# Comparative assessment of immunochromatographic test kits using low-molecular-weight antigens from cyst fluids of two different genotypes of Taenia solium for serodiagnosis of human cysticercosis

**Authors:** Lakkhana Sadaow, Penchom Janwan, Patcharaporn Boonroumkaew, Rutchanee Rodpai, Oranuch Sanpool, Tongjit Thanchomnang, Marcello Otake Sato, Pewpan M. Intapan, Hiroshi Yamasaki, Yasuhito Sako, Toni Wandra, Kadek Swastika, Wanchai Maleewong

PMC · DOI: 10.1051/parasite/2026003 · Parasite · 2026-01-23

## TL;DR

Researchers tested two types of rapid diagnostic kits for human cysticercosis using purified antigens from different Taenia solium genotypes and found them to be effective with high accuracy.

## Contribution

Development and evaluation of immunochromatography-based diagnostic kits using purified low-molecular-weight antigens from two T. solium genotypes.

## Key findings

- The American genotype-based ICT kit had 83.3% sensitivity and 93.6% specificity.
- The Asian genotype-based ICT kit showed 87.5% sensitivity and 98.6% specificity.
- Both kits demonstrated substantial agreement (Cohen’s kappa of 0.77) and better diagnostic specificity than a crude antigen-based ICT kit.

## Abstract

Human cysticercosis is a serious zoonosis caused by infection with larvae (cysticerci) of the pork tapeworm, Taenia solium. Infection can involve the nervous system, causing chronic headache and intracranial hypertension, focal neurological deficits, epileptic seizures, and paralysis. The disease is found in developing countries, where porcine cysticercosis is prevalent and undercooked pork is habitually consumed. This study aimed to develop immunochromatography-based test (ICT) kits, using low-molecular-weight antigens purified from cyst fluids of Latin American and Asian genotypes of T. solium. To evaluate the kits, we used 164 serum samples, including 24 from proven/confirmed cysticercosis cases, 110 from cases with other parasitoses, and 30 from healthy individuals. Diagnostic performances were calculated. The sensitivity, specificity, and accuracy were 83.3% (95% CI [62.6–95.3]), 93.6% (95% CI [88.1–97.0]), and 92.1% (95% CI [86.8–95.7]), respectively for the American genotype-based ICT kit, while for the Asian genotype-based ICT kit, they were 87.5% (95% CI [67.6–97.3]), 98.6% (95% CI [94.9–99.8]), and 97.0% (95% CI [93.0–99.0]), respectively. The sensitivity and specificity did not significantly differ between the two ICT kits (exact McNemar’s test; p > 0.05), with a concordance of 93.9%, represented by a Cohen’s kappa of 0.77 (p < 0.001), indicating substantial agreement. These results indicate that affinity-purified antigens from different geographical isolates can be used for the diagnosis of human cysticercosis. The diagnostic specificities were better than for a previously reported ICT kit that used crude antigen.

## Linked entities

- **Diseases:** cysticercosis (MONDO:0015484)
- **Species:** Taenia solium (taxon 6204)

## Full-text entities

- **Genes:** SLC12A3 (solute carrier family 12 member 3) [NCBI Gene 6559] {aka NCC, NCCT, TSC}, COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512] {aka COI, MTCO1}, CCL14 (C-C motif chemokine ligand 14) [NCBI Gene 6358] {aka CC-1, CC-3, CKB1, HCC-1, HCC-1(1-74), HCC-1/HCC-3}
- **Diseases:** trichinosis (MESH:D014235), pork tapeworm (MESH:D002590), parasitic diseases (MESH:D010272), headache (MESH:D006261), neurological deficits (MESH:D009461), T. solium taeniosis (MESH:D001260), intestinal helminthic infection (MESH:D007410), eosinophilic meningoencephalitis (MESH:D008590), CYSTICERCOSIS (MESH:D003551), gnathostomiasis (MESH:D058429), Neurocysticercosis (MESH:D020019), Gs1 (MESH:C537301), loiasis (MESH:D008118), alveolar echinococcosis (MESH:C536591), Anisakiasis (MESH:D017129), Fascioliasis (MESH:D005211), paralysis (MESH:D010243), Infection (MESH:D007239), toxocariasis (MESH:D014120), Taeniasis (MESH:D013622), cerebral sparganosis (MESH:D013031), parasitosis (MESH:D063726), amebiasis (MESH:D000562), intracranial hypertension (MESH:D019586), T. solium cyst (MESH:D003560), F. gigantica (OMIM:102510), amebic liver abscess (MESH:D008101), Infectious Diseases (MESH:D003141), angiostrongyliasis (MESH:C536369), cerebral paragonimiasis (MESH:D010237), TS (MESH:D005879), capillariasis (MESH:D017189), epilepsy (MESH:D004827), vesicular lesions (MESH:D012872), cystic echinococcosis (MESH:D004443)
- **Chemicals:** EDTA (MESH:D004492), NaCl (MESH:D012965), HEPES (MESH:D006531), gold (MESH:D006046), fatty acids (MESH:D005227), sugar (MESH:D000073893), Am (MESH:D000576), CHAPS (MESH:C028213), Tris-HCl (-)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Taenia saginata (beef tapeworm, species) [taxon 6206], Taenia solium (pig tapeworm, species) [taxon 6204], Fasciola gigantica (species) [taxon 46835], Paragonimus westermani (species) [taxon 34504], Paracapillaria philippinensis (species) [taxon 1457282]
- **Cell lines:** Hc1 — Homo sapiens (Human), Adult hepatocellular carcinoma, Cancer cell line (CVCL_W518)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12829318/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829318/full.md

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Source: https://tomesphere.com/paper/PMC12829318