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. 2007 Aug 16;7:96. doi: 10.1186/1471-2334-7-96

The pathogen recognition sensor, NOD2, is variably expressed in patients with pulmonary tuberculosis

Sanjay Lala 1,#, Keertan Dheda 2,3,✉,#, Jung-Su Chang 2, Jim F Huggett 2, Louise U Kim 2, Margaret A Johnson 4, Graham AW Rook 2, Satish Keshav 1, Alimuddin Zumla 2
PMCID: PMC2018706  PMID: 17705850

Abstract

Background

NOD2, an intracellular pathogen recognition sensor, modulates innate defences to muropeptides derived from various bacterial species, including Mycobacterium tuberculosis (MTB). Experimentally, NOD2 attenuates two key putative mycobactericidal mechanisms. TNF-α synthesis is markedly reduced in MTB-antigen stimulated-mononuclear cells expressing mutant NOD2 proteins. NOD2 agonists also induce resistance to apoptosis, and may thus facilitate the survival of MTB in infected macrophages. To further define a role for NOD2 in disease pathogenesis, we analysed NOD2 transcriptional responses in pulmonary leucocytes and mononuclear cells harvested from patients with pulmonary tuberculosis (PTB).

Methods

We analysed NOD2 mRNA expression by real-time polymerase chain-reaction in alveolar lavage cells obtained from 15 patients with pulmonary tuberculosis and their matched controls. We compared NOD2 transcriptional responses, in peripheral leucocytes, before and after anti-tuberculous treatment in 10 patients. In vitro, we measured NOD2 mRNA levels in MTB-antigen stimulated-mononuclear cells.

Results

No significant differences in NOD2 transcriptional responses were detected in patients and controls. In some patients, however, NOD2 expression was markedly increased and correlated with toll-like-receptor 2 and 4 expression. In whole blood, NOD2 mRNA levels increased significantly after completion of anti-tuberculosis treatment. NOD2 expression levels did not change significantly in mononuclear cells stimulated with mycobacterial antigens in vitro.

Conclusion

There are no characteristic NOD2 transcriptional responses in PTB. Nonetheless, the increased levels of NOD2 expression in some patients with severe tuberculosis, and the increases in expression levels within peripheral leucocytes following treatment merit further studies in selected patient and control populations.

Background

The innate immune system is postulated to play a crucial role in the elimination or control of Mycobacterium tuberculosis (MTB), which causes infectious tuberculosis [1,2]. These innate immune responses are triggered when MTB-derived molecules are sensed by toll-like receptors (TLRs), a family of membrane proteins, as well as by nucleotide-binding oligomerization domain 2 (NOD2; also known as CARD15), an intracellular pathogen recognition sensor. Activation of TLRs by MTB-antigens appears to be an important event in the control of infection. For example, mice that lack the toll-like receptor (TLR) adaptor molecule myeloid differentiation factor 88 (MyD88) are more susceptible to pneumonia following aerogenic infection with MTB [3].

The nature of these innate responses, however, appears complex and is not fully elucidated. For example, experimental studies show that MTB-induced TLR signalling effects both cellular activation [4] and apoptosis [5]. Similarly, the innate responses mediated by NOD2, in response to MTB-derived antigens, vary in different experimental systems.

NOD2 senses muramyl dipeptide (MDP) [6,7] a component of peptigoglycan that is found in mycobacterial cell walls. A recent in vitro study suggests that NOD2 is an essential recognition molecule for MTB [8], and pronounced cellular activation is noted in NOD2-transfected cells that are stimulated with MDP or heat-killed MTB preparations. Furthermore, cytokine production is inhibited in MTB-stimulated peritoneal macrophages obtained from NOD2-deficient mice and in human peripheral blood mononuclear cells (PBMCs) that express truncated NOD2 proteins [8]. On the other hand, MDP stimulation protects macrophages from apoptosis, which suggests that activation of NOD2 induces apoptosis resistance which facilitates the survival of MTB in macrophages [5].

