Background—Vascular endothelial E- selectin expression is induced by proinflammatory cytokines and contributes to accumulation of leucocytes in tissues.
Aims—To investigate the role of E-selectin in inflammatory bowel disease (IBD).
Methods—E-selectin expression was assessed in patients with ulcerative colitis and Crohn’s disease by measuring the concentration of circulating soluble E-selectin (sE-selectin) using ELISA, by immunohistochemistry of colonic biopsy specimens, and by abdominal immunoscintigraphy after injecting radiolabelled F(ab′)2 fragment of a monoclonal anti-E-selectin antibody. The value of scintigraphy using anti-E-selectin was judged by a prospective comparative study of autologous leucocyte scanning and E-selectin antibody scanning in 17 patients with IBD.
Results—Circulating sE-selectin was elevated in patients with clinically active disease. Tissue expression of E-selectin was enhanced in patients with active inflammation, with weak or absent expression in inactive disease and healthy controls. In-111 labelled anti-E-selectin scintiscans were compared with Tc-99m labelled leucocyte scans performed 24 hours earlier. Twelve patients had areas of active inflammation on leucocyte scan while 11 patients had positive E-selectin scans. The results of the two scans were concordant in 14 patients, with those positive for both (10/17) showing similar disease localisation and extent.
Conclusions—Tissue E-selectin and circulating sE-selectin are increased during active inflammatory bowel disease. Anti-E-selectin imaging with radiolabelled monoclonal antibody identified areas of inflammation in Crohn’s disease and ulcerative colitis. The technique should prove useful clinically for identifying the site and extent of disease.
- inflammatory bowel disease
- Crohn’s disease
- ulcerative colitis
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The vascular endothelium is an active participant in inflammatory processes. The response of endothelial cells to a variety of proinflammatory stimuli includes synthesis and expression of a number of cell surface antigens,1 many of which are also released into the bloodstream. E-selectin is a 115 kDa glycoprotein which is expressed on the luminal surface of endothelial cells in response to proinflammatory cytokines such as interleukin 1 (IL-1) and tumour necrosis factor (TNF), or bacterial lipopolysaccharide, and plays a major role in facilitating the emigration of leucocytes into the tissues.2-4
Accumulation of polymorphonuclear leucocytes from the circulation into the gut wall is an integral component of the inflammatory process in the chronic inflammatory bowel diseases (IBD), ulcerative colitis, and Crohn’s disease. E-selectin expression has been shown immunohistochemically in areas of active involvement of the gut.5-8 As expression of E-selectin is limited to activated endothelium,9 10 this molecule provides a potential target for in vivo detection and quantitation of disease activity.
Recent studies using animal models of inflammation have shown that intravenously injected radiolabelled anti-E-selectin monoclonal antibody is specifically taken up by activated endothelium, and that the degree of uptake can provide a quantitative measurement of E-selectin expression.11 12 Murine anti-E-selectin monoclonal antibody 1.2B6, labelled with In-111, can be used to image E-selectin expression, both in models of monoarthritis13-15 and in patients with rheumatoid arthritis,16 the specificity of anti-E-selectin uptake being shown by significantly more focal and intense images compared with those obtained with radiolabelled control IgG.
In this study we have explored the potential of this simple technique to image inflamed intestine in IBD. We have also confirmed E-selectin up regulation in ulcerative colitis and Crohn’s disease by measuring soluble E-selectin levels17 18 in the circulation and by detection of E-selectin expression immunohistologically in intestinal biopsy specimens.
Materials and methods
PATIENTS AND CONTROLS
For circulating soluble E-selectin, three groups were investigated: group I, Crohn’s disease (CD; 16 patients; nine men and seven women; median age 42.5 years, range 21–65); group II, ulcerative colitis (UC; 16 patients; eight men and eight women; median age 38 years, range 20–79); group III, controls (11 healthy volunteers; seven men and four women; median age 33 years, range 18–68). For imaging with monoclonal anti-E-selectin antibody two groups, both with active IBD, were investigated: group I, CD (seven patients; four men and three women; median age 33 years, range 21–51); group II, UC (10 patients; six men and four women; median age 38.5 years, range 22–79).
The diagnosis of UC and CD was based on clinical, radiological, endoscopic, and biopsy findings. Approval for the study was obtained from the Hammersmith Hospitals Trust Research Ethics Committee and the Administration of Radioactive Substances Advisory Committee (ARSAC). Each patient gave informed consent to participate in the study.
