Development and migration of protective CD8+ T cells into the nervous system following ocular herpes simplex virus-1 infection

Journal of Immunology

Volumn 174, Issue 5, 2005, Pages 2919-2925

  Lang, Anna ^a   Nikolich Žugich, Janko ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYFLUORESCEIN DIACETATE SUCCINIMIDYL ESTER; GAMMA INTERFERON; LEUKOSIALIN; VIRUS ANTIGEN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL ACTIVATION; CELL MATURATION; CELL MIGRATION; CELL PROLIFERATION; CONTROLLED STUDY; EYE INFECTION; FEMALE; HERPES SIMPLEX; HERPES SIMPLEX VIRUS 1; IMMUNOSURVEILLANCE; LYMPHOID ORGAN; MOUSE; NONHUMAN; PRIORITY JOURNAL; SENSORY GANGLION; T LYMPHOCYTE; TRIGEMINUS GANGLION; VIRUS ENCEPHALITIS; VIRUS REPLICATION;

EID: 14044271514     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.174.5.2919     Document Type: Article

References (53)

1. Lin, W. R., R. Jennings, T. L. Smith, M. A. Wozniak, and R. F. Itzhaki. 2001. Vaccination prevents latent HSV1 infection of mouse brain. Neurobiol. Aging 22:699.
2. Esiri, M. M. 1982. Herpes simplex encephalitis: an immunohistological study of the distribution of viral antigen within the brain. J. Neurol. Sci. 54:209.
3. Lewandowski, G., M. N. Zimmerman, L. L. Denk, D. D. Porter, and G. A. Prince. 2002. Herpes simplex type 1 infects and establishes latency in the brain and trigeminal ganglia during primary infection of the lip in cotton rats and mice. Arch. Virol. 147:167.
4. Schmutzhard, E. 2001. Viral infections of the CNS with special emphasis on herpes simplex infections. J. Neurol. 248:469.
5. Esiri, M. M., and A. H. Tomlinson. 1984. Herpes simplex encephalitis. Immunohistological demonstration of spread of virus via olfactory and trigeminal pathways after infection of facial skin in mice. J. Neurol. Sci. 64:213.
6. Lewandowski, G. 1997. Immunohistochemical examination of intracerebral T cell recruitment and adhesion molecule induction in herpes simplex virus-infected mice. Brain. Behav. Immun. 11:264.
7. Matsubara, S., and S. S. Atherton. 1997. Spread of HSV-1 to the suprachiasmatic nuclei and retina in T cell depleted BALB/c mice. J. Neuroimmunol. 80:165.
8. Kastrukoff, L., C. Long, P. C. Doherty, Z. Wroblewska, and H. Koprowski. 1981. Isolation of virus from brain after immunosuppression of mice with latent herpes simplex. Nature 291:432.
9. + T lymphocytes in the development of stress-induced herpes simplex encephalitis. J. Neuroimmunol. 140:13.
10. Kleinschmidt-DeMasters, B. K., and D. H. Gilden. 2001. The expanding spectrum of herpesvirus infections of the nervous system. Brain Pathol. 12:440.
11. Schiff, D., and M. K. Rosenblum. 1998. Herpes simplex encephalitis (HSE) and the immunocompromised: a clinical and autopsy study of HSE in the settings of cancer and human immunodeficiency virus-type 1 infection. Hum. Pathol. 29:215.
12. Ghiasi, H., S. Cai, G. C. Perng, A. B. Nesburn, and S. L. Wechsler. 2000. The role of natural killer cells in protection of mice against death and corneal scarring following ocular HSV-1 infection. Antiviral Res. 45:33.
13. + T cell subsets in the control of an acute herpes simplex virus infection of the skin and nervous system. J. Gen. Virol. 68:825.
14. Zhao, M., A. Azumi, and S. S. Atherton. 1995. T lymphocyte infiltration in the brain following anterior chamber inoculation of HSV-1. J. Neuroimmunol. 58:11.
15. + T cells are involved in protection against HSV-1 induced corneal scarring. Br. J. Ophthalmol. 84:408.
