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Schema {🗺️}

WebPage:
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         headline:Preliminary evidence of blunted humoral response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients treated with ocrelizumab
         description:Several concerns regard the immunogenicity of SARS-CoV-2 vaccines in people with multiple sclerosis (pwMS), since the majority of them is treated with immunomodulating/immunosuppressive disease modifying therapies. Here we report the first data on the humoral response to mRNA SARS-CoV-2 vaccine in a case series of 4 pwMS treated with ocrelizumab (OCR) as compared to a group of healthy subjects (HS). We collected serum samples at 0, 14, 21 days after the first dose and 7 days after the second dose of BNT162b2-mRNA-Covid-19 vaccine from 55 health-care workers and 4 relapsing pwMS on OCR, with no history of Covid-19 infection. Sera were tested using the LIAISON®SARS-CoV-2 TrimericS-IgG assay (DiaSorin-S.p.A.) for the detection of IgG antibodies to SARS-CoV-2 spike protein. The anti-spike IgGtiters were expressed in Binding Antibody Units (BAU), an international standard unit. At baseline all subjects were negative for anti-spike IgG. Seven days after the second dose of vaccine all HS mounted a significant humoral response (geometric mean 2010.4 BAU/mL C.I. 95% 1512.7-2672) while the 4 pwMS showed a lower response (range <4.81-175 BAU/mL). Humoral response to BNT162b2-mRNA-vaccine in pwMS treated with OCR was clearly blunted. Further data are urgently needed to confirm and expand these preliminary results and to develop strategies to optimize the response to SARSCoV-2 vaccines in pwMS on OCR.
         datePublished:2021-06-15T00:00:00Z
         dateModified:2021-06-15T00:00:00Z
         pageStart:3523
         pageEnd:3526
         sameAs:https://doi.org/10.1007/s10072-021-05397-7
         keywords:
            Multiple sclerosis
            COVID-19
            SARS-CoV-2 mRNA vaccine
            Ocrelizumab
            Humoral response
            Neurology
            Neuroradiology
            Neurosurgery
            Psychiatry
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      headline:Preliminary evidence of blunted humoral response to SARS-CoV-2 mRNA vaccine in multiple sclerosis patients treated with ocrelizumab
      description:Several concerns regard the immunogenicity of SARS-CoV-2 vaccines in people with multiple sclerosis (pwMS), since the majority of them is treated with immunomodulating/immunosuppressive disease modifying therapies. Here we report the first data on the humoral response to mRNA SARS-CoV-2 vaccine in a case series of 4 pwMS treated with ocrelizumab (OCR) as compared to a group of healthy subjects (HS). We collected serum samples at 0, 14, 21 days after the first dose and 7 days after the second dose of BNT162b2-mRNA-Covid-19 vaccine from 55 health-care workers and 4 relapsing pwMS on OCR, with no history of Covid-19 infection. Sera were tested using the LIAISON®SARS-CoV-2 TrimericS-IgG assay (DiaSorin-S.p.A.) for the detection of IgG antibodies to SARS-CoV-2 spike protein. The anti-spike IgGtiters were expressed in Binding Antibody Units (BAU), an international standard unit. At baseline all subjects were negative for anti-spike IgG. Seven days after the second dose of vaccine all HS mounted a significant humoral response (geometric mean 2010.4 BAU/mL C.I. 95% 1512.7-2672) while the 4 pwMS showed a lower response (range <4.81-175 BAU/mL). Humoral response to BNT162b2-mRNA-vaccine in pwMS treated with OCR was clearly blunted. Further data are urgently needed to confirm and expand these preliminary results and to develop strategies to optimize the response to SARSCoV-2 vaccines in pwMS on OCR.
      datePublished:2021-06-15T00:00:00Z
      dateModified:2021-06-15T00:00:00Z
      pageStart:3523
      pageEnd:3526
      sameAs:https://doi.org/10.1007/s10072-021-05397-7
      keywords:
         Multiple sclerosis
         COVID-19
         SARS-CoV-2 mRNA vaccine
         Ocrelizumab
         Humoral response
         Neurology
         Neuroradiology
         Neurosurgery
         Psychiatry
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            1590-1874
         volumeNumber:42
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         name:Springer International Publishing
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      author:
            name:Antonio Gallo
            url:http://orcid.org/0000-0002-2203-6237
            affiliation:
                  name:University of Campania “Luigi Vanvitelli”
                  address:
                     name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy
                     type:PostalAddress
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            email:[email protected]
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            name:Rocco Capuano
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                  name:University of Campania “Luigi Vanvitelli”
                  address:
                     name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy
                     type:PostalAddress
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            name:Giovanna Donnarumma
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            name:Elena Grimaldi
            affiliation:
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      name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Experimental Medicine, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Experimental Medicine, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Experimental Medicine, University of Campania “Luigi Vanvitelli”, Naples, Italy
      name:Department of Advanced Medical and Surgical Sciences, University of Campania “Luigi Vanvitelli”, Naples, Italy

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