Abstract
The murine gamma-herpesvirus 68 (MHV-68) provides a unique experimental model for dissecting immunity to large DNA viruses that persist in B lymphocytes. The analysis is greatly facilitated by the availability of genetically disrupted (-/-) mice that lack key host-response elements, and by the fact that MHV-68 is a lytic virus that can readily be manipulated for mutational analysis. The mutant virus strategy is being used, for example, to characterize the part played in vivo by an MHV-68-encoded chemokine-binding protein that may ultimately find an application in human therapeutics. Experiments with various -/- mice and monoclonal antibody depletion protocols have shown very clearly that type I interferons (IFNs) are essential for the early control of MHV-68 replication, while CD4+ T cells producing IFN-gamma function to limit the consequences of viral persistence. Virus-specific CD8+ effectors acting in the absence of the CD4+ subset seem initially to control the lytic phase in the lung following respiratory challenge, but are then unable to prevent the reactivation of replicative infection in epithelia and the eventual death of CD4+ T-cell-deficient mice. This could reflect the fact that the interaction between the CD8+ T cells and the virus-infected targets is partially compromised by the MHV-68 K3 protein, which inhibits antigen presentation by MHC class I glycoproteins. Immunization strategies focusing on the CD8+ T-cell response to epitopes expressed during the lytic phase of MHV-68 infection can limit virus replication, but are unable to prevent the establishment of latency. Other experiments with mutant viruses also suggest that there is a disconnection between lytic MHV-68 infection and latency. The massive nonspecific immunoglobulin response and the dramatic expansion of Vbeta4+ CD8+ T cells, which is apparently MHC independent, could represent some sort of 'smoke screen' used by MHV-68 to subvert immunity. Although MHV-68 is neither Epstein-Barr virus nor human herpesvirus-8, the results generated from this system suggest possibilities that may usefully be addressed with these human pathogens. Perhaps the main lesson learned to date is that all the components of immunity are likely to be important for the control of these complex viruses.
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- Alexander L., Denekamp L., Knapp A., Auerbach M. R., Damania B., Desrosiers R. C. The primary sequence of rhesus monkey rhadinovirus isolate 26-95: sequence similarities to Kaposi's sarcoma-associated herpesvirus and rhesus monkey rhadinovirus isolate 17577. J Virol. 2000 Apr;74(7):3388–3398. doi: 10.1128/jvi.74.7.3388-3398.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Altman J. D., Moss P. A., Goulder P. J., Barouch D. H., McHeyzer-Williams M. G., Bell J. I., McMichael A. J., Davis M. M. Phenotypic analysis of antigen-specific T lymphocytes. Science. 1996 Oct 4;274(5284):94–96. doi: 10.1126/science.274.5284.94. [DOI] [PubMed] [Google Scholar]
- Babcock G. J., Decker L. L., Volk M., Thorley-Lawson D. A. EBV persistence in memory B cells in vivo. Immunity. 1998 Sep;9(3):395–404. doi: 10.1016/s1074-7613(00)80622-6. [DOI] [PubMed] [Google Scholar]
- Belz G. T., Stevenson P. G., Castrucci M. R., Altman J. D., Doherty P. C. Postexposure vaccination massively increases the prevalence of gamma-herpesvirus-specific CD8+ T cells but confers minimal survival advantage on CD4-deficient mice. Proc Natl Acad Sci U S A. 2000 Mar 14;97(6):2725–2730. doi: 10.1073/pnas.040575197. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blaskovic D., Stanceková M., Svobodová J., Mistríková J. Isolation of five strains of herpesviruses from two species of free living small rodents. Acta Virol. 1980 Dec;24(6):468–468. [PubMed] [Google Scholar]
