Free Access
Reprod. Nutr. Dev.
Volume 43, Number 5, September-October 2003
Page(s) 439 - 457
References of  Reprod. Nutr. Dev. 43 (2003) 439-457
  1. Bramley AJ. Mastitis: physiology or pathology. Flem Vet J 1991, 62 Suppl. 1: 3-11.
  2. Waite R, Blackburn PS. The chemical composition and the cell count of milk. J Dairy Res 1957, 24: 328-339.
  3. Djabri B, Bareille N, Beaudeau F, Seegers H. Quarter milk somatic cell count in infected dairy cows: a meta-analysis. Vet Res 2002, 33: 335-357.
  4. Lee CS, Wooding FB, Kemp P. Identification, properties, and differential counts of cell populations using electron microscopy of dry cows secretions, colostrum and milk from normal cows. J Dairy Res 1980, 47: 39-50 [PubMed].
  5. Craven N. Generation of neutrophil chemoattractants by phagocytosing bovine mammary macrophages. Res Vet Sci 1983, 35: 310-317.
  6. Concha C, Holmberg O, Astrom G. Cells found in non-infected and staphylococcus-infected bovine mammary quarters and their ability to phagocytose fluorescentmicrospheres. Zentralbl Veterinarmed B 1986, 33: 371-378.
  7. Miller RH, Paape MJ, Fulton LA. Variation in milk somatic cells of heifers at first calving. J Dairy Sci 1991, 74: 3782-3790.
  8. Sordillo LM, Shafer-Weaver K, DeRosa D. Immunobiology of the mammary gland. J Dairy Sci 1997, 80: 1851-1865.
  9. Manlongat N, Yang TJ, Hinckley LS, Bendel RB, Krider HM. Physiologic-chemoattractantinduced migration of polymorphonuclear leukocytes in milk. Clin Diagn Lab Immunol 1998, 5: 375-381.
  10. Paape MJ, Guidry AJ. Effect of milking on leukocytes in the subcutaneous abdominal vein of the cow. J Dairy Sci 1969, 52: 998-1002.
  11. Hill AW. Somatic cells - Friends of foes? Flem Vet J 1991, 62 Suppl 1: 217-232.
  12. Riollet C, Rainard P, Poutrel B. Cell subpopulations and cytokine expression in cowmilk in response to chronic Staphylococcus aureus infection. J Dairy Sci 2001, 84: 1077-1084 [PubMed].
  13. Newbould FHS, Neave FK. The response of the bovine mammary gland to an infusion of staphylococci. J. Dairy Res 1965, 32: 163-170.
  14. Le Gall A, Plommet M. Observations sur la croissance des staphylocoques et la réaction leucocytaire au cours des premières heures de la mammite expérimentale de la brebis. Ann Biol Anim Biochim Biophys 1965, 5: 113-130.
  15. Shuster DE, Lee EK, Kehrli ME Jr. Bacterial growth, inflammatory cytokine production, and neutrophil recruitment during coliform mastitis in cows within ten days after calving, compared with cows at midlactation. Am J Vet Res 1996, 57: 1569-1575 [PubMed].
  16. Rainard P, Lautrou Y, Sarradin P, Coulibaly A, Poutrel B. The kinetics of inflammation and phagocytosis during bovine mastitis induced by Streptococcus agalactiae bearing the protein X. Vet Res Commun 1991, 15: 163-176 [PubMed].
  17. Vandeputte-Van Messom G, Burvenich C, Roets E, Massart-Leen AM, Heyneman R, Kremer WD, Brand A. Classification of newly calved cows into moderate and severe responders to experimentally induced Escherichia coli mastitis. J Dairy Res 1993, 60: 19-29 [PubMed].
  18. Hill AW. Factors influencing the outcome of Escherichia coli mastitis in the dairy cow. Res Vet Sci 1981, 31: 107-112.
  19. Colditz I, Watson D. Effect of immunisation on the early influx of neutrophils during staphylococcal mastitis in ewes. Res Vet Sci 1982, 33: 146-151.
