Development of a novel transgenic mouse for the study of interactions between CD4 and CD8 T cells during graft rejection

被引:166
作者
Ehst, BD
Ingulli, E
Jenkins, MK [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Pediat, Minneapolis, MN 55455 USA
关键词
adoptive transfer; ovalbumin; skin;
D O I
10.1046/j.1600-6135.2003.00246.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
The goal of this study was the development of a system in which the cooperative interactions between CD4 and CD8 T cells specific for defined peptides from a single minor histocompatibility antigen could be studied. A transgenic mouse strain that expresses chicken ovalbumin (Act-mOVA) on the surface of all cells in the body was produced as a source of tissues containing such an antigen. Skin grafts from Act-mOVA donors were rapidly and completely rejected by wildtype recipients, but only when both CD4 and CD8 T cells were present. CD4 T cells by themselves caused an incomplete form of rejection characterized by rapid but partial contraction of Act-mOVA grafts. CD8 T cells alone caused complete rejection of Act-mOVA skin grafts but only after a long delay. Adoptively transferred ovalbumin-specific TCR-transgenic CD4 and CD8 T cells were stimulated by Act-mOVA graft antigens and CD8 T-cell accumulation in the grafts was enhanced by specific CD4 T cells. These findings, together with the fact that the ligand for ovalbumin peptide-specific CD8 T cells can be detected in Act-mOVA tissues with an MHC-restricted antibody, make this an ideal system for the study of cooperation between CD4 and CD8 T cells.
引用
收藏
页码:1355 / 1362
页数:8
相关论文
共 45 条
  • [1] Ambrose H., 1987, HDB BIOL INVESTIGATI
  • [2] T cell tolerance and activation to a transgene-encoded tumor antigen
    Antoniou, A
    McCormick, D
    Scott, D
    Yeoman, H
    Chandler, P
    Mellor, A
    Dyson, J
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (05) : 1094 - 1102
  • [3] Arakelov A, 2000, SEMIN NEPHROL, V20, P95
  • [4] Defective TCR expression in transgenic mice constructed using cDNA-based α- and β-chain genes under the control of heterologous regulatory elements
    Barnden, MJ
    Allison, J
    Heath, WR
    Carbone, FR
    [J]. IMMUNOLOGY AND CELL BIOLOGY, 1998, 76 (01) : 34 - 40
  • [5] Help for cytotoxic-T-cell responses is mediated by CD40 signalling
    Bennett, SRM
    Carbone, FR
    Karamalis, F
    Flavell, RA
    Miller, JFAP
    Heath, WR
    [J]. NATURE, 1998, 393 (6684) : 478 - 480
  • [6] MAJOR HISTOCOMPATIBILITY COMPLEX DETERMINES SUSCEPTIBILITY TO CYTOTOXIC T-CELLS DIRECTED AGAINST MINOR HISTOCOMPATIBILITY ANTIGENS
    BEVAN, MJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1975, 142 (06) : 1349 - 1364
  • [7] Coordinate regulation of complex T cell populations responding to bacterial infection
    Busch, DH
    Pilip, IM
    Vijh, S
    Pamer, EG
    [J]. IMMUNITY, 1998, 8 (03) : 353 - 362
  • [8] Progressive loss of CD8(+) T cell-mediated control of a gamma-herpesvirus in the absence of CD4(+) T cells
    Cardin, RD
    Brooks, JW
    Sarawar, SR
    Doherty, PC
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (03) : 863 - 871
  • [9] Quantitative analysis of the immune response to mouse non-MHC transplantation antigens in vivo: The H60 histocompatibility antigen dominates over all others
    Choi, EY
    Yoshimura, Y
    Christianson, GJ
    Sproule, TJ
    Malarkannan, S
    Shastri, N
    Joyce, S
    Roopenian, DC
    [J]. JOURNAL OF IMMUNOLOGY, 2001, 166 (07) : 4370 - 4379
  • [10] CD8+ T cell subsets Tc1 and Tc2 cause different histopathologic forms of murine cardiac allograft rejection
    Delfs, MW
    Furukawa, Y
    Mitchell, RN
    Lichtman, AH
    [J]. TRANSPLANTATION, 2001, 71 (05) : 606 - 610