Table 3. Challenges for new serological tests for NCC diagnosis.
Test | Challenges |
Antibody test | Identify antigens or epitopes to maintain high sensitivity and specificity compared to native antigens. |
Increase the sensitivity for single brain lesion. | |
Identify antigens capable to differentiate exposure from infection. | |
Identify antigens capable to differentiate viable and non-viable cysticercosis. | |
Produce these antigens or epitopes in recombinant or synthetic way to have an easier and reproducible source of antigen. | |
Use these antigens or epitopes to develop a point of care test, to have a primary tool in field settings. | |
Antigen test | Produce MoAbs or nanobodies against T. solium metacestodes in order to increase sensitivity and specificity. |
Standardize a qualitative assay with a better reproducibility and repeatability. | |
Produce a test capable of differentiating viable and non-viable cysticercosis, with a high PPV for extraparenchymal NCC. | |
Assay needs to perform well in urine samples to avoid invasive and risky sampling methods. | |
Develop a point of care test, to have a primary tool in field settings. |
Note: NCC, neurocysticercosis.