|Prominent plasmacytosis following intravenous immunoglobulin correlates with clinical improvement in Guillain-Barré syndrome.|
|Jump to Full Text|
|PMID: 18461177 Owner: NLM Status: MEDLINE|
|BACKGROUND: High doses of pooled polyclonal IgG are commonly used to treat numerous autoimmune diseases. Their mode of action nevertheless remains only partially explained. At the same time, until now, no early biological marker has been able to predict their efficacy.
METHODOLOGY/PRINCIPAL FINDINGS: In a first pilot retrospective analysis, we reviewed white blood cell counts and blood smears in consecutive patients with autoimmune disease (n = 202) and non-autoimmune disease (n = 104). Autoimmune patients received either intravenous immunoglobulin (IVIg, n = 103), plasma exchange (n = 78) or no specific treatment (n = 21). We then prospectively monitored consecutive autoimmune patients with IVIg injection (n = 67), or without any specific treatment (n = 10) using the same routine laboratory tests, as well as flow cytometry. Both retrospective and prospective analyses identified large plasma-cell mobilization exclusively in IVIg-treated autoimmune patients 7 days after initiation of treatment. The majority of IVIg-mobilized plasma cells were immature HLA-DR(high)/CD138(low)/CXCR4(low) plasma cells expressing intracellular immunoglobulin G which were neither IVIg- nor human IgG-specific. Importantly, we found a strong negative correlation between the absolute number of IVIg-mobilized plasma cells and time to improve neurological function in both retrospective and prospective studies of Guillain-Barré syndrome (GBS), (r = -0.52, p = 0.0031, n = 30, r = -0.47, p = 0.0028, n = 40, respectively).
CONCLUSIONS/SIGNIFICANCE: IVIg promotes immature plasma-cell mobilization in patients with GBS, chronic inflammatory demyelinating polyneuropathy, myasthenia gravis and inflammatory myopathy. Prominent day 7 plasma-cell mobilization is a favourable prognostic marker in patients with GBS receiving IVIg treatment.
|Izumi Mori; Christophe Parizot; Karim Dorgham; Sophie Demeret; Zahir Amoura; Francis Bolgert; Guy Gorochov|
Related Documents :
|6472767 - Polyclonal immunoglobulins in malignant plasma cell dyscrasias.
7919807 - Evaluation of the immune response in symptomatic and asymptomatic human giardiasis.
18477847 - Melkersson-rosenthal syndrome and acquired c1 inhibitor deficiency.
1568647 - Activation of the classical complement pathway in spontaneous bacterial peritonitis.
24532617 - Evaluation of plethysmography for diagnosis of postintubation tracheal stenosis.
21571767 - Low-dose rituximab therapy for refractory thrombocytopenia in patients with systemic lu...
|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2008-05-07|
|Title: PloS one Volume: 3 ISSN: 1932-6203 ISO Abbreviation: PLoS ONE Publication Date: 2008|
|Created Date: 2008-05-07 Completed Date: 2008-08-28 Revised Date: 2013-06-05|
Medline Journal Info:
|Nlm Unique ID: 101285081 Medline TA: PLoS One Country: United States|
|Languages: eng Pagination: e2109 Citation Subset: IM|
|Institut National de la Santé et de la Recherche Médicale (INSERM) U543, Paris, France.|
|APA/MLA Format Download EndNote Download BibTex|
Aged, 80 and over
Cell Survival / drug effects
Guillain-Barre Syndrome / immunology*, pathology
Immunoglobulins, Intravenous / therapeutic use*
Plasma Cells / cytology, drug effects, immunology, pathology*
Severity of Illness Index
Journal ID (nlm-ta): PLoS ONE
Journal ID (publisher-id): plos
Journal ID (pmc): plosone
Publisher: Public Library of Science, San Francisco, USA
Mori et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Received Day: 6 Month: 11 Year: 2007
Accepted Day: 16 Month: 3 Year: 2008
collection publication date: Year: 2008
Electronic publication date: Day: 7 Month: 5 Year: 2008
Volume: 3 Issue: 5
E-location ID: e2109
PubMed Id: 18461177
Publisher Id: 07-PONE-RA-02678R2
|Prominent Plasmacytosis Following Intravenous Immunoglobulin Correlates with Clinical Improvement in Guillain-Barr? Syndrome Alternate Title:IVIg-Related Plasmacytosis|
1Institut National de la Sant? et de la Recherche M?dicale (INSERM) U543, Paris, France
2Laboratoire d'Immunologie Cellulaire et Tissulaire, Assistance Publique - H?pitaux de Paris (AP-HP) H?pital Piti?-Salp?tri?re, Paris, France
3Department of Neurology, Assistance Publique - H?pitaux de Paris (AP-HP) H?pital Piti?-Salp?tri?re, Paris, France
4Department of Internal Medicine, Assistance Publique - H?pitaux de Paris (AP-HP) H?pital Piti?-Salp?tri?re, Paris, France
5Universit? Pierre et Marie Curie-Paris 6 (UPMC), Paris, France
|Beijing Institute of Infectious Diseases, China
|Correspondence: * E-mail: email@example.com
Contributed by footnote: Conceived and designed the experiments: GG IM FB. Performed the experiments: IM. Analyzed the data: GG IM FB SD ZA. Contributed reagents/materials/analysis tools: GG IM CP KD. Wrote the paper: GG IM. Other: In charge of cytofluorometric analysis, ELISPOT assay, compiled data and prepared figures and wrote a primary draft of sections of the report: IM. In charge of flow cytometry setup: CP. In charge of fluorescein isothiocyanate conjugate of IVIg: KD. Examined, diagnosed and obtained samples from all patients included in the study: FB. Reviewed medical records, obtained samples for some patients: SD. Advised on study design and supervised the statistical analysis: ZA. Edited the report: SD, FB.
