B-cell depleting therapies may affect susceptibility to acute respiratory illness among patients with multiple sclerosis during the early COVID-19 epidemic in Iran

Mult Scler Relat Disord. 2020 Aug:43:102195. doi: 10.1016/j.msard.2020.102195. Epub 2020 May 13.

Abstract

Objective: To determine whether the course of COVID-19 is more severe in patients with MS and if MS disease-modifying treatments (DMTs) affect the risk of contracting the disease.

Methods: In a cross-sectional survey, data were collected by sending a questionnaire to 2000 patients with a demyelinating disease through an online portal system. Collected data included the current MS DMT and patient-reported disability level, history of recent sick contact, recent fever, respiratory symptoms, diagnosis with COVID-19, and the disposition after the diagnosis. We defined a COVID-19-suspect group as patients having fever and cough or fever and shortness of breath, or a presumptive diagnosis based on suggestive chest computed tomography. We calculated the proportion of COVID-19-suspect patients and compared their demographics, clinical characteristics, and DMT categories with the rest of survey-responders, using univariable and multivariable models.

Results: Out of 712 patients, 34 (4.8%) fulfilled our criteria for being in the COVID-19-suspect group. Only two patients required hospitalization. No patient required intensive care. In a multivariable model, disease duration (p-value=0.017), DMT category (p-value=0.030), and history of sick contact (p-values<0.001) were associated with the risk of being in the COVID-19-suspect group. Being on B-cell depleting antibodies (as compared to non-cell depleting, non-cell trafficking inhibitor DMTs) was associated with a 2.6-fold increase in the risk of being in the COVID-19-suspect group. (RR: 3.55, 95%CI: 1.45, 8.68, p-value=0.005).

Conclusions: The course of infection in patients with MS suspected of having COVID-19 was mild to moderate, and all patients had a full recovery. B-cell depleting antibodies may increase the susceptibility to contracting COVID-19.

Keywords: B-cell depleting therapies; COVID-19; DMTs; Multiple Sclerosis.

MeSH terms

  • Adult
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • B-Lymphocytes / immunology
  • Betacoronavirus
  • COVID-19
  • Coronavirus Infections / complications
  • Coronavirus Infections / epidemiology
  • Coronavirus Infections / immunology*
  • Coronavirus Infections / physiopathology
  • Cough
  • Cross-Sectional Studies
  • Crotonates / therapeutic use
  • Dimethyl Fumarate / therapeutic use
  • Disease Susceptibility
  • Dyspnea
  • Epidemics
  • Female
  • Fever
  • Fingolimod Hydrochloride / therapeutic use
  • Glatiramer Acetate / therapeutic use
  • Hospitalization / statistics & numerical data
  • Humans
  • Hydroxybutyrates
  • Immunocompromised Host / immunology*
  • Immunologic Factors / therapeutic use*
  • Intensive Care Units / statistics & numerical data
  • Interferons / therapeutic use
  • Iran / epidemiology
  • Lung / diagnostic imaging
  • Lymphocyte Depletion
  • Male
  • Multiple Sclerosis / complications
  • Multiple Sclerosis / drug therapy*
  • Multiple Sclerosis, Chronic Progressive / drug therapy
  • Multiple Sclerosis, Chronic Progressive / epidemiology
  • Multiple Sclerosis, Relapsing-Remitting / drug therapy
  • Multiple Sclerosis, Relapsing-Remitting / epidemiology
  • Natalizumab / therapeutic use
  • Nitriles
  • Pandemics
  • Pneumonia, Viral / complications
  • Pneumonia, Viral / epidemiology
  • Pneumonia, Viral / immunology*
  • Pneumonia, Viral / physiopathology
  • Rituximab / therapeutic use
  • SARS-CoV-2
  • Severity of Illness Index
  • Toluidines / therapeutic use
  • Tomography, X-Ray Computed

Substances

  • Antibodies, Monoclonal, Humanized
  • Crotonates
  • Hydroxybutyrates
  • Immunologic Factors
  • Natalizumab
  • Nitriles
  • Toluidines
  • teriflunomide
  • Rituximab
  • Glatiramer Acetate
  • Interferons
  • ocrelizumab
  • Dimethyl Fumarate
  • Fingolimod Hydrochloride