16. Morrison, L. A., and D. M. Knipe. 1997. Contributions of antibody and T cell subsets to protection elicited by immunization with a replication-defective mutant of herpes simplex virus type 1. Virology 239:315.
17. + T cell function is sufficient for clearance of infectious virus from trigeminal ganglia and establishment of herpes simplex virus type 1 latency in mice. Microb. Pathog. 27:387.
18. Deshpande, S. P., M. Zheng, S. Lee, and B. T. Rouse. 2002. Mechanisms of pathogenesis in herpetic immunoinflammatory ocular lesions. Vet. Microbiol. 86:17.
19. Deshpande, S. P., S. Lee, M. Zheng, B. Song, D. Knipe, J. A. Kapp, and B. T. Rouse. 2001. Herpes simplex virus-induced keratitis: evaluation of the role of molecular mimicry in lesion pathogenesis. J. Virol. 75:3077.
20. Deshpande, S., M. Zheng, S. Lee, K. Banerjee, S. Gangappa, U. Kumaraguru, and B. T. Rouse. 2001. Bystander activation involving T lymphocytes in herpetic stromal keratitis. J. Immunol. 167:2902.
21. Banerjee, K., S. Deshpande, M. Zheng, U. Kumaraguru, S. P. Schoenberger, and B. T. Rouse. 2002. Herpetic stromal keratitis in the absence of viral antigen recognition. Cell. Immunol. 219:108.
22. Sciammas, R., P. Kodukula, Q. Tang, R. L. Hendricks, and J. A. Bluestone. 1997. T cell receptor-γ/δ cells protect mice from herpes simplex virus type 1-induced lethal encephalitis. J. Exp. Med. 185:1969.
23. + T cells can block herpes simplex virus type 1 (HSV-1) reactivation from latency in sensory neurons. J. Exp. Med. 191:1459.
24. Liu, T., K. M. Khanna, B. N. Carriere, and R. L. Hendricks. 2001. Gamma interferon can prevent herpes simplex virus type 1 reactivation from latency in sensory neurons. J. Virol. 75:11178.
25. + T cells are selectively activated and retained in latently infected sensory ganglia. Immunity 18:593.
26. Ellison, A. R., L. Yang, C. Voytek, and T. P. Margolis. 2000. Establishment of latent herpes simplex virus type 1 infection in resistant, sensitive, and immunodeficient mouse strains. Virology 268:17.
27. Simmons, A., and D. C. Tscharke. 1992. Anti-CD8 impairs clearance of herpes simplex virus from the nervous system: implications for the fate of virally infected neurons. J. Exp. Med. 175:1337.
28. Bouley, D. M., S. Kanangat, W. Wire, and B. T. Rouse. 1995. Characterization of herpes simplex virus type-1 infection and herpetic stromal keratitis development in IFN-γ knockout mice. J. Immunol. 155:3964.
29. Cantin, E., B. Tanamachi, H. Openshaw, J. Mann, and K. Clarke. 1999. Gamma interferon (IFN-γ) receptor null-mutant mice are more susceptible to herpes simplex virus type 1 infection than IFN-γ ligand null-mutant mice. J. Virol. 73:5196.
30. Geiger, K. D., T. C. Nash, S. Sawyer, T. Krahl, G. Patstone, J. C. Reed, S. Krajewski, D. Dalton, M. J. Buchmeier, and N. Sarvetnick. 1997. Interferon-γ protects against herpes simplex virus type 1-mediated neuronal death. Virology 238:189.
31. + cell granules, restricts the spread of herpes simplex virus in the peripheral nervous systems of experimentally infected mice. J. Virol. 74:1029.
32. Chang, E., L. Galle, D. Maggs, D. M. Estes, and W. J. Mitchell. 2000. Pathogenesis of herpes simplex virus type 1-induced corneal inflammation in perforin-deficient mice. J. Virol. 74:11832.
33. + T cell responses and fail to contain virus infection of the central nervous system. J. Immunol. 166:1066.
34. Ghiasi, H., S. Cai, G. Perng, A. B. Nesburn, and S. L. Wechsler. 1999. Perform pathway is essential for protection of mice against lethal ocular HSV-1 challenge but not corneal scarring. Virus Res. 65:97.