Polyclonal IgG pooled from the serum of thousands of donors is widely used not only to confer passive protection to immune deficient patients but also as an anti-inflammatory agent . Intravenous immunoglobulin (IVIg) therapy is approved by Food and Drug Administration for the treatment of immune thrombocytopenic purpura, Kawasaki disease, primary immunodeficiency, bone marrow transplantation, chronic B-cell lymphocytic leukemia, and pediatric HIV infection . Off label use is common in several autoimmune conditions such as Guillain-Barr? syndrome (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), myasthenia gravis (MG), inflammatory myopathy (IM), and multiple sclerosis, making it a major drug expenditure item . Until now, there has existed no biological marker which may be used to evaluate the efficacy of this treatment. The lack of a biological marker is particularly troublesome when trying to evaluate the efficacy of IVIg during the course of chronic autoimmune diseases such as CIDP, MG and IM.
GBS is an autoimmune polyneuropathy, characterized by precedent infection and acutely progressive motor weakness. GBS affects 0.4?4.0 cases per 100,000 per year, and represents the most common cause of acute neuromuscular paralysis . Older age, preceding gastro-intestinal infection, and rapid onset of severe motor weakness have been demonstrated to be adverse prognostic factors , . Although IVIg has been shown to hasten the recovery of neurological function as efficiently as plasma exchange (PE), the mortality remains 5?10% in GBS , . Until now, it has been impossible to predict which patient will benefit from a single course of IVIg, and which will need a more individualized treatment.
We report here that IVIg induces a peripheral mobilization of plasma cells in GBS, CIDP, MG and IM patients 7 days after initiation of treatment. Our most remarkable finding is that prominent IVIg-mobilized plasmacytosis correlates with faster recovery of neurological function in patients with GBS.
The mode of action of IVIg remains only partially explained. We aimed to identify a biological marker to predict IVIg efficacy in autoimmune diseases.
Fifty consecutive patients with GBS (M/F 31/19, median age 57, range 15?84), hospitalized in our institution between June 2004 and June 2007, were prospectively recruited. Three control autoimmune disease groups consisted of consecutive patients with CIDP (12/2, 52, 30?73), MG (4/3, 70, 19?94), and IM (2/4, 30, 23?57). Only GBS, CIDP, and MG patients were na?ve of any previous immunomodulation therapy. Healthy bone marrow donors (2 men, 26, 32 years) and healthy controls (10/12, 39, 22?62) were enrolled in order to study medullary or circulating plasma cells.
Medical records of 157 GBS patients (91/66, 47, 15?83), referred to our institution between April 1990 and May 2004, were reviewed. We also analyzed medical records of consecutive autoimmune patients treated with IVIg (myasthenic respiratory crisis, 16/22, 58, 18?94, CIDP, 3/4, 55, 30?81) and consecutive non-autoimmune patients without immunomodulatory treatments (61/43, 53, 19?92, encephalitis n?=?30, cerebral abscess n?=?2, Lyme disease n?=?1, botulism n?=?1, status epilepticus n?=?35, cerebral vascular disease n?=?25, brain contusion n?=?2, amyotrophic lateral sclerosis n?=?8), admitted at our institution's neurological intensive care unit (ICU) for more than 14 days between April 1997 and May 2004.
All patients satisfied clinical diagnostic criteria of GBS , CIDP , MG  and IM . We excluded GBS patients with serious pre-existing disease (lymphoma n?=?1, colon cancer n?=?2, cholangiocarcinome n?=?1, hepatic abscess n?=?1, toxoplasmosis n?=?1).
The study was performed according to the Helsinki declaration. The ethics committee of Piti?-Salp?tri?re Hospital approved the study, and signed informed consent was obtained from all patients participating in the prospective study.
The same senior neurologist (F.B.) examined all GBS patients and assessed GBS disability-grade . GBS disability-grades were: 0?=?healthy, 1?=?minor symptoms and capable of running; 2?=?able to walk 5 m or more without assistance but unable to run; 3?=?able to walk 5 m across an open space with help; 4?=?chairbound/bedbound: unable to walk as in 3; 5?=?requiring assisted ventilation for at least part of the day; 6?=?dead. We evaluated treatment efficacy by time to one GBS disability-grade improvement, capacity to walk independently at 2 months, and the need for and duration of artificial ventilation time.
