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Cytotoxic T-lymphocyte tolerance to minor H-43a alloantigen is induced exclusively in the context of the self major histocompatibility complex class I H-2Kb molecules.

作者信息

Ishikawa H, Hino T, Kato H, Suzuki H, Saito K

机构信息

Department of Microbiology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Cell Immunol. 1987 Dec;110(2):436-42. doi: 10.1016/0008-8749(87)90136-5.

DOI:10.1016/0008-8749(87)90136-5
PMID:3500797
Abstract

We elucidated previously that cytotoxic T lymphocyte precursors (CTLp) against H-43a allo-antigen, which we had discovered as a new mouse minor H antigen, were primed in H-43b mice only in the context of self H-2Kb restriction element, and that anti-H-43a CTLp tolerance was induced in H-43b mice by injection with H-43a spleen cells (SC) from H-43 congenic mice, i.e., under the condition of disparity at only the H-43 locus. The present study attempted to determine whether the H-2Kb restriction element for anti-H-43a CTLp priming is also implicated in the induction of anti-H-43a CTLp tolerance. For this purpose, we used a newly established H-43b C3W (H-2k) strain which is H-43 congenic to H-43a C3H/HeN. When (C3W X B10.MBR)F1 (H-43b, H-2Kk/b, Ik/k, Dk/q) mice were injected with H-43a-bearing (C3H/HeN X B10.AKM)F1 (H-43a/b;H-2Kk/k,Ik/k,Dk/q)SC, their selfH-2Kb-restricted anti-H-43a CTLp were were primed (cross-priming). By contrast, injection of H-43a-bearing (C3H/HeN X B10.MBR)F1 (H-43a/b; H-2Kk/b,Ik/k, Dk/q)SC, which differ from (C3H/HeN x B10.AKM) F1 SC solely at H-2K and possess H-2Kb molecules, did not prime but specifically inactivated the anti-H-43a CTLp of (C3W x B10.MBR)F1 mice. These results indicate clearly that anti-H-43a CTLp tolerance is induced exclusively in the context of the H-2Kb element expressed on the antigenic H-43a SC.

摘要

相似文献

1
Cytotoxic T-lymphocyte tolerance to minor H-43a alloantigen is induced exclusively in the context of the self major histocompatibility complex class I H-2Kb molecules.
Cell Immunol. 1987 Dec;110(2):436-42. doi: 10.1016/0008-8749(87)90136-5.
2
Cytotoxic T lymphocyte response to minor H-43a alloantigen in H-43b mice. Privileged H-2Kb restriction to the response is not due to immunodominance or epistatic effect but due to Ir gene function of H-2Kb itself.H-43b小鼠中细胞毒性T淋巴细胞对次要H-43a同种抗原的应答。对该应答的特权性H-2Kb限制并非由于免疫显性或上位效应,而是由于H-2Kb自身的Ir基因功能。
J Immunol. 1988 Jan 1;140(1):44-51.
3
Cytotoxic T lymphocyte response to minor H-42a alloantigen in H-42b mice: clonal inactivation of the precursor cytotoxic T lymphocytes by veto-like spleen cells that express the H-42a antigen.H-42b小鼠对次要H-42a同种抗原的细胞毒性T淋巴细胞反应:表达H-42a抗原的类否决脾细胞对细胞毒性T淋巴细胞前体的克隆失活。
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4
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5
Effector mechanism in rejection of allografts expressing an isolated minor histocompatibility disparity. Importance of cytotoxic T lymphocytes in the rejection of H-43a allografts by H-43b mice.
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Cytotoxic T cell responses to minor H-43 alloantigens in H-43a and H-43b mice. Distinctive MHC class I restriction specificity and clonal inactivation are inherent properties of the H-43 system.
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7
The target minor H antigen for F1 cytotoxic T lymphocytes induced by Igh-congenic parental spleen cells is coded for by gene linked to H-2.由同基因亲本脾脏细胞诱导的F1细胞毒性T淋巴细胞的靶次要组织相容性抗原由与H-2相关的基因编码。
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Generation of cytotoxic T cells specific for minor histocompatibility antigens by cross challenge in vitro with H-2 disparate adherent cells.通过与H-2不相容的贴壁细胞进行体外交叉攻击产生针对次要组织相容性抗原的细胞毒性T细胞。
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Role of the H-2 complex in the induction of T cell tolerance to self minor histocompatibility antigens.H-2复合体在诱导T细胞对自身次要组织相容性抗原产生耐受性中的作用。
J Exp Med. 1983 Nov 1;158(5):1483-97. doi: 10.1084/jem.158.5.1483.
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In vivo priming of mouse CTL precursors directed to product of a newly defined minor H-42 locus is under a novel control of class II MHC gene.针对新定义的次要H-42位点产物的小鼠CTL前体的体内启动受II类MHC基因的新型调控。
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