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Article

Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis

by
Mark Lipphardt
,
Manuel Wallbach
and
Michael J. Koziolek
*
Department of Nephrology and Rheumatology, University Medical Center Göttingen, Robert-Koch-Str. 40, D-37075 Goettingen, Germany
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2020, 9(5), 1597; https://doi.org/10.3390/jcm9051597
Submission received: 11 May 2020 / Revised: 17 May 2020 / Accepted: 18 May 2020 / Published: 25 May 2020
(This article belongs to the Special Issue Apheresis in Neurological Disorders)
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Abstract

:
Multiple sclerosis (MS) is an inflammatory disease mainly affecting the central nervous system. In MS, abnormal immune mechanisms induce acute inflammation, demyelination, axonal loss, and the formation of central nervous system plaques. The long-term treatment involves options to modify the disease progression, whereas the treatment for the acute relapse has its focus in the administration of high-dose intravenous methylprednisolone (up to 1000 mg daily) over a period of three to five days as a first step. If symptoms of the acute relapse persist, it is defined as glucocorticosteroid-unresponsive, and immunomodulation by apheresis is recommended. However, several national and international guidelines have no uniform recommendations on using plasma exchange (PE) nor immunoadsorption (IA) in this case. A systematic review and meta-analysis was conducted, including observational studies or randomized controlled trials that investigated the effect of PE or IA on different courses of MS and neuromyelitis optica (NMO). One thousand, three hundred and eighty-three patients were included in the evaluation. Therapy response in relapsing-remitting MS and clinically isolated syndrome was 76.6% (95%CI 63.7–89.8%) in PE- and 80.6% (95%CI 69.3–91.8%) in IA-treated patients. Based on the recent literature, PE and IA may be considered as equal treatment possibilities in patients suffering from acute, glucocorticosteroid-unresponsive MS relapses.

1. Introduction

Multiple sclerosis (MS) is a disease which is defined as an inflammatory condition affecting the central nervous system. Its main course of damage is due to abnormal immune mechanisms, resulting in acute inflammation, demyelination, axonal loss, and the formation of central nervous systemplaques consisting of inflammatory cells [1,2].
The epidemiology of MS differs greatly depending on the geographic regions with a prevalence from high levels in North America and Europe (>100/100,000 inhabitants) to low rates in Eastern Asia and sub-Saharan Africa (2/100,000 population). Women are generally more affected than men [3].
Symptoms that occur with the onset of MS are very unspecific, since MS can affect all regions of the central nervous system and can make it hard for a physician to make an early diagnosis. Symptoms of MS include vision problems with a decreased visual acuity (VA) and a prolonged visual evoked potential (VEP), weakness, fatigue, spasms, ataxia, cognitive dysfunction, or numbness [4]. The occurrence of an optic neuritis in its typical form is considered to be associated with MS. However, it is also regarded as a demyelinating clinically isolated syndrome (CIS) with the risk to convert to MS, especially in the white population [5]. With such a variety of symptoms a thorough medical history and examination is essential to make the right diagnosis of MS. Blood tests, lumbar punctures, magnetic resonance imaging, and evoked potential tests help in the process of differentiating between other diseases [6]. Based on the symptoms and the progression of the disease MS is divided in four types: Relapsing-Remitting MS (RRMS), Secondary-Progressive MS (SPMS), Primary-Progressive MS (PPMS), and Progressive-Relapsing MS (PRMS).
MS can be characterized as a T-cell-driven disease with T helper (Th) cells, especially Th-1, Th-2, and Th-17 cells, as the main players in a various inflammatory cascade [7]. For instance, Th-1 cells are responsible for producing Interferon gamma (IFNγ) and tumor necrosis factor alpha (TNF-α) [8]. With the secretion of IFNy and TNF-α inflammation can be maintained by inhibiting Th-2 cell differentiation, since Th-2 cells produce anti-inflammatory cytokines like interleukin (IL)-4 and IL-13 [9,10]. Th-17 cells stimulate inflammation via secreting a vast number of various cytokines like IL-17, IL-21, IL-22, and IL-26 [11,12,13]. As a counterpart regulatory T (Treg) cells inhibit autoimmune responses [14]. In addition to that immunoglobulins (Ig) (especially IgG) are important in the pathogenesis of MS. Evidence of intrathecal Ig production and oligoclonal IgG bands contribute to the diagnosis of MS. Further differentiation shows various types of specific autoantibodies against myelin in subgroups of patients with MS, e.g., anti-myelin oligo-dendrocyte glycoprotein (anti-MOG) or anti-myelin basic protein (anti-MBP) [15]. Antibody-producing B-cells traveling between CNS, blood, and peripheral lymphatic organs clonally expanded B-cells and aggregated B-cells in meninges corroborate a pathophysiological role of B-cells and/or humoral immune answer in the pathogenesis of MS [16,17,18,19].
Based on the myelin protein loss, the geography and extension of plaques, the patterns of oligodendrocyte destruction, and the immunohistopathological evidence of complement activation Lucchinetti et al. described four different immunohistopathological patterns of demyelination in MS [20]. Patterns I and II showed close similarities to T-cell-mediated or T-cell plus antibody-mediated autoimmune encephalomyelitis. Patterns III and IV on the other hand were highly suggestive of a primary oligodendrocyte dystrophy.
Neuromyelitis optica (NMO) on the other hand is described as an idiopathic, severe, demyelinating disease of the central nervous system with the preference to affect the optic nerve and spinal cord. NMO has been considered as a variant of MS. However, with the analysis of clinical, laboratory, immunological, and pathological data the difference to MS is now acknowledged [21].
The treatment regime can be divided in treatment to modify the disease progression and treatment for the acute relapse. In the latter, the administration of high-dose intravenous methylprednisolone (up to 1000 mg daily) over a period of three to five days usually represents the first step in acute MS relapse treatment. A higher second high-dose intravenous methylprednisolone pulse with up to 2 g can be considered in unresponsive patients after an interval of 2 weeks [22,23,24]. Glucocorticoids may downregulate cellular cytotoxicity and lead to the death of activated B cells, but they will not modulate tissue destruction or conduction blockade by local antibody deposition [25]. If symptoms persist, the relapse is defined as glucocorticosteroid-unresponsive and immunomodulation by apheresis is recommended. However, several national and international guidelines have no uniform recommendations on using plasma exchange (PE) or immunoadsorption (IA) in this case. The American Society for Apheresis (ASFA) recommends PE for treatment to category II (“apheresis accepted as second-line therapy”) and IA for treatment to category III (“optimum role of apheresis therapy is not established”) [26]. The American Academy of Neurology also advises the use of PE for adjunctive treatment of relapsing forms of MS (Level B), while IA is not addressed [27,28]. The German guidelines are currently under reconstruction but formerly recommended both procedures as equivalent [29].
In this current issue, we review the use of IA and PE in treating, especially, the acute relapse of MS.