All non-ambulant GBS patients were treated on day of admission (day 0). PE was the first line treatment between April 1990 and April 1997, and IVIg (0.4 g/kg/day, Tegeline, LFB laboratories, Les Ulis, France) has been the preferred treatment since then. PE-treated GBS patients with more than 4 disability-grade received six 50 mL/kg PE (n?=?61), while patients with 3 disability-grade received only three PE courses (n?=?17). GBS patients received IVIg for 5 days if their disability-grade was at least 4 (n?=?81), or 3 days for grade 3 (n?=?17). All CIDP patients in the retrospective study showed respiratory failure (n?=?7), and therefore received IVIg for 4 days and oral prednisolone (1 mg/kg/day), while CIDP patients in the prospective study received IVIg only (n?=?14). All MG patients (n?=?45) received IVIg for 4 days and oral prednisolone (1 mg/kg/day). All IM patients (n?=?6) received IVIg for 4 days after receiving intravenous pulse methylprednisolone (1 g/day) for 3 days.
White blood cell count with 5 differentials was carried out on a XE2100 (SYXMEX) hematology analyzer, and plasma cell count was confirmed by blood smear exam after May Grunwald Giemsa staining.
Whole blood was collected at admission, and every 7 days during 28 days in the prospective population. Briefly, 200 ?l of heparinized whole blood was incubated for 20 minutes at room temperature with various combinations of monoclonal antibodies. The following antibodies were used: with anti-CD19 allophycocyanin mAb (clone HIB19), anti-CD27 phycoerythrin mAb (clone M-T271), anti-CD27 fluorescein isothiocyanate (FITC) mAb (clone M-T271), anti-CD45 FITC (clone 2D1), anti-CD138 peridinin chlorophyll protein-cyanin 5.5 mAb (clone MI15), anti-CXCR4 phycoerythrin mAb (clone 12G5), anti-HLA-DR phycoerythrin-cyanin 7 mAb (clone L243), anti-CD38 FITC mAb (clone HIT2), anti-IgG FITC mAb (clone G18-145), anti-IgM FITC mAb (clone G20-127) (all from Becton Dickson; San Diego; CA) and human IgG FITC (Sigma; St. Louis; USA). IVIg FITC was prepared by incubation of 20 ?l of 5 mg/ml FITC (Sigma) and 500 ?l of 2 mg/ml IVIg (LFB) solutions for 2 hours. Unbound FITC was removed by dialysis against 0.1 M Tris-Cl, 0.2 M NaCl (Sigma) pH 7.4 over 2 days. For intracellular staining, cells were fixed with 1% paraformaldehyde (Sigma) for 20 minutes at room temperature after surface staining, and then permeabilized with 0.1% saponin (Sigma) before intracellular staining. Analyses were performed using a FACS Calibur and CellQuest Pro software (Becton Dickson). Absolute numbers of various CD19+CD27high cell subsets were calculated per ?l of blood, based on the frequencies of CD45+CD19+CD27high cells among total CD45+ peripheral blood mononuclear cells (PBMCs).
Proportions of patients between groups were compared using Fisher exact test. Mean values between two groups were compared by use of Mann-Whitney U test. Correlation was analyzed using Spearman test. Time to one disability-grade improvement comparison between two groups was performed using the log-rank test. In all statistical analysis, p values <0.05 were considered as statistically significant. Data were analyzed using StatView? (SAS Institute, Cary, NC, USA).
GBS represents a particularly attractive study model of autoimmunity insofar as it represents an acutely progressive polyneuropathy. A precipitating infection is frequently suspected, and the date of onset of neurological symptom is known. It therefore seemed to us particularly interesting to study in those patients the variations of the different leukocyte subpopulations. We detected a very large population of circulating plasma cells in numerous GBS afflicted patients treated with IVIg. A retrospective analysis allowed us to determine that this plasmacytosis was maximal on the 7th day after initiating treatment (283 ? 343 cells/?l, n?=?30, mean ? SD; Figure 1A upper panel). This effect is likewise found in patients treated for CIDP or for MG (107 ? 31 cells/?l, n?=?6, 223 ? 272 cells/?l, n?=?21, respectively; Figure 1A middle and lower panels). Therefore, this anomaly does not seem linked to a particular pathologic condition, but rather to IVIg treatment.
