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The effects of anti-idiotypic antibody on antibody production and apoptosis of anti-dsDNA antibody producing cells.

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dc.contributor.authorLee, CH-
dc.contributor.authorSuh, CH-
dc.contributor.authorLee, J-
dc.contributor.authorKim, YT-
dc.contributor.authorLee, SK-
dc.date.accessioned2011-07-15T05:22:48Z-
dc.date.available2011-07-15T05:22:48Z-
dc.date.issued2003-
dc.identifier.issn0392-856X-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/3387-
dc.description.abstractOBJECTIVE: 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.
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dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHAntibodies, Anti-Idiotypic-
dc.subject.MESHAntibodies, Antinuclear-
dc.subject.MESHAntibody Formation-
dc.subject.MESHAntibody-Producing Cells-
dc.subject.MESHApoptosis-
dc.subject.MESHBlotting, Northern-
dc.subject.MESHBlotting, Western-
dc.subject.MESHCells, Cultured-
dc.subject.MESHDisease Models, Animal-
dc.subject.MESHElectrophoresis-
dc.subject.MESHEnzyme-Linked Immunosorbent Assay-
dc.subject.MESHFlow Cytometry-
dc.subject.MESHLupus Erythematosus, Systemic-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred MRL lpr-
dc.subject.MESHPrednisolone-
dc.subject.MESHSensitivity and Specificity-
dc.titleThe effects of anti-idiotypic antibody on antibody production and apoptosis of anti-dsDNA antibody producing cells.-
dc.typeArticle-
dc.identifier.pmid12846046-
dc.identifier.urlhttp://www.clinexprheumatol.org/article.asp?a=2054-
dc.contributor.affiliatedAuthor서, 창희-
dc.type.localJournal Papers-
dc.citation.titleClinical and experimental rheumatology-
dc.citation.volume21-
dc.citation.number3-
dc.citation.date2003-
dc.citation.startPage291-
dc.citation.endPage300-
dc.identifier.bibliographicCitationClinical and experimental rheumatology, 21(3). : 291-300, 2003-
dc.identifier.eissn1593-098X-
dc.relation.journalidJ00392856X-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Rheumatology
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