Studies of Tuberculosis (TB) case contacts are increasingly being utilised for understanding the relationship between M. tuberculosis and the human host and for assessing new interventions and diagnostic tests. We aimed to identify the incidence rate of new TB cases among TB contacts and to relate this to their initial Mantoux and ELISPOT test results.
Methods and Findings
After initial Mantoux and ELISPOT tests and exclusion of co-prevalent TB cases, we followed 2348 household contacts of sputum smear positive TB cases. We visited them at 3 months, 6 months, 12 months, 18 months and 24 months, and investigated those with symptoms consistent with TB. Those who were diagnosed separately at a government clinic had a chest x-ray. Twenty six contacts were diagnosed with definite TB over 4312 person years of follow-up (Incidence rate 603/100,000 person years; 95% Confidence Interval, 370–830). Nine index and secondary case pairs had cultured isolates available for genotyping. Of these, 6 pairs were concordant and 3 were discordant. 2.5% of non-progressors were HIV positive compared to 12% of progressors (HR 6.2; 95% CI 1.7–22.5; p = 0.010). 25 secondary cases had initial Mantoux results, 14 (56%) were positive ; 21 had initial ELISPOT results, 11 (52%) were positive; 15 (71%) of 21 tested were positive by one or the other test. Of the 6 contacts who had concordant isolates with their respective index case, 4 (67%) were Mantoux positive at recruitment, 3 (50%) were ELISPOT positive; 5 (83%) were positive by one or other of the two tests. ELISPOT positive contacts, and those with discordant results, had a similar rate of progression to those who were Mantoux positive. Those negative on either or both tests had the lowest rate of progression.
The incidence rate of TB disease in Gambian TB case contacts, after screening for co-prevalent cases, was 603/100,000 person years. Since initial ELISPOT test and Mantoux tests were each positive in only just over half of cases, but 71% were positive by one or other test, positivity by either might be the best indication for preventive treatment. These data do not support the replacement of the Mantoux test by an ELISPOT test in The Gambia or similar settings.
Citation: Hill PC, Jackson-Sillah DJ, Fox A, Brookes RH, de Jong BC, Lugos MD, et al. (2008) Incidence of Tuberculosis and the Predictive Value of ELISPOT and Mantoux Tests in Gambian Case Contacts. PLoS ONE 3(1): e1379. https://doi.org/10.1371/journal.pone.0001379
Academic Editor: Landon Myer, University of Cape Town, South Africa
Received: September 17, 2007; Accepted: November 23, 2007; Published: January 2, 2008
Copyright: © 2008 Hill 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 study was funded by the Medical Research Council (UK) and the European Commission. Neither funder had any role in conducting the study or preparing the manuscript.
Competing interests: RHB has a patent relating to ex vivo ELISPOT licensed through Oxford University. There are no other conflicts of interest.
Household contacts of tuberculosis (TB) cases have a relatively high prevalence of TB disease when screened  and a higher incidence rate of TB disease than the general population in the first years after exposure, the rate varying across different locations and populations–. It is likely that contacts of known TB cases contribute greatly to the overall TB disease burden in certain settings. For example, in West Africa, up to 45% of newly diagnosed TB cases have a known TB contact , . TB case contact studies are being engaged increasingly as platforms for studying TB and have potential in relation to the assessment of new diagnostic tests and interventions, including vaccines. However, more needs to be known about the epidemiology of TB in case contacts to assist in the planning and implementation of such studies.
Cross-sectional studies have suggested promise for interferon-gamma T cell based tests in the diagnosis M. tuberculosis infection and TB disease–. However, longitudinal studies suggest caution , , especially in interpreting a result when there is no known recent TB contact. Furthermore, it is not known what proportion of those who are TB case contacts, and become cases themselves, have a positive test from an initial screen. Recently, the British National Institute for Health and Clinical Excellence (NICE) published recommendations suggesting that the traditional Mantoux skin test and an interferon-gamma test be used in a two-step manner – the Mantoux test as a screening tool and an interferon-gamma test as confirmation . The evidence to support such an approach is lacking.
