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The need for better diagnostics for TB has been repeated so frequently that there is a danger of message fatigue. However, the unfortunate return of TB as the number 1 cause of death due to an infectious disease must surely serve as a further call to action for researchers, clinicians and funders to redouble our efforts.1 The fundamental issues with TB diagnosis deserve repeating: standard diagnosis of pulmonary TB relies primarily on sputum smear tests, which have limited sensitivity and specificity, and have not significantly changed for over 100 years.2 Recent data show that staining for acid-fast bacilli remains the most commonly used diagnostic method globally.3 The development of interferon-gamma release assays (IGRAs) and molecular amplification tests such as Xpert MTB/RIF assays has improved the landscape somewhat, but both are critically limited by cost and the need for extensive infrastructure. In addition, IGRAs do not distinguish latent from active TB, have limited robustness and perform worse in children than in adults.4–6 Recent data suggest that the roll-out and scale-up of the Xpert MTB/RIF assays in resource-limited settings have been far slower than anticipated.7 Importantly, molecular assays require relatively high numbers of bacilli to achieve adequate sensitivity. The diagnosis of extrapulmonary TB is often more challenging than pulmonary TB, frequently with low bacterial loads in difficult-to-access locations. Therefore, the majority of TB diagnoses still rely on smear and culture results of specimens taken by the least invasive route, and considerable clinical acumen is often required to determine the likelihood of TB in the face of negative culture results. Data from a recent global survey suggest that microbiologists and clinicians managing patients with TB require better diagnostic tests for TB to be developed, highlighting the significant limitations of existing tests.3
On this background, the study of Wang et al 8 published in Thorax provides a welcome addition to the literature on TB diagnosis. The group built on their previous observations that interleukin-27 (IL-27) may be a novel diagnostic marker of pleural TB, and also studied interferon-γ (IFN-γ) and adenosine deaminase (ADA) in patients with tuberculous and non-tuberculous pleural effusions. They then studied IL-27 in a second cohort before proceeding to a meta-analysis. They report excellent test performance with a specified cut-off value, finding IL-27 more accurate than ADA and equivalent to IFN-γ. Combination of IL-27 and ADA improved specificity, but at the expense of sensitivity. The authors conclude that in high TB prevalence settings, IL-27 could be used as a rule-in test to diagnose pleural TB and in low prevalence settings as a rule-out test. These findings potentially warrant further development.
The diagnosis of pleural TB has historically been difficult, in part due to the pathophysiology of the disease. Advanced pulmonary TB is characterised by tissue destruction, hypoxia and cavitation,9 with high bacterial loads within the cavity wall,10 whereas pleural TB has a relatively low bacterial load with extensive fluid collection.11 Consequently, pleural fluid culture is positive in fewer than 50% of cases.12 Previous gold standard diagnosis has centred on pleural biopsies, as histology showing granulomas on the pleural surface has greater specificity and sensitivity than pleural fluid microscopy and culture. However, pleural biopsy with Abrams needle has become an uncommon investigation, in part due to the low incidence of TB in high-resource countries, and many clinicians with access to thoracic surgery proceed directly to video-assisted thoracoscopic surgery to obtain diagnostic tissue. ADA, an enzyme used as a marker of T cell activation, showed initial promise as a novel diagnostic for pleural TB,13 but is not widely used in routine clinical practice in many countries.
The study by Wang et al inevitably raises further questions. First, the correct cut-off for IL-27 needs to be determined, as their meta-analysis included studies with concentrations ranging from 391 to 1007 ng/mL as diagnostic of pleural TB. Second, the utility of IL-27 will depend on the pretest probability, which itself results from the local TB epidemiology, and therefore the findings from high-incidence settings may not translate to lower incidence settings. Third, the difference between IL-27 and IFN-γ is not so striking that it is clear which should go forward as the optimal diagnostic test. Since IFN-γ is the read-out of IGRAs, this may drive more rapid development of next-generation IFN-γ assays to accurately measure concentrations, which would provide an advantage in investigating this analyte further. Finally, cytokine testing is not routinely performed even in major clinical service laboratories, unlike other analytes such as C reactive protein and albumin. Analysis of IFN-γ from QuantiFERON assays is usually batched for weekly analysis in most centres, as the number of tests does not justify daily analytical runs, and so how an occasional assay for IL-27 would be performed in laboratories in high-income settings is uncertain. In low-income settings, it seems even more unlikely that such tests will become routinely available without major advances in assay technology.
A further limitation of the approach described by Wang et al is that it requires thoracentesis, which is invasive compared with assays based on blood, saliva or urine. Unfortunately, Wang et al found that IL-27 concentrations in serum did not differ between patients with TB and the control patients with malignant or parapneumonic effusion in their study. Also, their approach would only be useful in a small proportion of patients with TB, as patients with isolated pleural TB constitute only 5%–10% of the total TB caseload in most settings.14 Therefore, how IL-27 as a novel diagnostic marker will move forward remains an open question. As an emerging diagnostic analyte, it faces precisely the same challenges as other putative biomarkers of TB, such as mass spectrometry or aptamer-identified biomarkers,15 16 matrix degradation products,17 or Mycobacterium tuberculosis-specific cytokine responses in blood,18 which have shown promise in individual studies but need development and further validation.
Ultimately, the goal for the TB diagnostic field must remain to achieve the criteria previously outlined for an ideal TB test: available at the point of care, cheap, stable in heat and humidity, requiring minimal training, no electricity and no reagents to be added.19 This represents a very high bar, and to date has remained elusive, but such an assay will be critical in accelerating the diagnosis of TB in high-incidence settings and therefore preventing transmission and containing the ongoing pandemic.20 The study by Wang et al is a step in the right direction, adding to the literature on potential emerging diagnostic biomarkers. The challenge is now to confirm the findings in further cohorts and develop novel analytical approaches that can move diagnostics based on emerging biomarkers from the research laboratory to the clinic.
Contributors MT and PTE wrote this editorial.
Funding Medical Research Council (grant no: MR/P023754/1).
Competing interests None declared.
Provenance and peer review Not commissioned; internally peer reviewed.
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