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BMC Neurology

, 19:190 | Cite as

Extensive immune reconstitution inflammatory syndrome in Fingolimod-associated PML: a case report with 7 Tesla MRI data

  • Tim Sinnecker
  • Jeffrie Hadisurya
  • Tilman Schneider-Hohendorf
  • Nicholas Schwab
  • Karsten Wrede
  • Oliver Gembruch
  • Ralf Gold
  • Kerstin Hellwig
  • Sara Pilgram-Pastor
  • Ortwin Adams
  • Philipp Albrecht
  • Hans-Peter Hartung
  • Orhan Aktas
  • Markus KraemerEmail author
Open Access
Case report
Part of the following topical collections:
  1. Demyelinating diseases

Abstract

Background

Progressive multifocal leukoencephalopathy (PML) is a rare complication of patients treated with fingolimod.

Case presentation

Routine MRI eventually led to diagnosis of asymptomatic early PML that remained stable after discontinuation of fingolimod. As blood lymphocyte counts normalized, signs of immune reconstitution inflammatory syndrome (IRIS) and renewed MS activity developed. Both, advanced laboratory and ultrahigh field MRI findings elucidated differences between PML and MS.

Conclusions

In our case, early discontinuation of fingolimod yielded a good outcome, lymphocyte counts reflected immune system activity, and paraclinical findings helped to differentiate between PML-IRIS and MS.

Keywords

Progressive multifocal leucencephalopathy Immune reconstitution inflammatory syndrome Fingolimod Multiple sclerosis 7 tesla MRI 

Abbreviations

CD8 cells

Cluster of differentition 8 cells

CSF

Cerebral spinal fluid

DMF

Dimethyl fumarate

EDSS

Expanded Disability Status Scale

IRIS

Immune reconstitution inflammatory syndrome

JCV

JC polyomavirus

MRI

Magnetic resonance imaging

MS

Multiple sclerosis

NK cells

Natural killer cells

PML

Progressive multifocal leukoencephalopathy

SWI

Susceptibility-weighted imaging

T

Tesla

T2*w

T2*-weighted imaging

Background

Progressive multifocal leukoencephalopathy (PML) is caused by JC polyomavirus (JCV), and represents a serious adverse complication of effective disease modifying multiple sclerosis (MS) therapies. In addition to natalizumab, PML has been reported during treatment with fingolimod [1]. MRI imaging is crucial to PML diagnosis, but the differentiation between PML, immune reconstitution inflammatory syndrome (IRIS), and renewed MS activity often proves to be very difficult [2].

We here report PML occurrence under sustained fingolimod-associated lymphopenia with development of IRIS after normalization of lymphocytes. Clinical, laboratory and neuroimaging findings including ultrahigh field MRI at 7 Tesla (7 T) are demonstrated to elucidate differentiating features between MS activity, early PML, and IRIS. The patient gave her consent on this publication. The study was conducted according to the principles expressed in the Declaration of Helsinki and 7 T-MRI examination was approved by the University Duisburg-Essen institutional review board.

Case presentation

A 41-year old woman was diagnosed with relapsing-remitting MS in December 2013. Initial treatment with interferon beta-1b (Extavia®, Betaferon®) was switched to fingolimod in February 2014 due to persistent disease activity. Anti-JCV-serum-antibodies were positive (Unilabs Copenhagen, Denmark). In November 2016 subclinical MRI activity occurred. At this time, the JCV antibody index value was 2.23. Fingolimod was continued, and the absolute lymphocyte count varied between 170/μl and 310/μl.

One year later, a routine 3 T MRI (14-11-2017) revealed a spotty C-band-shaped hyperintense left-parietal FLAIR lesion with patchy Gadolinium-enhancement, and a microcystic appearance on T2 weighted (T2w) images (Fig. 1 and Fig. 2). Few punctate “milky way”-like Gadolinium-enhancing lesions were present (Fig. 1). Clinically, a slight worsening of the pre-existing gait imbalance and ataxia as well as increased irritability and aggressiveness was noted. The Expanded Disability Status Scale (EDSS) score increased from 4.5 to 5.5.
Fig. 1

Overview on paraclinical findings and treatment decisions. The figure chronologically displays treatment decisions (first row), lymphocyte counts (second row), laboratory (third row), and MRI findings (fourth and fifth row). At baseline, only very few punctate milky way-like lesions were detectable (circle). After recovery of lymphocytes, new punctate milky way-like lesions developed (circle), and again ceased after corticosteroid pulse therapy (circle). The initial PML lesion in the left hemisphere was stable over time (see Fig. 2). Unfortunately, new MS-like lesions developed after discontinuation of fingolimod (white arrows). Anti-JCV antibody detection and quantification was performed at Unilabs Copenhagen, Denmark. JCV-DNA-PCR from CSF was performed at Institute of Virology, University Clinic of Duesseldorf.

