2000
DOI: 10.1016/s0304-4017(00)00231-4
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Evaluation of antigen-coating procedures of enzyme-linked immunosorbent assay method for detection of trypanosomal antibodies

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Cited by 11 publications
(5 citation statements)
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“…Compared with the freshly coated wells, there was also less variation in the precoated wells stored at either 4°C (coefficient of variation [CV] for positives, 21.5 versus 9.8; CV for negatives, 87.0 versus 23.6) or room temperature (CV for positives, 14.6 versus 8; CV for negatives, 88.7 versus 19.4). Similar assay stability has recently been reported for up to 12 months and at temperatures up to 50°C by Rebeski et al in a whole, fixed Trypanosoma congolense EIA (29,30).…”
Section: Vol 42 2004supporting
confidence: 51%
“…Compared with the freshly coated wells, there was also less variation in the precoated wells stored at either 4°C (coefficient of variation [CV] for positives, 21.5 versus 9.8; CV for negatives, 87.0 versus 23.6) or room temperature (CV for positives, 14.6 versus 8; CV for negatives, 88.7 versus 19.4). Similar assay stability has recently been reported for up to 12 months and at temperatures up to 50°C by Rebeski et al in a whole, fixed Trypanosoma congolense EIA (29,30).…”
Section: Vol 42 2004supporting
confidence: 51%
“…In particular PCR, which is a very sensitive technique for detecting trypanosomes (Moser et al, 1989;Masiga et al, 1992;Majiwa et al, 1994;Solano and Amsler-Delafosse, 1995;Reifenberg et al, 1997;Lefrançois et al, 1998), has limited use in routine diagnosis due to the need of specific laboratory facilities, common DNA cross-contamination, and high costs. While detection of trypanosome antigens lacks sensitivity and specificity (Desquesnes, 1996;Eisler et al, 1998;Rebeski et al, 1999), assays for detection of anti-trypanosome circulating antibodies have high measures of validity and are economical and applicable at a large scale (Reyna-Bello et al, 1998;Rebeski et al, 2000;Lejon et al, 2003).…”
Section: Introductionmentioning
confidence: 99%
“…no concentration steps needed). Furthermore, our previous work (Berrizbeitia et al , 2004) as well as that of Rebeski et al (2000) suggest that the fixed‐organism antigens can also be stable over prolonged periods at room temperature if stored with an appropriate desiccant. Although there were subtle differences between the performance of the fixed‐epimastigote and fixed‐trypomastigote EIAs, it is not clear whether or not the slight specificity advantage of the trypomastigote‐based test is clinically relevant or trumps the simpler protocol for growing epimastigotes in culture.…”
Section: Discussionmentioning
confidence: 90%