AI Article Synopsis

  • B-Cell Lymphoproliferative Disorders (B-LPDs) are characterized by the accumulation of B-cells in various parts of the body and present diagnostic challenges due to their similar features and varied outcomes.
  • Accurate diagnosis through immunophenotyping by flow cytometry is crucial, and the recent discovery of CD200's differential expression aids in distinguishing between similar disorders like chronic lymphocytic leukaemia (CLL) and mantle cell lymphoma (MCL).
  • A study analyzing 100 samples revealed that while all CLL cases expressed CD200, 6 MCL cases showed no expression, highlighting CD200’s potential role in improving clinical diagnosis and treatment strategies.

Article Abstract

B-Cell Lymphoproliferative Disorders (B-LPDs) are a group of heterogenous disorders characterised by the accumulation of B-cells in peripheral blood, bone marrow, lymph nodes and spleen. They have a variable disease course and outcome and many share similar features making differential diagnosis challenging. Therefore, accurate diagnosis is fundamental in particular for determining treatment options. Immunophenotyping by flow cytometry plays a crucial role in the diagnosis of B-LPDs. However, overlapping immunophenotyping patterns exist and the use of novel monoclonal antibodies has become increasingly important in immunophenotyping analysis. More recently differential expression of CD200 has been reported in various B-LPDs and that CD200 may improve the differentiation between chronic lymphocytic leukaemia (CLL) and mantle cell lymphoma (MCL). In this study CD200 expression is evaluated in different B-LPDs. A total of 100 samples were collected and analysed by immunophenotyping flow cytometry over a period of 1 year (2017-2018), by a panel of monoclonal antibodies including CD200. The percentage of CD200 and its expression intensity was evaluated and compared between different groups of B-LPDs. All of the 50 cases of CLL expressed CD200 with moderate to bright intensity, 6 MCL cases lacked the expression of CD200. Furthermore, all 5 cases of hairy cell leukaemia (HCL) expressed CD200. Out of all B-LPDs evaluated, CD200 expression in HCL cases was noted to be the brightest. The other 39 cases were not found to be B-LPDs. CD200 has an important role in differentiating CLL from MCL, HCL has a consistent bright expression of CD200. By adding CD200 to the combinations of markers in routine testing panel, Immunophenotyping by flow cytometry can be an effective tool in the diagnosis of B-LPDs especially in cases with atypical immunophenotyping pattern. Our result support that CD200 can be added to routine testing panel as it is useful in differentiating them.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563807PMC
http://dx.doi.org/10.3389/bjbs.2023.11573DOI Listing

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