- Brooks J. W., Hamilton-Easton A. M., Christensen J. P., Cardin R. D., Hardy C. L., Doherty P. C. Requirement for CD40 ligand, CD4(+) T cells, and B cells in an infectious mononucleosis-like syndrome. J Virol. 1999 Nov;73(11):9650–9654. doi: 10.1128/jvi.73.11.9650-9654.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Callan M. F., Tan L., Annels N., Ogg G. S., Wilson J. D., O'Callaghan C. A., Steven N., McMichael A. J., Rickinson A. B. Direct visualization of antigen-specific CD8+ T cells during the primary immune response to Epstein-Barr virus In vivo. J Exp Med. 1998 May 4;187(9):1395–1402. doi: 10.1084/jem.187.9.1395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cardin R. D., Brooks J. W., Sarawar S. R., Doherty P. C. Progressive loss of CD8+ T cell-mediated control of a gamma-herpesvirus in the absence of CD4+ T cells. J Exp Med. 1996 Sep 1;184(3):863–871. doi: 10.1084/jem.184.3.863. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang J., Renne R., Dittmer D., Ganem D. Inflammatory cytokines and the reactivation of Kaposi's sarcoma-associated herpesvirus lytic replication. Virology. 2000 Jan 5;266(1):17–25. doi: 10.1006/viro.1999.0077. [DOI] [PubMed] [Google Scholar]
- Chen Z. W., Craiu A., Shen L., Kuroda M. J., Iroku U. C., Watkins D. I., Voss G., Letvin N. L. Simian immunodeficiency virus evades a dominant epitope-specific cytotoxic T lymphocyte response through a mutation resulting in the accelerated dissociation of viral peptide and MHC class I. J Immunol. 2000 Jun 15;164(12):6474–6479. doi: 10.4049/jimmunol.164.12.6474. [DOI] [PubMed] [Google Scholar]
- Christensen J. P., Cardin R. D., Branum K. C., Doherty P. C. CD4(+) T cell-mediated control of a gamma-herpesvirus in B cell-deficient mice is mediated by IFN-gamma. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5135–5140. doi: 10.1073/pnas.96.9.5135. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christensen J. P., Doherty P. C., Branum K. C., Riberdy J. M. Profound protection against respiratory challenge with a lethal H7N7 influenza A virus by increasing the magnitude of CD8(+) T-cell memory. J Virol. 2000 Dec;74(24):11690–11696. doi: 10.1128/jvi.74.24.11690-11696.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christensen J. P., Doherty P. C. Quantitative analysis of the acute and long-term CD4(+) T-cell response to a persistent gammaherpesvirus. J Virol. 1999 May;73(5):4279–4283. doi: 10.1128/jvi.73.5.4279-4283.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christensen J. P., Marker O., Thomsen A. R. The role of CD4+ T cells in cell-mediated immunity to LCMV: studies in MHC class I and class II deficient mice. Scand J Immunol. 1994 Oct;40(4):373–382. doi: 10.1111/j.1365-3083.1994.tb03477.x. [DOI] [PubMed] [Google Scholar]
- Clambey E. T., Virgin H. W., 4th, Speck S. H. Disruption of the murine gammaherpesvirus 68 M1 open reading frame leads to enhanced reactivation from latency. J Virol. 2000 Feb;74(4):1973–1984. doi: 10.1128/jvi.74.4.1973-1984.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coppola M. A., Flaño E., Nguyen P., Hardy C. L., Cardin R. D., Shastri N., Woodland D. L., Blackman M. A. Apparent MHC-independent stimulation of CD8+ T cells in vivo during latent murine gammaherpesvirus infection. J Immunol. 1999 Aug 1;163(3):1481–1489. [PubMed] [Google Scholar]
- Coscoy L., Ganem D. Kaposi's sarcoma-associated herpesvirus encodes two proteins that block cell surface display of MHC class I chains by enhancing their endocytosis. Proc Natl Acad Sci U S A. 2000 Jul 5;97(14):8051–8056. doi: 10.1073/pnas.140129797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dal Canto A. J., Virgin H. W., 4th Animal models of infection-mediated vasculitis. Curr Opin Rheumatol. 1999 Jan;11(1):17–23. doi: 10.1097/00002281-199901000-00004. [DOI] [PubMed] [Google Scholar]
- Doherty P. C., Allan W., Eichelberger M., Carding S. R. Roles of alpha beta and gamma delta T cell subsets in viral immunity. Annu Rev Immunol. 1992;10:123–151. doi: 10.1146/annurev.iy.10.040192.001011. [DOI] [PubMed] [Google Scholar]
- Doherty P. C., Christensen J. P. Accessing complexity: the dynamics of virus-specific T cell responses. Annu Rev Immunol. 2000;18:561–592. doi: 10.1146/annurev.immunol.18.1.561. [DOI] [PubMed] [Google Scholar]
- Doherty P. C., Hamilton-Easton A. M., Topham D. J., Riberdy J., Brooks J. W., Cardin R. D. Consequences of viral infections for lymphocyte compartmentalization and homeostasis. Semin Immunol. 1997 Dec;9(6):365–373. doi: 10.1006/smim.1997.0094. [DOI] [PubMed] [Google Scholar]
