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All issues Volume 33 / No 1 (January-February 2002) Vet. Res., 33 1 (2002) 1-12 References
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Vet. Res.
Volume 33, Number 1, January-February 2002
Page(s) 1 - 12
DOI https://doi.org/10.1051/vetres:2001001
How to cite this article Vet. Res. (2002) 1-12
  1. Burvenich C., Dosogne H., Detilleux J., van Werven T., Is it possible to predict the severity of acute mastitis during early lactation through measurement of the activity of circulating polymorphonuclear cells ? Proceedings Journées Nationales GTV-INRA, 1999, pp. 43-52.
  2. Butcher E.C., Picker L.J., Lymphocyte homing and homeostasis, Science 272 (1996) 60-66 [CrossRef].
  3. Croitoru K., Bienenstock J., Characteristics and functions of mucosa-associated lymphoid tissue, in: Ogra P.L., Lamm M.E., McGhee J.R., Mestecky J., Strober W., Bienenstock J. (Eds.), Handbook of Mucosal Immunology, Academic Press, San Diego, CA, 1994, pp. 414-449.
  4. Cullor J.S., J5 Escherichia coli: a core antigen vaccine for coliform mastitis, Coliform mastitis symposium proceedings, Washington State University, College of Veterinary Medicine, 1993, pp. 30-35.
  5. De Cueninck B.J., Immune-mediated inflammation in the lumen of the bovine mammary gland, Int. Arch. Allergy Appl. Immunol. 59 (1979) 394-402 [PubMed].
  6. Dosogne H., Burvenich C., van Werven T., Roets E., Noordhuizen-Stassen E.N., Goddeeris B., Increased surface expression of CD11b receptors on polymorphonuclear leukocytes is not sufficient to sustain phagocytosis during Escherichia coli mastitis in early postpartum dairy cows, Vet. Immunol. Immunopathol. 60 (1997) 47-59 [PubMed].
  7. Dosogne H., Burvenich C., Freeman A.E., Kehrli M.E. Jr., Detilleux J.C., Sulon J., Beckers J.-F., Hoeben D., Pregnancy-associated glycoprotein and decreased polymorphonuclear leukocyte function in early post-partum dairy cows, Vet. Immunol. Immunopathol. 67 (1999) 47-54 [PubMed].
  8. Frost A.J., Hill A.W., Brooker B.E., The early pathogenesis of bovine mastitis due to Escherichia coli, Proc. R. Soc. Lond. B. Biol. Sci. 209 (1980) 431-439 [PubMed].
  9. Ginaldi L., De Martinis M., D'Ostilio A., Marini L., Loreto M.F., Quaglino D., The immune system in the elderly: III. Innate immunity, Immunol. Res. 20 (1999) 117-126 [PubMed].
  10. Gonzales R.N., Cullor J.S., Jasper D.E., Farver T.B., Brushnell R.B., Oliver M.N., Prevention of clinical coliform mastitis in dairy cows by a mutant Escherichia coli vaccine, Can. J. Vet. Res. 53 (1989) 301-305 [PubMed].
  11. Greisman S.E., Johnston C.A., Failure of antisera to J5 and R595 rough mutants to reduce endotoxemic lethality, J. Infect. Dis. 157 (1988) 54-64 [PubMed].
  12. Guidry A.J., O'Brien C.N., Current awareness of bovine mammary gland immunology, Flem. Vet. J. Suppl. 66 (1997) 341-358.
  13. Heyneman R., Burvenich C., Vercauteren R., Interaction between the respiratory burst activity of neutrophil leukocytes and experimentally induced Escherichia coli mastitis in cows, J. Dairy Sci. 73 (1990) 985-994 [PubMed].
  14. Hill A.W., Factors influencing the outcome of Escherichia coli mastitis in the dairy cow, Res. Vet. Sci. 31 (1981) 107 [PubMed].
  15. Hill A.W., Vaccination of cows with rough Escherichia coli mutants fails to protect against experimental intramammary bacterial challenge, Vet. Res. Commun. 15 (1991) 7 [CrossRef] [PubMed].
