Multiple Sclerosis (MS) is an autoimmune disease believed to be secondary to T cells autoreactive against myelin, leading to demyelination, neurodegeneration and, eventually, disability [1]. Four subtypes are described, depending on the behavior of the disease: relapsing–remitting, primary progressive, secondary progressive and relapsing progressive. The management is mainly based on disease modifying therapies (DMT) and steroids for acute attacks. Many DMT are available in clinical practice, including old (interferon β, alemtuzumab and glatiramer acetate) [2], and novel agents (natalizumab, daclizumab, ocrelizumab, etc.). The focus of these treatments is to decrease progression and minimize or delay the disability [2]. Despite the availability of these drugs, many patients progress and succumb to their disease. Autologous hematopoietic stem cell transplantation (ASCT) seems to be beneficial to patients in the relapsing–remitting with high inflammatory activity subgroup after failing the standard of care DMTs, and to those with aggressive MS who had developed severe disability in the prior 12 months [3]. Aplastic anemia (AA) is a form of bone marrow failure which is usually idiopathic, but can also develop because of infections, drugs (some are MS drugs) among other etiologies [4–6]. The treatment of AA depends on the severity of the disease and the age of the patient. Allogeneic Hematopoietic Stem Cell transplantation (allo-SCT) is the standard of care for young patients with severe AA [4]. We herein present two MS patients, who were allotransplanted for severe AA (Table 1).
Table 1.
Patients’ characteristics
| Case 1 | Case 2 | ||
|---|---|---|---|
| 1 | Age | 45 | 42 |
| 2 | Gender | Male | Female |
| 3 | Hematological Diagnosis | SAA | SAA |
| 4 | Karyotype | Normal | Normal |
| 5 | PNH | Small clone | Small clone |
| 6 | Patient HLA-DRB1 genotype | DRB1*03:01 | DRB1*15:01 |
| 7 | Donor type | MSD (male donor) | MSD (female donor) |
| 8 | Stem cell source | Bone marrow | PBSC |
| 9 | Conditioning | 1st HSCT FLU/CY 2nd HSCT FLU/CY/Alemtuzumab | Flu/Cy/ATG/TBI 200 |
| 10 | Stem cell dose (CD34) | 1st HSCT 1.46 × 106/kg 2nd HSCT 3.2 × 106/kg | 5.04 X106/kg |
| 11 | GvHD prophylaxis | MTX/CSA | MTX/CSA |
| 12 | Chimerism | Poor donor-lymphocyte engraftment improved after mega dose of stem cell boost | 100% |
| 13 | Graft failure | Yes 2 times | No |
| 14 | GvHD | Grade 1 liver GvHD post DLI | No GvHD |
| 15 | Duration from MS Diagnosis to SAA | 9 months | 5 years |
| 16 | MS type | Progressive relapsing MS | Relapsing remitting |
| 17 | Neurological signs and symptoms | Parapresis with sensory level | Parapresis with sensory level |
| 18 | Diagnostic MRI lesions pre- HSCT | Corpus callosum, and deep white matter spinal cord lesions | Supra and infra tentorial and spinal cord lesions |
| 19 | MS Treatment before HSCT | IFN-β 1a | IFN-β 1a |
| 20 | MS Treatment response | Poor response | Good response |
| 21 | MS course Post HCT | Slow progression | Stable disease |
| 22 | Residual disabilities | Yes | No |
| 23 | Interval from last Interferon dose to SAA development | One month | One month |
| 24 | EDSS Post HSCT | 6 | 4.5 |
MRI magnetic resonance imaging, TBI total body irradiation, PBSC peripheral blood stem cells, MS Multiple Sclerosis, HSCT hematopoietic stem cell transplantation, GvHD graft versus host disease, EDSS Expanded Disability Status Scale, ATG anti-thymocyte globulin
A 45-year-old man was diagnosed with severe AA in April 2014, after presenting with ecchymosis and epistaxis. His workup showed pancytopenia (ANC of 0.49 × 109/L, platelets of 10 × 109/L, hemoglobin of 6 g/dl) with 5% cellularity on the bone marrow biopsy. He underwent allo-SCT from his matched brother using fludarabine/cyclophosphamide (flu/cy) conditioning and bone marrow as a stem cell source. His course was complicated by mixed lymphoid chimerism. His GvHD prophylaxis consisted of short methotrexate (MTX) course and cyclosporine (CSA). Nine months post-transplant CSA tapering was started. However, 6 weeks after tapering he developed unsteady gait and, after an extensive workup, he was diagnosed with MS, based on the detection of typical MRI T2 lesions in periventricular, cortical and infratentorial areas of the brain, (Fig. 1) and oligoclonal bands in the CSF.