The role of NOD2 in the pathogenesis of human MTB-infection is unknown. In vitro, human PBMCs that express truncated NOD2 proteins synthesise significantly less cytokines after stimulation with MTB-derived antigens. Truncated NOD2 proteins are encoded by mutations in the NOD2 gene that predispose individuals to Crohn's disease, a granulomatous inflammatory bowel disease [9,10]. The prevalence of these Crohn's disease-associated mutations has not been fully described in all population groups where tuberculosis is endemic although these mutations are rare in African patients with tuberculosis [11].

To further define a role for NOD2 in disease pathogenesis, we analysed NOD2 mRNA transcriptional responses in pulmonary leucocytes and PBMCs harvested from patients with pulmonary tuberculosis (PTB) and healthy controls. We determined whether changes in NOD2 transcription, if present, are characteristic for patients with tuberculosis: increased transcriptional responses may suggest that MTB-infected macrophages are resistant to apoptosis whereas decreased transcriptional responses may suggest that cellular activation is diminished in infected macrophages. As various pathogen associated-molecular patterns (PAMPs) specifically alter host transcriptional responses [12], we analysed and correlated the transcriptional responses of other TLRs with NOD2 in patients with PTB.

Methods

Patients and samples

Fifteen HIV-negative patients with culture proven pulmonary tuberculosis (PTB), who donated blood and lung bronchoalveolar lavage (BAL) samples, were recruited in London, United Kingdom. All patients with PTB had pan-sensitive isolates, received standard short course chemotherapy (6 to 9 months) and demonstrated clinical and radiological response to anti-TB treatment. Control donors (n = 15) were healthy volunteers matched to the TB patients for age (within 4 years), sex and ethnicity. They were asymptomatic, had no risk factors for HIV infection (but were not formally tested), had normal chest radiographs and were assumed, based on antigen-specific (ESAT-6 and CFP-10) peripheral mononuclear cell IFN-γ responses, not to be latently infected (T SPOT TB, Oxford Immunotec, England) [13]. Control BAL samples were obtained from six control donors.

Whole blood (20 mL) was taken, after informed consent, within the first 2 weeks of anti-TB treatment (baseline). 2.5 mL whole blood was immediately transferred into PAXgene Blood RNA Tubes (Qiagen) for isolation and purification of intracellular RNA. The remaining blood, where relevant, was used for further experiments. Ten donors with PTB were bled again within 4 weeks of stopping chemotherapy. Approval was obtained from the Royal Free and UCLH hospital ethics committees.

BAL and Radiographic scoring

BAL fluid, obtained from a radiologically affected lung segment, was concentrated ~10 fold before analysis whilst cell pellets were immediately fixed in RNA stabilisation buffer. In control donors the right middle lobe was lavaged. When possible, lymphocyte counts in BAL were confirmed by flow cytometry (104 gated events) after staining ~7.5 × 105 cells with anti CD4-FITC, anti CD8-PE and anti CD3-PercP antibodies (BD Biosciences, UK). To determine the extent of pre-treatment radiological disease, two radiologists, blinded to patient details, scored chest radiographs for air space shadowing, reticular opacities and cavitation.

Enzyme-linked-immunospot (ELISPOT) assays

Peripheral T-cell IFN-γ ELISPOT responses to ESAT-6 and CFP-10 peptide pools were determined to exclude latent TB infection (T SPOT TB, Oxford Immunotec, England), as previously described [14,13,15].

Culture and infection of PBMCs with M. tuberculosis

PBMCs from five healthy control donors were separated from heparinized blood (50 ml) by Ficoll density gradient centrifugation, and cells were reconstituted at a final concentration of 1 × 106 cells/ml. To evaluate NOD2 gene regulation PBMCs were cultured for 66 hours in the presence of live H37RV M. tuberculosis, a clinical isolate (Beijing strain), live environmental mycobacterium (M. vaccae NCTC 11659) and medium alone. Cells were cultured in RPMI 1640 supplemented with 5% heat-inactivated human AB serum and 1% L-glutamine without antibiotics at 37°C and 5% CO2 in a category 3 laboratory and harvested at 18, 24, 48, and 66 h post-treatment. All strains were grown in Middlebrook 7H10 agar (Difco) containing 10% v/v oleic acid/albumin/dextrose/catalase supplement (BD Biosciences) in the category 3 laboratory. Mycobacteria were disaggregated by vigorous vortexing with glass beads and counted using a Neubauer hemocytometer as previously described [16]. A direct microscopic count was performed to determine mycobacterial concentration. PBMCs were infected with living mycobacteria at a dose of 1 organism per macrophage (10% monocytes in PBMC). The viability of mycobacteria was assessed by culturing the diluted bacteria on Middlebrook 7H10 agar.

