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The Effect of Lipopolysaccharide-Induced Mouse B Cell Activation on Schistosoma japonicum Development

TANG Hong-bin1,CHENG La-ying1,XIONG Tao2,DONG Hui-fen2 *,JIANG Ming-sen2   

  1. 1 Center for Animal Experiment of Wuhan University/Animal Biosafety Level-3 Laboratory,Wuhan 430071,China; 2 Department of Medical Parasitology,School of Basic Medical Science,Wuhan University,Wuhan 430071,China
  • Online:2015-10-30 Published:2016-01-06

Abstract:

Objective  To investigate the effect of lipopolysaccharide(LPS)-induced B cell activation on the development of Schistosoma japonicum.  Methods  Eighteen BALB/c nude mice deficient in T cells and 23 BALB/c SCID mice deficient in T and B cells were used in this study. Each was infected with 30±1 S. japonicum cercariae. The nude (n=9, NL group) and SCID(n=12, SL group) mice then received 2-3(every two weeks) intraperitoneal injections with LPS (100 μg/mL, 0.2 mL for each mouse). The remaining nude(n=9, N group) and SCID(n=11, S group) mice received PBS injection as control. The mice were sacrificed on days 28 and 36 after infection(n=4/5, 4/5, 5/6, 6/6 for N, NL, S and SL groups, respectively), and adult worms were collected by hepatic portal vein perfusion. The collecting rate of the adult worms was calculated, the body-length measured, and pairs of worms recorded. The liver tissue was collected and digested with 5% KOH, and the number of eggs per gram of liver tissue was calculated. The levels of TGF-β, IFN-γ and IL-10 in peripheral blood were evaluated. Spleen cell suspension was prepared for detecting the proportion of regulatory B cells(Bregs) in splenic lymphocytes.  Results  On day 28 after infection, the body-lengths of male worms in NL and N groups were (7.65±2.85) mm and (5.28±1.64) mm (P<0.01), and those of female worms were (9.64±1.99) mm and (7.49±1.63) mm (P<0.01), respectively. On day 36 after infection, the number of eggs per gram of liver tissue was significantly higher in the NL group than in the N group(1 088±297 vs 715±404, P<0.05), and significantly lower in the SL group than in the S group(217±33 vs 573±160, P<0.01). The proportions of CD1dhiCD5+CD19+ Bregs in N group on days 28 and 36 after infection were(12.73±0.96)% and(37.15±3.04)% (P<0.05), respectively, with no significant difference with that of NL group. The serum levels of TGF-β and IFN-γ on day 28 after infection were significantly different between N and NL groups(TGF-β, 101.75±46.72 vs 260.90±45.34 pg/mL; IFN-γ, 7.91±1.62 vs 14.11±3.72 pg/mL, both P<0.01). Similarly, significant difference was found for the plasma level of IL-10 on day 36 after infection between the S and N groups (41.85±3.14 vs 66.25±4.16 pg/mL, P<0.01), and between the SL and NL groups (44.48±3.87 vs 72.22±17.76 pg/mL, P<0.01), but not between the LPS groups and the control groups.  Conclusion  LPS can induce the release of cytokines (e.g. TGF-β) from B cells of mice infected with S. japonium, to facilitate the early development of adult female and male worms.

Key words: Schistosoma japonicum, B lymphocyte, Breg, IL-10, TGF-β, INF-γ