2. Effects of Apheresis Therapy

During PE, the patient’s plasma, including all plasma proteins, is removed and substituted by human albumin solution or fresh frozen plasma. The concept of IA involves a selective elimination of plasma proteins, e.g., antibodies, while sparing other plasma proteins [30]. Both techniques include an extracorporeal circulation circuit with systemic and/or local anticoagulation, as well as the need of a vascular access. The latter can either be peripheral venous, if individual vascular situation allows it, or by a central venous catheter. In IA, a secondary circuit is established in which a defined physico-chemical interaction of selected plasma proteins with a defined matrix should theoretically guarantee selective removal of circulating pathogens. In praxis, a bandwidth of proteins are removed [31,32] which are responsible for therapeutic effects but also possible side effects of IA. These effects differ with regard to used matrix of the adsorber, which physicians should be aware.
The exact mechanism by which apheresis treatment works is actually not fully understood. MS patients may benefit by the immediate removal of plasma antibodies, immune complexes and cytokines, induction of a redistribution of antibodies from the extravascular space, and subsequent immunomodulatory changes [30]. Here, cell types with receptors for immunoglobulins (Fc receptors), such as monocytes, macrophages, and natural killer cells, are especially of interest [25]. Besides effects on humoral immune system, experimental data suggest a reduction of circulating autoantigens and regulatory proteins [32] and induction of a higher relative quantity of Treg to Th17 cells [33], as well as a silencing of cellular autoimmune response [32].
Early active MS lesions with an immunohistopathological type II pattern, which are selectively associated with Ig’s and complement deposited along myelin sheaths, predict the best response to apheresis therapy in patients with steroid-unresponsive relapse [34], corroborating the hypothesis of effects on humoral immune response.

3. Plasma Exchange

3.1. Multiple Sclerosis (with Relapsing-Remitting and Progressive MS Sub-Sections)

The first study comparing the normal therapy regime with PE was performed by Khatri et al. in 1985 and included fifty-four patients with chronic progressive MS [35]. The results showed that patients with the additional PE have a higher improvement rate than patients with a “sham” PE. Following the study of Khatri et al., Weiner et al. enrolled 116 patients in a multicenter, randomized, double-blinded, controlled trial of 11 PE treatments in acute exacerbations of MS [36]. One of the main results showed patients treated with PE to have a significantly enhanced improvement after four weeks. In 1999, a study group of the Mayo Clinic conducted a randomized, sham-controlled, double-blinded study of PE in MS patients with severe neurological deficits after acute relapses, unresponsive to corticosteroids [37]. This study resulted in a moderate to greater improvement in neurological deficits in 42.1% of patients with true PE versus 5.9% of patients with sham PE. With the improved work with PE in the clinical setting, a variety of retrospective studies could demonstrate an improvement rate between 59–87.5% [38,39,40]. In a large study with 153 patients enrolled, Magana et al. identified 90 patients with moderate to marked functional neurological improvement within 6 months after treatment with PE [41].
An excellent and actual overview on apheresis in progressive MS forms is available in Reference [30]. So far, the ASFA recommends PE for treatment to category III: “Optimum role of apheresis therapy is not established. Decision making should be individualized” [26].

3.2. Clinically Isolated Syndrome

More recent studies set their focus not only on the relapsing-remitting and progressive MS sub-sections but also on the clinically isolated syndrome [42,43,44]. Therapy response rates ranged between 72–76%, therefore achieving a clinical response in the majority of patients.