In this study we followed a large number of TB case contacts for the development of TB disease and related their initial Mantoux and ELISPOT test results to the likelihood of progression to TB disease.
Materials and Methods
Between June 2002 and October 2004, TB cases and their household contacts were enrolled in a prospective cohort study in the Greater Banjul region of The Gambia, West Africa. We recruited, from the major government TB clinic and the Medical Research Council (MRC) outpatients' clinic, sputum smear positive pulmonary TB cases aged at least 15 years old, who had at least one household contact living with them. An index case was defined as the first TB case identified in a household. Household contacts were defined as individuals at least 6 months of age living the majority of the time on the same compound as the respective index TB case, sharing meals and identifying a common household head. Written informed consent was obtained from all adults in the study and parents/guardians of children under 15 years of age. The study was approved by the combined Gambia Government/MRC National Ethics Committee of The Gambia.
At the time of recruitment, contacts were interviewed and immediately afterwards had a blood sample taken for ELISPOT and HIV test, followed by a Mantoux test (2 Tuberculin Units [TU], PPD RT23 Statens Serum Institut, http:/www.ssi.dk). A maximum of 12 contacts had an ELISPOT test per day, others were randomly excluded. Those with symptoms, or a positive Mantoux test, were investigated for TB. The current policy in The Gambia is not to give Mantoux positive individuals preventive therapy. A co-prevalent TB case was defined as a household contact diagnosed with TB who had symptoms that commenced within 2 months of the recruitment of the respective index case. The results of the initial screening, yielding 33 co-prevalent cases, have been published elsewhere. We performed five follow-up visits (at 3, 6, 12, 18 and 24 months after recruitment) to each household and referred those with symptoms to the MRC TB clinic. All study participants had free access to the MRC TB clinic for treatment for any illness during this period. Any patients with symptoms of pulmonary disease received a chest X-ray and sputum analysis for AFB smear analysis and culture. If TB disease was bacteriologically confirmed, or clinically suspected in smear-negative or extra-pulmonary cases, patients were referred for a free standard six month TB treatment course to the Gambian National TB Treatment program. For those contacts who died, we designed a modified verbal autopsy form, focused on TB symptoms. This was administered by a trained field worker to family members and interpreted by clinicians.
Secondary Case definition
All contacts with symptoms, consistent with TB, that commenced at least 2 months after their respective index case was diagnossed, or with a positive Mantoux test (at least 10 mm of induration) at any follow-up time point, were considered to be possible secondary TB cases. They were asked to have a chest X-ray and provide sputum if they had a productive cough. All those initially Mantoux negative at recruitment were asked to have a repeat Mantoux test at 3 months. Those that were Mantoux positive were offered a chest X-ray. A diagnosis of a secondary TB case was based on the chest X-ray and sputum smear and culture results, and/or their response to a course of TB treatment if a trial of therapy had been considered appropriate. They were classified as having pulmonary or extra-pulmonary disease by consensus of two infectious diseases physicians and one paediatrician specialised in the diagnosis and management of TB cases.
An alternative strategy was devised with respect to those contacts who sought a diagnosis only at a government clinic, where sputum culture was not available. Names and ages of all TB cases treated at the government health clinics during the course of the study were recorded. Those that matched with contacts participating in our study, using an age category matching within 5 years, were re-visited to confirm whether they had had TB treatment or not. Those that confirmed having taken treatment, were asked to have a chest X-ray. Each radiograph was reviewed by the two infectious diseases physicians, and/or pediatrician when the participant was a child. After review, a consensus opinion regarding the diagnosis of a secondary TB case was formed . Those with no evidence of TB on chest X-ray were defined as ‘not definite’.
Sputum samples were prepared for smear using auramine-phenol, and cultured using Lowenstein-Jensen medium and the BACTEC 9000 MB system (Becton Dickinson) for identification of M. tuberculosis, as previously described. For molecular subtyping of index case isolates, we extracted mycobacterial DNA using CTAB and chloroform. We performed spoligotyping using membranes from Isogen Biosciences (http:/www.isogen-lifescience.com), as previously described. When the isolate of an index case and the isolate of a diseased contact from the same household shared the same spoligotype pattern (genotype), these were referred to as concordant genotypes. Isolates that shared the same spoligotype pattern except for one of 43 spacers, were also classified as concordant genotypes. All others were classified as discordant genotypes.
