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Vidas elfa

Manufactured by bioMérieux
Sourced in France

Vidas ELFA is an automated enzyme-linked fluorescent assay (ELFA) platform developed by bioMérieux for in vitro diagnostic testing. The system utilizes a unique combination of enzyme-linked immunoassay and fluorescent detection technology to provide qualitative, semi-quantitative, or quantitative results for a variety of analytes.

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Lab products found in correlation

2 protocols using vidas elfa

1

CD4+CD28null T cells in Multiple Sclerosis

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Peripheral blood samples (Li-Heparin coated tubes) were collected from 63 healthy controls (HC) and 227 MS patients in collaboration with the University Biobank Limburg (UBiLim). CMV and Epstein-Barr virus (EBV) status and titers (CMV IgG and EBV EBNA IgG) were determined in serum samples via Vidas ELFA (bioMérieux, Marcy l’Etoile, France) and Architect immunoassay (Abbott, Illinois, USA). Clinical data are presented in Table 1; there were no significant differences between CMV positive or negative donors, neither in MS patients nor in healthy controls.

Study subjects for CD4+CD28null T cell analysis.

MS patientsHealthy controls
CMV+CMV−CMV+CMV−
Number1001272439
Age (y)47 ± 1344 ± 1432 ± 932 ± 10
Male/Female (ratio)26/74 (0.35)35/92 (0.38)7/17 (0.41)14/25 (0.56)
EBV serostatus (−/border/+)0/2/642/0/87NA
Disease duration range1 mo–40 y0 mo–37 yNA
EDSS range0–70–7.5NA
Disease typeNA
 CIS56
 RR-MS6378
 CP-MS3243
Treatment#NA
 No treatment4656
 IFNβ2547
 Glatiramer acetate1510
 Natalizumab96
 Alemtuzumab24
 Teriflunomide/3
 Dimethyl fumarate2/
 Methotrexate11

#Within 3 months before blood collection.

MS, multiple sclerosis; EDSS, expanded disability status scale; CIS, clinically isolated syndrome; RR, relapsing remitting; CP, chronic progressive; IFNβ, interferon beta; CMV, cytomegalovirus; NA, not applicable.

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2

Varicella Zoster Vaccine Immune Response

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(#215830) due to off-label use of RZV. The study was registered at clinicaltrials.gov (NCT03685682).
After obtaining consent, participants received 2 intramuscular 0 . 5mL doses of RZV 2 to 6 months apart. Serum and PBMCs were collected prior to first dose of vaccine (V1), prior to second dose of vaccine (V2), and 4 weeks after the second dose (V3) (Figure 1). A negative prevaccination serostatus was confirmed by the VIDAS ELFA (enzyme linked fluorescent assay) VZV IgG assay (VIDAS, Biomerieux, France). Patients were followed up to 3 months after the second vaccine dose.
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