3.3. Optic Neuritis

Studies analyzing the use of PE in the setting of for severe steroid unresponsive optic neuritis were performed by Ruprecht et al. and Deschamps et al. [45,46]. Ruprecht et al. al. demonstrated an improvement of visual acuity in 70% of patients. Out of these seven patients, three continued to improve with their visual acuity, two remained at a stable state, whereas two patients suffered from worsening symptoms during the follow-ups [46].
In the study performed by Deschamps et al., thirty-four patients with a remaining visual acuity of 0.1 were treated with PE. Afterwards, the median visual acuity was 0.8 [45].
Studies on PE are summarized in Table 1. However, the reader must be aware that the comparability of the studies is limited by the different technical implementation of PE. This varied in frequency, treated plasma volume, and total number of PEs. As a result, the ASFA defined a corridor of technical implementation that recommended treatment of 1–1.5-fold plasma volume per session for a number of 5 to 7 treatments over a period of 10 to 14 days [26].

4. Immunoadsorption

4.1. Multiple Sclerosis (with Relapsing-Remitting and Progressive MS Sub-Sections)

IA was firstly introduced in the treatment of MS by de Andres et al. in 2000 [69]. They managed a prompt and unequivocal clinical response with a parallel decrease in IgG, fibrinogen, and C3 complement plasma levels in all three patients treated with IA. In the following years, retrospective studies confirmed the initial results of de Andres et al., showing improvement rates from 85–88.3% in MS patients receiving an IA therapy [70,71].

4.2. Clinically Isolated Syndrome

Studies incorporating patients with clinically isolated syndrome showed marked to moderate clinical response with a total gain of function in 66–100% of patients after treatment with immunoadsorption [42,72].

4.3. Neuromyelitis Optica

The first prospective study investigating effects of IA therapy in patients with MS with steroid-refractory optical neuritis showed an improvement of the mean visual acuity in 8 from 11 patients at day 180 ± 10 after IA [32]. A more recent study confirmed the efficacy and good tolerance of IA in relapses of MS patients with failure to respond to a steroid pulse therapy adequately. Moreover, the study established IA as first-line relapse treatment during pregnancy and breastfeeding [73].
The most commonly used column was a tryptophane-linked polyvinyl alcohol adsorber, but also a Sepharose-conjugated sheep antibodies to human IgG, as well as protein A column, have been used. Table 2 gives an overview about IA-studies in acute relapses of MS.

5. Plasma Exchange vs. Immunoadsorption

5.1. Multiple Sclerosis (with Relapsing-Remitting and Progressive MS Sub-Sections)

Recently, studies have been designed to compare the efficacy of PE versus IA. The most impressive work is that of Dorst et al. [42]. Sixty-one patients with acute relapse of multiple sclerosis or clinically isolated syndrome and without complete clinical remission of symptoms after at least one cycle of high-dose intravenous methylprednisolone were randomly assigned to receive IA (n = 31) or PE (n = 30). In the IA group (using a protein A adsorber), the 2.0-fold individual total plasma volume was processed on day 1, and the 2.5-fold on days 2–5. In the PE group, 2 L of plasma (corresponding to the 0.69 ± 0.12-fold individual total plasma volume) were removed each day and substituted by 5% human albumin solution. The median improvement of Multiple Sclerosis Functional Composite after 4 weeks compared to baseline was 0.385 (interquartile range (IQR) 0.200–0.675; p < 0.001) in the IA group and 0.265 (IQR 0.100–0.408; p < 0.001) in the PE group. Improvement in the IA group was significantly larger (p = 0.034) compared to PE. Response rates after 4 weeks were 86.7% in the IA group and 76.7% in the PE group. One deep venous thrombosis occurred in each group. One limitation in interpretation of this study, however, is that the apheresis dose applied was quite different in the two treatment arms and the observation period was relatively short.
Hohenstein et al. reported the successful use of IA with regenerating adsorbers in MS patients as a single center experience [78]. Faissner et al. compared PE and IA directly and demonstrated in a grouped analysis of patients treated with combined PE/ IA, PE, or IA alone, that all groups presented with a better result of visual evoked potentials, providing a valid treatment option in steroid-refractory MS-relapses [50].

5.2. Clinically Isolated Syndrome

Dorst et al. [42] also enrolled patients suffering from a clinically isolated syndrome in their recent study. The results are discussed above.

5.3. Neuromyelitis Optica

In a small cohort study, Faissner et al. showed equivalent results treating patients with neuromyelitis optica spectrum disorder with IA instead of PE, constituting IA as a valid therapeutic option [77]. Studies of our own also indicate PE and IA to be of equal efficacy and treatment safety [44,79]. We assessed 140 adult patients treated with PE (n = 73) or IA (n = 67) in steroid refractory multiple sclerosis or neuromyelitis optica. During our studies, we became aware of the fact that differences in body-mass-index, duration of disease, number of treatments, vascular access and treated plasma volumes between IA - and PE cohorts are a main concern for possible bias in the assessment of IA and PE as a treatment for MS patients. We also performed a retrospective single-center cohort study of pediatric patients with inflammatory CNS demyelinating disorders showing excellent tolerance and favorable outcomes of PE and IA in all pediatric patients [31].

