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Seroprevalence of SARS-CoV-2 in Patients with Multiple Sclerosis under Disease-Modifying Therapies: A Multi-Centre Study.
Sancho-Saldaña, Agustín; Gil-Sánchez, Anna; González-Mingot, Cristina; Peralta, Silvia; Solana, Maria Jose; Torres, Pascual; Juanes, Alba; Quibus, Laura; Ruiz, Emilio; Sanpedro, Eduardo; Quirant-Sánchez, Bibiana; Martínez-Cáceres, Eva; Ramo Tello, Cristina; Presas-Rodríguez, Silvia; García Rubio, Sebatián; Baron, Beatriz Pardiñas; Ramió-Torrentà, Lluís; Sotoca, Javier; González-Suárez, Inés; Eichau, Sara; Prieto-González, José M; Blasco Quilez, Maria Rosario; Sabín-Muñoz, Julia; Sánchez-López, Antonio José; Llorens Calatayud, Gloria; Calles, Carmen; Sempere, Ángel Pérez; Garcés, Moises; Carmona, Olga; Moral, Ester; Hervás, José Vicente; Blanco, Yolanda; Sola-Valls, Nuria; Tellez Lara, Nieves; Forero, Lucía; Brieva, Luis.
Affiliation
  • Sancho-Saldaña A; Neurology Department, Hospital Universitario Arnau de Vilanova, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Gil-Sánchez A; Neuroimmunology Group, Department of Medicine, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • González-Mingot C; Neuroimmunology Group, Department of Medicine, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Peralta S; Neurology Department, Hospital Universitario Arnau de Vilanova, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Solana MJ; Multiple Sclerosis Foundation from Lleida, 25198 Lleida, Spain.
  • Torres P; Neurology Department, Hospital Universitario Arnau de Vilanova, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Juanes A; Neuroimmunology Group, Department of Medicine, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Quibus L; Metabolic Physiopathology Group, Department of Experimental Medicine, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Ruiz E; Neuroimmunology Group, Department of Medicine, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Sanpedro E; Neurology Department, Hospital Universitario Arnau de Vilanova, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Quirant-Sánchez B; Neurology Department, Hospital Universitario Arnau de Vilanova, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Martínez-Cáceres E; Neurology Department, Hospital Universitario Arnau de Vilanova, Institut de Recerca Biomèdica de Lleida-IRBLleida, 25198 Lleida, Spain.
  • Ramo Tello C; Immunology Division, Hospital Germans Trias i Pujol, LCMN, 08916 Badalona, Spain.
  • Presas-Rodríguez S; Department of Cell Biology, Physiology, Immunology, Autonomous University, Bellaterra, 08193 Barcelona, Spain.
  • García Rubio S; Immunology Division, Hospital Germans Trias i Pujol, LCMN, 08916 Badalona, Spain.
  • Baron BP; Department of Cell Biology, Physiology, Immunology, Autonomous University, Bellaterra, 08193 Barcelona, Spain.
  • Ramió-Torrentà L; Multiple Sclerosis and Clinical Neuroimmunology Unit, Neurosciences Department, Hospital Germans Trias i Pujol, 08916 Badalona, Spain.
  • Sotoca J; Multiple Sclerosis and Clinical Neuroimmunology Unit, Neurosciences Department, Hospital Germans Trias i Pujol, 08916 Badalona, Spain.
  • González-Suárez I; Neurology Department, Hospital Universitario Miguel Servet, 50009 Zaragoza, Spain.
  • Eichau S; Neurology Department, Hospital Universitario Miguel Servet, 50009 Zaragoza, Spain.
  • Prieto-González JM; Girona Neuroimmunology and Multiple Sclerosis Unit, Neurology Department, Dr. Josep Trueta University Hospital, 17007 Girona, Spain.
  • Blasco Quilez MR; Neurodegeneration and Neuroinflammation Research Group, IDIBGI, 17190 Salt, Spain.
  • Sabín-Muñoz J; Medical Sciences Department, University of Girona, 17071 Girona, Spain.
  • Sánchez-López AJ; Neurology Department, Hospital Universitari MutuaTerrassa, 08035 Barcelona, Spain.
  • Llorens Calatayud G; Department of Neurology, Complejo Hospitalario Universitario de Vigo, Calle Clara Campoamor, 341, 36213 Vigo, Spain.
  • Calles C; Multiple Sclerosis Unit, Hospital Universitario Virgen Macarena, 41009 Seville, Spain.
  • Sempere ÁP; Fundación Instituto de Investigación Sanitaria de Santiago (IDIS), 15706 Santiago de Compostela, Spain.
  • Garcés M; Neuroimmunology Unit, Clínica Puerta de Hierro, Universidad Autónoma de Madrid, 28222 Madrid, Spain.
  • Carmona O; Neuroimmunology Unit, Clínica Puerta de Hierro, Universidad Autónoma de Madrid, 28222 Madrid, Spain.
  • Moral E; Biobank, Puerta de Hierro-Segovia de Arana Health Research Institute, 28222 Madrid, Spain.
  • Hervás JV; Neuroimmunology Unit, Puerta de Hierro-Segovia de Arana Health Research Institute, 28222 Madrid, Spain.
  • Blanco Y; Department of Neurology, Hospital Mateu Orfila, 07703 Mahón, Spain.
  • Sola-Valls N; Department of Neurology, Hospital Universitari Son Espases, 07120 Palma de Mallorca, Spain.
  • Tellez Lara N; Department of Neurology, Hospital General Universitario Dr. Balmis de Alicante, Universidad Miguel Hernández de Elche, 03202 Elche, Spain.
  • Forero L; Department of Neurology, Hospital Clínico Universitario Lozano Blesa, 50009 Zaragoza, Spain.
  • Brieva L; Department of Neurology, Fundació Salut Empordà, 17600 Girona, Spain.
J Clin Med ; 12(23)2023 Nov 23.
Article in En | MEDLINE | ID: mdl-38068295
ABSTRACT

