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Gastroenterol Hepatol (N Y). 2006 December; 2(12): 906–913.
PMCID: PMC5359938

Leukocytapheresis: An “Out-of-Body” Experience in Inflammatory Bowel Disease

Abstract

Leukocytapheresis has reemerged as a novel “nondrug” approach in the treatment of inflammatory bowel disease. The technique involves the extracorporeal passage of peripheral blood through a column of cellulose diacetate beads (Adacolumn) or a nonwoven polyester fiber filter (Cellsorba). The benefits accrued from the filtered extraction of granulocytes, monocytes (Adacolumn), and lymphocytes (Cellsorba) appear greater than the simple extraction of these cells. There appears to be an immunologic modulation of leukocytes and dendritic cells and a diminished response to proinflammatory cytokines. Unfortunately, blinded placebo-controlled trials are lacking. Nevertheless, the aggregate clinical experience detailed in this review suggests a relatively safe and attractive alternative to current inflammatory bowel disease therapies. Randomized, controlled sham trials are in progress.

Keywords: Leukocytapheresis, inflammatory cytokines, granulocytes, monocytes

Treatments for ulcerative colitis (UC) and Crohn’s disease (CD) appear to proliferate exponentially, but close scrutiny of their efficacy leads to the conclusion that a considerable portion of patients fail to benefit or are at risk for drug side effects or adverse events.1,2 One effort to avoid such drug toxicity and improve clinical benefit has focused on selective apheresis of leukocytes.3,4 Granulocytes, monocytes, and, to a lesser degree, lymphocytes, play a significant role in initiating and maintaining the inflammatory reaction of inflammatory bowel disease (IBD) by releasing proinflammatory cytokines, proteases, and other mediators of inflammation.5,6 Recognizing the significant concentrations of granulocytes and monocytes both in the circulation and inflamed tissues of IBD patients,7,8,9 selective leukocytapheresis (LCAP) has been employed to remove these cells from the host’s circulation before exiting into the inflamed tissue, with the aim of improving or modifying the cellular immune response.10,11

Although not a new concept, interest in extracorporeal LCAP has increased recently and stimulated several studies, primarily small uncontrolled studies. Although effectiveness has not as yet been substantiated by blinded placebo-controlled randomized clinical trials, the idea of a no-drug approach is appealing. The concept of taking something from the patient that is contributing to the disease and not giving a chemical or biologic therapy to the patient presents an attractive therapeutic alternative.

Leukocytapheresis Techniques

Most commonly with LCAP, peripheral blood is passed extracorporeally through a removable column or fiber filter that adsorbs leukocytes while the remaining blood is returned to the patient though a separate intravenous (IV) line. The two selective apheresis filters currently available are the Cellsorba system (Asahi Kasei Medical; Figure 1), which contains nonwoven polyester fibers that remove granulocytes and monocytes (90%), lymphocytes (70%), and some platelets,12 and the Adacolumn system (JIMRO; Figure 2), which contains cellulose diacetate beads that adhere to Fc gamma and complement receptors on granulocytes and monocytes, selectively removing them without significantly affecting lymphocytes or platelets (Figure 3).13 Alternatively, the centrifugal system uses one venous line to obtain blood and remove a buffy coat before reinfusing (multi-component system, Haemonetics).14 However, the fiber-and-column technique removes a 4-fold greater amount of leukocytes than centrifugation.15,16 A third, little-used technique is extracorporeal phototherapy in which blood removed from the patient is treated (with psoralen and ultraviolet irradiation) and then returned to the patient.17

Figure 1.
Cellsorba product design.
Figure 2.
Adacolumn product design.
Figure 3.
Adacolumn circuit: an outline of the extra-corporeal circulation through the Adacolumn device.

How Does LCAP Work?

