CCs. PPD gave comparable results to ESAT-6/CFP-10 ± TB7.7 antigens in whole blood IFN-γ release, making it a cheap alternative to the recombinant antigens.

Keywords: Latent Tb infection, IFN-γ release assay, TST, Sudan, Contact tracing

Background

Tuberculosis (TB) is a contagious and airborne disease of poverty that mostly affects young adults in their most productive years in developing countries. The vast majority of TB deaths are in the developing world with an estimated two million deaths annually. WHO reported that one third of the world population is infected with latent TB with 9.4 million new overt cases annually [1]. Five to 10% of individuals with latent TB progress to develop overt disease during their life time. Identification of people with latent TB infection (LTBI) will increase case detection rates and may dictate new treatment policies to control tuberculosis. In the absence of a gold standard test for identification of individuals with LTBI, different reports suggested tuberculin skin test (TST) or interferon-γ release assay (IGRA) as the best test [2-7].

The tuberculin skin test (TST) remains the most commonly used test for diagnosing latent TB infection (LTBI) that could indicate preventive treatment [2]. TST has a number of limitations: low sensitivity in immune-compromised patients and cross-reactivity with hypersensitivity in BCG-vaccinated and non-tuberculous mycobacterial (NTM) infections [3]. Recently a new diagnostic test IFN-γ release assay (IGRA) which measures the production of IFN-γ in whole blood upon stimulation with specific antigens has been introduced. These antigens (Early Secreted Antigenic Target-6; ESAT-6 and Culture Filtrate Protein-10; CFP-10), though unique to M. tuberculosis in the latent state, have been found in some non-tuberculous Mycobacteria and M. leprae. IFN-γ produced by T-cells plays a critical role in protective immunological responses to primary infection. The QuantiFERON-TB Gold In-Tube (QFT-GIT; Cellestis Ltd. Carnegie, Victoria, Australia) is the newest IGRA assay. In addition to the ESAT-6 and CFP-10 peptides, this test utilizes the TB7.7-M. tuberculosis specific peptide as well. Unfortunately, IGRAs cannot differentiate between active and past TB infections or between LTBI and tuberculosis [4-6].

This study aimed to determine LTBI point prevalence in a Sudanese population using TST and the IFN-γ release assay. The study also aimed to compare PPD and ESAT-6/CPF-10 ± TB7.7 antigens as stimulants for IFN-γ release in whole blood stimulation in vivo systems.

Methods

Scientific and ethical considerations

The study was approved and passed by the Ethics & Scientific Committees of the Institute of Endemic Diseases, University of Khartoum and the Ethics Committees of the Federal Ministry of Health, Khartoum. Written informed consents were obtained from all participating individuals. The national TB control program was heavily involved from the start of the study.

Study population

Index cases with smear-positive sputum pulmonary TB and at least one household contact were initially enrolled. House hold contacts (HHCs) of these cases were recruited based on the following inclusion criteria: age ≥15 years, living for more than six months at the same property as the respective index case, agreeing to participate and they/their guardian sign the informed consent. Sex-matched Community controls (CCs) were enrolled if: age ≥15 years, have no history of tuberculosis in his/her household, have no symptoms/signs of tuberculosis and has signed an informed consent.

Tuberculin skin testing

Tuberculin skin test (TST) was performed on all contacts by the administering 0.1 ml containing 5 tuberculin units (Razi Institute, Iran). Transverse induration was measured 72 hours later using the ballpoint pen technique. A reaction equal or more than 5 mm was considered as reactive [8].

Whole blood stimulation and IFN-γ release assay

For one hundred individuals whole blood stimulation and measurement of IFN-γ levels was conducted using QFT-G- in Tube Kit (Cellestis Ltd., Victoria, Australia) as per manufacturer’ instructions. Due to interruption of Kits supplies, M. tuberculosis recombinant antigens (ESAT-6/CFP-10, Cellestis Ltd., Victoria, Australia) and PPD were used in the rest of the volunteers (184 CCs), while IFN-γ production assay was performed using ELISA Kits from Komabiotech, Seoul, South Korea as per manufacturer’ instructions. The IFN-γ measurement kits were validated and compared at the QC Unit of the Institute of Endemic Diseases, University of Khartoum. Whole blood stimulation was performed as follows: one ml of blood was taken in each of four tubes: 1. ESAT-6/CFP-10 antigens 2. Phytohemagglutinin (PHA) for the positive control 3. No antigen for the negative control 4. Five PPD antigen units. The tubes were incubated for 24 hours at 37°C in Cellestis incubator (Cellestis Ltd., Victoria, Australia), and plasma was collected after centrifugation and stored at −20°C until assayed. A cut-off of 0.35 IU/mL for IFN-γ was applied.

