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

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

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.

MeSH terms

  • Animals
  • Antibody Formation / drug effects*
  • Antibody Specificity
  • Arthritis, Experimental / immunology
  • Arthritis, Experimental / pathology
  • Arthritis, Rheumatoid / immunology
  • Arthritis, Rheumatoid / therapy
  • Collagen Type II / chemistry*
  • Collagen Type II / pharmacology
  • Humans
  • Immune Tolerance / drug effects
  • Immunosuppression Therapy*
  • Male
  • Mice
  • Peptide Fragments / administration & dosage
  • Peptide Fragments / chemistry*
  • Peptide Fragments / pharmacology*
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / pharmacology*
  • Spleen / immunology
  • Spleen / pathology

Substances

  • Collagen Type II
  • Peptide Fragments
  • Recombinant Proteins