Procoagulatory State in Inflammatory Bowel Diseases Is Promoted by Impaired Intestinal Barrier Function

Pastorelli, Luca; Dozio, Elena; Pisani, Laura Francesca; Boscolo-Anzoletti, Massimo; Vianello, Elena; Munizio, Nadia; Spina, Luisa; Tontini, Gian Eugenio; Peyvandi, Flora; Corsi Romanelli, Massimiliano Marco; Vecchi, Maurizio

doi:https://doi.org/10.1155/2015/189341

Gastroenterology Research and Practice

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Abstract Introduction Materials and Methods Results Discussion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2015 | Article ID 189341 | https://doi.org/10.1155/2015/189341

Procoagulatory State in Inflammatory Bowel Diseases Is Promoted by Impaired Intestinal Barrier Function

Luca Pastorelli,^1,2Elena Dozio,²Laura Francesca Pisani,²Massimo Boscolo-Anzoletti,³Elena Vianello,²Nadia Munizio,¹Luisa Spina,¹Gian Eugenio Tontini,¹Flora Peyvandi,^3,4Massimiliano Marco Corsi Romanelli,^2,5and Maurizio Vecchi^1,2

Academic Editor: Gerassimos Mantzaris

Received29 Oct 2014

Revised27 Jan 2015

Accepted01 Feb 2015

Published12 Feb 2015

Abstract

Inflammatory and immune mediated disorders are risk factors for arterial and venous thromboembolism. Inflammatory bowel diseases (IBD) confer an even greater risk of thromboembolic events than other inflammatory conditions. It has been shown that IBD patients display defective intestinal barrier functions. Thus, pathogen-associated molecular patterns (PAMPs) coming from the intestinal bacterial burden might reach systemic circulation and activate innate immunity receptors on endothelial cells and platelets, promoting a procoagulative state. Aim of the study was to test this hypothesis, correlating the presence of circulating PAMPs with the activation of innate immune system and the activation of the coagulatory cascade in IBD patients. Specifically, we studied lipopolysaccharide (LPS), Toll-like receptor (TLR) 2, TLR4, and markers of activated coagulation (i.e., D-Dimer and prothrombin fragment ) in the serum and plasma of IBD patients. We found that LPS levels are increased in IBD and correlate with TLR4 concentrations; although a mild correlation between LPS and CRP levels was detected, clinical disease activity does not appear to influence circulating LPS. Instead, serum LPS correlates with both D-Dimer and measurements. Taken together, our data support the role of an impairment of intestinal barrier in triggering the activation of the coagulatory cascade in IBD.

1. Introduction

Cardiovascular events, including both arterial and venous thromboembolism, are a major cause of death and morbidity in Western countries [1]. Several cofactors influence the risk of cardiovascular events and, among these, inflammation seems to play a relevant role [2]. In fact, systemic and localized inflammatory processes can accelerate atherosclerosis and cause a hypercoagulative state [3]. As a matter of fact, the atherosclerotic plaque is ultimately an inflammatory lesion [4] where activated macrophages sustain the damage [5] and the inflammatory and coagulative molecular cascades are strictly linked and share several common mediators [3]. As such, it is not surprising that a wealth of epidemiologic data demonstrates an increased prevalence of thromboembolic complications in inflammatory and immune-mediated disorders [6]. Remarkably, it has been shown that, among many inflammatory and/or immune-mediated conditions, inflammatory bowel diseases (IBD), namely, ulcerative colitis (UC) and Crohn’s disease (CD), confer the most prominent risk of thromboembolism [7].

IBD are chronic and relapsing inflammatory diseases of the gut and their exact etiology is still obscure [8]; however, several key events in the pathogenesis of IBD are well recognized and studied. It is commonly accepted that the onset of IBD is linked to the presence of an altered intestinal permeability [9], a reduced mucosal innate immunity function [9], and an exaggerated adaptive immune response [10].

The increased incidence of thromboembolic events in IBD patients is likely to be multifactorial and the inflammatory process may have itself a role together with vitamin deficiencies (i.e., vitamin B12, vitamin B6, and folate) and other acquired factors [11–13]. Moreover, a defective intestinal mucosa barrier function may as well contribute to the procoagulative state, specifically in IBD patients. In fact, a leaky epithelial layer and/or a defective innate immune response impair gut capability to control intestinal bacterial burden, allowing bacterial components to penetrate into the intestinal mucosa [9], reach the systemic circulation, and come into contact with endothelial cells and platelets. Those bacterial components, such as lipopolysaccharide (LPS), may work as pathogen-associated molecular patterns (PAMPs), that is, molecules associated with different groups of microorganisms, and after being recognized by cells they activate a prompt innate immune response [14]. In fact, immune and nonimmune cells present on their membrane specific receptors deputed to recognize PAMPs, such as Toll-like receptors (TLRs) [14]. Apart from membrane-bound TLRs, soluble TLRs were also described. These molecules can be found in body fluids upon bacterial sensing [15–17] and, acting as decoy receptors for PAMPs, they negatively regulate membrane-bound TLR activation in order to prevent exaggerated innate immune activation [18–20]. Interestingly, soluble TLRs have been proposed as potential biomarkers for several inflammatory/infectious conditions, including IBD [21–26].

