Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Cell enrichment-free massive ex -vivo expansion of peripheral CD20(+) B cells via CD4O-CD4OL signals in non-human primates

Authors
Kim, Jung-SikByun, NariChung, HyunwooKim, Hyun-JeKim, Jong-MinChun, TaehoonLee, Won-WooPark, Chung-Gyu
Issue Date
22-Apr-2016
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
B cell; Ex-vivo expansion; Monkeys; CD40-D4OL signals
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.473, no.1, pp.92 - 98
Indexed
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
473
Number
1
Start Page
92
End Page
98
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/88901
DOI
10.1016/j.bbrc.2016.03.057
ISSN
0006-291X
Abstract
Non-human primates (NHPs) are valuable as preclinical resources that bridge the gap between basic science and clinical application. B cells from NHPs have been utilized for the development of B-cell targeted drugs and cell-based therapeutic modalities; however, few studies on the ex-vivo expansion of monkey B cells have been reported. In this study, we developed a highly efficient ex-vivo expansion protocol for monkey B cells resulting in 99% purity without the requirement for prior cell-enrichment procedures. To this end, monkey peripheral blood mononuclear cells (PBMCs) were stimulated for 12 days with cells constitutively expressing monkey CD4OL in expansion medium optimized for specific and massive expansion of B cells. The B cells expansion rates obtained were 2-5 times higher than those previously reported in humans, with rates ranging from 7.9 to 16.6 fold increase. Moreover, expanded B cells sustained high expression of co-stimulatory molecules including CD83 and CD86 until day 12 of culture, and the simple application of a brief centrifugation resulted in a CD20(+) B cell purity rate of greater than 99%. Furthermore, small amounts of CD3(+)CD2O(+)BT-like cells were generated and CD16 was expressed at moderate levels on expanded B cells. Thus, the establishment of this protocol provides a method to produce quantities of homogeneous, mature B cells in numbers sufficient for the in vitro study of B cell immunity as well as for the development of B cell-diagnostic tools and cell-based therapeutic modalities. (C) 2016 Elsevier Inc. All rights reserved.
Files in This Item
There are no files associated with this item.
Appears in
Collections
Graduate School > Department of Biotechnology > 1. Journal Articles

qrcode

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

Related Researcher

Researcher Chun, Tae hoon photo

Chun, Tae hoon
Department of Biotechnology
Read more

Altmetrics

Total Views & Downloads

BROWSE