In order to confirm an association between IVIg and the observed plasmacytosis, we analyzed GBS patients having received PE only. We ensured that treatments with PE (n?=?78) or IVIg (n?=?58) were administered in isolation of other therapies, notably the absence of associated steroids. Furthermore, the two groups were homogeneous in terms of prognostic factors, including age (p?=?0.98), previous diarrhoea (p?=?0.50) and intervals from disease onset to treatment initiation (p?=?0.09). We also included a third group of GBS patients (n?=?21) that received no specific treatment whatsoever over the course of their hospitalization, however this group would obviously represent patients who were less severely afflicted, compared with IVIg-treated patients (p?=?0.0008). In all these groups, we examined plasma-cell levels during a 14-day period following hospitalization. Peripheral blood plasmacytosis was not detected in patients treated with PE or in those without specific treatment (Figure 1B upper and middle panels). Importantly, the IVIg- and PE-treatment groups were homogeneous in terms of disability-grade at disease nadir (p?=?0.29) and rate of improvement of neurological function (p?=?0.84).
Although peripheral blood plasmacytosis was not detected in patients treated with PE, we were still concerned with the fact that this anomaly could simply reflect common infectious complications, and addressed this issue in two ways. Firstly, we verified that mean maximal plasma cell counts were not more elevated in IVIg-treated GBS patients with recorded infectious complications (pneumonia n?=?24, septicaemia n?=?1) than in the others during a 60-day period following hospitalization (278 ? 382 cells/?l, n?=?25 vs 307 ? 410 cells/?l, n?=?33, p?=?0.33, data not shown). Secondly, we reviewed medical records of consecutive non-autoimmune ICU-hospitalized patients who never received immunomodulation therapy but who were exposed to the same infectious hazards. In this non-autoimmune group, plasmacytosis was rarely detected (Figure 1B, lower panel), and mean plasma cell counts 7 days after admission (1.8 ? 17 cells/?l, n?=?96) were significantly less elevated than in IVIg-treated patients (GBS: 283 ? 343 cells/?l, n?=?30, p<0.0001, CIDP: 107 ? 31 cells/?l, n?=?6, p<0.0001, MG: 223 ? 272 cells/?l, n?=?21, p<0.0001, data not shown). Importantly, the presence of plasmacytosis in non-autoimmune patients was always associated with sepsis, and sepsis-related plasmacytosis never exceeded 200 cells/?l during the 14-day hospitalization (54?187 cells/?l, n?=?9). Altogether, it therefore seems reasonable to conclude that a prominent plasmacytosis exceeding 200 cells/?l 7 days after treatment was IVIg-induced.
We next examined if the data gathered during our retrospective analysis could be confirmed in a consecutive population of GBS, CIDP, MG and IM patients. Non-ambulant GBS patients and CIDP patients were treated with IVIg, whereas MG and IM patients received IVIg and steroids. Using flow cytometry, high CD27 expression on CD19+ B cells allows us to distinguish plasma cells from other CD19+ B cells (Figure 2A) , . A longitudinal analysis of these subpopulations was performed just prior to the start of treatment with IVIg and every 7 days during 1 month (Figure 2B). Compared to baseline values (day 0), one finds on the 7th day a very significant mobilization of circulating CD19+CD27high plasma cells in IVIg-treated patients (Figure 2). Importantly, IVIg-mobilized CD19+CD27high cell counts strongly correlated with plasma cell counts measured by blood smears (r?=?0.94, p<0.0001, n?=?67, data not shown), indicating that the same type of plasma cell was indeed monitored at day 7 of IVIg in both retrospective and prospective studies.
In comparison, levels of absolute CD19+CD27high plasma cell counts remained unchanged during the first week following admission in ambulant GBS patients without any specific treatment (5.9 ? 2.4 cells/?l vs 6.1 ? 4.2 cells/?l, n?=?10, p?=?0.53, data not shown).
The circulating plasma cells we observed could correspond to recently generated and/or highly differentiated plasma cells. Recently, downregulation of HLA-DR , and upregulation of CD138  and CXCR4 ,  have been shown to be characteristic features of mature plasma cells exiting from the bone marrow. We first verified that the IVIg-mobilized CD19+CD27high cells contained IgG, and co-expressed CD38 and CD138 (Figure S1A). In addition, their numbers were clearly proportional to the number of cells capable of secreting IgG antibodies in vitro in response to a non-specific stimulus (r?=?0.99, p?=?0.0028, n?=?6; Figure S1B and Methods S1).
We next revealed that the majority of IVIg-mobilized plasma cells were CXCR4low, CD138low, and HLA-DRhigh, and as such, relatively immature (Figure 3A left panel, B-C). Here, medullary cells from a healthy control were taken as reference in order to present CXCR4, CD138, and HLA-DR levels, typically associated with terminal differentiation into mature plasma cells in the bone marrow (Figure 3A, right panel).
We further clarified that plasma-cell mobilization was not the mere consequence of an immunization against IVIg. PBMCs were stained in vitro with fluorescently labeled IVIg or purified human IgG. As shown, mean fluorescence levels measured on CD19+CD27high cells before treatment remained unchanged 7 days after IVIg infusion (Figure 4 middle and right panels).
