Mucosal-Associated Invariant T Cells in Regenerative Medicine

被引:12
|
作者
Wakao, Hiroshi [1 ]
Sugimoto, Chie [1 ]
Kimura, Shinzo [1 ]
Wakao, Rika [2 ]
机构
[1] Dokkyo Med Univ, Int Epidemiol, Mibu, Tochigi, Japan
[2] PMDA, Off Regulatory Sci, Tokyo, Japan
来源
FRONTIERS IN IMMUNOLOGY | 2017年 / 8卷
基金
日本科学技术振兴机构;
关键词
mucosal-associated invariant T cells; induced pluripotent stem cells; infectious diseases; human immunodeficiency virus; cancer; cell therapy; regenerative medicine; drug resistance; CENTRAL-NERVOUS-SYSTEM; EMBRYONIC STEM-CELLS; MAIT CELLS; MULTIPLE-SCLEROSIS; HIV-INFECTION; NKT CELLS; INCREASED SUSCEPTIBILITY; BACTERIAL-INFECTION; MR1; TETRAMERS; ALPHA-CHAIN;
D O I
10.3389/fimmu.2017.01711
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although antibiotics to inhibit bacterial growth and small compounds to interfere with the productive life cycle of human immunodeficiency virus (HIV) have successfully been used to control HIV infection, the recent emergence of the drug-resistant bacteria and viruses poses a serious concern for worldwide public health. Despite intensive scrutiny in developing novel antibiotics and drugs to overcome these problems, there is a dilemma such that once novel antibiotics are launched in markets, sooner or later antibiotic-resistant strains emerge. Thus, it is imperative to develop novel methods to avoid this vicious circle. Here, we discuss the possibility of using induced pluripotent stem cell (iPSC)-derived, innate-like T cells to control infection and potential application of these cells for cancer treatment. Mucosal-associated invariant T (MAIT) cells belong to an emerging family of innate-like T cells that link innate immunity to adaptive immunity. MAIT cells exert effector functions without priming and clonal expansion like innate immune cells and relay the immune response to adaptive immune cells through production of relevant cytokines. With these characteristics, MAIT cells are implicated in a wide range of human diseases such as autoimmune, infectious, and metabolic diseases, and cancer. Circulating MAIT cells are often depleted by these diseases and often remain depleted even after appropriate remedy because MAIT cells are susceptible to activation-induced cell death and poor at proliferation in vivo, which threatens the integrity of the immune system. Because MAIT cells have a pivotal role in human immunity, supplementation of MAIT cells into immunocompromised patients suffering from severe depletion of these cells may help recapitulate or recover immunocompetence. The generation of MAIT cells from human iPSCs has made it possible to procure MAIT cells lost from disease. Such technology creates new avenues for cell therapy and regenerative medicine for difficult-to-cure infectious diseases and cancer and contributes to improvement of our welfare.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Mucosal-associated invariant T cells and disease
    Toubal, Amine
    Nel, Isabelle
    Lotersztajn, Sophie
    Lehuen, Agnes
    NATURE REVIEWS IMMUNOLOGY, 2019, 19 (10) : 643 - 657
  • [2] Development of mucosal-associated invariant T cells
    Koay, Hui-Fern
    Godfrey, Dale I.
    Pellicci, Daniel G.
    IMMUNOLOGY AND CELL BIOLOGY, 2018, 96 (06): : 598 - 606
  • [3] Mucosal-associated invariant T cells and disease
    Amine Toubal
    Isabelle Nel
    Sophie Lotersztajn
    Agnès Lehuen
    Nature Reviews Immunology, 2019, 19 : 643 - 657
  • [4] Antimicrobial activity of mucosal-associated invariant T cells
    Lionel Le Bourhis
    Emmanuel Martin
    Isabelle Péguillet
    Amélie Guihot
    Nathalie Froux
    Maxime Coré
    Eva Lévy
    Mathilde Dusseaux
    Vanina Meyssonnier
    Virginie Premel
    Charlotte Ngo
    Béatrice Riteau
    Livine Duban
    Delphine Robert
    Shouxiong Huang
    Martin Rottman
    Claire Soudais
    Olivier Lantz
    Nature Immunology, 2010, 11 : 701 - 708
  • [5] Mucosal-associated invariant T cells for cancer immunotherapy
    Li, Yan-Ruide
    Zhou, Kuangyi
    Wilson, Matthew
    Kramer, Adam
    Zhu, Yichen
    Dawson, Niels
    Yang, Lili
    MOLECULAR THERAPY, 2023, 31 (03) : 631 - 646
  • [6] Mucosal-associated invariant T cells in clinical diseases
    Reantragoon, Rangsima
    Boonpattanaporn, Norasate
    Corbett, Alexandra Jane
    McCluskey, James
    ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY, 2016, 34 (01): : 3 - 10
  • [7] Antimicrobial activity of mucosal-associated invariant T cells
    Le Bourhis, Lionel
    Martin, Emmanuel
    Peguillet, Isabelle
    Guihot, Amelie
    Froux, Nathalie
    Core, Maxime
    Levy, Eva
    Dusseaux, Mathilde
    Meyssonnier, Vanina
    Premel, Virginie
    Ngo, Charlotte
    Riteau, Beatrice
    Duban, Livine
    Robert, Delphine
    Rottman, Martin
    Soudais, Claire
    Lantz, Olivier
    NATURE IMMUNOLOGY, 2010, 11 (08) : 701 - U66
  • [8] Mucosal-Associated invariant T Cells in Autoimmune Diseases
    Chiba, Asako
    Murayama, Goh
    Miyake, Sachiko
    FRONTIERS IN IMMUNOLOGY, 2018, 9
  • [9] Invariant natural killer T cells and mucosal-associated invariant T cells in multiple sclerosis
    Bianchini, Elena
    De Biasi, Sara
    Simone, Anna Maria
    Ferraro, Diana
    Sola, Patrizia
    Cossarizza, Andrea
    Pinti, Marcello
    IMMUNOLOGY LETTERS, 2017, 183 : 1 - 7
  • [10] The dynamics of mucosal-associated invariant T cells in multiple sclerosis
    Sugimoto, Chie
    Hirotani, Makoto
    Yoshikiyo, Kazunori
    Koshimizu, Uichi
    Wakao, Rika
    Horinouchi, Takahiro
    Mazaki, Yuichi
    Higashi, Tsunehiko
    Fukazawa, Toshiyuki
    Fujita, Hiroyoshi
    Sasaki, Hidenao
    Wakao, Hiroshi
    SPRINGERPLUS, 2016, 5