Pour des raisons de limite de nombre de caractères, nous avons du tronquer la traduction du titre de cette publication.
Le voici en entier
"L'innocuité à long terme du rituximab induit une déplétion des lymphocytes B périphériques dans les maladies neurologiques auto-immunes."
Lu sur :https://www.ncbi.nlm.nih.gov/pubmed/29309416
Traduction disponible directement en cliquant en bas à droite de ce message sur l'expressionTraduire en
Long-term safety of rituximab induced peripheral B-cell depletion in autoimmune neurological diseases.
Memon AB1, Javed A2, Caon C1, Srivastawa S1, Bao F3, Bernitsas E1, Chorostecki J1,3, Tselis A1, Seraji-Bozorgzad N3, Khan O1,3.
PLoS One. 2018 Jan 8;13(1):e0190425. doi: 10.1371/journal.pone.0190425. eCollection 2018.
B-cells play a pivotal role in several autoimmune diseases, including patients with immune-mediated neurological disorders (PIMND), such as neuromyelitis optica (NMO), multiple sclerosis (MS), and myasthenia gravis (MG). Targeting B-cells has been an effective approach in ameliorating both central and peripheral autoimmune diseases. However, there is a paucity of literature on the safety of continuous B-cell depletion over a long period of time.
The aim of this study was to examine the long-term safety, incidence of infections, and malignancies in subjects receiving continuous therapy with a B-cell depleting agent rituximab over at least 3 years or longer.
This was a retrospective study involving PIMND who received continuous cycles of rituximab infusions every 6 to 9 months for up to 7 years. The incidence of infection related adverse events (AE), serious adverse events (SAE), and malignancies were observed.
There were a total of 32 AE and 4 SAE with rituximab treatment. The 3 SAE were noted after 9 cycles (48 months) and 1 SAE was observed after 11 cycles (60 months) of rituximab. There were no cases of Progressive multifocal leukoencephalopathy (PML) and malignancies observed throughout the treatment period. Rituximab was well tolerated without any serious infusion reactions. Also, rituximab was found to be beneficial in treating PIMND over a 7-year period.
This study demonstrates that long-term depletion of peripheral B-cells appears safe and efficacious in treating PIMND. Longer and larger prospective studies with rituximab are needed to carefully ascertain risks associated with chronic B-cell depletion, including malignancies. Recognizing that this is a small, retrospective study, such data nonetheless complement the growing literature documenting the safety and tolerability of B-cell depleting agents in neurological diseases.