Niiya Hironari, Lei Jin, Guo Yun, Azuma Taichi, Yakushijin Yoshihiro, Sakai Ikuya, Hato Takaaki, Tohyama Mikiko, Hashimoto Koji, Yasukawa Masaki
First Department of Internal Medicine, Ehime University School of Medicine Shitsukawa, Toon, Ehime, Japan.
Exp Hematol. 2006 May;34(5):642-53. doi: 10.1016/j.exphem.2006.02.001.
Monocyte-derived dendritic cells (DCs) play important roles in the immune response against infections and malignancies. Human herpesvirus 6 (HHV-6) infects monocytes and is reactivated in immunodeficient patients. To clarify the mechanisms of HHV-6-induced immunodeficiency, we investigated the effect of HHV-6 infection on differentiation of monocytes to DCs.
Monocytes were inoculated with or without HHV-6 and then allowed to differentiate to myeloid DCs in culture medium containing granulocyte-macrophage colony-stimulating factor and interleukin (IL)-4. The expression of cell surface molecules on DCs and the capacity of the DCs for antigen capture were examined by flow cytometric analysis. Alteration of antigen-presenting capacity induced by HHV-6 infection was examined.
The morphology of HHV-6-infected monocyte-derived DCs was distinctly different from that of the DCs derived from mock-infected monocytes. Although expression levels of DC-associated surface antigens, including CD80, CD83, and CD86, were significantly higher on HHV-6-infected monocyte-derived DCs than on DCs derived from mock-infected monocytes, antigen-presenting capacity was significantly lower in the former group. Addition of culture supernatant of HHV-6-infected monocytes resulted in suppression of the T-lymphocyte proliferative response, and anti-IL-10 neutralizing antibody partly inhibited this suppressive effect. The antigen-presenting capacity of DCs generated from a patient with severe HHV-6 reactivation was significantly lower than that of DCs generated from the same patient in the recovery phase.
HHV-6 infection induces immunodeficiency via impaired differentiation of DCs. These results present a new concept for the pathogenesis of HHV-6-induced immunodeficiency.
单核细胞衍生的树突状细胞(DCs)在针对感染和恶性肿瘤的免疫反应中发挥重要作用。人类疱疹病毒6型(HHV-6)感染单核细胞并在免疫缺陷患者中重新激活。为阐明HHV-6诱导免疫缺陷的机制,我们研究了HHV-6感染对单核细胞向DCs分化的影响。
将单核细胞接种有或无HHV-6,然后在含有粒细胞-巨噬细胞集落刺激因子和白细胞介素(IL)-4的培养基中使其分化为髓样DCs。通过流式细胞术分析检测DCs上细胞表面分子的表达以及DCs捕获抗原的能力。研究HHV-6感染诱导的抗原呈递能力的改变。
HHV-6感染的单核细胞衍生的DCs的形态与模拟感染的单核细胞衍生的DCs明显不同。尽管HHV-6感染的单核细胞衍生的DCs上DC相关表面抗原(包括CD80、CD83和CD86)的表达水平显著高于模拟感染的单核细胞衍生的DCs,但前一组的抗原呈递能力显著较低。添加HHV-6感染的单核细胞的培养上清液导致T淋巴细胞增殖反应受到抑制,抗IL-10中和抗体部分抑制了这种抑制作用。严重HHV-6再激活患者产生的DCs的抗原呈递能力明显低于同一患者恢复阶段产生的DCs。
HHV-6感染通过DCs分化受损诱导免疫缺陷。这些结果为HHV-6诱导的免疫缺陷的发病机制提出了一个新概念。