Project/Area Number |
59440017
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Research Category |
Grant-in-Aid for General Scientific Research (A)
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Allocation Type | Single-year Grants |
Research Field |
Applied veterinary science
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Research Institution | OBIHIRO UNIVERSITY |
Principal Investigator |
SUZUKI Naoyoshi Prof., Dept. Vet. Physiol. & Protozoan Immunol.,Obihiro University, 畜産学部, 教授 (10003071)
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Co-Investigator(Kenkyū-buntansha) |
SATO Motoyoshi Assist.Prof.,Dept. Vet. Clinical Radiology, Obihiro University, 畜産学部獣医放射線学講座, 講師 (50003140)
MIKAMI Masayuki Assoc.Prof.,Dept. Animal Science, Obihiro University, 畜産学部肉畜保蔵学講座, 助教授 (40003107)
SAITO Atsushi Assoc.Prof., Dept.Vet.Physiol. & Protozoan Immunol.,Obihiro University, 畜産学部家畜生理学講座, 助教授 (10002263)
MIURA Hiroyuki Prof.,Dept. Animal Science, Obihiro University, 畜産学部肉畜保蔵学講座, 教授 (90003079)
HIROSE Tsuneo Prof.,Dept. Vet. Clinical Radiology, Obihiro University, 畜産学部獣医放射線学講座, 教授 (60003076)
|
Project Period (FY) |
1984 – 1986
|
Project Status |
Completed (Fiscal Year 1986)
|
Budget Amount *help |
¥25,500,000 (Direct Cost: ¥25,500,000)
Fiscal Year 1986: ¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 1985: ¥6,000,000 (Direct Cost: ¥6,000,000)
Fiscal Year 1984: ¥15,500,000 (Direct Cost: ¥15,500,000)
|
Keywords | Long-term suspension culture / Toxoplasma gondii / Babesia rodhaini / Plasmodium berghei / Immunomodulator / TLA / Immunoregulator / Obioactin / オビオアクチン / BRM / 組織培養 / モジュレーター |
Research Abstract |
When animals (mice, rats and cattle) were pretreated with Toxoplasma lysate antigens(TLA), lymphokines such as IFN,MAF,MIF,TOXO-GIF appeared in their blood and they showed a strong non-specific resistance. In consequence, in order to clarify the defence mechanisms which can be induced by TLA against various infections, the mass cultivation of Toxoplasma organisms is necessary. Within the research period of this Grant, we established as the lst report in the world, a method of mass and long term propagation of Toxoplasma in suspension cultures for 30-60 days period and also found a technique for separation of the organisms from host cells automatically, using a microcomputer-controlled system. Then, TLA was used to examine the effect of immunomodulator in reducing clinical symptoms of Babesia, Plasmodium or Theileria infection in animals. In the main results obtained in our studies, non of the mice in the non-TLA treated control groups survived for more than 2 weeks after Babesia or Plasmodium infection, however, mice pretreated with TLA alone or together with lymphokiens or Obioactin survived in a high percentage. In the pretreated cattle infected with Theileria, the clinical symptoms and anemia were extremly slight as compared with those of the non-TLA treated cattle. When animals were treated with TLA, Thy-1 and <Lyt^1> positive and <Lyt^2> negative lymphocytes were found to accumulate remarkably in the thymus and spleen and there was a remarkable increase in the immune response of the host to infection with protozoan organisms.
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