期刊论文详细信息
Journal of Translational Medicine
Gene expression pattern of Treg and TCR Vγ subfamily T cells before and after specific immunotherapy in allergic rhinitis
Gehua Zhang1  Yangqiu Li2  Qintai Yang1  Yulian Chen1  Xuekun Huang1  Xiuli Wu2  Rui Zheng1 
[1] Department of Otorhinolaryngology-Head and Neck Surgery, The Third Affiliated Hospital, SUN Yat-sen University, Guangzhou 510630, China;Institute of Hematology, Medical College, Jinan University, Guangzhou 510632, China
关键词: γδ T cells;    Treg;    Foxp3;    Specific immunotherapy;    Allergic rhinitis;   
Others  :  821906
DOI  :  10.1186/1479-5876-12-24
 received in 2013-11-22, accepted in 2014-01-20,  发布年份 2014
PDF
【 摘 要 】

Background

T regulatory cell (Treg) plays a critical role in respiratory allergy and allergen-specific immunotherapy (SIT), and γδ T cells might participate in mediating Treg quantity and/or function in some immunological diseases. To further characterize whether γδ T cells could influence Treg in allergic rhinitis (AR) and SIT, we investigated the expression pattern of Treg’s Foxp3 gene and γδ T cell receptor (TCR) Vγ subfamily genes in peripheral blood mononuclear cells (PBMCs) of AR patients before and after SIT.

Methods

Eighteen AR patients undergoing effective SIT with house dust mite extract for one year were recruited. Visual Analogue Scale (VAS) was applied to evaluate the severity. Immunofluorescence quantification analysis was performed to determine the serum specific IgE (sIgE) content. Real-time PCR was used to detect the expression levels of Foxp3 and TCR Vγ subfamilies. Ten healthy volunteers were recruited as the controls.

Results

Nasal uni-VAS score after SIT was significantly lower than that before SIT, while serum sIgE content was similar before and after SIT. Expression levels of Foxp3 and TCR Vγ subfamilies in AR patients before treatment were significantly lower than those in healthy subjects. Expression levels of VγI and II were similar before and after SIT, while expression levels of Foxp3 and VγIII after SIT were significantly higher than those before. Before SIT, the significant positive correlation was observed between expression levels of Foxp3 and VγI, II, III, while negative correlation was observed between Foxp3, VγIII and VAS. After SIT, the significant positive correlation between expression levels of Foxp3 and VγIII and negative correlation between Foxp3, VγIII and VAS were observed.

Conclusions

Treg and Vγ subfamily T cells were in a dynamic equilibrium in AR patients before and after effective immunotherapy for one year. The early improvement of symptoms following immunotherapy might be independent of the serum sIgE content in AR patients, but associated with the reconstitution of T cell immunity.

【 授权许可】

   
2014 Zheng et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140712090321748.pdf 935KB PDF download
Figure 3. 66KB Image download
Figure 2. 71KB Image download
Figure 1. 60KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

