Proteasome inhibition: A novel mechanism to combat asthma

被引:86
作者
Elliott, PJ
Pien, CS
McCormack, TA
Chapman, ID
Adams, J
机构
[1] ProScript Inc, Cambridge, MA 02319 USA
[2] Quintiles Ltd, Edinburgh, Midlothian, Scotland
关键词
asthma; cell adhesion molecules; cytokines; delayed-type hypersensitivity; eosinophils; leukocytes; nuclear transcription factor-kappa B; proteasome; steroids;
D O I
10.1016/S0091-6749(99)70369-6
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Nuclear factor-kappa B (NF-kappa B) is a critical transcription factor required for the regulation of many genes involved in inflammatory responses to noxious stimuli, On activation, NF-kappa B induces the transcription of numerous proinflammatory cytokines, enzymes, and cellular adhesion molecules, Blockade of the proteasome with selective inhibitors attenuates the effects of NF-kappa B, leading to suppression of the inflammatory response, Objective: We sought to determine whether proteasome inhibitors would be active in a model of asthma, Methods: The mouse delayed-type hypersensitivity model was used to screen a panel of compounds for in vivo activity, The proteasome inhibitor, PS-519, was shown to be the most active in this model and was selected for further development. Allergen-induced pulmonary eosinophilia in Brown Norway rats was used subsequently to determine anti-inflammatory activity in an animal model. Results: Direct administration of PS-519 into the lungs significantly reduced leukocyte numbers, particularly the selective increase in eosinophils, Because steroids are the mainstay antiinflammatory therapy in asthma, and data is available to suggest their possible interaction to suppress the activation of NF-kappa B, rats were also treated by inhalation with combinations of a steroid and the proteasome inhibitor, In both the delayed-type hypersensitivity and the animal eosinophil. model, low doses of proteasome inhibitors were shown to be effective when given with low doses of steroids. Conclusion: Taken together, the present data suggest that proteasome inhibition may represent a novel strategy for the treatment of inflammatory lung diseases such as asthma.
引用
收藏
页码:294 / 300
页数:7
相关论文
共 71 条
[1]  
ASHERSON GL, 1968, IMMUNOLOGY, V15, P405
[2]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[3]   I-KAPPA-B - A SPECIFIC INHIBITOR OF THE NF-KAPPA-B TRANSCRIPTION FACTOR [J].
BAEUERLE, PA ;
BALTIMORE, D .
SCIENCE, 1988, 242 (4878) :540-546
[4]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[5]   NITRIC-OXIDE AND AIRWAY DISEASE [J].
BARNES, PJ .
ANNALS OF MEDICINE, 1995, 27 (03) :389-393
[6]   MOLECULAR MECHANISMS OF ANTIASTHMA THERAPY [J].
BARNES, PJ .
ANNALS OF MEDICINE, 1995, 27 (05) :531-535
[7]   Mechanisms of disease - Nuclear factor-kappa b - A pivotal transcription factor in chronic inflammatory diseases [J].
Barnes, PJ ;
Larin, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (15) :1066-1071
[8]   NF-kappa B: A pivotal role in asthma and a new target for therapy [J].
Barnes, PJ ;
Adcock, IM .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1997, 18 (02) :46-50
[9]   CELLULAR EVENTS IN THE BRONCHI IN MILD ASTHMA AND AFTER BRONCHIAL PROVOCATION [J].
BEASLEY, R ;
ROCHE, WR ;
ROBERTS, JA ;
HOLGATE, ST .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 139 (03) :806-817
[10]   EOSINOPHILIC INFLAMMATION IN ASTHMA [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
BARNEON, G ;
GHAVANIAN, N ;
ENANDER, I ;
VENGE, P ;
AHLSTEDT, S ;
SIMONYLAFONTAINE, J ;
GODARD, P ;
MICHEL, FB .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) :1033-1039