Faculty, Staff and Student Publications
Publication Date
8-13-2024
Journal
Biology
DOI
10.3390/biology13080613
PMID
39194551
PMCID
PMC11351582
PubMedCentral® Posted Date
August 2024
PubMedCentral® Full Text Version
Post-print
Abstract
It is common knowledge that immunoglobulin (Ig) is produced by B lymphocytes and mainly functions as an antibody. However, it has been shown recently that myeloblasts from acute myeloid leukemia (AML) could also express Ig and that AML-Ig played a role in leukemogenesis and AML progression. The difference between Ig from myeloblasts and B cells has not been explored. Studying the characteristics of the Ig repertoire in myeloblasts and B cells will be helpful to understand the function and significance of AML-Ig. We performed 5' RACE-related PCR coupled with PacBio sequencing to analyze the Ig repertoire in myeloblasts and B cells from Chinese AML patients. Myeloblasts expressed all five classes of IgH, especially Igγ, with a high expression frequency. Compared with B-Ig in the same patient, AML-Ig showed different biased V(D)J usages and mutation patterns. In addition, the CDR3 length distribution of AML-Ig was significantly different from those of B-Ig. More importantly, mutations of AML-IgH, especially Igμ, Igα, and Igδ, were different from that of B-IgH in each AML patient, and the mutations frequently occurred at the sites of post-translational modification. AML-Ig has distinct characteristics of variable regions and mutations, which may have implications for disease monitoring and personalized therapy.
Keywords
acute myeloid leukemia, myeloblast, immunoglobulin, V(D)J rearrangement patterns, somatic hypermutation, B cells
Published Open-Access
yes
Recommended Citation
Yan, Huige; Wu, Lina; Wang, Pingzhang; et al., "A Comparative Analysis of the Immunoglobulin Repertoire in Leukemia Cells and B Cells in Chinese Acute Myeloid Leukemia by High-Throughput Sequencing" (2024). Faculty, Staff and Student Publications. 2432.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/2432
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