key: cord-0001916-1px4aq89
authors: Griese, Matthias; Zarbock, Ralf; Costabel, Ulrich; Hildebrandt, Jenna; Theegarten, Dirk; Albert, Michael; Thiel, Antonia; Schams, Andrea; Lange, Joanna; Krenke, Katazyrna; Wesselak, Traudl; Schön, Carola; Kappler, Matthias; Blum, Helmut; Krebs, Stefan; Jung, Andreas; Kröner, Carolin; Klein, Christoph; Campo, Ilaria; Luisetti, Maurizio; Bonella, Francesco
title: GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders
date: 2015-08-12
journal: BMC Pulm Med
DOI: 10.1186/s12890-015-0083-2
sha: 35c1acec82c2f75a5d311b6adaceee30cbedaf6c
doc_id: 1916
cord_uid: 1px4aq89

BACKGROUND: The majority of cases with severe pulmonary alveolar proteinosis (PAP) are caused by auto-antibodies against GM-CSF. A multitude of genetic and exogenous causes are responsible for few other cases. Goal of this study was to determine the prevalence of GATA2 deficiency in children and adults with PAP and hematologic disorders. METHODS: Of 21 patients with GM-CSF-autoantibody negative PAP, 13 had no other organ involvement and 8 had some form of hematologic disorder. The latter were sequenced for GATA2. RESULTS: Age at start of PAP ranged from 0.3 to 64 years, 4 patients were children. In half of the subjects GATA2-sequence variations were found, two of which were considered disease causing. Those two patients had the typical phenotype of GATA2 deficiency, one of whom additionally showed a previously undescribed feature – a cholesterol pneumonia. Hematologic disorders included chronic myeloic leukemia, juvenile myelo-monocytic leukemia, lymphoblastic leukemia, sideroblastic anemia and two cases of myelodysplastic syndrome (MDS). A 4 year old child with MDS and DiGeorge Syndrome Type 2 was rescued with repetitive whole lung lavages and her PAP was cured with heterologous stem cell transplant. CONCLUSIONS: In children and adults with severe GM-CSF negative PAP a close cooperation between pneumologists and hemato-oncologists is needed to diagnose the underlying diseases, some of which are caused by mutations of transcription factor GATA2. Treatment with whole lung lavages as well as stem cell transplant may be successful.

Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by the progressive accumulation of surfactant in the alveoli of the lungs, leading to hypoxemic respiratory failure and, in severe cases, to death [1]. PAP is caused by (i) genetic diseases which result in dysfunction of surfactant or surfactant production (SFTPC, SFTPB, ABCA3, TTF1 deficiency) mainly presenting during infancy, by (ii) disruption of GM-CSF signaling from mutations in the receptor (GM-CSFRa, GM-CSFRb) or from acquired autoantibodies against GM-CSF, and by (iii) disorders that presumably impair surfactant clearance because of abnormal numbers or defective phagocytic functions of alveolar macrophages [2] . The latter are caused by inhaled particles or by hematologic disorders affecting macrophage precursors.

A broad spectrum of hematologic disorders have been associated with PAP, most frequently myelodysplastic syndrome (MDS), and more rarely acute (AML) and chronic myeloid leukaemia (CML), myelofibrosis, acute lymphoid leukaemia (ALL), adult T-cell leukaemia, aplastic anemia, lymphoma, multiple myeloma, plasmacytoma, essential thrombocytosis [3] , congenital dyserythropoietic anemia [4] , and status after unrelated stem cell transplant [5, 6] .

Up to now only mutations in one specific gene -GATA2have been associated with this form of PAP.

