Interferon-alpha-producing cells are localized in gut-associated lymphoid tissues in transmissible gastroenteritis virus (TGEV) infected piglets

Veterinary Research

Volumn 32, Issue 1, 2001, Pages 71-79

  Riffault, Sabine ^a   Carrat, Charles ^a   Van Reeth, Kristien ^b   Pensaert, Maurice ^b   Charley, Bernard ^a  

^a INRA Institut National de la Recherche Agronomique   (France)

^b GHENT UNIVERSITY   (Belgium)

Author keywords

Gut; Interferon; Lymphoid tissue; Pig; Transmissible gastroenteritis virus (TGEV)

Indexed keywords

ACRONICTA LEPORINA; ORYCTOLAGUS CUNICULUS; SUS SCROFA; TRANSMISSIBLE GASTROENTERITIS VIRUS;

ALPHA INTERFERON; VIRUS ANTIBODY; VIRUS ANTIGEN;

ANIMAL; ARTICLE; BIOSYNTHESIS; BLOOD; IMMUNOHISTOCHEMISTRY; IMMUNOLOGY; LEUKOCYTE; LYMPH NODE; MAJOR HISTOCOMPATIBILITY COMPLEX; MESENTERY; PEYER PATCH; SWINE; SWINE DISEASE; TIME; TISSUE DISTRIBUTION; TRANSMISSIBLE GASTROENTERITIS VIRUS;

ANIMALS; ANTIBODIES, VIRAL; ANTIGENS, VIRAL; GASTROENTERITIS, TRANSMISSIBLE, OF SWINE; IMMUNOHISTOCHEMISTRY; INTERFERON-ALPHA; LEUKOCYTES; LYMPH NODES; MAJOR HISTOCOMPATIBILITY COMPLEX; MESENTERY; PEYER'S PATCHES; SWINE; TIME FACTORS; TISSUE DISTRIBUTION; TRANSMISSIBLE GASTROENTERITIS VIRUS;

EID: 0035229923     PISSN: 09284249     EISSN: None     Source Type: Journal    
DOI: 10.1051/vetres:2001111     Document Type: Article

References (30)

