2012
DOI: 10.1097/bor.0b013e32834db4ee
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Myelodysplasia and autoimmunity

Abstract: The encouraging biological insights into the autoimmune component of MDS pathophysiology can lead to the development of novel forms of treatment for controlling MDS process. MDS with AIMs constitute an ideal model in the investigation of disordered immune function in preleukemic states.

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Cited by 30 publications
(22 citation statements)
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“…Among the hematopoietic neoplasms, MDS has been shown to be the most commonly associated disease with AID [21,27]. Associations between CMML and AID, including pyoderma gangrenosum, vasculitis, idiopathic thrombocytopenia, idiopathic eosinophilia and chronic inflammatory demyelinating polyneuropathy, are not uncommon [18,21,28].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Among the hematopoietic neoplasms, MDS has been shown to be the most commonly associated disease with AID [21,27]. Associations between CMML and AID, including pyoderma gangrenosum, vasculitis, idiopathic thrombocytopenia, idiopathic eosinophilia and chronic inflammatory demyelinating polyneuropathy, are not uncommon [18,21,28].…”
Section: Discussionmentioning
confidence: 99%
“…Some cytokine releases and clonal T-LGL/NK cell expansion during an autoimmune process could alter tissue microenvironments [47]. If the process occurred in MDS bone marrow, it would cause gene dysregulation in hematopoietic stem cells [27]. …”
Section: Discussionmentioning
confidence: 99%
“…Either way, both AA and MDS have a proportion of patients that have associated with clinical autoimmune phenomena 6,7 in addition to T cellmediated myelosuppression, and cytokine dysregulation in the bone marrow environment. Thus, the link of both disorders to an underlying autoimmune mechanism with an association with other autoimmune manifestations appears to be well established.…”
mentioning
confidence: 99%
“…Nonhematologic autoimmune disorders in MDS were fi rst described by Hamblin [6]. Castro et al reviewed 162 patients with MDS over a 6-month period, among whom rheumatic manifestations such as cutaneous vasculitis, lupus-like syndrome, or neuropathy was observed in 10% of the patients [1].…”
Section: Discussionmentioning
confidence: 99%