Department of Biomolecular Chemistry, Division of Allergy and Immunology, University of Wisconsin-Madison, Madison, WI 53706-0450, USA.
Clin Exp Allergy. 2010 Aug;40(8):1203-13. doi: 10.1111/j.1365-2222.2010.03546.x. Epub 2010 Jun 7.
Human rhinovirus (HRV) infections are a major cause of exacerbations in chronic respiratory conditions such as asthma and chronic obstructive pulmonary disease, but HRV-induced immune responses of the lower airway are poorly understood. Earlier work examining cytokine release following HRV infection has focused on epithelial cells because they serve as the principal site of viral replication, and internalization and replication of viral RNA appear necessary for epithelial cell mediator release. However, during HRV infection, only a small proportion of epithelial cells become infected. As HRV-induced cytokine levels in vivo are markedly elevated, this observation suggests that other mechanisms independent of direct viral infection may induce epithelial cell cytokine release.
Our aim was to test for the importance of interactions between human bronchial epithelial cells (HBECs) and monocytic cells in the control of mediator release during HRV exposure.
In vitro models of HRV serotype-16 (HRV16) infection of primary HBECs and human monocytic cells, in mono or co-culture, were used. We assessed HRV16-induced CXCL10 and CCL2 protein release via ELISA.
Co-culture of human monocytic and bronchial epithelial cells promoted a synergistic augmentation of CXCL10 and CCL2 protein release following HRV16 challenge. Transfer of conditioned media from HRV16-treated monocytic cells to epithelial cultures induced a robust release of CXCL10 by the epithelial cells. This effect was greatly attenuated by type I IFN receptor blocking antibodies, and could be recapitulated by IFN-alpha addition.
Our data indicate that epithelial CXCL10 release during HRV infection is augmented by a monocytic cell-dependent mechanism involving type I IFN(s). Our findings support a key role for monocytic cells in the amplification of epithelial cell chemokine production during HRV infection, and help to explain how an inflammatory milieu is created in the lower airways even in the absence of extensive viral replication and epithelial infection.
人类鼻病毒(HRV)感染是哮喘和慢性阻塞性肺疾病等慢性呼吸道疾病恶化的主要原因,但人们对 HRV 引起的下呼吸道免疫反应知之甚少。早期研究 HRV 感染后细胞因子释放的工作主要集中在上皮细胞上,因为它们是病毒复制的主要部位,病毒 RNA 的内化和复制似乎是上皮细胞介质释放所必需的。然而,在 HRV 感染期间,只有一小部分上皮细胞被感染。由于体内 HRV 诱导的细胞因子水平明显升高,这一观察结果表明,其他独立于直接病毒感染的机制可能诱导上皮细胞细胞因子释放。
我们旨在测试人支气管上皮细胞(HBEC)与单核细胞之间的相互作用在 HRV 暴露期间控制介质释放的重要性。
使用 HRV 血清型-16(HRV16)感染原代 HBEC 和人单核细胞的体外模型,分别进行单培养或共培养。我们通过 ELISA 评估 HRV16 诱导的 CXCL10 和 CCL2 蛋白释放。
共培养人单核细胞和支气管上皮细胞促进了 HRV16 攻击后 CXCL10 和 CCL2 蛋白释放的协同增强。将 HRV16 处理的单核细胞的条件培养基转移到上皮细胞培养物中,可诱导上皮细胞强烈释放 CXCL10。这一效应被 I 型 IFN 受体阻断抗体大大减弱,并且可以通过添加 IFN-α来重现。
我们的数据表明,上皮细胞 CXCL10 释放在 HRV 感染期间被单核细胞依赖性机制增强,该机制涉及 I 型 IFN(s)。我们的研究结果支持单核细胞在 HRV 感染期间放大上皮细胞趋化因子产生中的关键作用,并有助于解释即使在没有广泛病毒复制和上皮感染的情况下,如何在下呼吸道中产生炎症环境。