Abstract
The inflammatory response to viral infections is characteristically composed of mononuclear cells. The full development of this response is an immunologically specific event that is dependent on the presence of sensitized T lymphocytes [1–4]. These mononuclear inflammatory cells represent a variety of functional cell types indistinguishable, for the most part, on the basis of conventional morphology. Critical studies of the inflammatory response have, to date, been limited almost exclusively to examination of mice with infections of the central nervous system, lung, or liver with enveloped viruses. Under these circumstances, inflammatory infiltrates at various stages of development are known to consist of T lymphocytes of the helper/delayed-type hypersensitivity (Lyt-1) and cytotoxic/suppressor (Lyt-2) phenotypes, B lymphocytes at various stages of differentiation, natural killer (NK) cells, and monocyte/macrophages. Infections of other organs and/or of other species with different, particularly nonenveloped, viruses may generate inflammatory patterns different from those reviewed here.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
McFarland HF, Griffin DE, Johnson RT (1972) Specificity of the inflammatory response in viral encephalitis. I. Adoptive immunization of immunosuppressed mice infected with Sindbis virus. J Exp Med 136:216–226
Doherty PC, Zinkernagel RM (1974) T-cell-mediated immunopathology in viral infections. Transplant Rev 19:89–120
Blanden RV (1974) T cell response to viral and bacterial infection. Transplant Rev 19:56–88
Berger ML (1982) Immunologic requirements for the adoptive transfer of ectromelia virus meningitis. J Neuropath Exp Neurol 41:18–33
Doherty PC (1973) Quantitative studies of the inflammatory process in fatal viral meningoencephalitis. Am J Pathol 73:607–621
Hirsch RL, Griffin DE (1979) The pathogenesis of Sindbis virus infection in athymic nude mice. J Immunol 123:1215–1218
Brier AM, Snyderman R, Mergenhagen SE, Notkins AL (1970) Inflammation and herpes simplex virus: Release of a Chemotaxis generating factor from infected cells. Science 170:1104–1106
Ward PA, Cohen S, Flanagan TD (1972) Leukotactic factors elaborated by virus-infected tissues. J Exp Med 135:1095–1103
Mokhtarian F, Griffin DE, Hirsch RL (1982) Production of mononuclear chemotactic factors during Sindbis virus infection of mice. Infect Immun 35:965–973
Baringer JR, Griffith JF (1970) Experimental herpes simplex encephalitis: Early neuropathologic changes. J Neuropath Exp Neurol 29:89–104
Hirschberg H, Hirschberg T, Jaffe E, Thorsby E (1981) Antigen-presenting properties of human vascular endothelial cells: Inhibition by anti-HLA-DR antisera. Scand J Immunol 14:545–553
Doherty PC, Dunlop MBC, Parish CR, Zinkernagel R (1976) Inflammatory process in murine lymphocytic choriomeningitis is maximal in H-2K or H-2D compatible interactions. J Immunol 117:187–189
Berger ML (1982) The role of the major histocompatibility complex in the adoptive transfer of ectromelia virus meningitis. J Neuropathol Exp Neurol 41:34–44
Yap KL, Ada GL (1978) Cytotoxic T cells in the lungs of mice infected with an influenza virus. Scand J Immunol 7:73–80
Ennis FA, Wells MA, Butchko GM, Albrecht P (1978) Evidence that cytotoxic T cells are part of the host’s response to influenza pneumonia. J Exp Med 148:1241–1250
Leung KN, Ada GL (1980) Cells mediating delayed-type hypersensitivity in the lungs of mice infected with an influenza A virus. Scand J Immunol 12:393–400
Moench TR, Griffin DE (1984) Immunocytochemical identification and quantitation of mononuclear cells in cerebrospinal fluid, meninges, and brain during acute viral encephalitis. J Exp Med 159:77–88
Zinkernagel RM, Doherty PC (1979) MHC-restricted cytotoxic T cells: Studies on the biological role of polymorphic major transplantation antigens determining T-cell restriction-specificity, function, and responsiveness. Adv Immunol 27:51–171
Zinkernagel RM, Welsh RM (1976) H-2 compatibility requirement for virus-specific T cell-mediated effector functions in vivo. I. Specificity of T cells conferring antiviral protection against lymphocytic choriomeningitis virus is associated with H-2K and H-2D. J Immunol 117:1495–1502
