Autocrine IFN-γ Promotes Naive CD8 T Cell Differentiation and Synergizes with IFN-α To Stimulate Strong Function

被引:78
作者
Curtsinger, Julie M. [1 ]
Agarwal, Pujya [1 ]
Lins, Debra C. [1 ]
Mescher, Matthew F. [1 ]
机构
[1] Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
INTERFERON-GAMMA; CLONAL EXPANSION; MEMORY DEVELOPMENT; EFFECTOR FUNCTION; DENDRITIC CELLS; CUTTING EDGE; ANTIGEN; IL-12; BET; RECEPTOR;
D O I
10.4049/jimmunol.1102727
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autocrine IFN-gamma signaling is important for CD4 differentiation to Th1 effector cells, but it has been unclear whether it contributes to CD8 T cell differentiation. We show in this paper that naive murine CD8 T cells rapidly and transiently produce low levels of IFN-gamma upon stimulation with Ag and B7-1, with production peaking at similar to 8 h and declining by 24 h. The autocrine IFN-gamma signals for upregulation of expression of T-bet and granzyme B and induces weak cytolytic activity and effector IFN-gamma production. IFN-alpha acts synergistically with IFN-gamma to support development of strong effector functions, whereas IL-12 induces high T-bet expression and strong function in the absence of IFN-gamma signaling. Thus, IFN-gamma is not only an important CD8 T cell effector cytokine, it is an autocrine/paracrine factor whose contributions to differentiation vary depending on whether the response is supported by IL-12 or type I IFN. The Journal of Immunology, 2012, 189: 659-668.
引用
收藏
页码:659 / 668
页数:10
相关论文
共 44 条
[1]   T-bet is a STAT1-induced regulator of IL-12R expression in naive CD4+ T cells [J].
Afkarian, M ;
Sedy, JR ;
Yang, J ;
Jacobson, NG ;
Cereb, N ;
Yang, SY ;
Murphy, TL ;
Murphy, KM .
NATURE IMMUNOLOGY, 2002, 3 (06) :549-557
[2]   Gene Regulation and Chromatin Remodeling by IL-12 and Type I IFN in Programming for CD8 T Cell Effector Function and Memory [J].
Agarwal, Pujya ;
Raghavan, Arvind ;
Nandiwada, Sarada L. ;
Curtsinger, Julie M. ;
Bohjanen, Paul R. ;
Mueller, Daniel L. ;
Mescher, Matthew F. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (03) :1695-1704
[3]   Cutting edge: CD8 T cells specific for lymphocytic choriomeningitis virus require type IIFN receptor for clonal expansion [J].
Aichele, P ;
Unsoeld, H ;
Koschella, M ;
Schweier, O ;
Kalinke, U ;
Vucikuja, S .
JOURNAL OF IMMUNOLOGY, 2006, 176 (08) :4525-4529
[4]   IL-1 acts directly on CD4 T cells to enhance their antigen-driven expansion and differentiation [J].
Ben-Sasson, Shlomo Z. ;
Hu-Li, Jane ;
Quiel, Juan ;
Cauchetaux, Stephane ;
Ratner, Maya ;
Shapira, Ilana ;
Dinarello, Charles A. ;
Paul, William E. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (17) :7119-7124
[5]  
Curtsinger JM, 1999, J IMMUNOL, V162, P3256
[6]   Cutting edge: Type IIFNs provide a third signal to CD8 T cells to stimulate clonal expansion and differentiation [J].
Curtsinger, JM ;
Valenzuela, JO ;
Agarwal, P ;
Lins, D ;
Mescher, MF .
JOURNAL OF IMMUNOLOGY, 2005, 174 (08) :4465-4469
[7]   CD8 T cell clonal expansion and development of effector function require prolonged exposure to antigen, costimulation, and signal 3 cytokine [J].
Curtsinger, JM ;
Johnson, CM ;
Mescher, MF .
JOURNAL OF IMMUNOLOGY, 2003, 171 (10) :5165-5171
[8]   Signal 3 availability limits the CD8 T cell response to a solid tumor [J].
Curtsinger, Julie M. ;
Gerner, Michael Y. ;
Lins, Debra C. ;
Mescher, Matthew F. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (11) :6752-6760
[9]   Inflammatory cytokines as a third signal for T cell activation [J].
Curtsinger, Julie M. ;
Mescher, Matthew F. .
CURRENT OPINION IN IMMUNOLOGY, 2010, 22 (03) :333-340
[10]   CD4 T cell-dependent conditioning of dendritic cells to produce IL-12 results in CD8-mediated graft rejection and avoidance of tolerance [J].
Filatenkov, AA ;
Jacovetty, EL ;
Fischer, UB ;
Curtsinger, JM ;
Mescher, MF ;
Ingulli, E .
JOURNAL OF IMMUNOLOGY, 2005, 174 (11) :6909-6917