  20. Jain NC, Schalm OW, Lasmanis J. Experimentally induced coliform (Aerobacter aerogenes) mastitis in normal cows and in cows made neutropenic by an equine anti-bovine leukocyte serum. Am J Vet Res 1971, 32: 1929-1935 [PubMed].
  21. SchalmOW, Lasmanis J, JainNC. Conversion of chronic staphylococcal mastitis to acute gangrenous mastitis after neutropenia in blood and bone marrow produced by an equine anti-bovine leukocyte serum. Am J Vet Res 1976, 37: 885-890.
  22. Daley MJ, Oldham ER, Williams TJ, Coyle PA. Quantitative and qualitative properties of host polymorphonuclear cells during experimentally induced Staphylococcus aureus mastitis in cows. Am J Vet Res 1991, 52: 474-479 [PubMed].
  23. Schalm OW, Lasmanis J, Carroll E. Effect of pre-existing leukocytosis on experimental coliform (Aerobacter aerogenes) mastitis in cattle. Am J Vet Res 1964, 25: 83-89 [PubMed].
  24. SchalmOW, Lasmanis J, Carroll EJ. Experimental Streptococcus agalactiae mastitis in cattle: attempts to superimpose the organism in lactating glands harboring unrelated bacterial infections and in glands with experimentally induced sterile inflammation. Am J Vet Res 1967, 28: 685-695 [PubMed].
  25. Schalm OW, Carroll EJ, Lasmanis J. The leukocyte barrier and serologic investigations of experimental coliform (Aerobacter aerogenes) mastitis in cattle.AmJVetRes 1964, 25: 90-96.
  26. Dosogne H, Vangroenweghe F, Barrio B, Rainard P, Burvenich C. Decreased number and bactericidal activity against Staphylococcus aureus of the resident cells in milk of dairy cows during early lactation. J Dairy Res 2001, 68: 539-549 [CrossRef] [PubMed].
  27. Sandgren CH, Nordling K, Bjork I. Isolation and phagocytic properties of neutrophils and other phagocytes from nonmastitic bovine milk. J Dairy Sci 1991, 74: 2965-2975.
  28. Mehrzad J, Dosogne H, Meyer E, Heyneman R, Burvenich C. Respiratory burst activity of blood andmilk neutrophils in dairy cows during different stages of lactation. J Dairy Res 2001, 68: 399-415.
  29. Linde C, Holmberg O, Astrom G. The interference between coagulase negative staphylococci and Corynebacterium bovis and the common udder pathogens in the lactating cow. Nord Vet Med 1980, 32: 552-558 [PubMed].
  30. Bramley AJ. The effect of subclinical Staphylococcus epidermidis infection of the lactating bovine udder on its susceptibility to infection with Streptococcus agalactiae or Escherichia coli. Br Vet J 1978, 134: 146-151.
  31. Rainard P, Poutrel B. Effect of naturally occurring intramammary infections by minor pathogens on new infections by major pathogens in cattle. Am J Vet Res 1988, 49: 327-329.
  32. Poutrel B, Lerondelle C. Protective effect in the lactating bovine mammary gland induced by coagulase negative staphylococci against experimental Staphylococcus aureus infections. Ann Rech Vét 1980, 11: 327-332 [PubMed].
  33. Paape MJ, Wergin WP, Guidry AJ, Schultze WD. Phagocytic defense of the ruminant mammary gland. Adv Exp Med Biol 1981, 137: 555-578.
  34. Paape MJ, Schultze WD, Guidry AJ, Kortum WM, Weinland BT. Effect of an intramammary polyethylene device on the concentration of leukocytes and immunoglobulins in milk and on the leukocyte response to Escherichia coli endotoxin and challenge exposure with Staphylococcus aureus. Am J Vet Res 1981, 42: 774-783 [PubMed].
  35. Brooks BW, Barnum DA. The use of polyethylene intramammary device in protection of the lactating bovine udder against experimental infection with Staphylococcus aureus or Streptococcus agalactiae. Can J Comp Med 1982, 46: 267-269 [PubMed].