  16. Hoeben D., Monfardini E., Opsomer G., Burvenich C., Dosogne H., De Kruif A., Beckers J.-F., Chemiluminescence of bovine polymorphonuclear leukocytes during the periparturient period and relation with metabolic markers and bovine pregnancy-associated glycoprotein, J. Dairy Res. 67 (2000) 249-259 [CrossRef] [PubMed].
  17. Hogan J.S., Todhunter D.A., Tomita G.M., Smith K.L., Schoenberger P.S., Opsonic activity of bovine serum and mammary secretion after Escherichia coli J5 vaccination, J. Dairy Sci. 75 (1992) 72-77 [PubMed].
  18. Hogan J.S., Weiss W.P., Todhunter D.A., Smith K.L., Schoenberger P.S., Efficacy of an Escherichia coli J5 mastitis vaccine in an experimental challenge trial, J. Dairy Sci. 75 (1992) 415-422 [PubMed].
  19. Hogan J.S., Weiss W.P., Smith K.L., Todhunter D.A., Schoenberger P.S., Effects of an Escherichia coli J5 vaccine on mild clinical coliform mastitis, J. Dairy Sci. 78 (1995) 285-290 [PubMed].
  20. Hogan J.S., Smith K.L., Schoenberger P., Roming S., Thompson L., Antibody titer responses to intramammary immunization with Escherichia coli J5 bacterin, J. Dairy Sci. 80 (1997) 2398-2402 [PubMed].
  21. Hogan J.S., Bogacz V.L., Aslam M., Smith K.L., Efficacy of an Escherichia coli J5 bacterin administered to primigravid heifers, J. Dairy Sci. 82 (1999) 939-943 [PubMed].
  22. Kimura K., Goff J.P., Kehrli M.E. Jr., Effects of the presence of the mammary gland on expression of neutrophil adhesion molecules and myeloperoxidase activity in periparturient dairy cows, J. Dairy Sci. 82 (1999) 2385-2392 [PubMed].
  23. Kremer W.D.J., Noordhuizen-Stassen E.N., Grommers F.J., Daemen A.J.J.M., Henricks P.A.J., Burvenich C., Brand A., Preinfection chemotactic response of blood polymorphonuclear leukocytes to predict severity of Escherichia coli bovine mastitis, J. Dairy Sci. 76 (1993) 1568-1574 [PubMed].
  24. Lacey-VanKampen C., Mallard B.A., Effects of peripartum stress and disease on bovine lymphocyte subsets, Vet. Immunol. Immunopathol. 59 (1998) 79-92.
  25. Lammers A., van Vorstenbosch C.J., Erkens J.H.F., Smith H.E., The major bovine pathogens have different cell tropisms in cultures of bovine mammary gland cells, Vet. Microbiol. 80 (2001) 255-265 [CrossRef] [PubMed].
  26. Lipman L.J., de Nijs A., Lam T.J., Gaastra W., Identification of Escherichia coli strains from cows with clinical mastitis by serotyping and DNA polymorphism patterns with REP and ERIC primers, Vet. Microbiol. 43 (1995) 13-19 [CrossRef] [PubMed].
  27. Macatonia S.E., Hsieh C.S., Murphy K.M., O'Garra A., Dendritic cells and macrophages are required for Th1 development of CD4+ T cells from alpha beta TCR transgenic mice: IL-12 substitution for macrophages to stimulate IFN-gamma production is IFN-gamma-dependent, Int. Immunol. 5 (1993) 1119-1128 [CrossRef] [PubMed].
  28. Mackay C.R., Andrew D.P., Briskin M., Ringler D.J., Butcher E.C., Phenotype and migration properties of three major subsets of tissue homing T cells, Eur. J. Immunol. 26 (1996) 2433-2439 [PubMed].
  29. Mallard B.A., Wagter L.C., Ireland M.J., Dekkers J.C.M., Effects of growth hormone, insulin-like growth factor I and cortisol on periparturient antibody response profiles of dairy cattle, Vet. Immunol. Immunopathol. 60 (1997) 61-76 [PubMed].
