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The effects of anti-idiotypic antibody on antibody production and apoptosis of anti-dsDNA antibody producing cells.
DC Field | Value | Language |
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dc.contributor.author | Lee, CH | - |
dc.contributor.author | Suh, CH | - |
dc.contributor.author | Lee, J | - |
dc.contributor.author | Kim, YT | - |
dc.contributor.author | Lee, SK | - |
dc.date.accessioned | 2011-07-15T05:22:48Z | - |
dc.date.available | 2011-07-15T05:22:48Z | - |
dc.date.issued | 2003 | - |
dc.identifier.issn | 0392-856X | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/3387 | - |
dc.description.abstract | OBJECTIVE: Systemic lupus erythematosus is an autoimmune disease characterized by the production of anti-dsDNA antibody. Because the titer of anti-dsDNA antibody is correlated with disease severity, especially in lupus nephritis, controlling anti-dsDNA antibody production is important in the treatment of SLE. There are many regulatory mechanisms of autoantibody production; one of these is the interaction between idiotype and anti-idiotype antibody (anti-Id). The purpose of the present study was to assess the effect of anti-Id on anti-dsDNA antibody production and apoptosis and to study the mechanism of anti-Id induced apoptosis.
METHODS: After anti-dsDNA antibody producing hybridomas were treated with anti-Id, we checked the amount of anti-dsDNA antibody production, the rate of transcription, cellular proliferation, and apoptosis. Also, after treatment with anti-oxidant (N-acetyl-Lcysteine), phorbol esters with calcium ionophore and corticosteroids, we compared their effect on apoptosis with anti-Id. RESULTS: Two types of anti-dsDNA antibody producing hybridomas (G1-2, gamma and kappa chains; M2-10, mu and kappa chains) were treated with anti-Id and it was found that: (1) the amount of anti-dsDNA antibody production decreased; (2) the rate of transcription and cellular proliferation did not decrease; and (3) the level of apoptosis increased. The two cells expressed Fas and Fas-ligand, and the Fas of G1-2 was functional but that of M2-10 was not. The treatment of these cells with anti-Id resulted in no change in Fas-ligand and Bax expression, but the expression of Bcl-2 was decreased. In addition, treatment with antioxidant (N-acetyl-L-cysteine) inhibited anti-Id-induced apoptosis in G1-2 and M2-10. Phorbol esters with calcium ionophore also inhibited anti-Id induced apoptosis in M2-10. Corticosteroids induced apoptosis in both cells and showed similar results with anti-Id induced apoptosis. CONCLUSION: The anti-Id suppressed the production of anti-dsDNA antibody in two cells by inducing apoptosis, as did prednisolone. Furthermore, Bcl-2, oxygen-free radicals and protein kinase C might be involved in the induction of apoptosis by anti-Id. | - |
dc.language.iso | en | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Antibodies, Anti-Idiotypic | - |
dc.subject.MESH | Antibodies, Antinuclear | - |
dc.subject.MESH | Antibody Formation | - |
dc.subject.MESH | Antibody-Producing Cells | - |
dc.subject.MESH | Apoptosis | - |
dc.subject.MESH | Blotting, Northern | - |
dc.subject.MESH | Blotting, Western | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Disease Models, Animal | - |
dc.subject.MESH | Electrophoresis | - |
dc.subject.MESH | Enzyme-Linked Immunosorbent Assay | - |
dc.subject.MESH | Flow Cytometry | - |
dc.subject.MESH | Lupus Erythematosus, Systemic | - |
dc.subject.MESH | Mice | - |
dc.subject.MESH | Mice, Inbred MRL lpr | - |
dc.subject.MESH | Prednisolone | - |
dc.subject.MESH | Sensitivity and Specificity | - |
dc.title | The effects of anti-idiotypic antibody on antibody production and apoptosis of anti-dsDNA antibody producing cells. | - |
dc.type | Article | - |
dc.identifier.pmid | 12846046 | - |
dc.identifier.url | http://www.clinexprheumatol.org/article.asp?a=2054 | - |
dc.contributor.affiliatedAuthor | 서, 창희 | - |
dc.type.local | Journal Papers | - |
dc.citation.title | Clinical and experimental rheumatology | - |
dc.citation.volume | 21 | - |
dc.citation.number | 3 | - |
dc.citation.date | 2003 | - |
dc.citation.startPage | 291 | - |
dc.citation.endPage | 300 | - |
dc.identifier.bibliographicCitation | Clinical and experimental rheumatology, 21(3). : 291-300, 2003 | - |
dc.identifier.eissn | 1593-098X | - |
dc.relation.journalid | J00392856X | - |
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