Pathobiology of Severe Asthma

被引:89
作者
Bittar, Humberto E. Trejo [1 ]
Yousem, Samuel A. [1 ]
Wenzel, Sally E. [2 ]
机构
[1] Univ Pittsburgh, Med Ctr, Sch Med, Dept Pathol,Pulm Allergy & Crit Care Med Div,Dept, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Med Ctr, Sch Med, Asthma Inst,Pulm Allergy & Crit Care Med Div,Dept, Pittsburgh, PA 15260 USA
来源
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 10 | 2015年 / 10卷
关键词
airway; pathology; inflammation; histology; epithelium; interleukins; AIRWAY-SMOOTH-MUSCLE; BRONCHIAL EPITHELIAL-CELLS; ENDOTHELIAL GROWTH-FACTOR; INNATE LYMPHOID-CELLS; THYMIC STROMAL LYMPHOPOIETIN; SUBEPITHELIAL BASEMENT-MEMBRANE; BRONCHOALVEOLAR LAVAGE FLUID; INTRAEPITHELIAL MAST-CELLS; GENOME-WIDE ASSOCIATION; NECROSIS-FACTOR-ALPHA;
D O I
10.1146/annurev-pathol-012414-040343
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Severe asthma (SA) afflicts a heterogeneous group of asthma patients who exhibit poor responses to traditional asthma medications. SA patients likely represent 5-10% of all asthma patients; however, they have a higher economic burden when compared with milder asthmatics. Considerable research has been performed on pathological pathways and structural changes associated with SA. Although limitations of the pathological approaches, ranging from sampling, to quantitative assessments, to heterogeneity of disease, have prevented a more definitive understanding of the underlying pathobiology, studies linking pathology to molecular markers to targeted therapies are beginning to solidify the identification of select molecular phenotypes. This review addresses the pathobiology of SA and discusses the current limitations of studies, the inflammatory cells and pathways linked to emerging phenotypes, and the structural and remodeling changes associated with severe disease. In all cases, an effort ismade to link pathological findings to specific clinical/molecular phenotypes.
引用
收藏
页码:511 / 545
页数:35
相关论文
共 208 条
[1]   Corticosteroid-insensitive asthma: molecular mechanisms [J].
Adcock, IM ;
Lane, SJ .
JOURNAL OF ENDOCRINOLOGY, 2003, 178 (03) :347-355
[2]   Role of periostin, FENO, IL-13, lebrikzumab, other IL-13 antagonist and dual IL-4/IL-13 antagonist in asthma [J].
Agrawal, Swati ;
Townley, Robert G. .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2014, 14 (02) :165-181
[3]   MARKED GOBLET CELL HYPERPLASIA WITH MUCUS ACCUMULATION IN THE AIRWAYS OF PATIENTS WHO DIED OF SEVERE ACUTE ASTHMA ATTACK [J].
AIKAWA, T ;
SHIMURA, S ;
SASAKI, H ;
EBINA, M ;
TAKISHIMA, T .
CHEST, 1992, 101 (04) :916-921
[4]   Essential role of NKT cells producing IL-4 and IL-13 in the development of allergen-induced airway hyperreactivity [J].
Akbari, O ;
Stock, P ;
Meyer, E ;
Kronenberg, M ;
Sidobre, S ;
Nakayama, T ;
Taniguchi, M ;
Grusby, MJ ;
DeKruyff, RH ;
Umetsu, DT .
NATURE MEDICINE, 2003, 9 (05) :582-588
[5]   The Nonallergic Asthma of Obesity A Matter of Distal Lung Compliance [J].
Al-Alwan, Ali ;
Bates, Jason H. T. ;
Chapman, David G. ;
Kaminsky, David A. ;
DeSarno, Michael J. ;
Irvin, Charles G. ;
Dixon, Anne E. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 189 (12) :1494-1502
[6]   Variability of sputum inflammatory cells in asthmatic patients receiving corticosteroid therapy: A prospective study using multiple samples [J].
Al-Samri, Mohammed T. ;
Benedetti, Andrea ;
Prefontaine, David ;
Olivenstein, Ron ;
Lemiere, Catherine ;
Nair, Parameswaran ;
Martin, James G. ;
Hamid, Qutayba .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 125 (05) :1161-1163
[7]  
[Anonymous], 2000, Am J Respir Crit Care Med, V162, P2341
[8]   Cell-matrix and cell-cell interactions modulate apoptosis of bronchial epithelial cells [J].
Aoshiba, K ;
Rennard, SI ;
Spurzem, JR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1997, 272 (01) :L28-L37
[9]   IL-13-induced changes in the goblet cell density of human bronchial epithelial cell cultures: MAP kinase and phosphatidylinositol 3-kinase regulation [J].
Atherton, HC ;
Jones, G ;
Danahay, H .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 285 (03) :L730-L739
[10]  
Avdalovic Mark V, 2006, Am J Respir Crit Care Med, V174, P1069, DOI 10.1164/rccm.200506-848OC