Reverse transcription and real-time PCR

RNA was isolated from whole blood and from lavage cell pellets or cells using the Paxgene® and RNeasy® Kit, respectively. Reverse transcription and real-time PCR, to quantify mRNA encoding for NOD2 and NOD1, IL-4 and its splice variant IL-4δ2, IFN-γ, TLRs and several proteins involved in apoptosis (FLIP, FLICE, Bcl-2, Bax, Fas, FasL and Bfl-1), were performed on samples, as previously described, after quality control of RNA templates [17]. mRNA values were normalised to a validated housekeeping gene, human-acidic-ribosomal-protein (HuPO) [18,19]. Primer and probe sequences, excluding those which have been previously published [16,17], are shown in table 2.

Table 2.

Primer and probe sequences used to quantify gene expression by real-time PCR. Primer sequences for toll-like-receptor 2, 4, 6, 7 and 9 [17] and IL-4δ2 [18] have previously been published.

Genes * Probe sequence 5'-(FAM-TAMRA)-3'
◇ L primer-5'-3'
□ R primer-5'-3'		 Product size
IL-4 * AAACCTTCTGCAGGGCTGCGAC 71 bp
◇ GCTGCCTCCAAGAACACAAC
□ CTGTAGAACTGCCGGAGCAC
HuPO *TGCCAGTGTCTGTCTGCAGATTGG 105 bp
◇ GCTTCCTGGAGGGTGTCC
□ GGACTCGTTTGTACCCGTTG
NOD1 * CCTGGCTCCGACATCGGTGA 133 bp
◇ AAGCGAAGAGCTGACCAAAT
□ TCCCAGTTTAAGATGCGTGA
NOD2 * CCGAGGCATCTGCAAGCTCA 82 bp
◇ CTGCAAGGCTCTGTATTTGC
□ CTCGCAGTGAAGAGCACATT
TNF-α * CAGCCACTGGAGCTGCCCCT 102 bp
◇ AGCCCATGTTGTAGCAAACC
□ GCTGGTTATCTCTCAGCTCCA
FLIP * TGGATTGCTGCTTGGAGAACATTCC 114 bp
◇ GTTCAAGGAGCAGGGACAAG
□ ATCAGGACAATGGGCATAGG
FLICE * ACTTGGATGCAGGGGCTTTGACCAC 102 bp
◇ AAGTGCCCAAACTTCACAGC
□ GGGGCTTGATCTCAAAATGA
Bax * AAGTAGAAAAGGGCGACAACCCGGC 105 bp
◇ GAGAGGTCTTTTTCCGAGTGG
□ GCCTTGAGCACCAGTTTGCTG
Bfl-1 * CCACAACCTGGATCAGGTCCAAGCA 105 bp
◇ GGCTGGCTCAGGACTATCTG
□ TTTGGACTGAGAACGCAACA
Bcl-2 * CAAAGGCATCCCAGCCTCCGTTA 118 bp
◇ AGTACCTGAACCGGCACCT
□ TTCAGAGACAGCCAGGAGAAA
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Data analysis

Data was analysed using the Mann-Whitney U test, Wilcoxon matched pairs test, Spearman rank-sum correlation and linear regression on logged data.

Results

Demographic characteristics

Demographic details of matched TB patients (n = 15) and controls, shown in Table 1, indicate that there were no differences in baseline characteristics between these groups. All control patients had normal chest radiographs and had no laboratory evidence of latent TB infection with M. tuberculosis, as assessed by the antigen specific IFN-γ assay (T SPOT TB).

Table 1.

Demographic details and lavage cell counts at recruitment. Demographic details and radiographic scores are of 15 patients with pulmonary tuberculosis with their matched controls; the lavage cell counts are those of 10 patients and 6 controls. All participants were recruited in London, United Kingdom.