BACKGROUND:

The EMCOVID project conducted a multi-centre cohort study to investigate the impact of COVID-19 on patients with Multiple Sclerosis (pwMS) receiving disease-modifying therapies (DMTs). The study aimed to evaluate the seroprevalence and persistence of SARS-CoV-2 antibodies in MS patients enrolled in the EMCOVID database. The DMTs were used to manage MS by reducing relapses, lesion accumulation, and disability progression. However, concerns arose regarding the susceptibility of pwMS to COVID-19 due to potential interactions between SARS-CoV-2 and the immune system, as well as the immunomodulatory effects of DMTs.

METHODS:

This prospective observational study utilized data from a Multiple Sclerosis and COVID-19 (EMCOVID-19) study. Demographic characteristics, MS history, laboratory data, SARS-CoV-2 serology, and symptoms of COVID-19 were extracted for pwMS receiving any type of DMT. The relationship between demographics, MS phenotype, DMTs, and COVID-19 was evaluated. The evolution of SARS-CoV-2 antibodies over a 6-month period was also assessed.

RESULTS:

The study included 709 pwMS, with 376 patients providing samples at the 6-month follow-up visit. The seroprevalence of SARS-CoV-2 antibodies was higher among pwMS than the general population, with Interferon treatment being significantly associated with greater seroprevalence (16.9% vs. 8.4%; p 0.003). However, no other specific DMT showed a significant association with antibody presence. A total of 32 patients (8.5%) tested positive for IgG, IgM, or IgA antibodies against SARS-CoV-2 at baseline, but then tested negative at 6 months. Most of the pwMS in the cohort were asymptomatic for COVID-19 and, even among symptomatic cases, the prognosis was generally favourable.

CONCLUSION:

pwMS undergoing DMTs exhibited a higher seroprevalence of COVID-19 than the general population. Interferon treatment was associated with a higher seroprevalence, suggesting a more robust humoral response. This study provides valuable insights into the seroprevalence and persistence of SARS-CoV-2 antibodies in pwMS and contributes to our understanding of the impact of COVID-19 amongst this population.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Med Year: 2023 Document type: Article Affiliation country: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Med Year: 2023 Document type: Article Affiliation country: Spain