Statistical analysis

Statistical analyses were performed using Epidemiological Information (Epi Info) software version 3.4.3.0. The levels of IFN-γ cytokine and TST induration between the CCs and the HHCs were compared using student t-test and Chi-square. Pearson correlation test was used to compare TST and IFN-γ. P levels of <0.05 were considered significant. Kappa coefficient of agreement between TST and IGRA; PPD-induced IFN-γ release and ESAT-6/CFP-10 ± TB7.7-induced IFN-γ release for the study population was calculated as described by Cohen previously [9].

Results

A total of 284 consenting volunteers were enrolled in the study, ninety eight were House-Hold Contacts (HHCs) for 25 Index Cases and 186 were Community controls (CCs) with a male: female ratio of 1:4. The mean age of HHCs was 30 ± 11.0 years and that of CCs was 29 ± 10.0 years. Females were predominant in both HHCs and CCs, where they were four times more than males. All volunteers had history of BCG vaccination that was confirmed in the majority (>85%) by presence of a scar. TST induration and positivity were significantly different in HHCs compared to CCs (p = 0,000) (Table 1). Sixty per cent of HHCs had TST induration of <5 mm compared to 83% in CCs. Volunteers with TST induration of ≥10 mm were seen more frequent among HHCs (25.5%) compared to CCs (9%). Volunteers with TST of ≥ 15 mm were mainly seen in house hold contacts (p = 000). Nineteen of CCs could not be traced for TST reading in screening (Table 1).

Table 1.

Tuberculin skin test (TST) & Cytokines production in whole blood cultures [ESAT-6/CFP-10 & PPD] in the study population at screening

Variables
 House-Hold contacts
 Community controls**
 p value
  ( n = 98) ¤ (n = 186)  
  TST (mean ± SD)
 5 ±6
 2 ±3
 0.000*
< 5 mm
 59 (60.2%)
 139 (83.2%)
 0.000*
5 - 9 mm
 12 (12.2%)
 13 (7.8%)
 0.04*
10 - 14 mm
 13 (13.2%)§
 14 (8.4%)
 0.1
≥ 15 mm
 14 (14.4%)§
 01 (0.6%)
 0.000*
IFN-γ Mean level IU/ml:
  Purified Protein Derivative:
Mean ± SD
 0.5 ± 0.6
 0.3 ± 0.4
 0.4
< 0.35
 57/98 (58.2%)
 130/186 (69.9%)
 0.06
0.35-1.0
 28/98 (28.6%)
 44/186 (23.6%)
 0.1
1.1-2.0
 13/98 (13.2%)
 12/186 (6.5%)
 0.3
  ESAT-6 + CFP −10 ± TB7•7:
Mean ± SD
 0.5 ± 0.7
 0.2 ± 0.2
 0.000*
<0.35
 56/98 (57.1%)
 136/186(73.2%)
 0.03*
0.35 - 1.0
 18/98 (18.4%)§
 41/186 (22.2%)
 0.01*
1.1 - 2.0 24/98 (24.5%)§ 09/186 (4.6%) 0.2
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Continuous variable are expressed as means ± SD. *Significant difference (p < 0.05).

§There was a low correlation between IFN-γ level >0.35 IU/ml and TST ≥10 mm (r = 0.4).

All volunteers had history of BCG vaccination that was confirmed in the majority (>85%) by presence of a scar. **Nineteen CCs did not report for TST reading.