6. Meta-Analysis on Apheresis Effects on Demyelinating Diseases

6.1. Search Strategy and Inclusion Criteria

A systematic search was performed using Medline and Cochrane Library with combinations of the search terms “plasma exchange” OR “immunoadsorption” in combination with the terms “multiple sclerosis” OR “clinical isolated syndrome” OR “neuromyelitis optica” between 1980 and January 2020. Reports were screened independently for relevance based on title and abstract content by two authors (M.L. and M.J.K.). Randomized-controlled trials, as well as prospective cohort studies and retrospective studies and case series, were included if sufficient information on therapy response of PE or IA was provided. Studies with heterogeneous mixing MS, CIS, and/or NMO patients regarding therapy response were excluded if the treatment response was not specified separately in the individual indications. Moreover, case series with a case number less than five in the individual indication were also excluded. It should be mentioned as a limitation that there was no uniform definition of the term “therapy response” in the selected works and, with the exception of a few studies, the majority was retrospective data collection. The flow chart in Figure 1 summarizes the selection of studies in the meta-analysis.

6.2. Statistical Analysis

Analysis was performed using RevMan V.5.3 (Nordic Cochrane Centre, Copenhagen, Denmark, the Cochrane Collaboration, 2014). Data were quantitatively synthesized by an inverse-variance-weighted meta-analysis using a random-effect model because of the presence of heterogeneity. The normal approximation interval (sqrt(p(1-p)/n)) was used to generate the confidence interval for the therapy response rate. For studies where the normal approximation interval was zero, the confidence interval was set to one to calculate the random effect model. The 95% normal approximation confidence interval is provided in the meta-analyses.

7. Results

With the present search strategy and assessment of full-texts 690 studies, 40 observational and 1 randomized with a total of 1.383 patients could be analyzed. Figure 1 shows the flow chart of study selection.
Effects of PE can be summarized as follows: in relapsing-remitting MS and clinically isolated syndrome (12 studies and 398 patients) therapy response of 76.6% (95%CI 63.7–89.8%) (Figure 2A), in progressive MS (5 studies and 112 patients) therapy response of 53.9% (95%CI 29.5–78.4) (Figure 2B), in isolated optic neuritis (4 studies and 83 patients) therapy response of 71.5% (95%CI 56.4–86.6%) (Figure 2C), and in NMO (13 studies and 401 patients) therapy response of 72.5% (95%CI 61.0–83.9%) (Figure 2D).
Effects of IA can be summarized as follows: in relapsing-remitting MS and clinically isolated syndrome (9 studies and 352 patients), therapy response of 80.6% (95%CI 69.3–91.8%) (Figure 2E); and in NMO (2 studies and 37 patients), therapy response of 100% (95%CI 98.6–101.4%) (Figure 2F).

8. Safety Profile

8.1. General

Another important fact to consider is the treatment safety. The noted rates of side effects during those apheresis treatments are very heterogeneous. In the literature one can find complication rates from 4.2% until 25.6% [81,82,83,84]. In 2011, Köhler et al. postulated lower side effects using IA in patients suffering from myasthenia gravis [85]. They claim that a possible reason for the difference was due to the absence of albumin-substitution. Zoellner et al. designed a study to investigate the fibrinogen level and the occurrence of bleeding complications [86]. They demonstrated IA to have a lower degree of fibrinogen reduction as PE. Bleeding complications occurred in 1.3–3.1% of treatments. Schneider-Gold et al. reported allergic reactions, hypocoagulability, and bronchorespiratory infections with a significant higher frequency in the PE-only group as compared to the IA-only group or the both combined [87].

8.2. Multiple Sclerosis (with Relapsing-Remitting and Progressive MS Sub-Sections) and Clinically Isolated Syndrome

In the recent study performed by Dorst et al. [42], a general well tolerance was observed with 5 mild infections in the PE group and 4 mild allergic reactions in the IA group. Furthermore, courses of anemia and thrombocytopenia were documented with anemia being more frequent in the PE group and thrombocytopenia being more frequent in the IA group.

8.3. Multiple Sclerosis (with Relapsing-Remitting and Progressive MS Sub-Sections) and Neuromyelitis Optica

In our studies the complication rate was about 3.7% in over 780 apheresis cycles. Furthermore, we could not detect any differences regarding the safety profile of IA versus PE [44,79].
All in all, both IA and PE have a high tolerability regarding the safety profile. It should be added that the majority of the documented side effects are to be considered as mild. However, the use of IA and PE should be reserved to specialized centers familiar with technical procedure and experienced with this specialized patient population to ensure a high quality of treatment with low complication rates.

9. Treatment Predictors

9.1. General

One major predicting factor is the time to initiate apheresis treatment. Early initiation of apheresis correlates with a higher response rate as was shown by several study groups [44,60,80,88]. In the onset of sudden hearing loss, the early initiation of apheresis treatment was also beneficial [89].
Comparing the cumulative corticosteroid doses in apheresis-responders versus non-responders, no significant difference was shown, which makes a synergistic effect of apheresis and corticosteroids unlikely [44].

