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1.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-266287

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the clinical significance of plasmic L-plastin level in patients with colorectal cancer.</p><p><b>METHODS</b>From March 2008 to March 2009, plasma samples were collected from 40 patients and 40 healthy controls. Plasmic L-plastin level was measured by ELISA kit and was compared to TIMP-1.</p><p><b>RESULTS</b>Plasmic L-plastin level in patients with colorectal cancer was higher than that in healthy adults (1.662±0.386 vs. 0.485±0.085 μg/L, P<0.01). The sensitivity of L-plastin in the diagnosis of colorectal cancer was 67.5%, and the specificity was 80.6%. The Youden index was 0.481 and AUC was 0.772 (P<0.01). Plasmic L-plastin levels were associated with the tumor size (P=0.006), serosal penetration (F=4.687, P<0.05) and lymphatic metastasis (P<0.01). Compared to plasmic TIMP-1 level, L-plastin showed the same capability in indicating the depth of tumor. The specificity of L-plastin was better in indicating lymphatic metastasis (86% vs. 58%, χ2=4.2, P<0.05).</p><p><b>CONCLUSIONS</b>Plasmic L-plastin level may serve as a potential marker in colorectal cancer.</p>


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Case-Control Studies , Colorectal Neoplasms , Blood , Diagnosis , Enzyme-Linked Immunosorbent Assay , Membrane Glycoproteins , Blood , Microfilament Proteins , Blood , Sensitivity and Specificity , Tissue Inhibitor of Metalloproteinase-1 , Blood
2.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-326487

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of CD8(+)CD28(-) suppressor T cells(Ts) induced by dendritic cell(DC) with major histocompatibility complex 1(MHC-1) expression RNA interference on immune tolerance in rat intestinal transplantation.</p><p><b>METHODS</b>The expression level of CD8(+)CD28(-)Ts were successfully induced by DC with MHC-1 expression interfered by RNA interference technique under the stimulator of allograft antigen. Orthotopic intestinal transplantation was performed in 36 rats by modified three cuffs method. The recipients were randomly divided into three groups(12 rats in each group):group A was experimental group with CD8(+)CD28(-) Ts being administrated, mixed T cells were injected in group B, while in group C, NS were administrated. On the first day and the seventh day posttransplant, the 36 rats of the 3 groups were administrated through vena dorsalis penis respectively. Six rats were selected randomly from each group and the animals were sacrificed on the 14 th day postoperatively, serum levels of TGF-beta, IFN-gamma and the values of Na(+)-K(+)-ATPase activity of the intestinal graft were assayed and the intestinal pathologic morphology, intestinal allograft survival were observed concerning the remainders.</p><p><b>RESULTS</b>On the 14 th day after operation, the expression levels of TGF-beta and IFN-gamma in group A were significantly up-regulated as compared with those in group B and group C(P<0.05). Na(+)-K(+)-ATPase activity in group A was(6.3+/-1.0) kU/g, much higher than the levels of group B(3.6+/-0.9)kU/g and group C(2.9+/-1.3) kU/g and the differences were significant(P<0.05). The data suggested preliminarily that pathological scores of intestinal graft in group A were lower than those in group B and group C. The survival time of the recipients in group A was 32.0 days, much longer than that in group B (17.5 days, P<0.05) and group C(21.0 days, P<0.05).</p><p><b>CONCLUSION</b>CD8(+)CD28(-) Ts induced by DC with MHC-1 expression RNA interference can alleviate acute rejection and lead to immune tolerance in rat intestinal transplantation.</p>


Subject(s)
Animals , Male , Rats , Dendritic Cells , Allergy and Immunology , Metabolism , Immune Tolerance , Intestine, Small , Allergy and Immunology , Transplantation , Major Histocompatibility Complex , Allergy and Immunology , RNA Interference , Rats, Sprague-Dawley , Rats, Wistar , T-Lymphocytes, Regulatory , Allergy and Immunology , Transplantation Tolerance , Allergy and Immunology , Transplantation, Homologous , Allergy and Immunology
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