Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/14707
Title: Characterization of CMX-13 and evaluation of efficacy and mechanisms of action in animal model of autoimmunity
Authors: RAMGOLAM VINOD SATISCH
Keywords: Apoptosis, Allograft rejection, Immunosuppressant, Systemic Lupus Erythematosus, Chinese Medicine
Issue Date: 22-Mar-2005
Source: RAMGOLAM VINOD SATISCH (2005-03-22). Characterization of CMX-13 and evaluation of efficacy and mechanisms of action in animal model of autoimmunity. ScholarBank@NUS Repository.
Abstract: T-cells, which are inhibited in their apoptotic mechanism, induce Systemic Lupus Erythematosus (SLE). In our previous studies we have shown that CMX-13, a derivative from a Chinese Medicine, is a potent immunosuppressant. Here we have made an effort to elucidate the structure of the bioactive compound in CMX-13, the immunosuppressive mechanism in-vitro and in-vivo, and the effect of mRNA expression levels of cytokines in-vivo. Structure elucidation experiments suggest that CMX-13 is a hexapeptide. CMX-13 was able to accelerate apoptosis in Jurkat cells and PBMCs derived from SLE patients; improved pathogical factors significantly of the MRL-lpr/lpr mice SLE mouse model. However, no effect on the cytokine expression levels in moribund mice was observed. From these experiments we concluded that CMX-13 acts as an immunosuppressant by the induction of apoptosis on T-cells. We recommend further study on the effect of CMX-13 on the molecular mechanism of apoptosis.
URI: http://scholarbank.nus.edu.sg/handle/10635/14707
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