Abstract
The emergency represented by the COVID-19 pandemic represents a new challenge for clinicians who deal with autoimmune diseases because of patients undergoing immunosuppressive therapy. Few cases of Multiple Sclerosis (MS) patients receiving ocrelizumab who contracted COVID-19 with a benign course have recently been published. We present the case of a MS patient with mild COVID-19 who developed SARS-CoV-2 specific IgA without IgG ten weeks after infection. Patients on B-cell depleting drugs have a reduced antibody immune response to viral neoantigens. A relative sparing of mucosal-associated lymphoid tissues (MALT) could be responsible for IgA response in our patient.
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | N/A-N/A |
| Rivista | Multiple Sclerosis and Related Disorders |
| Volume | 44 |
| Numero di pubblicazione | 44 |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2020 |
All Science Journal Classification (ASJC) codes
- Neurologia
- Neurologia (clinica)
Keywords
- COVID-19
- IgA
- IgG
- Ocrelizumab
- Serology
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