The benefits of LCAP are more than just the removal of activated white blood cells. The “quantitative” removal of activated circulating leukocytes by these filters presumably reduces the concentration of inflammatory cells in diseased tissue. These diverted leukocytes are replaced by naïve leukocytes from the bone marrow or peripheral pooling sites.18 As a result, there is a decrease in leukocyte expression of adhesion molecules (L-selectin, integrins)19 and reactive oxygen species.20 Other mechanisms at work include immunologic modulation of leukocytes and dendritic cells and reduced cytokine production, with an altered response to proinflammatory cytokines and endotoxins.21 See Table 1.

Table 1.
Immune Modulation Effects of Leukocytapheresis

In addition, Adacolumn spares lymphocytes, which may be a benefit. Prior selective depletion of lymphocytes in CD patients not only showed no clinical advantage but the outcome was 21% poorer than in the control group.28 In both rheumatoid arthritis and CD there is an actual increase in lymphocytes, primarily CD4+ cells. These CD4+ cells, together with CD25+ T cells, inhibit T-cell activation and secrete an anti-inflammatory cytokine, interleukin (IL)-10, which aids in regulating a balanced immune response in the gut mucosa.29,30 The role of the circulatory immune complex in IBD is interrupted as well. Cellulose acetate beads in Adacolumn adsorb immunoglobulin (Ig)G and immune complex from plasma,31,32 which then bind to Fc gamma receptors on neutrophils and macrophages.33,34 The adsorbed IgG and immune complex generate complement activation fragments (C3a, C4a, C5a)7,31,33 as well as opsonins (C3b/C3bi, C4b/C4bi, C5), which then also adsorb to the column31,34,35 and bind leukocyte complement receptors CR1, CR2, and CR3 (MAC-1, CD11b, CD18) and CR4.36-38 Note that leukocyte adsorption is affected by complement opsonins, Fc gamma receptors, and complement receptors on leukocytes, especially neutrophils, monocytes, and macrophages. However, lymphocytes lack complement receptors except for B, T, and natural killer cells.37,39 Also, Fc gamma receptors are not usually expressed on lymphocytes, except for small segments of CD19+ B cells and CD56+ natural killer cells.40 This lack of expression might explain why Adacolumn selectively adsorbs granulocytes and not lymphocytes.

Ulcerative Colitis Experience and Disclaimer

The following chronology of experience with LCAP is plagued by the heterogeneity of the patient population, methodologic flaws of missing primary and secondary endpoints, inconsistent measures of disease activity varying from accepted validated instruments (eg, the Ulcerative Colitis Disease Activity Index [UCDAI] and the Inflammatory Bowel Disease Quality-of-Life index [IBDQ]) to simply the investigator’s subjective evaluation of improvement. Concomitant medications or changes in dosage or frequency of their use are frequently lacking in the record. There is only one sham (ie, placebo) study.41 Few studies are randomized and most trials are unblinded. Despite these drawbacks, the aggregate impression of the value of apheresis has earned its approval for use in UC by the Japanese ministry of health and a European commission of certification from a regulatory compliance organization (the TOV product service) in 1999.42

Adacolumn

The Adacolumn system employs a column of cellulose acetate beads that selectively adsorb 65% of granulocytes, 55% of monocytes, and 2% of lymphocytes; red blood cells and platelets are virtually unchanged, as are clotting factors.7 The following is a brief summary of the results of selected published studies on the use of Adacolumn (also referred to as granulocyte-monocyte adsorptive apheresis) for the treatment of UC; additional studies are listed in Table 2.