- Doherty P. C. The numbers game for virus-specific CD8+ T cells. Science. 1998 Apr 10;280(5361):227–227. doi: 10.1126/science.280.5361.227. [DOI] [PubMed] [Google Scholar]
- Doherty P. C., Topham D. J., Tripp R. A., Cardin R. D., Brooks J. W., Stevenson P. G. Effector CD4+ and CD8+ T-cell mechanisms in the control of respiratory virus infections. Immunol Rev. 1997 Oct;159:105–117. doi: 10.1111/j.1600-065x.1997.tb01010.x. [DOI] [PubMed] [Google Scholar]
- Doherty P. C., Topham D. J., Tripp R. A. Establishment and persistence of virus-specific CD4+ and CD8+ T cell memory. Immunol Rev. 1996 Apr;150:23–44. doi: 10.1111/j.1600-065x.1996.tb00694.x. [DOI] [PubMed] [Google Scholar]
- Dutia B. M., Allen D. J., Dyson H., Nash A. A. Type I interferons and IRF-1 play a critical role in the control of a gammaherpesvirus infection. Virology. 1999 Sep 1;261(2):173–179. doi: 10.1006/viro.1999.9834. [DOI] [PubMed] [Google Scholar]
- Dutia B. M., Clarke C. J., Allen D. J., Nash A. A. Pathological changes in the spleens of gamma interferon receptor-deficient mice infected with murine gammaherpesvirus: a role for CD8 T cells. J Virol. 1997 Jun;71(6):4278–4283. doi: 10.1128/jvi.71.6.4278-4283.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dutia B. M., Stewart J. P., Clayton R. A., Dyson H., Nash A. A. Kinetic and phenotypic changes in murine lymphocytes infected with murine gammaherpesvirus-68 in vitro. J Gen Virol. 1999 Oct;80(Pt 10):2729–2736. doi: 10.1099/0022-1317-80-10-2729. [DOI] [PubMed] [Google Scholar]
- Efstathiou S., Ho Y. M., Minson A. C. Cloning and molecular characterization of the murine herpesvirus 68 genome. J Gen Virol. 1990 Jun;71(Pt 6):1355–1364. doi: 10.1099/0022-1317-71-6-1355. [DOI] [PubMed] [Google Scholar]
- Egan M. A., Charini W. A., Kuroda M. J., Schmitz J. E., Racz P., Tenner-Racz K., Manson K., Wyand M., Lifton M. A., Nickerson C. E. Simian immunodeficiency virus (SIV) gag DNA-vaccinated rhesus monkeys develop secondary cytotoxic T-lymphocyte responses and control viral replication after pathogenic SIV infection. J Virol. 2000 Aug;74(16):7485–7495. doi: 10.1128/jvi.74.16.7485-7495.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ehlers B., Ulrich S., Goltz M. Detection of two novel porcine herpesviruses with high similarity to gammaherpesviruses. J Gen Virol. 1999 Apr;80(Pt 4):971–978. doi: 10.1099/0022-1317-80-4-971. [DOI] [PubMed] [Google Scholar]
- Ehtisham S., Sunil-Chandra N. P., Nash A. A. Pathogenesis of murine gammaherpesvirus infection in mice deficient in CD4 and CD8 T cells. J Virol. 1993 Sep;67(9):5247–5252. doi: 10.1128/jvi.67.9.5247-5252.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ensser A., Pflanz R., Fleckenstein B. Primary structure of the alcelaphine herpesvirus 1 genome. J Virol. 1997 Sep;71(9):6517–6525. doi: 10.1128/jvi.71.9.6517-6525.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Epstein M. A. Vaccination against Epstein-Barr virus: current progress and future strategies. Lancet. 1986 Jun 21;1(8495):1425–1427. doi: 10.1016/s0140-6736(86)91565-5. [DOI] [PubMed] [Google Scholar]
- Ewing C., Topham D. J., Doherty P. C. Prevalence and activation phenotype of Sendai virus-specific CD4+ T cells. Virology. 1995 Jun 20;210(1):179–185. doi: 10.1006/viro.1995.1329. [DOI] [PubMed] [Google Scholar]
- Falk K., Rötzschke O., Deres K., Metzger J., Jung G., Rammensee H. G. Identification of naturally processed viral nonapeptides allows their quantification in infected cells and suggests an allele-specific T cell epitope forecast. J Exp Med. 1991 Aug 1;174(2):425–434. doi: 10.1084/jem.174.2.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Flaño E., Woodland D. L., Blackman M. A. Requirement for CD4+ T cells in V beta 4+CD8+ T cell activation associated with latent murine gammaherpesvirus infection. J Immunol. 1999 Sep 15;163(6):3403–3408. [PubMed] [Google Scholar]
