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MOG antibody-associated encephalitis secondary to Covid-19: case report



While Covid-19 predominantly affects the respiratory system, neurological manifestations including encephalitis occur in some patients, possibly affecting the course and outcome of the disease. Here, we describe a unique case of a young man with Covid-19 and transient MOG-positive encephalitis, with a benign course.

Case presentation

A 22-year-old male, with PCR confirmed Covid-19 infection was admitted because of persistent headache. The clinical examination was normal. Neuropsychological testing revealed distinct executive deficits. Brain MRI and cerebrospinal fluid (CSF) analysis were suggestive for encephalitis. Further laboratory examination revealed a serum MOG antibody titre. The headache improved with analgetic treatment and i.v. methylprednisolone. Consequently, the MOG antibody titer decreased and MRI lesions were resolving. The patient made a full recovery, with no signs of deterioration over the following months.


Covid-19 manifestations in the CNS include encephalitis with variable course and prognosis. This case highlights a possible association between inflammation due to COVID-19 and transient secondary autoimmunity with transient MOG antibodies and atypical clinical presentation.

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SARS-CoV-2 was first identified in December 2019 in Wuhan, China [1]. Soon, it became clear that severely affected patients may also develop neurological symptoms and complications [2], including meningoencephalitis [3, 4]. Although typically causing fever, respiratory symptoms and myalgia, neurological syndromes in association with SARS-CoV-2 that may affect the course of the disease and outcome include inflammatory diseases such as Guillain-Barré syndrome (GBS), Miller-Fisher syndrome (MFS), (meningo-) encephalitis, and myelitis, as well as stroke, seizures, and myopathy [4, 5].

Case presentation

A previously healthy and asymptomatic 22-year-old male police officer was confirmed SARS-CoV-2 positive by PCR testing while in contact quarantine at home (= day 0). Ten days later, he was admitted to our hospital because of severe headache (verbal rating scale, VRS 8/10) that had started a week previously, few days after his positive test. He reported fever, neck stiffness, general weakness and a loss of smell and taste. He had been started on ASS, low-dose heparin, dexamethasone and aciclovir.

On physical examination at admission, he was fully oriented and had some neck rigidity. Further neurological examination was normal. Blood laboratory tests were unremarkable. Brain MRI (day 11) showed multiple disseminated pathological T2 and FLAIR hyperintensities, predominantly cortically, without any contrast enhancement (Fig. 1 A-D). Comprehensive neuropsychological assessment on day 16 showed no memory impairment, but mild impairment in executive functions (Table 1). CSF analysis revealed a pleocytosis with 31 cells per μl (normal range, nr, < 5). Total CSF protein was 39.9 mg/dL (nr, 15–45), CSF glucose 64 mg/dL (nr, 40–70), and lactate 11.8 mg/l (nr, 10–22). There was no intrathecal IgG synthesis An extensive search for infectious, paraneoplastic, and autoimmune causes of encephalitis was performed. SARS-CoV-2 and HSV 1, 2 PCR in the CSF were negative, as was serology for Lyme borreliosis and HIV. Serum and CSF studies revealed a serum myelin oligodendrocyte glycoprotein (MOG) antibody titre of 1:640 (live-cell assay, see Fig. 2), and a low metabotropic glutamate receptor 1 (mGluR1) antibody titre (fixed cell assay, 1:40; see also Table 2). Dexamethasone and aciclovir were discontinued. One thousand milligrams methylprednisolone i.v. per day was given for 5 days. The patient’s general condition and headache improved gradually after completing the treatment, corresponding to marked improvement in the brain MRI on day 17 (Fig. 1E). He was discharged home and gradually resumed work. At a follow-up visit (day 35), the patient felt well. There was no headache, no focal neurological deficits, and no meningism. Extensive follow-up neuropsychological assessment was entirely normal, with above average results in all dimensions (Table 1). Follow-up MRI showed a resolution of signal alterations (Fig. 1 F). The serum MOG antibody titre was reduced to 1:320, while further laboratory tests including mGluR1 antibody were normal. Upon telephone consultation after 2 months (day 63), he reported he felt well and was back to work in shifts, with no residual symptoms, no restrictions, and no medication.