Numbers in parenthesis indicate % TB Control
Age (median; range in years) 28; 18–52 28; 19–48
Sex (male) 9 (60) 8 (53)
Ethnicity
 Black African 9 (60) 8 (53)
 Indian 4 (26) 4 (26)
 Other 2 (14) 3 (21)
X-ray features
Cavitation 8 (53) 0
>50% airspace shadowing of total lung field 7 (47) 0
BAL (mean ± SE)
Total leucocytes (× 104/ml) 31 ± 8 12.8 ± 4.2
lymphocyte count (× 104/ml) 15 ± 4 2.7 ± 1.4
CD4: CD8 ratio 3.8 ± 1 2.55 ± 0.9
IFN-γ copy number 3390 [1525–7498] 13 [4–113]; p = 0.0005
Th1/Th2 ratio 3.5 [3.1–3.8] 1.1 [.4–1.8]; p = 0.0007
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Broncho-alveolar lavage (BAL) fluid analyses in patients with PTB and controls

BAL fluid recovered from patients with PTB were more cellular than controls, contained predominantly alveolar macrophages, and contained a significantly greater number of leucocytes and lymphocytes (Table 1). In PTB-affected patients, IFN-γ mRNA levels and the Th1/Th2 (IFN-γ/IL-4) ratio were significantly elevated compared to control subjects (Table 1).

Pulmonary leucocytes express NOD2 mRNA

NOD2 is most prominently expressed in circulating monocytes [10] and small intestinal Paneth cells [20]. Expression profiles in human pulmonary leucocytes have not previously been studied. We initially determined whether alveolar macrophages express NOD2 and measured NOD2 mRNA levels in pulmonary leucocytes present in BAL fluid [21]. We show that NOD2 mRNA expression levels are prominent in pulmonary leucocytes although expression levels did not differ between patients and controls (Figure 1). We also compared the expression levels of NOD1 mRNA (also known as CARD4), in pulmonary leucocytes obtained from patients and controls (Figure 1). NOD1 is an intracellular protein that is closely related to NOD2 but does not appear to play a role in the detection of mycobacterial antigens [8].

Figure 1.

Figure 1

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NOD1 and NOD2 mRNA expression in pulmonary leucocytes obtained from patients with tuberculosis and controls. NOD1 and NOD2 mRNA expression, measured by real-time RT-PCR, is similar in pulmonary leucocytes in 15 patients with tuberculosis compared to 6 healthy controls. To permit comparison between individuals, absolute copy numbers of NOD1 and NOD2 mRNA were measured during RT-PCR, using cDNA standards, and expressed relative to 106 mRNA copies of a validated housekeeping gene, HuPO.

Although there are no characteristic NOD2 transcriptional responses in patients with PTB, NOD2 mRNA was highly expressed in two patients. Both patients, who were of Somalian origin, and had severe tuberculosis: one patient had extensive pulmonary cavitatory disease and the other disseminated tuberculosis. We could not, however, identify more specific clinical variables to account for the high levels of NOD2 expression in these patients. Patients with cavitatory disease tended to have higher levels of NOD2 mRNA expression than those without pulmonary cavitation but these differences were not significant (Figure 2). There was no correlation between NOD2 mRNA levels and radiographic disease scores.

Figure 2.

Figure 2

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NOD2 gene expression in alveolar lavage cells from 15 subjects with tuberculosis (stratified by whether cavitation was detected on chest radiographs) and 6 healthy controls.

NOD2, and TLR2 and TLR4 mRNA expression correlate in pulmonary leucocytes obtained from patients with PTB

NOD2 regulates cellular responses to peptidoglycan-mediated activation of TLR2 [22]. Furthermore, mycobacterial TLR2 and NOD2 agonists synergistically induce cytokine release in PBMCs obtained from healthy volunteers and patients with Crohn's disease [8]. In pulmonary leucocytes obtained from patients with tuberculosis, NOD2 mRNA expression correlated with TLR2 (p = 0.02; figure 3A) and TLR4 (p = 0.01; figure 3B) but not with TLR6 mRNA expression (p = 0.17). These correlations were mainly due to the high levels of mRNA expression in the two previously mentioned patients. In healthy controls, there was no correlation between NOD2 and TLR2 or TLR4 mRNA expression in pulmonary leucocytes. NOD1 mRNA expression did not correlate with TLR2 or TLR4 mRNA expression in pulmonary leucocytes obtained from patients and controls.

