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Immunological characterization of Echinococcus granulosus cyclophilin, an allergen reactive with IgE and IgG4 from patients with cystic echinococcosis
Abstract
SUMMARY: By immunological screening of a cDNA library derived from protoscoleces of Echinococcus granulosus with IgE from patients with cystic echinococcosis (CE) and allergic manifestations, we isolated a protein identical to E. granulosus cyclophilin. The protein, named EA21, has close homology with Malassezia furfur cyclophilin allergen (Mal f 6) and with human cyclophilin. Using immunoblotting (IB) with a polyclonal antibody specific to EA21, we identified E. granulosus cyclophilin both in protoscoleces and in sheep hydatid fluid. Of the 58 sera from patients with CE, 29 (50%) were IgE positive to EA21, whereas, despite the high sequence homology, none were IgE positive to Mal f 6 or human cyclophilin. Only 26 of the 58 patients (45%) had IgG specific to EA21, whereas all patients (100%) had IgG specific to Mal f 6 and human cyclophilin. IB analysis showed that serum IgE-binding reactivity to EA21 differed significantly in patients with and without allergic reactions (20 of 25, 80%versus nine of 33, 27%; P < 10–4). Conversely, five of the 25 patients who had CE-related allergic manifestations (20%) and 21 of the 33 who did not (63%) had specific IgG4 (P = 10–3) and total IgG to EA21. EA21 induced a proliferative response in 15 of 19 (79%) patients’ PBMC regardless of the allergic manifestations, but it induced no IL-4 production. Overall, these findings suggest that E. granulosus cyclophilin is a conserved, constitutive, parasite protein that does not cross-react with cyclophilins from other organisms and is involved in the allergic symptoms related to CE.
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“Similarly, glutathione S-transferases from Schistosoma haematobium and cyclophilin from Echinococcus granulosus represent examples of conserved molecules that may contribute to cross-reactive antibody responses (Boumis et al. 2011; Ortona et al. 2002).”
From Parasites and allergies: a complex bidirectional relationship from evolutionary origins to modern therapeutics (2026) · cites this paper as Ortona et al. 2002
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Cited by
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Packi, K., Świerczewski, D., Klimczak, S., Ochab, D., Gałęziewska, J., Gromek, P., Kruczkowska, W., Płuciennik, E., Kałuzińska-Kołat, Ż., & Kołat, D. (2026) · Antonie van Leeuwenhoek · doi:10.1007/s10482-026-02425-4
Metadata
- Authors
- ORTONA, E., VACCARI, S., MARGUTTI, P., DELUNARDO, F., RIGANÒ, R., PROFUMO, E., BUTTARI, B., RASOOL, O., TEGGI, A., & SIRACUSANO, A.
- Venue
- Clinical and Experimental Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-04
- Volume
- 128
- Issue
- 1
- Pages
- 124-130
- ISSN
- 0009-9104
- 1365-2249
- Cited by
- 45
- References
- 0
- Language
- en
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- ORTONA, E., VACCARI, S., MARGUTTI, P., DELUNARDO, F., RIGANÒ, R., PROFUMO, E., BUTTARI, B., RASOOL, O., TEGGI, A., & SIRACUSANO, A. (2002). Immunological characterization of Echinococcus granulosus cyclophilin, an allergen reactive with IgE and IgG4 from patients with cystic echinococcosis. Clinical and Experimental Immunology. https://doi.org/10.1046/j.1365-2249.2002.01807.x