Deml Ludwig, Hüber Christian M, Barabas Sascha, Spindler Theresa, Cozzi Emanuele, Grossi Paolo
Lophius Biosciences GmbH, Regensburg, Germany.
Biotest AG, Dreieich, Germany.
Transplant Direct. 2021 Oct 22;7(11):e781. doi: 10.1097/TXD.0000000000001236. eCollection 2021 Nov.
Cytomegalovirus (CMV) immunoglobulin (CMVIG) is used for the prophylaxis of CMV infection after transplantation. Beyond providing passive CMV-specific immunity, CMVIG exerts enhancing and suppressive immunomodulatory functions. Although the anti-inflammatory activities of CMVIG have been extensively documented, its immunostimulatory activities remain poorly characterized.
This exploratory study analyzed the capacity of CMVIG to modulate cell-mediated innate and adaptive immunities in vitro on freshly isolated peripheral blood mononuclear cells (PBMCs) of CMV-seropositive and -seronegative healthy individuals, using interferon-γ (IFN-γ) enzyme-linked immunospot and intracellular cytokine staining assays.
We showed that CMVIG treatment increases the number of IFN-γ-secreting PBMCs of both CMV-seronegative and -seropositive individuals, indicating a global stimulatory effect on innate immune cells. Indeed, CMVIG significantly increased the frequency of natural killer cells producing the T helper cell 1-type cytokines tumor necrosis factor and IFN-γ. This was associated with the induction of interleukin-12-expressing monocytes and the activation of cluster of differentiation (CD) 4 and CD8 T cells, as measured by the expression of tumor necrosis factor and IFN-γ. Interestingly, stimulation of PBMCs from CMV-seropositive subjects with CMVIG-opsonized CMV antigens (phosphoprotein 65, CMV lysate) enhanced CD4 and CD8 T-cell activation, suggesting that CMVIG promotes the immunogenicity of CMV antigens.
Our data demonstrate that CMVIG can stimulate effector cells of both innate and adaptive immunities and promote the immunogenicity of CMV antigens. These immunostimulatory properties might contribute to the protective effect against CMV infection mediated by CMVIG.
巨细胞病毒免疫球蛋白(CMVIG)用于预防移植后巨细胞病毒(CMV)感染。除了提供被动的CMV特异性免疫外,CMVIG还发挥增强和抑制免疫调节功能。尽管CMVIG的抗炎活性已得到广泛记录,但其免疫刺激活性仍未得到充分表征。
本探索性研究使用干扰素-γ(IFN-γ)酶联免疫斑点法和细胞内细胞因子染色试验,分析了CMVIG在体外对CMV血清阳性和血清阴性健康个体新鲜分离的外周血单个核细胞(PBMC)的细胞介导的先天性和适应性免疫的调节能力。
我们发现,CMVIG治疗可增加CMV血清阴性和血清阳性个体中分泌IFN-γ的PBMC数量,表明对先天性免疫细胞具有全面的刺激作用。实际上,CMVIG显著增加了产生辅助性T细胞1型细胞因子肿瘤坏死因子和IFN-γ的自然杀伤细胞的频率。这与表达白细胞介素-12的单核细胞的诱导以及通过肿瘤坏死因子和IFN-γ的表达测量的分化簇(CD)4和CD8 T细胞的激活有关。有趣的是,用CMVIG调理的CMV抗原(磷蛋白65,CMV裂解物)刺激CMV血清阳性受试者的PBMC可增强CD4和CD8 T细胞的激活,表明CMVIG可促进CMV抗原的免疫原性。
我们的数据表明,CMVIG可刺激先天性和适应性免疫的效应细胞,并促进CMV抗原的免疫原性。这些免疫刺激特性可能有助于CMVIG介导的针对CMV感染的保护作用。