9.2. Multiple Sclerosis (with Relapsing-Remitting and Progressive MS Sub-Sections)

Magana et al. postulated the duration of the disease and preserved deep tendon reflexes as important clinical predictors [41]. A different approach was followed by the study group of Stork et al., who conducted a single-center cohort study with 69 MS patients, evaluating treatment response in relation to histopathologically defined immunopathological patterns of MS [34]. As early active demyelinating MS lesions can be divided in 3 different immunopathological patterns of demyelination, Stork et al. demonstrated that patients with pattern 1 and 2 are most likely to benefit from apheresis treatment, especially in patients with pattern 2 who show signs of a humoral immune response in particular. Patients with pattern 3 most likely do not benefit from apheresis treatment. During our studies, we also became aware of the fact that patients having a good response to apheresis treatment were significantly younger than non-responders [44]. This observation may be due to a decrease in remyelination efficiency, as proposed by Sim et al. [90]. A gender-related treatment benefit towards the female gender was identified in sub-groups of MS patients [44,91].

9.3. Neuromyelitis Optica

In a large study performed by Kleiter et al., it was shown that PE or IA exerts a better recovery from acute relapses in patients suffering from neuromyelitis optica if they had isolated myelitis [92]. More recent studies focused on the plasma anti-aquaporin-4 immunoglobulin G antibody as a positive predictor for treatment success with PE or IA in patients suffering from neuromyelitis optica spectrum disorder [12]. In both studies, particularly, patients with a positive anti-aquaporin-4 immunoglobulin G antibody responded well to the treatment with PE and IA. In addition to that, no advantage was revealed for either PE or IA. The disease specificity of anti-aquaporin-4 immunoglobulin G antibody is almost at 100% and clinical studies with immunohistochemical evidence suggest that this antibody plays a central role in the pathogenesis of neuromyelitis optica spectrum disorder [93].
These predictors can thus be summarized according to various variables. Table 3 provides a compilation.

10. Therapeutic Efficacy and Time Course

As for the time course of the therapeutic effect, the current literature agrees on regular neurological follow-ups after 6 months, manifesting a continuous and maximal clinical effect of the apheresis treatment [41,44,60,80]. Therapeutic effects over such a long period of time suggest immunomodulatory actions of apheresis rather than antibody removal on its own [95]. Those immunomodulatory actions happen most likely at the level of Th-cells and CNS-associated proteins, like the myelin basic protein. The prolonged therapeutic effect can be thought of as a clinical correlate of the immunomodulatory components of therapeutic apheresis. Furthermore, the duration of the apheresis induced therapeutic effect can be involved in the treatment process of initiating or changing disease-modifying drugs.

11. Conclusions

The focus of this current issue is the use and comparison of immunoadsorption and plasma exchange in the treatment of multiple sclerosis with the main concern of acute relapses.
Based on the studies of the current literature and performance of a meta-analysis, including 690 studies, 40 observational and 1 randomized with a total of 1383 patients, plasma exchange and immunoadsorption are treatment options of equal effectivity for acute glucocorticosteroid-unresponsive multiple sclerosis relapses.
For the meta-analysis randomized-controlled trials, prospective cohort studies, retrospective studies, and case series with sufficient information on therapy response of plasma exchange or immunoadsorption were included. Studies with heterogeneous mixing multiple sclerosis, clinically isolated syndrome, and/or neuromyelitis optica patients regarding therapy response were not included if the treatment response was not specified separately in the individual indications.
Plasma exchange has a therapy response of 76.6% in relapsing-remitting multiple sclerosis (RRMS) and clinically isolated syndrome (CIS), 53.9% in progressive multiple sclerosis (PMS), 71.5% in isolated optic neuritis, and 72.5% in neuromyelitis optica (NMO). Immunoadsorption (IA) has a therapy response of 80.6% in relapsing-remitting multiple sclerosis and clinically isolated syndrome and 100% in neuromyelitis optica.
Early treatment initiation with a median of 2–3 weeks and a patient age below 50 are considered to be beneficial regarding a treatment success. In addition to that, a treatment count of 5 to 7 with one plasma volume is also beneficial for treatment success, whereas patients suffering from progressive multiple sclerosis have a lower beneficial rate of apheresis therapy. Both immunoadsorption and plasma exchange have a high safety profile and a high tolerability regarding side effects.
Nevertheless, data situation is too heterogeneous regarding procedures and technical implementation to be finally assessed.

Author Contributions

Conceptualization, M.J.K.; Formal analysis, M.W.; Methodology, M.W.; Supervision, M.J.K.; Validation, M.L. and M.J.K.; Visualization, M.L.; Writing—original draft, M.L.; Writing—review & editing, M.W. and M.J.K. All authors have read and agreed to the published version of the manuscript.

