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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2009, Vol. 14 ›› Issue (10): 1142-1150.

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Study on the hypoglycemic mechanism of the fusion protein HSP65 -6 ×P277 in NOD mice

JIN Liang1, WANG Yu1, ZHU Ai-hua2, LIU Jing-jing1   

  1. 1Minigene Pharmacy Laboratory, School of Life Science &Technology, China Pharmaceutical University, Nanjing 210009, Jiangsu, China;
    2Key Laboratory of Biotechnology for Medicinal Plants of Jiangsu Province, Xuzhou Normal University, Shanghai Road, Xuzhou 221116, Jiangsu, China
  • Received:2009-06-05 Revised:2009-09-09 Published:2020-10-29
  • Contact: LIU Jing-jing, professor, majoring in gene engineering medi cine. Tel: 025-83271242 E-mail: minigene3 @yahoo.con.cn
  • About author:JIN Liang, male, PhD, majoring in gene engineering medicine. Tel: 18913812745 E-mail: jinboshi1975@yahoo.com.cn
  • Supported by:
    This work was support ed by China National Natural Science Fund Committee (Grant No.30701023, 30672464 and 30500458).

Abstract: AIM: To evaluate the hypoglycemic mechanism of the fusion protein HSP65 -6 ×P277 in NOD mice. METHODS: The fusion protein was used to immunize 4-week old female NOD mice with three i. n.inoculations in the absence of adjuvants.The effects of HSP65 -6 ×P277 on NOD mice were investigated by observing the change of blood glucose, cytokine levels, antibody types and degree of insulitis. RESULTS: The sera collected from HSP65 -6 ×P277 treated mice, contained relatively high levels of interleukin IL-4 but low levels of IL-2, and the antibody types were almost exclusively of the IgGl and IgG2b subclass, but at very low levels of IgG2a.T cells from HSP65 -6 ×P277 treated mice when incubated with HSP-peptide conjugate showed an increase in IL-10 secretion and a decrease in interferon (IFN)-γsecretion. HSP65 -6 ×P277 treatment reduced insulitis and T1DM incidence. CONCLUSION: The hypoglycemic mechanism of the fusion protein HSP65 -6 ×P277 is related to its inducing Th2 responses.

Key words: heat shock protein 65, P277, Th1/Th2 cells, cytokines

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