Finally, we sought to determine if IVIg-related plasmacytosis could serve as a marker of effectiveness of this treatment. Firstly, we plotted plasma cell counts 7 days post-IVIg and time to improvement of one GBS disability-grade, in order to assess the possible correlation between the number of IVIg-mobilized plasma cells and clinical improvement (Figure 5A). Retrospective analysis was limited to severely disabled patients in order to avoid bias related to potential deficiencies in minor symptom recording. We found a strong negative correlation between the absolute number of IVIg-mobilized plasma cells and time to improve one GBS disability-grade in both retrospective and prospective studies (r?=??0.52, p?=?0.0031, n?=?30, r?=??0.47, p?=?0.0028, n?=?40, respectively; Figure 5A).
Secondly, GBS patients were divided into two groups depending on whether they had or had not shown a significant plasmacytosis (? 200 plasma cells/?L) on the 7th day of treatment. Prominent plasmacytosis was noted in 12 out of 30 patients and 22 out of 40 severely disabled patients in retrospective and prospective analyses, respectively. Importantly, the two groups did not differ in any clinical prognostic factors, including intervals between motor deficit onset and treatment initiation (p?=?0.27, p?=?0.26, respectively), age (p?=?0.93, p?=?0.98, respectively), preceding diarrhoea (p>0.99, p?=?0.51, respectively), and rapid disease onset (p?=?0.44, p?=?0.40, respectively). Patients having shown a plasmacytosis greater than or equal to 200 plasma cells/?l on the 7th day of treatment recovered faster than those who had not shown such an expansion (p?=?0.011, p<0.0001, respectively; Figure 5B). More patients having presented with a prominent IVIg-related plasmacytosis achieved independent walking at day 56, compared with the others (p?=?0.0069, p?=?0.0095, respectively).
A more detailed analysis of the consecutive population revealed that patients exhibiting more than 200 IVIg-mobilized plasma cells/?l showed less severe GBS disability-grade at day 14 (3.1 ? 0.94 vs 4.2 ? 1.1, p?=?0.0031, data not shown). In addition, the patient group with a prominent IVIg-related plasmacytosis less frequently required mechanical ventilation (p?=?0.0073) and for shorter time than the group not showing IVIg-related plasmacytosis (18 ? 4.0 days, n?=?3 vs 39 ? 16 days, n?=?10, p?=?0.0034, data not shown).
Here we show that a prominent plasmacytosis was very frequently associated with administration of IVIg in autoimmune patients. More importantly, the level of circulating plasma cells on the 7th day of IVIg treatment correlated with clinical improvement in patients with GBS. These findings indicate that plasma cell count on the 7th day of IVIg will be useful to distinguish patients that have beneficial IVIg effects from those who would need more individualized treatment, and to reconsider the treatment regimen during the acute phase of GBS in the latter.
Low levels of circulating CD19+CD27high plasma cells were occasionally detected in healthy individuals (5.2 ? 2.4 cells/?l, n?=?22, data not shown) or in untreated autoimmune patients in our own study (Figure 2C). A fugacious plasmacytosis is in fact a well known physiological consequence of any recent antigenic stimulation , , , but typically much less than 100 lymphoplasmocytoid cells can be found in one microliter of blood in such occasions, even in autoimmune patients with active disease flares . Here, we verified that a prominent plasmacytosis was not a disease- or an infectious-related event. We also showed that IVIg-mobilized plasma cells were not IVIg-specific (Figure 4 middle panel), and therefore did not simply reflect an immunization against the infused products.
A very significant proportion of CD19+CD27high plasma cells on the 7th day of IVIg were detected in all GBS patients, as well as in other autoimmune patients (Figure 2C). GBS patients presented with significantly more day 7 plasma cells (31.2 ? 16.1% among CD19+ B cells, n?=?40), compared with other autoimmune patients (CIDP; 20.1 ? 15.4%, n?=?14, p?=?0.0092, MG; 8.3 ? 2.9%, n?=?7, p<0.0001, IM; 5.3 ? 2.7%, n?=?6, p<0.0001; Figure 2C left panel). The less prominent plasma-cell mobilization in MG and IM patients could be related to the fact that these patients received steroids either before or during IVIg infusion. However, GBS and CIDP groups were homogenous in terms of age, sex and treatment received. Therefore, we can only postulate that IVIg-related plasmacytosis would be more pronounced in the context of an ongoing immune response, compared to chronic conditions such as CIDP. In order to test that hypothesis, IVIg-related plasmacytosis should be measured in healthy controls.
