Detailed Information

Cited 1 time in webofscience Cited 1 time in scopus
Metadata Downloads

T cell receptor repertoires of ex vivo-expanded tumor-infiltrating lymphocytes from breast cancer patients

Authors
Park, IA[Park, In Ah]Rajaei, H[Rajaei, Hajar]Kim, YA[Kim, Young-Ae]Lee, H[Lee, Hyeonjin]Lee, H[Lee, Heejae]Seo, JH[Seo, Jeong-Han]Heo, SH[Heo, Sun-Hee]Song, IH[Song, In Hye]Gong, G[Gong, Gyungyub]Lee, HJ[Lee, Hee Jin]
Issue Date
Oct-2020
Publisher
HUMANA PRESS INC
Keywords
Breast cancer; Tumor-infiltrating lymphocytes; Expansion; T cell receptor
Citation
IMMUNOLOGIC RESEARCH, v.68, no.5, pp.233 - 245
Indexed
SCIE
SCOPUS
Journal Title
IMMUNOLOGIC RESEARCH
Volume
68
Number
5
Start Page
233
End Page
245
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/2897
DOI
10.1007/s12026-020-09150-8
ISSN
0257-277X
Abstract
A higher level of tumor-infiltrating lymphocytes (TILs) is associated with better prognosis in breast cancer patients. Adoptive transfer of lymphocytes coupled with conventional therapies has appealed to many clinicians and investigators as an effective treatment strategy for cancer patients, which necessitates efficient activation and expansion of cytotoxic T lymphocytes precisely targeting cancer cells. To comprehensively understand composition of TILs and to provide a grounding in adoptive T cell therapy, we analyzed the T cell receptor (TCR) repertoires in ex vivo-expanded TILs from nine breast cancer patients via next-generation sequencing. For the three of them, TCR repertoires of TILs gathered after the initial culture during 2 weeks were additionally analyzed and compared to those of TILs that underwent ex vivo rapid expansion procedure (REP). Diversity of TCR repertoire was variable among the patients. V/J segment usage in the clonotypes was similar among patients, with variable distribution of read counts for each V/J segment. The top 50% of most frequently observed VJ combinations was present in > 80% of the total clonotypes. Compared with TCGA data, the samples contained a similar amount of recurrent CDR3 sequences, but clonotype expansion was variable among the samples. In terms of clinicopathologic factor, presence of in vitro reactivity among triple-negative breast cancer cases seemed to be related to lower Shannon's index, butpvalue was not statistically significant. In addition, the proportion of CD45RO(+)cells out of CD8(+)T cells were negatively correlated with Shannon's diversity index for both TCR alpha and TCR beta chains (p = 0.010) via Spearman test. In this study, we identified a heterogeneous pattern of expanded T cell clones and stable usage of V/J segments in ex vivo-expanded TILs from breast cancer patients. Further large-scale studies are requisite to elucidate the clinical significance of TCR repertoires.
Files in This Item
There are no files associated with this item.
Appears in
Collections
Medicine > Department of Medicine > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE