Unique resistance of I/LnJ mice to a retrovirus is due to sustained interferon γ-dependent production of virus-neutralizing antibodies

被引:57
作者
Purdy, A [1 ]
Case, L [1 ]
Duvall, M [1 ]
Overstrom-Coleman, M [1 ]
Monnier, N [1 ]
Chervonsky, A [1 ]
Golovkina, T [1 ]
机构
[1] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
IFN-gamma; virus-neutralizing antibodies; retrovirus; infection; resistance;
D O I
10.1084/jem.20021499
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Selection of immune escape variants impairs the ability of the immune system to sustain an efficient antiviral response and to control retroviral infections. Like other retroviruses, mouse mammary tumor virus (MMTV) is not efficiently eliminated by the immune system of susceptible mice. In contrast, MMTV-infected I/Lnj mice are capable of producing IgG2a virus-neutralizing antibodies, sustain this response throughout their life, and secrete antibody-coated virions into the milk, thereby preventing infection of their progeny. Antibodies were produced in response to several MMTV variants and were cross-reactive to them. Resistance to MMTV infection was recessive and was dependent on interferon (IFN)-gamma production, because I/Lnj mice with targeted deletion of the INF-gamma gene failed to produce any virus-neutralizing antibodies. These findings reveal a novel mechanism of resistance to retroviral infection that is based on a robust and sustained IFN-gamma-dependent humoral immune response.
引用
收藏
页码:233 / 243
页数:11
相关论文
共 46 条
[21]   SUPERANTIGEN-REACTIVE CD4+ T-CELLS ARE REQUIRED TO STIMULATE B-CELLS AFTER INFECTION WITH MOUSE MAMMARY-TUMOR VIRUS [J].
HELD, W ;
SHAKHOV, AN ;
IZUI, S ;
WAANDERS, GA ;
SCARPELLINO, L ;
MACDONALD, HR ;
ACHAORBEA, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (02) :359-366
[22]   SUPERANTIGEN-INDUCED IMMUNE STIMULATION AMPLIFIES MOUSE MAMMARY-TUMOR VIRUS-INFECTION AND ALLOWS VIRUS TRANSMISSION [J].
HELD, W ;
WAANDERS, GA ;
SHAKHOV, AN ;
SCARPELLINO, L ;
ACHAORBEA, H ;
MACDONALD, HR .
CELL, 1993, 74 (03) :529-540
[23]   THE EFFECTS OF CHRONIC INFECTION WITH A SUPERANTIGEN-PRODUCING VIRUS [J].
IGNATOWICZ, L ;
KAPPLER, J ;
MARRACK, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (04) :917-923
[24]  
JANEWAY CA, 1989, COLD SH Q B, V54, P1
[25]  
Luther SA, 1997, J IMMUNOL, V159, P2807
[26]   T-CELL RECEPTOR V-BETA USE PREDICTS REACTIVITY AND TOLERANCE TO MLSA-ENCODED ANTIGENS [J].
MACDONALD, HR ;
SCHNEIDER, R ;
LEES, RK ;
HOWE, RC ;
ACHAORBEA, H ;
FESTENSTEIN, H ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
NATURE, 1988, 332 (6159) :40-45
[27]   T-CELL REACTIVITY AND TOLERANCE TO MLSA-ENCODED ANTIGENS [J].
MACDONALD, HR ;
GLASEBROOK, AL ;
SCHNEIDER, R ;
LEES, RK ;
PIRCHER, H ;
PEDRAZZINI, T ;
KANAGAWA, O ;
NICOLAS, JF ;
HOWE, RC ;
ZINKERNAGEL, RM ;
HENGARTNER, H .
IMMUNOLOGICAL REVIEWS, 1989, 107 :89-108
[28]   A MATERNALLY INHERITED SUPERANTIGEN ENCODED BY A MAMMARY-TUMOR VIRUS [J].
MARRACK, P ;
KUSHNIR, E ;
KAPPLER, J .
NATURE, 1991, 349 (6309) :524-526
[29]   Innate immunity: The virtues of a nonclonal system of recognition [J].
Medzhitov, R ;
Janeway, CA .
CELL, 1997, 91 (03) :295-298
[30]   CHANGING VIRUS-HOST INTERACTIONS IN THE COURSE OF HIV-1 INFECTION [J].
MIEDEMA, F ;
MEYAARD, L ;
KOOT, M ;
KLEIN, MR ;
ROOS, MTL ;
GROENINK, M ;
FOUCHIER, RAM ;
VANTWOUT, AB ;
TERSMETTE, M ;
SCHELLEKENS, PTA ;
SCHUITEMAKER, H .
IMMUNOLOGICAL REVIEWS, 1994, 140 :35-72