| Project/Area Number | 01480169 |
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| Research Category |
Grant-in-Aid for General Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
寄生虫学(含医用動物学）
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| Research Institution | Akita University |
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Principal Investigator |
YOSHIMURA Kentaro Akita University, Professor, 医学部, 教授 (90053058)
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| Co-Investigator(Kenkyū-buntansha) |
SHIMADA Hiroko Akita University, Research Associate, 医学部, 助手 (30235626)
ISHIDA Kazuto Akita University, Research Associate, 医学部, 助手 (60006731)
TANI Shigekazu Akita University, Research Associate, 医学部, 助手 (10006728)
ABE Tatsuya Akita University, Associate professor, 医学部, 助教授 (80128363)
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| Project Period (FY) |
1989 – 1991
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| Project Status |
Completed(Fiscal Year 1991)
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| Budget Amount *help |
¥6,600,000 (Direct Cost : ¥6,600,000)
Fiscal Year 1991 : ¥1,400,000 (Direct Cost : ¥1,400,000)
Fiscal Year 1990 : ¥1,400,000 (Direct Cost : ¥1,400,000)
Fiscal Year 1989 : ¥3,800,000 (Direct Cost : ¥3,800,000)
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| Keywords | Angiostrongylus cantonensis / eosinophil / eosinophil chemotactic factor / cerebrospinal fluid / monoclonal antibody / hypodense eosinophil / affinity chromatography / chemotactic assay / 間接蛍光抗体法 / Mesocestoides corti / ELISA / Western blotting / レセプタ- / モルモット / ラット |
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| Research Abstract |
This study deals with the possible mechanisms of local eosinophil infiltrations in Angiostrongylus cantonensis infections with special emphasis on parasite-derived eosinophil chemotactic factors and their receptors. The results obtained are sunearized as follows : Guinea-pig-eosinophils possess receptor (s) against eosinophil chemotactic factor (s) (ECF) derived from the young adult wores of A. cantonensis (YA), whereas rateosinophils are devoid of the receptor or, if any, the numbers of the receptor are few. The receptor is proteinaceous and reproducible. Hybridomas prepared from spleen cells of mice igmunized with partially Purified ECF-YA produced 2 kinds of sonoclonal antibodies (mabs) recognizing either 16.1 kD or 85 kD component in YA-whole wore extract. These mAbs were IgGl isotype. Both mAbs werespecifically reactive to ECF-YA, but failed to react to the respective whole worm extracts of A. cantonensis first stage larvae, Metastrangylus apri, Fasciola sp. and Spirometra erinace
… More
i plerocercoids. Several mAbs against 16.1 kD and 85 kD components all recognized the same corresponding epitopes on 16.1 kD and 85 kD antigens. Both anti-16.1 kD and anti-85 kD mAbs were capable of inhibiting eosinophil chemotactic activity of YA-whole worm extract but the former mAb gave a stronger inhibitory effect. The combination of both mAbs showed a stronger inhibitory effect than either mAb alone. Neither mAbs inhibited the chemotactic activity of ECFs derived from other helminth parasites. An affinity chromatography with anti-16.1 kD mAb succeeded in isolating a 16.1 kD antigen from YA-whole worm extracts. The ECF-YA was localized in the intestinal cytoplasm of the young adult worms. The ECF-YA can be discharged from the worms as an excretory and secretory product. Eosinophils in the cerebrospinal fluid (CSF) of mice infected with A. cantonensis were hypodense, while blood eosinophils from the same animals were normodense. Blood eosinophilia induced by the previous infection with other helminth parasite (Mesocestoides corti) failed to lead to CSF eosinophilia in subsequent A. cantonensis infection. CSF eosinophilia in A. cantonensis infection is probably provoked by ECF-YA and/or cytokines produced by lymphocytes sensitized with A. cantonensis antigens. Less
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