Staats Herman F, Kirwan Shaun M, Whisnant Carol C, Stephenson James L, Wagener Diane K, Majumder Partha P
Department of Pathology, Duke University Medical Center, Durham, NC 27710, USA.
Clin Vaccine Immunol. 2010 Mar;17(3):412-9. doi: 10.1128/CVI.00354-09. Epub 2010 Jan 27.
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 microg/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.
伤寒沙门氏菌Vi多糖被用作预防伤寒热的现有疫苗之一。接种Vi多糖疫苗后,通过酶联免疫吸附测定(ELISA)检测Vi特异性血清抗体可能会很复杂,因为Vi多糖与ELISA板的结合不佳,导致所测抗体反应的重现性较差。我们将Vi多糖化学偶联到荧光珠上,并进行研究以确定基于珠子的免疫测定是否提供了一种可重现的方法来测量疫苗诱导的抗Vi血清IgG抗体。与ELISA相比,Vi珠子免疫测定的背景较低,因此信噪比更高。Vi珠子免疫测定用于评估印度加尔各答市996名受试者接种疫苗前后的血清抗Vi IgG。由于该地区是伤寒沙门氏菌的流行地区,大约45%的受试者在接种疫苗前具有抗Vi血清IgG的保护水平(即抗Vi IgG为1微克/毫升),接种疫苗后近98%的受试者具有抗Vi血清IgG的保护水平。我们的结果表明,基于珠子的免疫测定提供了一种有效、可重现的方法来测量接种Vi多糖疫苗前后的血清抗Vi IgG反应。