In GBS patients, the magnitude of IVIg-related plasmacytosis correlated with improvement of neurological function, including achievement of independent locomotion and discontinuation of mechanical ventilation. Importantly, clinical prognostic factors were demonstrated to be homogenous between patients with a prominent IVIg-related plasmacytosis and the others, indicating that IVIg-mobilized plasma cells could be served as a biological prognostic marker. Recently, a prognostic scoring system for GBS has been reported to predict the capacity of independent locomotion at 6 months . This scoring system is based on age, previous episode of diarrhoea and GBS disability-grade at 2 weeks of treatment. We evaluated how day 7 plasmacytosis performs, compared with this score (Erasmus GBS outcome score). In the consecutive population we studied, we show that the group of patients with a prominent IVIg-related plasmacytosis will recover faster than the others according to classic criteria (ventilation time, ability to walk independently at 2 months and 6 months). We show that the Erasmus GBS outcome score in that group could also have predicted a more favourable evolution, compared with the other (p?=?0.0018). As stated above, retrospective analysis was limited to severely disabled patients in order to avoid bias related to minor symptom recording. In that retrospective population-based study, we also show that the group of patients with a prominent IVIg-related plasmacytosis will recover faster than the other. Interestingly, we found that the Erasmus GBS outcome score would not have predicted a more favourable evolution in that group (p?=?0.55). Therefore, plasma-cell monitoring appears to have an added value over the Erasmus GBS outcome score for the prognostic evaluation of severe GBS patients.
Further observations in the 5 GBS patients who relapsed within 28 days after IVIg give further comfort to the prognostic value of day 7 plasmacytosis. These patients had significantly less circulating day 7 plasma cells, compared with the others (68 ? 72 cells/?l, n?=?5 vs 369 ? 426 cells/?l, n?=?35, p?=?0.0079), and were treated with several courses of IVIg. Despite repeating IVIg treatment, 2 such refractory patients died 28 days and 100 days after the first IVIg course. It is therefore unlikely that repeating IVIg treatment in refractory patients will be adequate. Cost would be reduced, and treatment could be optimized by defining which patients would benefit from an alternative treatment instead of receiving several IVIg courses. However, more patients need to be studied before we can recommend not repeating IVIg infusion in the absence of plasmacytosis after the first IVIg course.
The mobilization of a large number of plasma cells concurrently with clinical improvement might seem surprising. The detection of these cells is rather typically associated with autoimmune disease flares, for instance in multiple sclerosis and systemic lupus erythematosus , . Our data, as counter-intuitive as they may seem, are nevertheless in good agreement with proposed models of plasma-cell dynamics during humoral immune responses . According to the later, newly generated plasmablasts enter into competition with older cells for their medullary niches. Similarly, we would like to propose that following IVIg treatment, a large ?wave? of mobilized cells induces a significant renewal of the repertoire of antibody-secreting cells. A ?re-equilibration? of the repertoire of circulating antibodies in favour of non-pathogenic antibodies could then ensue. As stated above, it is strongly suspected that antibody-secreting plasma cells which cross-react with nervous structures are induced during a preceding infectious episodes , and reside in the survival niches of the bone marrow in patients with GBS . One can imagine that a proportion of these cells, among others, would be chased from the marrow by a wave of new polyclonal immigrants , . Given the long half-life of antibodies, this mechanism may be difficult to reconcile with the rapid mode of action of IVIg. Other mechanisms have been proposed to account for the anti-inflammatory effect of IVIg , . It is now generally accepted that IVIg has multiple therapeutic effects that would act in concert . IVIg could, for instance, directly influence plasma-cell survival , . Plasma-cell mobilization could nevertheless have a long lasting impact on the pool of long-lived plasma cells that are not affected by classic immunomodulation treatments . This particular mode of action of IVIg could explain its superiority over steroids in certain indications such as GBS , , . Interestingly, it is notable that Pemphigus Vulgaris patients who do not respond to steroids plus immunosuppressive agents can nevertheless respond to IVIg .
IVIg promotes immature plasma-cell mobilization in patients with GBS, CIDP, MG and IM (Figure 3C). Even if it has been demonstrated that IVIg could accelerate the in vitro maturation of B lymphocytes , the origin of the mobilized plasma cells  and the mechanism through which this treatment induces their mobilization remain unclear. It will therefore be interesting to determine how IVIg is able to influence the maturation, the migration, and ultimately the replenishment of plasma cells.
In spite of IVIg treatment, approximately 20% of the patients with GBS are unable to walk without assistance after 1 year , . Day 7 plasma-cell monitoring will be helpful to predict which patients will improve after IVIg treatment, and therefore will prompt the early implementation of more individualized therapeutic strategies in such patients at a greater risk of poor outcome.
IVIg-mobilized CD19+CD27high plasma cells were IgG-secreting cells. (A) A representative 4-colour cytofluorometric analysis of GBS PBMCs 7 days after initiation of IVIg infusion. Intracellular analysis revealed that post-IVIg CD19+CD27high plasma cells (gated as indicated) were intracellular IgG+IgM? and membrane CD38+CD138+ (insets). (B) Correlation between flow cytometry-enumerated CD19+CD27high cells and ELISPOT-enumerated IgG-secreting cells (SCs) in 6 GBS patients treated with IVIg. Cytofluorometric analysis and ELISPOT assay were simultaneously performed 7 days post-IVIg infusion. Correlation was analyzed using Spearman test.
