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
[51]   Multidimensional endotyping in patients with severe asthma reveals inflammatory heterogeneity in matrix metalloproteinases and chitinase 3-like protein 1 [J].
Hinks, Timothy S. C. ;
Brown, Tom ;
Lau, Laurie C. K. ;
Rupani, Hitasha ;
Barber, Clair ;
Elliott, Scott ;
Ward, Jon A. ;
Ono, Junya ;
Ohta, Shoichiro ;
Izuhara, Kenji ;
Djukanovic, Ratko ;
Kurukulaaratchy, Ramesh J. ;
Chauhan, Anoop ;
Howarth, Peter H. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 138 (01) :61-75
[52]   Asthmatics able to step down from inhaled corticosteroid treatment without loss of asthma control have low serum eotaxin/CCL11 [J].
Hoffmann, Hans Jurgen ;
Nielsen, Lars Peter ;
Harving, Henrik ;
Heinig, John H. ;
Dahl, Ronald .
CLINICAL RESPIRATORY JOURNAL, 2008, 2 (03) :149-157
[53]   Asthma as a chronic disease of the innate and adaptive immune systems responding to viruses and allergens [J].
Holtzman, Michael J. .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (08) :2741-2748
[54]   TOTAL EOSINOPHIL COUNTS IN MANAGEMENT OF BRONCHIAL-ASTHMA [J].
HORN, BR ;
ROBIN, ED ;
THEODORE, J ;
VANKESSEL, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1975, 292 (22) :1152-1155
[55]   Recent developments regarding periostin in bronchial asthma [J].
Izuhara, Kenji ;
Matsumoto, Hisako ;
Ohta, Shoichiro ;
Ono, Junya ;
Arima, Kazuhiko ;
Ogawa, Masahiro .
ALLERGOLOGY INTERNATIONAL, 2015, 64 :S3-S10
[56]   Eotaxin in serum of patients with asthma or chronic obstructive pulmonary disease:: relationship with eosinophil cationic protein and lung function [J].
Jahnz-Rózyk, K ;
Plusa, T ;
Mierzejewska, J .
MEDIATORS OF INFLAMMATION, 2000, 9 (3-4) :175-179
[57]   Periostin is a systemic biomarker of eosinophilic airway inflammation in asthmatic patients [J].
Jia, Guiquan ;
Erickson, Richard W. ;
Choy, David F. ;
Mosesova, Sofia ;
Wu, Lawren C. ;
Solberg, Owen D. ;
Shikotra, Aarti ;
Carter, Richard ;
Audusseau, Severine ;
Hamid, Qutayba ;
Bradding, Peter ;
Fahy, John V. ;
Woodruff, Prescott G. ;
Harris, Jeffrey M. ;
Arron, Joseph R. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 130 (03) :647-+
[58]   Activation states of blood eosinophils in asthma [J].
Johansson, M. W. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2014, 44 (04) :482-498
[59]   Eosinophil β1 integrin activation state correlates with asthma activity in a blind study of inhaled corticosteroid withdrawal [J].
Johansson, MW ;
Barthel, SR ;
Swenson, CA ;
Evans, MD ;
Jajour, NN ;
Mosher, DF ;
Busse, WW .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 117 (06) :1502-1504
[60]   Increased periostin associates with greater airflow limitation in patients receiving inhaled corticosteroids [J].
Kanemitsu, Yoshihiro ;
Matsumoto, Hisako ;
Izuhara, Kenji ;
Tohda, Yuji ;
Kita, Hideo ;
Horiguchi, Takahiko ;
Kuwabara, Kazunobu ;
Tomii, Keisuke ;
Otsuka, Kojiro ;
Fujimura, Masaki ;
Ohkura, Noriyuki ;
Tomita, Katsuyuki ;
Yokoyama, Akihito ;
Ohnishi, Hiroshi ;
Nakano, Yasutaka ;
Oguma, Tetsuya ;
Hozawa, Soichiro ;
Nagasaki, Tadao ;
Ito, Isao ;
Oguma, Tsuyoshi ;
Inoue, Hideki ;
Tajiri, Tomoko ;
Iwata, Toshiyuki ;
Izuhara, Yumi ;
Ono, Junya ;
Ohta, Shoichiro ;
Tamari, Mayumi ;
Hirota, Tomomitsu ;
Yokoyama, Tetsuji ;
Niimi, Akio ;
Mishima, Michiaki .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 132 (02) :305-+