Both endothelial cells and platelets possess innate immunity receptors, such as TLR2 and TLR4 [27–29], that, after being activated by PAMPs, promote cell activation and the subsequent release of different procoagulative molecules, all of them triggering the molecular pathways of coagulation.

In the present paper, we evaluated the potential link between decreased intestinal barrier function and activation of coagulation in IBD. To this aim we explored the correlation between circulating LPS, soluble TLR2 and TLR4 serum levels, and sensitive markers of activated coagulation (i.e., D-Dimer and prothrombin fragment ) [30], thus evaluating the final steps of the coagulatory cascade.

2. Materials and Methods

2.1. Patients

After having read and signed a specific informed consent, 58 consecutive IBD patients (35 CD and 23 UC) followed up at the Gastroenterology and Gastrointestinal Endoscopy Unit of the IRCCS Policlinico San Donato and 20 healthy controls were enrolled in the study. Blood was collected from all IBD patients and all control subjects. All IBD diagnoses had been confirmed by standardized clinical, endoscopic, and histologic criteria [31, 32]. Disease activity was assessed using the Harvey-Bradshaw Index (HBI) for CD patients [33] and the Mayo scores for UC [34]. Patients with proctitis were excluded from the study. The demographic and clinical characteristics of the patients are reported in Table 1. The study was designed to respect the ethical guidelines of the Declaration of Helsinki. The Internal Review Board of the local Ethical Committee approved the study protocol (Ethical Committee Protocol number # 2025, ASL Milano-2, approved on June 14, 2007).

2.2. Blood Sampling and Serum and Plasma Collection

Peripheral blood was collected by venipuncture of an antecubital vein without any blood stasis using sterilized needles in BD vacutainer SST II Advance for serum collection and in BD vacutainer with sodium citrate for plasma collection. A 3 mL blood tube was used for serum and plasma separation after centrifugation at 2370 g for 15 min at room temperature. Serum and plasma were stored at −80°C in 0.5 mL aliquots until the time of assays.

2.3. C Reactive Protein Measurement

C reactive protein (CRP) levels were measured by a commercially available immunoturbidimetric assay (Roche Diagnostic, Germany).

2.4. TLR2 and TLR4 Protein Quantification in Serum

The measurement of TLR2 and TLR4 was performed by means of commercially available sandwich enzyme immunoassay (R&D System, USA, and USCN Life Sciences Inc., China, resp.), following manufacturers’ instructions.

2.5. LPS Quantification

The Endpoint Chromogenic Limulus Amebocyte Lysate (LAL) Test (Lonza) was used as a quantitative test for LPS, according to manufacturer’s instructions. Briefly, serum was diluted 1 : 10 with LAL reagent water (LRW), heat inactivated in a water bath for 15 minutes at 70°C, and then diluted 1 : 2 in LRW. The test was performed in a microplate at 37°C in heating block. Each sample was tested in duplicate. Fifty μL of diluted sample was mixed with 50 μL of the LAL supplied in the test kit and incubated at 37°C (±1°C) for 10 minutes. One hundred μL of substrate solution was then mixed with the LAL sample and incubated at 37°C (±1°C) for an additional 6 minutes. The reaction was stopped with 100 μL acetic acid 25% v/v in water. The absorbance of the sample was determined spectrophotometrically at 405–410 nm.

2.6. D-Dimer and F1 + 2 Dosage

D-Dimer HS kit (Instrumentation Laboratory, Spain) was used for the quantitative determination of D-Dimer in human citrated plasma, following manufacturer’s instructions. Briefly, the D-dimer HS 500 latex reagent is a suspension of polystyrene latex particles of uniform size coated with the F(ab′)₂ fragment of a monoclonal antibody highly specific for the D-Dimer domain included in fibrin soluble derivatives. Plasma containing D-Dimer was mixed with the latex reagent and the reaction buffer, obtaining agglutination directly proportional to the D-Dimer concentration.

ENzygnost sandwich ELISA test (Siemens, Germany) was used to measure prothrombin fragment , according to manufacturer’s instructions.

2.7. Statistical Analysis

Data were analyzed by use of a computerized program (GraphPad Prism, GraphPad Software Inc., San Diego, CA). Statistical methods employed included the use of Mann-Whitney Test and Spearman Correlation Test. Data are presented as the median and interquartile range. The statistical significance was set at .