(10.10 MB TIF)
Click here for additional data file (pone.0002109.s001.png)
(0.03 MB DOC)
Click here for additional data file (pone.0002109.s002.doc)
Competing Interests: The authors have declared that no competing interests exist.
Funding: This study was financially supported by Assistance Publique - Hopitaux de Paris (CIB Piti?-Salp?tri?re) and by grants from INSERM and Laboratoire fran?ais du Fractionnement et des Biotechnologies (LFB-Biom?dicaments).
We thank H. Merle-Beral and K. Maloum for reviewing cytological analysis, V. Leblond for advice on bone marrow analysis, D. Ramani for reviewing medical records, C. Fieschi, and A. Mathian for discussions and advices, N. Haddad and M. Le Garff for supervision of early ELISPOT assay, D.R. Raphael and N. Gowlland for editing the manuscript.
|1.||Kazatchkine MD,Kaveri SV. 2001;Immunomodulation of autoimmune and inflammatory diseases with intravenous immune globulin.N Engl J Med 345:747–755. [pmid: 11547745]|
|2.||G?rcan HM. 2007;Efficacy of various intravenous immunoglobulin therapy protocols in autoimmune and chronic inflammatory disorders.Ann Pharmacother 41:812–823. [pmid: 17440006]|
|3.||Govoni V,Granieri E. 2001;Epidemiology of the Guillain-Barr? syndrome.Curr Opin Neurol 14:605–613. [pmid: 11562572]|
|4.||Visser LH,Schmitz PI,Meulstee J,van Doorn PA,van der Mech? FG. 1999;Prognostic factors of Guillain-Barr? syndrome after intravenous immunoglobulin or plasma exchange. Dutch Guillain-Barr? Study Group.Neurology 53:598–604. [pmid: 10449126]|
|5.||van Koningsveld R,Steyerberg EW,Hughes RA,Swan AV,van Doorn PA,et al. 2007;A clinical prognostic scoring system for Guillain-Barr? syndrome.Lancet Neurol 6:589–594. [pmid: 17537676]|
|6.||van der Mech? FG,Schmitz PI. 1992;A randomized trial comparing intravenous immune globulin and plasma exchange in Guillain-Barr? syndrome. Dutch Guillain-Barr? Study Group.N Engl J Med 326:1123–1129. [pmid: 1552913]|
|7.||Plasma Exchange/Sandoglobulin Guillain-Barr? Syndrome Trial Group. 1997;Randomised trial of plasma exchange, intravenous immunoglobulin, and combined treatments in Guillain-Barr? syndrome.Lancet 349:225–230. [pmid: 9014908]|
|8.||Asbury AK,Cornblath DR. 1990Assessment of current diagnostic criteria for Guillain-Barr? syndrome.Ann Neurol 27 Suppl :S21–24.|
|9.||Ad Hoc Subcommittee of the American Academy of Neurology AIDS Task Force. 1991;Research criteria for diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP).Neurology 41:617–618. [pmid: 2027473]|
|10.||Victor M,Ropper AH. 2001Myasthenia gravis and related disorders of the neuromuscular junction.Victor M,Ropper AHAdams and Victor's principles of neurology (7th ed) New York: McGraw-Hill Inc; :1536–1539.|
|11.||Bohan A,Peter JB,Bowman RL,Pearson CM. 1977;Computer-assisted analysis of 153 patients with polymyositis and dermatomyositis.Medicine (Baltimore) 56:255–286. [pmid: 327194]|
|12.||Hughes RA,Newsom-Davis JM,Perkin GD,Pierce JM. 1978;Controlled trial prednisolone in acute polyneuropathy.Lancet 2:750–753. [pmid: 80682]|
|13.||Klein U,Rajewsky K,Kuppers R. 1998;Human immunoglobulin (Ig)M+IgD+ peripheral blood B cells expressing the CD27 cell surface antigen carry somatically mutated variable region genes: CD27 as a general marker for somatically mutated (memory) B cells.J Exp Med 188:1679–1689. [pmid: 9802980]|
|14.||Odendahl M,Jacobi A,Hansen A,Feist E,Hiepe F,et al. 2000;Disturbed peripheral B lymphocyte homeostasis in systemic lupus erythematosus.J Immunol 165:5970–5979. [pmid: 11067960]|
|15.||Odendahl M,Mei H,Hoyer BF,Jacobi AM,Hansen A,et al. 2005;Generation of migratory antigen-specific plasma blasts and mobilization of resident plasma cells in a secondary immune response.Blood 105:1614–1621. [pmid: 15507523]|
|16.||Medina F,Segundo C,Campos-Caro A,Gonzalez-Garcia I,Brieva JA. 2002;The heterogeneity shown by human plasma cells from tonsil, blood, and bone marrow reveals graded stages of increasing maturity, but local profiles of adhesion molecule expression.Blood 99:2154–2161. [pmid: 11877292]|
