Lupus & antiphospholipid syndrome
Screening for Neoehrlichia mikurensis and other emerging tick-borne pathogens in Swedish patients with systemic lupus erythematosus receiving B-cell-targeted therapies
Authors' conclusion
Evidence suggests that B-cell-targeted therapies may raise eTBD risk; however, none of the individuals with SLE included herein was found to be infected, despite the documented presence of these pathogens in Southeastern Sweden. Our findings contrast with those from Norwegian immunocompromised patients, but are in line with data from the Danish nationwide Rheumatological Database, including patients with arthritis receiving tumour necrosis factor inhibitors. Hypothetically, higher doses of glucocorticoids impair B-cell function and increase the risk of eTBD further. Nevertheless, routine eTBD screening of patients with SLE in Southeastern Sweden is not supported by our data.
Study context
- Population
- Patients with systemic lupus erythematosus (SLE) receiving rituximab or belimumab in Region Östergötland, a tick-endemic region of Southeastern Sweden, with comparator patients with quiescent disease on hydroxychloroquine treatment onlySLE patients receiving rituximab or belimumab, biobanked sera (n = 143) collected during 2015–2024
- Participants
- 48 patients
- Comparison
- SLE patients receiving rituximab or belimumab vs patients with quiescent disease on hydroxychloroquine treatment only
- RITUXIMAB OR BELIMUMABn = 48
- HYDROXYCHLOROQUINE ONLYn = 50
- Outcome
- Pathogen-specific DNA for Neoehrlichia mikurensis, Borrelia burgdorferi sensu lato, Borrelia miyamotoi, Anaplasma phagocytophilum, Spiroplasma ixodetis, and Babesia spp.
Methodological detailscomparators: patients with quiescent disease on hydroxychloroquine treatment only
- Comparators: patients with quiescent disease on hydroxychloroquine treatment only
Main finding
As reported in the abstract
- No pathogen-specific DNA for the examined emerging tick-borne diseases (eTBDs) was detected in serum samples from the included patients
Original publication
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