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Fundamentals of Cancer Medicine |
R&D Systems, Inc., Minneapolis, Minnesota, USA
Mary Dietz, R&D Systems, Inc., 614 McKinley Place NE, Minneapolis, Minnesota, USA. Telephone: 612-379-2956; Fax: 612-379-6580; e-mail: maryd{at}rndsystems.com
For years the large double stranded DNA viruses were thought to contain numerous "non-essential" genes. These genes are now found to code proteins used by the virus to counteract the host immune response. Genomic mapping of these viruses and the identification of sequence homology to cellular proteins has led to suggested functions for these gene products [1-4]. These viral genes are thought to have been captured from host cells during viral evolution and modified to confer an advantage in viral replication, survival or transmission (Table 1
).
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receptor (R) homolog, called M-T7, that can bind rabbit IFN- and inhibit its antiviral activities [5]. Viral IFN-R homologs have been found in several species of poxviruses, and interferon-responsive elements are found in the gamma herpes virus family [6]. IFN-, a primary mediator of host defense against viral and non-viral pathogens, activates macrophages and enhances the expression of major histocompatibility complex (MHC) class I and II glycoproteins in order to aid in viral antigen presentation, and it induces the expression of anti-viral effector proteins in the cell. The production of a soluble cellular homolog to the IFN-R by the virus would prevent triggering of the host cell response by binding to and blocking the host-produced IFN-. The host defense use of IFN is also targeted by the production of virus-associated RNA genes (VA RNA) in the adenovirus to block the IFN-induced autophosphorylation of double-stranded RNA-activated inhibitor of translation (DAI) and thereby blocking the antiviral effect of interferon. The presentation of viral antigen by the MHC class I molecule also can be disrupted by viral homologs. E3-gp19K from adenovirus binds strongly to class I MHC molecules in the endoplasmic reticulum, preventing their translocation to the surface [1, 7]. ML18 from human cytomegalovirus produces a class I homolog that binds ß2-microglobulin, a subunit of class I MHC molecules required for transport to the cell surface [8].
Other soluble cell-receptor homologs include the myxoma virus, M-T2, a cellular tumor necrosis factor (TNF)-receptor homolog that binds and inhibits TNF [9]. Similar TNF-receptor homologs have been detected in cowpox and variola [2]. B15R from the vaccinia virus is a secreted interleukin 1 (IL)-1 receptor type II homolog that binds and inhibits the action of IL-1ß [10, 11]. TNF and IL-1 are early promoters of inflammation, and blocking their action stops initiation of inflammatory response. The action of TNF is stopped also by the intracellular inhibitors E3-14.7K, E3-10.4/14.5K, and E1B-19K from adenoviruses by disruption of signal transduction after TNF binds to the cell-surface receptor [7]. The cowpox virus gene crmA blocks the IL-1 induced inflammatory response by inhibiting the cleavage of pro-IL-1ß to the active form [12]. CrmA is one member of the serine proteinase inhibitors that has been identified in poxvirus and orthopoxvirus [13]. Viruses thus have mechanisms that counteract extracellular and intracellular aspects of the host defense system.
Other inhibitors of host-defense strategies involve blocking the complement pathways by production of viral proteins that bind complement subunits and inhibit the complement-mediated lysis of infected cells [1, 6, 13, 14]. Epstein-Barr virus encodes BCFR1, an IL-10 homolog [15], produced to suppress the Th1 cellular immune response and turn the response to Th2, which is less effective. Many DNA viruses have genes that encode apoptosis-inhibiting proteins, such as BHRF1 in Epstein-Barr virus, a Bcl-2 homolog that blocks the apoptotic response of the host [6, 16-18]. Viruses also produce homologs of the human type D cyclin genes that may trigger kinase activity that effectively blocks host regulation of cell proliferation [18-20].
Chemokines play a key role in the initial host reaction to infection and injury. Viral genomes have sequences homologous to those of chemokines and chemokine receptors. There are three chemokine receptor homologs, US28, US27 and ML33 in the cytomegalovirus genome. US28-transfected cells can bind a wide range of chemokines, including MCP-1, RANTES, and MIP-1
[21, 22]. Although US27 is thought to arise from gene duplication of US28, no ligand has been identified. M33 is the mouse cytomegalovirus equivalent of the human CMV ML33. Mutation of M33 had no effect on infection of mouse fibroblasts in vitro, but in vivo there was much less virus in the salivary glands of mice infected with the mutant than the wild-type virus. It was suggested that M33 is important in the movement of virus through infected cells to the salivary glands to assist in viral transmission to new hosts [8].
Human herpesvirus-8 (HHV-8), a gammaherpesvirus, also known as Kaposi's sarcoma-associated herpesvirus, is present in almost all AIDS-KS lesions and the rare B-cell primary effusion (body-cavity based) lymphoma associated with KS [6]. HHV-8 contains several genes with sequence homology to many cellular proteins such as chemokines (ORF K4, K6 and K4.1), human IL-6 (ORF K2), interferon regulatory factor (ORF K9), Bcl-2 (ORF 16), cyclin D (ORF 72), and an IL-8-like receptor (ORF 74) [3, 6, 16, 19, 20]. These viral proteins may contribute to mechanisms that block the host defense and contribute to virus-induced neoplasia. HHV-8 vIL-6 has been shown to have biological properties similar to human IL-6 [3, 23]. The chemokine homologs, named vMIP-I and vMIP-II, weakly block HIV infections and induce angiogenesis [3, 24]. vMIP-II (also called vMIP-1ß) binds predominantly to CCR-3, the eotaxin receptor, causing human eosinophil activation as measured by intracellular calcium mobilization and chemotaxis [24]. These observations may be significant to the association of HHV-8 with Kaposi's sarcoma, body-cavity-based or pleural effusion lymphoma, and multicentric Castleman's disease, a polyclonal lymphoproliferation associated with increased vascularity [6, 23, 25]. It has been hypothesized that HHV-8 plays a role in the development of these diseases.
Understanding the function of viral homologs and the role they play in the establishment of infection and disease may greatly assist in understanding the host response mechanisms involved in reaction to infection and disease. Some specific activities have been demonstrated for some of the viral-encoded proteins, but the actual in vivo functions are uncertain.
References
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