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Article Dans Une Revue Neurology Année : 2019

Prospective validation of the PML risk biomarker l-selectin and influence of natalizumab extended intervals

Jonathan Ciron

Résumé

Low l-selectin (CD62L) on CD4+ T cells after cryopreservation has been introduced in 2013 as a risk biomarker for the development of progressive multifocal leukoencephalopathy (PML) during natalizumab treatment or HIV infection. The biomarker has been reproduced retrospectively in some international cohorts, but not in others, potentially because of its sensitivity to biomaterial quality, assay protocols, and the time point of testing. With regard to current approaches to PML risk reduction, natalizumab extended interval dosing is thought to improve immune surveillance and reduce PML risk, whereas clinical efficacy seems unaffected.
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Dates et versions

hal-03001614 , version 1 (12-11-2020)

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Nicholas Schwab, Tilman Schneider-Hohendorf, Béatrice Pignolet, Florence Bucciarelli, Lise Scandella, et al.. Prospective validation of the PML risk biomarker l-selectin and influence of natalizumab extended intervals. Neurology, 2019, 93 (12), pp.550-554. ⟨10.1212/WNL.0000000000008135⟩. ⟨hal-03001614⟩
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