The mean IFN-γ production level for the ESAT-6/CFP-10 ± TB7.7 whole blood stimulation was significantly different for the HHCs (0.5 ± 0.7 IU/ml) compared to the CCs (0.2 ± 0.2 IU/ml) (p = 0.000). These recombinant antigens stimulation gave IFN-γ production levels of ≥0.35 IU/ml in 42.9% (42/98) of HHCs compared to 26.9% (50/186) of CCs (p = 0.01) only in the 0,35-1,0 range. Fifty seven percent of the HHCs were not reactive in whole blood IFN-γ production compared to more than seventy percent in the CCs (p = 0.03). In PPD-whole blood stimulation, IFN-γ production levels of ≥ 0.35 IU/ml were 41.8% (41/98) and 30.1% (56/186) for HHCs and CCs respectively (p = 0.06 not significant).

IFN-γ productions levels induced by ESAT-6/CPF-10 ± TB7•7 antigens were not significantly different from those produced by PPD in HHCs and CCs (p = 0.7). Kappa co-efficient of agreement between PPD-induced IFN-γ release and ESAT-6/CFP-10 ± TB7.7-induced IFN-γ release for the study population was calculated at 1 (Table 1).

No correlation between TST and IFN-γ production levels in HHCs and CCs could be detected (r = 0.4).

TST induration of ≥ 10 mm gave a LTBI a point prevalence of 327 cases/1000 individuals among HHCs compared to 126 cases/1000 individuals among CCs (p = 0.000). PPD-induced IFN-γ release assay gave an LTBI point prevalence of 418 cases/1000 individuals among HHCs compared to 301 cases/1000 individuals among CCs (p =0.06). On the other hand ESAT-6/CFP-10 ± TB7.7-induced IFN-γ gave an LTBI point prevalence of 429 cases/1000 individuals among HHCs compared to 268 cases/1000 individuals among CCs (p = 0.01). Overall, LTBI point prevalence was calculated in the study population for TST (induration ≥ 10 mm), PPD-IFN-γ induced and ESAT-6/CPF-10 ± TB7•7 assays at 453/1000, 719/1000 and 678/1000 respectively (Table 1).

The Cohen’s co-efficient of agreement between TST and IGRA for the study population was calculated at 0.52.

Discussion

Tuberculosis control programs in developing countries are greatly haunted by low case detection rates and latent TB infections that constitute hidden pools that continuously feed new cases. Accurate diagnosis of LTBI and appropriate treatment of probable cases-to-be reduce the risk of progression to overt disease and increase case detection rates [7,10]. However the role of preventive treatment in high burden countries needs to be assessed. Furthermore, testing of adult contacts is controversial in high incidence countries [11]. At present time there is no gold standard test for the detection of individuals with LTBI and TST has been the most widely used diagnostic tool in the detection of LTBI for more than a century. TST is a simple and cheap test but has reduced specificity as BCG vaccination may affect the results as in our population. TST is an in vivo test that measures skin induration response due to cytokines/chemokines secretion (IL- 4, IFN-γ, tumor necrosis factor-α, IL-10, IL-12 and G-CSF) [2]. On the other hand, whole blood IFN-γ release assays are highly specific for latent M. tuberculosis, but are expensive, need special equipment and expertise and are not widely available in developing countries. In addition, these tests have limited predictive values to identify those patients who will develop overt tuberculosis [12-23]. IFN-γ release assay (IGRAs) measure only IFN-γ production, a T helper 1 response, so it remains possible that positive TST results might capture an immune response in truly infected individuals that are missed by the IFN-γ release assay [14].

In the absence of a gold standard test for LTBI, we took LTBI point prevalence as an objective measure of LTBI. In our study, IFN-γ release assays were more frequently positive in HHCs than the TST, a result that may indicate a better sensitivity. These data are in agreement with previous studies that reported that IFN-γ release assay is better than TST in detecting individuals with LTBI [12-22]. Lowering the TST induration to ≥ 5 mm gave an LBTI point prevalence that is comparable to IFN-γ release assay test in previous reports [20-22].