The ex-vivo ELISPOT assays for IFN-γ were performed on fresh samples onsite as previously described. Pooled sequential 15-mer peptides, overlapping by 10 amino-acid residues, of ESAT-6 and CFP-10 proteins (ABC, Imperial College, London, UK) were used as stimulatory antigens at 5 µg/ml. The positive control was phytohaemaglutinin (PHA; Sigma-Aldrich, UK). All antigens were tested in duplicate wells. Assays were scored by an ELISPOT counter (AID-GmbH, Strassberg, Germany). Positive test wells were pre-defined as containing at least eight spot forming units (SFU) more than negative control wells. For a positive ESAT-6/CFP-10 result it was necessary for at least one of the pools of overlapping peptides to be positive. PHA wells were set to at least 150 SFU/well/2×105 above negative control wells. Negative control wells were required to have less than 20 SFU. These criteria are the same as we have previously documented and are more stringent than those recommended for the commercial T-spot assay.
Testing for HIV-1 and HIV-2 infection was by competitive ELISA (Wellcome Laboratories, Dartford, Kent, Uk) and Western blot (Diagnostics Pasteur, http:/www.sanofipasteur.com) as previously described. Those individuals who tested positive were referred to the onsite MRC HIV clinic for clinical care and follow-up, being eligible for consideration for free anti-retroviral therapy according to set criteria.
Data management and statistical analysis
The number of SFU in each ELISPOT well were automatically entered into a database. All other data were entered using double data entry into an ACCESS database and checked for errors. We used Cox proportional hazards regression to assess the relationship between risk factors and rate of progression to disease in TB contacts, having confirmed non-violation of the proportional hazards assumption. Results were reported as unadjusted and adjusted hazard ratios (HR) and their 95% confidence intervals (CI). All statistical analyses were conducted using Stata software (version 8; Stata Corp, http://www.statacom).
Of the 2381 contacts of 317 sputum smear and culture positive TB cases, 33 were excluded from follow-up, having been identified as co-prevalent cases. Figure 1 shows the numbers of contacts assessed at each of the five follow-up points over 2 years: 24 died and 191 were lost to the study through migration out of the study area; 82–93% of those resident at each time point were assessed for symptoms of TB. Twenty six contacts were diagnosed with as secondary TB cases over 4312 person years of follow-up. A further 6 contacts were treated for TB but the diagnosis was considered not definite. Of the 24 who died duriing follow-up: four were HIV positive, two of whom had been a TB suspect but had normal chest X-rays; 11 clearly died of a non-TB cause; five had some history on verbal autopsy suspicious for TB, four of these had been investigated during follow-up and had normal investigations; and a verbal autopsy was not possible for four.
Figure 2 shows the period from enrolment to the time when the contact first became a TB suspect: 14 were diagnosed in the first 6 months after the co-prevalent window period, the other 12 were distributed over the next 17 months. Table 1 shows the characteristics of those who progressed to disease versus those who did not. Progressors had a similar gender and ethnicity split than those who did not progress. Interestingly there was not a strong relationship with sleeping proximity to a TB case. As expected, while only 2.5% of non-progressors were HIV positive, 12% (3 of 24) progressors were HIV positive at recruitment. This difference was significant in the univariable (HR 6.0; 95% CI 1.8–20.0; p = 0.020) and multivariable analysis (HR 6.2; 95% CI 1.7–22.5; p = 0.010), and accounted for some of the age difference between progressors and non-progressors. No information was available regarding the level of immunosuppression of the HIV positive progressors. BCG scar was not significantly associated with protection against progression to disease.
Table 2 provides details of each individual TB secondary case in relation to their recruitment Mantoux and ELISPOT results. At recruitment, 14 (56%) of 25 that were tested, and later diagnosed as cases, were Mantoux positive; 11 (52%) of 21 tested were ELISPOT positive; and 15 (71%) of 21 tested were positive by one or the other of the two tests. The agreement, in the secondary cases, between the two tests at recruitment was 61.9% (kappa = 0.24). Nine index case and secondary case pairs had cultured isolates available for molecular genotyping. Of these, 6 pairs were concordant and 3 were discordant. Of the 6 contacts who had concordant isolates with their respective index case, 4 (67%) were Mantoux positive at recruitment, 3 (50%) were ELISPOT positive and 5 (83%) were positive by one or other of the two tests.
