Low telomerase activity in CD4+ regulatory T cells in patients with severe chronic GVHD after hematopoietic stem cell transplantation

被引:37
|
作者
Kawano, Yutaka [1 ,2 ,3 ]
Kim, Haesook T. [4 ,5 ,6 ]
Matsuoka, Ken-ichi [1 ,2 ,3 ]
Bascug, Gregory [1 ,2 ]
McDonough, Sean [1 ,2 ]
Ho, Vincent T. [1 ,2 ,3 ]
Cutler, Corey [1 ,2 ,3 ]
Koreth, John [1 ,2 ,3 ]
Alyea, Edwin P. [1 ,2 ,3 ]
Antin, Joseph H. [1 ,2 ,3 ]
Soiffer, Robert J. [1 ,2 ,3 ]
Ritz, Jerome [1 ,2 ,3 ,5 ,7 ]
机构
[1] Dana Farber Canc Inst, Div Hematol Malignancies, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA USA
[5] Dana Farber Canc Inst, Canc Vaccine Ctr, Boston, MA USA
[6] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[7] Harvard Stem Cell Inst, Boston, MA USA
基金
美国国家卫生研究院;
关键词
VERSUS-HOST-DISEASE; CHROMOSOME INSTABILITY; INDUCED APOPTOSIS; GRAFT; HTERT; ACTIVATION; CANCER; LENGTH; RISK; DYSFUNCTION;
D O I
10.1182/blood-2011-06-362137
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CD4(+)CD25(+)Foxp3(+) regulatory T cells (Treg) play an important role in the control of chronic graft-versus-host disease (cGVHD). In this study, we examined telomere length and telomerase activity of Treg and conventional CD4(+) T cells (Tcon) in 61 patients who survived more than 2 years after allogeneic hematopoietic stem cell transplantation. Cell proliferation and expression of Bcl-2 were also measured in each subset. Treg telomere length was shorter and Treg telomerase activity was increased compared with Tcon (P < .0001). After transplantation, Treg were also more highly proliferative than Tcon (P < .0001). Treg number, telomerase activity, and expression of Bcl-2 were each inversely associated with severity of cGVHD. These data indicate that activation of telomerase is not sufficient to prevent telomere shortening in highly proliferative Treg. However, telomerase activation is associated with increased Bcl-2 expression and higher Treg numbers in patients with no or mild cGVHD. In contrast, patients with moderate or severe cGVHD have fewer Treg with lower levels of telomerase activity and Bcl-2 expression. These results suggest that failure to activate Treg telomerase may restrict proliferative capacity and increase apoptotic susceptibility, resulting in the loss of peripheral tolerance and the development of cGVHD. (Blood. 2011; 118(18):5021-5030)
引用
收藏
页码:5021 / 5030
页数:10
相关论文
共 50 条
  • [41] Galectin-3 expression in donor T cells reduces GvHD severity and lethality after allogeneic hematopoietic cell transplantation
    Mohammadpour, Hemn
    Tsuji, Takemasa
    MacDonald, Cameron R.
    Sarow, Joseph L.
    Rosenheck, Hanna
    Daneshmandi, Saeed
    Qiu, Jingxin
    Choi, Jee Eun
    Matsuzaki, Junko
    Witkiewicz, Agnieszka K.
    Attwood, Kristopher
    Blazar, Bruce R.
    Odunsi, Kunle
    Repasky, Elizabeth A.
    McCarthy, Philip L.
    CELL REPORTS, 2023, 42 (03):
  • [42] B and T Lymphocyte Attenuator Mediates Inhibition of Tumor-Reactive CD8+ T Cells in Patients After Allogeneic Stem Cell Transplantation
    Hobo, Willemijn
    Norde, Wieger J.
    Schaap, Nicolaas
    Fredrix, Hanny
    Maas, Frans
    Schellens, Karen
    Falkenburg, J. H. Frederik
    Korman, Alan J.
