IL-21 restricts T follicular regulatory T cell proliferation through Bcl-6 mediated inhibition of responsiveness to IL-2

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作者
Christoph Jandl
Sue M. Liu
Pablo F. Cañete
Joanna Warren
William E. Hughes
Alexis Vogelzang
Kylie Webster
Maria E. Craig
Gulbu Uzel
Alexander Dent
Polina Stepensky
Bärbel Keller
Klaus Warnatz
Jonathan Sprent
Cecile King
机构
[1] Garvan Institute of Medical Research,Department of Immunology
[2] St Vincent’s Clinical School,Department of Medicine
[3] University of NSW,Division of Immunology and Genetics
[4] John Curtin School of Medical Research,Department of Microbiology and Immunology
[5] The Australian National University,undefined
[6] Institute of Endocrinology and Diabetes,undefined
[7] The Children’s Hospital at Westmead,undefined
[8] Sydney,undefined
[9] School of Women’s and Children’s Health,undefined
[10] University of New South Wales,undefined
[11] Laboratory of Clinical Infectious Diseases,undefined
[12] National Institute of Allergy and Infectious Diseases,undefined
[13] National Institutes of Health,undefined
[14] Indiana University School of Medicine,undefined
[15] Pediatric Hematology-Oncology and Bone Marrow Transplantation,undefined
[16] Hadassah Hebrew University Hospital,undefined
[17] Kiryat Hadassah,undefined
[18] Center for Chronic Immunodeficiency (CCI),undefined
[19] University Medical Center and University of Freiburg,undefined
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摘要
T follicular regulatory (Tfr) cells control the magnitude and specificity of the germinal centre reaction, but how regulation is contained to ensure generation of high-affinity antibody is unknown. Here we show that this balance is maintained by the reciprocal influence of interleukin (IL)-2 and IL-21. The number of IL-2-dependent FoxP3+ regulatory T cells is increased in the peripheral blood of human patients with loss-of-function mutations in the IL-21 receptor (IL-21R). In mice, IL-21:IL-21R interactions influence the phenotype of T follicular cells, reducing the expression of CXCR4 and inhibiting the expansion of Tfr cells after T-cell-dependent immunization. The negative effect of IL-21 on Tfr cells in mice is cell intrinsic and associated with decreased expression of the high affinity IL-2 receptor (CD25). Bcl-6, expressed in abundance in Tfr cells, inhibits CD25 expression and IL-21-mediated inhibition of CD25 is Bcl-6 dependent. These findings identify a mechanism by which IL-21 reinforces humoral immunity by restricting Tfr cell proliferation.
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