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Strongyloides ratti antigenic components recognized by IgE antibodies in immunoblotting as an additional tool for improving the immunodiagnosis in human strongyloidiasis
Rodrigues, Rosângela Maria; Sopelete, Mônica Camargo; Silva, Deise Aparecida de Oliveira; Cunha-Júnior, Jair Pereira; Taketomi, Ernesto Akio; Costa-Cruz, Julia Maria.
  • Rodrigues, Rosângela Maria; Universidade Federal de Uberlândia. Instituto de Ciências Biomédicas. Departamento de Imunologia, Microbiologia e Parasitologia. Uberlândia. BR
  • Sopelete, Mônica Camargo; Universidade Federal de Uberlândia. Instituto de Ciências Biomédicas. Departamento de Imunologia, Microbiologia e Parasitologia. Uberlândia. BR
  • Silva, Deise Aparecida de Oliveira; Universidade Federal de Uberlândia. Instituto de Ciências Biomédicas. Departamento de Imunologia, Microbiologia e Parasitologia. Uberlândia. BR
  • Cunha-Júnior, Jair Pereira; Universidade Federal de Uberlândia. Instituto de Ciências Biomédicas. Departamento de Imunologia, Microbiologia e Parasitologia. Uberlândia. BR
  • Taketomi, Ernesto Akio; Universidade Federal de Uberlândia. Instituto de Ciências Biomédicas. Departamento de Imunologia, Microbiologia e Parasitologia. Uberlândia. BR
  • Costa-Cruz, Julia Maria; Universidade Federal de Uberlândia. Instituto de Ciências Biomédicas. Departamento de Imunologia, Microbiologia e Parasitologia. Uberlândia. BR
Mem. Inst. Oswaldo Cruz ; 99(1): 89-93, Feb. 2004. ilus, graf
Article in English | LILACS | ID: lil-356450
RESUMO
IgE antibody response in human strongyloidiasis was evaluated by enzyme-linked immunosorbent assay (ELISA) and immunoblotting (IB) using Strongyloides ratti saline extract as heterologous antigen. A total of 50 serum samples of patients who were shedding S. stercoralis larvae in feces (group I, copropositive), 38 of patients with other intestinal parasites (group II), and 38 of subjects with negative results in three parasitologic assays (group III, copronegative) were analyzed. Levels of IgE anti-Strongyloides expressed in ELISA Index (EI) were significantly higher in patients of group I (1.32) than in group II (0.51) and group III (0.81), with positivity rates of 54 percent, 0 percent, and 10.5 percent, respectively. Fifteen S. ratti antigenic components were recognized in IB-IgE by sera of group I, with frequency ranging from 8 percent to 46 percent. In group II, only two antigenic bands (101, 81 kDa) were detected in a frequency of 10 percent and no reactivity was found in group III. Sera with EI values > 1.5 recognized five from 13 specific antigenic bands (70, 63, 61, 44, 7 kDa). It can be concluded that these five antigenic components recognized by IB-IgE using S. ratti antigen might be employed as an additional tool for improving the immunodiagnosis in human strongyloidiasis.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Strongyloidiasis / Antibodies, Helminth / Strongyloides ratti / Antigens, Helminth Limits: Animals / Humans Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2004 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal de Uberlândia/BR

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Full text: Available Index: LILACS (Americas) Main subject: Strongyloidiasis / Antibodies, Helminth / Strongyloides ratti / Antigens, Helminth Limits: Animals / Humans Language: English Journal: Mem. Inst. Oswaldo Cruz Journal subject: Tropical Medicine / Parasitology Year: 2004 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal de Uberlândia/BR