TANG Hong-bin, CHENG La-ying, XIONG Tao, DONG Hui-fen, JIANG Ming-sen
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2015 Oct;33(5):338-44.
To investigate the effect of lipopolysaccharide (LPS)-induced B cell activation on the development of Schistosoma japonicum.
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.
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 CD(hi)CD5(+)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-y 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-y, 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.
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.
探讨脂多糖(LPS)诱导的B细胞活化对日本血吸虫发育的影响。
本研究使用了18只缺乏T细胞的BALB/c裸鼠和23只缺乏T细胞和B细胞的BALB/c SCID小鼠。每只小鼠感染30±1条日本血吸虫尾蚴。然后,裸鼠(n = 9,NL组)和SCID小鼠(n = 12,SL组)每2周腹腔注射2 - 3次LPS(100μg/mL,每只小鼠0.2 mL)。其余裸鼠(n = 9,N组)和SCID小鼠(n = 11,S组)注射PBS作为对照。感染后第28天和第36天处死小鼠(N、NL、S和SL组分别为4/5、4/5、5/6、6/6),通过肝门静脉灌注收集成虫。计算成虫收集率,测量虫体长度,并记录虫对数量。收集肝脏组织,用5% KOH消化,计算每克肝脏组织中的虫卵数。评估外周血中TGF-β、IFN-γ和IL-10的水平。制备脾细胞悬液,检测脾淋巴细胞中调节性B细胞(Bregs)的比例。
感染后第28天,NL组和N组雄虫体长分别为(7.65±2.85)mm和(5.28±1.64)mm(P<0.01),雌虫体长分别为(9.64±1.99)mm和(7.49±1.63)mm(P<0.01)。感染后第36天,NL组每克肝脏组织中的虫卵数显著高于N组(1088±297 vs 715±404,P<0.05),SL组显著低于S组(217±33 vs 573±160,P<0.01)。感染后第28天和第36天,N组CD(hi)CD5(+)CD19(+) Bregs的比例分别为(12.73±0.96)%和(37.15±3.04)%(P<0.05),与NL组无显著差异。感染后第28天,N组和NL组血清中TGF-β和IFN-γ水平有显著差异(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,均P<0.01)。同样,感染后第36天,S组和N组血浆中IL-10水平有显著差异(41.85±3.14 vs 66.25±4.16 pg/mL,P<0.01),SL组和NL组也有显著差异(44.48±3.87 vs 72.22±17.76 pg/mL,P<0.01),但LPS组与对照组之间无显著差异。
LPS可诱导感染日本血吸虫小鼠的B细胞释放细胞因子(如TGF-β),促进雌雄成虫的早期发育。