GATA2 is a zinc finger transcription factor essential for differentiation of immature hematopoietic cells [7] . Among many other functions GATA2 regulates the phagocytosis of alveolar macrophages [8] . Alveolar macrophages treated with the sense GATA-2 expression construct show an increase in their phagocytic activity by up to 280 % compared to the antisense construct [9] . GATA2 deficiency is a recently described disorder of hematopoiesis, lymphatics, and immunity, caused by heterozygous mutations leading to haplo-insufficiency of the transcription factor GATA2. The disease presents with a complex array of diagnoses and symptoms of varying extent including MDS, AML, chronic myelomonocytic leukemia (CMML), severe viral, disseminated mycobacterial and invasive fungal infections, pulmonary arterial hypertension, warts, panniculitis, human papillomavirus (HPV) positive tumors, Epstein-Barr virus (EBV) positive tumors, venous thrombosis, lymphedema, sensorineural hearing loss, miscarriage and hypothyroidism [6] . PAP has been reported in about 18 % of all subjects with GATA2 deficiency [6, 10] . However, not much is known on the severity and clinical course of PAP in these subjects, which were exclusively adults. Pneumologists treating patients with severe PAP not caused by autoantibodies against GM-CSF frequently do not know the cause of these rare conditions [11] .

Here, we investigate a cohort of children and adults with severe and chronic PAP and hematologic disease for the presence of GATA2 mutations. GATA2 mutations were identified in a minority of patients only. One child with a GATA2 variant was successfully treated initially by therapeutic whole lung lavages (WLL) and eventually by stem cell transplant.

All subjects with PAP diagnosed based on the characteristic phenotype by lung biopsy or bronchoalveolar lavage (BAL) and CT scan findings were identified from the kids-lung-register (http://www.kinderlungenregister.de/ index.php/en/) within the child-EU project (European Register and Biobank on Childhood Interstitial Lung Diseases, European Commission, FP7, GA 305653).

In order to differentiate subgroups of PAP, all patients with GM-CSF-Ra or Rb mutations [12] and a high GM-CSF autoantibody level were excluded. 21 subjects were identified of whom 13 (11 adults, 2 children) had pulmonary involvement only. 8 subjects suffered from PAP and a hematologic disease -diagnosed by standard proceduresand were selected for further analysis (Fig. 1) .

The GATA2 gene was analysed by Sanger sequencing. Genomic DNA was isolated from EDTA blood samples using the QIAamp DNA Blood Mini Kit (Qiagen) and PCR amplified using HotStarTaq polymerase (Qiagen). PCR products were purified with the MinElute 96 UF PCR Purification Kit (Qiagen). Primers used for PCR and sequencing reactions are shown in Table 1 . Sequencing was performed by GATC Biotech AG (Konstanz, Germany).

In subject 4 800 ng of genomic DNA extracted from formalin fixed tissue were fragmented to an average size of 200 bp and desired fragment sizes were obtained with Agencourt® AMPure® XP beads (Beckman Coulter). Sequencing libraries were prepared using Accel-NGS-1S Library Kit (Swift Biosciences, Ann Harbor, MI), sequenced on the HiSeq 1500 (Illumina) and aligned to the human genome assembly (hg19). The GATA2 locus was covered by 86 reads.

Follow-up data of the patients were collected until October 2014. The study was approved by the institutional review board, the ethics commission of the medical faculty of the Ludwig-Maximilians University, Munich, Germany (EK 026-06). All parents or guardians gave their written informed consent, the children gave assent.

Age at onset of PAP ranged from 0.4 to 64 years. Half of the patients were children (Table 2 ). Beside chronic respiratory insufficiency due to PAP, all patients suffered from recurrent respiratory tract infections or exacerbations. These were mainly common cold viral infections, in some cases non-tuberculous mycobacteria, herpes simplex virus (HSV), and cytomegalovirus (CMV) were identified. All patients were immunodeficient: in three patients primary immunodeficiency syndromes were identified: two with a monocyte deficiency not further specified (no. 2, 4) and one with a Di George type II syndrome with combined Table 1 Sequences of primers used for amplification of the GATA2 gene   Exon  Forward  Reverse   #1  CCC GCA AAG TGA TGT CG  CAA ACG GAC CAA GCG ATT C   #2  ACC TCG TGG TGG GAC TTT G  GAT CCT ACA TCC GGG The hallmark of all patients of this study was severe PAP with continuous need of oxygen (Table 2 ). All but two subjects (no. 4, 5) were treated symptomatically with repetitive therapeutic WLL to improve respiratory insufficiency. Treatment was eventually not successful in 3 patients who died from respiratory failure, complicated by infection or acute respiratory distress syndrome (ARDS).