3. Results

3.1. Circulating LPS Is Increased in IBD Patients and Correlates with TLR2 and TLR4 Serum Concentration in UC

In order to evaluate the penetration of PAMPs in the blood flow, as a result of a defective intestinal barrier function in IBD, we measured circulating LPS in the sera of IBD patients versus control subjects. LPS levels were more elevated in CD (0.400 (95% CI 0.333–0.540) EU/mL) and UC (0.430 (95% CI 0.276–0.677) EU/mL) patients compared with controls (0.325 (95% CI 0.264–0.411) EU/mL; and , resp.) (Figure 1(a)). When performing a subanalysis of CD patients according to their disease location, as described by the Montreal classification [35], we detected significantly increased LPS levels in patients with colonic disease (0.420 (95% CI 0.350–0.620) EU/mL) compared to controls () (Figure 1(a)). Then, we measured serum concentration of TLR2, as putative aspecific marker of systemic innate immune activation. Similarly to LPS, we found more abundant TLR2 in CD (517.21 (95% CI 412.07–890.73) pg/mL) and UC (447.60 (95% CI 339.90–704.41) pg/mL) sera versus controls (281.15 (95% CI 122.23–412.05) pg/mL; and , resp.) (Figure 1(b)). Interestingly, only CD patients with colonic or ileocolonic involvement showed increased TLR2 levels (512.80 (95% CI 436.92–778.27) and 656.72 (95% CI 578.43–1195.55) pg/mL, resp.; and , resp.) compared to controls. We next analyzed the correlation between LPS and TLR2 levels; although we did not find any correlation between these two variables, when considering the whole IBD patients (Figure 1(c)) or CD patients (Figure 1(d)), a significant correlation (, ) was observed when we considered UC patients separated from CD ones (Figure 1(d)). In addition, subanalysis of CD patients according to disease location did not reveal any further association (data not shown). We also evaluated the correlation between serum TLR4 (Figure 2(a)), that is, the principal innate immune receptor for LPS, and circulating LPS, and we detected a significant correlation (, ) (Figure 2(b)); interestingly, when we repeated the analysis dividing patients according to their disease, we found more robust correlation for UC (, ) and CD with colonic involvement (L2 + L3) (, ) than for CD as a whole (, ) (Figure 2(c)).

(a)

(b)

(c)

(d)

Figure 1

Circulating LPS and TLR2 are increased in IBD and correlate with each other in UC. Concentrations of LPS and TLR2 were measured in the sera of IBD (both UC and CD) patients and healthy controls (CONT). (a) LPS serum levels in CONT, UC, and CD patients (left panel) and CD locations according to Montreal classification (right panel). (b) TLR2 serum levels in CONT, UC, and CD patients (left panel) and CD locations according to Montreal classification (right panel). (c) Correlation between circulating levels of LPS and TLR2 in IBD patients. (d) Correlation between circulating levels of LPS and TLR2 in UC (left panel) and CD (right panel) patients. Horizontal bars in (a) and (b) represent median and interquartile range. Statistical analysis was performed by means of Mann-Whitney Test and Spearman Correlation Test. was considered statistically significant.

(a)

(b)

(c)

Figure 2

TLR4 serum correlates with circulating LPS in IBD patients. Concentrations of LPS and TLR4 were measured in the sera of IBD (both UC and CD) patients. (a) TLR4 serum levels in UC and CD patients (left panel) and CD locations according to Montreal classification (right panel). (b) Correlation between circulating levels of LPS and TLR4 in IBD patients. (c) Correlation between circulating levels of LPS and TLR4 in UC (left panel), CD (central panel) patients, and CD patients with colonic and ileocolonic involvement (L2 + L3 according to Montreal classification) (right panel). Horizontal bars in (a) represent median and interquartile range. Statistical analysis was performed by means of Spearman Correlation Test. was considered statistically significant.

3.2. LPS Levels Correlate with Biochemical but Not Clinical Activity in IBD Patients, Whereas TLR2 and TLR4 Levels Are Independent of Disease Activity

In order to evaluate whether or not circulating LPS, TLR2, and TLR4 were merely markers of systemic inflammation or disease activity, we analyzed the correlation between those variables with a biochemical activity marker, that is, CRP, and two commonly used clinical activity indexes, such as the Mayo score for UC and the Harvey-Bradshaw Index for CD. Our analysis was able to demonstrate only a weak correlation between circulating LPS and CRP concentrations (, ) (Figure 3). We observed no correlation at all when subanalysis for disease and disease location was performed (data not shown), suggesting that LPS, TLR2, and TLR4 levels are mostly independent of disease activity. No correlations have been observed with the clinical indexes (i.e., Mayo score and Harvey-Bradshaw Index) (Figure 3).

