Generation and expansion of regulatory human CD4(+) T-cell clones specific for pancreatic islet autoantigens

Dromey, JA; Lee, BH; Yu, H; Young, HE; Thearle, DJ; Jensen, KP; Mannering, SI; Harrison, LC

Author(s): Dromey, JA; Lee, BH; Yu, H; Young, HE; Thearle, DJ; Jensen, KP; Mannering, SI; Harrison, LC;
Details: Publication Year 2011-02,Volume 36,Issue #1,Page 47-55
Journal Title: JOURNAL OF AUTOIMMUNITY
Publication Type: Journal Article
Abstract: Autoantigen-specific regulatory T cells (Treg) are a potential cell therapy for human autoimmune disease, provided they could be generated in adequate numbers and with stable function. To this end, we determined the feasibility of cloning and expanding human CD4(+) Treg specific for the type 1 diabetes autoantigens. GAD65 and proinsulin. Blood CD4(+) cells stimulated to divide in response to GAD65 (in three healthy individuals) or proinsulin (in one type 1 diabetic) were flow sorted into single cells and cultured on feeder cells in the presence of anti-CD3 monoclonal antibody, IL-2 and IL-4. Clones were expanded over 4-6 weeks and screened for autoantigen-dependent suppression of tetanus toxoid-specific T-cell proliferation. Suppression by Treg clones was then confirmed against autoantigen-specific non-Treg clones. Of a total of 447 clones generated, 98 (21.9%) had autoantigen-dependent suppressor function. Treg clones were anergic but proliferated to autoantigen after addition of IL-2 or in co-culture with stimulated bulk T cells, without loss of suppressor function. Treg clones were stored over liquid N-2, thawed and further expanded over 12 days, whereupon they exhibited decreased suppressor function. Expansion of Treg clones overall was in the order 10(7)-10(8)-fold. Treg clones were not distinguished by markers of conventional CD4(+)CD25(+) Treg and suppressed independently of cell cell contact but not via known soluble suppressor factors. This study demonstrates that autoantigen-specific CD4(+) Treg clones with potential application as a cell therapy for autoimmune disease can be generated and expanded from human blood. (C) 2010 Elsevier Ltd. All rights reserved.
Publisher: ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
Keywords: IN-VITRO; NOD MICE; FOXP3; DISEASE; PROLIFERATION; SUPPRESSION; EXPRESSION; INDUCTION; HEALTHY; INSULIN
Publisher's Version: https://doi.org/10.1016/j.jaut.2010.10.005
Terms of Use/Rights Notice: Refer to copyright notice on published article.

Creation Date: 2011-02-01 12:00:00