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Haptens can serve as surrogate transplantation antigens in a manner that demonstrates H-2 restriction of graft rejection.
J Exp Med. 1983 Apr 1;157(4):1354-9. doi: 10.1084/jem.157.4.1354.
2
Induction of H-2-restricted contact hypersensitivity by hapten-derivatized skin grafts. Evidence that the immunogenic signal includes H-2 determinants derived from the skin.
Transplantation. 1984 Feb;37(2):195-201. doi: 10.1097/00007890-198402000-00015.
3
The induction of tolerance to DNFB contact sensitivity using hapten modified lymphoid cells. I. Cellular requirements for rapid induction of tolerance.
Cell Immunol. 1980 May;51(2):360-9. doi: 10.1016/0008-8749(80)90267-1.
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Genetic restrictions for the induction of suppressor T cells by hapten-modified lymphoid cells in tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitivity. Role of the H-2D region of the major histocompatibility complex.
J Exp Med. 1978 Mar 1;147(3):788-99. doi: 10.1084/jem.147.3.788.
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Suppressor cells in tolerance to contact sensitivity active against hapten-syngeneic and hapten-allogeneic determinants.
J Exp Med. 1977 Jul 1;146(1):49-58. doi: 10.1084/jem.146.1.49.
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Induction of tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitivity with hapten-modified lymphoid cells. II. Selective tolerance in F1 mice of T cell subsets recognizing 1-fluoro-2,4-dinitrobenzene associated with parental major histocompatibility complex antigens.
J Exp Med. 1980 Apr 1;151(4):959-64. doi: 10.1084/jem.151.4.959.
8
Keratinocyte-derived, CD80-mediated costimulation is associated with hapten-specific IgE production during contact hypersensitivity to TH1 haptens.
J Allergy Clin Immunol. 2005 Feb;115(2):383-90. doi: 10.1016/j.jaci.2004.11.019.
9
Influence of contact sensitivity to DNFB on the induction of carrier-determined tolerance to DNP.
Cell Immunol. 1976 Oct;26(2):135-40. doi: 10.1016/0008-8749(76)90357-9.
10
Desensitization of contact allergy to DNFB in mice. III. Characteristics of immediate desensitization induced by haptenated spleen cells.
Cell Immunol. 1986 Apr 1;98(2):279-88. doi: 10.1016/0008-8749(86)90288-1.
引用本文的文献
1
Cloned LYT-2+ cytolytic T lymphocytes destroy allogeneic tissue in vivo.
J Exp Med. 1984 Jan 1;159(1):234-43. doi: 10.1084/jem.159.1.234.
本文引用的文献
1
Evidence for major histocompatibility complex restriction in transplantation immunity.
Proc Natl Acad Sci U S A. 1982 Jan;79(1):171-4. doi: 10.1073/pnas.79.1.171.
2
The vascular bed as the primary target in the destruction of skin grafts by antiserum. I. Resistance of freshly placed xenografts of skin to antiserum.
J Exp Med. 1981 Nov 1;154(5):1319-31. doi: 10.1084/jem.154.5.1319.
3
H-2 restriction of T cells causing lethal graft-versus-host disease across minor histocompatibility barriers in mice.
Transplant Proc. 1981 Mar;13(1 Pt 2):1217-9.
4
Cells mediating graft rejection in the mouse. I. Lyt-1 cells mediate skin graft rejection.
J Exp Med. 1981 May 1;153(5):1044-57. doi: 10.1084/jem.153.5.1044.
5
Maturation of cytotoxic effector cells at the site of allograft rejection.
Transplant Proc. 1981 Mar;13(1 Pt 2):1105-7.
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The vascular bed as the primary target in the destruction of skin grafts by antiserum. II. Loss of sensitivity to antiserum in long-term xenografts of skin.
J Exp Med. 1981 Nov 1;154(5):1332-41. doi: 10.1084/jem.154.5.1332.
8
Active clonal deletion in neonatal H-2 tolerance.
Ann N Y Acad Sci. 1982;392:276-90. doi: 10.1111/j.1749-6632.1982.tb36113.x.
9
Epidermal Langerhans cell density determines whether contact hypersensitivity or unresponsiveness follows skin painting with DNFB.
J Immunol. 1980 Jan;124(1):445-53.
10
Cell-mediated immunity: delayed-type hypersensitivity and cytotoxic responses are mediated by different T-cell subclasses.
J Exp Med. 1976 Jun 1;143(6):1534-9. doi: 10.1084/jem.143.6.1534.
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