(a)

(b)

(c)

Figure 3

Circulating LPS correlates with biochemical but not clinical activity in IBD patients. Concentrations of LPS, TLR2, TLR4, and CRP were measured in the sera of IBD (both UC and CD) patients. Clinical activity of UC and CD was evaluated using Mayo score and Harvey-Bradshaw Index. (a) Correlation between CRP serum levels and circulating LPS, TLR2, and TLR4 in IBD patients. (b) Correlation between Mayo score and circulating LPS, TLR2, and TLR4 in UC patients. (c) Correlation between Harvey-Bradshaw Index and circulating LPS, TLR2, and TLR4 in CD patients. Statistical analysis was performed by means of Spearman Correlation Test. was considered statistically significant.

3.3. Concentrations of Circulating LPS Correlate with Plasma Levels of Markers of Activated Coagulation

We also measured the plasma concentrations of D-Dimer and prothrombin fragment , which are well known markers of activated coagulation and are increased in procoagulative states. LPS levels significantly correlated with both D-Dimer (, ) and concentrations (, ) (Figure 4); however, no correlation was found between TLR2 or TLR4 and those coagulation markers (Figure 4). On the other hand, when we analyzed only data obtained in UC patients, we not only confirmed the correlation between LPS and both D-Dimer (, ) and (, ), but also detected good correlations between TLR2 and D-Dimer (, ), TLR4 and D-Dimer (, ), and TLR4 and (, ) (Figure 5). When all CD patients were considered for analysis, no significant correlation was found; remarkably, when only patients with colonic disease (L2 and L3) were taken into account, correlations between D-Dimer and and LPS levels were confirmed (, , and , , resp.) (Figure 6).

(a)

(b)

Figure 4

Circulating LPS correlates with markers of activated coagulation in IBD patients. Concentrations of LPS, TLR2, and TLR4 and levels of D-Dimer and prothrombin fragment were measured in the sera and plasma, respectively, of IBD patients. (a) Correlation between D-Dimer plasma levels and serum LPS, TLR2, and TLR4 in IBD patients. (b) Correlation between prothrombin fragment and circulating LPS, TLR2, and TLR4 in IBD patients. Statistical analysis was performed by means of Spearman Correlation Test. was considered statistically significant.

(a)

(b)

Figure 5

Circulating LPS, TLR2, and TLR4 correlate with markers of activated coagulation in UC patients. Concentrations of LPS, TLR2, and TLR4 and levels of D-Dimer and prothrombin fragment were measured in the sera and plasma, respectively, of UC patients. (a) Correlation between D-Dimer plasma levels and serum LPS, TLR2, and TLR4 in UC patients. (b) Correlation between prothrombin fragment and circulating LPS, TLR2, and TLR4 in UC patients. Statistical analysis was performed by means of Spearman Correlation Test. was considered statistically significant.

(a)

(b)

Figure 6

Circulating LPS correlates with markers of activated coagulation in CD patients with colonic involvement. Concentrations of LPS and levels of D-Dimer and prothrombin fragment were measured in the sera and plasma, respectively, of CD patients. (a) Correlation between D-Dimer plasma levels and serum LPS in all CD patients (left panel), CD patients with exclusive ileal involvement (L1 according to Montreal classification) (central panel), and CD patients with colonic involvement (L2 + L3 according to Montreal classification). (b) Correlation between prothrombin fragment and circulating LPS in all CD patients (left panel), CD patients with exclusive ileal involvement (L1 according to Montreal classification) (central panel), and CD patients with colonic involvement (L2 + L3 according to Montreal classification). Statistical analysis was performed by means of Spearman Correlation Test. was considered statistically significant.

4. Discussion

Since 1972, when Shorter et al. postulated that a primary defect in gut permeability and barrier function may lead to the onset of persistent inflammation in the gut and to the development of IBD [36], a growing body of evidence has demonstrated that the impairment of intestinal barrier function is a common feature in IBD patients leading to derangements in both epithelial permeability to gut antigens and early mucosal innate immune responses, protecting from microorganisms penetration and bacterial translocation [8, 9]. Interestingly, genetic studies demonstrated a strong correlation between the carriage of polymorphisms of genes regulating intestinal epithelial paracellular permeability and the risk of developing UC [37, 38], whereas being carrier of innate immunity-related gene polymorphisms increases the susceptibility to CD [38].

Patients suffering from IBD, and particularly UC [39], are more prone to incur into thromboembolic events [40], similarly to patients affected by other inflammatory and immune-related disorders [6]; however, the only presence of an ongoing inflammatory process does not explain by itself this phenomenon. In fact, it has been shown that the risk of thromboembolism is more elevated in IBD than rheumatoid arthritis, a disease often characterized by a prominent systemic inflammation [7], thus suggesting that some gut specific mechanisms may be involved. Besides deficiencies of vitamins involved in the proper regulation of coagulatory homeostasis, such as vitamin B6, vitamin B12, and folic acid [11–13], the alteration of intestinal barrier function may be a cofactor promoting a procoagulative state in IBD.

