Artículos de revistas
Immune mediators associated to male infertility in a mouse model of DNA immunization with the sperm protease proacrosin
Fecha
2016-11Registro en:
Russi, Romina; Garcia, Maria Ines; Vignatti, Paulina; Veiga, Maria Florencia; Vazquez, Monica Hebe; et al.; Immune mediators associated to male infertility in a mouse model of DNA immunization with the sperm protease proacrosin; Elsevier Ireland; Journal Of Reproductive Immunology.; 118; 11-2016; 28-35
0165-0378
1872-7603
CONICET Digital
CONICET
Autor
Russi, Romina
Garcia, Maria Ines
Vignatti, Paulina
Veiga, Maria Florencia
Vazquez, Monica Hebe
Veaute, Carolina Melania Isabel
Resumen
The immune response has relevant physiological functions both in the male and female reproductive system, and must be tightly controlled to achieve a successful pregnancy. Several immune factors have been related to infertility, among them humoral and cellular immune responses triggered by sperm antigens. The present study was aimed at evaluating the immune profile induced by DNA immunization against the sperm protease proacrosin in CF1 male mice and its effect upon fertility. Immunized animals exhibited higher anti-proacrosin antibodies levels than controls (indirect ELISA), both in serum (p<0.01) and in seminal vesicle fluid (SVF; p<0.05). IgG2a levels were higher than IgG1 in serum (p<0.01) and similar in SVF. IL-10 and TGF-β1 mRNA levels were lower in testis (p<0.05), whereas TNF-α and IFN-γ transcript levels were increased in SV tissue (p<0.05). Immunized mice showed a trend toward higher IFN-γ concentration in serum and SVF than controls. Male fertility rate was diminished in immunized mice (p<0.01) and inversely correlated with serum and SVF anti-proacrosin IgG levels (p<0.001). Immunized animals also had fewer pups born than controls (p<0.01). To our knowledge, this is the first report on DNA immunization done in CF1 mice. Injection of proacrosin DNA induces an immune response in the male reproductive tract characterized by high levels of specific antibodies and cytokine changes. These factors may alter the crucial balance of the genital tract microenvironment required for adequate fertilization and pregnancy.