The effect of cyclosporine on asymmetric antibodies and serum transforming growth factor beta1 in abortion-prone model of mice CBA/J x DBA/2

authors:

avatar Seyed Mohammad Moazzeni , * , avatar bizhan sadighi-moghaddam


how to cite: Moazzeni S M , sadighi-moghaddam B. The effect of cyclosporine on asymmetric antibodies and serum transforming growth factor beta1 in abortion-prone model of mice CBA/J x DBA/2. koomesh. 2015;16(4):e151248. 

Abstract

Introduction: One of the common causes of recurrent spontaneous abortion is interference of immunological factors. Administration of cyclosporine, as an immunosuppressive drug, has reportedly reduc the rate of abortion in abortion-prone model of mice CBA/J mated DBA/2 male mice. On the other hand, asymmetric antibodies and TGF-β1 have been considered as an important factor in successful pregnancy outcomes. Intravaginal administration of TGF-β has also been reported to reduce the resorption rate in the same mouse model. In this study, the immunomodulatory effects of cyclosporine on serum level of asymmetric antibodies (AAbs) and T cell growth factor beta (TGF-β1) were investigated. Material and Methods: Female CBA/J mice were mated with male DBA/2. The pregnant females were divided into two groups: 1- test group received intraperitoneal injection of 1mg/kg cyclosporine (n=7), 2- control group received intraperitoneal injection of Phosphate Buffered Saline (PBS) (n=7). Both groups received treatments on the 5th day of pregnancy. Serum samples were collected on the 13.5th day of pregnancy, when the percentage of abortion was also calculated. Results: The percentage of AAbs and abortion rate were significantly reduced in cyclosporine group (P0.05). Conclusion: Our study showed that despite the significant reduction in percentage of AAbs and no significant difference in serum level of TGF-β1, the abortion rate was markedly reduced in cyclosporine group. So other mechanisms of immunomodulation and reduction of abortion rate except asymmetric antibodies and TGF-β1 should be involved in this mouse model following cyclosporine administration.