Acknowledgments

This publication is dedicated to the work of G. A. Müller, who always promoted apheresis therapy during his time as a full professor at the chair of Nephrology Göttingen, Germany.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

ASFAAmerican society for apheresis
CISClinical isolated syndrome
IgImmunoglobulin
ILInterleukin
IFNγInterferon gamma
NMONeuromyelitis optica
MSMultiple Sclerosis
PEPlasma exchange
PPMSPrimary-Progressive MS
PRMSProgressive-Relapsing MS
RRMSRelapsing remitting MS
SPMSSecondary-Progressive MS
Th T helper
TregT regulatory
TNF-αTumor necrosis factor alpha
VAVisual acuity
VEPVisual evoked potential

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Figure 1. Flow chart of study selection. MS = multiple sclerosis, NMO = neuromyelitis optica, PE = plasma exchange, IA = immunoadsorption.
Figure 1. Flow chart of study selection. MS = multiple sclerosis, NMO = neuromyelitis optica, PE = plasma exchange, IA = immunoadsorption.
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Figure 2. The 95% normal approximation confidence interval is provided in the meta-analyses. The given SE correspond to normal approximation confidence interval (sqrt(p(1-p)/n)). (A) Effects of PE in RRMS and CIS. (B) Effects of PE in PMS. (C) Effects of PE in opticus neuritis. (D) Effects of PE in NMO. (E) Effects of IA in RRMS and CIS. (F) Effects of IA in NMO. RRMS = relapsing-remitting multiple sclerosis, CIS = clinically isolated syndrome, PMS = progressive multiple sclerosis, SE = standard error, IV = instrumental variables. Figure 2A: Correia et al. [51], Dorst et al. [42], Ehler et al. [49], Ehler at al. [43], Faissner et al. [50], Habek et al. [38], Lipphardt et al. [44], Magana et al. [41], Meca-Lallana et al. [48], Schilling et al. [39], Trebst et al. [40], Yücesan et al. [47]. Figure 2B: Giedraitiene et al. [54], Hauser et al. [52], Khatri et al. [35], Magana et al. [41], Medenica et al. [53]. Figure 2C: Deschamps et al. [45], Merle et al. [56], Roesner et al. [55], Ruprecht et al. [46]. Figure 2D: Abboud et al. [61], Aungsmart et al. [62], Jiao et al. [64], Kim et al. [60], Kleiter et al. [67], Kumar et al. [66], Lim et al. [59], Magana et al. [41], Mori et al. [65], Song et al. [68], Srisupa-Olan et al. [63], Wang et al. [58], Watanabe et al. [57]. Figure 2E: Dorst et al. [42], Heigl et al. [70], Hoffmann et al. [73], Koziolek et al. [32], Llufriu et al. [80], Mauch et al. [71], Schimrigk et al. [75], Schimrigk et al. [76], Trebst et al. [72]. Figure 2F: Faissner et al. [77], Kleiter et al. [67].
Figure 2. The 95% normal approximation confidence interval is provided in the meta-analyses. The given SE correspond to normal approximation confidence interval (sqrt(p(1-p)/n)). (A) Effects of PE in RRMS and CIS. (B) Effects of PE in PMS. (C) Effects of PE in opticus neuritis. (D) Effects of PE in NMO. (E) Effects of IA in RRMS and CIS. (F) Effects of IA in NMO. RRMS = relapsing-remitting multiple sclerosis, CIS = clinically isolated syndrome, PMS = progressive multiple sclerosis, SE = standard error, IV = instrumental variables. Figure 2A: Correia et al. [51], Dorst et al. [42], Ehler et al. [49], Ehler at al. [43], Faissner et al. [50], Habek et al. [38], Lipphardt et al. [44], Magana et al. [41], Meca-Lallana et al. [48], Schilling et al. [39], Trebst et al. [40], Yücesan et al. [47]. Figure 2B: Giedraitiene et al. [54], Hauser et al. [52], Khatri et al. [35], Magana et al. [41], Medenica et al. [53]. Figure 2C: Deschamps et al. [45], Merle et al. [56], Roesner et al. [55], Ruprecht et al. [46]. Figure 2D: Abboud et al. [61], Aungsmart et al. [62], Jiao et al. [64], Kim et al. [60], Kleiter et al. [67], Kumar et al. [66], Lim et al. [59], Magana et al. [41], Mori et al. [65], Song et al. [68], Srisupa-Olan et al. [63], Wang et al. [58], Watanabe et al. [57]. Figure 2E: Dorst et al. [42], Heigl et al. [70], Hoffmann et al. [73], Koziolek et al. [32], Llufriu et al. [80], Mauch et al. [71], Schimrigk et al. [75], Schimrigk et al. [76], Trebst et al. [72]. Figure 2F: Faissner et al. [77], Kleiter et al. [67].
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Table
Table 1. Studies on plasma exchange (PE) in treatment of relapsing-remitting multiple sclerosis (RRMS), clinically isolated syndrome (CIS), progressive MS, isolated optic neuritis, and neuromyelitis optica (NMO). EDSS = Expanded Disability Status Scale.
Table 1. Studies on plasma exchange (PE) in treatment of relapsing-remitting multiple sclerosis (RRMS), clinically isolated syndrome (CIS), progressive MS, isolated optic neuritis, and neuromyelitis optica (NMO). EDSS = Expanded Disability Status Scale.
“Relapsing-Remitting Multiple Sclerosis” and “Clinically Isolated Syndrome”
CitationYearnDesignNo. of TreatmentsTreated Plasma Volume (mL)OutcomeLimitation
