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Sökning: id:"swepub:oai:prod.swepub.kib.ki.se:138798037" > Rituximab in multip...

Rituximab in multiple sclerosis: Frequency and clinical relevance of anti-drug antibodies

Dunn, N (författare)
Karolinska Institutet
Juto, A (författare)
Karolinska Institutet
Ryner, M (författare)
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Manouchehrinia, A (författare)
Karolinska Institutet
Piccoli, L (författare)
Fink, K (författare)
Karolinska Institutet
Piehl, F (författare)
Karolinska Institutet
Fogdell-Hahn, A (författare)
Karolinska Institutet
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 (creator_code:org_t)
2017-08-01
2018
Engelska.
Ingår i: Multiple sclerosis (Houndmills, Basingstoke, England). - : SAGE Publications. - 1477-0970 .- 1352-4585. ; 24:9, s. 1224-1233
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Rituximab is a chimeric monoclonal anti-CD20 B-cell-depleting antibody increasingly used off-label in multiple sclerosis (MS). The clinical relevance of anti-drug antibodies (ADAs) against rituximab in MS is unknown. Objective: To determine frequency of ADA in relation to B-cell counts, allergic reactions and clinical efficacy in a large cohort of MS-treated patients. Methods: Cross-sectional study with collection of serum samples from 339 MS patients immediately before a scheduled rituximab infusion. ADAs were detected using an in-house–validated electrochemiluminescent immunoassay and a commercial enzyme-linked immunosorbent assay (ELISA) to compare methods. Data on patient demographics and clinical outcomes were retrieved from the Swedish MS Registry and patient records. Results: ADAs were detected in 37% of relapsing–remitting MS and 26% in progressive forms of MS. Presence of ADAs decreased with increasing number of rituximab infusions. There was a significant association between both presence and titres of ADAs and incomplete B-cell depletion, but not with infusion/adverse reactions or clinical outcomes at the group level. Only five patients terminated rituximab during follow-up, four of which were ADA positive. Conclusion: Rituximab treatment is associated with a high degree of ADAs, which correlates with efficacy of B-cell depletion; however, the clinical relevance of ADAs remains uncertain.

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