Crohn’s disease activity was assessed by the Crohn’s Disease Activity Index (CDAI)19 which assesses eight clinical variables. Remission was defined by a score of less than 150 and severe illness by a score of more than 450. The patients with ulcerative colitis were clinically assessed as being in remission or having mild, moderate, or severe disease, as described by Truelove and Witts.20
MONOCLONAL ANTIBODY LABELLING WITH111In
1.2B6 is a mouse IgG1 monoclonal antibody and recognises porcine and human E-selectin.21 The F(ab′)2 fragment was produced by pepsin digestion of the whole antibody and further purified by protein A affinity chromatography and dialysis. The purity of F(ab′)2 was assessed by non-reducing sodium dodecyl sulphate-polyacrylamide gel electrophoresis, and a single band was identified. The immunoreactivity of F(ab′)2 was confirmed by enzyme linked immunosorbent assay (ELISA) on cultured endothelial cells.
Antibodies were labelled with 111In using the method of Danpure et al.22 The F(ab′)2 was coupled with diethylenetriaminepentaacetic acid (DTPA) bicyclic anhydride (Sigma Chemical Co, Dorset, UK) at pH 8.0, pooled, filtered through a 2 μm microfilter (Ministart, Sartorius GmbH, Gottingen, Germany) and stored at 4°C in 20 μl aliquots. On the day of the experiment, 20–25 MBq of carrier free 111In chloride (Amersham International, Amersham, UK) was brought to pH 6.0 by addition of 45 μl of 3.8% sodium citrate, pH 7.4, and was added to a 20 μl (1 mg/ml) aliquot of antibody. After 30 minutes at room temperature, free 111In was removed by passage through a Sephadex G50 column. The radiopharmaceutical purity, assessed using thin layer chromatography on silica gel (ITLC-SG; Gelman Sciences, Ann Arbor, Michigan, USA) with phosphate buffered saline (PBS) solution as the solvent, was 98.4 (1.4)%. The injected dose was 12.4 (1) MBq.
LEUCOCYTE LABELLING WITH99mTc
Autologous polymorphonuclear leucocytes (PMN) were separated from 96 ml of venous blood and labelled with Tc-99m hexamethylpropyleneamine oxime (HMPAO; hexametazime (CERETEC); Amersham International, UK), using a modification of the method of Danpureet al.22 The blood was drawn in two 60 ml syringes containing 10 ml of acid citrate dextrose (ACD; National Institute of Health formula A). ACD mixed blood (40 ml) was centrifuged at 3000 rpm for 15 minutes to obtain cell free plasma for washing and resuspension of labelled white cells. Remaining ACD-blood was mixed with hydroxyethyl starch (Hespan, 6% in saline solution; Dupont Pharm, Letchworth, UK) and was left for about one hour at room temperature. Leucocyte rich, platelet rich supernatant was removed and centrifuged for five minutes at 150 g to obtain a pellet containing leucocytes. Leucocytes were labelled using 250 MBq of freshly prepared 99mTc HMPAO. The labelled PMNs were washed and suspended in 5 ml of cell free plasma. The mean labelling efficiency was 75% and the injected dose was 170 (15) MBq. The number of PMN injected was 1.4 × 108 and the cell purity was more than 90% with less than 4% non-viable cells, as assessed by trypan blue and ethidium bromide/acridine orange stain in PBS.
Anterior, posterior, and pelvic outlet images were obtained one, four, and 24 hours after intravenous injection of 99mTc labelled leucocytes, using a gammacamera equipped with a low energy, general purpose collimator. 111In labelled anti-E-selectin monoclonal antibody was administered 24 hours after the99mTc leucocyte injection and images were obtained using a medium energy collimator at one, four, and 24 hours and in some cases 48 hours post-injection.
EVALUATION OF IMAGES
Images were evaluated without knowledge of clinical data by experienced nuclear medicine physicians. The distribution of uptake of anti-E-selectin was compared with that of 99mTc PMN. For the localisation of disease activity with labelled PMN, intestinal segments were considered pathological when labelled PMN showed abnormal localisation at one hour, and PMN imaging at 24 hours was used to outline the colon but not for diagnostic purposes. In the case of111In labelled anti-E-selectin, intestinal localisation at any time (four, 24, 48 hours) was considered abnormal.
