| Project/Area Number |
11670237
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
寄生虫学(含医用動物学)
|
|---|
| Research Institution | AKITA UNIVERSITY |
|---|
Principal Investigator |
SHIMADA Hiroko Akita University, School of Medicine, Research Associate, 医学部, 助手 (30235626)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
YOSHIMURA Kentaro Akita University, School of Medicine, Professor, 医学部, 教授 (90053058)
ISHIDA Kazuto Akita University, School of Medicine, Research Associate, 医学部, 助手 (60006731)
|
|---|
| Project Period (FY) |
1999 – 2000
|
| Project Status |
Completed (Fiscal Year 2000)
|
| Budget Amount *help |
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2000: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1999: ¥2,600,000 (Direct Cost: ¥2,600,000)
|
|---|
| Keywords | Angiostrongylus cantonensis / CD4^+T-cell / Morbidity / Interferon-γ / IL-4 / BALB / c / T cell blot / Nitric oxide / T blot / SAS-PAGE / X線 / magnetic microbeads / 抗IL-4モノクローナル抗体 / 好酸球増多 |
|---|
| Research Abstract |
There are murine strain dependent differences in susceptibility and host morbidity to Angiostrongylus cantonensis infection. The body weight reduction in A.cantonensis-infected BALB/c mice starting at around day 15 post-infection (p.i.) is CD4^+T cell-dependent. The aim of this study is, therefore, to determine the mechanism (s) of CD4^+T cell-mediated host morbidity of A.cantonensis-infected BALB/c strain mice. The results are as follows : 1. An attempt to induce A.cantonensis antigen specific Th1/Th2 clones from splenic CD4^+T cells separated from A.cantonensis-infected BALB/c mice at days 15-16 p.i. by the standard procedure was unsuccessful. Drastic improvement of the method is now planning. 2. It is unlikely that both IL-4 and interferon-γ are related to host morbidity, since body weight reduction was observed in mice treated with anti-IL-4 monoclonal antibody and in interferon-γ knockout mice. 3. Nitric oxide is not involved in the host morbidity in BALB/c mice, since body weight changes in A.cantonensis-infected BALB/c mice cannot be affected by the intraperitoneal administration of aminoguanidine, inhibitor of iNOS, in vivo. 4. Splenic CD4^+T cells separated from A.cantonensis-infected BALB/c mice at days 13-20 p.i. showed significant proliferative activity to young adult worm antigen proteins with molecular weights of 56, 48, 40, 31-22 kDa. 5. BALB/c mice infected with X-ray-irradiated third stage larvae yielded a lower worm recovery, but showed body weight reduction. It indicates that the body weight reduction probably is not related to the worm load, but closely associated with CD4^+T cell-mediated inflammatory responses in the brain with pleocytosis in the cerebrospinal fluid.
|