- Gompels U. A., Craxton M. A., Honess R. W. Conservation of gene organization in the lymphotropic herpesviruses herpesvirus Saimiri and Epstein-Barr virus. J Virol. 1988 Mar;62(3):757–767. doi: 10.1128/jvi.62.3.757-767.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Greensill J., Sheldon J. A., Renwick N. M., Beer B. E., Norley S., Goudsmit J., Schulz T. F. Two distinct gamma-2 herpesviruses in African green monkeys: a second gamma-2 herpesvirus lineage among old world primates? J Virol. 2000 Feb;74(3):1572–1577. doi: 10.1128/jvi.74.3.1572-1577.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grusby M. J., Johnson R. S., Papaioannou V. E., Glimcher L. H. Depletion of CD4+ T cells in major histocompatibility complex class II-deficient mice. Science. 1991 Sep 20;253(5026):1417–1420. doi: 10.1126/science.1910207. [DOI] [PubMed] [Google Scholar]
- Gulland F. M., Reid H. W., Buxton D., Lewis J. C., Kock R. A., Kirkwood J. K. Malignant catarrhal fever in a roan antelope (Hippotragus equinus) at Regent's Park. Vet Rec. 1989 Jan 14;124(2):42–43. doi: 10.1136/vr.124.2.42. [DOI] [PubMed] [Google Scholar]
- Hamilton-Easton A. M., Christensen J. P., Doherty P. C. Turnover of T cells in murine gammaherpesvirus 68-infected mice. J Virol. 1999 Sep;73(9):7866–7869. doi: 10.1128/jvi.73.9.7866-7869.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hardy C. L., Silins S. L., Woodland D. L., Blackman M. A. Murine gamma-herpesvirus infection causes V(beta)4-specific CDR3-restricted clonal expansions within CD8(+) peripheral blood T lymphocytes. Int Immunol. 2000 Aug;12(8):1193–1204. doi: 10.1093/intimm/12.8.1193. [DOI] [PubMed] [Google Scholar]
- Henle G., Henle W., Diehl V. Relation of Burkitt's tumor-associated herpes-ytpe virus to infectious mononucleosis. Proc Natl Acad Sci U S A. 1968 Jan;59(1):94–101. doi: 10.1073/pnas.59.1.94. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holloway S. A., Lindquester G. J., Studdert M. J., Drummer H. E. Identification, sequence analysis and characterisation of equine herpesvirus 5 glycoprotein B. Arch Virol. 1999;144(2):287–307. doi: 10.1007/s007050050504. [DOI] [PubMed] [Google Scholar]
- Husain S. M., Usherwood E. J., Dyson H., Coleclough C., Coppola M. A., Woodland D. L., Blackman M. A., Stewart J. P., Sample J. T. Murine gammaherpesvirus M2 gene is latency-associated and its protein a target for CD8(+) T lymphocytes. Proc Natl Acad Sci U S A. 1999 Jun 22;96(13):7508–7513. doi: 10.1073/pnas.96.13.7508. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hyland L., Sangster M., Sealy R., Coleclough C. Respiratory virus infection of mice provokes a permanent humoral immune response. J Virol. 1994 Sep;68(9):6083–6086. doi: 10.1128/jvi.68.9.6083-6086.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ishido S., Wang C., Lee B. S., Cohen G. B., Jung J. U. Downregulation of major histocompatibility complex class I molecules by Kaposi's sarcoma-associated herpesvirus K3 and K5 proteins. J Virol. 2000 Jun;74(11):5300–5309. doi: 10.1128/jvi.74.11.5300-5309.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacoby R. O., Buxton D., Reid H. W. The pathology of wildebeest-associated malignant catarrhal fever in hamsters, rats and guinea-pigs. J Comp Pathol. 1988 Jan;98(1):99–109. doi: 10.1016/0021-9975(88)90034-5. [DOI] [PubMed] [Google Scholar]
- Kapadia S. B., Molina H., van Berkel V., Speck S. H., Virgin H. W., 4th Murine gammaherpesvirus 68 encodes a functional regulator of complement activation. J Virol. 1999 Sep;73(9):7658–7670. doi: 10.1128/jvi.73.9.7658-7670.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kitamura D., Roes J., Kühn R., Rajewsky K. A B cell-deficient mouse by targeted disruption of the membrane exon of the immunoglobulin mu chain gene. Nature. 1991 Apr 4;350(6317):423–426. doi: 10.1038/350423a0. [DOI] [PubMed] [Google Scholar]
- Kuroda M. J., Schmitz J. E., Charini W. A., Nickerson C. E., Lifton M. A., Lord C. I., Forman M. A., Letvin N. L. Emergence of CTL coincides with clearance of virus during primary simian immunodeficiency virus infection in rhesus monkeys. J Immunol. 1999 May 1;162(9):5127–5133. [PubMed] [Google Scholar]