Yap KL, Ada GL, McKenzie IFC (1978) Transfer of specific cytotoxic T lymphocytes protects mice inoculated with influenza virus. Nature 273:238
Oppenheim JJ (1981) Lymphokines. In Oppenheim JJ, Rosenstreich DL, Potter M (eds), Cellular Immunity and Inflammation. Elsevier, New York, p 259
Nash AA, Phelan J, Wildy P (1981) Cell-mediated immunity in herpes simplex virus-infected mice: H-2 mapping of the delayed-type hypersensitivity response and the antiviral T cell response. J Immunol 126:1260–1262
Zinkernagel RM (1976) H-2 restriction of virus-specific T cell mediated effector function in vivo. II. Adoptive transfer of delayed-type hypersensitivity to murine lymphocytic choriomeningitis virus is restricted by the K and D region of H-2. J Exp Med 144:766–787
Leung KN, Ada GL (1980) Two T-cell populations mediate delayed-type hypersensitivity to murine influenza virus infection. Scand J Immunol 12:481–487
Liew FY (1982) Regulation of delayed-type hypersensitivity to pathogens and alloantigens. Immunol Today 3:18–23
Edidin M (1972) The tissue distribution and cellular location of transplantation antigens. In Kahan BD, Reisfeld RA (eds) Transplantation Antigens. Academic Press, New York, p 125
Hurwitz JL, Korngold R, Doherty PC (1983) Specific and nonspecific T cell recruitment in viral meningitis: Possible implications for autoimmunity. Cell Immunol 76:397–401
Johnson RT (1971) Inflammatory response to viral infection. In Immunological Disorders of the Nervous System, Vol 69. Res Pub Assoc Res Nerv Ment Dis, p 305
Kitamura T (1975) Hematogenous cells in experimental Japanese encephalitis. Acta Neuropathol 32:341–353
Blinzinger K, Herrlinger H, Luh S, Anzil AP (1978) Ultrastructural cytochemical demonstration of peroxidase-positive monocyte granules: An additional method for studying the origin of mononuclear cells in encephalitic lesions. Acta Neuropathol 43:55–61
Askenase PW, Bursztajn S, Gershon MD, Gershon RK (1980) T cell-dependent mast cell degranulation and release of serotonin in murine delayed-type hypersensitivity. J Exp Med 152:1358–1374
Mokhtarian F, Griffin DE (1984) Role of mast cells in virus induced CNS inflammation. Cell. Immunol, (in press)
Owens SL, Osebold JW, Zee YC (1981) Dynamics of B-lymphocytes in the lungs of mice exposed to aerosolized virus. Infect Immun 23:231–238
Esiri MM (1980) Poliomyelitis: Immunoglobulin-containing cells in the central nervous system in acute and convalescent phases of the human disease. Clin Exp Immunol 40:42–48
Esiri MM, Oppenheimer DR, Brownell B, Haire M (1982) Distribution of measles antigen and immunoglobulin-containing cells in the CNS in subacute sclerosing panencephalitis (SSPE) and atypical measles encephalitis. J Neurol Sci 53:29–43
Griffin DE (1981) Immunoglobulin in the cerebrospinal fluid: Changes during acute viral encephalitis in mice. J Immunol 126:27–31
Gerhard W, Koprowski H (1977) Persistence of virus-specific memory B cells in mice CNS. Nature 266:360–361
Leung KN, Ada GL (1981) Induction of natural killer cells during murine influenza virus infection. Immunobiology 160:352–366
Doherty PC, Korngold R (1983) Characteristics of poxvirus-induced meningitis: Virus-specific and nonspecific cytotoxic effectors in the inflammatory exudate. Scand J Immunol 17:1–7
Herberman RB, Djeu JY, Kay D, Ortaldo JR, Riccardi C, Bonnard GD, Holden HT, Fagnani R, Santoni A, Puccetti P (1979) Natural killer cells: Characteristics and regulation of activity. Immunol Rev 44:43–70
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1984 Springer-Verlag New York Inc.
About this chapter
Cite this chapter
Griffin, D.E. (1984). The Inflammatory Response to Acute Viral Infections. In: Notkins, A.L., Oldstone, M.B.A. (eds) Concepts in Viral Pathogenesis. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-5250-4_7
Download citation
DOI: https://doi.org/10.1007/978-1-4612-5250-4_7
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4612-9756-7
Online ISBN: 978-1-4612-5250-4
eBook Packages: Springer Book Archive