Predictive value of TNF-α, IFN-γ, and IL-10 for tuberculosis among recently exposed contacts in the United States and Canada

Tuberculosis (TB) is the leading infectious cause of death worldwide, with > 10 million new cases annually and 1.5 million deaths [1]. A better understanding of the immunologic and epidemiologic profiles associated with Mycobacterium tuberculosis infection and disease after TB exposure can help focus TB control efforts. Identification of surrogate markers of protective immunity against M. tuberculosis infection and TB disease can also aid development of new TB vaccines.

Immune responses among persons with TB disease have been the subject of multiple studies. Interferon-gamma (IFN-γ) and tumor necrosis factor alpha (TNF-α) are essential for protection against mycobacterial infections [2]. TNF-α response to M. tuberculosis antigens may be elevated and IFN-γ response depressed at the time of TB diagnosis, with a later decline in TNF-α and elevation of IFN-γ associated with successful resolution of disease [3‐5]. Further, an increase in TNF-α has been observed among persons with previously treated TB disease at the time of relapse [5]. Interleukin 10 (IL-10) may impair host resistance to M. tuberculosis infection [6]. IL-10 is known to be elevated early in the course of TB disease, and is believed to function as an inhibitor to regulate and help prevent the potentially destructive effects of an over vigorous immune response [7].

IFN-γ response is well established as an immune correlate of M. tuberculosis infection. A study from Uganda reported that elevation in IFN-γ responses are predictive of subsequent tuberculin skin test (TST) conversion in Bacillus Calmette-Guérin (BCG) vaccinated but not among unvaccinated household contacts [8]. Elevated IFN-γ response has been closely correlated with a positive TST and TB exposure intensity, and thus by inference, with latent M. tuberculosis infection [9‐13].

Evidence from recent studies reveals that IFN-γ responses can also be predictive of subsequent TB disease. In an intriguing study from Colombia, investigators observed a trend toward increased risk for TB disease among contacts with upper quartile elevations of IFN-γ [14]. In a study of contacts in Germany, a higher predictive value for TB was observed among contacts with positive IFN-γ release assays (IGRA) compared with TST [15]. In a cohort study in South Africa, IGRA conversion from negative to positive among adolescents was correlated with a positive predictive value (PPV) for subsequent TB disease of 2.8% [16, 17]. In a 2012 meta-analysis, positive IGRAs had a PPV for TB of 2.7% [18]. Longitudinal studies of exposed contacts have not had sufficient power to determine whether measurable differences in IFN-γ responses can predict which persons with latent TB infection will ultimately develop TB disease. Additionally, direct comparisons of IFN-γ profiles among persons with TB disease and those having latent TB infection are rare, and information on cytokine responses other than IFN-γ is limited. Recently, a transcriptomic signature of progression from latent to active TB with a sensitivity of 39–54% was reported [19].

We conducted a prospective study of contact investigations at health departments in the United States and Canada. We previously described rates, timing, and risk factors for TB disease among contacts [20, 21]. Here, we examine the immune response profiles of 3 cytokines believed to influence immunity to TB—TNF-α, IFN-γ, and IL-10—in the same contact cohort.

We prospectively enrolled culture-confirmed adult TB patients and their close contacts at 9 US and Canadian sites participating in the Tuberculosis Epidemiologic Studies Consortium [22] (see published Methods [20]). Contacts were identified, enrolled, interviewed, offered human immunodeficiency virus (HIV) testing, and screened for LTBI and TB from 2002 to 2006, then followed with TB registry matches performed annually for 4 years after last site enrollment at 8 sites and annually for 2 years at one site (final follow-up February 2011) [20]. Since enrollment occurred over a 4-year period, contacts enrolled earlier in the study had a longer tuberculosis registry match observation period, with 100% observed for at least 4 years and 94% for at least 5 years after exposure [20]. HIV prevalence in the parent study contact cohort was 2% [23]. While a standard protocol was used for conducting contact investigations, the staff at the study sites did not use a standard protocol for patient management, which included efforts to prevent secondary cases by investigation and treatment of contacts with LTBI [20]. Exposure hours were calculated by careful interview of both the index patient and each contact to determine hours per day, week, and month of shared indoor living space. These were then added over the course of the entire infectious period to determine the total number of exposure hours. The date of TB diagnosis was defined as the start date for TB treatment.