Autoantibodies against GM-CSF were determined in order to characterize PAP further, they were negative in all patients (Table 3) . Serum levels of GM-CSF were not significantly increased in the patients with serum available. 4 of the 8 patients had sequence anomalies in GATA2 ( Table 3) . Two of these, a synonymous variant and a missense variant were predicted not to be damaging by Polyphen-2 [13] and SIFT [14] . The other two were heterozygous point mutations predicted to be deleterious, both of these patients had a phenotype characteristic for GATA2 deficiency.

The courses of cases 2, 4, 7 and 8 are reported in more detail to illustrate characteristic presentations.

A 34 year old male patient presented with disseminated Mycobacterium avium intracellulare infection, including the lungs, chronic labial herpes including a positive serum HSV PCR, and M. Bowen of the skin. Cellular immunodeficiency was suspected based on absent monocytes; the patient was HIV-negative. 3 years later the patient developed respiratory insufficiency, the CT scan showed consolidations suspicious of cryptogenic organizing or atypical pneumonia. Several courses of antibiotic therapy were followed by two pulses of cyclophosphamide; the patient deteriorated further, CT scan showed bilateral interstitial thickening and crazy-paving pattern. Open lung biopsy revealed PAP. Bone marrow aspiration was normal. He was treated symptomatically with WLL under ECMO (extracorporeal membrane oxygenation) support, developed anuric acute renal failure, and died from acute cardiac failure. The patient carried the mutation p.Y377D in the GATA2 gene.

A 38 year old female patient presented with recurrent bronchitis and sinusitis, breathlessness during exercise, and interstitial markings on chest x-ray. An open lung biopsy was performed, histology revealed PAP associated with cholesterol pneumonia. Liver and bone marrow biopsies were normal. In the following months she developed progressive peripheral edema and cardiac insufficiency with mild pulmonary hypertension. She further developed a pseudomembranous glomerulonephritis with nephrotic syndrome and a Pseudomonas urosepsis at 39 years. At 40 years cellular immunodeficiency was demonstrated based on the absence of monocytes. She developed condylomatous lesions of the vulva and HPVassociated (types 16 and 28) vulva intraepithelial neoplasia grade 2-3 (VIN2-VIN3), which was resected. Her course was determined by chronic respiratory failure (at rest 4LO2/min; PaO2 45 mmHg (normal > 86), normal PaC02). However, no WLL were performed as the patient was lost on follow up at 43 years. The patient carried the mutation p.R398W in the GATA2 gene.

Case no. 7 A 4.5 year old girl with Di George Syndrome type II from deletion of 10p (OMIM 601362) with severe immunodeficiency, single right kidney, inner ear deafness, [15] , with good clinical and radiological response over a period of one year (Fig. 2) . A HLA-identical (10/10) unrelated-stem cell donor was identified at the age of 10 years and she received allogeneic stem cell transplant. Within a few weeks after transplant, PAP and respiratory distress resolved (Fig. 2) .