[36]1989116Double-blind, multi-center, randomized11n.a.Significant improvement after 4 weeksNo plasmapheresis protocol specifications
[37]199936Double-blind73000Therapy response in 42% of patientsPatient collective with heterogenous MS-types
[39]200513Retrospective53000Therapy response in 71% of patientsSmall number of subjects
[47]20076Retrospective41.0-fold plasma volumeTherapy response in 100% of patientsSmall number of subjects
[40]200920Retrospective3–71.5-fold plasma volumeTherapy response in 76% of patients regarding visual acuitySmall number of subjects
[38]20104Retrospective52750Therapy response in 75% of patientsno placebo, Small number of subjects, the study was observational in character
[41]2011153Retrospective7n.a.Therapy response in 59% of patientsPatient collective with heterogenous MS-types
[48]201315Retrospective≥71.0-fold plasma volumeTherapy response in 93.3% of patientsRRMS + CIS
[49]201411RetrospectiveMedian 7 (3–8)3000 (2200–3500)Therapy response in 91% of patientsCIS only
[43]201590Retrospective3–81.0-fold plasma volumeTherapy response in 72% of patientsThe lack of a control group
[50]201616Retrospectiven.a.2000Therapy response in 91% of patients regarding visual evoked potentialSmall number of subjects and a higher expanded disability status scale in patients in the PE only group
[51]201846RetrospectiveMean 7.39 sessionsn.a.Complete therapy response in 41% of patients and partial therapy response in 39% of patientsPatient collective with heterogenous MS-types
[44]201942Retrospective4–11Mean 2930 median 2000Therapy response in 73% of patientspatients without sufficient follow-up data had a significantly higher patient age and longer duration of disease
[42]201930Double-blind, randomized, uni-centerOn 5 days0.69 ± 0.12-fold individual total plasma volumeTherapy response in 76% of patientsLack of blinding and small number of subjects
“Progressive Multiple Sclerosis”
CitationYearnDesignNo. of TreatmentsTreated Plasma Volume (mL)OutcomeLimitation
[52]198318Prospective, randomized4–5n.a.Therapy response in 27.8% of patientsSmall number of subjects, no plasmapheresis protocol specifications
[35]198554Double-blind controlled20n.a.Therapy response in 54% of patientsNo plasmapheresis protocol specifications
[53]199424Prospective8n.a.Therapy response in 87.5% of patientsSmall number of subjects, no plasmapheresis protocol specifications
[41]201110Retrospective7n.a.Therapy response in 30% of patientsSmall number of subjects
[54] 20156open-label, single-center proof of concept study42000–2500Therapy response in 66.7% of patientsSmall number of subjects
“Isolated Optic Neuritis”
CitationYearnDesignNo. of TreatmentsTreated Plasma Volume (mL)OutcomeLimitation
[46]200410Retrospectiven.a.n.a.Therapy response in 70% of patientsSmall number of subjects
[55]201223Retrospective5~3000Therapy response in 70% of patientsheterogenous
[56]201216Retrospective51.0-fold plasma volumeTherapy response in 87.5% of patientsSmall number of subjects
[45]201634RetrospectiveMedian 5, range 5–101.5-fold body mass volumeTherapy response in 56% of patients regarding visual acuityThe lack of a control group
“Neuromyelitis Optica”
CitationYearnDesignNo. of TreatmentsTreated Plasma Volume (mL)OutcomeLimitation
[57]20076Retrospective3–52000–3000Therapy response in 50% of patientsSmall number of subjects
[58]20115Retrospective≥51.0-fold plasma volumeTherapy response in 80% of patientsSmall number of subjects
[41]201126Retrospective7n.a.Therapy response in 42.3% of patientsHistorical cohort study
[59]201331Retrospectiven.a.n.a.Therapy response in 65% of patientsNo study controlled treatment regimes
[60]201315Retrospective61.0–1.5-fold plasma volumeTherapy response in 78% of patientsSmall number of subjects
[61]201665Retrospective5–71.5-fold plasma volumeTherapy response in 65% of patientsSelection bias; use of EDSS scores as the primary outcome measure
[62]201721Retrospective5n.a.Therapy response in 81% of patientsUse of EDSS scores as the primary outcome measure
[63]201828Retrospective51000Therapy response in 42.9% of patientsUse of EDSS scores as the primary outcome measure
[64]201829Retrospective2–71.0-fold plasma volumeTherapy response in 82.8% of patientsHeterogenous treatment protocols
[65]20189Retrospective71.0-fold plasma volumeTherapy response in 75% of patientsSmall number of subjects
[66]20185Retrospective5 (3–7)1.0-fold plasma volumeTherapy response in 80% of patientsSmall number of subjects
[67]2018146Retrospective≥3n.a.Therapy response in 86% of patientsHeterogenous treatment protocols
[68]201915Retrospective2–3n.aTherapy response in 100% of patientsSmall number of subjects
Table
Table 2. Studies on immunoadsorption in treatment of relapsing-remitting multiple sclerosis (RRMS), clinically isolated syndrome (CIS) and neuromyelitis optica (NMO).
