Biological treatments and connective tissue disease associated interstitial lung disease

被引:51
作者
Panopoulos, Stylianos T. [1 ]
Sfikakis, Petros P. [1 ]
机构
[1] Univ Athens, Sch Med, Dept Propedeut & Internal Med 1, Laikon Hosp, GR-11527 Athens, Greece
关键词
biological treatments; connective tissue disease; interstitial lung disease; pulmonary fibrosis; NECROSIS-FACTOR-ALPHA; SYSTEMIC-LUPUS-ERYTHEMATOSUS; B-CELL DEPLETION; HUMAN DERMAL FIBROBLASTS; RHEUMATOID-ARTHRITIS; PULMONARY-FIBROSIS; INFLIXIMAB TREATMENT; RITUXIMAB THERAPY; FOLLOW-UP; T-CELLS;
D O I
10.1097/MCP.0b013e3283483ea5
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Purpose of review There is no specific therapy for interstitial lung disease associated with connective tissue diseases (CTDs-ILD), a potentially fatal condition for some of these patients. This article reviews currently available information on the effects on CTDs-ILD of biological treatments that are increasingly used with considerable success in various systemic diseases. Recent findings A beneficial effect of antitumor necrosis factor (TNF) agents on CTDs-ILD has been described in sporadic patients with rheumatoid arthritis (RA), systemic sclerosis (SSc) and systemic lupus erythematosus (SLE). However, and despite the fact that there was no clear evidence of pulmonary toxicity of these agents in randomized-controlled trials comprising thousands of patients with RA and spondylarthropathies, new onset or exacerbation of preexisting ILD with high mortality rates has so far been observed in 144 RA patients following anti-TNF treatment in clinical practice. Likewise, administration of the B-cell depleting anti-CD20 antibody rituximab was beneficial for ILD in SSc patients but associated with new-onset ILD in isolated patients with RA and SLE. Pertinent information on other biological treatments is currently lacking. Summary Data on the therapeutic role of biological agents in CTDs-ILD is preliminary and controversial. Although preexisting ILD is not a contraindication for these agents, until more information is available their administration should be stopped when new pulmonary symptoms occur.
引用
收藏
页码:362 / 367
页数:6
相关论文
共 52 条
[1]   Fatal exacerbation of fibrosing alveolitis associated with systemic sclerosis in a patient treated with adalimumab [J].
Allanore, Y. ;
Devos-Francois, G. ;
Caramella, C. ;
Boumier, P. ;
Jounieaux, V. ;
Kahan, A. .
ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (06) :834-835
[2]  
Antoniou KM, 2007, CLIN EXP RHEUMATOL, V25, P23
[3]  
Apostolaki M, 2010, CURR DIR AUTOIMMUN, V11, P1, DOI 10.1159/000289195
[4]   Adverse events and efficacy of TNF-α blockade with infliximab in patients with systemic lupus erythematosus: long-term follow-up of 13 patients [J].
Aringer, Martin ;
Houssiau, Frederic ;
Gordon, Caroline ;
Graninger, Winfried B. ;
Voll, Reinhard E. ;
Rath, Eva ;
Steiner, Guenter ;
Smole, Josef S. .
RHEUMATOLOGY, 2009, 48 (11) :1451-1454
[5]   Infliximab treatment in a patient with rheumatoid arthritis and pulmonary fibrosis [J].
Bargagli, E ;
Galeazzi, M ;
Rottoli, P .
EUROPEAN RESPIRATORY JOURNAL, 2004, 24 (04) :708-708
[6]   Infliximab treatment in a patient with systemic sclerosis associated with lung fibrosis and pulmonary hypertension [J].
Bargagli, Elena ;
Galeazzi, Mauro ;
Bellisai, Francesca ;
Volterrani, Luca ;
Rottoli, Paola .
RESPIRATION, 2008, 75 (03) :346-349
[7]   B cell depletion in diffuse progressive systemic sclerosis: safety, skin score modification and IL-6 modulation in an up to thirty-six months follow-up open-label trial [J].
Bosello, Silvia ;
De Santis, Maria ;
Lama, Gina ;
Spano, Cristina ;
Angelucci, Cristiana ;
Tolusso, Barbara ;
Sica, Gigliola ;
Ferraccioli, Gianfranco .
ARTHRITIS RESEARCH & THERAPY, 2010, 12 (02)
[8]   Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management [J].
Castelino, Flavia V. ;
Varga, John .
ARTHRITIS RESEARCH & THERAPY, 2010, 12 (04)
[9]   Systemic sclerosis Th2 cells inhibit collagen production by dermal fibroblasts via membrane-associated tumor necrosis factor α [J].
Chizzolini, C ;
Parel, Y ;
De Luca, C ;
Tyndall, A ;
Åkesson, A ;
Scheja, A ;
Dayer, JM .
ARTHRITIS AND RHEUMATISM, 2003, 48 (09) :2593-2604