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环磷酰胺诱导的耐受性在预先用Galα1-3Galβ-4-GlcNAc抗原致敏的α1,3-半乳糖基转移酶基因敲除小鼠中的应用。

Application of cyclophosphamide-induced tolerance in alpha1,3-galactosyltransferase knockout mice presensitized with Gal alpha 1-3Gal beta-4-GlcNAc antigens.

作者信息

Onzuka Tatsushi, Shimizu Ichiro, Tomita Yukihiro, Iwai Toshiro, Okano Shinji, Tominaga Ryuji

机构信息

Department of Cardiovascular Surgery, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

Surg Today. 2008;38(9):807-14. doi: 10.1007/s00595-007-3715-1. Epub 2008 Aug 28.


DOI:10.1007/s00595-007-3715-1
PMID:18751946
Abstract

PURPOSE: Hyperacute rejection (HAR) mediated by the natural antibody (nAb) against Gal alpha 1-3Gal beta-4-GlcNAc (alpha Gal) is the major obstacle in xenogeneic organ transplantation. Previously, we reported the acceptance of donor heart grafts in anti-alpha Gal nAb-producing galactosyltransferase knockout (GalT KO) mice after cyclophosphamide (CP)-induced tolerance conditioning. In the present study, we applied our tolerance induction conditioning in presensitized recipient mice. METHODS: GalT KO (alpha Gal(-/-), H-2(b/d)) recipient mice were presensitized with alpha Gal(+) rabbit red blood cells (RRBCs). Presensitized or nonsensitized recipient mice were treated with CP-induced tolerance conditioning, consisting of AKR (alpha Gal(+/+), H-2(k)) spleen cells (SC), CP, busulfan (BU), and AKR bone marrow cells (BMC). We assessed the survival of donor hearts and skin grafts and analyzed the production of anti-alpha Gal Abs by flow cytometry. RESULTS: Donor mixed chimerism was achieved in the presensitized GalT KO mice treated with CP-induced tolerance conditioning. In parallel with the disappearance of anti-alpha Gal Abs, permanent acceptance of donor heart grafts and skin grafts was observed in presensitized and GalT KO mice treated with CP-induced tolerance conditioning. CONCLUSIONS: Both B-cell and T-cell tolerance was achieved in the presence of a higher titer of anti-alpha Gal Abs after treatment with CP-induced tolerance conditioning.

摘要

目的:由针对Galα1-3Galβ-4-GlcNAc(αGal)的天然抗体(nAb)介导的超急性排斥反应(HAR)是异种器官移植的主要障碍。此前,我们报道了在环磷酰胺(CP)诱导的耐受性预处理后,产生抗αGal nAb的半乳糖基转移酶敲除(GalT KO)小鼠接受供体心脏移植。在本研究中,我们将耐受性诱导预处理应用于预先致敏的受体小鼠。 方法:用αGal(+)兔红细胞(RRBCs)对GalT KO(αGal(-/-),H-2(b/d))受体小鼠进行预先致敏。对预先致敏或未致敏的受体小鼠进行CP诱导的耐受性预处理,包括AKR(αGal(+/+),H-2(k))脾细胞(SC)、CP、白消安(BU)和AKR骨髓细胞(BMC)。我们评估了供体心脏和皮肤移植的存活情况,并通过流式细胞术分析了抗αGal抗体的产生。 结果:在接受CP诱导的耐受性预处理的预先致敏的GalT KO小鼠中实现了供体混合嵌合。随着抗αGal抗体的消失,在接受CP诱导的耐受性预处理的预先致敏和GalT KO小鼠中观察到对供体心脏移植和皮肤移植的永久接受。 结论:在CP诱导的耐受性预处理后,在抗αGal抗体滴度较高的情况下实现了B细胞和T细胞耐受性。

相似文献

[1]
Application of cyclophosphamide-induced tolerance in alpha1,3-galactosyltransferase knockout mice presensitized with Gal alpha 1-3Gal beta-4-GlcNAc antigens.

Surg Today. 2008

[2]
Sequential analysis of anti-alpha Gal natural antibody-producing B cells in GalT knockout mice in cyclophosphamide-induced tolerance.

Scand J Immunol. 2006-6

[3]
Tolerization of Gal alpha 1,3Gal-reactive B cells in pre-sensitized alpha 1,3-galactosyltransferase-deficient mice by nonmyeloablative induction of mixed chimerism.

Xenotransplantation. 2001-11

[4]
Efficacy and limitations of cyclophosphamide-induced tolerance against alphaGal antigen.

Scand J Immunol. 2005-9

[5]
Mixed chimerism induced without lethal conditioning prevents T cell- and anti-Gal alpha 1,3Gal-mediated graft rejection.

J Clin Invest. 1999-8

[6]
T cell and B cell tolerance to GALalpha1,3GAL-expressing heart xenografts is achieved in alpha1,3-galactosyltransferase-deficient mice by nonmyeloablative induction of mixed chimerism.

Transplantation. 2001-6-15

[7]
Requirement of a higher degree of chimerism for skin allograft tolerance in cyclophosphamide-induced tolerance.

Transpl Int. 2005-5

[8]
Mixed chimerism, heart, and skin allograft tolerance in cyclophosphamide-induced tolerance.

Transplantation. 2000-9-27

[9]
Lewis rat pancreas, but not cardiac xenografts, are resistant to anti-gal antibody mediated hyperacute rejection.

Transplantation. 2001-5-27

[10]
Antibody-mediated T-cell reduction or increased levels of chimerism overcome resistance to cyclophosphamide-induced tolerance in NKT-deficient mice.

Scand J Immunol. 2010-8

引用本文的文献

[1]
Current status of and prospects for the English medical journal Surgery Today.

Surg Today. 2010-12

本文引用的文献

[1]
Application of chimerism-based drug-induced tolerance to rat into mouse xenotransplantation.

Scand J Immunol. 2006-10

[2]
Humoral immunity is the dominant barrier for allogeneic bone marrow engraftment in sensitized recipients.

Blood. 2006-11-15

[3]
Sequential analysis of anti-alpha Gal natural antibody-producing B cells in GalT knockout mice in cyclophosphamide-induced tolerance.

Scand J Immunol. 2006-6

[4]
Decay-accelerating factor prevents acute humoral rejection induced by low levels of anti-alphaGal natural antibodies.

Transplantation. 2006-1-15

[5]
Efficacy and limitations of cyclophosphamide-induced tolerance against alphaGal antigen.

Scand J Immunol. 2005-9

[6]
''Homologous restriction'' in complement lysis: roles of membrane complement regulators.

Xenotransplantation. 2005-7

[7]
Heart transplantation in baboons using alpha1,3-galactosyltransferase gene-knockout pigs as donors: initial experience.

Nat Med. 2005-1

[8]
Acute vascular rejection of xenografts: roles of natural and elicited xenoreactive antibodies in activation of vascular endothelial cells and induction of procoagulant activity.

Transplantation. 2004-6-15

[9]
Characterization of human CD55 and CD59 transgenic pigs and kidney xenotransplantation in the pig-to-baboon combination.

Transplantation. 2004-5-15

[10]
Gal alpha 1,3Gal expression on porcine pancreatic islets, testis, spleen, and thymus.

Xenotransplantation. 2004-1

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