Functional characterization of double-negative T cells isolated from leukoreduction filter residues.
10.3724/zdxbyxb-2025-0625
- Author:
Zhiqiang XIANG
1
,
2
;
Yue WU
3
;
Kaiyu HUANG
3
;
Fuqiang WU
3
;
Ju LIN
4
;
Lieyong SANG
5
;
Liming YANG
6
Author Information
1. Department of Pharmacy, School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China. xiangzq@
2. com.
3. Wyze Biotech CO., Ltd., Shaoxing 312065, Zhejiang Province, China.
4. Shaoxing Municipal Blood Center, Shaoxing 312071, Zhejiang Province, China.
5. Shaoxing Municipal Blood Center, Shaoxing 312071, Zhejiang Province, China. 363729994@qq.com.
6. Wyze Biotech CO., Ltd., Shaoxing 312065, Zhejiang Province, China. lyang@wyzebiotech.com.
- Publication Type:Journal Article
- Keywords:
Cell activity;
Cell culture;
Double negative T cells;
Leukocyte reduction filter;
Leukoreduction filter residues
- From:
Journal of Zhejiang University. Medical sciences
2025;():1-9
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVES:To characterize the biological properties of double-negative T (DNT) cells isolated from leukoreduction filter residues.
METHODS:Leukoreduction filters containing residues from 400 mL whole blood units (n=6) were collected from a blood center. Filters were back-flushed with normal saline, and the eluate was concentrated to obtain leukoreduction filter residues. Leukocytes in the residues were counted by dual-fluorescence staining. DNT cells were then isolated from the residues using antibody-mediated adsorption and density gradient centrifugation. Both cryopreserved and fresh unstimulated DNT cells derived from the residues were subjected to in vitro culture. Following culture, cells were assessed for expansion fold, viability, immunophenotype, differentiation status, and cytotoxicity against target cells using dual-fluorescence staining and flow cytometry, with comparisons made to DNT cells derived from whole blood.
RESULTS:The leukocyte recovery rate achieved through reverse flushing of the leukocyte reduction filter was (41.9±14.7)%. Compared to whole blood, the DNT cell starting material obtained from filter residues showed no significant difference in total T-cell content (P>0.05). However, the viability and purity of the resulting DNT cell starting materials were significantly lower (both P<0.05). After 17 days of culture, DNT cells from filter residues and whole blood showed no significant differences in expansion fold, immunophenotype, differentiation status, or cytotoxicity toward target cells (all P>0.05). However, the viability of DNT cells from residues was significantly lower than that of whole blood-derived DNT cells [(86.0±4.2)% vs. (92.2±1.2)%, P<0.05]. After thawing (post 3 or 15 days of cryopreservation) and 17 days of culture, DNT cell starting materials from residues showed comparable immunophenotype, expansion fold, and differentiation status to their non-cryopreserved counterparts from the same source (all P>0.05). However, the viability of DNT cells cryopreserved for 3 days [92.4% (91.8%, 92.8%)] and the cytotoxicity against target cells of those cryopreserved for 15 days [91.3% (89.4%, 95.1%)] were significantly higher than those of non-cryopreserved DNT cells [87.8% (82.0%, 89.0%) and 70.9% (67.3%, 80.2%), respectively] (P<0.05).
CONCLUSIONS:DNT cells derived from leukoreduction filter residues exhibited highly comparable characteristics to those from whole blood in terms of expansion, purity, differentiation, and biological potency. Furthermore, their biological activity post-cryopreservation and revival remained largely similar to non-cryopreserved cells. These findings suggest that leukoreduction filter residues represent a promising alternative source of starting material for manufacturing off-the-shelf, allogeneic DNT cell therapeutics.
