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Neurological autoimmune diseases following vaccinations against SARS-CoV-2: a case series.
Kaulen, Leon D; Doubrovinskaia, Sofia; Mooshage, Christoph; Jordan, Berit; Purrucker, Jan; Haubner, Carmen; Seliger, Corinna; Lorenz, Hanns-Martin; Nagel, Simon; Wildemann, Brigitte; Bendszus, Martin; Wick, Wolfgang; Schönenberger, Silvia.
  • Kaulen LD; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Doubrovinskaia S; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Mooshage C; Department of Neuroradiology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Jordan B; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Purrucker J; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Haubner C; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Seliger C; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Lorenz HM; Division of Rheumatology, Department of Internal Medicine V, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Nagel S; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Wildemann B; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Bendszus M; Department of Neuroradiology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Wick W; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
  • Schönenberger S; Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.
Eur J Neurol ; 29(2): 555-563, 2022 02.
Article in English | MEDLINE | ID: covidwho-1476180
ABSTRACT
BACKGROUND AND

PURPOSE:

Population-based studies suggest that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines may trigger immune-mediated thrombotic thrombocytopenia (VITT) raising concerns for other autoimmune responses. The aim was to characterize neurological autoimmunity after SARS-CoV-2 vaccinations.

METHODS:

In this single-centre prospective case study patients with neurological autoimmunity in temporal association (≤6 weeks) with SARS-CoV-2 vaccinations and without other triggers are reported. Clinical, laboratory and imaging data were collected with a median follow-up of 49 days.

RESULTS:

In the study period 232,603 inhabitants from the main catchment area of our hospital (Rhein-Neckar-Kreis, county) received SARS-CoV-2 vaccinations. Twenty-one cases (new onset n = 17, flares n = 4) diagnosed a median of 11 days (range 3-23) following SARS-CoV-2 vaccinations (BNT162b2 n = 12, ChAdOx1 n = 8, mRNA-1273 n = 1) were identified. Cases included VITT with cerebral venous sinus thrombosis (n = 3), central nervous system demyelinating diseases (n = 8), inflammatory peripheral neuropathies (n = 4), myositis (n = 3), myasthenia (n = 1), limbic encephalitis (n = 1) and giant cell arteritis (n = 1). Patients were predominantly female (ratio 3.21) and the median age at diagnosis was 50 years (range 22-86). Therapy included administration of steroids (n = 15), intravenous immunoglobulins in patients with Guillain-Barré syndrome or VITT (n = 4), plasma exchange in cases unresponsive to steroids (n = 3) and anticoagulation in VITT. Outcomes were favourable with partial and complete remissions achieved in 71% and 24%, respectively. Two patients received their second vaccination without further aggravation of autoimmune symptoms under low-dose immunosuppressants.

CONCLUSIONS:

In this study various neurological autoimmune disorders encountered following SARS-CoV-2 vaccinations are characterized. Given the assumed low incidence and mostly favourable outcome of autoimmune responses, the benefits of vaccinations outweigh the comparatively small risks.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peripheral Nervous System Diseases / Guillain-Barre Syndrome / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Adult / Aged / Female / Humans / Middle aged / Young adult Language: English Journal: Eur J Neurol Journal subject: Neurology Year: 2022 Document Type: Article Affiliation country: Ene.15147

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Peripheral Nervous System Diseases / Guillain-Barre Syndrome / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Adult / Aged / Female / Humans / Middle aged / Young adult Language: English Journal: Eur J Neurol Journal subject: Neurology Year: 2022 Document Type: Article Affiliation country: Ene.15147