ASSAY OF SOLUBLE E SELECTIN
Acid citrate dextrose containing venous blood (5 ml) was centrifuged at 3000 rpm for 15 minutes to isolate cell free plasma. Quantitative estimation of soluble E-selectin was performed in triplicate using sandwich ELISA.18 Briefly, 96 well polyvinyl plates (Greiner, UK; 655061) were coated with monoclonal mouse antihuman antibody and were kept overnight at 4°C. The next morning plates were washed multiple times and blocked with 1% bovine serum albumin for two hours at 37°C. Plates were then incubated with plasma and multiple dilutions of known amounts of E-selectin (later used to plot a standard curve to quantitate samples) at 37°C for two hours. After multiple washes plates were again incubated at 37°C with biotinylated mouse antihuman monoclonal antibody. Two hours later plates were washed and incubated with peroxidase conjugated reagents A&B (Sigma, UK) for one hour at room temperature. After further washes plates were developed with orthophenylenediamine and the reaction was stopped with 2 M H2SO4. Colour intensity was measured using an ELISA reader at 492 nm.
IMMUNOHISTOLOGICAL ASSESSMENT OF BIOPSY SPECIMENS
Cryostat sections of biopsy samples from colon and small intestine were immunostained using a modified peroxidase method.23 Briefly, 5 μm thick frozen sections were cut by cryostat and air dried for at least one hour. Sections were fixed in acetone and endogenous peroxidase activity was blocked by H2O2. Monoclonal anti-E-selectin antibody was added to the sections in a humid chamber and kept at 4°C overnight. This was followed by polyclonal sheep antimouse peroxidase conjugated antibody for one hour at room temperature. After this slides were immersed in 3,3-diaminobenzidine solution for 15 minutes, washed, immersed in haematoxylin for one minute, washed, dehydrated and cleaned before mounting coverslips. Sections were washed with PBS two to three times after each step. The degree of inflammation and the intensity of E-selectin expression in tissue sections was scored by an experienced observer blinded to the clinical diagnosis of patients. A semiquantitative scale of 0 (no detectable staining), + (weak staining of occasional vessels), ++ (widespread moderately stained vessels), +++ (widespread strongly stained vessels) was used. A similar semiquantitative analysis was used for the extent of polymorphonuclear leucocyte infiltration in the lamina propria of the mucosa.
The Mann-Whitney U test was used to assess the differences between patient groups. Simple linear regression and Pearson’s product moment correlation were used to identify the relation of variables with disease activity as determined by the CDAI and Truelove and Witts’ criteria.19 20
CIRCULATING SOLUBLE E SELECTIN
sE-selectin was measured in peripheral blood of 43 individuals (fig 1). sE-selectin values in the serum of 11 healthy donors ranged from 18 to 53 ng/ml (mean (SD) 41 (14) ng/ml). Values were redetermined at three months in six volunteers and did not show any statistically significant variation. The serum levels of sE-selectin of patients with inactive UC (eight patients) and CD (eight patients) did not differ significantly from normal (37 (21) and 35 (13) ng/ml respectively). However, in both active UC (eight patients) and CD (eight patients) there were significantly elevated levels of sE-selectin (98 (22) and 89 (16) ng/ml respectively) compared with healthy controls (both p<0.001) and patients with inactive disease (both p<0.001). The relation between disease activity and circulating sE-selectin was explored. In CD, there was a significant correlation between CDAI and circulating sE-selectin levels (r=0.715, p<0.001). Disease activity in UC was measured as mild, moderate, and severe using the Truelove and Witts’ criteria. sE-selectin levels correlated well with disease activity.
Previous studies of patients with arthritis have shown that in the absence of active synovial inflammation, labelled anti-E-selectin antibody accumulates in bone marrow, liver, and spleen producing background similar to that seen in leucocyte scanning (fig 2). Excretion of radioparticles is also seen in the urinary bladder.
Seventeen patients with IBD were sequentially imaged with99mTc labelled leucocytes and 24 hours later with111In labelled anti-E-selectin F(ab′)2 fragment (table 1). Twelve of these patients had areas of active inflammation detectable by leucocyte scanning, and 11 patients had anti-E-selectin scans in which abnormal localisation in areas of bowel was imaged (positive scans). Ten of the 13 patients with clinically active disease showed similar areas of disease isotope uptake with each type of scan (fig 3). One patient with a recent relapse of UC was positive with anti-E-selectin scanning alone, while two patients had positive leucocyte but negative anti-E-selectin scans. In four patients with clinically inactive disease, both types of scan were negative. Thus results were concordant for both detection and extent of inflammation in 10/13 patients with clinically active disease, and were also concordant in all four patients with inactive disease.
A major difference in the scan appearances with the two techniques concerned migration of radioactivity after initial localisation to bowel. As has been well recognised previously, labelled leucocytes are excreted into the intestinal lumen after initial localisation in the wall, and thereafter move distally with the faecal stream. This is known to render interpretation of the disease extent unreliable if scans are performed at time intervals of greater than four hours after reinjection of leucocytes (fig 4). In contrast areas identified by anti-E-selectin images stayed well localised in early and late scans and indeed were intensified further with time (fig 5).
