Natalizumab granule cell neuronopathy: FDG-PET in diagnosis and immune reconstitution with G-CSF

Case report: clinical course.

A 31-year-old Caucasian female diagnosed in 1990 with relapsing-remitting MS on natalizumab since 2008 was admitted twice between July and September 2015, with progressive unsteadiness, dysarthria, and diplopia. Her serum anti-JCV antibody index was 2.41. Following concerns about possible progressive multifocal leukoencephalopathy (PML), her natalizumab was stopped in July 2015 (figure, A). She was treated with IV methylprednisolone, and the second course was followed up with oral prednisolone, to reduce her risk of immune reconstitution inflammatory syndrome (IRIS). Despite unchanged imaging (figure, B), in September 2015, a lumbar puncture found JCV-DNA viral load measured at 5,000 copies/mL.

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Figure (A) Diagrammatic representation of disease course, EDSS, JCV CSF viral load, and treatments

(A) The disease was managed with interferon beta-1a (Rebif®) (2007–2009), but this was changed to monthly infusions of natalizumab in January 2009 because of disease breakthrough while on treatment. On starting natalizumab, her EDSS was 2.5; despite testing positive for anti-JCV antibody, her treatment was continued until July 2015, with a stable EDSS 2.0 and no further relapses. Her EDSS went up to 6.0 in July and to 8.0 in November. After treatment with G-CSF, her EDSS decreased to 6.5. (B) Diagram showing sequential MRI slices. Axial slices of T2 FLAIR sequences. Upper panel (B.a) demonstrates the unchanged multiple foci of abnormal signal in the cerebral white matter. Lower panel (B.b) demonstrates progressive cerebellar volume loss in particular between September 2015 and November 2015. The red arrow identifies an area of high signal in the pons. (C) FDG-PET. Brain PET FDG identifying small patches of hypometabolism (blue arrows) in the left inferior cerebellar cortex and right posterior cerebellar cortex, performed on December 31, 2015. EDSS = Expanded Disability Status Scale; FDG-PET = fluorodeoxyglucose PET; FLAIR = Fluid attenuation inversion recovery; G-CSF = granulocyte-colony stimulating factor; JCV = JC virus.

Her clinical condition deteriorated and she became bedbound, and, in November 2015, her Expanded Disability Status Scale (EDSS) measured 8.0 on admission. A repeat CSF sample measured a viral load of 17,000 copies/mL of JCV-DNA. Repeat MRI did not identify features consistent with PML but did show progressive cerebellar volume loss (figure, B.b). A fluorodeoxyglucose-PET (FDG-PET) demonstrated patchy hypometabolism in the cerebellum (figure, C). Based on these results, a diagnosis of GCN without PML was made. Mirtazapine was started, and prednisolone was stopped. Although not traditionally used, a 5-day trial of G-CSF was prescribed. Over the next 6 weeks, she showed progressive improvement in speech and mobility, and her EDSS improved to 7.0. A repeat CSF in January 2016 showed that the viral load had dropped to 250 copies/mL JCV-DNA.

In February 2016, she experienced severe nausea. Her MRI showed high signal in the brainstem, in particular the pons (figure, B.b red arrow), felt to be consistent with IRIS. She declined steroids feeling this treatment was not warranted, given her overall clinical improvement. To date, her most recent imaging demonstrated a stable appearance and her latest EDSS is 6.5 (figure, A).

Discussion.

This is the first case to describe the use of FDG-PET to aid diagnosis and the use of G-CSF to promote immune reconstitution in an MS patient with GCN. Although our understanding of PML after natalizumab is improving, our understanding of GCN after natalizumab is limited.

Difficulty in diagnosing early GCN is highlighted here, where progressive cerebellar atrophy was identified retrospectively, long after JCV-DNA was confirmed in the CSF. The presence of early cerebellar symptoms in patients treated with natalizumab requires early and regular imaging for cerebellar atrophy, in particular progression of atrophy,⁶ with or without lumbar punctures for JCV-DNA detection.⁷ The use of FDG-PET here is novel, demonstrating hypometabolism within both hemispheres of the cerebellum and enabling clear anatomical localization of the problem. Hypometabolism is an expected finding given the pathologic findings of neuronal cell loss in GCN, whereas in IRIS one may have expected more activity resulting from influx of immune cells. Limitations of this include the delay in performing the scan and the absence of serial imaging. FDG-PET could potentially be useful if used earlier; however, further studies into the utility of FDG-PET in this context are needed.

This patient was not a candidate for plasmapheresis because she had been off natalizumab for 3 months and it would have been cleared from her system. In addition, plasma exchange has been shown to be ineffective in natalizumab-associated PML cases.⁸ Faced with progressive clinical deterioration and rising JCV-DNA in the CSF despite steroids, it was decided to start G-CSF, a glycoprotein, which primarily stimulates the production, mobilization, and survival of neutrophils, to initiate immune reconstitution in December 2016. Stefoski highlighted the clinical benefit of G-CSF in PML in 8/16 patients, with the desired response of immune-boosting leukocytosis and lymphocytosis resulting in IRIS in 16/18 patients.⁵ This is the first case to describe the use of G-CSF in the treatment of GCN but similar to its prior use, our patient developed IRIS approximately 6 months after natalizumab and 2 months after G-CSF. This was managed conservatively because of no significant clinical worsening.

This case highlights that the use of a novel diagnostic tool in GCN and hypometabolism on FDG-PET in the cerebellum could be used to support the early diagnosis of GCN. We also demonstrate as had been shown in preliminary case reports in PML that the use of G-CSF in these patients may be helpful in GCN.