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Homogeneous Expansion of Human T-Regulatory Cells Via Tumor Necrosis Factor Receptor 2
Okubo, Yoshiaki ; Mera, Toshiyuki ; Wang, Limei ; Faustman, Denise L
Scientific reports, 2013-11-06, Vol.3 (1), p.3153-3153
[Peer Reviewed Journal]
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Title:
Homogeneous Expansion of Human T-Regulatory Cells Via Tumor Necrosis Factor Receptor 2
Author:
Okubo, Yoshiaki
;
Mera, Toshiyuki
;
Wang, Limei
;
Faustman, Denise L
Subjects:
Tumor necrosis factor receptors
;
Graft-versus-host reaction
;
Immunoregulation
;
Therapeutic applications
;
Hypersensitivity
;
Clinical trials
;
Cytotoxicity
;
T cell receptors
;
Lymphocytes T
;
Cell surface
;
Asthma
;
CD4 antigen
;
Progeny
;
Tumor necrosis factor receptor 2
;
Infectious diseases
;
Tumor necrosis factor
;
Tumor necrosis factor-TNF
;
Autoimmune diseases
;
Surface markers
;
Index Medicus
Is Part Of:
Scientific reports, 2013-11-06, Vol.3 (1), p.3153-3153
Description:
T-regulatory cells (Tregs ) are a rare lymphocyte subtype that shows promise for treating infectious disease, allergy, graft-versus-host disease, autoimmunity, and asthma. Clinical applications of Tregs have not been fully realized because standard methods of expansion ex vivo produce heterogeneous progeny consisting of mixed populations of CD4 + T cells. Heterogeneous progeny are risky for human clinical trials and face significant regulatory hurdles. With the goal of producing homogeneous Tregs , we developed a novel expansion protocol targeting tumor necrosis factor receptors (TNFR) on Tregs . In in vitro studies, a TNFR2 agonist was found superior to standard methods in proliferating human Tregs into a phenotypically homogeneous population consisting of 14 cell surface markers. The TNFR2 agonist-expanded Tregs also were functionally superior in suppressing a key Treg target cell, cytotoxic T-lymphocytes. Targeting the TNFR2 receptor during ex vivo expansion is a new means for producing homogeneous and potent human Tregs for clinical opportunities.
Publisher:
London: Nature Publishing Group
Language:
English
Identifier:
ISSN:
2045-2322
EISSN:
2045-2322
DOI:
10.1038/srep03153
PMID:
24193319
Source:
© ProQuest LLC All rights reserved
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