The current and future role of biomarkers in type 2 cytokine-mediated asthma management

被引:80
作者
Pavord, I. D. [1 ]
Afzalnia, S. [2 ]
Menzies-Gow, A. [3 ]
Heaney, L. G. [4 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Resp Med Unit, Oxford, England
[2] Roche Prod Ltd, Welwyn Garden City, Herts, England
[3] Royal Brompton Hosp, Lung Div, London, England
[4] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Ctr Expt Med, Belfast, Antrim, North Ireland
关键词
EXHALED NITRIC-OXIDE; C-REACTIVE PROTEIN; EOSINOPHILIC AIRWAY INFLAMMATION; OBSTRUCTIVE PULMONARY-DISEASE; RANDOMIZED CONTROLLED-TRIAL; ALPHA MONOCLONAL-ANTIBODY; REGULATED CHEMOKINE TARC; CHITINASE-LIKE PROTEIN; INNATE LYMPHOID-CELLS; DIFFICULT ASTHMA;
D O I
10.1111/cea.12881
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Assessment and management of asthma is complicated by the heterogeneous pathophysiological mechanisms that underlie its clinical presentation, which are not necessarily reflected in standardized management paradigms and which necessitate an individualized approach to treatment. This is particularly important with the emerging availability of a variety of targeted forms of therapy that may only be appropriate for use in particular patient subgroups. The identification of biomarkers can potentially aid diagnosis and inform prognosis, help guide treatment decisions and allow clinicians to predict and monitor response to treatment. Biomarkers for asthma have been identified from a variety of sources, including airway, exhaled breath and blood. Biomarkers from exhaled breath include fractional exhaled nitric oxide, measurement of which can help identify patients most likely to benefit from inhaled corticosteroids and targeted anti-immunoglobulin E therapy. Biomarkers measured in blood are relatively non-invasive and technically more straightforward than those measured from exhaled breath or directly from the airway. The most well established of these are the blood eosinophil count and serum periostin, both of which have demonstrated utility in identifying patients most likely to benefit from targeted anti-interleukin and anti-immunoglobulin E therapies, and in monitoring subsequent treatment response. For example, serum periostin appears to be a biomarker for responsiveness to inhaled corticosteroid therapy and may help identify patients as suitable candidates for anti-IL-13 treatment. The use of biomarkers can therefore potentially help avoid unnecessary morbidity from high-dose corticosteroid therapy and allow the most appropriate and cost-effective use of targeted therapies. Ongoing clinical trials are helping to further elucidate the role of established biomarkers in routine clinical practice, and a range of other circulating novel potential biomarkers are currently being investigated in the research setting.
引用
收藏
页码:148 / 160
页数:13
相关论文
共 122 条
[1]   Exhaled nitric oxide in diagnosis and management of respiratory diseases [J].
Abba, Abdullah A. .
ANNALS OF THORACIC MEDICINE, 2009, 4 (04) :173-181
[2]   Treatable traits: toward precision medicine of chronic airway diseases [J].
Agusti, Alvar ;
Bel, Elisabeth ;
Thomas, Mike ;
Vogelmeier, Claus ;
Brusselle, Guy ;
Holgate, Stephen ;
Humbert, Marc ;
Jones, Paul ;
Gibson, Peter G. ;
Vestbo, Jorgen ;
Beasley, Richard ;
Pavord, Ian D. .
EUROPEAN RESPIRATORY JOURNAL, 2016, 47 (02) :410-419
[3]   Elevated level of serum osteopontin in school-age children with asthma [J].
Akelma, A. Z. ;
Cizmeci, M. N. ;
Kanburoglu, M. K. ;
Bozkaya, D. ;
Catal, F. ;
Mete, E. ;
Kutukoglu, I. ;
Namuslu, M. .
ALLERGOLOGIA ET IMMUNOPATHOLOGIA, 2014, 42 (04) :275-281
[4]   ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005 [J].
American Thoracic Society ;
European Respiratory Society .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (08) :912-930
[5]  
[Anonymous], 2014, THORAX, V69, P1
[6]  
Arron Joseph R, 2013, Ann Am Thorac Soc, V10 Suppl, pS206, DOI 10.1513/AnnalsATS.201303-047AW
[7]  
Asthma UK, 2016, ASTHM FACTS STAT
[8]   Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework [J].
Atkinson, AJ ;
Colburn, WA ;
DeGruttola, VG ;
DeMets, DL ;
Downing, GJ ;
Hoth, DF ;
Oates, JA ;
Peck, CC ;
Schooley, RT ;
Spilker, BA ;
Woodcock, J ;
Zeger, SL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (03) :89-95
[9]   Type-2 innate lymphoid cells in human allergic disease [J].
Barlow, Jillian L. ;
McKenzie, Andrew N. J. .
CURRENT OPINION IN ALLERGY AND CLINICAL IMMUNOLOGY, 2014, 14 (05) :397-403
[10]   Novel biomarkers for asthma stratification and personalized therapy [J].
Bartminski, Grzegorz ;
Crossley, Matthew ;
Turcanu, Victor .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2015, 15 (03) :415-430