Njenga M K, Pease L R, Wettstein P, Mak T, Rodriguez M
Department of Immunology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
Lab Invest. 1997 Jul;77(1):71-84.
Cells of the central nervous system (CNS) normally do not express detectable levels of major histocompatibility complex (MHC) Class I antigens. However, MHC Class I expression can be induced after virus infection. We tested the hypothesis that virus-induced Class I expression is mediated by lymphocytes or cytokines using lymphocyte- and cytokine-deficient mice. We used Theiler's murine encephalomyelitis virus (TMEV), which induces CNS demyelination that maps genetically to the D region of MHC Class I and is associated with high levels of Class I products. TMEV infection of severe combined immunodeficiency (SCID) and recombination activation gene-1-deficient mice, which lack B and T lymphocytes, resulted in equivalent H-2D and H-2K expression in brain and spinal cord, according to analysis of the area and intensity of immunoperoxidase staining. Class I antigens were demonstrated as early as 6 hours after infection, and they were more widely distributed than viral RNA, indicating that expression was induced indirectly via a soluble factor. To determine whether cytokines induced the expression, we infected mice lacking receptors for interferon-alpha/beta (IFN-alpha/beta R (-/-)), interferon-gamma (IFN-gamma R(-/-)), and tumor necrosis factor-alpha (TNFRp55(-/-)). TMEV-infected IFN-gamma R(-/-) and TN-FRp55(-/-) mice expressed Class I antigens in the CNS, whereas IFN-alpha/beta R(-/-) mice did not, establishing that IFN-alpha/beta mediated the expression. In contrast to the equivalent expression in SCID mice, we observed greater area and higher intensity of H-2D versus H-2K antigens in infected SCID mice reconstituted with normal spleen cells. Collectively, the data indicate that after TMEV infection, early generalized MHC Class I expression is mediated by IFN-alpha/beta independently of lymphocytes, but the differential regulation of H-2D over H-2K may be controlled by B and/or T lymphocytes.
中枢神经系统(CNS)的细胞通常不表达可检测水平的主要组织相容性复合体(MHC)I类抗原。然而,病毒感染后可诱导MHC I类抗原的表达。我们使用淋巴细胞和细胞因子缺陷小鼠来检验病毒诱导的I类抗原表达是由淋巴细胞或细胞因子介导的这一假说。我们使用了泰勒氏鼠脑脊髓炎病毒(TMEV),该病毒可诱导中枢神经系统脱髓鞘,其基因定位到MHC I类的D区域,并与高水平的I类产物相关。根据免疫过氧化物酶染色的面积和强度分析,严重联合免疫缺陷(SCID)小鼠和重组激活基因-1缺陷小鼠(缺乏B和T淋巴细胞)感染TMEV后,脑和脊髓中H-2D和H-2K的表达相当。I类抗原在感染后6小时就被检测到,并且其分布比病毒RNA更广泛,这表明表达是通过可溶性因子间接诱导的。为了确定细胞因子是否诱导了这种表达,我们感染了缺乏α/β干扰素受体(IFN-α/βR(-/-))、γ干扰素受体(IFN-γR(-/-))和肿瘤坏死因子-α受体(TNFRp55(-/-))的小鼠。感染TMEV的IFN-γR(-/-)和TN-FRp55(-/-)小鼠在中枢神经系统中表达I类抗原,但IFN-α/βR(-/-)小鼠不表达,这表明IFN-α/β介导了这种表达。与SCID小鼠中的等量表达相反,在用正常脾细胞重建的感染SCID小鼠中,我们观察到H-2D抗原相对于H-2K抗原的面积更大且强度更高。总体而言,数据表明,TMEV感染后早期广泛的MHC I类抗原表达由IFN-α/β独立于淋巴细胞介导,但H-2D相对于H-2K的差异调节可能由B和/或T淋巴细胞控制。