    Olive, Daniel
    van der Voort, Robbert
    Dolstra, Harry
    JOURNAL OF IMMUNOLOGY, 2012, 189 (01): : 39 - 49
  • [43] Harnessing T Cells to Control Infections After Allogeneic Hematopoietic Stem Cell Transplantation
    Basso, Sabrina
    Compagno, Francesca
    Zelini, Paola
    Giorgiani, Giovanna
    Boghen, Stella
    Bergami, Elena
    Bagnarino, Jessica
    Siciliano, Mariangela
    Del Fante, Claudia
    Luppi, Mario
    Zecca, Marco
    Comoli, Patrizia
    FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [44] Maturation and Phenotypic Heterogeneity of Human CD4+Regulatory T Cells From Birth to Adulthood and After Allogeneic Stem Cell Transplantation
    Matos, Tiago R.
    Hirakawa, Masahiro
    Alho, Ana C.
    Neleman, Lars
    Graca, Luis
    Ritz, Jerome
    FRONTIERS IN IMMUNOLOGY, 2021, 11
  • [45] CD137 Agonist Therapy Can Reprogram Regulatory T Cells into Cytotoxic CD4+ T Cells with Antitumor Activity
    Akhmetzyanova, Ilseyar
    Zelinskyy, Gennadiy
    Littwitz-Salomon, Elisabeth
    Malyshkina, Anna
    Dietze, Kirsten K.
    Streeck, Hendrik
    Brandau, Sven
    Dittmer, Ulf
    JOURNAL OF IMMUNOLOGY, 2016, 196 (01): : 484 - 492
  • [46] The anti-CXCL4 antibody depletes CD4(+)CD25(+)FOXP3(+) regulatory T cells in CD4+ T cells from chronic osteomyelitis patients by the STAT5 pathway
    Huang, Kai
    Ge, Shuyu
    ANNALS OF PALLIATIVE MEDICINE, 2020, 9 (05) : 2723 - +
  • [47] Circulating endothelial cells and endothelial progenitor cells as potential predictors of acute GVHD after allogeneic hematopoietic stem cell transplantation
    Takamatsu, Akiko
    Nakashima, Yasuhiro
    Haji, Shojiro
    Tsuda, Mariko
    Masuda, Toru
    Kimura, Daisaku
    Shiratsuchi, Motoaki
    Ogawa, Yoshihiro
    EUROPEAN JOURNAL OF HAEMATOLOGY, 2022, 109 (02) : 146 - 153
  • [48] CD4+FOXP3+ Regulatory T Cell Therapies in HLA Haploidentical Hematopoietic Transplantation
    Mancusi, Antonella
    Piccinelli, Sara
    Velardi, Andrea
    Pierini, Antonio
    FRONTIERS IN IMMUNOLOGY, 2019, 10
  • [49] CD4+ invariant natural killer T cells protect from murine GVHD lethality through expansion of donor CD4+CD25+FoxP3+ regulatory T cells
    Schneidawind, Dominik
    Pierini, Antonio
    Alvarez, Maite
    Pan, Yuqiong
    Baker, Jeanette
    Buechele, Corina
    Luong, Richard H.
    Meyer, Everett H.
    Negrin, Robert S.
    BLOOD, 2014, 124 (22) : 3320 - 3328
  • [50] Mixed chimerism established by hematopoietic stem cell transplantation is maintained by host and donor T regulatory cells
    Kinsella, Francesca A. M.
    Zuo, Jianmin
    Inman, Charlotte F.
    Pearce, Hayden
    Maggs, Luke
    Eldershaw, Suzy E.
    Chan, Y. L. Tracey
    Nunnick, Jane
    Nagra, Sandeep
    Griffiths, Mike
    Craddock, Charles
    Malladi, Ram
    Moss, Paul
    BLOOD ADVANCES, 2019, 3 (05) : 734 - 743