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慢性移植物抗宿主病中细胞成分的复杂相互作用。

Complex interactions of cellular players in chronic Graft-versus-Host Disease.

机构信息

Department of Dermatology, Medical University of Vienna, Vienna, Austria.

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.

出版信息

Front Immunol. 2023 Jun 26;14:1199422. doi: 10.3389/fimmu.2023.1199422. eCollection 2023.


DOI:10.3389/fimmu.2023.1199422
PMID:37435079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10332803/
Abstract

Chronic Graft-versus-Host Disease is a life-threatening inflammatory condition that affects many patients after allogeneic hematopoietic stem cell transplantation. Although we have made substantial progress in understanding disease pathogenesis and the role of specific immune cell subsets, treatment options are still limited. To date, we lack a global understanding of the interplay between the different cellular players involved, in the affected tissues and at different stages of disease development and progression. In this review we summarize our current knowledge on pathogenic and protective mechanisms elicited by the major involved immune subsets, being T cells, B cells, NK cells and antigen presenting cells, as well as the microbiome, with a special focus on intercellular communication of these cell types extracellular vesicles as up-and-coming fields in chronic Graft-versus-Host Disease research. Lastly, we discuss the importance of understanding systemic and local aberrant cell communication during disease for defining better biomarkers and therapeutic targets, eventually enabling the design of personalized treatment schemes.

摘要

慢性移植物抗宿主病是一种危及生命的炎症性疾病,影响异基因造血干细胞移植后的许多患者。尽管我们在了解疾病发病机制和特定免疫细胞亚群的作用方面取得了重大进展,但治疗选择仍然有限。迄今为止,我们缺乏对受影响组织中不同细胞参与者之间相互作用的全面了解,以及在疾病发展和进展的不同阶段。在这篇综述中,我们总结了我们目前对主要涉及的免疫亚群(即 T 细胞、B 细胞、NK 细胞和抗原呈递细胞)以及微生物组引发的致病和保护机制的了解,特别关注这些细胞类型的细胞间通讯,以及细胞外囊泡作为慢性移植物抗宿主病研究中的新兴领域。最后,我们讨论了了解疾病过程中全身和局部异常细胞通讯的重要性,以确定更好的生物标志物和治疗靶点,最终能够设计个性化的治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/4d7352c84d7f/fimmu-14-1199422-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/87836cd7fc0f/fimmu-14-1199422-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/59a9abc61907/fimmu-14-1199422-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/e806464107b7/fimmu-14-1199422-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/a1d0d3b2c301/fimmu-14-1199422-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/4d7352c84d7f/fimmu-14-1199422-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/87836cd7fc0f/fimmu-14-1199422-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/59a9abc61907/fimmu-14-1199422-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/e806464107b7/fimmu-14-1199422-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/a1d0d3b2c301/fimmu-14-1199422-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bab0/10332803/4d7352c84d7f/fimmu-14-1199422-g005.jpg

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引用本文的文献

[1]
Targeting hypoxia-inducible factor 1α in chronic graft-versus-host disease to enhance graft-versus-leukemia responses: implications for nanotherapeutics.

Front Immunol. 2025-7-28

[2]
Chronic Graft-versus-host Disease, Part 1: How Preclinical Models Shape Our Understanding of Biology and Pave the Way for Future Therapeutic Interventions.

Transplantation. 2025-6-24

[3]
Oral Chronic Graft-Versus-Host Disease: Pathogenesis, Diagnosis, Current Treatment, and Emerging Therapies.

Int J Mol Sci. 2024-9-27

[4]
The role and novel use of natural killer cells in graft-versus-leukemia reactions after allogeneic transplantation.

Front Immunol. 2024

[5]
Osteoclasts and Probiotics Mediate Significant Expansion, Functional Activation and Supercharging in NK, γδ T, and CD3+ T Cells: Use in Cancer Immunotherapy.

Cells. 2024-1-24

本文引用的文献

[1]
The Role of Extracellular Vesicles (EVs) in Chronic Graft vs. Host Disease, and the Potential Function of Placental Cell-Derived EVs as a Therapeutic Tool.

Int J Mol Sci. 2023-5-1

[2]
Combinatorial inhibition of Tec kinases BTK and ITK is beneficial in ameliorating murine sclerodermatous chronic graft versus host disease.

Bone Marrow Transplant. 2023-8

[3]
Single-cell landscape analysis unravels molecular programming of the human B cell compartment in chronic GVHD.

JCI Insight. 2023-6-8

[4]
Hematopoietic stem cell-derived Tregs are essential for maintaining favorable B cell lymphopoiesis following posttransplant cyclophosphamide.

JCI Insight. 2023-4-24

[5]
Ambient oxygen levels regulate intestinal dysbiosis and GVHD severity after allogeneic stem cell transplantation.

Immunity. 2023-2-14

[6]
Graft-versus-host disease is locally maintained in target tissues by resident progenitor-like T cells.

Immunity. 2023-2-14

[7]
Ibrutinib for First-Line Treatment of Chronic Graft-Versus-Host Disease: Results From the Randomized Phase III iNTEGRATE Study.

J Clin Oncol. 2023-4-1

[8]
Optimizing multiplexed imaging experimental design through tissue spatial segregation estimation.

Nat Methods. 2023-3

[9]
A Phase I Trial of SYK Inhibition with Fostamatinib in the Prevention and Treatment of Chronic Graft-Versus-Host Disease.

Transplant Cell Ther. 2023-3

[10]
Cell-based therapy in prophylaxis and treatment of chronic graft-versus-host disease.

Front Immunol. 2022

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