Table 2.
Selected Studies of Adacolumn for Treatment of UC

A combined Japanese and UK trial of granulocyte-monocyte adsorptive apheresis in 33 patients reported remission rates of 81% in steroid-refractory and 88% steroid-naive patients. Eleven cycles of apheresis over 11 weeks were used. Maintenance of remission occurred in 26 of 33 (78%) patients at 12 months and 14 of 25 patients became steroid-free with few adverse events.43

A disconcerting lack of benefit over a steroid comparator group occurred in 19 UC patients given prednisone and apheresis (4 with the Haemonetics centrifugal system, 15 with Adacolumn), with a clinical response of 68.4% with apheresis versus 75% with prednisone alone. Fifteen LCAP and 11 prednisone patients required colectomy. A problem with interpretation of these results exists because the apheresis group had a significantly higher initial prednisone requirement, indicating more severe disease. Clinical remission (Seo index) occurred in 6 of 19 apheresis patients (31.6%) versus 12 of 16 prednisone patients (75%). These results, although limited by a small sample size, bring into question the value of apheresis as initial therapy for severe UC.44

Maintenance of remission with intermittent every-2-week Adacolumn apheresis for 12 months was as effective in 7 of 10 UC patients as 6-mercaptopurine (6-MP) was in 6 of 10 patients. Three apheresis patients relapsed at 4, 5, and 12 months versus 3 6-MP patients at 4, 10, and 11 months; 1 6-MP patient was excluded after liver abnormalities. Apheresis appeared comparable to 6-MP in maintaining remission in this limited study.45

Twenty steroid-refractory and 10 steroid-dependent Japanese UC patients received 5 apheresis sessions with Adacolumn over 4 weeks. Twenty-four patients (55%) entered remission. Nine (20%) responded and 11 (25%) were unchanged. Only 2 of 10 “severe” steroid-refractory patients underwent remission but 7 of 10 “moderate” refractory patients did so. Steroids could be tapered in 9 of 10 steroid-dependent patients.46

Fifteen IBD patients intolerant or refractory to all prior IBD therapy were entered into an open-label pilot granulocyte/monocyte apheresis program with Adacolumn given in 5 sessions. Eleven of 15 UC patients completed the sessions; 4 patients responded (UCDAI reduction of >3 points), and 1 entered remission (UCDAI <2) with overall improvement in IBDQ scores. CD patient response was more impressive in 14 of 15 patients completing the 5 sessions. Eight CD patients (57%) responded and 5 entered remission. No device-related serious adverse events were noted. This initial US experience shows promise for refractory IBD patients.47

Twenty steroid-naïve active UC patients were treated with Adacolumn for an average of 6 to 10 sessions at 2 sessions per week. Seventeen patients (85%) entered remission with a decrease in C-reactive protein (CRP), total white blood cell count (WBC), polymorphonuclear leukocytes (PMNs), and monocytes. An elevated lymphocyte count and soluble tumor necrosis factor (TNF) receptors I and II were noted in the return blood flow to the patient after filtration. Sixty percent maintained in remission at 8 months.48

In a Scandinavian apheresis experience of 100 patients, remission occurred in 44 patients and a response was seen in 24 patients, for an overall response rate of 68%. Of the patients, 52 had UC, 44 had CD, and 4 had indeterminate colitis. The mean time to response was 7 weeks after 5 weekly sessions, and mean time to relapse was 5.5 months. A total of 27 of 50 patients discontinued steroids. Adverse events were minor but 1 patient had a pulmonary embolism using a central venous catheter.49

Semiweekly granulocyte and monocyte apheresis in place of weekly sessions resulted in a remarkable 73.1% remission rate (38/52 patients) with only 15.9 days to achieving remission versus a 46.7% remission rate (21/45 patients) and 28.1 days until remission in those utilizing a weekly schedule. Each group received a total of 10 treatments. If substantiated in future trials, the semiweekly program would immeasurably enhance compliance and overall patient acceptance.50

Five weeks (5 cycles) of Adacolumn apheresis in 12 patients with moderately active UC resulted in clinical remission in 8 patients, endoscopic and histologic improvement in 11 patients, and steroid withdrawal in 9. All 12 patients showed significant improvement in quality of life scores.51

Cellsorba

The Cellsorba system utilizes 2 filters. The unwoven fiber filter traps 90% of leukocytes (100% granulocytes, 60% lymphocytes, 35% platelets) but a “rebound” increase of 170% of initial leukocyte count occurs 20 minutes post-procedure, which then normalizes within 24 hours.35,41 The following is a brief summary of the results of selected published studies on the use of Cellsorba for the treatment of UC; additional studies are listed in Table 3.