  30. Mallard B.A., Dekkers J.C., Ireland M.J., Leslie K.E., Sharif S., Lacey Vankampen C., Wagter L., Wilkie B.N., Alteration in immune responsiveness during the peripartum period and its ramification on dairy cow and calf health, J. Dairy Sci. 81 (1998) 585-595 [PubMed].
  31. Morris D.D., Cullor J.S., Whitlock R.H., Wickstrom M., Corbeil L.B., Endotoxemia in neonatal calves given antiserum to a mutant Escherichia coli (J5), Am. J. Vet. Res. 47 (1986) 2554-2565 [PubMed].
  32. Nickerson S.C., Pankey J.W., Boddie N.T., Distribution, location, and ultrastructure of plasma cells in the uninfected, lactating bovine mammary gland, J. Dairy Res. 51 (1984) 209-217 [PubMed].
  33. Park Y.H., Fox L.K., Hamilton M.J., Davis W.C., Bovine mononuclear leukocyte subpopulations in peripheral blood and mammary gland secretions during lactation, J. Dairy Sci. 75 (1992) 998-1006 [PubMed].
  34. Parsons K.R., Howard C.J., Jones B.V., Sopp P., Investigation of bovine gut associated lymphoid tissue (GALT) using monoclonal antibodies against bovine lymphocytes, Vet. Pathol. 26 (1989) 396-408 [PubMed].
  35. Persson K., Carlsson A., Hambleton C., Guidry A.J., Immunoglobulins, lysozyme and lactoferrin in the teat and udder of the dry cow during endotoxin-induced inflammation, J. Vet. Med. B 39 (1992) 165-174.
  36. Rebelatto M.C., Mead C., HogenEsch H., Lymphocyte populations and adhesion molecule expression in bovine tonsils, Vet. Immunol. Immunopathol. 73 (2000) 15-29 [PubMed].
  37. Renjifo X., Howard C., Kerkhofs P., Denis M., Urbain J., Moser M., Pastoret P.P., Purification and characterization of bovine dendritic cells from peripheral blood, Vet. Immunol. Immuno- pathol. 60 (1997) 77-88.
  38. Rieser C., Ramoner R., Holtl L., Rogatsch H., Papesh C., Stenzl A., Bartsch G., Thurnher M., Mature dendritic cells induce T-helper type-1-dominant immune responses in patients with metastatic renal cell carcinoma, Urol. Int. 63 (2000) 151-159 [CrossRef].
  39. Riollet C., Rainard P., Poutrel B., Kinetics of cells and cytokines during immune-mediated inflammation in the mammary gland of cows systemically immunized with Staphylococcus aureus $\alpha$-toxin, Inflamm. Res. 49 (2000) 486 [CrossRef] [PubMed]- 496.
  40. Salmon H., Mammary gland immunology and neonate protection in pigs, in: Mol J.A., Clegg R.A. (Eds.), Biology of the mammary gland, Kluwer Academic / Plenum Publishers, New York, 2000, pp. 279-286.
  41. Sanchez-Carlo V., Wilson R.A., McDonald J.S., Packer R.A., Biochemical and serologic properties of Escherichia coli isolated from cows with acute mastitis, Am. J. Vet. Res. 45 (1984) 1771-1774 [PubMed].
  42. Satoshi H., Suzuki-Miki K., Takeyoshi I., Maki I., Takashi K., Nobuhisa N., Yamamoto-Noriko T., Meijin T., Effects of paternal lymphocyte immunization on peripheral Th1/Th2 balance and TCR Vbeta and Vgamma repertoire usage of patients with recurrent spontaneous abortions, Am. J. Reprod. Immunol. 43 (2000) 107-115 [PubMed].
  43. Schuhbauer D.M., Mitchison N.A., Mueller B., Interaction within clusters of dendritic cells and helper T cells during initial Th1/Th2 commitment, Eur. J. Immunol. 30 (2000) 1255-1262 [PubMed].
  44. Shafer-Weaver K.A., Corl C.M., Sordillo L.M., Shifts in bovine CD4+ subpopulations increase T-helper-2 compared with T-helper-1 effector cells during the postpartum period, J. Dairy Sci. 82 (1999) 1696-1706 [PubMed].