1. Artursson K., Lindersson M., Varela N., Scheynius A., Alm G.V., Interferon-alpha production and tissue localization of interferon-alpha/beta producing cells after intradermal administration of Aujeszky's disease virus-infected cells in pigs, Scand. J. Immunol. 41 (1995) 121-129.
2. Baudoux P., Carrat C., Besnardeau L., Charley B., Laude H., Coronavirus pseudoparticles formed with recombinant M and E proteins induce alpha interferon synthesis by leukocytes, J. Virol. 72 (1998) 8636-8643.
3. Belardelli F., Gresser I., The neglected role of type I interferon in the T-cell response: implications for its clinical use, Immunol. Today 17 (1996) 369-372.
4. Bogdan C., The function of type I interferons in antimicrobial immunity, Curr. Opin. Immunol. 12 (2000) 419-424.
5. Capobianchi M.R., Facchini J., Di Marco P., Antonelli G., Dianzani F., Induction of alpha interferon by membrane interaction between viral surface and peripheral blood mononuclear cells, Proc. Soc. Exp. Biol. Med. 178 (1985) 551-556.
6. Cella M., Jarrossay D., Facchetti F., Alebardi O., Nakajima H., Lanzavecchia A., Colonna M., Plasmacytoid monocytes migrate to inflamed lymph nodes and produce large amounts of type I interferon, Nat. Med. 5 (1999) 919-923.
7. Charley B., Laude H., Induction of alpha interferon by transmissible Gastroenteritis Coronavirus: role of transmembrane glycoprotein E1, J. Virol. 62 (1988) 8-11.
8. de Arce H.D., Artursson K., L'Haridon R., Perers A., La Bonnardière C., Aim G.V., A sensitive immunoassay for porcine interferon-α, Vet. Immunol. Immunopathol. 30 (1992) 319-327.
9. Eloranta M.L., Alm G.V., Splenic marginal metallophilic macrophages and marginal zone macrophages are the major interferon-alpha/beta producers in mice upon intravenous challenge with herpes simplex virus, Scand. J. Immunol. 49 (1999) 391-394.
10. Eloranta M.L., Sandberg K., Alm G.V., The interferon-alpha/beta responses of mice to herpes simplex virus studied at the blood and tissue level in vitro and in vivo, Scand. J. Immunol. 43 (1996) 356-360.
11. Fitzgerald-Bocarsly P., Human Natural Interferon-α producing cells, Pharmacol. Ther. 60 (1993) 39-62.
12. Gobi A.E., Funa K., Alm G.V., Different induction patterns of mRNA for IFN-alpha and -beta in human mononuclear leukocytes after in vitro stimulation with herpes simplex virus-infected fibroblasts and Sendai virus, J. Immunol. 140 (1988) 3605-3609.
13. Grage-Griebenow E., Flad H.D., Ernst M., Fc gamma receptor I (CD64)-negative human monocytes are potent accessory cells in viral antigen-induced T cell activation and exhibit high IFN-alpha-producing capacity, J. Leukocyte Biol. 60 (1996) 389-396.
14. Kadowaki N., Antonenko S., Lau J.Y., Liu Y.J., Natural interferon alpha/beta-producing cells link innate and adaptive immunity, J. Exp. Med. 192 (2000) 219-226.
15. La Bonnardière C., Laude H., High interferon titer in newborn pig intestine during experimentally induced viral enteritis, Infect. Immun. 32 (1981) 28-31.
16. Laude H., Chapsal J.M., Gelfi J., Labiau S., Grosclaude J., Antigenic structure of transmissible gastroenteritis virus. I. Properties of monoclonal antibodies directed against virion proteins, J. Gen. Virol. 67 (1986) 119-130.
17. Laude H., Gelfi J., Lavenant L., Charley B., Single amino acid changes in the viral glycoprotein M affect induction of alpha interferon by coronavirus TGEV, J. Virol. 66 (1992) 743-749.
18. Lebon P., Commoy-Chevalier M.J., Robert-Galliot B., Chany C., Different mechanisms for α and β interferon induction, Virology 119 (1982) 504-507.
19. Lunney J.K., Characterization of swine leukocyte differentiation antigens, Immunol. Today 14 (1993) 147-148.
20. McPherson G.G., Liu L.M., Dendritic cells and Langerhans cells in the uptake of mucosal antigens, Curr. Top. Microbiol. Immunol. 236 (1999) 33-53.
21. Muller U., Steinhoff U., Reis L.F.L., Hemmi S., Pavlovir J., Zinkernagel R.M., Aguet M., Functional role of type I and type II IFNs in antiviral defense, Science 264 (1994) 1918-1921.
22. Pensaert M., Haelterman E.O., Burnstein T., Transmissible gastroenteritis of swine: virus-intestinal cell interactions. I. Immunofluorescence, histopathology and virus production in the small intestine through the course of infection, Arch. Gesamte Virusforsch. 31 (1970) 321-334.
23. Riffault S., Eloranta M.L., Carrat C., Sandberg K., Charley B., Alm G., Herpes simplex virus induces appearance of interferon-alpha/beta-producing cells and partially interferon-alpha/beta-dependent accumulation of leukocytes in murine regional lymph nodes, J. Interferon Cytok. Res. 16 (1996) 1007-1014.
24. Riffault S., Carrat C., Besnardeau L., La Bonnardière C., Charley B., In vivo induction of interferon-α in pig by non-infectious coronavirus: tissue localization and in situ phenotypie characterization of interferon-α producing cells, J. Gen. Virol. 78 (1997) 2483-2487.
25. Siegal F.P., Kadowaki N., Shodell M., Fitzgerald-Bocarsly P.A., Shah K., Ho S., Antonenko S., Liu Y.J., The nature of the principal type 1 interferon-producing cells in human blood, Science 284 (1999) 1835-1837.
26. Splichal I., Bonneau M., Charley B., Ontogeny of interferon alpha secreting cells in the porcine fetal hernatopoietic organs, Immunol. Lett. 43 (1994) 203-208.
27. Splichal I., Rehakova Z., Sinkora M., Sinkora J., Trebichavsky I., Laude H., Charley B., In vivo study of interferon alpha secreting cells in pig fetal lymphohematopoietic organs following in utero TGEV coronavirus injection, Res. Immunol. 148 (1997) 241-250.
28. Svensson H., Johannisson A., Nikkila T., Aim G.V., Cederblad B., The cell surface phenotype of human natural interferon-alpha producing cells as determined by flow cytometry, Scand. J. Immunol. 44 (1996) 164-172.
29. Tomasi T.B., Introduction, an overview of the mucosal system, in: Ogra P.L., Mestecky J., Lamm M.E., Strober W., McGhee J.R., Bienenstock J. (Eds.), Handbook of mucosal immunology, Acad. Press, San Diego, 1994.
30. van den Broek M.F., Muller U., Huang S., Zinkernagel R.M., Aguet M., Immune defence in mice lacking type I and/or type II interferon receptors, Immunol. Rev. 148 (1995) 5-18.