Thymosins: chemistry and biological properties in health and disease

被引:22
作者
Goldstein, AL [1 ]
Badamchian, M [1 ]
机构
[1] George Washington Univ, Dept Biochem & Mol Biol, Sch Med & Hlth Sci, Washington, DC 20037 USA
关键词
actin; angiogenesis; chemokines; cytokines; neuroendocrine; T cells; thymic peptides; thymosin alpha(1); thymosin beta(4); wound healing;
D O I
10.1517/eobt.4.4.559.29800
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This paper will review the historical background that has generated our present interest in the actions of the thymosins in biological therapy. It will also discuss the multiple actions of the thymosins in the immune, endocrine and central nervous systems. The isolation from the thymus gland of the thymosins, a family of biologically active molecules with hormone-like properties, was first described in 1966 by AL Goldstein and A White. Since that time, significant progress has been made in understanding the role of the thymosins in immunity and the nature of the growth factors, cytokines and chemokines they modulate. The thymosins include a family of biochemically and functionally distinct polypeptides with clinically important physiological properties. In the early 1970s, preclinical studies establishing the immunorestorative effects of a partially purified thymosin preparation termed thymosin fraction 5 (TF5) provided the scientific foundation for the first clinical trials with TF5 in 1974. TF5 was effective in turning on the immune systems of a number of children with DiGeorge syndrome and other thymic dysplasias. These trials led to further interest in the active components in TF5 and to the chemical characterisation of the biologically active thymosins. Several of these molecules are showing significant promise in the clinic in the areas of cancer, infectious diseases and wound healing.
引用
收藏
页码:559 / 573
页数:15
相关论文
共 59 条
[1]   REDUCTION IN INCIDENCE OF WASTING DISEASE IN NEONATALLY THYMECTOMIZED CBA/W MICE BY INJECTION OF THYMOSIN [J].
ASANUMA, Y ;
GOLDSTEIN, AL ;
WHITE, A .
ENDOCRINOLOGY, 1970, 86 (03) :600-+
[2]   Thymosin β4 reduces lethality and down-regulates inflammatory mediators in endotoxin-induced septic shock [J].
Badamchian, M ;
Fagarasan, MO ;
Danner, RL ;
Suffredini, AF ;
Damavandy, H ;
Goldstein, AL .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2003, 3 (08) :1225-1233
[3]   Thymosin α1 is a time and dose-dependent antagonist of dexamethasone-induced apoptosis of murine thymocytes in vitro [J].
Baumann, CA ;
Badamchian, M ;
Goldstein, AL .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 2000, 22 (12) :1057-1066
[4]  
BEARD J, 1899, LANCET, P144
[5]   Role of thymosin β4 in tumor metastasis and angiogenesis [J].
Cha, HJ ;
Jeong, MJ ;
Kleinman, HK .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (22) :1674-1680
[6]   A pilot study of the safety and efficacy of thymosin α1 in augmenting immune reconstitution in HIV-infected patients with low CD4 counts taking highly active antiretroviral therapy [J].
Chadwick, D ;
Pido-Lopez, J ;
Pires, A ;
Imami, N ;
Gotch, F ;
Villacian, JS ;
Ravindran, S ;
Paton, NI .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2003, 134 (03) :477-481
[7]  
DALAKAS MC, 1980, NEW ENGL J MED, V302, P1092
[8]   COMBINATION TREATMENT WITH ZIDOVUDINE, THYMOSIN-ALPHA(1) AND INTERFERON-ALPHA IN HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION [J].
GARACI, E ;
ROCCHI, G ;
PERRONI, L ;
DAGOSTINI, C ;
SOSCIA, F ;
GRELLI, S ;
MASTINO, A ;
FAVALLI, C .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1994, 24 (01) :23-28
[9]   Anti-inflammatory effects in the skin of thymosin-β4 splice-variants [J].
Girardi, M ;
Sherling, MA ;
Filler, RB ;
Shires, J ;
Theodoridis, E ;
Hayday, AC ;
Tigelaar, RE .
IMMUNOLOGY, 2003, 109 (01) :1-7
[10]  
Giuliani C, 2000, EUR J IMMUNOL, V30, P778, DOI 10.1002/1521-4141(200003)30:3<778::AID-IMMU778>3.0.CO