Table 3 shows the incidence rate of progression to disease according to recruitment Mantoux and ELISPOT results. Those contacts who were ELISPOT positive and those who were ELISPOT negative at recruitment had a similar rate of progression to disease as those who were Mantoux postive and negative respectively. Those negative on either or both tests had the lowest incidence rate of progression. Of note, those with discordant results had a similar rate of progression to those who were positive on either test. Taking into consideration the 21 cases with ELISPOT and Mantoux results at recruitment in relation to current international guidelines for preventive therapy: 15 would have been captured by accepting a positive result on one or both tests, 11 would have been captured by either the Mantoux or ELISPOT test, but only 7 would have been captured by a requirement to be positive on both tests–over half (8 of 15) that were intially positve by either test had discordant results at recruitment. Using Cox regression modelling, the crude and adjusted Hazard ratios for a positive test in relation to becoming a secondary case were: 1.9 (95% CI: 1.0–4.7) and 1.8 (95% CI 0.8–4.1) respectively for the Mantoux test and 1.9 (0.8–4.5) and 1.8 (0.8–4.2) for the ELISPOT test.
After an initial screen for co-prevalent disease, we actively followed over 2000 household contacts of sputum smear positive TB cases for a total of 4312 person years. Twenty-six secondary cases were identified, giving an incidence rate of 603/100,000 person years. HIV positivity, despite a low prevalence in this population, was the one significant risk factor for progression to TB disease. We were able to calculate the incidence rates of secondary disease in relation to initial Mantoux and ELISPOT results and to show how many secondary cases were ‘captured’ by a positive test. Only 15 (71%) of the 21 secondary cases with recruitment results were positive on either test. Furthermore 4 Mantoux positive secondary cases were ELISPOT negative and 4 ELISPOT positive secondary cases were Mantoux negative. The results of this study have implications for the design of trials of new interventions, particularly vaccines, in Africa, and the revision of current guidelines for TB control.
The 33 (1.5%) co-prevalent cases and the 26 secondary cases identified in this study population can be compared with the number identified in other TB case contact studies, although few have presented incidence rates of secondary disease - which can only be calculated when the total person time of follow-up is known. Guwatudde et al  conducted a case contact study in Uganda, following 1206 contacts of 423 TB cases for 2 years. As in our study, over half of the TB cases in these African TB contacts were found at an initial screen - they identified 51 (4.2%) co-prevalent cases and 25 secondary cases. The median age of the secondary cases was 31 years and 13 (52%) were HIV positive. The higher rate of HIV positivity compared to our study explains a large part of the higher prevalence of cases at screening and the larger relative number of secondary cases at follow-up. Furthermore, a higher proportion (66% vs 38%) of the Ugandan contacts were Mantoux positive at recruitment, suggesting a higher background rate of M. tuberculosis infection. Egsmose et al , as part of a study in rural Kenya, found that 17 (4.3%) of 392 TB case contacts became ‘tubercle bacilli excretor’ TB cases within one year, after exclusion of those diagnosed with TB before enrolment. Puffer et al  followed 1358 household contacts of 298 ‘sputum positive’ American TB cases in the 1940s for 8754 person years and identified 30 cases of clinical TB: the overall attack rate of clinical TB was 690/100,000 person years. Ferebee et al  found 479 (1.9%) cases of TB in 25,512 American household contacts of TB cases (not limited to sputum smear positive cases) in the 1950s. Of the remaining contacts 12,594 were assigned not to receive isoniazid: in this group, 107 (0.8%) secondary cases were identified over one year of follow-up; 62 of these had pulmonary disease.