Fig. 1

Serial MRI examinations. A-D, at initial examination (d 11 after PCR diagnosis), FLAIR (A) showed increased signal intensity bilaterally, in the cortex and basal ganglia. B DWI showed only a small area of restricted diffusion in the right insular cortex. C There was no signal enhancement after i.v. gadolinium. D-F T2 images showing signal hyperintensities before (d 11) (D) and improvement after 5 days of i.v. methylprednisolone (d17; E). F Full resolution (d 35)

Table 1 Neuropsychological tests
Fig. 2

Live cell assay for the determination of antibodies against MOG. MOG-transfected human embryonic kidney cells (HEK, marked by the co-transfected intracellular green fluorescent protein [6] are bound by the MOG antibodies visualized by a red fluorochrome. Nuclear counterstaining in blue. Bar: 20 μm

Table 2 Serological examination and findings


We report a young male with PCR confirmed oligosymptomatic, clinically mild Covid-19 disease, and meningoencephalitis confirmed by brain MRI and CSF analysis. While several recent works reported on autoantibody findings in Covid-19 patients, this is, to our knowledge, the first report of a mildly affected adult with CSF and MRI confirmed meningoencephalitis and serum anti-MOG antibodies that decreased over time. The serum MOG antibody titre is above the threshold of 1:160 that has been suggested by experts in the field [8]. The lack of detectability in CSF is not surprising: The MOG antibody serum titre was 1:640, close to the immunoglobulin G ratio (CSF:serum) of 1:440. This means that only very few MOG antibodies crossed the blood-CSF barrier. It is known that MOG antibodies are usually not intrathecally synthesized [8]. Taken together, these pieces of information support the credibility to the MOG antibody titre results. According to an influential publication, a MOG antibody serum titre of 1:640 is “low positive” (1:160–1:640). For mGluR1 antibodies, no formal cut-off has been suggested. Nevertheless, by experience, the 1:40 serum titre appears too low to be relevant. Comparing this patient with the largest existing mGluR1 antibody series shows that he neither had the typical cerebellar ataxia nor the typical standard CSF abnormalities nor CSF antibodies against mGluR1 [9].

SARS-CoV-2 has only scarcely been found in the CSF, suggesting that Covid-associated neuropathology is caused by mechanisms different from direct viral toxicity [10]. Autoreactive antibodies targeting the CNS may mediate CNS and PNS damage. Thus, studies have looked for autoantibodies in Covid-19 patients. Franke et al. observed CSF-IgG binding to brain structures in all of their 11 severely ill Covid-19 patients with neurological symptoms examined, yet none with a defined antigenic target [11]. Recently, Fleischer et al. described neurological symptoms in 60% of their 102 SARS-CoV-2 positive patients. Of those tested, 35% were reported to harbor serum autoantibodies against diverse neuronal and glial epitopes (no titers given), without specific clinical correlations [12]. Without giving further details, or neuroimaging data, they did not find a correlation between severity of disease and presence of anti-MOG antibodies. In this case report, the MOG antibodies were tested by a live-cell assay and had a titre ≥1:160, which is an internationally accepted threshold for positivity [8, 13]. The monophasic disease course with multifocal fluffy T2/FLAIR hyperintense brain lesions correlated well to a MOG antibody-associated disease [13]. Vraka and colleagues reported a severely ill 13 months infant in the UK with altered consciousness, seizures, and fever [14]. The girl had received MMR vaccination a month before and had a febrile illness ten days previously. She required intubation and intensive care treatment. SARS-CoV-2 and adenovirus PCRs were positive, as were anti-MOG antibodies; there was no statement as to the method and titre. Cerebral MRI showed bilateral widespread white matter lesions including the splenium of the corpus callosum. She did not make a full recovery [14]. Due to the various confounders, it remains unclear if and how in this case MOG antibodies may have been connected to the SARS-CoV-2 infection, the MRI lesions, and the pathology in this infant [14]. Peters and co-workers recently presented the case of a 23-years old man with cognitive decline, unilateral headaches, dysesthesias and fever. After a positive SARS-CoV-2 test, he had generalized seizures. The brain MRI showed left hemispheric hyperintensity, as well as leptomeningeal enhancement. Serum MOG IgG antibodies were positive at 1:100. i. v. steroid treatment resulted in a marked improvement of cognitive function and MRI findings [15].

A Medline search (“[covid or covid-19 or SARS or SARS-CoV-2] and encephalitis and MOG”) conducted on 27 August 2021 yielded only two results (cited as refs. [14, 15] and discussed above), both published in 2021, and one review citing one case of MOG-associated myelitis. In addition, there are few heterogeneous case reports of optic neuritis with positive MOG-antibodies associated with Sars-CoV2 infection [16].

