The expression of exogenous ADA gene in T-lymphocytes of children with recurrent respiratory tract infectious diseases

Qu Shen , You Yingjian , Wang Xiaolin , Shen Guanxin , Deng Yaozhu , He Shanshu

Current Medical Science ›› 1996, Vol. 16 ›› Issue (3) : 143 -147.

PDF
Current Medical Science ›› 1996, Vol. 16 ›› Issue (3) : 143 -147. DOI: 10.1007/BF02908794
Article

The expression of exogenous ADA gene in T-lymphocytes of children with recurrent respiratory tract infectious diseases

Author information +
History +
PDF

Abstract

The adenosine deaminase (ADA) activities in blood lymphocytes of 41 normal children and 17 with recurrent respiratory tract infections were examined, and the T-lymphocytes of two children whose ADA activities were obviously lower than those of others were culturedin vitro. Then the exogenous human ADA gene was transfected into these cells by means of lipofectin mediated gene transfer. The results showed that the ADA activities in cultured T-lymphocytes were raised and the immunological were also improved.

Keywords

adenosine deaminase / lymphocyte / gene expression / gene therapy / recurrent respiratory tract infection

Cite this article

Download citation ▾
Qu Shen, You Yingjian, Wang Xiaolin, Shen Guanxin, Deng Yaozhu, He Shanshu. The expression of exogenous ADA gene in T-lymphocytes of children with recurrent respiratory tract infectious diseases. Current Medical Science, 1996, 16(3): 143-147 DOI:10.1007/BF02908794

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

GiblettE R, AndersonJ E, CohenF, et al. . Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity. Lacncet, 1972, 2: 1067-1067

[2]

CarsonD A, CarreraC J. Immunodeficiency secondary to adenosine deficiency and purine neucleoside phosphorylation deficiency. Semin Hematol, 1990, 27(3): 260-260

[3]

YasuharaA. Serum adenosine deaminase activity in the differentiation of respiratory diseases in children. Clin Chim Acta, 1986, 161(3): 341-341

[4]

1988, 3(5): 249

[5]

1991, 9(5):298

[6]

1996, 16(1): 5

[7]

1981, 1 (2):18

[8]

1995, 3(6): 8

[9]

SanesJ R, RubensteinJ L R, NicdasJ F. Use of a recombinant retrovirus to study post-implantation lineage in mouse embryos. EMBO J, 1986, 5: 133-133

[10]

AndersonW F. Human gene therapy. Science, 1992, 256: 09-09

[11]

LimB, WilliamsD A, OrkinS H, et al. . Retrovirus mediated gene transfer of human adenosine deamenase: Expression of functional enzyme in murine hematorpoictic stem cell in vivo. Mol Cell Biol, 1987, 7(10): 3459-3459

[12]

BraakmanE, Van BeusechemV W, Van KrimpenB A, et al. . Genetic correction of cultured T cells from an adenosine deaminas deficient patient. Eur J Immunol, 1992, 19(1): 63-63

[13]

KantoffP W, KohnD B, MitsuyaH, et al. . Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirusmediated gene transfer. Proc Natl Acad Sci USA, 1986, 83: 6563-6563

[14]

Lipofectin ADA T, 1994, 23(2): 89

AI Summary AI Mindmap
PDF

73

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/