Severe enterovirus infections in patients with immune-mediated inflammatory diseases receiving anti-CD20 monoclonal antibodies

Gregoire Martin de Fremont, Helene Chabrolles, Audrey Mirand, Anne Sophie L'Honneur,Nicolas Mele, Bertrand Dunogue, David Boutboul, Meryem Farhat, Eric Hachulla, Mouna Lazrek, Virginie Rieu, Alexis Mathian, Helene Chaussade, Aurelie Ruet, Sonia Burrel, Fabienne Coury-Lucas, Isabelle Schuffenecker, Adrien Lemaignen, Karl Stefic, Maelle le Besnerais, Marion Carrette, Luc Mouthon, Veronique Avettand-Fenoel, Benjamin Terrier, Jerome Hadjadj

RMD OPEN(2024)

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Abstract
Objective Patients with X linked agammaglobulinemia are susceptible to enterovirus (EV) infections. Similarly, severe EV infections have been described in patients with impaired B-cell response following treatment with anti-CD20 monoclonal antibodies (mAbs), mostly in those treated for haematological malignancies. We aimed to describe severe EV infections in patients receiving anti-CD20 mAbs for immune-mediated inflammatory diseases (IMIDs).Methods Patients were included following a screening of data collected through the routine surveillance of EV infections coordinated by the National Reference Center and a review of the literature. Additionally, neutralising antibodies were assessed in a patient with chronic EV-A71 meningoencephalitis.Results Nine original and 17 previously published cases were retrieved. Meningoencephalitis (n=21/26, 81%) associated with EV-positive cerebrospinal fluid (n=20/22, 91%) was the most common manifestation. The mortality rate was high (27%). EV was the only causal agents in all reported cases. Patients received multiple anti-CD20 mAbs infusions (median 8 (5-10)), resulting in complete B-cell depletion and moderate hypogammaglobulinemia (median 4.9 g/L (4.3-6.7)), and had limited concomitant immunosuppressive treatments. Finally, in a patient with EV-A71 meningoencephalitis, a lack of B-cell response to EV was shown.Conclusion EV infection should be evoked in patients with IMIDs presenting with atypical organ involvement, especially meningoencephalitis. Anti-CD20 mAbs may lead to impaired B-cell response against EV, although an underlying primary immunodeficiency should systematically be discussed.
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Key words
autoimmune diseases,rituximab,antirheumatic agents,B-lymphocytes
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