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[重组人II型胶原蛋白肽250-270的体液免疫抑制研究]

[Study of the humoral immune suppression of recombinant human collagen type II peptide 250-270].

作者信息

Wang Hong-Kun, Zhu Ping, Li Xiao-Yan, Zheng Zhao-Hui, Jia Jun-Feng, Ding Jin, Fan Chun-Mei

机构信息

Department of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2006 Nov;22(6):742-4.

Abstract

AIM

To investigate the modulation of rhC II 250-270 peptide on special humoral immune response in the course of oral administration.

METHODS

ELISA was used to determine antigen-specific antibodies in mice sera. The frequency of anti-C II and anti-C II (250-270) antibody-forming spleen cells was measured by ELISPOT.

RESULTS

The level of C II- and C II (250-270)- specific IgG in serum from the mice fed with rhC II (250-270) were (0.82+/-0.02) and (0.84+/-0.04) respectively, and lower significantly than those of collagen-induced arthritis (CIA) control group. The anti-C II (250-270) antibody responses were suppressed obviously (P<0.01). The frequency of antibody-forming cells in the spleen from rhC II (250-270)-fed mice were (158+/-9 counts/well) and (181+/-10 counts/well) respectively, and also were reduced significantly when compared with that in CIA control group (247+/-16 counts/well)(P<0.05).

CONCLUSION

Oral rhC II (250-270) could induce specific suppression of humoral responds in CIA. These findings together with a better understanding of the mechanisms of oral tolerance and regulation of humoral immune response in CIA, will help the development of innovative therapeutic intervention for rheumatoid arthritis.

摘要

目的

研究重组人CⅡ250 - 270肽在口服给药过程中对特异性体液免疫反应的调节作用。

方法

采用ELISA法测定小鼠血清中的抗原特异性抗体。通过ELISPOT检测抗CⅡ和抗CⅡ(250 - 270)抗体形成脾细胞的频率。

结果

喂食重组人CⅡ(250 - 270)的小鼠血清中CⅡ和CⅡ(250 - 270)特异性IgG水平分别为(0.82±0.02)和(0.84±0.04),显著低于胶原诱导性关节炎(CIA)对照组。抗CⅡ(250 - 270)抗体反应明显受到抑制(P<0.01)。喂食重组人CⅡ(250 - 270)的小鼠脾脏中抗体形成细胞的频率分别为(158±9个/孔)和(181±10个/孔),与CIA对照组(247±16个/孔)相比也显著降低(P<0.05)。

结论

口服重组人CⅡ(250 - 270)可诱导对CIA中体液反应的特异性抑制。这些发现以及对口服耐受机制和CIA中体液免疫反应调节的更好理解,将有助于类风湿关节炎创新治疗干预措施的开发。

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