- Lee B. J., Santee S., Von Gesjen S., Ware C. F., Sarawar S. R. Lymphotoxin-alpha-deficient mice can clear a productive infection with murine gammaherpesvirus 68 but fail to develop splenomegaly or lymphocytosis. J Virol. 2000 Mar;74(6):2786–2792. doi: 10.1128/jvi.74.6.2786-2792.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li H., Dyer N., Keller J., Crawford T. B. Newly recognized herpesvirus causing malignant catarrhal fever in white-tailed deer (Odocoileus virginianus). J Clin Microbiol. 2000 Apr;38(4):1313–1318. doi: 10.1128/jcm.38.4.1313-1318.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Li H., Snowder G., O'Toole D., Crawford T. B. Transmission of ovine herpesvirus 2 among adult sheep. Vet Microbiol. 2000 Jan;71(1-2):27–35. doi: 10.1016/s0378-1135(99)00160-1. [DOI] [PubMed] [Google Scholar]
- Liu L., Flaño E., Usherwood E. J., Surman S., Blackman M. A., Woodland D. L. Lytic cycle T cell epitopes are expressed in two distinct phases during MHV-68 infection. J Immunol. 1999 Jul 15;163(2):868–874. [PubMed] [Google Scholar]
- Liu L., Usherwood E. J., Blackman M. A., Woodland D. L. T-cell vaccination alters the course of murine herpesvirus 68 infection and the establishment of viral latency in mice. J Virol. 1999 Dec;73(12):9849–9857. doi: 10.1128/jvi.73.12.9849-9857.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lucin P., Pavić I., Polić B., Jonjić S., Koszinowski U. H. Gamma interferon-dependent clearance of cytomegalovirus infection in salivary glands. J Virol. 1992 Apr;66(4):1977–1984. doi: 10.1128/jvi.66.4.1977-1984.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McMichael A. J., O'Callaghan C. A. A new look at T cells. J Exp Med. 1998 May 4;187(9):1367–1371. doi: 10.1084/jem.187.9.1367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morgan A. J., Finerty S., Lovgren K., Scullion F. T., Morein B. Prevention of Epstein-Barr (EB) virus-induced lymphoma in cottontop tamarins by vaccination with the EB virus envelope glycoprotein gp340 incorporated into immune-stimulating complexes. J Gen Virol. 1988 Aug;69(Pt 8):2093–2096. doi: 10.1099/0022-1317-69-8-2093. [DOI] [PubMed] [Google Scholar]
- Murali-Krishna K., Altman J. D., Suresh M., Sourdive D. J., Zajac A. J., Miller J. D., Slansky J., Ahmed R. Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. Immunity. 1998 Feb;8(2):177–187. doi: 10.1016/s1074-7613(00)80470-7. [DOI] [PubMed] [Google Scholar]
- Murali-Krishna K., Lau L. L., Sambhara S., Lemonnier F., Altman J., Ahmed R. Persistence of memory CD8 T cells in MHC class I-deficient mice. Science. 1999 Nov 12;286(5443):1377–1381. doi: 10.1126/science.286.5443.1377. [DOI] [PubMed] [Google Scholar]
- Nash A. A., Sunil-Chandra N. P. Interactions of the murine gammaherpesvirus with the immune system. Curr Opin Immunol. 1994 Aug;6(4):560–563. doi: 10.1016/0952-7915(94)90141-4. [DOI] [PubMed] [Google Scholar]
- Parry C. M., Simas J. P., Smith V. P., Stewart C. A., Minson A. C., Efstathiou S., Alcami A. A broad spectrum secreted chemokine binding protein encoded by a herpesvirus. J Exp Med. 2000 Feb 7;191(3):573–578. doi: 10.1084/jem.191.3.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peacock J. W., Bost K. L. Infection of intestinal epithelial cells and development of systemic disease following gastric instillation of murine gammaherpesvirus-68. J Gen Virol. 2000 Feb;81(Pt 2):421–429. doi: 10.1099/0022-1317-81-2-421. [DOI] [PubMed] [Google Scholar]
- Polić B., Hengel H., Krmpotić A., Trgovcich J., Pavić I., Luccaronin P., Jonjić S., Koszinowski U. H. Hierarchical and redundant lymphocyte subset control precludes cytomegalovirus replication during latent infection. J Exp Med. 1998 Sep 21;188(6):1047–1054. doi: 10.1084/jem.188.6.1047. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollock J. L., Presti R. M., Paetzold S., Virgin H. W., 4th Latent murine cytomegalovirus infection in macrophages. Virology. 1997 Jan 6;227(1):168–179. doi: 10.1006/viro.1996.8303. [DOI] [PubMed] [Google Scholar]