The data presented in this paper strongly support this novel hypothesis. In fact, in order to assess intestinal permeability to PAMPs and bacterial translocation from the gut, we measured circulating LPS and found higher concentrations of this bacterial component in the sera of IBD patients (Figure 1(a)). Consistent with the data previously presented by Candia et al. [26], IBD patients also presented higher serum levels of TLR2, as a sign of innate immune activation (Figures 1(b), 1(c), and 1(d)). Remarkably, serum TLR2 was recently described to correlate with the presence of prosthetic joint infection in patients undergoing revision of joint arthroplasty, because of suspected local infection [23]; thus, circulating TLR2 may be considered a marker of the presence of bacterial components in the blood flow. Moreover, high levels of soluble TLR2 were shown in the sera of patients affected by psoriasis [21] and systemic lupus erythematosus [25], diseases in which innate immunity plays a major pathogenetic role [41, 42]. As such, high levels of soluble TLR2 may reflect the activation of innate inflammatory responses.

LPS levels correlated with the serum concentrations of TLR4, which is the innate immune receptor deputed to LPS recognition (Figure 2). This may be a sign of an increased expression and activation of TLR4, because of LPS binding.

Apart from a very modest correlation between LPS and CRP levels, LPS, TLR2, and TLR4 concentrations did not appear to be influenced by biochemical and clinical disease activity (Figure 3), suggesting that their levels may be influenced, for the great part, by intestinal permeability.

Both TLR2 and TLR4 are expressed by platelets and endothelial cells [27–29]; moreover the binding of their respective ligands causes the procoagulatory activation of these cell populations. More in detail, TLR2 signaling in platelets leads to a thromboinflammatory response, through the activation of phosphoinositide 3-kinase [43], cyclooxygenase, and purinergic P2Y1 and P2Y12 receptors [44] and alpha-granule release [45], whereas LPS-TLR4 binding enhances classical agonist-induced platelet aggregation [46, 47]. The TLR2 and TLR4 signaling on endothelial cells strongly activates NF-κB [5, 29], leading to the release of proinflammatory mediators, which can activate the coagulatory cascade. Nonetheless, the pathogenesis of atherosclerotic plaques is mediated by the presence of activated macrophages within the plaque, which also respond vigorously to TLR stimulation releasing proinflammatory cytokines [48].

Given the multiplicity of cell types and pathways involved in the activation of coagulation mediated by TLRs, we decided to measure the activation products of the coagulation and fibrinolysis, that is, the fibrin degradation product D-Dimer and prothrombin fragment , as they describe closely the overall activation of the coagulatory cascade [30]. Remarkably, LPS levels significantly correlated with both D-Dimer and (Figure 4), clearly suggesting that circulating PAMPs may function as triggers for the activation of coagulation.

It may be worthy to note that the correlation between circulating LPS and markers of activated coagulation was stronger when considering only UC patients (Figures 1(d), 2(c), and 5) and CD patients with colonic or ileocolonic disease (L2 and L3 according to Montreal classification [35]) (Figure 6). These data suggest that the presence of colonic disease is the key risk factor for coagulatory unbalance that may follow bacterial translocation from the gut; indeed, the colon has to cope with a significantly greater bacterial burden than the rest of the gastrointestinal tract; as such it is rational that a break-down of intestinal barrier function in this site might lead to a more prominent bacterial penetration/translocation.

Moreover, in order to explain the differences we found in UC versus CD, other issues should be taken into account: CD patients often display greater signs of systemic inflammation rather than UC; as such, data coming from CD patients may suffer from the noise resulting from inflammation-driven activation of coagulation; as an alternative, PAMPs-mediated coagulatory activation may have a different relevance or follow different pathways in UC versus CD, also considering that genetic data suggest different defects in intestinal barrier function in those two diseases [38].

Taken together, our data support the novel hypothesis that intestinal barrier defects contribute to the development of a procoagulatory state in IBD. Our results need to be confirmed with future studies; in fact, the correlations we observed in human patients do not demonstrate the biological importance of the phenomenon we are postulating. A further limitation of our study is that we are using very simple markers in order to explore extremely complex systems. Indeed, experiments on animal models of intestinal inflammation are warranted in order to provide the final demonstration of our hypothesis and mechanistically dissect it and evaluate its real biologic relevance.

Conflict of Interests

None of the authors has any conflict of interests related to this paper/work to declare.

Acknowledgments

The authors acknowledge Dr. Rossella Bader for her important technical support. This work was supported by the Italian Ministry of University and Research PRIN Grant 2007K4HZEJ_004 (MV).