All health departments defined negative TSTs as < 5 mm and positive TSTs as > 5 mm induration. TST conversion was defined as a first TST < 5 mm and a subsequent TST > 5 mm.

Whole blood was collected in heparinized tubes at the study sites and shipped to Case Western Reserve University (Cleveland, Ohio) overnight at room temperature, then diluted 10-fold with RPMI-1640 medium and dispensed into 24-well tissue culture plates. Wells remained un-stimulated or they received M. tuberculosis (H37Rv) culture filtrate protein (CFP) (5 μg/mL) or phytohemagglutinin (PHA) (10 μg/mL). Cell-free supernatants were collected after 24-h (TNF-α) and 5-day (IFN-γ and IL-10) incubation at 37^o C with 5% CO₂ and stored frozen at –70^o C until use. TNF-α, IFN-γ, and IL-10 levels in thawed supernatants were assessed by using enzyme linked immunosorbent assay kits from Endogen, R&D Systems and Biosource, respectively. The lower limit of detection for the assays was < 2 pg/mL, < 5 pg/mL and <  0.2 pg/mL, respectively.

Epidemiologic characteristics and CFP-stimulated (CFPS) TNF-α, IFN-γ, and Il-10 concentrations were evaluated for enrolled contacts. Univariate analyses were performed using χ² or Fisher’s exact test. Multivariate logistic regression was performed by using backward elimination. SAS® 9.1 was used for all analyses. P-values <.05 were considered statistically significant.

Contacts with known HIV infection were excluded because of concerns that HIV might affect their immune responses and the risk for developing TB disease.

The protocol was approved by the institutional review boards at CDC and all participating project sites.

In our study, CFPS cytokine responses were evaluated for contacts after exposure to an infectious TB patient. A total of 60 exposed contacts were diagnosed with TB disease, representing 4.7% of all enrolled contacts; for 19 of these, specimens were collected from two months to three years before TB diagnosis. The majority of previous reports have been limited to assessment of CFPS cytokine responses after rather than before TB diagnosis [3‐5, 7, 9, 24‐26]. Further, most previous studies have included limited numbers of TB patients and a convenience sample of healthy control subjects. The detailed epidemiologic data collected prospectively on our study population provide a unique opportunity to evaluate immune correlates of protection, infection, and disease.

CFPS TNF-α and IFN-γ responses were significantly higher for contacts with co-prevalent TB than for contacts without TB. In multivariate analyses that examined CFPS cytokine responses and epidemiologic factors related to exposure and TB disease risk, elevated CFP IFN-γ or TNF-α responses were independent predictors of co-prevalent TB. These findings indicate that CFPS TNF-α and IFN-γ responses might be useful tools for predicting active TB and prompt consideration of their use during contact investigation.

Our study also identified algorithms based on immunologic and epidemiologic factors with higher PPVs for subsequent incident TB disease than reported for IFN-γ release assays (2.7%) or TSTs (1.5%) [18]. Transcriptomic signatures have also shown promising results, but have not been tested in combination with clinical and epidemiologic factors; further, reports to date have included co-prevalent TB as well as incident TB cases [19, 27]. In an algorithm combining young age, positive TST results, and elevated CFPS TNF-α, IFN-γ, and IL-10 responses, the estimate of PPV for incident TB disease in our study was 25%, which was high compared with PPV for all exposed contacts (1.5%), contacts with a positive TST (3%), or young age alone (1%). Of note, these algorithms are based on very small samples, and there was wide variability around the point estimates. Further studies with a larger sample size are needed to more fully explore the PPV for incident TB diagnosis of algorithms which combine epidemiologic and immunologic factors.

