Related Experiment Video
Updated: Aug 28, 2025

15:07
VDJ-Seq: Deep Sequencing Analysis of Rearranged Immunoglobulin Heavy Chain Gene to Reveal Clonal Evolution Patterns of B Cell Lymphoma
Published on: December 28, 2015
26.8K
Gastric DLBCL clonal evolution as function of patient age
Irina Iosselevitch1, Hilla Tabibian-Keissar2, Iris Barshack1,2,3
1The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.
Frontiers in Immunology
|September 15, 2022
Summary
Gastric Diffuse Large B cell lymphoma (DLBCL) development varies with age. Contrary to expectations, elderly patients exhibited a more diverse repertoire of gastric B cell clones than younger individuals.
Area of Science:
- Oncology
- Immunology
- Gastroenterology
Background:
- Diffuse Large B cell lymphoma (DLBCL) is the most common and aggressive non-Hodgkin lymphoma (NHL).
- Gastric DLBCL, a subtype affecting the stomach, remains under-investigated, particularly concerning age-related changes.
- DLBCL incidence peaks in individuals over 50 but can affect younger patients.
Purpose of the Study:
- To investigate age-related alterations in the development of gastric Diffuse Large B cell lymphoma (gastric DLBCL).
- To analyze the clonal diversity of gastric B cells in relation to patient age.
Main Methods:
- Amplification and sequencing of immunoglobulin (Ig) heavy chain variable region genes.
- Analysis of nine preserved gastric DLBCL biopsies from patients aged 25 to 89 years.
- Comparative analysis of clonal repertoire diversity between young and elderly DLBCL patients.
Main Results:
- Malignant clone identification from biopsies proved less certain than previously assumed.
- The repertoire of gastric B cell clones was found to be more diverse in elderly DLBCL patients compared to younger ones.
- This diversity finding contrasts with prior expectations regarding age and lymphoma development.
Conclusions:
- Age significantly influences the clonal diversity of gastric B cells in DLBCL.
- Understanding these age-related changes is crucial for further investigation into gastric DLBCL pathogenesis.
- The study highlights the need for refined methods in malignant clone identification in lymphoma biopsies.
Keywords:
B lymphocytesImmunoglobulin (Ig)agingantigen receptor repertoiregastric diffuse large B cell lymphoma (DLBCL)high-throughput sequencing (HTS)lineage treessomatic hypermutation
