Development of spontaneous airway changes consistent with human asthma in mice lacking T-bet

被引:498
作者
Finotto, S
Neurath, MF
Glickman, JN
Qin, SX
Lehr, HA
Green, FHY
Ackerman, K
Haley, K
Gatte, PR
Szabo, SJ
Drazen, JM
De Sanctis, GT
Glimcher, LH
机构
[1] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Pulm & Crit Care, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Gastroenterol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[5] Millenium Pharmaceut, Cambridge, MA 02138 USA
[6] Univ Mainz, Dept Pathol, D-55131 Mainz, Germany
[7] Univ Calgary, Dept Pathol & Lab Med, Calgary, AB T2N 4N1, Canada
[8] Univ Mainz, Med Clin 1, D-55131 Mainz, Germany
关键词
D O I
10.1126/science.1065544
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human asthma is associated with airway infiltration by T helper 2 (T(H)2) lymphocytes. We observed reduced expression of the T(H)1 transcription factor, T-bet, in T cells from airways of patients with asthma compared with that in T cells from airways of nonasthmatic patients, suggesting that loss of T-bet might be associated with asthma. Mice with a targeted deletion of the T-bet gene and severe combined immunodeficient mice receiving CD4(+) cells from T-bet knockout mice spontaneously demonstrated multiple physiological and inflammatory features characteristic of asthma, Thus, T-bet deficiency, in the absence of allergen exposure, induces a murine phenotype reminiscent of both acute and chronic human asthma.
引用
收藏
页码:336 / 338
页数:3
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