Abstract
Vaccinia virus recombinants expressing the three major bovine herpes virus-1 (BHV-1) glycoproteins gI, gIII and gIV were used to identify the major target antigens for BHV-1-specific CTL isolated from immune cattle. Peripheral blood mononuclear cells (PBMC) expanded in vitro in the presence of interleukin-2 (IL-2) and lysed both gIII- and gIV-infected target cells. Secondary in vitro stimulation of PBMC was also performed in the presence of either fixed BHV-1-infected autologous fibroblasts or ultraviolet (UV)-inactivated virus. Both methods of antigen presentation allowed the proliferation of BHV-1-specific CTL but the target glycoprotein for these CTL differed depending on the method of stimulation. Vaccinia-gIV-infected targets were lysed predominantly when PBMC were stimulated by fixed infected fibroblasts, whilst PBMC stimulated by UV-inactivated virus lysed mostly vaccinia-gIII-infected targets. This observation could be explained by a different processing pathway of BHV-1 antigens in each cell type involved.
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Selected References
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- Baldwin C. L., Teale A. J., Naessens J. G., Goddeeris B. M., MacHugh N. D., Morrison W. I. Characterization of a subset of bovine T lymphocytes that express BoT4 by monoclonal antibodies and function: similarity to lymphocytes defined by human T4 and murine L3T4. J Immunol. 1986 Jun 15;136(12):4385–4391. [PubMed] [Google Scholar]
- Campos M., Rossi C. R. In vitro induction of cytotoxic lymphocytes from infectious bovine rhinotracheitis virus hyperimmune cattle. Am J Vet Res. 1986 Nov;47(11):2411–2414. [PubMed] [Google Scholar]
- Carter J. J., Weinberg A. D., Pollard A., Reeves R., Magnuson J. A., Magnuson N. S. Inhibition of T-lymphocyte mitogenic responses and effects on cell functions by bovine herpesvirus 1. J Virol. 1989 Apr;63(4):1525–1530. doi: 10.1128/jvi.63.4.1525-1530.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cook C. G., Splitter G. A. Comparison of bovine mononuclear cells with other species for cytolytic activity against virally-infected cells. Vet Immunol Immunopathol. 1989 Feb;20(3):239–261. doi: 10.1016/0165-2427(89)90004-4. [DOI] [PubMed] [Google Scholar]
- Cranage M. P., Kouzarides T., Bankier A. T., Satchwell S., Weston K., Tomlinson P., Barrell B., Hart H., Bell S. E., Minson A. C. Identification of the human cytomegalovirus glycoprotein B gene and induction of neutralizing antibodies via its expression in recombinant vaccinia virus. EMBO J. 1986 Nov;5(11):3057–3063. doi: 10.1002/j.1460-2075.1986.tb04606.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cullen S. E., Kindle C. S., Shreffler D. C., Cowing C. Differential glycosylation of murine B cell and spleen adherent cell Ia antigens. J Immunol. 1981 Oct;127(4):1478–1484. [PubMed] [Google Scholar]
- Eugui E. M., Emery D. L. Genetically restricted cell-mediated cytotoxicity in cattle immune to Theileria parva. Nature. 1981 Mar 19;290(5803):251–254. doi: 10.1038/290251a0. [DOI] [PubMed] [Google Scholar]
- Glass E. J., Spooner R. L. Generation and characterisation of bovine antigen-specific T cell lines. J Immunol Methods. 1990 Apr 17;128(2):267–275. doi: 10.1016/0022-1759(90)90219-l. [DOI] [PubMed] [Google Scholar]
- Glorioso J., Kees U., Kümel G., Kirchner H., Krammer P. H. Identification of herpes simplex virus type 1 (HSV-1) glycoprotein gC as the immunodominant antigen for HSV-1-specific memory cytotoxic T lymphocytes. J Immunol. 1985 Jul;135(1):575–582. [PubMed] [Google Scholar]
- Lanzavecchia A. Antigen-specific interaction between T and B cells. Nature. 1985 Apr 11;314(6011):537–539. doi: 10.1038/314537a0. [DOI] [PubMed] [Google Scholar]
- Lawman M. J., Griebel P., Hutchings D. L., Davis W. C., Heise J., Qualtiere L., Babiuk L. A. Generation of IL-2 dependent bovine cytotoxic T lymphocyte clones reactive against BHV-1 infected target cells: loss of genetic restriction and virus specificity. Viral Immunol. 1987;1(3):163–176. doi: 10.1089/vim.1987.1.163. [DOI] [PubMed] [Google Scholar]
- Liang X. P., Babiuk L. A., van Drunen Littel-van den Hurk S., Fitzpatrick D. R., Zamb T. J. Bovine herpesvirus 1 attachment to permissive cells is mediated by its major glycoproteins gI, gIII, and gIV. J Virol. 1991 Mar;65(3):1124–1132. doi: 10.1128/jvi.65.3.1124-1132.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mackett M., Smith G. L., Moss B. General method for production and selection of infectious vaccinia virus recombinants expressing foreign genes. J Virol. 1984 Mar;49(3):857–864. doi: 10.1128/jvi.49.3.857-864.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mackett M., Smith G. L. Vaccinia virus expression vectors. J Gen Virol. 1986 Oct;67(Pt 10):2067–2082. doi: 10.1099/0022-1317-67-10-2067. [DOI] [PubMed] [Google Scholar]
