1999 Fiscal Year Final Research Report Summary
MOLECULAR MECHANISM OF THE THIRD TYPE OF CELL DEATH AND ITS APPLICATION FOR SPECIFIC IMMUNOSUPPRESSIVE THERAPY
| Project/Area Number |
09557048
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 展開研究 |
|---|
| Research Field |
内科学一般
|
|---|
| Research Institution | EHIME UNIVERSITY |
|---|
Principal Investigator |
ASANO Yoshihiro EHIME UNIVERSITY, SCHOOL OF MEDICINE, PROFESSOR, 医学部, 教授 (70114353)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
SUMITA Kohsuke EHIME UNIVERSITY, SCHOOL OF MEDICINE, RESEARCH ASSOCIATE, 医学部, 助手 (20281454)
KANOH Makoto EHIME UNIVERSITY, SCHOOL OF MEDICINE, ASSISTANT PROFESSOR, 医学部, 講師 (10116923)
SHINOMIYA Hirota EHIME UNIVERSITY, SCHOOL OF MEDICINE, ASSOCIATE PROFESSOR, 医学部, 助教授 (80162618)
|
|---|
| Project Period (FY) |
1997 – 1999
|
| Keywords | fractionated irradiation / immunological tolerance / cell death / MHC molecules / pluripotent stem cells |
|---|
| Research Abstract |
A monoclonal antibody (mAb), RE2, directly kill activated lymphocytes without participation of complement through a novel pathway of call death. The present study was carried out to clarify the mechanism of and participating molecules of this novel type of cell death and to establish specific immunosuppressive method using this mAb. Using expression cloning method, we cloned the genes coding for the molecules reactive with the mAb. MHC class I molecules (KィイD1kィエD1 and KィイD1bィエD1) were turned out to be target molecules of RE2 mAb. However, antibody specific to KィイD1kィエD1, 11-4.1, did not induce cell death in the activated lymphocytes. Therefore, we think that the unknown molecule(s) associated with KィイD1kィエD1 or KィイD1bィエD1 is responsible for this novel type of cell death.
Alloantigen-specific tolerance was successfully induced by fractionated irradiation together with injection of alloantigen. We think the combined treatment of animals with fractionated irradiation and RE2-administration may provide a stable method of tolerance induction.
|
-
-
-
-
-
-
-
[Publications] Taki, S., T. Sato, K. Ogasawara, T. Fukuda, M. Sato, S. Hide, G. Suzuki, M. Mitsuyama, E-H. Shin, S. Kojima, T. Taniguchi, and Y. Asano: "Multi-stage regulation of Th1-type immune responses by the transcription factor IRF-1"Immunity. 6. 673 (1997)
Description
「研究成果報告書概要(欧文)」より
-
[Publications] Tan, R. S-P., A. U. Kara, C. Feng, and Y. Asano: "Nitoric oxide is not essential in the protection of Plasmodium berghei blood stage murine malaria infection in IRF-1 (interferon regulatory factor-1) deficient mice"9th International Congress of Parasitology, eds., Tada, I., Kojima, S., and Tsuji, M., Monduzzi Editore, Italy. 1003-1007 (1998)
Description
「研究成果報告書概要(欧文)」より
-
-
-
-
-
