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Role of persistence of antigen and indirect recognition in the maintenance of tolerance to renal allografts

机译:抗原的持久性和间接识别在维持肾脏同种异体移植耐受性中的作用

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摘要

BACKGROUND: We have previously shown that a 12-day treatment with cyclosporine A (CyA) facilitates induction of tolerance to class-I disparate kidneys, as demonstrated by acceptance of second, donor-matched kidneys without immunosuppression. In the present study, we have examined 1) the duration of tolerance in the absence of donor antigen and 2) the pathway of antigen recognition determining maintenance or loss of tolerance. METHODS: Seventeen miniature swine received class-I mismatched kidneys with 12 days of CyA, and received second donor-matched kidneys without immunosuppression at 0, 1, 3, or 4 months after nephrectomy of the primary graft. Five were sensitized 6 weeks after nephrectomy of the primary graft, three with donor-matched skin grafts, and two with donor class-I peptides to eliminate direct pathway involvement. In addition, two long-term tolerant animals received class-I peptides. RESULTS: Rejection of second grafts required at least a 3 month absence of donor antigen. Although donor-matched skin grafts in animals tolerant to kidneys induced antidonor cytotoxic T lymphocyte responses, second renal transplants revealed no evidence of sensitization. In contrast, immunization of recipients with donor class-I peptides after nephrectomy of the primary graft led to loss of tolerance at both T-cell and B-cell levels, as evidenced by rejection of the second graft in 5 days and development of antidonor immunoglobulin G. Peptide immunization of long-term tolerant in recipients bearing long-term renal grafts did not break tolerance. CONCLUSIONS: These data indicate that the renal allograft is required for the indefinite maintenance of tolerance, that indirect antigen presentation is capable of breaking tolerance, and that in tolerant animals, direct antigen presentation may suppress rejection, allowing tolerance to persist.
机译:背景:我们先前已经证明,用环孢菌素A(CyA)治疗12天有助于诱导对I类异种肾脏的耐受性,这是通过接受第二只供体匹配的肾脏而没有免疫抑制所证实的。在本研究中,我们检查了1)在没有供体抗原的情况下耐受的持续时间,以及2)确定维持或丧失耐受性的抗原识别途径。方法:17只小型猪接受了I类错配的肾脏,并伴有12天的CyA,并且在初次移植肾后0、1、3或4个月接受了第二只供体匹配的肾脏,但没有免疫抑制。在初次肾移植术后6周,对五名患者进行了敏化,对三名进行了供体匹配的皮肤移植,并对三名进行了I类供体肽消除,以消除直接通路的参与。另外,两只长期耐受的动物接受了I类肽。结果:第二次移植的排斥至少需要三个月没有供体抗原。尽管在耐受肾脏的动物体内匹配供体的皮肤移植物诱导了抗供体的细胞毒性T淋巴细胞反应,但第二次肾脏移植并未显示出致敏的迹象。相比之下,一次移植肾切除后用供体I类肽免疫受体会导致T细胞和B细胞水平的耐受性丧失,这在5天内第二次移植排斥和抗供体免疫球蛋白的发展中得到了证明。 G.接受长期肾移植的接受者的长期耐受性肽免疫未破坏耐受性。结论:这些数据表明无限期维持耐受性需要同种异体肾移植,间接抗原呈递能够破坏耐受性,在耐受性动物中,直接抗原呈递可以抑制排斥反应,从而使耐受性得以持续。

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