It is possible that we have underestimated the true number of secondary cases in this study. Some of those who died may have had TB, although this appeared unlikely in most from the verbal autopsies. We also excluded some of those who had undergone TB treatment, because they did not meet our criteria for diagnosis. Some of these individuals may well have had TB disease. We have also shown that some cases preferentially access the government clinic for diagnosis in The Gambia, even with free access to the MRC study clinic. While we are confident that we have captured those that were diagnosed at the government clinic, we suspect strongly that stigma is a significant impediment to the acknowledgement of both symptoms and to seeking a TB diagnosis and treatment in The Gambia and many other African settings. Furthermore, as identified by Guwatudde et al, the limitations of current diagnostic tools make an underestimation of the true number of secondary cases possible, especially in relation to the difficult diagnosis of TB in children. Under-diagnosis of secondary TB in children would lead to a selection bias, if present, and has implications for the interpretation of age as a predictor of progression to disease.
This study sheds new light on the appropriateness of major TB guidelines, in particular the NICE guidelines – the results do not support the two-step appraoch that is advocated, at least in settings such as The Gambia. Using such an approach, only seven of the 21 progressors in our study, that were initially tested by both tests, would have been eligible for preventive treatment. This compares to 15 who were positive on one or other test. These results were consistent with those obtained when considering only the initial results of those six contacts with an isolate concordant by genotyping with that of their respective index case. Few data from other studies are available to shed more light on this issue. In a retrospective study of practice in 120 child TB suspects in Newcastle, Taylor et al identified 5 TB cases: 4 had a positive Mantoux test at the beginning of the investigations, 3 had a positive Quantiferon T cell assay test. This, together with the results presented here, suggest caution in the application of the NICE guidelines.
One might consider, as an alternative strategy, preventive treatment for those who are positive on either test. A possible approach would be to treat all those who are Mantoux positive, then perform a T cell based test on those who are Mantoux negative, treating those with a positive result. Thus, instead of testing all Mantoux positive individuals with a T cell assay as is recommended, one would test all Mantoux negative individuals. These issues can be considered in terms of numbers needed to treat to prevent one TB case. From our results, 60 Mantoux positive contacts need to be treated to prevent a case, compared to 59 ELISPOT positive contacts and 90 contacts overall (ie. regardless of test result). Taking those positive by skin test plus those skin test negative contacts that are ELISPOT positve, 56 would need to be treated to prevent one TB case. These calculations assume 100% efficacy of prophylactic treatment, which would be expected to be less than 90% in reality .
It would be important to consider repeating each test in those initially negative as we have previously shown that some who later become cases, converted to a positive test 3 months after the initial screen . Furthermore, it is of note that even those TB case contacts that were both Mantoux and ELISPOT negative had an incidence rate of secondary disease of 400/100,000 person years. This compares to the incidence rate of all cases of TB of 242/100,000 per year for the whole Gambian population (http://www.who.int/globalatlas/predefinedreports/tb/PDF_Files/gmb.pdf), regardless of Mantoux and/or ELISPOT status prior to progression to disease. One could therefore make a case, in making policy for prophylactic treatment, for treating all those who have a known contact with a sputum smear positive TB case in The Gambia and similar settings. International guidelines presently suggest such a strategy only in Mantoux negative individuals with a particular susceptibility to develop TB disease. Of relevance to The Gambia and other African countries in particular, HIV positive individuals cleary fall into this category.
The results of the molecular genotyping provide insights into the TB case contact model as a platform for TB research in The Gambia: six (67%) of the nine pairs of index cases and secondary cases with isolates available were concordant. Therefore, the other three secondary cases acquired their M. tuberculosis from someone other than their respective index case, most probably from outside their household. The mix of intra- and extra- household transmission likely varies according to the degree of TB endemnicity in the general population. In highly endemic suburbs of Capetown, South Africa, for example, isolates match on molecular subtyping in less than half (46%) of households with two TB patients, and the authors estimated that only 19% of M. tuberculosis transmission occurs within households . Therefore, one should be cautious when interpreting findings from TB case contact studies, taking into account the level of community transmission outside households and molecular genotyping on index case and secondary case isolates should be performed when possible.