A recent systematic review and meta-analysis including all literature published until 24 October 2020 [17] found no reports on Covid-19-associated MOG positive encephalitis. However, in this systematic review, the average incidence of encephalitis a complication of covid-19 was estimated to be 0.2%, with a high rate of co-morbidities, and a mortality rate of 13.4% in affected patients [17].

Even though the primary target of SARS-CoV-2 is the respiratory system, the virus has also been recognized as a neuroinfectious agent. Several cases of possible encephalitis and para- or post-viral immune mediated neurological syndromes have been described in COVID-19 patients [18, 19]. Support for autoimmune mechanisms in “Neuro-Covid” also comes from a recent post-mortem case series reporting neuropathological changes predominantly in the brainstem and cerebellum, compatible with autoimmune encephalitis [20]. Potential pathogenetic mechanisms include molecular mimicry between viral proteins and neuronal autoantigens and delayed stimulation of post-viral autoimmunity similar to NMDA receptor encephalitis following herpes simplex virus (HSV) encephalitis [13].

MOG is a glycoprotein located on the myelin surface. The concept of inflammatory CNS disease associated with antibodies against MOG has evolved to include a wide variety of syndromes. MOG antibodies are more prevalent in demyelinating disorders (e.g., optic neuritis, ADEM), but can also be associated with encephalitis without demyelination [13]. However, little is known about secondary autoimmune encephalitis associated with SARS-CoV-2 infection. In view of this, in our case MOG antibodies might be either an immunological epiphenomenon or reflect possible secondary autoimmunity as yet another neurological feature of this deadly virus. It will remain crucial to collect further data on neurological manifestations worldwide, and to better understand the pathology and devise rational, pathogenesis-oriented treatment.


We describe a unique case of a young man with Covid-19 and transient MOG-positive encephalitis, with a benign course. Covid-19 manifestations in the CNS include encephalitis with variable course and prognosis. This case highlights a possible association between inflammation due to COVID-19 and transient secondary autoimmunity.

Availability of data and materials

The data generated or analyzed during this study are included in this article.



Severe acute respiratory syndrome coronavirus 2


Myelin oligodendrocyte glycoprotein


metabotropic glutamate receptor 1


Cerebrospinal fluid


Verbal rating scale


Guillain-Barré syndrome


Miller-Fisher syndrome


Measles, mumps, and rubella


Acute disseminated encephalomyelitis


Polymerase chain reaction


Magnetic resonance imaging


Fluid-attenuated inversion recovery


N-methyl-D-aspartate receptor


  1. 1.

    Zhu N, Zhang D, Wang W, et al. A novel coronavirus from patients with pneumonia in China. N Engl J Med. 2019;382:727–33.

    Article  Google Scholar 

  2. 2.

    Mao L, Jin H, Wang M, et al. Neurologic manifestations of hospitalized patients with coronavirus disease 2019 in Wuhan, China. JAMA Neurol. 2020;77:683–90.

    Article  Google Scholar 

  3. 3.

    Rogers JP, Chesney E, Oliver D, Pollak TA, McGuire P, Fusar-Poli P, et al. Psychiatric and neuropsychiatric presentations associated with severe coronavirus infections: a systematic review and meta-analysis with comparison to the COVID-19 pandemic. Lancet Psychiatry. 2020;7:611–27.

    Article  Google Scholar 

  4. 4.

    Berlit P, Bösel J, Gahn G, Isenmann S, Meuth SG, Nolte CH, et al. "Neurological manifestations of COVID-19" - guideline of the German society of neurology. Neurol Res Pract. 2020;2:51.

    Article  Google Scholar 

  5. 5.

    Helms J, Kremer S, Merdji H, Clere-Jehl R, Schenck M, Kummerlen C, et al. Neurologic features in severe SARS-CoV-2 infection. N Engl J Med. 2020;382:2268–70.

    Article  Google Scholar 

  6. 6.

    Di Pauli F, Mader S, Rostasy K, Schanda K, Bajer-Kornek B, Ehling R, et al. Temporal dynamics of anti-MOG antibodies in CNS demyelinating diseases. Clin Immunol. 2011;138:247–54.

    Article  Google Scholar 

  7. 7.