Eight patients also underwent colonoscopic examination within two weeks prior to scanning although this was not a formal part of the study. This opportunity was taken to evaluate the results of anti-E-selectin scans and colonoscopic appearance. In all instances there was concordance between scans and colonoscopic appearance with respect to distribution of disease in the colon. In one patient in whom colonoscopic examination did not permit ileal examination, ileal inflammation was detected on the scan; in others more proximal areas of ileal inflammation were detected with the scan. Histological examination of the biopsy specimens of endoscopically active areas taken during colonoscopy confirmed the diagnosis of active inflammatory bowel disease. Table 2 summarises the results.
Intestinal tissue specimens were obtained from five patients without inflammatory or neoplastic bowel disease, and from nine patients (four active and five inactive) with inflammatory bowel disease, five of whom also participated in the E-selectin imaging study. Of the imaged patients, three had clinically active disease and all were positive on E-selectin scan. Among these patients immunohistological examination of biopsy specimens, taken during colonoscopy or from surgically resected samples, showed strong widespread expression of E-selectin (fig 6). Two patients, who had clinically inactive disease at the time of imaging, were negative on scans and immunohistochemical examination of the tissue taken during colonoscopic examination showed weak or undetectable E-selectin expression. Table 3 presents the details of these five patients, together with the sE-selectin levels, and assessment of the degree of polymorphonuclear infiltration in the biopsy specimens. One patient with clinically active disease did not participate in the imaging study; however immunohistochemical examination of biopsy specimens taken during colonoscopy showed widespread expression of E-selectin. Similarly three of five patients with clinically inactive disease, who did not participate in the imaging study, showed minimal or undetectable E-selectin expression on immunohistology. Thus of the nine patients studied immunohistologically, all four with active disease had E-selectin expression detected; of the five with clinically inactive disease, weak expression was detected in one. Four of five healthy volunteers had no E-selectin positive blood vessels and one had minimal labelling.
There are well recognised problems in defining the extent and activity of IBD, especially in Crohn’s disease. For example the rectum, which is the area of gut mucosa most readily available for inspection and sampling, may be endoscopically normal during relapse either due to the effects of local treatment in ulcerative colitis or disease distribution in Crohn’s disease. Assessment of the whole colon in ulcerative colitis and Crohn’s disease by colonoscopy and histology is often inadvisable in active disease and radiological examination of the small and large intestine may fail to reflect inflammatory activity.
The technique of leucocyte scanning was developed against this background, and in specialised centres has been shown to be effective in identifying the presence and site of active inflammation in IBD.24-27 Leucocyte scanning has also been developed for the quantitation of disease activity, and applied in clinical trials of drug and dietary therapy. Various authors have reported good correlation between the site and extent of labelled leucocyte accumulation and the results of endoscopy, histology, and radiology.28-31 However there are several disadvantages of leucocyte scanning techniques. The most obvious are the requirements for adequate numbers of circulating leucocytes and for in vitro manipulation of autologous blood with its associated risks of infection. The preparation of labelled leucocytes requires technical expertise, and this in particular seems to have limited the adoption of the technique beyond specialist centres. With respect to accuracy, a constraint of the use of leucocyte scanning in IBD is the fact that leucocytes that have migrated to inflamed bowel transmigrate into the intestinal lumen within a few hours, making the use of early scans essential to avoid overestimation of the extent of disease (fig 4). In addition, if the readily available 99mTc HMPAO technique is used to label leucocytes, urinary excretion of isotope into the bladder renders assessment of the pelvis more difficult and biliary excretion contributes to the appearance of bowel radioactivity in delayed views.
Despite these shortcomings many specialist centres have recognised leucocyte scanning as a reliable technique for the diagnosis and assessment of inflammatory bowel disease, but a simpler alternative technique is clearly desirable. This study was designed to explore an approach which does not require in vitro manipulation of autologous blood, is neither technically demanding nor time consuming, and which could be available to non-specialist centres. Previous approaches aimed at simplifying scintigraphic techniques have included the use of labelled antigranulocyte monoclonal antibody, chemotactic peptides, simple colloids phagocytosed by leucocytes, and human immunoglobulin.32-36 Unfortunately none of these agents has fulfilled their early promise, either due to insufficient selective uptake into inflammatory sites or problems with non-specific binding, but the data presented here show that antibody scanning for E-selectin offers a convenient and effective approach.