This results of this study have implications for research, clinical and public health practice. The incidence rate that we have documented here can form a guide for those choosing to use a TB case contact study platform for research. While approximately 5 to 6% of Mantoux or ELISPOT positive TB case contacts develop TB within 2 years in The Gambia, the majority are already cases at initial screening and it is clear that multi-site studies, with a higher overall case yield, may be needed to answer certain research questions. Such consortia are already being established. For example a Gates Grand Challenge project across multiple African sites utilises a TB case contact study model. Two key conclusions can be drawn from the ELISPOT and Mantoux test results. Firstly, it seems that certain individuals respond preferentially to one or the other test, at least in the early stages of M. tuberculosis infection. This may be due to varying incubation periods, as we have indicated previously, or there may be a more fundamental immunological basis. Thus, both tests may be best used together at an initial screen – perhaps to test first with Mantoux and all those that are negative with ELISPOT-this takes advantage of the likelihood that ELISPOT is probably not subject to the booster phenomenon. Secondly, where contact with an index case continues throughout treatment and conversion of both the Mantoux and ELISPOT tests occur over time, repeated testing should be considered. At a wider public health policy level, these results do not support replacement of the Mantoux test with a T cell based test for the diagnosis of TB infection, at least in settings such as The Gambia.
We thank the study participants for their involvement in this study and our field and laboratory assistants for their hard work.
Conceived and designed the experiments: PH AF RA KM TC RB SD. Performed the experiments: PH AF ML SH TC RB DJ IA AA BD. Analyzed the data: DJ PH AF ML SH RB SD IA AA BD. Wrote the paper: DJ PH RA KM. Other: Enrolled patients: PH. Wrote the first draft of the paper: PH.
- 1. Jackson-Sillah D, Hill PC, Fox A, Brookes RH, Donkor SA, et al. (2007) Screening for tuberculosis among 2381 household contacts of sputum-smear-positive cases in The Gambia. Trans R Soc Trop Med Hyg 101: 594–601.
- 2. Guwatudde D, Nakakeeto M, Jones-Lopez EC, Maganda A, Chiunda A, et al. (2003) Tuberculosis in household contacts of infectious cases in Kampala, Uganda. Am J Epidemiol 158: 887–898.
- 3. Egsmose T, Ang'awa JO, Poti SJ (1965) The use of isoniazid among household contacts of open cases of pulmonary tuberculosis. Bull World Health Organ 33: 419–433.
- 4. Puffer RR, Zeidberg LD, Dillon A, Gass RS, Hutcheson RH (1952) Tuberculosis attack and death rates of household associates; the influence of age, sex, race, and relationship. Am Rev Tuberc 65: 111–127.
- 5. Ferebee SH, Mount FW (1962) Tuberculosis morbidity in a controlled trial of the prophylactic use of isoniazid among household contacts. Am Rev Respir Dis 85: 490–510.
- 6. Lienhardt C, Fielding K, Sillah JS, Bah B, Gustafson P, et al. (2005) Investigation of the risk factors for tuberculosis: a case-control study in three countries in West Africa. Int J Epidemiol 34: 914–923.
- 7. Hill PC, Jackson-Sillah DJ, Donkor SA, Otu J, Adegbola RA, et al. (2006) Risk factors for tuberculosis: a clinic-based case control study in The Gambia. BMC Public Health 6: 156.
- 8. Ewer K, Deeks J, Alvarez L, Bryant G, Waller S, et al. (2003) Comparison of T-cell-based assay with tuberculin skin test for diagnosis of Mycobacterium tuberculosis infection in a school tuberculosis outbreak. Lancet 361: 1168–1173.
- 9. Mazurek GH, LoBue PA, Daley CL, Bernardo J, Lardizabal AA, et al. (2001) Comparison of a whole-blood interferon gamma assay with tuberculin skin testing for detecting latent Mycobacterium tuberculosis infection. JAMA 286: 1740–1747.
- 10. Pai M, Gokhale K, Joshi R, Dogra S, Kalantri S, et al. (2005) Mycobacterium tuberculosis infection in health care workers in rural India: comparison of a whole-blood interferon gamma assay with tuberculin skin testing. JAMA 293: 2746–2755.
