Rituximab therapy in autoimmune pulmonary alveolar proteinosis

Borie R., Debray M-P., Laine C., Aubier M., Crestani B.

Source: Eur Respir J 2009; 33: 1503-1506
Journal Issue: June
Disease area: Interstitial lung diseases

Congress or journal article abstractFull text journal articlePDF journal article, handout or slides

Rating: 0
You must login to grade this presentation.

Share or cite this content

Citations should be made in the following way:
Borie R., Debray M-P., Laine C., Aubier M., Crestani B.. Rituximab therapy in autoimmune pulmonary alveolar proteinosis. Eur Respir J 2009; 33: 1503-1506

You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.

Member's Comments

No comment yet.
You must Login to comment this presentation.


Related content which might interest you:
Plasmapheresis for treatment of pulmonary alveolar proteinosis
Source: Eur Respir J 2009; 33: 1220-1222
Year: 2009



Inhaled GM-CSF for autoimune pulmonary alveolar proteinosis
Source: Short video statement 2020
Year: 2020

Pulmonary alveolar proteinosis
Source: Respipedia Article
Year: 2017

Treatment of severe pulmonary alveolar proteinosis using inhaled GM-CSF
Source: Annual Congress 2010 - Rare diffuse lung diseases
Year: 2010

Successful treatment by GMCSF of pulmonary alveolar proteinosis relapsing after a first GMCSF course
Source: Eur Respir J 2004; 24: Suppl. 48, 670s
Year: 2004

Aerosol granulocyte-macrophage colony-stimulating factor for pulmonary alveolar proteinosis
Source: Eur Respir J 2006; 27: 585-593
Year: 2006



Treatment of pulmonary alveolar proteinosis (PAP) with administration of GM-CSF
Source: Eur Respir J 2002; 20: Suppl. 38, 447s
Year: 2002

Reduced GM-CSF autoantibody in improved lung of autoimmune pulmonary alveolar proteinosis
Source: Eur Respir J 2012; 39: 777-780
Year: 2012


Inhaled GM-CSF in pulmonary alveolar proteinosis (PAP) patient refractory to plasmapheresis combined with multiple whole lung lavages (WLL)
Source: International Congress 2016 – Orphan diseases I
Year: 2016

Inhaled sargramostim and whole lung lavage (WLL) as therapy of autoimmune pulmonary alveolar proteinosis (aPAP)
Source: International Congress 2016 – Orphan diseases I
Year: 2016

Granulocyte-macrophage colony stimulating factor inhalation therapy as a treatment for pulmonary alveolar proteinosis
Source: Eur Respir J 2003; 22: Suppl. 45, 377s
Year: 2003

Neutralizing capacity of autoantibody against GM-CSF in patients with autoimmune pulmonary alveolar proteinosis
Source: International Congress 2018 – Pitfalls in the diagnosis and management of rare diffuse parenchymal lung diseases (DPLDs)
Year: 2018


An open-label trial of rituximab therapy in pulmonary alveolar proteinosis
Source: Eur Respir J 2011; 38: 1361-1367
Year: 2011



Alveolar lipoproteinosis syndromes
Source: Eur Respir Mon 2011; 54: 171-186
Year: 2011


Intercurrent intractable factors in autoimmune pulmonary alveolar proteinosis
Source: Annual Congress 2009 - Various backgrounds in diffuse parenchymal lung disease
Year: 2009


The analysis of alveolar macrophage form in secondary pulmonary alveolar proteinosis complicated with myelodysplastic syndrome.
Source: International Congress 2017 – Rare diseases
Year: 2017

PAS-negative pulmonary alveolar proteinosis
Source: Annual Congress 2008 - Rare clinical cases
Year: 2008

Pulmonary alveolar proteinosis: failure of treatment by bronchoscopic lobar lavages and GM-CSF treatment in a child
Source: Eur Respir J 2003; 22: Suppl. 45, 309s
Year: 2003

Mini-whole lung lavage to treat pulmonary alveolar proteinosis (PAP)
Source: Virtual Congress 2020 – Addressing unresolved questions in rare diffuse parenchymal lung diseases: interdisciplinary research is the key
Year: 2020


The role of apoptosis in idiopathic pulmonary alveolar proteinosis
Source: Annual Congress 2006 - Usefulness of broncoalveolar lavage (BAL) in interstitial lung diseases
Year: 2006