Cytokines and transcription factors that regulate T helper cell differentiation: New players and new insights

被引:284
作者
Agnello, D
Lankford, CSR
Bream, J
Morinobu, A
Gadina, M
O'Shea, JJ
Frucht, DM
机构
[1] NIAMSD, Mol Immunol & Inflammat Branch, NIH, Bethesda, MD 20802 USA
[2] US FDA, Div Monoclonal Antibodies, Ctr Biol Evaluat & Res, Bethesda, MD 20014 USA
[3] Queens Univ Belfast, Dept Microbiol & Immunol, Belfast, Antrim, North Ireland
关键词
T helper (T-H) cells; differentiation; T(H)1 cells; T(H)2 cells; interferon-gamma; interleukin (IL)-4; IL-12; IL-23; IL-27; Stat1; Stat4; Stat6; GATA-3; c-Maf; NFATs;
D O I
10.1023/A:1023381027062
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The differentiation of naive CD4(+) T cells into subsets of T helper cells is a pivotal process with major implications for host defense and the pathogenesis of immune-mediated diseases. Though the basic paradigm was discovered more than 15 years ago, new discoveries continue to be made that offer fresh insights into the regulation of this process (1). T helper (T-H)1 cells produce interferon (IFN)-gamma, promoting cell-mediated immunity and control of intracellular pathogens. We now know that T(H)1 differentiation is regulated by transcription factors such as T-bet, Stat1, and Stat4, as well as cytokines such as IL-12, IL-23, IL-27, type I IFNs, and IFN-gamma. In contrast, T(H)2 cells produce IL-4, which promotes allergic responses and is important in host defense against helminths. The transcription factors Stat6, GATA-3, c-Maf, NFATs, and the cytokine IL-4 promote T(H)2 differentiation. These key regulators of T-H differentiation are the subject of this review.
引用
收藏
页码:147 / 161
页数:15
相关论文
共 176 条
  • [1] Functional diversity of helper T lymphocytes
    Abbas, AK
    Murphy, KM
    Sher, A
    [J]. NATURE, 1996, 383 (6603) : 787 - 793
  • [2] T-bet is a STAT1-induced regulator of IL-12R expression in naive CD4+ T cells
    Afkarian, M
    Sedy, JR
    Yang, J
    Jacobson, NG
    Cereb, N
    Yang, SY
    Murphy, TL
    Murphy, KM
    [J]. NATURE IMMUNOLOGY, 2002, 3 (06) : 549 - 557
  • [3] Modulation of chromatin structure regulates cytokine gene expression during T cell differentiation
    Agarwal, S
    Rao, A
    [J]. IMMUNITY, 1998, 9 (06) : 765 - 775
  • [4] Cell-type-restricted binding of the transcription factor NFAT to a distal IL-4 enhancer in vivo
    Agarwal, S
    Avni, O
    Rao, A
    [J]. IMMUNITY, 2000, 12 (06) : 643 - 652
  • [5] Abrogation of bronchial eosinophilic inflammation and airway hyperreactivity in signal transducers and activators of transcription (STAT)6-deficient mice
    Akimoto, T
    Numata, F
    Tamura, M
    Takata, Y
    Higashida, N
    Takashi, T
    Takeda, K
    Akira, S
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (09) : 1537 - 1542
  • [6] Cutting edge:: The common γ-chain is an indispensable subunit of the IL-21 receptor complex
    Asao, H
    Okuyama, C
    Kumaki, S
    Ishii, N
    Tsuchiya, S
    Foster, D
    Sugamura, K
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 167 (01) : 1 - 5
  • [7] Ausubel LJ, 1997, J IMMUNOL, V159, P2502
  • [8] TH cell differentiation is accompanied by dynamic changes in histone acetylation of cytokine genes
    Avni, O
    Lee, D
    Macian, F
    Szabo, SJ
    Glimcher, LH
    Rao, A
    [J]. NATURE IMMUNOLOGY, 2002, 3 (07) : 643 - 651
  • [9] INTERLEUKIN-12 (IL-12) INDUCES TYROSINE PHOSPHORYLATION OF JAK2 AND TYK2 - DIFFERENTIAL USE OF JANUS FAMILY TYROSINE KINASES BY IL-2 AND IL-12
    BACON, CM
    MCVICAR, DW
    ORTALDO, JR
    REES, RC
    O'SHEA, JJ
    JOHNSTON, JA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (01) : 399 - 404
  • [10] INTERLEUKIN-12 INDUCES TYROSINE PHOSPHORYLATION AND ACTIVATION OF STAT4 IN HUMAN-LYMPHOCYTES
    BACON, CM
    PETRICOIN, EF
    ORTALDO, JR
    REES, RC
    LARNER, AC
    JOHNSTON, JA
    O'SHEA, JJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) : 7307 - 7311