Novel biomarkers in asthma: chemokines and chitinase-like proteins

被引:43
作者
Hartl, Dominik [1 ]
Lee, Chun G. [1 ]
Da Silva, Carla A. [1 ]
Chupp, Geoffrey L. [1 ]
Elias, Jack A. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Pulm & Crit Care Med Sect, New Haven, CT 06520 USA
关键词
asthma; biomarker; chemokine; chemokine (C-C motif) ligand 17; chitinase-like protein; ACTIVATION-REGULATED CHEMOKINE; ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS; ACIDIC MAMMALIAN CHITINASE; EXHALED NITRIC-OXIDE; INTERFERON-GAMMA; SERUM YKL-40; BRONCHOALVEOLAR LAVAGE; T-CELLS; AIRWAY INFLAMMATION; MESSENGER-RNA;
D O I
10.1097/ACI.0b013e32831f8ee0
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose of review Allergic asthma is a frequent lung disease in Western civilizations and is characterized by airway inflammation and tissue remodeling. Without early diagnosis and specific treatment, asthma results in a loss of lung function, impaired quality of life and the risk to die from uncontrolled asthma attacks. Thus, there is a need for specific biomarkers to detect asthma as soon as possible and to initiate the correct clinical treatment. Recent findings Recent studies have highlighted the potential role of the chemokine (C-C motif) ligand 17 and the chitinase-like protein YKL-40 as novel biomarkers in asthma. Patient studies suggest that these proteins could be useful to identify asthmatics, to characterize disease severity or both in patients with asthma. Functional studies indicate that these molecules are more than correlated epiphenomena and instead contribute in significant ways to asthma pathogenesis. Summary Assessments of chemokine (C-C motif) ligand 17 and YKL-40 may allow physicians to more accurately diagnose and predict the course of asthma and thereby allow therapy to be appropriately tailored for a given patient.
引用
收藏
页码:60 / 66
页数:7
相关论文
共 133 条
[1]  
Adcock Ian M., 2004, Current Drug Targets - Inflammation and Allergy, V3, P257, DOI 10.2174/1568010043343660
[2]   Regulated production of the T helper 2-type T-cell chemoattractant TARC by human bronchial epithelial cells in vitro and in human lung xenografts [J].
Berin, MC ;
Eckmann, L ;
Broide, DH ;
Kagnoff, MF .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 24 (04) :382-389
[3]   The role of TARC in the pathogenesis of allergic asthma [J].
Berin, MC .
DRUG NEWS & PERSPECTIVES, 2002, 15 (01) :10-16
[4]  
Bleau G, 1999, EXS, V87, P211
[5]   Allergy and asthma [J].
Bochner, BS ;
Busse, WW .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2005, 115 (05) :953-959
[6]   CLONING OF A CDNA-ENCODING CHITOTRIOSIDASE, A HUMAN CHITINASE PRODUCED BY MACROPHAGES [J].
BOOT, RG ;
RENKEMA, GH ;
STRIJLAND, A ;
VANZONNEVELD, AJ ;
AERTS, JMFG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) :26252-26256
[7]   Identification of a novel acidic mammalian chitinase distinct from chitotriosidase [J].
Boot, RG ;
Blommaart, EFC ;
Swart, E ;
Ghauharali-van der Vlugt, K ;
Bijl, N ;
Moe, C ;
Place, A ;
Aerts, JMFG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (09) :6770-6778
[8]  
Brightling Christopher E, 2005, Treat Respir Med, V4, P309, DOI 10.2165/00151829-200504050-00002
[9]   The value of FeNO measurement in asthma management: the motion for - Yes, it's NO or, the wrong end of the Stick! [J].
Bush, Andrew ;
Eber, Ernst .
PAEDIATRIC RESPIRATORY REVIEWS, 2008, 9 (02) :127-131
[10]   Advances in immunology - Asthma [J].
Busse, WW ;
Lemanske, RF .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (05) :350-362