ABSTRACT
Objective To provide supportive evidences for the diagnosis of primary major depres-sive disorder (MDD) by analyzing the alterations of proinflammatory cytokines such as IL-1α, IL-6, IL-18, TNF-αas well as the total complement activity (CH50) in serum samples.Methods Hamilton Depression Rating Scale ( HAMD) was used to rate the severity of depression with the patients who were diagnosed as primary MDD.Enzyme-linked immunosorbent assay (ELISA) was used to detect the levels of IL-1α, IL-6, IL-18 and TNF-αand the CH50 in serum samples from 49 patients and 40 healthy subjects .Results Pa-tients with MDD showed significantly different levels of IL-6, IL-18, TNF-αand CH50 in serum samples as compared with that in healthy subjects (P0.05).There were significant gender differ-ences with levels of IL-1αamong the patients with MDD (P0.05). Conclusion The changes of CH50 and certain proinflammatory cytokines such as IL-6, IL-18 and TNF-αmight be involved in the progression of MDD , suggesting the possibility of using them as indicators for the di-agnosis of MDD.
ABSTRACT
HIV infection in children conditions a serious immunodeficiency with special characteristic that distinguish it from the adult, causing a global immune deficit. This constitutes a cases and controls study between Cuban paediatric patients infected with HIV by vertical transmission and a control group of supposedly healthy children. The both groups were characterized from the clinical point of view and markers were used for evaluated the immunologic and virologycal state. Clinically 75% of patients present a pattern of precocious progression, from total only two stay asymptomatic. All HIV infected children receive antirretroviral treatment and three of them present values of viral load bigger than 100,000 cp/mL. The immune alterations found in the HIV infected children compared with healthy children were: a cellular immune depletion with diminish counts of lymphocytes subsets of T CD4+, CD16+/CD56 + and CD19+, an increase in subsets of CD3+, CD8+, CD8+/CD38+, CD3+/ CD95+ and a hipergammaglobulinemia to prevalence of immunoglobulin gamma IgG (p < 0.05). On the other hand, they were not significantly differences in the serum levels of both C3 and C4, as well as in the haemolytic activity of the roads classic and it alternates of the complement system. This finding allowed us to a better attention and treatment of paediatric HIV patients.
La infección por el virus de la inmunodeficiencia humana (VIH) en niños condiciona una grave inmunodeficiencia con características especiales que la distinguen del adulto, ocasionando un déficit inmune global. Se realizó un estudio de casos y controles de los pacientes pediátricos cubanos infectados por transmisión vertical con el VIH comparado con niños supuestamente sanos. Ambos grupos se caracterizaron desde el punto de vista clínico y se emplearon marcadores que evaluaron el estado inmunológico y virológico. Clínicamente 75% de los pacientes infectados por VIH presentan un patrón de progresión precoz, y dos se mantienen asintomáticos. A todos los niños infectados se les suministró tratamiento antirretroviral y tres presentan valores de carga viral mayores de 100,000 cp/mL. Las alteraciones inmunes encontradas en los pacientes VIH+ fueron: una inmunodepresión celular con conteos de subpoblaciones linfoides T CD4+, CD16+/CD56 + y CD 19+ disminuidas significativamente con respecto al grupo control (p < 0.05). Además, se encontró un aumento de linfocitos CD3+, CD8+, CD8+/CD38+, CD3+/CD95+ y una hipergammaglobulinemia a predominio de inmunoglobulina gamma IgG en la comparación estadística (p < 0.05). Por otra parte, no se encontraron diferencias significativas en los niveles séricos de C3 y C4, así como en la actividad hemolítica de las vías clásica y alterna del sistema del complemento. Este conocimiento nos permitió sentar pautas para contribuir al manejo y tratamiento de los pacientes pediátricos infectados por VIH.
Subject(s)
Child , Child, Preschool , Female , Humans , Infant , Male , HIV Infections/immunology , Infectious Disease Transmission, Vertical , Case-Control Studies , Complement Activation , Cuba , /analysis , /analysis , Disease Progression , HIV Infections/transmission , Hypergammaglobulinemia/etiology , Lymphocyte Count , T-Lymphocyte Subsets , Viral LoadABSTRACT
Summary: The expression of CH50 polypoptide in bladder cancer cell line BIU-87 and the effects on the invasion ability of BIU-87 were investigated. The eukaryotic expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfection in vitro. The expression of CH50 polypeptide was detected by using immunohistochemical S-P method. The expression of the transfected gene was identified by RT-PCR. Cell invasion assay kit was applied to detect the effect of CH50 polypeptide on the invasion ability of BIU-87. The results showed that the BIU-87 cells transfected with pCH510 could express the CH50 polypeptide, while in the control group, no CH50 polypeptide was detectable. In the transfection group, the invasion ability of BIU-87 in vitro was lower than in control group (P<0.05). It was concluded that CH50 polypeptide was successfully expressed in BIU-87 cells by gene transfection, by which the in vitro invasion ability of BIU-87 was inhibited.
ABSTRACT
Objective: To investigate the expression and identification of CH50 polypeptide in bladder cancer cell line BIU-87 by gene transfection. Methods:The eukaryotic expressing vector pCH510 of polypeptide CH50 was introduced into BIU-87 cells by gene transfection Lipofectimine TM2000.The expressed product was identified by immunohistochemistry and Western blot method. The expression of the transfected gene was identified by RT-PCR. Results:The BIU-87 cells could produce CH50 polypeptide by transfection. Conclusion:When the vector of pCH510 was transfected into BIU-87 cells in vitro, the cell adhension characteristic would be changed.