- Presti R. M., Pollock J. L., Dal Canto A. J., O'Guin A. K., Virgin H. W., 4th Interferon gamma regulates acute and latent murine cytomegalovirus infection and chronic disease of the great vessels. J Exp Med. 1998 Aug 3;188(3):577–588. doi: 10.1084/jem.188.3.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Price G. E., Gaszewska-Mastarlarz A., Moskophidis D. The role of alpha/beta and gamma interferons in development of immunity to influenza A virus in mice. J Virol. 2000 May;74(9):3996–4003. doi: 10.1128/jvi.74.9.3996-4003.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Price G. E., Ou R., Jiang H., Huang L., Moskophidis D. Viral escape by selection of cytotoxic T cell-resistant variants in influenza A virus pneumonia. J Exp Med. 2000 Jun 5;191(11):1853–1867. doi: 10.1084/jem.191.11.1853. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reid H. W., Rowe L. The attenuation of a herpes virus (malignant catarrhal fever virus) isolated from hartebeest (Alcelaphus buselaphus cokei Gunther). Res Vet Sci. 1973 Jul;15(1):144–146. [PubMed] [Google Scholar]
- Rickinson A. B., Moss D. J. Human cytotoxic T lymphocyte responses to Epstein-Barr virus infection. Annu Rev Immunol. 1997;15:405–431. doi: 10.1146/annurev.immunol.15.1.405. [DOI] [PubMed] [Google Scholar]
- Sangster M. Y., Mo X. Y., Sealy R., Coleclough C. Matching antibody class with pathogen type and portal of entry: cognate mechanisms regulate local isotype expression patterns in lymph nodes draining the respiratory tract of mice inoculated with respiratory viruses, according to virus replication competence and site of inoculation. J Immunol. 1997 Aug 15;159(4):1893–1902. [PubMed] [Google Scholar]
- Sangster M. Y., Topham D. J., D'Costa S., Cardin R. D., Marion T. N., Myers L. K., Doherty P. C. Analysis of the virus-specific and nonspecific B cell response to a persistent B-lymphotropic gammaherpesvirus. J Immunol. 2000 Feb 15;164(4):1820–1828. doi: 10.4049/jimmunol.164.4.1820. [DOI] [PubMed] [Google Scholar]
- Sarawar S. R., Brooks J. W., Cardin R. D., Mehrpooya M., Doherty P. C. Pathogenesis of murine gammaherpesvirus-68 infection in interleukin-6-deficient mice. Virology. 1998 Sep 30;249(2):359–366. doi: 10.1006/viro.1998.9309. [DOI] [PubMed] [Google Scholar]
- Sarawar S. R., Cardin R. D., Brooks J. W., Mehrpooya M., Hamilton-Easton A. M., Mo X. Y., Doherty P. C. Gamma interferon is not essential for recovery from acute infection with murine gammaherpesvirus 68. J Virol. 1997 May;71(5):3916–3921. doi: 10.1128/jvi.71.5.3916-3921.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sarawar S. R., Cardin R. D., Brooks J. W., Mehrpooya M., Tripp R. A., Doherty P. C. Cytokine production in the immune response to murine gammaherpesvirus 68. J Virol. 1996 May;70(5):3264–3268. doi: 10.1128/jvi.70.5.3264-3268.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scherer M. T., Ignatowicz L., Winslow G. M., Kappler J. W., Marrack P. Superantigens: bacterial and viral proteins that manipulate the immune system. Annu Rev Cell Biol. 1993;9:101–128. doi: 10.1146/annurev.cb.09.110193.000533. [DOI] [PubMed] [Google Scholar]
- Simas J. P., Efstathiou S. Murine gammaherpesvirus 68: a model for the study of gammaherpesvirus pathogenesis. Trends Microbiol. 1998 Jul;6(7):276–282. doi: 10.1016/s0966-842x(98)01306-7. [DOI] [PubMed] [Google Scholar]
- Slifka M. K., Ahmed R. Long-term humoral immunity against viruses: revisiting the issue of plasma cell longevity. Trends Microbiol. 1996 Oct;4(10):394–400. doi: 10.1016/0966-842X(96)10059-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith P. M., Wolcott R. M., Chervenak R., Jennings S. R. Control of acute cutaneous herpes simplex virus infection: T cell-mediated viral clearance is dependent upon interferon-gamma (IFN-gamma). Virology. 1994 Jul;202(1):76–88. doi: 10.1006/viro.1994.1324. [DOI] [PubMed] [Google Scholar]
- Speck S. H., Virgin H. W. Host and viral genetics of chronic infection: a mouse model of gamma-herpesvirus pathogenesis. Curr Opin Microbiol. 1999 Aug;2(4):403–409. doi: 10.1016/s1369-5274(99)80071-x. [DOI] [PubMed] [Google Scholar]
