Ahmed Elshafa Hassan, Brooks Eric, Sloan Shelby, Schlotter Sarah, Jeney Frankie, Hale Claire, Mao Charlene, Zhang Xiaoli, McLaughlin Eric, Shindiapina Polina, Shire Salma, Das Manjusri, Prouty Alexander, Lozanski Gerard, Mamuye Admasu T, Abebe Tamrat, Alinari Lapo, Caligiuri Michael A, Baiocchi Robert A
Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH 43210, USA.
Comprehensive Cancer Center, The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, OH 43210, USA.
Vaccines (Basel). 2021 May 26;9(6):555. doi: 10.3390/vaccines9060555.
Epstein-Barr virus (EBV) is a human herpes virus that infects over 90% of the world's population and is linked to development of cancer. In immune-competent individuals, EBV infection is mitigated by a highly efficient virus-specific memory T-cell response. Risk of EBV-driven cancers increases with immune suppression (IS). EBV-seronegative recipients of solid organ transplants are at high risk of developing post-transplant lymphoproliferative disease (PTLD) due to iatrogenic IS. While reducing the level of IS may improve EBV-specific immunity and regression of PTLD, patients are at high risk for allograft rejection and need for immune-chemotherapy. Strategies to prevent PTLD in this vulnerable patient population represents an unmet need. We have previously shown that BZLF1-specific cytotoxic T-cell (CTL) expansion following reduced IS correlated with immune-mediated PTLD regression and improved patient survival. We have developed a vaccine to bolster EBV-specific immunity to the BZLF1 protein and show that co-culture of dendritic cells (DCs) loaded with a αDEC205-BZLF1 fusion protein with peripheral blood mononuclear cells (PMBCs) leads to expansion and increased cytotoxic activity of central-effector memory CTLs against EBV-transformed B-cells. Human-murine chimeric Hu-PBL-SCID mice were vaccinated with DCs loaded with αDEC205-BZLF1 or control to assess prevention of fatal human EBV lymphoproliferative disease. Despite a profoundly immunosuppressive environment, vaccination with αDEC205-BZLF1 stimulated clonal expansion of antigen-specific T-cells that produced abundant IFNγ and significantly prolonged survival. These results support preclinical and clinical development of vaccine approaches using BZLF1 as an immunogen to harness adaptive cellular responses and prevent PTLD in vulnerable patient populations.
爱泼斯坦-巴尔病毒(EBV)是一种人类疱疹病毒,全球超过90%的人口都曾感染过该病毒,它与癌症的发生有关。在免疫功能正常的个体中,EBV感染可通过高效的病毒特异性记忆T细胞反应得到缓解。EBV驱动的癌症风险会随着免疫抑制(IS)而增加。由于医源性免疫抑制,实体器官移植的EBV血清阴性受者发生移植后淋巴细胞增生性疾病(PTLD)的风险很高。虽然降低免疫抑制水平可能会改善EBV特异性免疫和PTLD的消退,但患者发生同种异体移植排斥反应和需要免疫化疗的风险很高。在这一脆弱患者群体中预防PTLD的策略仍是未满足的需求。我们之前已经表明,免疫抑制降低后BZLF1特异性细胞毒性T细胞(CTL)的扩增与免疫介导的PTLD消退及患者生存率提高相关。我们开发了一种疫苗来增强针对BZLF1蛋白的EBV特异性免疫,并表明用负载αDEC205-BZLF1融合蛋白的树突状细胞(DC)与外周血单核细胞(PMBC)共培养可导致中央效应记忆CTL针对EBV转化的B细胞的扩增和细胞毒性活性增加。用人鼠嵌合的Hu-PBL-SCID小鼠接种负载αDEC205-BZLF1或对照的DC,以评估对致命性人类EBV淋巴细胞增生性疾病的预防作用。尽管存在深度免疫抑制环境,但用αDEC205-BZLF1疫苗接种可刺激产生大量IFNγ的抗原特异性T细胞的克隆扩增,并显著延长生存期。这些结果支持以BZLF1作为免疫原的疫苗方法的临床前和临床开发,以利用适应性细胞反应并预防脆弱患者群体中的PTLD。