ABSTRACT
Apolymerase chain reaction [PCR], based on insertion sequence IS6110,was developed to detect mycobacterium tuberculosis complex organisms in the blood samples of 56 tuberculosis patients and 34 healthy controls.the erly secreted antigenic target 6-KDa[ESAT-6] are used to stimulate T lymphocyte subsets from tuberculosis infected patients and the correltion of these immune responses to the genetic factoes[HLATYPE] which determined the host immune response is evaluated.ESAT-6 derived peptides:P1[1.05 +/- 0.084],P2[1.08 +/- 0.094],P3[1.02 +/- 0.086],P5[0.98 +/- 0.117] and P7[1.26 +/- 0.152] were significantly higer in the infected group than in non-infected one. Besides, 33ptients and 12 controls were tested for HL-DRB HLA DQB and HLA-DPB Only type HLA-DEB 15was significan tly associated with tuberculosis infection using the Chi-square test[X[2]=0.04311]. By using the relative risk some HL types were relatively more susceptible to be associated with tuberculosis infection. HLA-DR typing of patients showed that they covered a large spectrum of HLA-DR molecules encoded by HLA-DEB1,-DRB3,-DRB4,and DRB5genes.however,HLA-DQ typing showed that they HLA-DQB1 molecules, HLA-DP typing of patients showed that covered a large spectrum of HLA-DP molecules encoded by HLA-DPB1.
Subject(s)
Humans , Male , Female , HLA Antigens/genetics , Polymerase Chain Reaction/bloodABSTRACT
Colonisation of the small intestine by V. cholerae, a typical non-invasive pathogen, is an important early step in the pathogenesis of cholera. In the present study, trial to make cholera whole-cell vaccine with addition of recombinant B subunit of cholera toxin [rCTB] was-done. Cholera chB gene was cloned into pQE expression vector. Large-scale culture was done for preparative rCTB production and purification. Commercial CTB from V. cholerae was used for induction of polyclonal anti-CTB antibodies in mice. These polyclonal antibodies were used to test the antigenicity and identity of rCTB. Cholera whole-cell vaccine was prepared by resuspending equal volumes of dead Inaba and Ogawa vaccine strains in PBS. Orochol E Berna was used as control vaccine. Mice were divided into 4 groups [20 mice each]; group 1 [G1]: control unimmunised, group 2 [62]: rCTB immunized, group 3 [G3]: rCTB + killed Inaba and Ogawa immunised, and group 4 [G4]: Orochol immunized. Sera and faeces from all groups were collected and used in evaluation of anti-rCTB antibody levels. The spleens of animals were aseptically removed and used in lymphoproliferative assay. Small bacterial cultures revealed the presence of specific band at approximately 12-12.5 KDa in induced culture. Anti-commercial CTB antibodies were successfully prepared and used in Western blot analysis and verified the presence and antigenicity of rCTB. Large scale production and purification of rCTB resulted in 12.9 mg protein. Both serum and secretory antibody level in mice of G2 was significantly less than in mice of both G3 and G4. G3 was significantly higher than 62, while there was no significant difference between G3 and G4. G4 was significantly higher than G2, while there was no significant difference between G4 and G3. Stimulation index of splenic cells in G 1 was not significantly different from that of G2, while it was significantly lower than GB and G4. SI of G2 was significantly lower than G3 and G4. G3 was significantly higher than G1, G2, and G4. G4 was significantly higher than 01 and 02, but it was significantly lower than G3. The results in this study showed the ability of rCT B to induce immune responses in the presence of cholera bacteria more than if used alone. The inclusion of rCTB in addition to vibrios, increased systemic, intestinal, and cellular responses. Depending on previous studies, adding any new cholera strain which are present or will appear in future is possible. In addition, other vaccines [either killed bacteria or vaccine subunit] can be added to the formula indicated in this study