Figure 3.

Figure 3

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NOD2 mRNA expression correlates with TLR2 and TLR4 mRNA expression in pulmonary leucocytes harvested from patients with tuberculosis. A significant correlation was observed between mRNA molecules encoding NOD2 and toll-like receptor (TLR) 2 (p = 0.02) [A] and TLR4 (p = 0.01) [B] in pulmonary leucocytes harvested from patients with tuberculosis. To permit correlations, absolute copy numbers of NOD2 and TLR2, TLR4 and TLR6 mRNA were measured during RT-PCR, using cDNA standards, and expressed relative to 106 mRNA copies of a validated housekeeping gene HuPO.

NOD2 expression increases in whole blood following anti-tuberculous therapy

In whole blood, both NOD2 and NOD1 mRNA expression increased following treatment, although only increases in NOD2 mRNA expression were significant (Figure 4).

Figure 4.

Figure 4

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NOD1 and NOD2 mRNA expression in peripheral blood cells obtained from patients with tuberculosis, before and after anti-tuberculous treatment. NOD1 and NOD2 mRNA expression was analysed, by real-time RT-PCR, in peripheral blood cells isolated from patients with tuberculosis and matched controls. To permit comparison between individuals, absolute copy numbers of NOD2 (4A) and NOD1 (4B) mRNA were measured during RT-PCR, using cDNA standards, and expressed relative to 106 mRNA copies of a validated housekeeping gene HuPO. NOD2 but not NOD1 mRNA levels increased significantly after treatment.

Signalling pathways activated by NOD2

Following activation by MDP, NOD2 triggers downstream cellular responses mediated through NF-κB and mitogen-activated protein kinase (MAPK) activation [23]. This results in the production of various cytokines, such as TNFα and IL-4, which are important in regulating immune responses to MTB [1,17]. We therefore compared NOD2 mRNA with the transcriptional responses of selected cytokines in BAL-derived cells obtained from patients with PTB (n = 15) and controls (n = 6). Although there were clear differences in the expression of some cytokines (IFNγ, IL-4 and its splice variant and antagonist, IL-4δ2) in patients with TB and controls, there was no correlation between expression of these cytokines and NOD2. There was also no correlation between NOD2 and TNFα transcriptional responses in patients and controls. In addition, NOD2 mRNA expression did not correlate with expression of mRNA encoding several proteins involved in apoptosis (FLIP, FLICE, Bcl-2, Bax, Fas, FasL and Bfl-1) although high levels of mRNA encoding the anti-apoptotic protein FLICE were measured in BAL-derived cells obtained from the two patients with elevated NOD2 mRNA levels.

NOD2 mRNA expression is not regulated in PMBC freshly inoculated with live strains of mycobacteria

We exposed PBMCs from five healthy volunteers, who did not have laboratory evidence of tuberculosis infection (as established by antigen-specific IFN-γ assays [14,13,15]), to pathogenic strains of live mycobacteria (H37RV and Beijing strain) and an environmental mycobacterium (M. vaccae NCTC 11659), to determine if NOD2 mRNA expression levels are regulated by. In general, mycobacteria induced modest, but non-significant changes, in NOD2 mRNA expression (Figure 5A). Mycobacteria induced marked increases in NOD2 mRNA expression in one volunteer (Figure 5B) although mycobacterial stimulation did not regulate NOD2 mRNA expression significantly in PBMC extracted from the other volunteers (Figure 5C–F). In these studies, NOD2 mRNA expression levels varied widely and did not correlate with any specific mycobacterial strain.

Figure 5.