E-selectin provides an attractive target for imaging inflammation in IBD. The molecule, on the endothelial surface of blood vessels, is reliably detected by monoclonal antibody. E-selectin is up regulated during inflammation and its expression is thought to reflect the effects of proinflammatory cytokines (for example, IL-1 or TNF), or possibly bacterial lipopolysaccharide, on the activation state of endothelial cells. The inflamed mucosa in IBD has been shown to express IL-1 and TNF-α by multiple techniques including immuno- histochemistry.2-4 We have shown that enhanced E-selectin expression in IBD can be localised by radiolabelled antibody scanning, and that the results show good concordance with scans obtained with labelled leucocytes. This concordance was apparent both for patients with colonic and for those with small intestinal disease. In a limited analysis of regional E-selectin expression detected by scintigraphy with regional colonoscopic appearances, good correlation was also found. At this stage, we have not performed a series of studies in other inflammatory diseases of the bowel such as bacillary dysentery or diverticulitis. There is however no reason to anticipate that the up-regulation of E-selectin in the bowel should be limited to the chronic idiopathic inflammatory bowel diseases that we have studied; indeed in one individual with HIV associated diarrhoea in whom the technique was applied, notable terminal ileal accumulation of anti-E-selectin was identified, and a diagnosis of cytomegalovirus infection and cryptosporidiosis eventually established. The study in this individual also exemplifies one potential advantage of monoclonal antibody scintigraphy as compared with leucocyte scanning: avoidance of ex vivo manipulation of blood from potentially infectious patients.
In this study the anti-E-selectin monoclonal antibody was labelled with111In in order to allow comparison within 24 hours with99mTc labelled leucocyte scans; preliminary observations indicate that more focal and intense images of anti-E-selectin localisation can, as would be expected, be obtained using99mTc labelling and we are currently developing this aspect further. It is also clear that before the technique will be widely used, further developments of monoclonal technology are desirable. Although murine antibodies can be safely administered, particularly as antibody fragments when unbound antibody can be excreted rapidly, the use of humanised or chimeric antibodies minimises further the risk of an untoward immunological reaction.
Expression of E-selectin in active IBD was not only shown locally in inflamed tissues, but was also increased in plasma in the form of the circulating soluble molecule (sE-selectin). While the majority of endothelial cell surface E-selectin is thought to be removed from the cell surface by internalisation, a proportion is shed and this probably accounts for the circulating soluble form.37 It is of interest that levels of sE-selectin were significantly increased in active IBD, and it is possible that sE-selectin measurements might be useful clinically in IBD for long term monitoring. Some studies have not found a difference in soluble E-selectin levels among patients with active disease as compared with those with inactive or no disease,38 but more recent studies report the same findings as our study.39 40 It may be that measuring circulating sE-selectin could be used for planning investigations in patients with inflammatory bowel disease and to determine when anti-E-selectin scanning will be useful in the assessment of disease, a hypothesis which requires further evaluation. The demonstration of vascular endothelial E-selectin expression in active disease immunohistochemically, with absent or weak expression in inactive disease and healthy volunteers, suggests that E-selectin is an attractive candidate for further development in the diagnosis and treatment of inflammatory processes; there are currently no data as to whether alternative vascular cell adhesion molecules (VCAM) could be developed as targets in a similar way. Both VCAM-1 and intercellular adhesion molecule (ICAM) 1 may have a degree of constitutive expression in normal mucosa, and VCAM-1 may not be overexpressed in inflammatory bowel disease.39
In conclusion, we have shown the feasibility of using anti-E-selectin monoclonal antibody to evaluate patients with IBD. This imaging technique has a number of advantages over radiolabelled leucocyte scanning, and further work is in progress towards developing the technique for general use. We anticipate that the use of99mTc labelled anti-E-selectin antibody will improve image quality in comparison with 111In. With further study, the analysis of scans should allow quantitation of E-selectin expression, by expressing regional uptake as a proportion of injected dose, or by comparison of gut uptake with another region of uptake such as bone marrow. Besides the importance of the study for the identification of inflammatory activity in IBD, this report also paves the way towards the potential use of antibodies to adhesion molecules for therapeutic purposes. A recent study has shown improvement in acetic acid induced inflammatory bowel disease in rats after administration of anti-ICAM-1 antibodies.41 Targeting antibody to adhesion molecules in inflamed endothelium in man has been shown in our study to be feasible, and the strategy can in the future be developed to address combinations of antigen and antibody aimed at preventing leucocyte accumulation.
This work was supported by the National Association for Colitis and Crohn’s Disease UK, the Hammersmith Hospitals Trust Special Trustees, and the Medical Research Council of the UK.
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