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自然杀伤细胞:不只是慢性血管排斥反应的追随者,也是其启动者。

NK Cells: Not Just Followers But Also Initiators of Chronic Vascular Rejection.

机构信息

CIRI, INSERM U1111, Université Claude Bernard Lyon I, CNRS UMR5308, Ecole Normale Supérieure de Lyon, University of Lyon, Lyon, France.

Hospices Civils de Lyon, Edouard Herriot Hospital, Department of Transplantation, Nephrology and Clinical Immunology, Lyon, France.

出版信息

Transpl Int. 2024 Oct 16;37:13318. doi: 10.3389/ti.2024.13318. eCollection 2024.


DOI:10.3389/ti.2024.13318
PMID:39479216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11521863/
Abstract

Chronic graft rejection represents a significant threat to long-term graft survival. Early diagnosis, understanding of the immunological mechanisms and appropriate therapeutic management are essential to improve graft survival and quality of life for transplant patients. Knowing which immune cells are responsible for chronic vascular rejection would allow us to provide effective and appropriate treatment for these patients. It is now widely accepted that natural killer (NK) cells play an important role in chronic vascular rejection. They can either initiate chronic vascular rejection by recognizing missing self on the graft or be recruited by donor-specific antibodies to destroy the graft during antibody-mediated rejection. Whatever the mechanisms of activation of NK cells, they need to be primed to become fully activated and damaging to the graft. A better understanding of the signaling pathways involved in NK cell priming and activation would pave the way for the development of new therapeutic strategies to cure chronic vascular rejection. This review examines the critical role of NK cells in the complex context of chronic vascular rejection.

摘要

慢性移植物排斥反应是长期移植物存活的重大威胁。早期诊断、了解免疫机制和适当的治疗管理对于提高移植患者的移植物存活率和生活质量至关重要。了解哪些免疫细胞负责慢性血管排斥反应,将使我们能够为这些患者提供有效和适当的治疗。现在广泛认为,自然杀伤 (NK) 细胞在慢性血管排斥反应中发挥重要作用。它们可以通过识别移植物上的缺失自我来启动慢性血管排斥反应,也可以被供体特异性抗体募集,在抗体介导的排斥反应期间破坏移植物。无论 NK 细胞激活的机制如何,它们都需要被预先激活才能完全激活并对移植物造成损害。更好地了解 NK 细胞的激活和激活所涉及的信号通路将为开发新的治疗策略来治愈慢性血管排斥反应铺平道路。这篇综述探讨了 NK 细胞在慢性血管排斥反应这一复杂背景下的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/f3f60e173099/ti-37-13318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/caa4813b266e/ti-37-13318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/41d89444c6da/ti-37-13318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/f3f60e173099/ti-37-13318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/caa4813b266e/ti-37-13318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/41d89444c6da/ti-37-13318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f692/11521863/f3f60e173099/ti-37-13318-g003.jpg

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引用本文的文献

[1]
Targeting CD38 in Antibody-Mediated Rejection.

Transpl Int. 2025-5-15

[2]
Antibody-mediated rejection-treatment standard.

Nephrol Dial Transplant. 2025-8-1

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本文引用的文献

[1]
The role of antibody glycosylation in autoimmune and alloimmune kidney diseases.

Nat Rev Nephrol. 2024-10

[2]
A Randomized Phase 2 Trial of Felzartamab in Antibody-Mediated Rejection.

N Engl J Med. 2024-7-11

[3]
Influence of immunosuppressive drugs on natural killer cells in therapeutic drug exposure in liver transplantation.

Hepatobiliary Surg Nutr. 2023-12-1

[4]
Natural killer cell functional genetics and donor-specific antibody-triggered microvascular inflammation.

Am J Transplant. 2024-5

[5]
Transcriptomic signatures of chronic active antibody-mediated rejection deciphered by RNA sequencing of human kidney allografts.

Kidney Int. 2024-2

[6]
Examining the impact of immunosuppressive drugs on antibody-dependent cellular cytotoxicity (ADCC) of human peripheral blood natural killer (NK) cells and gamma delta (γδ) T cells.

Transpl Immunol. 2024-2

[7]
Transcriptional and spatial profiling of the kidney allograft unravels a central role for FcyRIII+ innate immune cells in rejection.

Nat Commun. 2023-7-19

[8]
Interleukin-21 promotes Type-1 activation and cytotoxicity of CD56CD16 natural killer cells during kidney allograft antibody-mediated rejection showing a new link between adaptive and innate humoral allo-immunity.

Kidney Int. 2023-10

[9]
Afucosylation of HLA-specific IgG1 as a potential predictor of antibody pathogenicity in kidney transplantation.

Cell Rep Med. 2022-11-15

[10]
Diminished cell proliferation promotes natural killer cell adaptive-like phenotype by limiting FcεRIγ expression.

J Exp Med. 2022-11-7

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