- Stevenson P. G., Belz G. T., Altman J. D., Doherty P. C. Changing patterns of dominance in the CD8+ T cell response during acute and persistent murine gamma-herpesvirus infection. Eur J Immunol. 1999 Apr;29(4):1059–1067. doi: 10.1002/(SICI)1521-4141(199904)29:04<1059::AID-IMMU1059>3.0.CO;2-L. [DOI] [PubMed] [Google Scholar]
- Stevenson P. G., Belz G. T., Castrucci M. R., Altman J. D., Doherty P. C. A gamma-herpesvirus sneaks through a CD8(+) T cell response primed to a lytic-phase epitope. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9281–9286. doi: 10.1073/pnas.96.16.9281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stevenson P. G., Cardin R. D., Christensen J. P., Doherty P. C. Immunological control of a murine gammaherpesvirus independent of CD8+ T cells. J Gen Virol. 1999 Feb;80(Pt 2):477–483. doi: 10.1099/0022-1317-80-2-477. [DOI] [PubMed] [Google Scholar]
- Stevenson P. G., Doherty P. C. Kinetic analysis of the specific host response to a murine gammaherpesvirus. J Virol. 1998 Feb;72(2):943–949. doi: 10.1128/jvi.72.2.943-949.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stevenson P. G., Doherty P. C. Non-antigen-specific B-cell activation following murine gammaherpesvirus infection is CD4 independent in vitro but CD4 dependent in vivo. J Virol. 1999 Feb;73(2):1075–1079. doi: 10.1128/jvi.73.2.1075-1079.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stevenson P. G., Efstathiou S., Doherty P. C., Lehner P. J. Inhibition of MHC class I-restricted antigen presentation by gamma 2-herpesviruses. Proc Natl Acad Sci U S A. 2000 Jul 18;97(15):8455–8460. doi: 10.1073/pnas.150240097. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stewart J. P., Micali N., Usherwood E. J., Bonina L., Nash A. A. Murine gamma-herpesvirus 68 glycoprotein 150 protects against virus-induced mononucleosis: a model system for gamma-herpesvirus vaccination. Vaccine. 1999 Jan;17(2):152–157. doi: 10.1016/s0264-410x(98)00190-x. [DOI] [PubMed] [Google Scholar]
- Stewart J. P., Usherwood E. J., Ross A., Dyson H., Nash T. Lung epithelial cells are a major site of murine gammaherpesvirus persistence. J Exp Med. 1998 Jun 15;187(12):1941–1951. doi: 10.1084/jem.187.12.1941. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sunil-Chandra N. P., Arno J., Fazakerley J., Nash A. A. Lymphoproliferative disease in mice infected with murine gammaherpesvirus 68. Am J Pathol. 1994 Oct;145(4):818–826. [PMC free article] [PubMed] [Google Scholar]
- Sunil-Chandra N. P., Efstathiou S., Nash A. A. Murine gammaherpesvirus 68 establishes a latent infection in mouse B lymphocytes in vivo. J Gen Virol. 1992 Dec;73(Pt 12):3275–3279. doi: 10.1099/0022-1317-73-12-3275. [DOI] [PubMed] [Google Scholar]
- Thomson S. A., Elliott S. L., Sherritt M. A., Sproat K. W., Coupar B. E., Scalzo A. A., Forbes C. A., Ladhams A. M., Mo X. Y., Tripp R. A. Recombinant polyepitope vaccines for the delivery of multiple CD8 cytotoxic T cell epitopes. J Immunol. 1996 Jul 15;157(2):822–826. [PubMed] [Google Scholar]
- Thomson S. A., Sherritt M. A., Medveczky J., Elliott S. L., Moss D. J., Fernando G. J., Brown L. E., Suhrbier A. Delivery of multiple CD8 cytotoxic T cell epitopes by DNA vaccination. J Immunol. 1998 Feb 15;160(4):1717–1723. [PubMed] [Google Scholar]
- Thorley-Lawson D. A., Miyashita E. M., Khan G. Epstein-Barr virus and the B cell: that's all it takes. Trends Microbiol. 1996 May;4(5):204–208. doi: 10.1016/s0966-842x(96)90020-7. [DOI] [PubMed] [Google Scholar]
- Topham D. J., Doherty P. C. Clearance of an influenza A virus by CD4+ T cells is inefficient in the absence of B cells. J Virol. 1998 Jan;72(1):882–885. doi: 10.1128/jvi.72.1.882-885.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Topham D. J., Doherty P. C. Longitudinal analysis of the acute Sendai virus-specific CD4+ T cell response and memory. J Immunol. 1998 Nov 1;161(9):4530–4535. [PubMed] [Google Scholar]
