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Derivatives of human beta-Casein fragments (54-59) exhibit highly potent immunosuppressant activity.

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Puri, A
Bhattacharya, M
Tripathi, L M
Haq, W
 
Date 2010-09-09T08:52:31Z
2010-09-09T08:52:31Z
2009
 
Identifier International Immunopharmacology, 9 (9) 2009, 1092-1096
http://hdl.handle.net/123456789/589
 
Description Human β-casein fragment (54-59) having the amino acid sequence Val-Glu-Pro-Ile-Pro-Tyr, has shown potent immunostimulant activity. Several analogs of this hexapeptide have been synthesized with modification at the N-terminal region and two analogs, viz. peptide I and peptide II have shown significant immunosuppressant activity in-vivo mouse model. Effect on cell mediated immunity (CMI) and humoral immunity was studied in mouse/SRBC model. Both the peptides failed to stimulate immune response in vivo and showed inhibition of CMI and humoral response to sheep red blood cells (SRBC). Peptides showed inhibition in alloantigen induced lymphocyte proliferation, i.e., mixed lymphocyte reaction (MLR) in vitro. Treatment with peptides inhibited the production of interferon-γ (IFN-γ), and increased the production of interleukin-4 (IL-4) as well as improved the skin graft survival. Cyclosporine a known immunosuppressant showed similar effect on mouse model. Present study thus provides a lead for the development of safe and effective immunosuppressant.
 
Format 121401 bytes
application/pdf
 
Language en
 
Subject human beta-casein fragments
Immunosuppressant peptide
immunomodulator
Lymphocytes proliferation
 
Title Derivatives of human beta-Casein fragments (54-59) exhibit highly potent immunosuppressant activity.
 
Type Article