References

W. Rosamond, K. Flegal, K. Furie et al., “Heart disease and stroke statistics—2008 update: a report from the American heart association statistics committee and stroke statistics subcommittee,” Circulation, vol. 117, no. 4, pp. e25–e46, 2008.
View at: Publisher Site | Google Scholar
C. T. Esmon, “Inflammation and thrombosis,” Journal of Thrombosis and Haemostasis, vol. 1, no. 7, pp. 1343–1348, 2003.
View at: Publisher Site | Google Scholar
J. Petaja, “Inflammation and coagulation. An overview,” Thrombosis Research, vol. 127, supplement 2, pp. S34–S37, 2011.
View at: Publisher Site | Google Scholar
J. Frostegård, “Immunity, atherosclerosis and cardiovascular disease,” BMC Medicine, vol. 11, no. 1, article 117, 2013.
View at: Publisher Site | Google Scholar
K. J. Moore, F. J. Sheedy, and E. A. Fisher, “Macrophages in atherosclerosis: a dynamic balance,” Nature Reviews Immunology, vol. 13, no. 10, pp. 709–721, 2013.
View at: Publisher Site | Google Scholar
B. Zoller, X. Li, J. Sundquist, and K. Sundquist, “Autoimmune diseases and venous thromboembolism: a review of the literature,” American Journal of Cardiovascular Disease, vol. 2, no. 3, pp. 171–183, 2012.
View at: Google Scholar
W. Miehsler, W. Reinisch, E. Valic et al., “Is inflammatory bowel disease an independent and disease specific risk factor for thromboembolism?” Gut, vol. 53, no. 4, pp. 542–548, 2004.
View at: Publisher Site | Google Scholar
A. Kaser, S. Zeissig, and R. S. Blumberg, “Inflammatory bowel disease,” Annual Review of Immunology, vol. 28, pp. 573–621, 2010.
View at: Publisher Site | Google Scholar
L. Pastorelli, C. D. Salvo, J. R. Mercado, M. Vecchi, and T. T. Pizarro, “Central role of the gut epithelial barrier in the pathogenesis of chronic intestinal inflammation: iessons learned from animal models and human genetics,” Frontiers in Immunology, vol. 4, article 280, Article ID Article 280, 2013.
View at: Publisher Site | Google Scholar
M. Zaeem Cader and A. Kaser, “Recent advances in inflammatory bowel disease: mucosal immune cells in intestinal inflammation,” Gut, vol. 62, no. 11, pp. 1653–1664, 2013.
View at: Publisher Site | Google Scholar
S. Saibeni, L. Spina, and M. Vecchi, “Exploring the relationships between inflammatory response and coagulation cascade in inflammatory bowel disease,” European Review for Medical and Pharmacological Sciences, vol. 8, no. 5, pp. 205–208, 2004.
View at: Google Scholar
S. Saibeni, M. Cattaneo, M. Vecchi et al., “Low vitamin B₆ plasma levels, a risk factor for thrombosis, in inflammatory bowel disease: role of inflammation and correlation with acute phase reactants,” The American Journal of Gastroenterology, vol. 98, no. 1, pp. 112–117, 2003.
View at: Publisher Site | Google Scholar
M. Cattaneo, M. Vecchi, M. L. Zighetti et al., “High prevalence of hyperhomocysteinemia in patients with inflammatory bowel disease: a pathogenic link with thromboembolic complications?” Thrombosis and Haemostasis, vol. 80, no. 4, pp. 542–545, 1998.
View at: Google Scholar
T. H. Mogensen, “Pathogen recognition and inflammatory signaling in innate immune defenses,” Clinical Microbiology Reviews, vol. 22, no. 2, pp. 240–273, 2009.
View at: Publisher Site | Google Scholar
E. LeBouder, J. E. Rey-Nores, N. K. Rushmere et al., “Soluble forms of Toll-like receptor (TLR)2 capable of modulating TLR2 signaling are present in human plasma and breast milk,” Journal of Immunology, vol. 171, no. 12, pp. 6680–6689, 2003.
View at: Publisher Site | Google Scholar
K. I. Iwami, T. Matsuguchi, A. Masuda, T. Kikuchi, T. Musikacharoen, and Y. Yoshikai, “Cutting edge: naturally occurring soluble form of mouse toll-like receptor 4 inhibits lipopolysaccharide signaling,” Journal of Immunology, vol. 165, no. 12, pp. 6682–6686, 2000.
View at: Publisher Site | Google Scholar
I. Muñoz, M. P. Sepulcre, J. Meseguer, and V. Mulero, “Molecular cloning, phylogenetic analysis and functional characterization of soluble Toll-like receptor 5 in gilthead seabream, Sparus aurata,” Fish & Shellfish Immunology, vol. 35, no. 1, pp. 36–45, 2013.
View at: Publisher Site | Google Scholar