- 11. Hill PC, Brookes RH, Fox A, Fielding K, Jeffries DJ, et al. (2004) Large-scale evaluation of enzyme-linked immunospot assay and skin test for diagnosis of Mycobacterium tuberculosis infection against a gradient of exposure in The Gambia. Clin Infect Dis 38: 966–973.
- 12. Hill PC, Brookes RH, Adetifa IM, Fox A, Jackson-Sillah D, et al. (2006) Comparison of enzyme-linked immunospot assay and tuberculin skin test in healthy children exposed to Mycobacterium tuberculosis. Pediatrics 117: 1542–1548.
- 13. Ewer K, Millington KA, Deeks JJ, Alvarez L, Bryant G, et al. (2006) Dynamic Antigen-specific T-Cell Responses after Point-Source Exposure to Mycobacterium tuberculosis. Am J Respir Crit Care Med 174: 831–839.
- 14. Pai M, Joshi R, Dogra S, Mendiratta DK, Narang P, et al. (2006) Serial testing of health care workers for tuberculosis using interferon-gamma assay. Am J Respir Crit Care Med 174: 349–355.
- 15. 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 Med 4: e192.
- 16. Tuberculosis: clinical diagnosis and management of tuberculosis, and measures for its prevention and control (2006). London: National Institute for Health and Clinical Excellence. Clinical Guideline 33.
- 17. Adegbola RA, Hill P, Baldeh I, Otu J, Sarr R, et al. (2003) Surveillance of drug-resistant Mycobacterium tuberculosis in The Gambia. Int J Tuberc Lung Dis 7: 390–393.
- 18. van Embden JD, Cave MD, Crawford JT, Dale JW, Eisenach KD, et al. (1993) Strain identification of Mycobacterium tuberculosis by DNA fingerprinting: recommendations for a standardized methodology. J Clin Microbiol 31: 406–409.
- 19. Kamerbeek J, Schouls L, Kolk A, van Agterveld M, van Soolingen D, et al. (1997) Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol 35: 907–914.
- 20. Jeffries DJ, Hill PC, Fox A, Lugos M, Jackson-Sillah DJ, et al. (2006) Identifying ELISPOT and skin test cut-offs for diagnosis of Mycobacterium tuberculosis infection in The Gambia. Int J Tuberc Lung Dis 10: 192–198.
- 21. Ferrara G, Losi M, D'Amico R, Roversi P, Piro R, et al. (2006) Use in routine clinical practice of two commercial blood tests for diagnosis of infection with Mycobacterium tuberculosis: a prospective study. Lancet 367: 1328–1334.
- 22. Schim van der Loeff MF, Sarge-Njie R, Ceesay S, Awasana AA, Jaye P, et al. (2003) Regional differences in HIV trends in The Gambia: results from sentinel surveillance among pregnant women. AIDS 17: 1841–1846.
- 23. Jeffries DJ, Donkor S, Brookes RH, Fox A, Hill PC (2004) Design and implementation of relational databases relevant to the diverse needs of a tuberculosis case contact study in the Gambia. Int J Tuberc Lung Dis 8: 1095–1099.
- 24. Taylor RE, Cant AJ, Clark JE (2007) Potential impact of NICE tuberculosis guidelines in paediatric TB screening. Arch Dis Child (In press).
- 25. Ferebee SH (1970) Controlled chemoprophylaxis trials in tuberculosis. A general review. Bibl Tuberc 26: 28–106.
- 26. (2005) Guidelines for the investigation of contacts of persons with infectious tuberculosis. Recommendations from the National Tuberculosis Controllers Association and CDC. MMWR Recomm Rep 54: 1–47.
- 27. Verver S, Warren RM, Munch Z, Richardson M, van der Spuy GD, et al. (2004) Proportion of tuberculosis transmission that takes place in households in a high-incidence area. Lancet 363: 212–214.
- 28. Kaufmann SH, Parida SK (2007) Changing funding patterns in tuberculosis. Nat Med 13: 299–303.
- 29. Hill PC, Jeffries DJ, Brookes RH, Fox A, Jackson-Sillah D, et al. (2007) Using ELISPOT to expose false positive skin test conversion in tuberculosis contacts. PLoS ONE 2: e183.