Fig. 2

3 T and 7 T MR imaging findings in early fingolimod-associated PML. The first row displays MRI images at baseline (a-c) and last follow up (d). At baseline, T2 weighted imaging (a) revealed a new C-shaped lesion with near microcystic appearance (zoom) that clearly infiltrates the short association fibres (“U fibres”). The lesion exhibited a patchy, irregular contrast enhancement (white arrow) on contrast enhanced T1 weighted images (b). The lesion was hyperintense on FLAIR (c, black arrow). The imaging pattern was strongly suggestive for PML. Thus, fingolimod was stopped immediately. Half year later, the size of the PML lesion remained unchanged (d, black arrow). The second and third row shows highly resolving 7 T MRI images. T2*w imaging with a resolution of 0.25 × 0.25mm2 delineates a small PML lesion (e). The PML lesion is T2*w hyperintense (black arrows), infiltrates the short association fibres (“U fibres”), and appears diffusely delineated against the white matter. Moreover, T2*w hypointense areas are visible within the surrounding cortex (black arrowhead). This finding is more pronounced on susceptibility weighted imaging (SWI, f, black arrowheads, “dark” signal). Unwrapped phase maps (g) showed positive phase changes (white arrowheads, “bright” signal) indicating paramagnetic effects. A minimal intensity projection map (MIP, h) of SWI illustrates SWI hypointense signal along white matter fibre tracts. Moreover, 7 T MRI differentiated between MS- and PML- associated lesions. On the one hand, 7 T T2* weighted MRI visualized a distinct central vein within MS-like lesions (J, white arrows). On top of that, numerous punctate contrast enhancing milky way-like lesions (I-L) were visible. Much of contrast enhancing lesions did not show a central vessel on T2*w images (i and j, black arrows). A very small vessel was faintly visible in other punctate lesions (j and k, black arrowheads). l demonstrates contrast-enhancement of the lesion displayed in K

PML was suspected on the background of atypical lesions on MRI, and subsequently confirmed by detection JCV-DNA in CSF (39 copies/ml, Institute of Virology, Heinrich-Heine-University Duesseldorf; serum JCV antibody index value: 5.23).

Laboratory findings revealed sustained grade 3 lymphopenia (310/μl, CD4+ count 27/μl, CD8+ count 71/μl). Flow cytometry of peripheral blood confirmed a reduction of lymphocytes with reduced proportions of NK cells (CD56+ count 56/μl), as compared to fingolimod-treated control MS patients (Fig. 3a-b). However, the CD4/CD8 ratio and the naïve/memory distribution of T cells was comparable to fingolimod-treated control MS patients (Fig. 3c-d) [3]. The PML biomarker CD62L (L-selectin) was strongly reduced compared to healthy controls and in the lower range of fingolimod-treated MS patients (Fig. 3e) [4]. LFA-1 expression on CD4 T cells was strongly elevated indicating recent cellular activation (Fig. 3f) [5].
Fig. 3

Flow cytometry of peripheral blood-derived mononuclear cells. Peripheral blood mononuclear cells (PBMC) of the patient at the time point of PML diagnosis were analyzed using ten color flow cytometry and compared to four healthy donors (HD) and three Fingolimod-treated control MS patients. (a) The proportions of monocytes (CD14+) and lymphocytes (CD3+) among all viable PBMC. (b) Proportions of B- (CD19+), NK- (CD56+), NK T- (CD56+, CD3+), as well as T- (CD56-, CD3+) cells of all viable lymphocytes. (c) The ratio of CD4+ to CD8+ T cells of all CD3+ T cells. (d) Proportions of naïve (CD62L+, CD45RA+), central-memory (CD62L+, CD45RA-) and effector-memory (CD62L-, CD45RA-) CD4+ T cells. (e) Percentage of CD62L+ cells of viable CD4+ T cells. (f) Mean fluorescence intensity of CD11a on viable CD4+ T cells. Two-way ANOVA with Tukey’s multiple comparisons test was performed for (a, b and d). One-way ANOVA with Tukey’s multiple comparisons test was performed for (c, e and f). * = p < 0.05; ** = p < 0.01; *** = p < 0.001; **** = p < 0.0001

Fingolimod was immediately suspended and mirtazapine 30 mg per day was started. Repeated 3 T control MRIs revealed an increasing number of “milky way”-like punctate Gadolinium-enhancing lesions (Fig. 1) in both hemispheres. Concurrently the immune system reconstituted within one month as blood lymphocyte counts normalized (13-12-2018: 1260/μl). Two weeks later, 3 T MRI (27-12-2017) showed substantially more Gadolinium-enhancing punctate lesions (Fig. 1). At this time, JCV-PCR was negative in CSF suggesting IRIS rather than progression of PML, therefore an intravenous corticosteroid pulse therapy was administered (Fig. 1).