S. L. Zunt, L. V. Burton, L. I. Goldblatt, E. E. Dobbins, and M. Srinivasan, “Soluble forms of Toll-like receptor 4 are present in human saliva and modulate tumour necrosis factor-α secretion by macrophage-like cells,” Clinical and Experimental Immunology, vol. 156, no. 2, pp. 285–293, 2009.
View at: Publisher Site | Google Scholar
A.-C. Raby, E. le Bouder, C. Colmont et al., “Soluble TLR2 reduces inflammation without compromising bacterial clearance by disrupting TLR2 triggering,” Journal of Immunology, vol. 183, no. 1, pp. 506–517, 2009.
View at: Publisher Site | Google Scholar
R.-S. Chang, Y.-C. Wang, and S.-T. Kao, “Soluble toll-like receptor 4 reversed attenuating effect of Chinese herbal Xiao-Qing-Long-Tang on allergen induced nerve growth factor and thymic stromal lymphopoietin,” Experimental and Therapeutic Medicine, vol. 6, no. 5, pp. 1199–1207, 2013.
View at: Publisher Site | Google Scholar
K. Kondelkova, J. Krejsek, L. Borska et al., “Membrane and soluble Toll-like receptor 2 in patients with psoriasis treated by Goeckerman therapy,” International Journal of Dermatology, vol. 53, no. 11, pp. e512–e517, 2014.
View at: Publisher Site | Google Scholar
H.-B. Yang, K.-Q. Xie, J.-M. Deng, and S.-M. Qin, “Expression of soluble toll-like receptors in pleural effusions,” Chinese Medical Journal, vol. 123, no. 16, pp. 2225–2230, 2010.
View at: Publisher Site | Google Scholar
E. Galliera, L. Drago, C. Vassena et al., “Toll-like receptor 2 in serum: a potential diagnostic marker of prosthetic joint infection?” Journal of Clinical Microbiology, vol. 52, no. 2, pp. 620–623, 2013.
View at: Publisher Site | Google Scholar
A. Zhao, C. Blackburn, J. Chin, and M. Srinivasan, “Soluble toll like receptor 2 (TLR-2) is increased in saliva of children with dental caries,” BMC Oral Health, vol. 14, no. 1, article 108, 2014.
View at: Publisher Site | Google Scholar
M. E. Houssen, R. H. El-Mahdy, and D. A. Shahin, “Serum soluble toll-like receptor 2: a novel biomarker for systemic lupus erythematosus disease activity and lupus-related cardiovascular dysfunction,” International Journal of Rheumatic Diseases, 2014.
View at: Publisher Site | Google Scholar
E. Candia, D. Díaz-Jiménez, P. Langjahr et al., “Increased production of soluble TLR2 by lamina propria mononuclear cells from ulcerative colitis patients,” Immunobiology, vol. 217, no. 6, pp. 634–642, 2012.
View at: Publisher Site | Google Scholar
F. Cognasse, H. Hamzeh, P. Chavarin, S. Acquart, C. Genin, and O. Garraud, “Evidence of Toll-like receptor molecules on human platelets,” Immunology and Cell Biology, vol. 83, no. 2, pp. 196–198, 2005.
View at: Publisher Site | Google Scholar
F. X. Zhang, C. J. Kirschning, R. Mancinelli et al., “Bacterial lipopolysaccharide activates nuclear factor-kappaB through interleukin-1 signaling mediators in cultured human dermal endothelial cells and mononuclear phagocytes,” The Journal of Biological Chemistry, vol. 274, no. 12, pp. 7611–7614, 1999.
View at: Publisher Site | Google Scholar
E. Faure, O. Equils, P. A. Sieling et al., “Bacterial lipopolysaccharide activates NF-κB through toll-like receptor 4 (TLR-4) in cultured human dermal endothelial cells. Differential expression of TLR-4 and TLR-2 in endothelial cells,” The Journal of Biological Chemistry, vol. 275, no. 15, pp. 11058–11063, 2000.
View at: Publisher Site | Google Scholar
M. D. Boisclair, H. Ireland, and D. A. Lane, “Assessment of hypercoagulable states by measurement of activation fragments and peptides,” Blood Reviews, vol. 4, no. 1, pp. 25–40, 1990.
View at: Publisher Site | Google Scholar
E. F. Stange, S. P. L. Travis, S. Vermeire et al., “European evidence-based Consensus on the diagnosis and management of ulcerative colitis: definitions and diagnosis,” Journal of Crohn's & Colitis, vol. 2, no. 1, pp. 1–23, 2008.
View at: Publisher Site | Google Scholar
A. Dignass, G. van Assche, J. O. Lindsay et al., “The second European evidence-based Consensus on the diagnosis and management of Crohn's disease: current management,” Journal of Crohn's & Colitis, vol. 4, no. 1, pp. 28–62, 2010.
View at: Publisher Site | Google Scholar
R. F. Harvey and J. M. Bradshaw, “A simple index of Crohn's-disease activity,” The Lancet, vol. 1, no. 8167, p. 514, 1980.
View at: Google Scholar