  36. Corlett NJ, Peters RR, Paape MJ, Schultze WD. Effect of intramammary device on new infection rate, milk yield, and milk somatic cell counts in Maryland dairy herds. J Dairy Sci 1984, 67: 2571-2579 [PubMed].
  37. CorlettNJ, PaapeMJ, King RL. Effect of surface and composition of intramammary device on stripping milk somatic cell count. J Dairy Sci 1983, 66 (Suppl 1): 204-205.
  38. Bright SA, Schultze WD, Paape MJ, Peters RR. Effect of intramammary devices on the outcome of induced Escherichia coli infection of bovine mammary quarters. Am J Vet Res 1987, 48: 1290-1294 [PubMed].
  39. Postle DS, Roguinsky M, Poutrel B. Induced staphylococcal infections in the bovine mammary gland. Am J Vet Res 1978, 39: 29-35.
  40. Serieys F. Relation entre concentration cellulaire du lait individuel, production laitière, et sensibilité des vaches aux infections mammaires. Ann Rech Vet 1985, 16: 271-277 [PubMed].
  41. Hill AW, Shears AL, Hibbitt KG. The pathogenesis of experimental Escherichia coli mastitis in newly calved dairy cows. Res Vet Sci 1979, 26: 97-101 [PubMed].
  42. De Cueninck BJ. Immune-mediated inflammation in the lumen of the bovine mammary gland. Int Arch Allergy Appl Immunol 1979, 59: 394-402.
  43. Herbelin C, Poutrel B, Gilbert FB, Rainard P. Immune recruitment and bactericidal activity of neutrophils in milk of cows vaccinated with staphylococcal alpha-toxin. J Dairy Sci 1997, 80: 2025-2034.
  44. Rainard P. Experimental mastitis with Escherichia coli: sequential response of leukocytes and opsonic activity in milk of immunised and unimmunised cows. Ann Rech Vet 1983, 14: 281-286.
  45. 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 1990, 73: 985-994 [PubMed].
  46. Lohuis JA, Schukken YH, Henricks PA, Heyneman R, Burvenich C, Verheijden JH, Van Miert AS, Brand A. Preinfection functions of blood polymorphonuclear leukocytes and the outcome of experimental Escherichia coli mastitis in the cow. J Dairy Sci 1990, 73: 342-350 [PubMed].
  47. Kremer WD, Noordhuizen-Stassen EN, Grommers FJ, Daemen AJ, Henricks PA, Brand A, Burvenich C. Preinfection chemotactic response of blood polymorphonuclear leukocytes to predict severity of Escherichia coli mastitis. J Dairy Sci 1993, 76: 1568-1574 [PubMed].
  48. Van Werven T, Noordhuizen-Stassen EN, Daemen AJ, Schukken YH, 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 1997, 80: 67-74 [PubMed].
  49. Suriyasathaporn W, Heuer C, Noordhuizen- Stassen EN, Schukken YH. Hyperketonemia and the impairment of udder defense: a review. Vet Res 2000, 31: 397-412.
  50. Beaudeau F, Fourichon C, SeegersH, Bareille N. Risk of clinical mastitis in dairy herds with a high proportion of low individual milk somaticcell counts. Prev Vet Med 2002, 53: 43-54.
  51. Suriyasathaporn W, Schukken YH, Nielen M, Brand A. Low somatic cell count: a risk factor for subsequent clinical mastitis in a dairy herd. J Dairy Sci 2000, 83: 1248-1255.
  52. Rainard P, Poutrel B. Dynamics of nonclinical bovine intramammary infections with major and minor pathogens. Am J Vet Res 1982, 43: 2143-2146.
  53. Paape MJ, Wergin WP, Guidry AJ, Pearson RE. Leukocytes-second line of defense against invading mastitis pathogens. J Dairy Sci 1979, 62: 135-153.