A full-term boy with normocytic anemia (Hb 13.1 g/dL) presented after a few weeks with paleness, fatigue, tachydyspnea, and failure to thrive. At the age of four month the hemoglobin level had decreased to 5.3 g/dL and a sideroblastic anemia was diagnosed. No genetic cause was identified; Pearson syndrome and mutations in ALAS2 and SLC25A38 were excluded. His bone marrow showed massive erythroid hyperplasia with dyserythropoiesis and marked depression of myeloid cells. Pulmonary infiltrates were initially interpreted as pneumonia. At the age of 5 months a CMV infection was successfully treated with ganciclovir. At 8 months he developed respiratory failure (PaO2 60 mmHg, PaCO2 55 mmHg) with bilateral pulmonary infiltrates. The diagnosis of PAP was made by analysis of BAL fluid and open lung biopsy. From the age 8 to 23 months the boy underwent 11 therapeutic WLLs, improving his general condition and gas exchange. Currently he maintains oxygen-saturation levels above 92 % under oxygen support 0.5-1 l of O2/min). The anemia is stable with Hb levels between 7.5 and 9.0 g/dL. The molecular cause of very rare sideroblastic anemia was not revealed, the associated depression of myeloid cells was likely the cause of PAP. GATA2 deficiency was not causal, as the patient showed no GATA2 variant in our investigations; potential intronic variations were not investigated.

This study shows that GATA2 mutations in patients with hematologic diseases and severe PAP occur at a relatively low frequency. GATA2 analysis may help to diagnose the underlying hematologic condition. Severe PAP in children due to MDS can be cured by stem cell transplant. Severe PAP is a rare but serious complication of hematologic disorders. Here we differentiated two groups of diseases having in common a presentation with significant chronic respiratory insufficiency and recurrent pulmonary tract infections or exacerbations. These groups included (i) patients with GATA2 deficiency, a protean disorder of hematopoiesis, lymphatics, and immunity [6] , and (ii) patients with functionally or numerically reduced alveolar macrophages and/or their respective mononuclear precursors due to CML, JMML, cALL, MDS or sideroblastic anemia in the absence of disease causing GATA2 mutations.

GATA2 deficiency has a broad phenotype encompassing immunodeficiency, MDS/AML, pulmonary disease, and vascular/lymphatic dysfunction. A precise history and knowledge of the disease course may help to select potential candidates with high confidence for specific genetic diagnostic. GATA2 gene mutations were associated with PAP in two cases; p.Y377D is a novel missense mutation demonstrated here to present with the classical mono-MAC syndrome [16] . p.R398W has previously been described in six patients, of whom 2 had a PAP [6] . Here we add the histopathological feature of cholesterol pneumonia to this phenotype. Of interest, further heterozygous variations in GATA2 were identified in two other subjects; however these were predicted to be non-disease causing ( Table 3) . As not all subjects with a specific GATA2 mutation causing GATA2 deficiency develop PAP [6] , additional factors are involved which determine PAP. Patients with the same GATA2 mutation need to be investigated further and experimental models will help to better understand the molecular defect(s) leading to PAP. Similarly, in non-GATA2 deficient patients with PAP and hematologic abnormalities, the mechanism of PAP development is unknown. Currently, their PAP is presumed to be due to reduced monophagocytic function in the alveoli to clear surfactant [17] . Best proof for the critical role of bonemarrow derived alveolar macrophages for surfactant homeostasis is provided by the correction of PAP by SCT. This was shown here for the first time in a young child. Shortly, i.e. within days after take of SCT, there was clearing of PAP, superseding rapidly the need for therapeutic WLLs (Fig. 1) .

Here we also show that WLLs are feasible also for children, even at very young age, with small sized airways and in the presence of severe respiratory distress, using techniques we have established previously [18] . WLL can be used to symptomatically treat all types of PAP and to bridge until the underlying condition can be cured or alternative treatments have been implemented.

Due to relative immune deficiency state and irrespective of the cause, the impact of infections should be considered Fig. 2 Long term course of a child suffering from DiGeorge syndrome type II and PAP due to MDS with monosomy 7, trisomy 8, and a GATA2 missense variant. Successful treatment by therapeutic WLLs, and definitive treatment of the PAP by SCT. (a) clinical course (b,c) CT1 at presentation (d,e) CT2 after first 2 whole lung lavages (f) CXR 1 before SCT (g) CXR2 7 weeks after SCT and (h) CXR3 1 year after SCT carefully. It is likely that with often severe respiratory tract infections PAP may be triggered to deteriorate. Thus we recommend early diagnosis and proper antimicrobial treatment, in particular of organisms characteristic for these often lethal conditions, including mycobacteria, nocardia, herpes viruses, and fungi [6, 19, 20] . In addition and concordant with the immune deficiency the extensive usage of systemic corticosteroids should be cautioned, as there is so far no evidence of their beneficial effect in PAP. Extensive usage might enhance immune deficiency and weaken antimicrobial defense further [15] .