Figure 5

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NOD2 mRNA expression in live mycobacteria stimulated-peripheral blood cells obtained from healthy volunteers. NOD2 mRNA levels varied widely in healthy donor derived-PBMCs that were stimulated with live mycobacterial strains [A = combined data and B to F individual data]. NOD2 mRNA expression was analysed, by real-time RT-PCR, in peripheral blood cells isolated from healthy donors. To permit comparison between individuals, absolute copy numbers of NOD2 mRNA were measured during RT-PCR, using cDNA standards, and expressed relative to 106 mRNA copies of a validated housekeeping gene HuPO. Lower numbers of PBMCs were harvested from Donors 1 and 3, and these cells were not stimulated with Mycobacterium vaccae. MV = M, vaccae; H37 = H37RV strain and CPA = Beijing strain.

Discussion

NOD2, a member of the phylogenetically conserved NLR (NACHT-leucine-rich repeat) family, is an essential pattern recognition sensor for MTB-derived antigens. Mycobacterial antigens fail to induce an appropriate increase in TNF-α synthesis in human PBMC that express mutant NOD2 proteins and in murine macrophages lacking NOD2 [8]. The gene mutations that encode mutant NOD2 proteins, however, appear to be rare in patients with tuberculosis. NOD2 agonists may also modulate innate responses to MTB by inducing resistance to apoptosis that facilitates the survival of MTB in infected macrophages [5]. Thus, NOD2 may play a role in attenuating two key putative mycobactericidal pathways. To further define a role for NOD2 in disease pathogenesis, we analysed NOD2 transcriptional responses in pulmonary leucocytes and mononuclear cells harvested from patients with pulmonary tuberculosis (PTB).

Our gene expression studies revealed that there are no characteristic NOD2 transcriptional responses in pulmonary leucocytes obtained from patients with tuberculosis. NOD2 mRNA levels in patients generally compared with those in control donors. Nonetheless, increased NOD2 levels, which correlate with TLR2 and TLR4 expression, were noted in some patients with severe infection. This observation, coupled with the increases in NOD2 expression in peripheral leucocytes following treatment, suggest further study in a larger group of patients to confirm a role for NOD2 in PTB. In the present study, we only measured total leucocyte and lymphocyte counts in bronchoalveolar lavage fluid. As NOD2 is most prominently expressed in monocytes, with very little expression in neutrophils and lymphocytes, it is most likely that monocytes account for the overwhelming majority of NOD2 expression [24].

We did not quantify the number of epithelial cells present in broncho-alveolar fluid and we cannot determine the effect of mycobacterial infection on NOD2 expression in respiratory epithelial cells. Baseline NOD2 expression levels in primary respiratory epithelial cells is low [25] although NOD2 mRNA expression is enhanced in immortalised human bronchial epithelial cells that are infected with Streptococcus pneumoniae[25]. It would therefore be important to determine the relative contribution of respiratory epithelial cells and monocytes to the increases in NOD2 expression seen in some patients.

In the present study, NOD2 mRNA expression levels were similar in patients (who often have active disease for many weeks prior to diagnosis) and controls. This does not exclude a role for NOD2 during the early stages of MTB infection, when M. tuberculosis encounters the alveolar macrophage and innate immune pathways are first activated. It is also possible, however, that the absolute levels of NOD2 expression may not play a role in determining susceptibility to MTB infection. Rather, structural variants of NOD2 proteins may modulate host immune responses as suggested by in vitro studies [8]. Thus, studies are required to confirm whether individuals with gene mutations encoding for mutant NOD2 proteins are predisposed to MTB-infection. The lack of an association between Crohn's disease-associated NOD2 gene mutations and tuberculosis in African patients [11] does not exclude a role for NOD2 in MTB-infection because NOD2 gene mutations are probably rare in African populations [10]. It would be instructive, therefore, to determine whether NOD2 gene mutations are associated with MTB-infection in Caucasian populations, where these mutations occur with much greater frequency.