|17.||Nakayama T,Hieshima K,Izawa D,Tatsumi Y,Kanamaru A,et al. 2003;Cutting edge: profile of chemokine receptor expression on human plasma cells accounts for their efficient recruitment to target tissues.J Immunol 170:1136–1140. [pmid: 12538668]|
|18.||Muehlinghaus G,Cigliano L,Huehn S,Peddinghaus A,Leyendeckers H,et al. 2005;Regulation of CXCR3 and CXCR4 expression during terminal differentiation of memory B cells into plasma cells.Blood 105:3965–3971. [pmid: 15687242]|
|19.||Thomson PD,Harris NS. 1977;Detection of plaque-forming cells in the peripheral blood of actively immunized humans.J Immunol 118:1480–1482. [pmid: 321692]|
|20.||Stevens RHME,Morrow C,Saxon A. 1979;Characterization of a circulating subpopulation of spontaneous antitetanus antibody producing cells following in vivo booster immunization.J Immunol 122:2498–2504. [pmid: 312871]|
|21.||Cepok S,Rosche B,Grummel V,Vogel F,Zhou D,et al. 2005;Short-lived plasma blasts are the main B cell effector subset during the course of multiple sclerosis.Brain 128:1667–1676. [pmid: 15800022]|
|22.||Yuki N,Susuki K,Koga M,Nishimoto Y,Odaka M,et al. 2004;Carbohydrate mimicry between human ganglioside GM1 and Campylobacter jejuni lipooligosaccharide causes Guillain-Barr? syndrome.Proc Natl Acad Sci U S A 101:11404–11409. [pmid: 15277677]|
|23.||Radbruch A,Muehlinghaus G,Luger EO,Inamine A,Smith KG,et al. 2006;Competence and competition: the challenge of becoming a long-lived plasma cell.Nat Rev Immunol 6:741–750. [pmid: 16977339]|
|24.||Bernasconi NL,Traggiai E,Lanzavecchia A. 2002;Maintenance of serological memory by polyclonal activation of human memory B cells.Science 298:2199–2202. [pmid: 12481138]|
|25.||Siragam V,Crow AR,Brinc D,Song S,Freedman J,et al. 2006;Intravenous immunoglobulin ameliorates ITP via activating Fc gamma receptors on dendritic cells.Nat Med 12:688–692. [pmid: 16715090]|
|26.||Nimmerjahn F,Ravetch JV. 2007;The antiinflammatory activity of IgG: the intravenous IgG paradox.J Exp Med 204:11–15. [pmid: 17227911]|
|27.||Gold R,Stangel M,Dalakas MC. 2007;Drug Insight: the use of intravenous immunoglobulin in neurology?therapeutic considerations and practical issues.Nat Clin Pract Neurol 3:36–44. [pmid: 17205073]|
|28.||Xiang Z,Cutler AJ,Brownlie RJ,Fairfax K,Lawlor KE,et al. 2007;FcgammaRIIb controls bone marrow plasma cell persistence and apoptosis.Nat Immunol 8:419–429. [pmid: 17322888]|
|29.||Ravetch JV,Nussenzweig M. 2007;Killing some to make way for others.Nat Immunol 8:337–339. [pmid: 17375094]|
|30.||Hoyer BF,Moser K,Hauser AE,Peddinghaus A,Voigt C,et al. 2004;Short-lived plasmablasts and long-lived plasma cells contribute to chronic humoral autoimmunity in NZB/W mice.J Exp Med 199:1577–1584. [pmid: 15173206]|
|31.||Guillain-Barr? Syndrome Steroid Trial Group. 1993;Double-blind trial of intravenous methylprednisolone in Guillain-Barr? syndrome.Lancet 341:586–590. [pmid: 8094828]|
|32.||van Koningsveld R,Schmitz PI,van der Mech? FG,Visser LH,Meulstee J,et al. 2004;Effect of methylprednisolone when added to standard treatment with intravenous immunoglobulin for Guillain-Barr? syndrome: randomized trial.Lancet 363:192–196. [pmid: 14738791]|
|33.||Ahmed AR. 2004;Treatment of autoimmune mucocutaneous blistering diseases with intravenous immunoglobulin therapy.Expert Opin Investig Drugs 13:1019–1032.|
|34.||de Grandmont MJ,Racine C,Roy A,Lemieux R,Neron S. 2003;Intravenous immunoglobulins induce the in vitro differentiation of human B lymphocytes and the secretion of IgG.Blood 101:3065–3073. [pmid: 12480708]|
|35.||Vassilev T,Yamamoto M,Aissaoui A,Bonnin E,Berrih-Aknin S,et al. 1999;Normal human immunoglobulin suppresses experimental myasthenia gravis in SCID mice.Eur J Immunol 29:2436–2442. [pmid: 10458757]|
Previous Document: Gender differences in the mu rhythm of the human mirror-neuron system.
Next Document: The use of mosquito nets and the prevalence of Plasmodium falciparum infection in rural South Centra...