2007
DOI: 10.3960/jslrt.47.31
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MALT Lymphoma : Recent Advances in Aetiology and Molecular Genetics

Abstract: Mucosa-associated lymphoid tissue (MALT) lymphoma is a common low grade B-cell lymphoma arising from a background of chronic inflammatory disease at a number of mucosal sites. Those originating in the stomach are causatively linked to Helicobacter pylori infection and eradication of the bacterium with antibiotics leads to long-term complete regression of the lymphoma in ∼ 70% of cases. Now, there is further evidence of linking Campylobacter jejuni, Borrelia burgdorferi and Chlamydia psittaci infection with imm… Show more

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Cited by 126 publications
(102 citation statements)
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“…psittaci elementary bodies in the PBMCs were found viable and infectious and capable to grow in vitro and to be isolated from patients with OAMZL [79]. Taken together, the fact that C. psittaci can be isolated and grown in vitro from biological samples of OAL patients, improves the evidence level supporting this bacte-ria-lymphoma association and fulfills the second Koch's postulate hitherto reserved for H. pylori for gastric lymphoma [81].…”
Section: The Role Ofsupporting
confidence: 53%
“…psittaci elementary bodies in the PBMCs were found viable and infectious and capable to grow in vitro and to be isolated from patients with OAMZL [79]. Taken together, the fact that C. psittaci can be isolated and grown in vitro from biological samples of OAL patients, improves the evidence level supporting this bacte-ria-lymphoma association and fulfills the second Koch's postulate hitherto reserved for H. pylori for gastric lymphoma [81].…”
Section: The Role Ofsupporting
confidence: 53%
“…13,15 The optimal treatment approach for localized nongastric MALT lymphoma is still evolving. Micro-organisms have been implicated in the pathogenesis of MALT lymphoma arising from some locations, 16 with successful treatment by using antibiotics, most notably doxycycline for orbital MALT lymphomas. [17][18][19] However, the results are still premature to consider it as a primary modality of therapy because durable remission has only been documented in 48% in a cohort of 27 patients treated 19 and that a uniformly high response rate has not been reported by other investigators.…”
Section: Discussionmentioning
confidence: 99%
“…Malt1 gene is localized in a break point of chromosome 18q21 and t(11;18)(q21;q21) generates API2-MALT1 fusion protein, whereas t(14;18)(q32;q21) juxtaposes Malt1 gene to the immunoglobulin locus and upregulates its expression [41,43,44]. Although transient transfection of wild type MALT1 does not significantly activate NF-κB, overexpression of its oncogenic form potently activates NF-κB in vitro [42,45].…”
Section: Cbm Proteins In Antigen Receptor Signalingmentioning
confidence: 99%