[Effects of soluble egg antigen and adult worm antigen of Schistosoma japonicum on differentiation of effector B cells of mice].

Objective: To observe the differentiation ability of effector B cells induced by soluble egg antigen (SEA) and soluble adult worm antigen (SWAP) of Schistosoma japonicum.

Methods: The mouse spleen mononuclear cells and CDl9+ B cells sorted by beadg were stimulated by SEA, SWAP and lipopolysaccharide (LPS), respectively. The ratios of CD19+ IL-6+ cells and CD19+ IFN-gamma+ cells were analyzed by flow cytometry after 72 hours. At the same time, the cytokines IL-6 and IFN-gamma levels in the cultured supernatants were detected by ELISA. The mouse was immunized with the mixture of SEA or SWAP or LPS and the incomplete Freund' s adjuvant for three times, respectively. The mouse spleen mononuclear cells were isolated at the seventh day after the last immunization. The ratios of CD19+ IL-6+ cells and CD19 IFN-gama+ cells were analyzed, and the cytokines IL-6 and IFN-gamma+ levels in the culture supernatants were detected.

Results: The ratio of CD19 IL-6+ cells in spleen mononuclear cells and splenic B cells was significantly increased in the groups stimulated by SEA and LPS (P < 0.05), and the cytokines IL-6 level in the CD193 cells culture supernatants were significantly increased (P < 0.01). Furthermore, the ratio of CD19+ IL-6+ cells and the cytokines IL-6 level were significantly increased in the SEA immunized group (P < 0.01). SWAP could induce a significantly higher ratio of the CD19+ IFN-gamma+ cells in spleen cells, instead of in splenic CD19+ B cells (P < 0.05). The CD19+ IFN-gamma+ cells and the cytokine IFN-gamma level in the culture supernatants in the SWAP immunized group were significantly higher than those in the SEA and PBS immunized groups (P C 6.01).

Conclusions: SEA preferentially induces the increase of CDl9+ IL-6+ cells in mouse spleen cells; while SWAP preferentially induces the CD19 + IFN-gamma+ cells' production of mouse spleen cells, depending on the effects of other immune cells.