Natural and synthetic thymic peptides as therapeutics for immune dysfunction

被引:51
作者
Morozov, VG [1 ]
Khavinson, VK [1 ]
机构
[1] Inst Bioregulat & Gerontol, St Petersburg, Russia
来源
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY | 1997年 / 19卷 / 9-10期
关键词
thymus; thymic factors; Thymalin (R); Thymogen (R); Vilon (R); immunoregulation; immunomodulation; immunotherapy;
D O I
10.1016/S0192-0561(97)00058-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural thymic peptides have been isolated from calf thymus by mild acid extraction. Pharmaceutical containing natural peptides (Thymalin(R)) was put into practice as immunocorrector. One of the immunomodulatory molecules (L-Glu-L-Trp) has been isolated from Thymalin by reversed-phase high performance liquid chromatography. Pharmaceutical containing this agent (Thymogen(R)) was designed on the base of synthesized dipeptide. A novel immunomodulatory dipeptide was synthesized and termed Vilon(R). Both natural and synthetic pharmaceuticals activated T-cell differentiation, T-cell recognition of peptide-MHC complexes, induced the changes in intracellular composition of cyclic nucleotides and cytokine [interleukin (IL-2), interferon (IFN)] excretion of blood lymphocytes. Synthetic dipeptides activated neutrophil chemotaxis and phagocytosis. They had no influence on antioxidant response in thymocytes in comparison with natural peptides. Thymalin and Thymogen were used in persons with chronic pathology and immune dysfunction. The results indicate that thymic peptides participate in the regulating mechanisms of inflammatory processes as cytokine antagonists and show the difference between natural and synthetic products. It is important for the drugs designed to prevent immune dysfunction development. (C) 1998 Published by Elsevier Science Ltd on behalf of the International Society for Immunopharmacology.
引用
收藏
页码:501 / 505
页数:5
相关论文
共 20 条
[1]   EFFECT OF LOW-MOLECULAR-WEIGHT FACTORS OF THYMUS AND PINEAL-GLAND ON LIFE-SPAN AND SPONTANEOUS TUMOR-DEVELOPMENT IN FEMALE MICE OF DIFFERENT AGE [J].
ANISIMOV, VN ;
LOKTIONOV, AS ;
KHAVINSON, VK ;
MOROZOV, VG .
MECHANISMS OF AGEING AND DEVELOPMENT, 1989, 49 (03) :245-257
[2]   PROTEIN-DEGRADATION AND MODIFICATION - INTRODUCTION AND OVERVIEW [J].
BERGAMINI, E .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1992, 663 :43-47
[3]  
BIRR C, 1994, INFEC DIS T, V15, P143
[4]   BINDING OF CHEMOTACTIC COLLAGEN-DERIVED PEPTIDES TO FIBROBLASTS - RELATIONSHIP TO FIBROBLAST CHEMOTAXIS [J].
CHIANG, TM ;
POSTLETHWAITE, AE ;
BEACHEY, EH ;
SEYER, JM ;
KANG, AH .
JOURNAL OF CLINICAL INVESTIGATION, 1978, 62 (05) :916-922
[5]   THYMOSIN-ALPHA-1 - ISOLATION AND SEQUENCE-ANALYSIS OF AN IMMUNOLOGICALLY ACTIVE THYMIC POLYPEPTIDE [J].
GOLDSTEIN, AL ;
LOW, TLK ;
MCADOO, M ;
MCCLURE, J ;
THURMAN, GB ;
ROSSIO, J ;
LAI, CY ;
CHANG, D ;
WANG, SS ;
HARVEY, C ;
RAMEL, AH ;
MEIENHOFER, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (02) :725-729
[6]  
GRINTSEVICH I I, 1984, Radiobiologiya, V24, P537
[7]   METHYL INOSINE MONOPHOSPHATE (MIMP), A NEW PURINE IMMUNOMODULATOR FOR HIV-INFECTION [J].
HADDEN, JW ;
GINERSOROLLA, A ;
HADDEN, EM .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1991, 13 :49-54
[8]  
HADDEN JW, 1986, ADV IMMUNOPHARMACOL, P487
[9]  
HADDEN JW, 1985, SERONO S IMMUNOPHARM, P183
[10]  
KHAVINSON VK, 1981, IMMUNOLOGIA, V5, P28