We were surprised to find significantly higher levels of NOD2 mRNA expression in peripheral leucocytes obtained from patients who completed anti-tuberculosis therapy. Firstly, we hypothesise that this could have been due to translocation of antigen-specific leucocytes predominantly to the site of disease (lungs) with few NOD2 expressing leucocytes in the peripheral compartment, and reversal of this profile after treatment. However, the lack of preferential NOD2 upregulation in the lung makes this unlikely. Secondly, we speculate that MTB infection may subvert protective innate responses by downregulating NOD2 expression, whose levels therefore increase after successful chemotherapy. We might expect this to occur in parallel with TNF-α as this cytokine up-regulates NOD2 mRNA expression in various cell lineages including PBMC [26,27]. However, in keeping with the observations of other investigators [28,29], we did not observe increased TNF-α mRNA expression after treatment completion. We did not investigate the relationship between NOD2 and soluble TNF-α receptors, which may modulate TNF-α levels. Thirdly, it is intriguing to speculate that increased levels of NOD2 mRNA, which occur with completion of TB treatment, is a correlate of protective immunity. Similar longitudinal changes may occur with IFN-γ [17,29,30] and the Th1-like splice variant IL-4δ2 [17], which both increase significantly with anti-TB treatment. In keeping with these observations IL-4δ2 mRNA levels are also increased in healthy subjects with latent MTB infection who contain the disease [31,32]. Longitudinal studies in TB infected patients, however, would be required to address the role of NOD2 in this context. Interestingly, preliminary data indicate that mycobacterial antigens regulate the expression of NOD2 splice variants [33] and further studies are required to clarify their role in tuberculosis.

A significant limitation of this study is that we did not study MTB-specific responses in subjects with known NOD2 gene mutations. However, we found these patients difficult to recruit in our clinical setting. We also acknowledge that real time PCR measures steady state mRNA levels only and not the activity of NOD2 protein, which is physiologically active at concentrations too low to detect by immunoassay. This study was powered to detect a 0.5 log change in NOD2 mRNA levels although smaller changes may be biologically meaningful. However, mRNA levels in patients and controls were similar and we found no trends suggesting that inter-group difference might be present.

Conclusion

Overall, our findings show that there are no characteristic NOD2 transcriptional responses in pulmonary leucocytes obtained from patients with PTB. Nonetheless, the increased levels of NOD2 mRNA expression in peripheral leucocytes obtained from patients completing treatment and correlation between NOD2 and TLR2 and TLR4 mRNA expression in pulmonary leucocytes obtained from some patients with severe tuberculosis does not exclude a role for NOD2 in disease pathogenesis. The role of mutant NOD2 proteins in MTB-infection in different ethnic groups needs to be defined.

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

SL contributed to formulation of study design, conducted some of the relevant experiments, analysed the data, and contributed to writing and critical appraisal of the manuscript. KD contributed to formulation of study design, conducted some of the relevant experiments, recruited the patients, analysed the data, and contributed to writing and critical appraisal of the manuscript. JC conducted some of the relevant experiments and contributed to data analysis. LUK conducted some of the relevant experiments and contributed to data analysis. JFH conducted some of the relevant experiments and contributed to data analysis. MAJ, SK, GAWR and AZ contributed to formulation of study design, facilitated patient recruitment, analysed the data, and contributed to writing and critical appraisal of the manuscript. All the authors have read and approved the final manuscript.

Pre-publication history

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

http://www.biomedcentral.com/1471-2334/7/96/prepub

Acknowledgments

Acknowledgements

The authors would like to thank the TB clinic and bronchoscopy staff at the Royal Free Hospital NHS trust for facilitating patient recruitment, the radiologists for scoring the x-rays, and the patients and volunteers that took part in the study. This work was, in part, supported by the SA Research Chairs Initiative (KD), sponsored by the South African NRF and DST. SL was supported by a Crohn's in Childhood Research Association (CICRA) Research Fellowship.

Contributor Information

Sanjay Lala, Email: s.lala@mweb.co.za.

Keertan Dheda, Email: keertandheda@yahoo.co.uk.

Jung-Su Chang, Email: susanchangtw@yahoo.com.

Jim F Huggett, Email: j.huggett@ucl.ac.uk.

Louise U Kim, Email: l.kim@ucl.ac.uk.

Margaret A Johnson, Email: Margaret.Johnson@royalfree.nhs.uk.

Graham AW Rook, Email: g.rook@ucl.ac.uk.

Satish Keshav, Email: satish.keshav@royalfree.nhs.uk.

Alimuddin Zumla, Email: a.i.zumla@googlemail.com.

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