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IL-10 modified mRNA monotherapy prolongs survival after composite facial allografting through the induction of mixed chimerism.白细胞介素-10修饰的信使核糖核酸单一疗法通过诱导混合嵌合体延长复合面部移植后的生存期。
Mol Ther Nucleic Acids. 2023 Feb 16;31:610-627. doi: 10.1016/j.omtn.2023.02.016. eCollection 2023 Mar 14.
2
Donor derived hematopoietic stem cell niche transplantation facilitates mixed chimerism mediated donor specific tolerance.供者来源造血干细胞龛移植促进嵌合状态介导的供者特异性免疫耐受。
Front Immunol. 2023 Feb 16;14:1093302. doi: 10.3389/fimmu.2023.1093302. eCollection 2023.
3
The intragraft vascularized bone marrow induces secondary donor-specific mystacial pad allograft tolerance.移植物内血管化骨髓诱导次级供体特异性触须垫同种异体移植耐受。
Front Immunol. 2022 Dec 12;13:1059271. doi: 10.3389/fimmu.2022.1059271. eCollection 2022.
4
Reciprocal Donor-Recipient Strain Combinations Present Different Vascularized Composite Allotransplantation Outcomes in Rodent Models.同种异体供受者菌株组合在啮齿动物模型中呈现出不同的血管化复合组织移植结果。
Plast Reconstr Surg. 2023 Jun 1;151(6):1220-1231. doi: 10.1097/PRS.0000000000010099. Epub 2023 May 24.
5
Foxp3+ regulatory T cell therapy for tolerance in autoimmunity and solid organ transplantation.Foxp3+ 调节性 T 细胞治疗自身免疫和实体器官移植中的免疫耐受。
Front Immunol. 2022 Nov 17;13:1055466. doi: 10.3389/fimmu.2022.1055466. eCollection 2022.
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Tolerance of a Vascularized Composite Allograft Achieved in MHC Class-I-mismatch Swine Mixed Chimerism.在 MHC Ⅰ类错配猪混合嵌合体中实现血管化复合移植物的耐受。
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7
The Effect of Narrow-Band Ultraviolet B Irradiation on the Vascularized Composite Allotransplantation Rat Model.窄带紫外线 B 照射对血管化复合组织同种异体移植大鼠模型的影响。
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8
Tocilizumab-induced Leukoencephalopathy with a Reversible Clinical Course.托珠单抗诱发的白质脑病,临床病程可逆。
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Immunosuppression maintenance in vascularized composite allotransplantation: what is just right?血管化复合组织移植中的免疫抑制维持:何为恰到好处?
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血管化复合组织同种异体移植中诱导耐受的现状。

The current state of tolerance induction in vascularized composite allotransplantation.

机构信息

Department of Surgery, Division of Plastic and Reconstructive Surgery, University of Colorado Denver/Anschutz Medical Campus, Aurora, Colorado, USA.

出版信息

Curr Opin Organ Transplant. 2024 Dec 1;29(6):368-375. doi: 10.1097/MOT.0000000000001176. Epub 2024 Sep 20.

DOI:10.1097/MOT.0000000000001176
PMID:39422587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11537808/
Abstract

PURPOSE OF REVIEW

Significant advancements have been made in the field of vascularized composite allotransplantation (VCA); however, like solid organ transplantation, bypassing the recipient's immune response remains a significant obstacle to long-term allograft survival. Therefore, strategies to overcome acute and chronic rejection and minimize immunosuppressive therapy are crucial for the future of VCA. This review highlights recent attempts to induce tolerance in VCA and discusses key findings through a clinical lens.

RECENT FINDINGS

Promising VCA tolerance protocols are being investigated, with five recent studies illustrating various successes. These preclinical approaches demonstrate a correlation between the presence of donor-derived T cells and VCA tolerance, the importance of using clinically available reagents within preclinical protocols, and the ability to induce sustained tolerance through nonmyeloablative methods. Furthermore, environmental factors, such as NB-UVB light are being investigated for their immunomodulation properties and may influence VCA graft rejection.

SUMMARY

To widen the scope of VCA, minimization of immunosuppression is needed. Overall, tolerance induction protocols should have a low-toxicity level, minimally invasive induction therapies, and utilize short-term immunosuppressive medications. By examining the milestones of recent studies, researchers can gain new technical approaches to immune modulation and make data-driven amendments to tolerance protocols in preparation for clinical translation.

摘要

目的综述:血管化复合组织移植(VCA)领域取得了重大进展;然而,与实体器官移植一样,绕过受者免疫反应仍然是长期移植物存活的重大障碍。因此,克服急性和慢性排斥反应并最小化免疫抑制治疗的策略对于 VCA 的未来至关重要。本综述重点介绍了诱导 VCA 耐受的最新尝试,并从临床角度讨论了关键发现。

最近的发现:目前正在研究有前途的 VCA 耐受方案,最近的五项研究说明了各种成功。这些临床前方法表明供体细胞的存在与 VCA 耐受之间存在相关性,在临床前方案中使用临床可用试剂的重要性,以及通过非清髓性方法诱导持续耐受的能力。此外,还在研究环境因素,如 NB-UVB 光,以了解其免疫调节特性,这些特性可能会影响 VCA 移植物排斥。

总结:为了扩大 VCA 的范围,需要最小化免疫抑制。总体而言,诱导耐受的方案应具有低毒性、微创诱导治疗,并使用短期免疫抑制药物。通过检查最近研究的里程碑,研究人员可以获得新的免疫调节技术方法,并对耐受方案进行数据驱动的修正,为临床转化做准备。