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The serum samples collected at all time points were tested using a viral microneutralization assay as previously described,, and using a strain that is antigenically similar to the vaccine strain (A/Netherlands/602/09) at Viroclinics Biosciences (Rotterdam).
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Thus, a laboratory comparison of the 2-day enzyme-linked immunosorbent assay (ELISA) and 3-day hemagglutination (HA) microneutralization (MN) protocols, using A(H1N1 pdm09, A(H3N2), and A(H5N1) viruses, was performed by the CONSISE Laboratory Working Group.
Neutralizing antibody titers for prototype HAdVs −5, −26, −35 and −48 were determined using a modified microneutralization assay [36].
Testing was done by using a standardized microneutralization assay.
Antibodies to each DENV type were measured at the Translational Medicine Branch Pilot Bioproduction Facility, WRAIR using a quantitative microneutralization assay (MN50) performed in Vero cells as previously described.
Samples were tested using a standard microneutralization assay for antibodies to poliovirus types 1, 2, and 3 according to established protocols at the Global Polio Specialized Laboratory, Centers for Disease Control and Prevention.
The Translational Medicine Branch, Pilot Bioproduction Facility of WRAIR conducted the analyses using a quantitative microneutralization assay (MN50) performed in Vero cells, as previously described.
Viral RNAs were extracted from pelleted virions using a QIAamp Viral RNA Mini Kit (Qiagen).
This process was repeated four times, and then the supernatants were used for determining the neutralization titers, using a microneutralization assay with A/reassortants/NYMC X-179A/California/07/2009(H1N1) virus and MDCK cells according to standard procedures [41].
YF neutralizing antibody titers were measured using a microneutralization assay.
Virus neutralization was determined using a microneutralization assay on heat-inactivated sera as described previously [ 14, 16].
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