Table 3.
Selected Studies of Cellsorba for treatment of UC

Thirteen patients (8 with UC and 5 with CD) were treated with Cellsorba for 5 sessions then 5 monthly treatments (averaging 3 L filtration per session), resulting in 11 patients (84.6%) improving and 6 achieving remission at the completion of the 5 monthly sessions. Eight patients (61.5%) maintained their response without additional therapy.18

LCAP with Cellsorba improved the clinical and endoscopic picture of 2 steroid-resistant UC patients after 6 sessions. The same authors expanded on this experience, noting that 12 of 13 UC patients entered remission and 4 CD patients improved.57

In a multicenter open-label trial, 4 of 7 steroid-dependent or -resistant UC patients on a monthly apheresis program achieved remission for 12 months, and then remained steroid-free.58

Five patients with active UC received 6 sessions of LCAP with Cellsorba that resulted in clinical, histologic, and endoscopic improvement. An excess of CD83+ dendritic cells were found in the filtered buffy coats. LCAP also led to downregulation of IL-6 and IL-8.26

In the only placebo-controlled study with LCAP (Cellsorba), 10 treated patients and 9 patients in a sham group received 5 weekly sessions of apheresis followed by 2 more at 4-week intervals. Eight of 10 LCAP-treated patients showed significant improvement on the clinical activity index versus 3 of 9 sham-treated patients. Four sham-treated patients and 1 LCAP-treated patient reported adverse events, none of them severe. There was a statistically significant greater reduction in steroid use in the LCAP group.59

Other Techniques and Comparative Studies

Avoiding extracorporeal circulation (“off-line” leukapheresis), a 400 cc sample of peripheral blood was passed through a leukocyte “elimination” filter for 5 sessions (2000 cc treated) and reinfused, with subsequent clinical and endoscopic improvements in 1 patient. No follow-up series was reported, or adverse events.62

Fifty steroid-resistant UC patients received LCAP using a centrifugal cell separator (Haemonetics) for 5 weekly sessions. Twenty-six of 38 patients (68.4%) improved their stool frequency (<4/day), 17/30 (56.7%) “normalized” their CRP, 26/45 (57.7%) showed endoscopic remission, and 20/37 (54.1%) had histologic improvement. Overall, 74% (37/50) had improvement in their disease activity.58

A pilot study using an LCAP centrifugal procedure resulted in 13 of 14 corticosteroid-resistant patients entering remission within 4 weeks after apheresis and remaining in remission for 8 months without additional steroids. One of the 14 patients required a colectomy. Two adhesion molecules (L-selectin and VLA4a) on the surface decreased.19

Of 23 corticosteroid-resistant UC patients given centrifugal LCAP, 18 (78.3%) achieved remission within 4 weeks with confirmatory endoscopic and histologic benefit. No significant adverse events were reported.63

Honma and colleagues used both filtration and centrifugation to achieve remission in 23 of 25 steroid-resistant, moderate to severe UC patients for 5 weekly infusions. Details are lacking in this uncontrolled study regarding assessment of remission and outcome. A maintenance program of apheresis at 4-week intervals failed to improve a 50% relapse rate at two years. Steroids were tapered, 5-ASA/sulfasalazine were maintained, but no immunomodulating medications were reported. In addition, assessments of relapse were poorly described.64

Apheresis therapy in moderate to severe UC was studied with 3 different filter systems. Granulocyte apheresis (Adacolumn) showed 60% efficacy (3 remissions, 3 responses), LCAP (Cellsorba) was 70% effective (4 remissions, 3 responses), and mononuclear apheresis separating lymphocytes from monocytes was 90% effective (8 remissions, 1 response) with a longer lasting effect than other systems. Poor results were noted if the neutrophil count increased by 140% with decreased CD4 cells and a rise in inflammatory cytokines; this did not occur with the mononuclear apheresis system.65