K. W. Schroeder, W. J. Tremaine, and D. M. Ilstrup, “Coated oral 5-aminosalicylic acid therapy for mildly to moderately active ulcerative colitis: a randomized study,” The New England Journal of Medicine, vol. 317, no. 26, pp. 1625–1629, 1987.
View at: Publisher Site | Google Scholar
J. Satsangi, M. S. Silverberg, S. Vermeire, and J.-F. Colombel, “The Montreal classification of inflammatory bowel disease: controversies, consensus, and implications,” Gut, vol. 55, no. 6, pp. 749–753, 2006.
View at: Publisher Site | Google Scholar
R. G. Shorter, K. A. Huizenga, and R. J. Spencer, “A working hypothesis for the etiology and pathogenesis of nonspecific inflammatory bowel disease,” The American Journal of Digestive Diseases, vol. 17, no. 11, pp. 1024–1032, 1972.
View at: Publisher Site | Google Scholar
A. I. Thompson and C. W. Lees, “Genetics of ulcerative colitis,” Inflammatory Bowel Diseases, vol. 17, no. 3, pp. 831–848, 2011.
View at: Publisher Site | Google Scholar
C. W. Lees, J. C. Barrett, M. Parkes, and J. Satsangi, “New IBD genetics: common pathways with other diseases,” Gut, vol. 60, no. 12, pp. 1739–1753, 2011.
View at: Publisher Site | Google Scholar
G. C. Nguyen and J. Sam, “Rising prevalence of venous thromboembolism and its impact on mortality among hospitalized inflammatory bowel disease patients,” The American Journal of Gastroenterology, vol. 103, no. 9, pp. 2272–2280, 2008.
View at: Publisher Site | Google Scholar
H. Yuhara, C. Steinmaus, D. Corley et al., “Meta-analysis: the risk of venous thromboembolism in patients with inflammatory bowel disease,” Alimentary Pharmacology and Therapeutics, vol. 37, no. 10, pp. 953–962, 2013.
View at: Publisher Site | Google Scholar
W. R. Swindell, P. E. Stuart, M. K. Sarkar et al., “Cellular dissection of psoriasis for transcriptome analyses and the post-GWAS era,” Acta Veterinaria Scandinavica, vol. 7, article 27, 2014.
View at: Publisher Site | Google Scholar
D. Salem, R. Subang, P. Laplante, J. Levine, and J. Rauch, “The dual role of innate immunity in antiphospholipid syndrome and systemic lupus erythematosus,” Lupus, vol. 23, no. 12, pp. 1327–1331, 2014.
View at: Publisher Site | Google Scholar
P. Blair, S. Rex, O. Vitseva et al., “Stimulation of Toll-like receptor 2 in human platelets induces a thromboinflammatory response through activation of phosphoinositide 3-kinase,” Circulation Research, vol. 104, no. 3, pp. 346–354, 2009.
View at: Publisher Site | Google Scholar
H. Kälvegren, C. Skoglund, C. Helldahl, M. Lerm, M. Grenegård, and T. Bengtsson, “Toll-like receptor 2 stimulation of platelets is mediated by purinergic P2X1-dependent Ca2+ mobilisation, cyclooxygenase and purinergic P2Y1 and P2Y12 receptor activation,” Thrombosis and Haemostasis, vol. 103, no. 2, pp. 398–407, 2010.
View at: Publisher Site | Google Scholar
S. Rex, L. M. Beaulieu, D. H. Perlman et al., “Immune versus thrombotic stimulation of platelets differentially regulates signalling pathways, intracellular protein-protein interactions, and α-granule release,” Thrombosis and Haemostasis, vol. 102, no. 1, pp. 97–110, 2009.
View at: Publisher Site | Google Scholar
G. Zhang, J. Han, E. J. Welch et al., “Lipopolysaccharide stimulates platelet secretion and potentiates platelet aggregation via TLR4/MyD88 and the cGMP-dependent protein kinase pathway,” The Journal of Immunology, vol. 182, no. 12, pp. 7997–8004, 2009.
View at: Publisher Site | Google Scholar
G. T. Brown and T. M. McIntyre, “Lipopolysaccharide signaling without a nucleus: kinase cascades stimulate platelet shedding of proinflammatory IL-1β-rich microparticles,” The Journal of Immunology, vol. 186, no. 9, pp. 5489–5496, 2011.
View at: Publisher Site | Google Scholar
L. Chávez-Sánchez, J. E. Espinosa-Luna, K. Chávez-Rueda, M. V. Legorreta-Haquet, E. Montoya-Díaz, and F. Blanco-Favela, “Innate immune system cells in atherosclerosis,” Archives of Medical Research, vol. 45, no. 1, pp. 1–14, 2014.
View at: Publisher Site | Google Scholar

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Copyright © 2015 Luca Pastorelli et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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