Interleukin-16 in a mouse model of allergic asthma

作者: J.J. de Bie

DOI:

关键词:

摘要: Allergic asthma is a disease which affects an increasing number of people. Patients with this illness suffer from variable airflow obstruction and increased airway responsiveness to variety stimuli. Furthermore, inflammatory response in the lungs occurs, accompanied by enhanced mucus production (10). In serum these patients levels IgE antibodies can be detected (reviewed 238, 239). Currently, several different drugs are available for people who asthma. These medicines include corticosteroids, b2-agonists, leukotriene antagonists phosphodiesterase inhibitors (240-244). Corticosteroids most effective used drug at moment treatment reduce component hyperresponsiveness (245). However, corticosteroids not very selective affect whole range non-inflammatory cells (246-248). More importantly, all that allergic do cure but only clinical symptoms disorder. Therefore, current research focused on development strategies treat asthmatics more causal level their illness. It now widely accepted T-helper type 2 (Th2) lymphocytes play role (10, 249, 250). Th2 produce limited set cytokines including interleukin-3 (IL3), IL4, IL5, IL9, IL10 IL13. Both human asthmatic murine models subsets have been (8, 9) it extensively documented produced crucial symptoms. New could therefore aimed specifically targeting T cell subset or (18, 251, 252).

参考文章(259)
Teri J. Liegler, Daniel P. Stites, HIV-1 gp120 and anti-gp120 induce reversible unresponsiveness in peripheral CD4 T lymphocytes. Journal of Acquired Immune Deficiency Syndromes. ,vol. 7, pp. 340- 348 ,(1994)
Schleimer Rp, Effects of glucocorticosteroids on inflammatory cells relevant to their therapeutic applications in asthma The American review of respiratory disease. ,vol. 141, ,(1990)
Bruce N. Rehlaender, Moo J. Cho, Antibodies as Carrier Proteins Pharmaceutical Research. ,vol. 15, pp. 1652- 1656 ,(1998) , 10.1023/A:1011936007457
Okunieff P, Höckel M, de Bie J, Terris Dj, Dunphy Ep, Oxygen distributions partly explain the radiation response of human squamous cell carcinomas. The British journal of cancer. Supplement. ,vol. 27, ,(1996)
J. Matthews, M. P. Coogan, J. L. Kut, M. R. I. Young, M. A. Wright, M. E. Young, Stimulation of splenic T-lymphocyte function by endogenous serotonin and by low-dose exogenous serotonin. Immunology. ,vol. 80, pp. 395- 400 ,(1993)
Peter J. Barnes, Molecular Mechanisms of Anti-Asthma Therapy Pharmacological Sciences: Perspectives for Research and Therapy in the Late 1990s. pp. 403- 409 ,(1995) , 10.1007/978-3-0348-7218-8_41