Partial plasma cell differentiation as a mechanism of lost major histocompatibility complex class II expression in diffuse large B-cell lymphoma
Blood, ISSN: 0006-4971, Vol: 119, Issue: 6, Page: 1459-1467
2012
- 51Citations
- 44Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations51
- Citation Indexes51
- 51
- CrossRef34
- Captures44
- Readers44
- 44
Article Description
Loss of major histocompatibility complex class II (MHC II) expression is associated with poor patient outcome in diffuse large B-cell lymphoma (DLBCL). As MHC II molecules are lost with plasmacytic differentiation in normal cells, we asked whether MHC II loss in DLBCL is associated with an altered differentiation state. We used gene expression profiling, quantum dots, and immunohistochemistry to study the relationship between MHC II and plasma cell markers in DLBCL and plasmablastic lymphoma (PBL). Results demonstrate that MHC II(−) DLBCL immunophenotypically overlap with PBL and demonstrate an inverse correlation between MHC II and plasma cell markers MUM1, PRDM1/Blimp1, and XBP1s. In addition, MHC II expression is significantly higher in germinal center-DLBCL than activated B cell-DLBCL. A minor subset of cases with an unusual pattern of mislocalized punctate MHC II staining and intermediate levels of mRNA is also described. Finally, we show that PBL is negative for MHC II. The results imply a spectrum of MHC II expression that is more frequently diminished in tumors derived from B cells at the later stages of differentiation (with complete loss in PBL). Our observations provide a possible unifying concept that may contribute to the poor outcome reported in all MHC II(−) B-cell tumors.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0006497120461105; http://dx.doi.org/10.1182/blood-2011-07-363820; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84856882081&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/22167754; https://ashpublications.org/blood/article/119/6/1459/30166/Partial-plasma-cell-differentiation-as-a-mechanism; https://ashpublications.org/blood/article-pdf/119/6/1459/1357301/zh800612001459.pdf; http://www.bloodjournal.org/content/119/6/1459; http://www.bloodjournal.org/content/119/6/1459.abstract; http://www.bloodjournal.org/content/119/6/1459.full.pdf; http://www.bloodjournal.org/content/119/6/1459?sso-checked=true; http://www.bloodjournal.org/cgi/doi/10.1182/blood-2011-07-363820
American Society of Hematology
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