- Topham D. J., Tripp R. A., Sarawar S. R., Sangster M. Y., Doherty P. C. Immune CD4+ T cells promote the clearance of influenza virus from major histocompatibility complex class II -/- respiratory epithelium. J Virol. 1996 Feb;70(2):1288–1291. doi: 10.1128/jvi.70.2.1288-1291.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tripp R. A., Hamilton-Easton A. M., Cardin R. D., Nguyen P., Behm F. G., Woodland D. L., Doherty P. C., Blackman M. A. Pathogenesis of an infectious mononucleosis-like disease induced by a murine gamma-herpesvirus: role for a viral superantigen? J Exp Med. 1997 May 5;185(9):1641–1650. doi: 10.1084/jem.185.9.1641. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Usherwood E. J., Ross A. J., Allen D. J., Nash A. A. Murine gammaherpesvirus-induced splenomegaly: a critical role for CD4 T cells. J Gen Virol. 1996 Apr;77(Pt 4):627–630. doi: 10.1099/0022-1317-77-4-627. [DOI] [PubMed] [Google Scholar]
- Usherwood E. J., Roy D. J., Ward K., Surman S. L., Dutia B. M., Blackman M. A., Stewart J. P., Woodland D. L. Control of gammaherpesvirus latency by latent antigen-specific CD8(+) T cells. J Exp Med. 2000 Oct 2;192(7):943–952. doi: 10.1084/jem.192.7.943. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Usherwood E. J., Stewart J. P., Robertson K., Allen D. J., Nash A. A. Absence of splenic latency in murine gammaherpesvirus 68-infected B cell-deficient mice. J Gen Virol. 1996 Nov;77(Pt 11):2819–2825. doi: 10.1099/0022-1317-77-11-2819. [DOI] [PubMed] [Google Scholar]
- Virgin H. W., 4th, Latreille P., Wamsley P., Hallsworth K., Weck K. E., Dal Canto A. J., Speck S. H. Complete sequence and genomic analysis of murine gammaherpesvirus 68. J Virol. 1997 Aug;71(8):5894–5904. doi: 10.1128/jvi.71.8.5894-5904.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Virgin H. W., Speck S. H. Unraveling immunity to gamma-herpesviruses: a new model for understanding the role of immunity in chronic virus infection. Curr Opin Immunol. 1999 Aug;11(4):371–379. doi: 10.1016/s0952-7915(99)80063-6. [DOI] [PubMed] [Google Scholar]
- Wang G. H., Garvey T. L., Cohen J. I. The murine gammaherpesvirus-68 M11 protein inhibits Fas- and TNF-induced apoptosis. J Gen Virol. 1999 Oct;80(Pt 10):2737–2740. doi: 10.1099/0022-1317-80-10-2737. [DOI] [PubMed] [Google Scholar]
- Weck K. E., Barkon M. L., Yoo L. I., Speck S. H., Virgin HW I. V. Mature B cells are required for acute splenic infection, but not for establishment of latency, by murine gammaherpesvirus 68. J Virol. 1996 Oct;70(10):6775–6780. doi: 10.1128/jvi.70.10.6775-6780.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weck K. E., Dal Canto A. J., Gould J. D., O'Guin A. K., Roth K. A., Saffitz J. E., Speck S. H., Virgin H. W. Murine gamma-herpesvirus 68 causes severe large-vessel arteritis in mice lacking interferon-gamma responsiveness: a new model for virus-induced vascular disease. Nat Med. 1997 Dec;3(12):1346–1353. doi: 10.1038/nm1297-1346. [DOI] [PubMed] [Google Scholar]
- Wilson A. D., Lövgren-Bengtsson K., Villacres-Ericsson M., Morein B., Morgan A. J. The major Epstein-Barr virus (EBV) envelope glycoprotein gp340 when incorporated into Iscoms primes cytotoxic T-cell responses directed against EBV lymphoblastoid cell lines. Vaccine. 1999 Mar 5;17(9-10):1282–1290. doi: 10.1016/s0264-410x(98)00351-x. [DOI] [PubMed] [Google Scholar]
- Yu Z., Manickan E., Rouse B. T. Role of interferon-gamma in immunity to herpes simplex virus. J Leukoc Biol. 1996 Oct;60(4):528–532. doi: 10.1002/jlb.60.4.528. [DOI] [PubMed] [Google Scholar]
- Zajac A. J., Blattman J. N., Murali-Krishna K., Sourdive D. J., Suresh M., Altman J. D., Ahmed R. Viral immune evasion due to persistence of activated T cells without effector function. J Exp Med. 1998 Dec 21;188(12):2205–2213. doi: 10.1084/jem.188.12.2205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Berkel V., Preiter K., Virgin H. W., 4th, Speck S. H. Identification and initial characterization of the murine gammaherpesvirus 68 gene M3, encoding an abundantly secreted protein. J Virol. 1999 May;73(5):4524–4529. doi: 10.1128/jvi.73.5.4524-4529.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Dyk L. F., Hess J. L., Katz J. D., Jacoby M., Speck S. H., Virgin HW I. V. The murine gammaherpesvirus 68 v-cyclin gene is an oncogene that promotes cell cycle progression in primary lymphocytes. J Virol. 1999 Jun;73(6):5110–5122. doi: 10.1128/jvi.73.6.5110-5122.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]