Table 2. Studies on immunoadsorption in treatment of relapsing-remitting multiple sclerosis (RRMS), clinically isolated syndrome (CIS) and neuromyelitis optica (NMO).
“RRMS” and “CIS”
CitationYearnDesignNo. of TreatmentsTreated Plasma Volume (mL)Matrix of AdsorberOutcomeLimitation
[69]20003Retrospective5–6n.a.n.a.Therapy response in 100% of patientssmall number of subjects
[74]200512Prospective141.5-fold plasma volumeSepharose-conjugated sheep antibodies to human immunoglobulin (IgG)No significant therapy responsesmall number of subjects and patient collective with heterogenous MS-types
[71]201114Retrospective5–6n.a.TryptophanTherapy response in 85% of patientssmall number of subjects
[75]201224RetrospectiveMean 5 (range 3–6)2000–2500TryptophanTherapy response in 83% of patientssmall number of subjects and patient collective with heterogenous MS-types
[72]201210Retrospective5–72500TryptophanTherapy response in 66% of patientssmall number of subjects
[32]201211Prospective52500TryptophanTherapy response in 72% of patientssmall number of subjects
[70]201360Retrospective62000TryptophanTherapy response in 88% of patientsonly qualitative data regarding the therapeutic success and clinical data on tolerability were available
[76]2016147Retrospectiven.a.2000–2500TryptophanTherapy response in 71% of patientsExpanded Disability Status Scale was used to measure a change in relapse-related disability
[73]201823RetrospectiveMean 5.82031 ± 230TryptophanTherapy response in 83% of patientsLack of a control group; use of immunoadsorption was limited in some study centers
[44]201932Retrospective5–72000–2500TryptophanTherapy response in 65% of patientspatients without sufficient follow-up data had a significantly higher patient age and longer duration of disease
[42]201931Prospective, double-blind, randomized, uni-centerOn 5 days2.0-fold total plasma volume on day 1, and the 2.5-fold total plasma volume on day 2–5protein ATherapy response in 100% of patientsLack of blinding and small number of subjects
“NMO”
CitationYearnDesignNo. of TreatmentsTreated Plasma Volume (mL)Matrix of AdsorberOutcomeLimitation
[77]201610RetrospectiveMean 5.2 (3–7)2000–2500TryptophanTherapy response in 100% of patientsSmall number of subjects
[67]201827Retrospective≥3n.a.Tryptophan or Protein ATherapy response in 100% of patientsHeterogenous treatment protocols
Table
Table 3. Predictors of apheresis response. EDSS = Expanded Disability Status Scale; MRI = magnetic resonance imaging. * Pediatric patients only.
Table 3. Predictors of apheresis response. EDSS = Expanded Disability Status Scale; MRI = magnetic resonance imaging. * Pediatric patients only.
“Multiple Sclerosis” (with Relapsing-Remitting and Progressive MS Sub-Sections)
ClassificationPredictorCitationMeaning
Clinical signs and symptomsEDSS ≤ 5[43]Indicates good apheresis response
Preserved deep tendon reflexes[41]Indicates good apheresis response
DemographicsYounger age[44]Indicates good apheresis response
Female[37,91]Indicates good apheresis response
Histological classification and localizationGadolinium positive MRI lesions[43]Indicates good apheresis response
Histological type 1 and 2 pattern[34]Indicates good apheresis response
Histological type 3 pattern[34]Indicates poor apheresis response
Pre-treatmentNo disease modifying drugs[43]Indicates good apheresis response
Short duration of disease[41]Indicates good apheresis response
“Neuromyelitis Optica”
ClassificationPredictorCitationMeaning
Histological classification and localizationIsolated myelitis[85]Indicates good apheresis response
Laboratory valuesAnti-aquaporin-4 IgG positive[12]Indicates good apheresis response
“Mixed”
ClassificationPredictorCitationMeaning
ApheresisEarly initiation[44,60,80,88]Indicates good apheresis response
Clinical signs and symptomsLower baseline scores on the EDSS, visual outcome, and gait scales[94] *Indicates good apheresis response
Pre-treatmentCumulative corticosteroid doses[44]Irrelevant for apheresis response

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Lipphardt, M.; Wallbach, M.; Koziolek, M.J. Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis. J. Clin. Med. 2020, 9, 1597. https://doi.org/10.3390/jcm9051597

AMA Style

Lipphardt M, Wallbach M, Koziolek MJ. Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis. Journal of Clinical Medicine. 2020; 9(5):1597. https://doi.org/10.3390/jcm9051597

Chicago/Turabian Style

Lipphardt, Mark, Manuel Wallbach, and Michael J. Koziolek. 2020. "Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis" Journal of Clinical Medicine 9, no. 5: 1597. https://doi.org/10.3390/jcm9051597

APA Style

Lipphardt, M., Wallbach, M., & Koziolek, M. J. (2020). Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis. Journal of Clinical Medicine, 9(5), 1597. https://doi.org/10.3390/jcm9051597

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