The next MRI (10-01-2018) showed slightly less lesions and Gadolinium-enhancement. Clinically, the EDSS score improved to 4.5 (improved gait balance and ataxia).

Ultrahigh field MRI at 7 T was done and visualized the initial C-shaped PML lesion in great anatomical detail (Fig. 2e-h). In addition, T2*w and SWI hypointense (“dark”) areas corresponding to positive (“bright”) MR phase changes and thus indicating paramagnetic susceptibility changes were visible within the surrounding cortex and neighboring white matter fiber tracts (Fig. 2e-h).

Moreover, numerous punctate contrast enhancing milky way-like lesions were detectable on 7 T T1w and T2*w images. Several of these did not present with a central vessel, while a very small vessel was faintly visible in a small proportion of punctate lesions. In contrast, a relatively large central vein was observed within MS-like lesions (Fig. 2i-l).

Follow-up MRIs in March and May 2018 showed new nodular- and ring-like contrast enhancing white matter lesions typical of MS plaques (Fig. 1). Presuming MS activity, immunomodulation with glatiramer acetate was started. The initial left parietal PML lesion did not enlarge at all (Fig. 2d).

Discussion and conclusions

We here report a case of early fingolimod-associated PML in a patient with MS. The diagnosis was suspected on the background of typical signs of PML in routine MRI and confirmed by positive JCV-DNA-PCR in CSF. After discontinuation of fingolimod, the initial small PML lesion was stable over time and did not enlarge centrifugally into large flame-like PML lesions, which are characteristic for natalizumab-associated PML. Nevertheless, as blood lymphocyte counts normalized and JCV DNA was no longer detectable in CSF, signs of IRIS and renewed MS activity developed. The time interval between PML onset and return of MS disease activity appeared relatively short in comparison to natalizumab-associated PML. Moreover, 7 T MRI revealed distinct imaging patterns and thus helped to differentiate between PML, IRIS and renewed MS activity.

In detail, paramagnetic susceptibility changes as indicated by “dark” signal on SWI/T2*w and “bright” signal on phase maps adjacent to the PML lesion were observed. Their origin is largely unknown, but loss of diamagnetic myelin or iron release by dying oligodendrocytes as an very early sign of JCV infiltration have been discussed.

In addition, we observed numerous “milky way”-like lesions. It has been suggested that these alterations may serve as an early imaging marker for PML [6]. 7 T MRI may add to this finding since a distinct central vein seems to be less frequently detectable within “milky way”-like lesions [7] versus (even small) MS lesions [8].

The origin of “milky way”-like lesions is unknown. One hypothesis is that they highlight an overwhelming immune response, presumably within perivascular spaces. Of note, the absence of a central vessel on highly resolving gradient echo MR images does not contradict the perivascular distribution hypothesis of milky way-like lesions as such sequences do not allow for the visualization of vessels that contain oxygenated blood or are to small for detection (e.g. venules). Other authors have described punctate or milky way–like lesions as areas of active JC virus replication in early PML [7]. Our own observations support both hypotheses as milky-way-like lesions were present from the start (favors the latter), and more milky-way-like lesions developed after normalization of lymphocytes (favors the former). A comparative histopathological and MRI study would have the potential to improve our understanding of milky-way-like lesions. One case report included a histopathological analysis of seven tissue fragments (needle biopsy) in a fingolimod-associated PML patient with milky-way-like lesions on MRI. The study described small inflammatory foci that were in line with a mild host response against JCV infection [9].

Similar to the other recently reported cases [1], our patient presented with lymphopenia (grade 4, in our case) indicating that it may have played a critical role in PML-IRIS development, as suggested from findings on dimethyl fumarate (DMF), where prolonged lymphopenia accounts for most PML cases [10]. However, in contrast to prior hypotheses regarding reduced CD8 cell counts as a potential cause for DMF-PML [11], our case presented with an unaltered CD4/CD8 ratio (in line with the other fingolimod-PML cases [1]), but reduced NK cell numbers.

In summary, in this case PML lesion enlargement stopped after discontinuation of fingolimod in parallel to normalization of lymphocyte counts, and development of signs of IRIS. Our imaging findings support the idea of using ultrahigh field MRI including highly resolving T2*w and SWI to support the diagnosis of PML, and to differentiate from MS activity and IRIS.

Notes

Acknowledgments

Not applicable.

Authors’ information

Not applicable.

Authors’ contributions

TS, JH, TSH performed data acquisition and analysis and drafted the manuscript. NS, KW, OG, SPP, OAd performed data acquisition and analysis and revised the manuscript. RG, KH, PA, HPH, OAk revised the manuscript for intellectual content and helped with the interpretation of the data. MK conceived the study, performed data acquisition and analysis and drafted the manuscript. All authors read and approved the manuscript.