Ogawa and associates conducted a comparator study of Cellsorba and Adacolumn. Seven of 13 patients (53.8%) using Cellsorba responded versus 9 of 13 (69%) using Adacolumn. A faster response was seen with Cellsorba and concomitant steroids (1.75 weeks) versus Adacolumn (2.5 weeks). Adverse events included headaches in 5 patients. The authors concluded that both systems are safe and useful in UC.66

Crohn’s Disease Experience

Considerably less experience has been reported in patients with CD and leukocytapheresis. See Table 4 for a summary of published studies.

Table 4.
Studies of Apheresis for Treatment of Crohn’s Disease

Maintenance of Remission/Response

Difficulties abound in evaluating reports of maintenance efficacy. The literature often precludes evaluation of one device’s advantage over another when results are commingled.59,72 Control patients are usually nonexistent. Remission assessment and primary and secondary outcomes are not delineated. Most studies are unblinded. Maintenance studies are troubled by various assessments of relapse and concomitant medications are not recorded.

The literature is conflicted regarding a maintenance benefit. Some reports are highly suggestive of a prolonged remission or response in a maintenance experience,43,48,53,66 others are unfavorable.23,72 Honma’s initial success by inducing remission in 23 of 25 severe steroid-resistant UC patients was not sustained over 2 years despite monthly sessions compared to the steroid monotherapy group.64 The only controlled placebo (ie, sham) study with 5 of 10 UC patients entering remission after 5 weekly sessions was not extended beyond 8 weeks after the initial therapy.59

Questions remain unanswered as to whether a different patient population (eg, those who are not so severely ill or refractory to therapy), more frequent sessions, or concomitant immunomodulators or biological therapy would prolong remission rates.

Apheresis appears to play a promising role as an apparently safe modality in the induction of remission. Whether this holds true for maintenance of remission awaits further long-term studies.

Adverse Effects

Adverse effects have been remarkably few and, when encountered, extremely mild. In one study,73 a decline in WBC to 61.8% of baseline with Adacolumn occurred within 15 minutes. After 60 minutes, the WBC count returned to baseline. However, plasma C3a concentrations increased from 123±61 mg/mL at baseline to 417±96 mg/mL at 60 minutes, indicating activation of the complement system and anaphylatoxin production. This is of questionable clinical significance.

Nagase and colleagues reviewed 1,978 LCAP sessions between 1992 and 1997. Moderate reactions occurred in 31 sessions (1.6%) involving 15 patients (16%). These included nausea, fever, chills, nasal obstruction, palpitations, and respiratory or chest symptoms. There was prompt recovery without sequelae after a transient interruption of administration or medical therapy. Although a 46% incidence of clotting in the filter IV lines occurred, most were of little significance and this has not been reported in the subsequent experience with LCAP.74 There is only 1 report of a significant event, by Ljung and associates.49 A pulmonary embolus occurred in a patient in which a central venous catheter was used for apheresis.

Conclusion

Leukocytapheresis appears promising as a “no-drug” therapy in active IBD. Unfortunately, the accumulated IBD literature lacks placebo-controlled trials (often lacking primary or secondary endpoints) and is hampered by heterogenic populations with a mixture of concomitant medications. The data for maintenance of initial benefit are still scant and conflicted. Nevertheless, the impressive response and remission rates are enhanced by the extremely low incidence of adverse events, suggesting it is a safe therapy meriting further investigation. Selective apheresis given more frequently than once weekly may offer a more expeditious remission rate resulting in time and indirect cost savings. A randomized placebo-controlled trial is underway in the United States. Whether its role in combination with immunomodulators and/or biologic therapies would enhance its efficacy in maintaining remission awaits further study.

Acknowledgement

The author is grateful to Drs. Bruce Sands and Maria Abreu for their comments and to Gail Torodash for secretarial assistance.

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