Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia.
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Summary
This novel clinical syndrome links susceptibility to mycobacterial, viral, and fungal infections with malignancy and can be transmitted in an autosomal dominant pattern.
- Type
- article
- Published
- 2010-02-25
- Cited by
- 333
- References
- 72
- OpenAlex
- https://openalex.org/W1990196345
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:6756669
Keywords
Lymphocytopenia, Immunology, Biology, Medicine, Pathology
References
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- Papillomaviruses in the causation of human cancers - a brief historical account.
- Treatment of refractory disseminated nontuberculous mycobacterial infection with interferon gamma. A preliminary report.
- Pulmonary alveolar proteinosis as a terminal complication in myelodysplastic syndromes: a report of four cases detected on autopsy.
- Phagocytosis of Staphylococcus aureus by Macrophages Exerts Cytoprotective Effects Manifested by the Upregulation of Antiapoptotic Factors
- Pulmonary alveolar proteinosis and disseminated Mycobacterium avium infection.
- Direct evidence for a bone marrow origin of the alveolar macrophage in man.
- The order of expression of transcription factors directs hierarchical specification of hematopoietic lineages.
- The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases.
- Pulmonary alveolar proteinosis is a disease of decreased availability of GM-CSF rather than an intrinsic cellular defect.
- Kaposi sarcoma-associated herpesvirus/human herpesvirus 8 and lymphoproliferative disorders
- The prolonged life-span of alveolar macrophages.
- Clinical manifestations and infectious complications of hairy-cell leukaemia.
- The immunobiology of cancer immunosurveillance and immunoediting.
- Sibling cases of Mycobacterium avium complex disease associated with hematological disease
- Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
Cited by
- Myeloid malignancies with somatic GATA2 mutations can be associated with an immunodeficiency phenotype
- Bone marrow failure synd romes and refractory cytopenia of childhood
- Homeostasis of Langerhans and dendritic cells in health and disease
- Primary immunodeficiency update II: Syndromes associated with mucocutaneous candidiasis and non-infectious cutaneous manifestations
- Expression des histones déméthylases dans les cellules hématopoïétiques humaines et les leucémies aiguës
- Pediatric myelodysplastic syndromes
- Myeloid Growth Factors Promote Resistance to Mycobacterial Infection by Curtailing Granuloma Necrosis through Macrophage Replenishment
- A study of biomarker analysis in association with type 1 diabetes and their shared features in rheumatoid arthritis
- Host susceptibility to non-tuberculous mycobacterial infections.
- GATA2 Germline Mutations Impair GATA2 Transcription, Causing Haploinsufficiency: Functional Analysis of the p.Arg396Gln Mutation
- The immunopathogenesis of ankylosing spondylitis
- Contribution of the GATA2 transcription factor to the development and progression of myeloid disorders
- Learning from other diseases: protection and pathology in chronic fungal infections
- Management of Uterine Bleeding During Hematopoietic Stem Cell Transplantation
- Genetic Control of Susceptibility to Candida albicans in SM/J Mice
- ANEMIA OF CENTRAL ORIGIN
- GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia
- Tissue resident macrophages self-maintain locally throughout adult life with minimal contribution from circulating monocytes
- Varicella zoster virus immunity: A primer.
- Opportunistic yeast pathogens: reservoirs, virulence mechanisms, and therapeutic strategies
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