    Bien CG, Bien CI, Dogan Onugoren M, De Simoni D, Eigler V, Haensch CA, et al. Routine diagnostics for neural antibodies, clinical correlates, treatment and functional outcome. J Neurol. 2020;267:2101–14.

    CAS  Article  Google Scholar 

  8. 8.

    Reindl M, Waters P. Myelin oligodendrocyte glycoprotein antibodies in neurological disease. Nat Rev Neurol. 2019;15:89–102.

    CAS  Article  Google Scholar 

  9. 9.

    Spatola M, Petit Pedrol M, Maudes E, et al. Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis. Neurology. 2020;95:e3012–25.

    CAS  Article  Google Scholar 

  10. 10.

    Neumann B, Schmidbauer ML, Dimitriadis K, et al. Cerebrospinal fluid findings in COVID-19 patients with neurological symptoms. J Neurol Sci. 2020;418:117090.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Franke C, Ferse C, Kreye J, Reincke SM, Sanchez-Sendin E, Rocco A, et al. High frequency of cerebrospinal fluid autoantibodies in COVID-19 patients with neurological symptoms. Brain Behav Immun. 2021;93:415–9.

    CAS  Article  Google Scholar 

  12. 12.

    Fleischer M, Köhrmann M, Dolff S, et al. Observational cohort study of neurological involvement among patients with SARS-CoV-2 infection. Ther Adv Neurol Disord. 2021;14:1–14.

    Article  Google Scholar 

  13. 13.

    Armangue T, Olivé-Cirera G, Martínez-Hernandez E, Sepulveda M, Ruiz-Garcia R, Muñoz-Batista M, et al. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study. Lancet Neurol. 2020;19:234–46.

    CAS  Article  Google Scholar 

  14. 14.

    Vraka K, Ram D, West S, Chia WYE, et al. Two Paediatric patients with encephalopathy and concurrent COVID-19 infection: two sides of the same coin? Case Rep Neurol Med. 2021.

  15. 15.

    Peters J, Alhasan S, Vogels Chantal BF, Grubaugh ND, Farhadian S, Longbrake EE. MOG-associated encephalitis following SARS-COV-2 infection. Mult Scler Relat Disord. 2021.

  16. 16.

    Kogure C, Kikushima W, Fukuda Y, et al. Myelin oligodendrocyte glycoprotein antibody-associated optic neuritis in a COVID-19 patient: a case report. Medicine (Baltimore). 2021;100(19):e25865.

    CAS  Article  Google Scholar 

  17. 17.

    Siow I, Lee KS, Zhang JJY, Saffari SE, Ng A. Encephalitis as a neurological complication of COVID-19: a systematic review and meta-analysis of incidence, outcomes, and predictors. Eur J Neurol. 2021.

  18. 18.

    Toscano G, Palmerini F, Ravaglia S, Ruiz L, Invernizzi P, Cuzzoni MG, et al. Guillain-Barré syndrome associated with SARS-CoV-2. N Engl J Med. 2020;382:2574–6.

    Article  Google Scholar 

  19. 19.

    Guilmot A, Maldonado S, Sellimi A, Bronchain M, Hanseeuw B, Belkhir L, et al. Immune mediated neurological syndromes in SARS CoV 2 infected patients. J Neurol. 2021;268:751–7.

    CAS  Article  Google Scholar 

  20. 20.

    Matschke J, Lütgehetmann M, Hagel C, Sperhake JP, Schröder AS. Edler C at al. Neuropathology of patients with COVID-19 in Germany: a post-mortem case series. Lancet Neurol. 2020;19:919–29.

    CAS  Article  Google Scholar 

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We acknowledge the patient for his consent to share these findings.


The authors declare that they have no sources of funding related to the manuscript.

Author information




ED and SI interviewed, examined, and treated the patient. ED, SI, CB and CGB contributed to the design and depth of the manuscript. SI reviewed the patient’s records to synthesize the case report. SI and ED carried out the literature search and review. SI and ED selected relevant MRI images. CB contributed Fig. 2. CGB researched background information. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Stefan Isenmann.

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Durovic, E., Bien, C., Bien, C.G. et al. MOG antibody-associated encephalitis secondary to Covid-19: case report. BMC Neurol 21, 414 (2021).

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  • COVID-19
  • Encephalitis
  • MOG antibody
  • Methylprednisolone
  • Neuropsychology
  • SARS-CoV-2