TY - JOUR
T1 - Serodiagnosis of neurocysticercosis using synthetic 8-KD proteins
T2 - Comparison of assay formats
AU - Scheel, Christina M.
AU - Khan, Azra
AU - Hancock, Kathy
AU - Garcia, Hector H.
AU - Gonzalez, Armando E.
AU - Gilman, Robert H.
AU - Tsang, Victor C.W.
AU - Mayta, H.
AU - Lopez, M. T.
AU - Silva, M.
AU - Rodriguez, S.
AU - Noh, J.
PY - 2005/10
Y1 - 2005/10
N2 - The assay of choice for serological detection of cysticercosis in humans and pigs is the enzyme-linked immunoelectrotransfer blot (EITB), a Western blot assay that relies on the use of seven lentil-lectin-purified glycoproteins (LLGPs) derived from Taenia solium metacestodes. The EITB is has a sensitivity of 98% and a specificity of 100% in detecting cysticercosis, yet scarcity of native source material and the labor-intensive process of metacestode purification hinder its practicality. These limitations have necessitated the reproduction of the EITB antigens in synthetic forms. Four chemically synthesized LLGP antigens, TS14, TS18var1, TSRS1, and TSRS2var1, were assayed individually by enzyme-linked immunosorbent assay (ELISA) and Western blot for immunoreactivity against a large cohort of sera from clinically defined neurocysticercosis patients. The sensitivity and specificity of all four of these antigens using the ELISA format were well below the standards set by the LLGP EITB, whereas results of the Western blot format closely mirrored those of the LLGP EITB.
AB - The assay of choice for serological detection of cysticercosis in humans and pigs is the enzyme-linked immunoelectrotransfer blot (EITB), a Western blot assay that relies on the use of seven lentil-lectin-purified glycoproteins (LLGPs) derived from Taenia solium metacestodes. The EITB is has a sensitivity of 98% and a specificity of 100% in detecting cysticercosis, yet scarcity of native source material and the labor-intensive process of metacestode purification hinder its practicality. These limitations have necessitated the reproduction of the EITB antigens in synthetic forms. Four chemically synthesized LLGP antigens, TS14, TS18var1, TSRS1, and TSRS2var1, were assayed individually by enzyme-linked immunosorbent assay (ELISA) and Western blot for immunoreactivity against a large cohort of sera from clinically defined neurocysticercosis patients. The sensitivity and specificity of all four of these antigens using the ELISA format were well below the standards set by the LLGP EITB, whereas results of the Western blot format closely mirrored those of the LLGP EITB.
UR - http://www.scopus.com/inward/record.url?scp=26844483492&partnerID=8YFLogxK
U2 - 10.4269/ajtmh.2005.73.771
DO - 10.4269/ajtmh.2005.73.771
M3 - Artículo
C2 - 16222024
AN - SCOPUS:26844483492
SN - 0002-9637
VL - 73
SP - 771
EP - 776
JO - American Journal of Tropical Medicine and Hygiene
JF - American Journal of Tropical Medicine and Hygiene
IS - 4
ER -