The PPV for TB disease of CFPS TNF-α, IFN-γ, and IL10 responses singly and in combination without considering epidemiologic factors was considerably lower (4–6%); however, this is in fact double or triple the expected disease rate (1–3%) among exposed contacts [20, 28‐30]. Further, CFPS TNF-α, IFN-γ, and IL10 responses singly and in combination had high NPVs for both co-prevalent TB (97–99%) and incident TB (99–100%), indicating a potential for using these responses as a tool to identify a subgroup of contacts with a high certainty of not currently having TB nor of being diagnosed with TB in the future.

Our findings provide evidence that TNF-α and IFN-γ have the potential to help predict the diagnosis of co-prevalent TB at the time of contact investigation. TNF-α and IFN-γ may thus be useful adjuncts to current diagnostic methods, which consist primarily of symptom-based screening with chest radiograph followed by sputum examination and culture, and can take from days to weeks to complete. On the basis of our findings, elevation of either TNF-α or IFN-γ responses should heighten suspicion of TB, particularly if both are elevated, the patient has clinical symptoms of TB, a positive TST, or is of young age. Further, the absence of TNF-α elevation in a single measurement soon after TB exposure could be used to define a group at low risk for TB.

The role of TNF-α as a pro-inflammatory cytokine essential to host defense against TB is well-established [3‐5, 31, 32]. Previous studies have evaluated cytokine responses among patients with TB at various times after treatment initiation [5, 24‐26]. The majority of studies reported that TNF-α levels are higher among TB patients than control subjects evaluated soon after treatment initiation [5, 24‐26], with a subsequent decline to levels similar to those of control subjects associated with successful resolution of disease [5]. In one report, the ratio of TNF-α to IL-10 was determined to be useful in distinguishing latent TB infection from active disease [32]. In our study, contacts who were diagnosed with incident TB over a 4-year follow-up had substantially higher CFPS TNF-α responses at baseline than contacts who remained disease free. This novel finding suggests that elevation in CFPS TNF-α responses could help predict subsequent development of active TB. This univariate finding was not supported by the multivariate analysis, however, and thus is not conclusive. The multivariate result may have been influenced by the very small number of persons in our study who subsequently developed TB. Additional studies with larger numbers are needed to further explore the possible role of elevation in CFPS TNF-α responses as a predictor for subsequent development of active TB. Our findings provide new information revealing that measurement of TNF-α might be helpful in predicting which exposed contacts will be diagnosed with TB at an earlier time than current diagnostic algorithms [33]. Further, these findings put into new context the increase in TNF-α among persons with previously treated TB at the time of relapse observed in an earlier report [5] by raising the question of whether measurement of TNF-α could help to predict TB relapse.

IFN-γ is known to play an important role in host defense against M. tuberculosis. In the majority of studies, IFN-γ levels have been reported to be low soon after TB diagnosis, with a subsequent increase reflecting successful resolution of disease [3, 25, 34]. IFN-γ assays lack optimal sensitivity for TB disease, however, with elevations among only an estimated 70–90% of active TB cases [9, 26]. Furthermore, although measurement of IFN-γ responses can be useful for diagnosing both latent TB infection and TB disease, current assays cannot discriminate between the 2 conditions. In our study, IFN-γ responses were significantly higher among contacts with co-prevalent TB compared with contacts without TB, but were similar for contacts with co-prevalent TB and those who were TST-positive without TB. Our findings indicate that measuring IFN-γ responses might be helpful in predicting active TB weeks to months earlier than current diagnostic algorithms (which rely on follow-up skin testing of contacts who were initially skin test negative 8–10 weeks after exposure) [34] and in identifying which exposed contacts have been infected with M. tuberculosis, but cannot identify which contacts with latent TB infection will subsequently develop TB.

