Plasmapheresis for treatment of pulmonary alveolar proteinosis

被引:50
作者
Luisetti, M. [1 ]
Rodi, G. [2 ]
Perotti, C. [3 ]
Campo, I.
Mariani, F.
Pozzi, E.
Trapnell, B. C. [4 ]
机构
[1] Univ Pavia, Policlin San Matteo, Clin Malattie Apparato Resp, Fdn IRCCS,Inst Resp Dis, I-27100 Pavia, Italy
[2] Univ Pavia, Intens Care Unit 1, IRCCS San Matteo Hosp Fdn, I-27100 Pavia, Italy
[3] Univ Pavia, Serv Immunohematol & Transfus Med, IRCCS San Matteo Hosp Fdn, I-27100 Pavia, Italy
[4] Cincinnati Childrens Hosp Med Ctr, Div Pulm Biol, Cincinnati, OH USA
关键词
Autoantibodies; granulocyte-macrophage colony-stimulating factor; surfactant; whole lung lavage; GM-CSF; AUTOANTIBODIES; LAVAGE;
D O I
10.1183/09031936.00097508
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Whole lung lavage (WLL) is currently the standard therapy for pulmonary alveolar proteinosis (PAP). Nevertheless, some PAP frequently. The present paper reports a patient despite three WLL treatments over 10 months. with autoimmune PAP with persistent disease Plasmapheresis with ten 1.5-L plasma exchanges was performed, which lowered the serum granulocyte-macrophage colony-stimulating colony-stimulating factor (GM-CSF) autoantibody level from 250 mu g.mL(-1) to 156 mu g.mL(-1) 80 weeks after completion of plasmapheresis. However, this decrease was not accompanied by clinical improvement and the patient required additional WLL therapy. The results confirm that minor reductions in serum granulocyte-macrophage colony-stimulating factor autoantibody levels from plasmapheresis are not reflected in clinical improvement in the severity of lung disease in pulmonary alveolar proteinosis.
引用
收藏
页码:1220 / 1222
页数:3
相关论文
共 7 条
[1]   Bronchoalveolar lavage fluid composition in alveolar proteinosis - Early changes after therapeutic lavage [J].
Alberti, A ;
Luisetti, M ;
Braschi, A ;
Rodi, G ;
Iotti, G ;
Sella, D ;
Poletti, V ;
Benori, V ;
Baritussio, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (03) :817-820
[2]   Long-term durable benefit after whole lung lavage in pulmonary alveolar proteinosis [J].
Beccaria, M ;
Luisetti, M ;
Rodi, G ;
Corsico, A ;
Zoia, MC ;
Colato, S ;
Pochetti, P ;
Braschi, A ;
Pozzi, E ;
Cerveri, I .
EUROPEAN RESPIRATORY JOURNAL, 2004, 23 (04) :526-531
[3]  
Bendtzen K, 2007, NEW ENGL J MED, V356, P2001
[4]   Anti-GM-CSF titer predicts response to GM-CSF therapy in pulmonary alveolar proteinosis [J].
Bonfield, TL ;
Kavuru, MS ;
Thomassen, MJ .
CLINICAL IMMUNOLOGY, 2002, 105 (03) :342-350
[5]   Plasmapheresis, GM-CSF, and alveolar proteinosis [J].
Kavuru, MS ;
Bonfield, TL ;
Thomassen, MJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (07) :1036-1036
[6]   Pulmonary alveolar proteinosis [J].
Trapnell, BC ;
Whitsett, JA ;
Nakata, K .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (26) :2527-2539
[7]   High-affinity autoantibodies specifically eliminate granulocyte-macrophage colony-stimulating factor activity in the lungs of patients with idiopathic pulmonary alveolar proteinosis [J].
Uchida, K ;
Nakata, K ;
Trapnell, BC ;
Terakawa, T ;
Hamano, E ;
Mikami, A ;
Matsushita, I ;
Seymour, JF ;
Oh-Eda, M ;
Ishige, I ;
Eishi, Y ;
Kitamura, T ;
Yamada, Y ;
Hanaoka, K ;
Keicho, N .
BLOOD, 2004, 103 (03) :1089-1098