Funding

There was no funding.

Ethics approval and consent to participate

The study was conducted according to the principles expressed in the Declaration of Helsinki and was approved by the local university (Duisburg-Essen) institutional review board.

Consent for publication

Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images and videos. A copy of the written consent is available for review by the Editor of this journal.

Competing interests

Tim Sinnecker has received travel support from Roche and Actelion, and is employee of the Medical Image Analysis Center in Basel, Switzerland.

Jeffrie Hadisurya has received travel funding from Novartis, Teva, Bayer and Biogen.

Tilman Schneider-Hohendorf has received research and travel support from Biogen and Novartis.

Nicholas Schwab has received travel funding from Novartis, and Biogen.

Karsten Wrede reports no disclosures.

Oliver Gembruch reports no disclosures.

Ralf Gold received speaker’s and board honoraria from Baxter, Bayer Schering, Biogen Idec, CLB Behring, Genzyme, Merck Serono, Novartis, Roche, Stendhal, Talecris, TEVA. His department received grant support from Bayer Schering, BiogenIdec, Genzyme, Merck Serono, Novartis, TEVA. He possesses stock options from Merck Serono and Roche.

Kerstin Hellwig reports grants and honoriaria from Biogen, Novartis, Roche, Bayer Healthcare, Teva, Sanofi and Merck.

Sara Pilgram-Pastor reports no disclosures.

Ortwin Adams reports no disclosures.

Philipp Albrecht reports grants, personal fees and non-financial support from Allergan, Biogen, Ipsen, Merz Pharmaceuticals, Novartis, and Roche, personal fees and non-financial support from Bayer Healthcare, and Merck, and non-financial support from Sanofi-Aventis/Genzym.

Hans-Peter Hartung has received fees for serving on steering commitees from Biogen Idec, GeNeuro, Sanofi Genzyme, Merck, Novartis Pharmaceuticals, Octapharma, Opexa Therapeutics, Teva Pharmaceuticals, MedImmune, Bayer HealthCare, Forward Pharma, and Roche, fees for serving on advisory boards from Biogen Idec, Sanofi Genzyme, Merck, Novartis Pharmaceuticals, Octapharma, Opexa Therapeutics, Teva Pharmaceuticals, and Roche, and lecture fees from Biogen Idec, Sanofi Genzyme, Merck, Novartis Pharmaceuticals, Octapharma, Opexa Therapeutics, Teva Pharmaceuticals, MedImmune, and Roche.

Orhan Aktas has received, with approval by the Heinrich Heine University, advisor fees or honoraria from Almirall, Bayer HealthCare, Biogen, MedImmune, Merck, Novartis, and Teva; research support from Bayer HealthCare, Biogen, Novartis, Roche, and Teva.

Markus Kraemer has received, by approval by his hospital, honoria from Bayer Schering, Biogen Idec, Merck Pharma Novartis Pharma, Teva Pharma, Roche Pharma und Shire Deutschland.

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Copyright information

© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  • Tim Sinnecker
    • 1
    • 2
  • Jeffrie Hadisurya
    • 3
  • Tilman Schneider-Hohendorf
    • 4
  • Nicholas Schwab
    • 4
  • Karsten Wrede
    • 5
    • 6
  • Oliver Gembruch
    • 5
    • 6
  • Ralf Gold
    • 7
  • Kerstin Hellwig
    • 7
  • Sara Pilgram-Pastor
    • 8
  • Ortwin Adams
    • 9
  • Philipp Albrecht
    • 10
  • Hans-Peter Hartung
    • 10
  • Orhan Aktas
    • 10
  • Markus Kraemer
    • 3
    • 10
    Email author
  1. 1.Department of NeurologyUniversitätsspitalBaselSwitzerland
  2. 2.Medical Image Analysis Center BaselBaselSwitzerland
  3. 3.Department of NeurologyAlfried Krupp von Bohlen und Halbach HospitalEssenGermany
  4. 4.Clinic of Neurology with Institute of Translational NeurologyUniversity Hospital MünsterMünsterGermany
  5. 5.Department of NeurosurgeryUniversity Hospital Essen, University Duisburg-EssenEssenGermany
  6. 6.Erwin L. Hahn Institute for Magnetic Resonance ImagingUniversity Duisburg-EssenEssenGermany
  7. 7.Department of Neurology, St. Josef HospitalRuhr-University BochumBochumGermany
  8. 8.Department of NeuroradiologyAlfried Krupp HospitalEssenGermany
  9. 9.Institute of Virology, Medical FacultyHeinrich-Heine University DüsseldorfDüsseldorfGermany
  10. 10.Department of Neurology, Medical FacultyHeinrich-Heine University DüsseldorfDüsseldorfGermany

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