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移植肺后病毒再激活前,交叉反应性抗病毒 T 细胞增加。

Cross-reactive anti-viral T cells increase prior to an episode of viral reactivation post human lung transplantation.

机构信息

Department of Medicine, Monash University, Central Clinical School, The Alfred Centre, Melbourne, Victoria, Australia.

出版信息

PLoS One. 2013;8(2):e56042. doi: 10.1371/journal.pone.0056042. Epub 2013 Feb 6.

DOI:10.1371/journal.pone.0056042
PMID:23405250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3566045/
Abstract

Human Cytomegalovirus (CMV) reactivation continues to influence lung transplant outcomes. Cross-reactivity of anti-viral memory T cells against donor human leukocyte antigens (HLA) may be a contributing factor. We identified cross-reactive HLA-A02:01-restricted CMV-specific cytotoxic T lymphocytes (CTL) co-recognizing the NLVPMVATV (NLV) epitope and HLA-B27. NLV-specific CD8+ T cells were expanded for 13 days from 14 HLA-A02:01/CMV seropositive healthy donors and 11 lung transplant recipients (LTR) then assessed for the production of IFN-γ and CD107a expression in response to 19 cell lines expressing either single HLA-A or -B class I molecules. In one healthy individual, we observed functional and proliferative cross-reactivity in response to B*27:05 alloantigen, representing approximately 5% of the NLV-specific CTL population. Similar patterns were also observed in one LTR receiving a B27 allograft, revealing that the cross-reactive NLV-specific CTL gradually increased (days 13-193 post-transplant) before a CMV reactivation event (day 270) and reduced to basal levels following viral clearance (day 909). Lung function remained stable with no acute rejection episodes being reported up to 3 years post-transplant. Individualized immunological monitoring of cross-reactive anti-viral T cells will provide further insights into their effects on the allograft and an opportunity to predict sub-clinical CMV reactivation events and immunopathological complications.

摘要

人类巨细胞病毒(CMV)的再激活继续影响肺移植的结果。抗病毒记忆 T 细胞对供体人类白细胞抗原(HLA)的交叉反应可能是一个促成因素。我们鉴定了与 HLA-B27 共识别 NLVPMVATV(NLV)表位的 HLA-A02:01 限制性 CMV 特异性细胞毒性 T 淋巴细胞(CTL)。从 14 名 HLA-A02:01/CMV 血清阳性的健康供体和 11 名肺移植受者(LTR)中,使用 NLV 特异性 CD8+T 细胞在 13 天内扩增,然后评估其对表达单一 HLA-A 或 -B 类 I 分子的 19 个细胞系产生 IFN-γ和 CD107a 表达的情况。在一名健康个体中,我们观察到针对 B*27:05 同种异体抗原的功能和增殖交叉反应,代表 NLV 特异性 CTL 群体的大约 5%。在接受 B27 同种异体移植的 LTR 中也观察到了类似的模式,表明交叉反应性 NLV 特异性 CTL 在 CMV 再激活事件(第 270 天)之前逐渐增加(移植后第 13-193 天),并在病毒清除后(第 909 天)降至基础水平。肺功能保持稳定,移植后 3 年内未报告急性排斥反应。对交叉反应性抗病毒 T 细胞的个体化免疫监测将进一步深入了解它们对移植物的影响,并提供预测亚临床 CMV 再激活事件和免疫病理并发症的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b0/3566045/088e3a13ec97/pone.0056042.g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b0/3566045/088e3a13ec97/pone.0056042.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b0/3566045/050be106a8f3/pone.0056042.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b0/3566045/2906b2d4e53b/pone.0056042.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b0/3566045/d19a49ab4b6c/pone.0056042.g003.jpg
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