Fig. 1.
MRI brain showing T2 and FLAIR Abnormal signal hyperintensity in deep white matter tracts cerebral parenchyma—case 1
After neurological evaluation and an initial observation phase, he was started on interferon beta-1a (IFN-β 1a). However, a month after the first dose, he developed pancytopenia, and an extensive workup showed hypocellular bone marrow (5%) with full donor chimerism (infectious, nutritional deficiencies, and autoimmune causes were ruled out). Simultaneously, his MS symptoms got worse, the expanded disability status scale (EDSS) was 6.5 and an MRI showed new spinal cord demyelinating lesions. He then underwent a second allo-SCT from the same donor using FCC conditioning and mycofenolate mofetil (MMF) for GvHD prophylaxis. He engrafted by day 14 and his sensory symptoms improved as well.
His second post-transplant course was complicated by poor graft function and mixed chimerism (Fig. 2) which eventually led to graft failure that did not respond to immune manipulation and donor lymphocyte infusion (DLI). Ten months after his second transplant he received a stem cell mega dose (total 22.11 × 108/kg nucleated cells infused, including 11.25 × 106/kg CD34 stem cells and 39.98 × 107/kg CD3 + /kg). Currently, 56 months after his stem cell boost, he remains in remission of the severe AA, and his MS is stable, with an EDSS of 6, and no further clinical or radiological progression.
Fig. 2.
Showing chimerism post second HSCT—case 1
A 42-year-old woman, diagnosed with MS in 2014, started on IFN-β 1a with good control, and no further relapses. In 2019, she was diagnosed with AA, after presenting with vaginal bleeding, and was found to have pancytopenia (WBC 3.49 × 109/L, HGB 81 g/L ANC 0.33 × 109/L, platelet 3 × 109/L). IFN-β 1a was suspended, and she was started on horse ATG at 40 mg/m2 and CSA, with no improvement. She then underwent matched sibling donor allo-SCT in 2020, with Flu/Cy/ATG/TBI conditioning. She engrafted quickly with full donor chimerism and, currently, 27 months post allo-SCT, she is off immunosuppression, with no further progression of her MS, despite being off MS medications since the AA diagnosis.
The association of MS and SAA has been reported in the literature [7]. The HLA Class II DRB1 antigen DR15 (common alleles *1501, *1502) is observed with a frequency between 20 and 30% in various ethnic populations [8], and has been implicated in the pathogenesis of both AA and MS. Allo-SCT is a standard intervention for young AA patients with a matched sibling, and for the majority of the other AA patients after failing immunosuppressive therapy (IST), even in the absence of a matched sibling donor. Auto-HSCT is a standard option for patients with RRMS after failing one line of DMT [3]. Auto-HSCT is also considered an option, even before failing a full course of DMT, for patients with aggressive RRMS who developed severe disability in the preceding 12 months [3]. It is now considered as a standard, whereas allo-HSCT is generally not recommended or performed only in selected highly refractory cases with an HLA identical sibling donor [9]. Allo-HSCT for MS is rarely performed. GvHD associated with allo-HSCT usually affects the skin, gut, and liver, and only rarely the CNS, in which case there is often a significant systemic GvHD elsewhere [10]. CNS involvement of GvHD is controversial, especially since clinical manifestations of CNS GvHD are heterogeneous [11–14]. Patients with chronic GvHD affecting the CNS may present with stroke-like episodes, MS, transverse myelitis, or acute disseminated encephalomyelitis-like disorders, encephalitis, and other nonspecific neurological symptoms [15]. MS-like relapsing–remitting disease has been reported at ten months after allogeneic HSCT [16]. In the absence of GvHD affecting other organs, that presentation fulfilled neither the international consensus diagnostic criteria for neuromyelitis optica spectrum disorder nor the Grauer et al. criteria for the CNS manifestations of GvHD [17, 18].
Our cases highlight the association of MS and AA. These cases also highlight the issue of CNS GvHD and how to differentiate this from MS.
Data availability
Raw data were generated at King Faisal specialist hospital. Derived data supporting the findings of this study are available from the corresponding author [Alfadil,Haroon] on request.
Declarations
Conflict of Interest
The authors declare that they have no conflict of interest.
Footnotes
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Raw data were generated at King Faisal specialist hospital. Derived data supporting the findings of this study are available from the corresponding author [Alfadil,Haroon] on request.