Virus Elimination in Acute Lymphocytic Choriomeningitis Virus Infection Correlation with Virus‐Specific Delayed‐Type Hypersensitivity rather than Cytotoxicity

The immunological effector mechanism responsible for the elimination of virus in murine acute non‐fatal extracranial lymphocytic choriomeningitis virus infection was studied. In this infection virus clearance is generally regarded as the result of a direct action of virus‐specific cytotoxic T cells (Tc cells) on virus‐producing target cells in the infected mouse. However, by manipulating the antiviral immune response by pretreatment with various doses of cyclophosphamide, we found lack of correlation between Te‐cell activity and the clearance of virus. In contrast, we observed a conspicuous correlation between the host's ability to mount a virus‐specific delayed‐type hypersensitivity (DTH) response and its capacity to combat virus. Moreover, pretreatment with silica and carragheenan prolonged viraemia without impairment of the peak Tc‐cell response. These findings indicate that Tc cells have little or no capacity to eliminate virus, at least in the absence of an inflammatory response, and our findings suggest that virus clearance reflects a DTH‐like process.

[1]  A. Thomsen,et al.  Fatal Meningitis following Lymphocytic Choriomeningitis Virus Infection Reflects Delayed‐Type Hypersensitivity Rather than Cytotoxicity , 1983, Scandinavian journal of immunology.

[2]  H. Ertl,et al.  An Analysis of Effector T Cell Generation and Function in Mice Exposed to Influenza A or Sendai Viruses , 1981, Immunological reviews.

[3]  Y. L. Lin,et al.  Biological properties of an influenza A virus-specific killer T cell clone. Inhibition of virus replication in vivo and induction of delayed- type hypersensitivity reactions , 1981, The Journal of experimental medicine.

[4]  M. Simon,et al.  Effector T lymphocytes in lymphocytic choriomeningitis virus-infected mice. Cytolytic activity of Lyt-23 spleen cells in vitro does not correlate with elimination of infectious virus from spleens , 1981, The Journal of experimental medicine.

[5]  A. Thomsen,et al.  Concanavalin A‐mediated in Vitro Activation of a Secondary Cytotoxic T‐Cell Response in Virus‐primed Splenocytes , 1980, Scandinavian journal of immunology.

[6]  R. Welsh,et al.  Natural Killer Cell Response to Lymphocytic Choriomeningitis Virus in Beige Mice , 1980, Scandinavian journal of immunology.

[7]  P. Hochman,et al.  Do Natural Killer Cells Engage in Regulated Reactions Against Self to Ensure Homeostasis? , 1979, Immunological reviews.

[8]  Glaser,et al.  Regulation of specific cell-mediated cytotoxic response against SV40- induced tumor associated antigens by depletion of suppressor T cells with cyclophosphamide in mice , 1979, The Journal of experimental medicine.

[9]  R M Zinkernagel,et al.  MHC-restricted cytotoxic T cells: studies on the biological role of polymorphic major transplantation antigens determining T-cell restriction-specificity, function, and responsiveness. , 1979, Advances in immunology.

[10]  M. V. Doyle,et al.  Interactions between viruses and lymphocytes. I. In vivo replication of lymphocytic choriomeningitis virus in mononuclear cells during both chronic and acute viral infections. , 1978, Journal of immunology.

[11]  G. Shearer,et al.  Depressive effect of silica particles on F1 hybrid anti-parent cell-mediated lympholysis induced in vitro. , 1978, Cellular immunology.

[12]  K. Bro-Jørgensen The interplay between lymphocytic choriomeningitis virus, immune function, and hemopoiesis in mice. , 1978, Advances in virus research.

[13]  A. Starzinski-Powitz,et al.  The role of T cells in anti-herpes simplex virus immunity. I. Induction of antigen-specific cytotoxic T lymphocytes. , 1977, Journal of immunology.

[14]  R. Zinkernagel,et al.  Antiviral protection by virus-immune cytotoxic T cells: infected target cells are lysed before infectious virus progeny is assembled , 1977, The Journal of experimental medicine.

[15]  A. Starzinski-Powitz,et al.  Cyclophosphamide-sensitive T lymphocytes suppress the in vivo generation of antigen-specific cytotoxic T lymphocytes , 1977, The Journal of experimental medicine.

[16]  R. Zinkernagel,et al.  Major transplantation antigens, viruses, and specificity of surveillance T cells. , 1977, Contemporary topics in immunobiology.

[17]  R. Zinkernagel H-2 restriction of virus-specific T-cell-mediated effector functions in vivo. II. Adoptive transfer of delayed-type hypersensitivity to murine lymphocytic choriomeningits virus is restriced by the K and D region of H-2 , 1976, The Journal of experimental medicine.

[18]  P. Alexander,et al.  Mechanisms of extracellular killing of nucleated mammalian cells by macrophages. , 1976 .

[19]  R. Zinkernagel,et al.  15 – Lymphocyte–Macrophage Interactions and Macrophage Activation in the Expression of Antimicrobial Immunity in Vivo , 1976 .

[20]  H. McFarland,et al.  THE ROLE OF THE INFLAMMATORY RESPONSE IN VIRAL INFECTIONS , 1975 .

[21]  K. Bro-Jørgensen,et al.  TWO POPULATIONS OF T LYMPHOCYTES IMMUNE TO THE LYMPHOCYTIC CHORIOMENINGITIS VIRUS , 1974, The Journal of experimental medicine.

[22]  R. Blanden,et al.  Macrophage activation in mice infected with ectromelia or lymphocytic choriomeningitis viruses. , 1973, The Australian journal of experimental biology and medical science.

[23]  O. Marker,et al.  STUDIES ON CELL-MEDIATED IMMUNITY TO LYMPHOCYTIC CHORIOMENINGITIS VIRUS IN MICE , 1973, The Journal of experimental medicine.

[24]  R. Graham,et al.  Spectrum and possible mechanism of carrageenan cytotoxicity. , 1971, The American journal of pathology.

[25]  A. C. Allison,et al.  AN EXAMINATION OF THE CYTOTOXIC EFFECTS OF SILICA ON MACROPHAGES , 1966, The Journal of experimental medicine.