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胎儿和出生后的睾丸作为供体组织表现出免疫豁免权。

Fetal and postnatal testis shows immunoprivilege as donor tissue.

作者信息

Statter M B, Foglia R P, Parks D E, Donahoe P K

机构信息

Department of Surgery, Massachusetts General Hospital, Boston 02114.

出版信息

J Urol. 1988 Jan;139(1):204-10. doi: 10.1016/s0022-5347(17)42354-8.

DOI:10.1016/s0022-5347(17)42354-8
PMID:3275800
Abstract

We evaluated the immunogenicity of the testis by transplanting adult, postnatal, and fetal rat testicular tissue into outbred adult female and male rats for 10 days. Testis grafts were evaluated morphometrically and histologically, and selectively compared to renal grafts previously reported in part. Testis grafts from days 15 to 21 of gestation, and from three, nine, 12 and 15 days after birth showed an overall increase in growth, with maintenance of architecture and minimal lymphocytic infiltrate. In contrast, only fetal renal tissue from days 15 to 17 demonstrated an increase in growth with maintenance of architecture and minimal lymphocytic infiltrate; grafts from later in gestation grew only slightly and showed progressive deterioration in architecture with an increasing lymphocytic infiltrate. Fifteen day fetal testis grafts were also implanted for longer intervals up to 45 days. The fetal testis grafts implanted for 20 and 30 days showed an increase in size with maintenance of architecture and minimal lymphocytic infiltrate. The observed fetal and postnatal testis growth in the non-immunosuppressed adult host makes compelling further studies directed at determining those factors contributing to the decreased immunogenicity of this organ.

摘要

我们通过将成年、出生后及胎鼠睾丸组织移植到远交系成年雌性和雄性大鼠体内10天,评估了睾丸的免疫原性。对睾丸移植物进行了形态计量学和组织学评估,并与之前部分报道的肾移植物进行了选择性比较。妊娠第15至21天以及出生后第3、9、12和15天的睾丸移植物总体生长增加,结构维持且淋巴细胞浸润极少。相比之下,只有妊娠第15至17天的胎儿肾组织生长增加,结构维持且淋巴细胞浸润极少;妊娠后期的移植物生长仅轻微,结构逐渐恶化且淋巴细胞浸润增加。15天龄胎儿睾丸移植物也植入更长时间,长达45天。植入20天和30天的胎儿睾丸移植物大小增加,结构维持且淋巴细胞浸润极少。在未免疫抑制的成年宿主中观察到的胎儿和出生后睾丸生长,促使我们进行进一步研究,以确定导致该器官免疫原性降低的因素。

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Fetal and postnatal testis shows immunoprivilege as donor tissue.胎儿和出生后的睾丸作为供体组织表现出免疫豁免权。
J Urol. 1988 Jan;139(1):204-10. doi: 10.1016/s0022-5347(17)42354-8.
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Can fetal and newborn allografts survive in an immunocompetent host?胎儿和新生儿的同种异体移植物能在具有免疫活性的宿主中存活吗?
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Nat Med. 2015 Aug;21(8):869-79. doi: 10.1038/nm.3889. Epub 2015 Jul 13.
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Structural, cellular and molecular aspects of immune privilege in the testis.睾丸免疫豁免的结构、细胞和分子方面。
Front Immunol. 2012 Jun 11;3:152. doi: 10.3389/fimmu.2012.00152. eCollection 2012.
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Pig embryonic pancreatic tissue as a source for transplantation in diabetes: transient treatment with anti-LFA1, anti-CD48, and FTY720 enables long-term graft maintenance in mice with only mild ongoing immunosuppression.
猪胚胎胰腺组织作为糖尿病移植的来源:用抗LFA1、抗CD48和FTY720进行短暂治疗可使小鼠在仅进行轻度持续免疫抑制的情况下长期维持移植。
Diabetes. 2009 Jul;58(7):1585-94. doi: 10.2337/db09-0112. Epub 2009 Apr 28.
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Hepatic reconstruction from fetal porcine liver cells using a radial flow bioreactor.使用径向流生物反应器从胎猪肝细胞进行肝脏重建。
World J Gastroenterol. 2008 May 7;14(17):2740-7. doi: 10.3748/wjg.14.2740.
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Embryonic pig pancreatic tissue transplantation for the treatment of diabetes.胚胎猪胰腺组织移植治疗糖尿病。
PLoS Med. 2006 Jul;3(7):e215. doi: 10.1371/journal.pmed.0030215.
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Embryonic pig liver, pancreas, and lung as a source for transplantation: optimal organogenesis without teratoma depends on distinct time windows.胚胎猪肝脏、胰腺和肺作为移植来源:无畸胎瘤的最佳器官发生取决于不同的时间窗。
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Springer Semin Immunopathol. 1998;19(3):311-22. doi: 10.1007/BF00787228.
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[Prospects for clinical transplantation of the testis as an organ and as a tissue].[睾丸作为器官和组织进行临床移植的前景]
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