Department of Medicine, Monash University, Central Clinical School, The Alfred Centre, Melbourne, Victoria, Australia.
PLoS One. 2013;8(2):e56042. doi: 10.1371/journal.pone.0056042. Epub 2013 Feb 6.
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.
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。