  45. Smith J.L., Hogan J.S., Smith K.L., Efficacy of intramammary immunization with an Escherichia coli J5 bacterin, J. Dairy Sci. 82 (1999) 2582-2588 [PubMed].
  46. Soltys J., Quinn M., Selective recruitment of T-cell subsets to the udder during Staphylococcal and Streptococcal mastitis: analysis of lymphocyte subsets and adhesion molecule expression, Infect. Immun. 67 (1999) 6293-6302 [PubMed].
  47. Sordillo L.M., Peel J.E., Effect of interferon-) on the production of tumor necrosis factor during acute Escherichia coli mastitis, J. Dairy Sci. 75 (1992) 2119-2125 [PubMed].
  48. Taylor B.C., Dellinger J.D., Cullor J.S., Stott J.L., Bovine milk lymphocytes display the phenotype of memory T cells and are predominantly CD8+, Cell. Immunol. 156 (1994) 245-253 [CrossRef] [PubMed].
  49. Tomita G.M., Nickerson S.C., Owens W.E., Wren B., Influence of route of vaccine administration against experimental intramammary infection caused by Escherichia coli, J. Dairy Sci. 81 (1998) 2159-2164 [PubMed].
  50. Tomita G.M., Ray C.H., Nickerson S.C., Owens W.E., Gallo G.F., A comparison of two commercially available Escherichia coli J5 vaccines against E. coli intramammary challenge, J. Dairy Sci. 83 (2000) 2276-2281 [PubMed].
  51. Tyler J.W., Cullor J.S., Osburn B.I., Bushnell R.B., Fenwick B.W., Relationship between serologic recognition of Escherichia coli O111: B4 (J5) and clinical coliform mastitis in cattle, Am. J. Vet. Res. 49 (1988) 1950-1954 [PubMed].
  52. Tyler J.W., Cullor J.S., Thurmond M.C., Douglas V.L., Dellinger J.D., Humoral response in neonatal calves following immunization with Escherichia coli (strain J5): the effects of adjuvant, age and colostral passive interference, Vet. Immunol. Immunopathol. 23 (1989) 333-344 [PubMed].
  53. Tyler J.W., Cullor J.S., Spier S.J., Smith B.P., Immunity targeting common core antigens of Gram-negative bacteria, J. Vet. Int. Med. 4 (1990) 17-25.
  54. Vandeputte-Van Messom G., Burvenich C., Roets E., Massart-Leën A.-M., Heyneman R., Kremer W.D.J., Brand A., Classification of newly calved cows into moderate and severe responders to experimentally induced Escherichia coli mastitis, J. Dairy Res. 60 (1993) 19-29 [PubMed].
  55. Van Werven T., Noordhuizen-Stassen E.N., Daemen A.J.J.M., Schukken Y.H., Brand A., Burvenich C., Preinfection in vitro chemotaxis, phagocytosis, oxidative burst, and expression of CD11/CD18 receptors and their predictive capacity on the outcome of mastitis induced in dairy cows with Escherichia coli, J. Dairy Sci. 80 (1997) 67-74 [PubMed].
  56. Wagter L.C., Mallard B.A., Dekkers J.C.M., Leslie K.E., Wilkie B.N., Characterization of immune responsiveness and disease occurrence during the peripartum period. J. Dairy Sci. 79 Suppl. 1 (1996) 119 (abstr.).
  57. Washington E.A., Katerelos M., Cahill R.N.P., Kimpton W.G., Differences in the tissue-specific homing of $\alpha\beta$ and $\gamma\delta$ T cells to gut and peripheral lymph nodes, Int. Immunol. 6 (1994) 1891-1897 [CrossRef] [PubMed].
  58. Wegmann T.G., Lin H., Guilbert L., Mosmann T.R., Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a Th2 phenomenon ? Immunol. Today 14 (1993) 353-356 [CrossRef] [PubMed].
  59. Young Y.H., Sheep immunology and goat peculiarities. Leukocyte migration, in: Pastoret P.P., Griebel P., Bazin H., Govaerts A. (Eds.), Handbook of Vertebrate Immunology, Academic Press, London, 1998, pp. 493-496.