【 参考文献 】
  • [1]Nouri-Aria KT: Foxp3 expressing regulatory T-cells in allergic disease. Adv Exp Med Biol 2009, 665:180-194.
  • [2]Kay AB: Allergy and allergic diseases. Second of two parts. N Engl J Med 2001, 344:109-113.
  • [3]Cook L, Miyahara N, Jin N, Wands J, Taube C, Roark CL, Potter TA, Gelfand EW, O’Brien RL, Born WK: Evidence that CD8+ dendritic cells enable the development of γδ T cells that modulate airway hyperresponsiveness. J Immunol 2008, 181:309-319.
  • [4]Yang Q, Li P, Li Y, Wu X, Huang X, Chen Y, Zhang G: Effects of immunotherapy on the distribution and clonality of TCR Vγ and Vδ subfamily T cells in allergic rhinitis patients. J Med Biochem 2012, 31:94-99.
  • [5]Korematsu S, Tanaka Y, Nagakura T, Minato N, Izumi T: Human gammadelta T cells modulate the mite allergen-specific T-helper type 2-skewed immunity. Clin Exp Allergy 2007, 37:1681-1687.
  • [6]Petermann F, Rothhammer V, Claussen MC, Haas JD, Blanco LR, Heink S, Prinz I, Hemmer B, Kuchroo VK, Oukka M, Korn T: Gammadelta T cells enhance autoimmunity by restraining regulatory T cell responses via an interleukin-23-dependent mechanism. Immunity 2010, 33:351-363.
  • [7]Bousquet J, Khaltaev N, Cruz A, Denburg J, Fokkens W, Togias A, Zuberbier T, Baena-Cagnani C, Canonica G, van Weel C: World health organization; GA (2) LEN; AllerGen. allergic rhinitis and its impact on asthma (ARIA) 2008 update (in collaboration with the world health organization, GA (2) LEN and AllerGen). Allergy 2008, 63:8-160.
  • [8]Mailing HJ: Immunotherapy as an effective tool in allergy treatment. Allergy 1998, 53:461-472.
  • [9]Chen S, Zha X, Yang L, Li B, Liye Z, Li Y: Deficiency of CD3gamma, delta, epsilon, and zeta expression in T cells from AML patients. Hematology 2011, 16:31-36.
  • [10]Bousquet P, Combescure C, Neukirch F, Klossek J, Mechin H, Daures JP, Bousquet J: Visual analog scales can assess the severity of rhinitis graded according to ARIA guidelines. Allergy 2007, 62:367-372.
  • [11]Xuan L, Wu X, Zhang Y, Fan Z, Ling Y, Huang F, Zhang F, Zhai X, Liu Q: Granulocyte colony-stimulating factor affects the distribution and clonality of TRGV and TRDV repertoire of T cells and graft-versus-host disease. J Transl Med 2011, 9:215. BioMed Central Full Text
  • [12]Li B, Liu S, Niu Y, Fang S, Wu X, Yu Z, Chen S, Yang L, Li Y: Altered expression of the TCR signaling related genes CD3 and FcepsilonRIgamma in patients with aplastic anemia. J Hematol Oncol 2012, 5:6. BioMed Central Full Text
  • [13]Spector S, Wallace D, Nicklas R, Portnoy J, Blessing-Moore J, Bernstein D, Cox L, Oppenheimer J, Lang D, Schuller D: Comments on allergic rhinitis and its impact on asthma (ARIA) guidelines. J Allergy Clin Immunol 2011, 127:1641-1642.
  • [14]Akdis CA, Akdis M: Mechanisms of allergen-specific immunotherapy. J Allergy Clin Immunol 2011, 127:18-27.
  • [15]Burks A, Calderon MA, Casale T, Cox L, Demoly P, Jutel M, Nelson H, Akdis CA: Update on allergy immunotherapy: American Academy of Allergy, Asthma & Immunology/European Academy of Allergy and Clinical Immunology/PRACTALL consensus report. J Allergy Clin Immunol 2013, 131:1288-1296.
  • [16]Sakaguchi S, Sakaguchi N, Asano M, Itoh M, Toda M: Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases. J Immunol 1995, 155:1151-1164.
  • [17]Hori S, Nomura T, Sakaguchi S: Control of regulatory T cell development by the transcription factor Foxp3. Science 2003, 299:1057-1061.
  • [18]Provoost S, Maes T, van Durme YM, Gevaert P, Bachert C, Schmidt-Weber CB, Brusselle GG, Joos GF, Tournoy KG: Decreased FOXP3 protein expression in patients with asthma. Allergy 2009, 64:1539-1546.
  • [19]Takai T, Ikeda S: Barrier dysfunction caused by environmental proteases in the pathogenesis of allergic diseases. Allergol Int 2011, 60:25-35.
  • [20]Szczepanik M, Nowak B, Askenase P, Ptak W: Cross-talk between gammadelta T lymphocytes and immune cells in humoral response. Immunology 1998, 95:612.
  • [21]Beetz S, Wesch D, Marischen L, Welte S, Oberg HH, Kabelitz D: Innate immune functions of human gammadelta T cells. Immunobiology 2008, 213:173-182.
  • [22]Cai Y, Shen X, Ding C, Qi C, Li K, Li X, Jala VR, Zhang H-G, Wang T, Zheng J: Pivotal role of dermal IL-17-producing γδ T cells in skin inflammation. Immunity 2011, 35:596-610.
  文献评价指标  
  下载次数:4次 浏览次数:21次