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Development of a Bead Immunoassay To Measure Vi Polysaccharide-Specific Serum IgG after Vaccination with the Salmonella enterica Serovar Typhi Vi Polysaccharide ▿

机译:接种沙门氏菌血清型伤寒沙门氏菌Vi多糖疫苗后可测量Vi多糖特异性血清IgG的珠粒免疫分析方法的开发▿

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摘要

Vi polysaccharide from Salmonella enterica serotype Typhi is used as one of the available vaccines to prevent typhoid fever. Measurement of Vi-specific serum antibodies after vaccination with Vi polysaccharide by enzyme-linked immunosorbent assay (ELISA) may be complicated due to poor binding of the Vi polysaccharide to ELISA plates resulting in poor reproducibility of measured antibody responses. We chemically conjugated Vi polysaccharide to fluorescent beads and performed studies to determine if a bead-based immunoassay provided a reproducible method to measure vaccine-induced anti-Vi serum IgG antibodies. Compared to ELISA, the Vi bead immunoassay had a lower background and therefore a greater signal-to-noise ratio. The Vi bead immunoassay was used to evaluate serum anti-Vi IgG in 996 subjects from the city of Kolkata, India, before and after vaccination. Due to the location being one where Salmonella serotype Typhi is endemic, approximately 45% of the subjects had protective levels of anti-Vi serum IgG (i.e., 1 μg/ml anti-Vi IgG) before vaccination, and nearly 98% of the subjects had protective levels of anti-Vi serum IgG after vaccination. Our results demonstrate that a bead-based immunoassay provides an effective, reproducible method to measure serum anti-Vi IgG responses before and after vaccination with the Vi polysaccharide vaccine.
机译:鼠伤寒沙门氏菌血清型伤寒病毒的Vi多糖被用作预防伤寒的可用疫苗之一。通过酶联免疫吸附测定(ELISA)接种Vi多糖后,对Vi特异性血清抗体的测量可能会很复杂,因为Vi多糖与ELISA板的结合力较差,导致所测抗体反应的再现性较差。我们将Vi多糖化学缀合到荧光珠上,并进行研究以确定基于珠的免疫测定法是否提供了可重复性的方法来测量疫苗诱导的抗Vi血清IgG抗体。与ELISA相比,Vi珠免疫分析的背景较低,因此信噪比更高。在注射之前和之后,使用Vi bead免疫测定法评估了来自印度加尔各答市的996位受试者的血清抗Vi IgG。由于该位置是伤寒沙门氏菌血清型的地方,约有45%的受试者在接种疫苗前具有抗Vi血清IgG的保护水平(即1μg/ ml的抗Vi IgG),近98%的受试者接种疫苗后具有抗Vi血清IgG的保护水平。我们的结果表明,基于珠的免疫测定提供了一种有效,可重复的方法,可以在接种Vi多糖疫苗之前和之后测量血清抗Vi IgG应答。

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