35. Manickan, E., and B. T. Rouse. 1995. Roles of different T-cell subsets in control of herpes simplex virus infection determined by using T-cell-deficient mouse-models. J. Virol. 69:8178.
36. Mueller, S. N., W. Heath, J. D. McLain, F. R. Carbone, and C. M. Jones. 2002. Characterization of two TCR transgenic mouse lines specific for herpes simplex virus. Immunol. Cell. Biol. 80:156.
37. Altman, J. D., P. A. Moss, P. J. Goulder, D. H. Barouch, M. G. McHeyzer-Williams, J. I. Bell, A. J. McMichael, and M. M. Davis. 1996. Phenotypic analysis of antigen-specific T lymphocytes. Science 274:94.
38. Jones, C. M., S. C. Cose, R. M. Coles, A. C. Winterhalter, A. G. Brooks, W. R. Heath, and F. R. Carbone. 2000. Herpes simplex virus type 1-specific cytotoxic T-lymphocyte arming occurs within lymph nodes draining the site of cutaneous infection. J. Virol. 74:2414.
39. Bonneau, R. H., L. A. Salvucci, D. C. Johnson, and S. S. Tevethia. 1993. Epitope specificity of H-2Kb-restricted, HSV-1-, and HSV-2-cross-reactive cytotoxic T lymphocyte clones. Virology 195:62.
40. Hanke, T., F. L. Graham, K. L. Rosenthal, and D. C. Johnson. 1991. Identification of an immunodominant cytotoxic T-lymphocyte recognition site in glycoprotein B of herpes simplex virus by using recombinant adenovirus vectors and synthetic peptides. J. Virol. 65:1177.
41. + T cells. J. Immunol. 150:2346.
42. Murali-Krishna, K., J. D. Altman, M. Suresh, D. J. Sourdive, A. J. Zajac, J. D. Miller, J. Slansky, and R. Ahmed. 1998. Counting antigen-specific CD8 T cells: a reevaluation of bystander activation during viral infection. Immunity 8:177.
43. Masopust, D., and L. Lefrancois. 2003. CD8 T-cell memory: the other half of the story. Microb. Infect. 5:221.
44. + T cells can clear established lyric infections from skin and nerves and can partially limit the early spread of virus after cutaneous inoculation. J. Immunol. 172:392.
45. Yamagami, S., M. R. Dana, and T. Tsuru. 2002. Draining lymph nodes play an essential role in alloimmunity generated in response to high-risk corneal transplantation. Cornea 21:405.
46. Coles, R. M., S. N. Mueller, W. R. Heath, F. R. Carbone, and A. G. Brooks. 2002. Progression of armed CTL from draining lymph node to spleen shortly after localized infection with herpes simplex virus 1. J. Immunol. 168:834.
47. Mueller, S. N., C. M. Jones, C. M. Smith, W. R. Heath, and F. R. Carbone. 2002. Rapid cytotoxic T lymphocyte activation occurs in the draining lymph nodes after cutaneous herpes simplex virus infection as a result of early antigen presentation and not the presence of virus. J. Exp. Med. 195:651.
48. Wong, P., and E. G. Pamer. 2001. Cutting edge: antigen-independent CD8 T cell proliferation. J. Immunol. 166:5864.
49. + T cell differentiation: initial antigen encounter triggers a developmental program in naive cells. Nat. Immunol. 2:415.
50. + dendritic cells but not by Langerhans cells. Science 301:1925.
51. + dendritic cells are generally involved in priming CTL immunity to viruses. J. Immunol. 172:1996.
52. Zhao, X., E. Deak, K. Soderberg, M. Linehan, D. Spezzano, J. Zhu, D. M. Knipe, and A. Iwasaki. 2003. Vaginal submucosal dendritic cells, but not Langerhans cells, induce protective Th1 responses to herpes simplex virus-2. J. Exp. Med. 197:153.
53. Iwasaki, A. 2003. The role of dendritic cells in immune responses against vaginal infection by herpes simplex virus type 2. Microb. Infect. 5:1221.