Shared and distinct roles of T peripheral helper and T follicular helper cells in human diseases
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作者:
Hiroyuki Yoshitomi
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机构:Kyoto University,Department of Immunology, Graduate School of Medicine
Hiroyuki Yoshitomi
Hideki Ueno
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机构:Kyoto University,Department of Immunology, Graduate School of Medicine
Hideki Ueno
机构:
[1] Kyoto University,Department of Immunology, Graduate School of Medicine
[2] Kyoto University,Institute for the Advanced Study of Human Biology
[3] Icahn School of Medicine at Mount Sinai,Department of Microbiology
[4] Global Health and Emerging Pathogens Institute,undefined
[5] Icahn School of Medicine at Mount Sinai,undefined
来源:
Cellular & Molecular Immunology
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2021年
/
18卷
关键词:
peripheral helper T cells;
T follicular helper cells;
CXCL13, Autoantibodies;
autoimmune diseases;
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摘要:
The interactions of CD4+ T cells and B cells are fundamental for the generation of protective antibody responses, as well as for the development of harmful autoimmune diseases. Recent studies of human tissues and blood samples have established a new subset of CD4+ B helper T cells named peripheral helper T (Tph) cells. Unlike T follicular helper (Tfh) cells, which interact with B cells within lymphoid organs, Tph cells provide help to B cells within inflamed tissues. Tph cells share many B helper-associated functions with Tfh cells and induce B cell differentiation toward antibody-producing cells. The differentiation mechanism is also partly shared between Tph and Tfh cells in humans, and both Tfh and Tph cells can be found within the same tissues, including cancer tissues. However, Tph cells display features distinct from those of Tfh cells, such as the expression of chemokine receptors associated with Tph cell localization within inflamed tissues and a low Bcl-6/Blimp1 ratio. Unlike that of Tfh cells, current evidence shows that the target of Tph cells is limited to memory B cells. In this review, we first summarize recent findings on human Tph cells and discuss how Tph and Tfh cells play shared and distinct roles in human diseases.
机构:
Australian Natl Univ, John Curtin Sch Med Res, Canberra, ACT 2601, AustraliaAustralian Natl Univ, John Curtin Sch Med Res, Canberra, ACT 2601, Australia
Vinuesa, Carola G.
Fagarasan, Sidonia
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机构:
RIKEN, Yokohama Inst, Ctr Integrat Med Sci IMS RCAI, Yokohama, Kanagawa 2300045, JapanAustralian Natl Univ, John Curtin Sch Med Res, Canberra, ACT 2601, Australia
Fagarasan, Sidonia
Dong, Chen
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机构:
Tsinghua Univ, Beijing 100084, Peoples R China
Univ Texas Houston, MD Anderson Canc Ctr, Houston, TX 77030 USAAustralian Natl Univ, John Curtin Sch Med Res, Canberra, ACT 2601, Australia
机构:
Univ Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Shelby Interdisciplinary Biomed Res Bldg, Birmingham, AL 35294 USA
Birmingham Vet Affairs Med Ctr, Birmingham, AL 35233 USAUniv Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Shelby Interdisciplinary Biomed Res Bldg, Birmingham, AL 35294 USA
Mountz, John D.
Hsu, Hui-Chen
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机构:
Univ Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Shelby Interdisciplinary Biomed Res Bldg, Birmingham, AL 35294 USAUniv Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Shelby Interdisciplinary Biomed Res Bldg, Birmingham, AL 35294 USA
Hsu, Hui-Chen
Ballesteros-Tato, Andre
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机构:
Univ Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Shelby Interdisciplinary Biomed Res Bldg, Birmingham, AL 35294 USAUniv Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Shelby Interdisciplinary Biomed Res Bldg, Birmingham, AL 35294 USA
Ballesteros-Tato, Andre
JOURNAL OF IMMUNOLOGY,
2019,
202
(06):
: 1649
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1658