After confirming the diagnosis of PAP either by a combination of characteristic CT scan and BAL findings and trans-bronchial or open lung biopsy, it is important to determine the etiology of PAP. As more than 90 % of PAP in adulthood is caused by autoantibodies against GM-CSF [1, 21, 22] , this condition has to be initially excluded by analysis of serum [23, 24] . None of our patients had increased levels of GM-CSF autoantibodies. Serum levels of GM-CSF are low in autoimmune PAP [25] , whereas elevated values can be found in congenital GM-CSFRa or GM-CSFRb defects and possibly in other forms of PAP. Thus, particularly in children these other entities need to be excluded. In our cohort of patients with severe PAP and hematologic diseases, serum GM-CSF level were low to intermediate, supporting some up regulation of GM-CSF. Next, genetic analysis of GATA2 is helpful in order to diagnose the underlying hematologic entity more precisely, in particular in patients who meet the broad but characteristic phenotype of GATA2 deficiency [6] . This diagnostic algorithm for PAP will allow differentiating important subgroups and may help to identify further genetic abnormalities, known or suspected to be associated with PAP.

When investigating a patient with severe PAP, the pneumologist should be aware of the wide range of diseases which can cause secondary PAP and consider interdisciplinary involvement of a hemato-oncologist. Conversely, hemato-oncologists should include PAP in the differential diagnosis of respiratory failure associated with pulmonary interstitial changes in hematologic diseases. 

ATB-binding cassette sub-family A member 3; ALL: Acute lymphoid leukemia; AML: Acute myeloid leukemia; ARDS: Acute respiratory distress syndrome; BAL: Bronchoalveolar lavage; cALL: common acute lymphoblastic leukemia; CML: Chronic myeloid leukemia; CMML: Chronic myelomonocytic leukemia

ECMO: Extracorporeal membrane oxygenation; GM-CSF: Granulocyte macrophage colony-stimulating factor; HPV: Human papilloma virus

HSV: Herpes simplex virus; JMML: Juvenile myelomonocytic leukemia

MDS: Myelodysplastic syndrome; PAP: Pulmonary alveolar proteinosis

SFTPB: Gene encoding for Surfactant protein B; SFTBC: Gene encoding for Surfactant protein C; TTF1: Thyroid transcription factor 1; WLL: Whole lung lavage. References 1. Seymour JF, Presneill JJ. Pulmonary alveolar proteinosis: progress in the first 44 years

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The work of MG was kindly supported by Else-Kroener-Fresenius Stiftung (MG 2013_A72), by the German Federal Ministry of Education and Research (EuPAPNet project inside ERARE, number 01GM1011A), European Register and Biobank on Childhood Interstitial Lung Diseases (European Commission, FP7, GA 305653, chILD-EU).

The authors declare that they have no competing interests.Authors' contributions MG designed the study, collected the cases, analysed the data and wrote the draft of the manuscript. He is the guarantor of the entire manuscript. UC, AMH, JL, KK, BF, ML, CS, CK and MG contributed and evaluated patients and performed chart review, ZR, AS, BH, SK, CKr, and JA performed laboratory analyses, CU, CKr and BF critically revised the manuscript, DT provided tissue samples and performed histopathological analyses, AS, TW, UC and FB contributed to the long term collection of subjects, patient recruitment and evaluation. All contributors read and agreed to the final version of the manuscript.Author's information This paper is devoted to Prof. Maurizio Luisetti's outstanding contribution to the field of human alveolar proteinosis.