1992
DOI: 10.1111/j.1365-3024.1992.tb00035.x
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Characterization of monoclonal antibodies against eosinophil chemotactic factors from young adult worms of Angiostrongylus cantonensis

Abstract: Two kinds of IgG1 monoclonal antibodies against eosinophil chemotactic factors (ECFs) derived from Angiostrongylus cantonensis young adult worms (YA) were established. Western blot analyses demonstrated that one monoclonal antibody recognized a 16.1 kD component of YA-whole worm extract, and the other an 85 kD component. These antibodies did not show any cross reactions against several helminth antigens, as assessed by ELISA. The chemotactic activity of YA-whole worm extract for guinea-pig-eosinophils was sign… Show more

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Cited by 9 publications
(4 citation statements)
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“…The patients’ peripheral blood and stool samples were investigated over a few consecutive days. For the serological testing, we extracted the crude antigens from adult worms of F. hepatica and F. gigantica isolated from infected cattle and then connected the antigens to panels according to Ishida et al [17] and Chen et al [18]. Briefly, worms washed in phosphate-buffered saline (PBS, pH7.4) were individually homogenized with a tissue homogenizer for 3 minutes.…”
Section: Methodsmentioning
confidence: 99%
“…The patients’ peripheral blood and stool samples were investigated over a few consecutive days. For the serological testing, we extracted the crude antigens from adult worms of F. hepatica and F. gigantica isolated from infected cattle and then connected the antigens to panels according to Ishida et al [17] and Chen et al [18]. Briefly, worms washed in phosphate-buffered saline (PBS, pH7.4) were individually homogenized with a tissue homogenizer for 3 minutes.…”
Section: Methodsmentioning
confidence: 99%
“…However, only four to five antigen bands ( 29 kDa, 31 kDa, 55 kDa, 85-99 kDa, 200-204 kDa) can be considered as relevant for the serological diagnosis of A. cantonensis [11][12][13]. In our patient, four specific antigen bands (IgG) were seen.The specificity of A. cantonensis Western blot among helminthiasis is critical and cross-reactivity is inevitable.…”
Section: Discussionmentioning
confidence: 86%
“…Whole worm antigens of A. cantonensis , P. westermani , T. spiralis and plerocercoids of Spirometra spp. were prepared following the standard protocol according to Ishida et al [45] and Chen et al [43]. Briefly, parasites were washed in phosphate-buffered saline (PBS), pH7.4 3 times, then homogenized in PBS with a tissue homogenizer (Bio-Gen PRO200 Homogenizer, PRO Scientific Inc., Oxford, CT, USA) for 3 minutes.…”
Section: Methodsmentioning
confidence: 99%