A tool that enhances identification of persons at highest risk for TB disease might enable health departments to better prioritize public health investigations of persons exposed to infectious TB. Thus, interventions could be targeted at the limited number of persons truly at risk, thereby increasing the efficiency and effectiveness of public health prevention measures and reducing costs. Our findings indicate a potential role for both CFPS TNF-α and IFN-γ responses as adjunctive diagnostic tools for TB disease. IFN-γ response assays are already in clinical use, but primarily for diagnosing latent TB infection. Although our findings are intriguing, further evidence for the clinical utility of incorporating CFPS TNF-α responses into diagnostic algorithms for TB as well as development of a TB-specific commercial assay for TNF-α will be necessary before measurement of CFPS TNF-α responses can be routinely incorporated into clinical care.

Our study provides new evidence to support immune-mediated mechanisms for the link between immune compromising medical conditions such as diabetes and steroid use, excess alcohol use, smoking, and illicit drug use and increased risk for TB. Persons with immunocompromising medical conditions are known to be at higher risk for TB than normal hosts [35]. Excess alcohol use, cigarette smoking, illicit drug use, and older or younger age have also been linked to increased TB risk, with immune-mediated mechanisms postulated [36‐44]. Excess alcohol use is associated with decreased production of TNF-α [37, 38], and exposure to cigarette smoke has been associated in mouse models with decreased production of TNF-α and IFN-γ as well as increased production of IL-10 [39, 40]. In our study, CFPS TNF-α and IFN-γ responses were lower for persons with immunocompromising medical conditions and substance use than for those without such conditions, indicating that these conditions might affect the human immune response through both TNF-α and IFN-γ cytokine response pathways. Furthermore, whereas CFPS TNF-α and IFN-γ responses were higher among contacts with TB compared with contacts without TB for normal hosts, no difference in responses was observed for either cytokine among contacts with immunocompromising medical conditions or substance abuse, indicating that these conditions might blunt both the TNF-α and IFN-γ immune responses to TB.

CFPS TNF-α responses among our study population were substantially higher among persons of black versus non-black race across all outcome groups. These novel findings are intriguing, particularly in light of established differences in TB rates among persons in the United States by race/ethnicity [45]. Further studies are needed to validate these findings, and to determine whether variation in CFPS TNF-α cytokine responses by race is associated with functional changes which affect susceptibility, immune response, and TB risk following M. tuberculosis exposure. These findings also have implications for considering race/ethnicity in vaccine trials using cytokine-based surrogate markers.

Our study has certain limitations. Blood specimens were not obtained at the same time point after exposure for all contacts, which might affect variability of responses; not all eligible contacts agreed to participate in the immunologic study; the number of contacts with TB was relatively limited; and we did not account for clustering of TB by index case in the multivariable analysis. Although we cannot exclude the possibility that our study failed to detect one or more cases among contacts no longer under follow-up, the number missed is expected to be quite small since follow-up completeness was 100% at 4 years, and 94% at 5 years; further, 92% of all cases occurred before or within the first year after the end of exposure, followed by a steep decline in subsequent years [20]. Therefore, our epidemiological data suggest that very few secondary cases among contacts were missed either before or after the 5-year post exposure time point. Our findings that most secondary cases occur soon after exposure and could not have been prevented even with timely contact investigation [20], the fact that only one third of contacts with LTBI completed treatment [46], and evidence that most contacts who initiated treatment did so > 3 months after exposure (M Reichler personal communication), when the risk of progression to tuberculosis is already lower, suggest that the impact of LTBI treatment on the rates and timing of tuberculosis in our study is not expected to be large. Despite the limitations, substantial epidemiologic data of good quality were collected in addition to CFPS cytokine responses, a strength of the study.

Our study findings confirm that IFN-γ and TNF-α are immune correlates of TB disease, and demonstrate that cytokine concentrations and epidemiologic factors at the time of contact investigation may predict co-prevalent tuberculosis, and may also be useful to rule out development of active TB based on absence of cytokine elevation In our study, we observed differences in CFPS cytokine responses by age, race, underlying medical condition, and substance abuse, highlighting the value of examining immunologic correlates of M. tuberculosis infection and disease in the context of clinical and epidemiologic factors. Further studies are needed to validate these findings and to explore the role of other cytokines and chemokines involved in immune defense against M. tuberculosis.