Phase 1b randomized, double-blind study of namilumab, an anti-granulocyte macrophage colony-stimulating factor monoclonal antibody, in mild-to-moderate rheumatoid arthritis [PDF]
Change from baseline in swollen (a) and tender (b) joint counts. *Error bars show upper SE for placebo and lower SE for namilumab. SE standard error, SJC swollen joint count, TJC tender joint count.
A. Batalov +47 more
core +3 more sources
Pulmonary alveolar proteinosis (PAP) and anti‐PL‐7 antibody‐positive interstitial lung disease (ILD) share early radiographic similarities, yet their treatments differ significantly. This article reports a rare case of dual anti‐PL‐7 and anti‐GM‐CSF autoantibody positivity, initially misdiagnosed as anti‐synthetase syndrome due to interstitial ...
Beili Liu +5 more
wiley +1 more source
Autoimmune pulmonary alveolar proteinosis prior to myelodysplastic syndrome
We report the first case of autoimmune pulmonary alveolar proteinosis (PAP) associated with and preceding myelodysplastic syndrome. A 74‐year‐old female with a history of polymyalgia rheumatica presented with six months history of progressive exertional ...
Chuan Tai Foo +2 more
doaj +1 more source
Niche signals and transcription factors involved in tissue-resident macrophage development [PDF]
Tissue-resident macrophages form an essential part of the first line of defense in all tissues of the body. Next to their immunological role, they play an important role in maintaining tissue homeostasis. Recently, it was shown that they are primarily of
Bonnardel, Johnny +2 more
core +2 more sources
Insuficiencia respiratoria neonatal asociada a mutación en el gen de la proteína C del surfactante [PDF]
La insuficiencia respiratoria en el recién nacido a término durante las primeras semanas de vida extrauterina es una situación poco frecuente. Entre sus causas se incluyen las enfermedades difusas del intersticio pulmonar, un grupo heterogéneo de ...
Alava, E. (Enrique) de +4 more
core +1 more source
Transfer RNA and small molecule therapeutics for aminoacyl‐tRNA synthetase diseases
Aminoacyl‐tRNA synthetases catalyze the ligation of a specific amino acid to a cognate tRNA—a reaction that lays the foundations for deciphering the genetic code. Pathogenic alleles in these synthetases can lead to dominant or recessive disorders, for which little or no disease‐specific treatments exist.
Tristan N. Samuels +8 more
wiley +1 more source
Impact of A Multidisciplinary Team Discussion for Genetic Lung Fibrosis
ABSTRACT Background and Objective Approximately 30% of individuals diagnosed with familial pulmonary fibrosis (FPF) exhibit a pathogenic variant upon genetic analysis. We established a genetic Multidisciplinary Discussion (geneMDD) aimed to enhance expertise in diagnosing and managing FPF.
Giovanni Franco +30 more
wiley +1 more source
In this study, we report the history of a 40-year-old man with a primary cerebral abscess caused by Nocardia abscessus that led to the discovery of autoimmune pulmonary alveolar lipoproteinosis (anti-granulocyte-macrophage colony-stimulating factor [GM ...
Charlotte Berthoux +6 more
semanticscholar +1 more source
A case of uncomplicated pulmonary alveolar proteinosis evolving to pulmonary fibrosis
Pulmonary alveolar proteinosis (PAP) is a rare syndrome characterised by intra-alveolar accumulation of surfactant components and cellular debris, with minimal interstitial inflammation or fibrosis.
A. Chroneou +4 more
doaj +1 more source
Venoarterial extracorporeal membrane oxygenation (ECMO) for support during whole lung lavage for pulmonary alveolar proteinosis. [PDF]
INTRODUCTION ECMO as support during whole lung lavage (WLL) for pulmonary alveolar proteinosis is reserved for severe cases where oxygenation is inadequate to support the patient using the ventilator alone.
Cavarocchi, Nicholas C +4 more
core +2 more sources

