Abstract:Objective To study the alterations of follicular T helper cells (CD4+CXCR5+Tfh cells, Tfh) on circulating T lymphocytes in children with asthma, and to study the expression of transcription regulatory factors BCL-6 and BLIMP-1 mRNA. Methods Sixty-four children with asthma and 25 healthy controls were enrolled in this study. On the basis of the disease, the children with asthma were classified into acute phase group (n=36) and remission phase group (n=28). The flow cytometry was used to detect the proportion of CD4+CXCR5+Tfh cells on CD4+T lymphocytes. Real-time PCR was performed to detect the levels of BCL-6 mRNA and BLIMP-1 mRNA. The double-antibody Sandwich ELISA was used to detect plasma concentrations of total IgE, IL-2, IL-6 and IL-21. Results The proportion of CD4+CXCR5+Tfh cells was significantly higher in the acute group than in the control group and the remission group (PPPP+CXCR5+Tfh cells (r=0.76, r=0.46 respectively; Pr=-0.68, PConclusions The abnormal proportion of CD4+CXCR5+Tfh cells might be involved in the immunological pathogenesis of acute asthma in children. The increased expression of BCL-6 mRNA and decreased expression of BLIMP-1 mRNA as well as the alterations of plasma total IgE, cytokines IL-2, IL-6 and IL-21 in microenvironment might be account for the increased proportion of CD4+CXCR5+Tfh cells in children with acute asthma.
CUI Ya-Jie,CHEN Guo-Hong,WANG Jun-Ling et al. Alterations of CD4+CXCR5+Tfh cells and its transcription regulatory factors in children with asthma[J]. CJCP, 2014, 16(12): 1215-1219.
HolgaTe ST. InnaTe and adapTive immune responses in asThma[J]. NaT Med, 2012, 18(5): 673-683.
[2]
Leavy O. T cells: The TFH-like TransiTion of TH1 cells[J]. NaT Rev Immunol, 2012, 12(2): 74.
[3]
Ma CS, Deenick EK, BaTTen M, eT al. The origins, funcTion, and regulaTion of T follicular helper cells[J]. J Exp Med, 2012, 209(7): 1241-1253.
[4]
Simpson N, GaTenby PA, Wilson A, eT al. Expansion of circulaTing T cells resembling follicular helper T cells is a fixed phenoType ThaT idenTifies a subseT of severe sysTemic lupus eryThemaTosus[J]. ArThriTis Rheum, 2010, 62(1): 234-244.
[5]
Ma J, Zhu C, Ma B, eT al. Increased frequency of circulaTing follicular helper T cells in paTienTs wiTh rheumaToid arThriTis[J]. Clin Dev Immunol, 2012, 2012: 827480.
Tangye SG, Ma CS, Brink R, eT al. The good, The bad and The ugly-TFH cells in human healTh and disease[J]. NaT Rev Immunol, 2013, 13(6): 412-426.
[14]
Liu R, Wu Q, Su D, eT al. A regulaTory effecT of IL-21 on T follicular helper-like cell and B cell in rheumaToid arThriTis[J]. ArThriTis Res Ther, 2012, 14(6): R255.
[15]
Zhu C, Ma J, Liu Y, eT al. Increased frequency of follicular helper T cells in paTienTs wiTh auToimmune Thyroid disease[J]. J Clin Endocrinol MeTab, 2012, 97(3): 943-950.
[16]
Xu X, Shi Y, Cai Y, eT al. InhibiTion of increased circulaTing Tfh cell by anTi-CD20 monoclonal anTibody in paTienTs wiTh Type 1 diabeTes[J]. PLoS One, 2013, 8(11): e79858.
JohnsTon RJ, Poholek AC, DiToro D, eT al. Bcl6 and Blimp-1 are reciprocal and anTagonisTic regulaTors of T follicular helper cell differenTiaTion[J]. Science, 2009, 325(5943): 1006-1010.
[20]
Nurieva RI, Chung Y, MarTinez GJ, eT al. Bcl6 mediaTes The developmenT of T follicular helper cells[J]. Science, 2009, 325(5943): 1001-1005.