Role for macrophage migration inhibitory factor in asthma

被引:182
作者
Mizue, Y
Ghani, S
Leng, L
McDonald, C
Kong, P
Baugh, J
Lane, SJ
Craft, J
Nishihira, J
Donnelly, SC
Zhu, Z
Bucala, R
机构
[1] Yale Univ, Sch Med, Dept Med, Anlyan Ctr, New Haven, CT 06520 USA
[2] Sapporo Immunodiagnost, Sapporo, Hokkaido 0010922, Japan
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, Dublin 4, Ireland
[4] Tallaght Hosp, Dublin, Ireland
[5] Hokkaido Univ, Dept Mol Biochem, Sapporo, Hokkaido 060, Japan
关键词
cytokine; genetic polymorphism; innate immunity;
D O I
10.1073/pnas.0507189102
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
Macrophage migration inhibitory factor (MIF) is an immunologic regulator that is expressed in inflammatory and autoimmune disorders. We investigated MIF's role in asthma using genetic approaches in a mouse model and in a cohort of asthma patients. Mice genetically deficient in MIF that were primed and aerosol-challenged with ovalbumin showed less pulmonary inflammation and lower airway hyperresponsiveness than genetically matched, wild-type controls. MIF deficiency also resulted in lower titers of specific IgE, IgG(1), and IgG(2a), and decreased pulmonary, T(H)2 cytokine levels. IL-5 concentrations were lower and corresponded to decreased eosinophil numbers in bronchoalveolar lavage fluid. T cell studies also showed a lower level of antigen-specific responses in MIF-KO versus wild-type mice. In an analysis of 151 white patients with mild, moderate, or severe asthma (Global Initiative for Asthma criteria), a significant association was found between mild asthma and the low-expression, 5-CATT MIF allele. Pharmacologic inhibition of MIF may be beneficial and could be guided by the MIF genotype of affected individuals.
引用
收藏
页码:14410 / 14415
页数:6
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