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首页> 外文期刊>The Journal of general virology >Delineating the role of CD4+ T cells in the activation of human cytomegalovirus-specific immune responses following immunization with Ad-gBCMVpoly vaccine: implications for vaccination of immunocompromised individuals
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Delineating the role of CD4+ T cells in the activation of human cytomegalovirus-specific immune responses following immunization with Ad-gBCMVpoly vaccine: implications for vaccination of immunocompromised individuals

机译:在用Ad-gBCMVpoly疫苗免疫后描述CD4 + T细胞在活化人巨细胞病毒特异性免疫反应中的作用:对免疫受损个体的疫苗接种的影响

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Reconstitution of the virus-specific CD8+ T-cell response is crucial for the prevention of human cytomegalovirus (CMV)-associated pathogenesis in transplant patients and human immunodeficiency virus-infected individuals. Although adoptive T-cell immunotherapy has been used successfully in various clinical settings, prophylactic vaccination remains the most amenable strategy to prevent CMV disease. However, vaccination in clinical settings where the host is severely immunocompromised due to the loss of CD4+ T cells remains a significant challenge. This study investigated the efficacy of a chimeric CMV vaccine in a model setting that allowed studies on the generation of CD8+ T-cell memory responses in a transient CD4+ T-cell-deficient setting similar to that seen in immunocompromised patients. Immunization with an adenoviral CMV vaccine under transient helpless (complete CD4+ T-cell depletion) or help-deficient (partial CD4+ T-cell depletion) conditions demonstrated that induction of the effector CD8+ T-cell and humoral responses was almost completely eliminated under helpless conditions, and was gradually regained with the recovery of CD4+ T cells. However, this response failed to protect the host from viral infection, suggesting that lack of CD4+ T cells during vaccination can significantly impair the priming and maturation of CMV-specific immune responses. Furthermore, although the induction of CMV-specific immune responses was also significantly reduced in a help-deficient environment, these primed effector cells could mature normally and generate long-term polyfunctional memory responses capable of restricting virus replication in vivo. These results highlight the importance of monitoring CD4+ T-cell numbers before vaccination for the successful implementation of a CMV vaccine in an immunocompromised setting.
机译:病毒特异性CD8 + T细胞应答的重构对于预防移植患者和人类免疫缺陷病毒感染者的人类巨细胞病毒(CMV)相关发病机理至关重要。尽管过继性T细胞免疫疗法已在各种临床环境中成功使用,但预防接种仍是预防CMV疾病的最可行策略。但是,在临床环境中,由于CD4 + T细胞丢失导致宿主严重免疫功能低下的疫苗接种仍然是一项重大挑战。这项研究调查了嵌合CMV疫苗在模型环境中的功效,该模式允许研究在短暂的CD4 + T细胞缺陷状态下类似于免疫功能低下患者所见的CD8 + T细胞记忆反应的产生。在短暂的无助(完全CD4 + T细胞耗竭)或无帮助(部分CD4 + T细胞耗竭)条件下用腺病毒CMV疫苗免疫证明,在无助条件下几乎完全消除了效应CD8 + T细胞和体液反应的诱导。 ,并随着CD4 + T细胞的恢复逐渐恢复。但是,这种反应无法保护宿主免受病毒感染,这表明疫苗接种过程中CD4 + T细胞的缺乏会严重损害CMV特异性免疫反应的引发和成熟。此外,尽管在缺乏帮助的环境中,CMV特异性免疫反应的诱导也显着减少,但是这些引发的效应细胞可以正常成熟,并产生能够限制病毒在体内复制的长期多功能记忆反应。这些结果强调了在免疫接种前成功监测CMV疫苗接种前监测CD4 + T细胞数量的重要性。

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