Identification, Isolation, and Functional Assay of Regulatory T Cells

被引:41
作者
Azimi, Maryam [1 ]
Aslani, Saeed [1 ]
Mortezagholi, Sahar [2 ]
Salek, Amir [3 ]
Javan, Mohammad Reza [4 ]
Rezaiemanesh, Alireza [1 ]
Ghaedi, Mojgan [5 ]
Gholamzad, Mehrdad [3 ]
Salehi, Eisa [1 ]
机构
[1] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran, Iran
[2] Tabriz Univ Med Sci, Sch Med, Dept Immunol, Tabriz, Iran
[3] Tarbiat Modares Univ, Dept Immunol, Fac Med Sci, Tehran, Iran
[4] Zabol Univ Med Sci, Dept Biochem & Immunol, Fac Med, Zabol, Iran
[5] Univ Tehran Med Sci, Sch Publ Hlth, Dept Immunol, Tehran, Iran
关键词
Cell isolation; functional assay; regulatory T cells; therapeutic tool; IN-VITRO; CD69; EXPRESSION; SUPPRESSIVE FUNCTION; AUTOIMMUNE-DISEASES; FOXP3; CLINICAL-TRIALS; SELF-TOLERANCE; IL-7; RECEPTOR; BONE-MARROW; PROLIFERATION;
D O I
10.1080/08820139.2016.1193869
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Two categories of regulatory T cells (Tregs), nTreg and iTreg, play vital roles in orchestrating the integrity of a host in the course of an immune response. Tregs commonly belong to CD4+ CD25+ T cells and they are characterized by a transcription factor - forkhead box P3 (FoxP3). Within the space of the last few years, interests have been drawn to Tregs as a therapeutic tool in several settings like autoimmune disease, transplantation, and tumor disorders. As a consequence, to assess the functional properties of Tregs, namely through their ability to suppress other cells, cytokine expression, and proliferation in a variety of conditions, it is mandatory to gain better approaches to this end. This would be beneficial in designing better-than-ever therapeutic methods with regard to Tregs properties. Gaining better insights into the underlying mechanisms of immune regulation, by means of straightforward and less time-consuming techniques, will hopefully permit the therapeutic application of these cells in the control of human disorders. This review aims at going through the basic methods for Treg isolation as well the efficiency of the commonly exerted in vitro assays of Tregs-mediated immune suppression.
引用
收藏
页码:584 / 602
页数:19
相关论文
共 128 条
[1]
MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF A MURINE LIGAND FOR CD40 [J].
ARMITAGE, RJ ;
FANSLOW, WC ;
STROCKBINE, L ;
SATO, TA ;
CLIFFORD, KN ;
MACDUFF, BM ;
ANDERSON, DM ;
GIMPEL, SD ;
DAVISSMITH, T ;
MALISZEWSKI, CR ;
CLARK, EA ;
SMITH, CA ;
GRABSTEIN, KH ;
COSMAN, D ;
SPRIGGS, MK .
NATURE, 1992, 357 (6373) :80-82
[2]
Quantifying lymphocyte kinetics in vivo using carboxyfluorescein diacetate succinimidyl ester (CFSE) [J].
Asquith, B ;
Debacq, C ;
Florins, A ;
Gillet, N ;
Sanchez-Alcaraz, T ;
Mosley, A ;
Willems, L .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2006, 273 (1590) :1165-1171
[3]
CD4+CD25high regulatory cells in human peripheral blood [J].
Baecher-Allan, C ;
Brown, JA ;
Freeman, GJ ;
Hafler, DA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1245-1253
[4]
Cutting edge: Foxp3-mediated induction of pim 2 allows human T regulatory cells to preferentially expand in rapamycin [J].
Basu, Samik ;
Golovina, Tatiana ;
Mikheeva, Tatiana ;
June, Carl H. ;
Riley, James L. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (09) :5794-5798
[5]
Rapamycin selectively expands CD4+CD25+FoxP3+ regulatory T cells [J].
Battaglia, M ;
Stabilini, A ;
Roncarolo, MG .
BLOOD, 2005, 105 (12) :4743-4748
[6]
Rapamycin promotes expansion of functional CD4+CD25+FOXP3+ regulatory T cells of both healthy subjects and type 1 diabetic patients [J].
Battaglia, Manuela ;
Stabilini, Angela ;
Migliavacca, Barbara ;
Horejs-Hoeck, Jutta ;
Kaupper, Thomas ;
Roncarolo, Maria-Grazia .
JOURNAL OF IMMUNOLOGY, 2006, 177 (12) :8338-8347
[7]
Regulatory T Cell Immunotherapy for Type 1 Diabetes: A Step Closer to Success? [J].
Bayry, Jagadeesh ;
Gautier, Jean-Francois .
CELL METABOLISM, 2016, 23 (02) :231-233
[8]
All-trans retinoic acid mediates enhanced T reg cell growth, differentiation, and gut homing in the face of high levels of co-stimulation [J].
Benson, Micah J. ;
Pino-Lagos, Karina ;
Rosemblatt, Mario ;
Noelle, Randolph J. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (08) :1765-1774
[9]
FEASIBILITY OF PROLIFERATION STUDIES USING THE BRDU AND MTT ASSAYS WITH A HEAD AND NECK-CARCINOMA CELL-LINE [J].
BERGLER, W ;
PETROIANU, G ;
SCHADEL, A .
ORL-JOURNAL FOR OTO-RHINO-LARYNGOLOGY AND ITS RELATED SPECIALTIES, 1993, 55 (04) :230-235
[10]
Natural versus adaptive regulatory T cells [J].
Bluestone, JA ;
Abbas, AK .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (03) :253-257