- Marshall R. L., Rodriguez L. L., Letchworth G. J., 3rd Characterization of envelope proteins of infectious bovine rhinotracheitis virus (bovine herpesvirus 1) by biochemical and immunological methods. J Virol. 1986 Mar;57(3):745–753. doi: 10.1128/jvi.57.3.745-753.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Misra V., Blumenthal R. M., Babiuk L. A. Proteins Specified by bovine herpesvirus 1 (infectious bovine rhinotracheitis virus). J Virol. 1981 Nov;40(2):367–378. doi: 10.1128/jvi.40.2.367-378.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morrison L. A., Braciale V. L., Braciale T. J. Antigen form influences induction and frequency of influenza-specific class I and class II MHC-restricted cytolytic T lymphocytes. J Immunol. 1988 Jul 15;141(2):363–368. [PubMed] [Google Scholar]
- Morrison W. I., Goddeeris B. M., Brown W. C., Baldwin C. L., Teale A. J. Theileria parva in cattle: characterization of infected lymphocytes and the immune responses they provoke. Vet Immunol Immunopathol. 1989 Feb;20(3):213–237. doi: 10.1016/0165-2427(89)90003-2. [DOI] [PubMed] [Google Scholar]
- Nyaga P. N., McKercher D. G. Pathogenesis of bovine herpesvirus-1 (BHV-1) infections: interactions of the virus with peripheral bovine blood cellular components. Comp Immunol Microbiol Infect Dis. 1979;2(4):587–602. doi: 10.1016/0147-9571(79)90100-0. [DOI] [PubMed] [Google Scholar]
- Reddehase M. J., Cox J. H., Koszinowski U. H. Frequency analysis of cytolytic T cell precursors (CTL-P) generated in vivo during lethal rabies infection of mice. I. Distinction of CTL-P with different interleukin 2 sensitivity. Eur J Immunol. 1982 Jun;12(6):519–523. doi: 10.1002/eji.1830120613. [DOI] [PubMed] [Google Scholar]
- Reddehase M. J., Koszinowski U. H. Significance of herpesvirus immediate early gene expression in cellular immunity to cytomegalovirus infection. Nature. 1984 Nov 22;312(5992):369–371. doi: 10.1038/312369a0. [DOI] [PubMed] [Google Scholar]
- Scheerlinck J. P., Burssens G., Brys L., Michel A., Hauser P., De Baetselier P. Differential presentation of hepatitis B S-preS(2) particles and peptides by macrophages and B-cell like antigen-presenting cells. Immunology. 1991 May;73(1):88–94. [PMC free article] [PubMed] [Google Scholar]
- Splitter G. A., Eskra L., Abruzzini A. F. Cloned bovine cytolytic T cells recognize bovine herpes virus-1 in a genetically restricted, antigen-specific manner. Immunology. 1988 Jan;63(1):145–150. [PMC free article] [PubMed] [Google Scholar]
- Splitter G. A., Eskra L. Bovine T lymphocyte response to bovine herpesvirus-1: cell phenotypes, viral recognition and acid-labile interferon production. Vet Immunol Immunopathol. 1986 Mar;11(3):235–250. doi: 10.1016/0165-2427(86)90004-8. [DOI] [PubMed] [Google Scholar]
- Taswell C. Limiting dilution assays for the determination of immunocompetent cell frequencies. I. Data analysis. J Immunol. 1981 Apr;126(4):1614–1619. [PubMed] [Google Scholar]
- Witmer L. A., Rosenthal K. L., Graham F. L., Friedman H. M., Yee A., Johnson D. C. Cytotoxic T lymphocytes specific for herpes simplex virus (HSV) studied using adenovirus vectors expressing HSV glycoproteins. J Gen Virol. 1990 Feb;71(Pt 2):387–396. doi: 10.1099/0022-1317-71-2-387. [DOI] [PubMed] [Google Scholar]
- Yasukawa M., Inatsuki A., Kobayashi Y. Differential in vitro activation of CD4+CD8- and CD8+CD4- herpes simplex virus-specific human cytotoxic T cells. J Immunol. 1989 Sep 15;143(6):2051–2057. [PubMed] [Google Scholar]
- Zarling J. M., Moran P. A., Burke R. L., Pachl C., Berman P. W., Lasky L. A. Human cytotoxic T cell clones directed against herpes simplex virus-infected cells. IV. Recognition and activation by cloned glycoproteins gB and gD. J Immunol. 1986 Jun 15;136(12):4669–4673. [PubMed] [Google Scholar]
- van Drunen Littel-van den Hurk S., Zamb T., Babiuk L. A. Synthesis, cellular location, and immunogenicity of bovine herpesvirus 1 glycoproteins gI and gIII expressed by recombinant vaccinia virus. J Virol. 1989 May;63(5):2159–2168. doi: 10.1128/jvi.63.5.2159-2168.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- van Drunen Littel-van den Hurk S., van den Hurk J. V., Babiuk L. A. Topographical analysis of bovine herpesvirus type-1 glycoproteins: use of monoclonal antibodies to identify and characterize functional epitopes. Virology. 1985 Jul 15;144(1):216–227. doi: 10.1016/0042-6822(85)90319-8. [DOI] [PubMed] [Google Scholar]
