TY - JOUR
T1 - Improved Diagnosis of Viable Parenchymal Neurocysticercosis by Combining Antibody Banding Patterns on Enzyme-Linked Immunoelectrotransfer Blot (EITB) with Antigen Enzyme-Linked Immunosorbent Assay (ELISA)
AU - the Cysticercosis Working Group in Peru (CWGP)
AU - Arroyo, Gianfranco
AU - Bustos, Javier A.
AU - Lescano, Andres G.
AU - Gonzales, Isidro
AU - Saavedra, Herbert
AU - Pretell, E. Javier
AU - Castillo, Yesenia
AU - Perez, Erika
AU - Dorny, Pierre
AU - Gilman, Robert H.
AU - O'Neal, Seth E.
AU - Gonzalez, Armando E.
AU - Garcia, Hector H.
AU - Verastegui, Manuela
AU - Zimic, Mirko
AU - Sanchez, Sofia
AU - Martinez, Manuel
AU - Mayta, Holger
AU - Santivañez, Saul
AU - Pajuelo, Monica
AU - Lopez, Maria T.
AU - Gomez-Puerta, Luis
AU - Vargas-Calla, Ana
AU - Gonzalez-Gustavson, Eloy
AU - Moyano, Luz M.
AU - Gamboa, Ricardo
AU - Vilchez, Percy
AU - Muro, Claudio
AU - Nash, Theodore
AU - Friedland, Jon
N1 - Publisher Copyright:
© 2022 American Society for Microbiology. All Rights Reserved.
PY - 2022/2
Y1 - 2022/2
N2 - The diagnosis of neurocysticercosis (NCC) depends on neuroimaging and serological confirmation. While antibody detection by enzyme-linked immunoelectrotransfer blot (EITB) fails to predict viable NCC, EITB banding patterns provide information about the host's infection course. Adding antigen enzyme-linked immunosorbent assay (Ag-ELISA) results to EITB banding patterns may improve their ability to predict or rule out of viable NCC. We assessed whether combining EITB banding patterns with Ag-ELISA improves discrimination of viable infection in imaging-confirmed parenchymal NCC. EITB banding patterns were grouped into classes using latent class analysis. True-positive and false-negative Ag-ELISA results in each class were compared using Fisher's exact test. Four classes were identified: 1, EITB negative or positive to GP50 alone (GP50 antigen family); 2, positive to GP42-39 and GP24 (T24/42 family), with or without GP50; and 3 and 4, positive to GP50, GP42-39, and GP24 and reacting to bands in the 8-kDa family. Most cases in classes 3 and 4 had viable NCC (82% and 88%, respectively) compared to classes 2 and 1 (53% and 5%, respectively). Adding positive Ag-ELISA results to class 2 predicted all viable NCC cases (22/22 [100%]), whereas 11/40 patients (27.5%) Ag-ELISA negative had viable NCC (P, 0.001). Only 1/4 patients (25%) Ag-ELISA positive in class 1 had viable NCC, whereas 1/36 patients (2.8%) Ag-ELISA negative had viable NCC (P = 0.192). In classes 3 and 4, adding Ag-ELISA was not contributory. Combining Ag-ELISA with EITB banding patterns improves discrimination of viable from nonviable NCC, particularly for class 2 responses. Together, these complement neuroimaging more appropriately for the diagnosis of viable NCC.
AB - The diagnosis of neurocysticercosis (NCC) depends on neuroimaging and serological confirmation. While antibody detection by enzyme-linked immunoelectrotransfer blot (EITB) fails to predict viable NCC, EITB banding patterns provide information about the host's infection course. Adding antigen enzyme-linked immunosorbent assay (Ag-ELISA) results to EITB banding patterns may improve their ability to predict or rule out of viable NCC. We assessed whether combining EITB banding patterns with Ag-ELISA improves discrimination of viable infection in imaging-confirmed parenchymal NCC. EITB banding patterns were grouped into classes using latent class analysis. True-positive and false-negative Ag-ELISA results in each class were compared using Fisher's exact test. Four classes were identified: 1, EITB negative or positive to GP50 alone (GP50 antigen family); 2, positive to GP42-39 and GP24 (T24/42 family), with or without GP50; and 3 and 4, positive to GP50, GP42-39, and GP24 and reacting to bands in the 8-kDa family. Most cases in classes 3 and 4 had viable NCC (82% and 88%, respectively) compared to classes 2 and 1 (53% and 5%, respectively). Adding positive Ag-ELISA results to class 2 predicted all viable NCC cases (22/22 [100%]), whereas 11/40 patients (27.5%) Ag-ELISA negative had viable NCC (P, 0.001). Only 1/4 patients (25%) Ag-ELISA positive in class 1 had viable NCC, whereas 1/36 patients (2.8%) Ag-ELISA negative had viable NCC (P = 0.192). In classes 3 and 4, adding Ag-ELISA was not contributory. Combining Ag-ELISA with EITB banding patterns improves discrimination of viable from nonviable NCC, particularly for class 2 responses. Together, these complement neuroimaging more appropriately for the diagnosis of viable NCC.
KW - Ag-ELISA
KW - EITB banding patterns
KW - Taenia solium
KW - viable NCC
UR - http://www.scopus.com/inward/record.url?scp=85124809599&partnerID=8YFLogxK
U2 - 10.1128/jcm.01550-21
DO - 10.1128/jcm.01550-21
M3 - Original Article
C2 - 34851685
AN - SCOPUS:85124809599
SN - 0095-1137
VL - 60
JO - Journal of Clinical Microbiology
JF - Journal of Clinical Microbiology
IS - 2
M1 - e01550-21
ER -