Low correlation between TST and IFN-γ release assay has been reported in this study as well as in many other studies [19,21,22]. On the other hand, many other studies have reported moderate to strong positive correlation between the TST and IFN-γ release assay tests. These later studies presented TST as the least cost-effective, while others reported that TST followed by IGRA as highly cost effective [22,24-26]. It is worth mentioning that a study from South Africa suggested that TST was more effective in identifying LTBI than three generations of a whole blood IFN-γ release assay tests in countries with high TB burden [27]. Park and colleagues found that the cost effectiveness of the different testing strategies for LTBI was very variable especially between tests reagents [28]. The cost of QFT (IGRA) per person was reported to be between $20 and $30, while that of TST was ~ $5. In our setting, the cost of the TST process and IGRA were calculated at around $2 and $20 respectively, cheaper than that reported elsewhere. The cost of individuals having to come back for TST reading can easily be offset by the comparatively high cost of the IGRA tests. TST and IGRA were shown to have moderate agreement in the study population, presenting it as a cheaper alternative when cost constitutes a limitation for TB control programs in developing countries [29,30].

This study showed that IGRA positivity and TST reactivity were associated with close exposure to index cases (IC) as evidenced by the significant differences in reactivity of IFN-γ release tests/TST among HHCs and CCs. These results are concordant with previous reports. The low prevalence of LTBI among CCs probably indicates lower than national average prevalence of TB in the study area. Sudan is a vast country and prevalence rates vary considerably between different counties [1].

In the absence of a gold standard test for the diagnosis of LTBI, developing countries with high burden of TB have been relying on TST to diagnose LTBI especially in children, where treatment of LTBI diagnosed by TST has been shown to reduce the risk of progression to active TB by 60-90% [31,32].

In this study IFN-γ release test results gave a high LTBI point prevalence that is comparable to that reported from India and Ethiopia [33,34].

Purified Protein Derivative (PPD) gave similar results to ESAT-6/CFP-10 ± TB7.7 in whole blood IFN-γ release assay, with an almost perfect degree of agreement, making it a cheap alternative to recombinant antigens. This is in concordance with previous reports by Brock and colleagues [32] where they reported comparable levels of sensitivities for the QuantiFERON-TB test based on M. tuberculosis-PPD and that based on ESAT-6 or CFP-10 antigens. These findings can markedly reduce the high cost of IFN-γ-release assay tests. However we didn’t find a significant difference in terms of PPD IFN-γ whole blood assays levels between HHCs and CCs, which may imply a significant overlap between the values in these BCG-vaccinated populations due to lower specificity of PPD.

Conclusion

IFN-γ release assay (IGRA) using PPD or ESAT-6/CFP-10 give higher LTBI point prevalence compared to TST, which may indicate better sensitivity but the high cost of IGRA could be a concern for some developing countries. Although a less specific test, Purified Protein Derivative (PPD) gave comparable results to ESAT-6/CFP-10 ± TB7.7 in whole blood IFN-γ release assay, making it a cheap alternative to recombinant antigens.

Abbreviations

LTBI: Latent TB Infection; TST: Tuberculin skin test; IFN-γ: Interferon-gamma; IGRA: Interferon gamma release assay.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

AOS, EAG conceived and wrote the study proposal, prepared the necessary scientific and ethics approvals and contributed to volunteers’ recruitment, TST testing and wrote the manuscript. KAM, AOS carried the blood collections and the immunological tests. AMM, AAB, AHA, FMI & AME were involved in volunteers’ recruitment, care and follow-up, participated in manuscript writing and revision. All authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2458/13/1128/prepub

Contributor Information

Amani Osman Shakak, Email: amaniosman@hotmail.com.

Eltahir Awad Gasim Khalil, Email: eltahirgasim@yahoo.ca.

Ahmed Mudawi Musa, Email: musaam2003@yahoo.co.uk.

Kawthar Abd Eljalil Mohamed Salih, Email: kawthar_80@hotmail.com.

Abd Elgadir Ali Bashir, Email: abdelgadir50@yahoo.com.

Ala Hassan Ahmed, Email: drahahmed@hotmail.com.

Fath Elrahman Mohamed Idris, Email: drfidris@hotmail.com.

Ahmed Mohamed Elhassan, Email: ahmedelhassan85@gmail.com.

Acknowledgment

The investigating team would like to thank the administrations of the Faculty of Medicine, University of Shendi and the Department of Clinical Pathology & Immunology, Institute of Endemic Diseases, University of Khartoum for provision of logistic and financial supports.

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