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相似文献

1
[Allograft "acceptance" and tolerance: a new concept].
Bull Acad Natl Med. 1998;182(1):79-85; discussion 85-6.
2
Functional relevance of donor-derived hematopoietic microchimerism only for induction but not for maintenance of allograft acceptance.供体来源的造血微嵌合体的功能相关性仅在于诱导而非维持同种异体移植物的接受。
Transplant Proc. 1999 Feb-Mar;31(1-2):920-1. doi: 10.1016/s0041-1345(98)01836-3.
3
Microchimerism in a human hand allograft.
Lancet. 1999 Nov 20;354(9192):1820-1. doi: 10.1016/s0140-6736(05)70589-4.
4
Peripheral microchimerism in long-term cadaveric-kidney allograft recipients.
Lancet. 1994 Jun 11;343(8911):1468-9. doi: 10.1016/s0140-6736(94)92583-6.
5
The functional relevance of passenger leukocytes and microchimerism for heart allograft acceptance in the rat.过客白细胞和微嵌合体对大鼠心脏同种异体移植接受的功能相关性。
Nat Med. 1999 Nov;5(11):1292-7. doi: 10.1038/15248.
6
Role of microchimerism on long-term graft survival after donor-specific transfusion in a rat heart transplantation model.微嵌合体在大鼠心脏移植模型中供体特异性输血后长期移植物存活中的作用。
Transplant Proc. 1998 Nov;30(7):3862-4. doi: 10.1016/s0041-1345(98)01266-4.
7
Peripheral blood microchimerism does not correlate with the state of graft acceptance in HLA-DRB1 mismatched renal transplant recipients.外周血微嵌合体与HLA-DRB1错配肾移植受者的移植物接受状态无关。
Transplant Proc. 1998 Feb;30(1):7-8. doi: 10.1016/s0041-1345(97)01161-5.
8
Use of CTLA4Ig for induction of mixed chimerism and renal allograft tolerance in nonhuman primates.使用CTLA4Ig诱导非人类灵长类动物的混合嵌合体形成和同种异体肾移植耐受。
Am J Transplant. 2014 Dec;14(12):2704-12. doi: 10.1111/ajt.12936. Epub 2014 Nov 13.
9
Donor cell microchimerism in kidney transplantation: Implications for graft function.供体细胞微嵌合体在肾移植中的作用:对移植物功能的影响。
Int J Immunogenet. 2020 Dec;47(6):494-500. doi: 10.1111/iji.12492. Epub 2020 Sep 2.
10
Microchimerism and graft tolerance: cause or effect?
Lancet. 1997 May 10;349(9062):1336-7. doi: 10.1016/s0140-6736(97)22019-2.

本文引用的文献

1
Homograft sensitivity. An expression of the immunologic origins and consequences of individuality.同种移植敏感性。个体免疫起源及后果的一种表现。
Physiol Rev. 1959 Oct;39:811-59. doi: 10.1152/physrev.1959.39.4.811.
2
THE REVERSAL OF REJECTION IN HUMAN RENAL HOMOGRAFTS WITH SUBSEQUENT DEVELOPMENT OF HOMOGRAFT TOLERANCE.人类肾移植排斥反应的逆转及随后同种移植耐受性的发展
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3
Lymphoid/nonlymphoid compartmentalization of donor leukocyte chimerism in rat recipients of heart allografts, with or without adjunct bone marrow.在接受或未接受辅助性骨髓移植的心脏同种异体移植大鼠受者中,供体白细胞嵌合体的淋巴细胞/非淋巴细胞分区情况
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4
The discovery of MHC restriction.主要组织相容性复合体(MHC)限制的发现。
Immunol Today. 1997 Jan;18(1):14-7. doi: 10.1016/s0167-5699(97)80008-4.
5
Chimerism and transplantation tolerance: cause and effect.
Immunol Today. 1996 Dec;17(12):584-7; discussion 588. doi: 10.1016/s0167-5699(96)10069-4.
6
The lost chord: microchimerism and allograft survival.失落的和弦:微嵌合体与同种异体移植存活
Immunol Today. 1996 Dec;17(12):577-84; discussion 588. doi: 10.1016/s0167-5699(96)10070-0.
7
On immunological memory.论免疫记忆。
Annu Rev Immunol. 1996;14:333-67. doi: 10.1146/annurev.immunol.14.1.333.
8
Neonatal tolerance revisited: turning on newborn T cells with dendritic cells.重新审视新生儿耐受性:利用树突状细胞激活新生T细胞。
Science. 1996 Mar 22;271(5256):1723-6. doi: 10.1126/science.271.5256.1723.
9
Immunology taught by viruses.病毒传授的免疫学。
Science. 1996 Jan 12;271(5246):173-8. doi: 10.1126/science.271.5246.173.
10
Cell migration and chimerism after whole-organ transplantation: the basis of graft acceptance.全器官移植后的细胞迁移与嵌合现象:移植物接受的基础
Hepatology. 1993 Jun;17(6):1127-52.

[Allograft "acceptance" and tolerance: a new concept].

作者信息

Starzl T E

机构信息

Transplantation Institute, University of Pittsburgh Medical Center, Pennsylvania 15213, USA.

出版信息

Bull Acad Natl Med. 1998;182(1):79-85; discussion 85-6.

PMID:9622934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3005769/
Abstract

Discovery of microchimerism in kidney and liver transplantation provided an important framework for a better understanding of allograft acceptance, for analysis of management problems and for therapeutically oriented transplanted research. In these new concept correlations with infectious diseases caused by non cytopathic microorganisms, previous enigmas, immunologic reaction, counter argument and general immunologic implications are discussed.

摘要