THE EFFECT OF HBV-TF ON THE IMMUNOLOGICAL FUNCTION OF THE SAME SPACIES GOATS / 西安交通大学学报(医学版)

The goats were injected with hepatitis B virus-transfer factor (HBV-TF), which was made from the immune spleen of the same spacies goats immunized with HBsAg After that, we measured the goats cellular immunity and humoral immunity by cheching up the serum anti-HBs level and lymphocyte transformation assay by ~3H-Thymidine (~3H-TdR) incorporation assay. The experiments showed that HBV-TF has the capacity of passing the specific cellular immunity from immune animals to no immune animals. The animals receiving HBV-TF showed a typical skin delay hypersensitivity to specific antigen and augument the effect of lymphocyte transformation in the presence of HBsAg. HBV-TF can also remove the inhibition of lymphocyte transformation caused by HBsAg, Both HBV-TF and N-TF can increase the number of goats blood leucocytes. However HBV-TF and N-TF have no effect on animal's humoral immunity.

DIRECT ELISA FOR THE EARLY DIAGNOSIS OF HFRS / 西安交通大学学报(医学版)

The antigen of hemorrhagic fever with renal syndrome (HFRS) virus in the infected suckling mouse brains was purified by a combined method—Protamin sulfate sedimentation and sucrose cushion uhracentrifugation. The Purified antigen was labeled with horseradish peroxidase (HRP). A kind of IgM antibody capture ELISA that used HRP—labeled antigen of HFRS Virus, i.e, direct ELISA, was successfully established for the detection of specific IgM antibody in sera from patients with HFRS. Compared with IgM antibody capture ELISA that used HRP—labeled IgG antibody to HFRS virus ,direct ELISA was similar in sensitivity to it,but direct ELISA could completely avoid the interference caused by rheumatoid factor (RF) as well as could reduce one step immune reaction. 87 serum samples from patients with HFRS(diagnosed clinically) in various stages, including 37 from Patients with HFRS in early stage(from 1 to 5 days after the onset of HFRS)were detected by direct ELISA . The positive rates of specific IgM antibody were 96.5% and 91.8%, respectively. We think that direct ELISA that uses HRP—labeled antigen provides a more specific,simpler and faster method for early di—agnosis of HFRS.