The dual nature of retinoic acid in pemphigus and its therapeutic potential: Special focus on all-trans Retinoic Acid

被引:9
作者
Tavakolpour, Soheil [1 ,2 ]
Daneshpazhooh, Maryam [2 ]
Mahmoudi, Hamid Reza [2 ]
Balighi, Kamran [2 ]
机构
[1] Iran Univ Med Sci, Tehran, Iran
[2] Univ Tehran Med Sci, Autoimmune Bullous Dis Res Ctr, Tehran, Iran
关键词
Pemphigus; All-trans-Retinoic Acid; Regulatory T cells; Regulatory B cells; Retinoic acid; REGULATORY T-CELLS; VITAMIN-A; TGF-BETA; B-CELLS; AUTOANTIBODY PRODUCTION; IGE PRODUCTION; TH17; CELLS; AUTOIMMUNE; DIFFERENTIATION; EXPRESSION;
D O I
10.1016/j.intimp.2016.04.031
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The efficient treatment of pemphigus With no certain side effect remained a controversial issue. Although there are various options for controlling disease severity, the majority of them may cause serious side effects. Retinoic acid (RA), an active metabolite converted from vitamin A, plays an active role in immune functions. Effects of RA, especially all-trans-Retinoic Acid (ATRA) on different types of cells involved in immune responses were analyzed in vitro and in vivo. RAs could affect the differentiation of T helper (Th) cells, B cells responses, stabilization of both natural regulatory. T cells (nTregs) and regulatory B cells (Bregs) populations, and regulating the expression of critical genes in immune responses. The role of RA, based on major immune cells involved in pemphigus has not been addressed so far. In this study, we sought to determine the possible effects of RA, with a special focus on ATRA in pemphigus. All the evidences of ATRA effects on the immune system were collected and their association with the pemphigus was analyzed. According to the previous results, ATRA causes a decline in Th17 populations; increase in CD4+ induced regulatory T cells (iTregs), stabilization of nTregs, and promotion of suppressive B cells, which are critical in the improvement of pemphigus. Nevertheless, it also causes shifting of the Th1:Th2 balance toward Th2 cells, which is not favorable for pemphigus patients. In conclusion, ATRA acts via different ways in pemphigus. Due to increase in the suppressive function via iTregs, nTregs, and Bregs, it is suggested that patients with pemphigus may benefit from systemic ATRA therapy. To clarify this issue, further studies, such as clinical trials are needed. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:180 / 186
页数:7
相关论文
共 88 条
[61]  
Tavakolpour S., 2016, RECEPT CLIN INVEST, V3, pe1173
[63]   Interleukin 4 inhibition as a potential therapeutic in pemphigus [J].
Tavakolpour, Soheil ;
Tavakolpour, Vahid .
CYTOKINE, 2016, 77 :189-195
[64]   Vitamin A Impairs the Reprogramming of Tregs into IL-17-Producing Cells during Intestinal Inflammation [J].
Tejon, Gabriela ;
Manriquez, Valeria ;
De Calisto, Jaime ;
Flores-Santibanez, Felipe ;
Hidalgo, Yessia ;
Crisostomo, Natalia ;
Fernandez, Dominique ;
Sauma, Daniela ;
Rodrigo Mora, J. ;
Bono, Maria R. ;
Rosemblatt, Mario .
BIOMED RESEARCH INTERNATIONAL, 2015, 2015
[65]   RETINOIDS ENHANCE IGA PRODUCTION BY LIPOPOLYSACCHARIDE-STIMULATED MURINE SPLEEN-CELLS [J].
TOKUYAMA, H ;
TOKUYAMA, Y .
CELLULAR IMMUNOLOGY, 1993, 150 (02) :353-363
[66]   The regulatory effects of all-trans-retinoic acid on isotype switching:: Retinoic acid induces IgA switch rearrangement in cooperation with IL-5 and inhibits IgG1 switching [J].
Tokuyama, H ;
Tokuyama, Y .
CELLULAR IMMUNOLOGY, 1999, 192 (01) :41-47
[67]   Deficient CD4+CD25high T regulatory cell function in patients with active systemic lupus erythematosus [J].
Valencia, Xavier ;
Yarboro, Cheryl ;
Illei, Gabor ;
Lipsky, Peter E. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (04) :2579-2588
[68]   All-trans Retinoic Acid Inhibits Type 1 Diabetes by T Regulatory (Treg)-Dependent Suppression of Interferon-γ-Producing T-cells Without Affecting Th17 Cells [J].
Van, Yang-Hau ;
Lee, Wen-Hui ;
Ortiz, Serina ;
Lee, Mi-Heon ;
Qin, Han-Jun ;
Liu, Chih-Pin .
DIABETES, 2009, 58 (01) :146-155
[69]  
VANVLASSELAER P, 1992, J IMMUNOL, V148, P2062
[70]   Loss of functional suppression by CD4+CD25+ regulatory T cells in patients with multiple sclerosis [J].
Viglietta, V ;
Baecher-Allan, C ;
Weiner, HL ;
Hafler, DA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (07) :971-979