  54. Russell MW, Reiter B. Phagocytic deficiency of bovine milk leucocytes: an effect of casein. J Reticuloendothel Soc 1975, 18: 1-13.
  55. Mehrzad J, Duchateau L, Pyorala S, Burvenich C. Blood and milk neutrophil chemiluminescence and viability in primiparous and pluriparous dairy cows during late pregnancy, around parturition and early lactation. J Dairy Sci 2002, 85: 3268-3276 [PubMed].
  56. Newbould FH. The effect of added serum and glucose, and some inherent factors, on phagocytosis in vitro by milk leukocytes from several cows. Can J Comp Med 1973, 37: 189-194 [PubMed].
  57. Goldberg JJ, Pankey JW, Politis I, Zavizion B, Bramley AJ. Effect of oxygen tension on killing of Escherichia coli by bovine polymorphonuclear neutrophil leucocytes in vitro. J Dairy Res 1995, 62: 331-338 [PubMed].
  58. Craven N,Williams MR. Defences of the bovine mammary gland against infection and prospects for their enhancement. Vet Immunol Immunopathol 1985, 10: 71-127.
  59. Jain NC, Lasmanis J. Phagocytosis of serum-resistant and serum-sensitive coliform bacteria (Klebsiella) by bovine neutrophils from blood and mastitic milk. Am J Vet Res 1978, 39: 425-427 [PubMed].
  60. Newbould FH. Enhancement of phagocytosis in bovine milk leukocytes in vitro. Can J Comp Med 1970, 34: 261-264.
  61. Guidry AJ, Paape MJ, Pearson RE, Williams WF. Effect of local immunization of the mammary gland on phagocytosis and intracellular kill of Staphylococcus aureus by polymorphonuclear neutrophils. AmJVetRes 1980, 41: 1427-1431.
  62. Hill AW, Heneghan DJ, Field TR,Williams MR. Increase in specific opsonic activity in bovine milk following experimental Escherichia coli mastitis. Res Vet Sci 1983, 35: 222-226 [PubMed].
  63. Jain NC, Jasper DE, Dellinger JD. Experimental bovine mastitis due to mycoplasma. Cornell Vet 1969, 59: 10-28.
  64. Howard CJ, Taylor G, Collins J, Gourlay RN. Interaction of Mycoplasma dispar and Mycoplasma agalactiae subsp. bovis with bovine alveolar macrophages and bovine lacteal polymorphonuclear leukocytes. Infect Immun 1976, 14: 11-17 [PubMed].
  65. Rainard P, Poutrel B. Deposition of complement components on Streptococcus agalactiae in bovine milk in the absence of inflammation. Infect Immun 1995, 63: 3422-3427 [PubMed].
  66. Paape MJ, Guidry AJ, Kirk ST, Bolt DJ. Measurement of phagocytosis of 32P-labeled Staphylococcus aureus by bovine leukocytes: lysostaphin digestion and inhibitory effect of cream. Am J Vet Res 1975, 36: 1737-1743 [PubMed].
  67. PaapeMJ, Guidry AJ. Effect of fat and casein on intracellular killing of Staphylococcus aureus by milk leukocytes. Proc Soc Exp Biol Med 1977, 155: 588-593 [PubMed].
  68. Russell MW, Brooker BE, Reiter B. Inhibition of the bactericidal activity of bovine polymorphonuclear leucocytes and related systems by casein. Res Vet Sci 1976, 20: 30-35.
  69. Cooray R. Casein effects on the myeloperoxidase- mediated oxygen-dependent bactericidal activity of bovine neutrophils. Vet Immunol Immunopathol 1996, 51: 55-65.
  70. Hill AW, Heneghan DJ, Williams MR. The opsonic activity of bovine milk whey for the phagocytosis and killing by neutrophils of encapsulated and non-encapsulated Escherichia coli. Vet Microbiol 1983, 8: 293-300 [CrossRef] [PubMed].
  71. Leigh JA, Field TR. Killing of Streptococcus uberis by bovine neutrophils following growth in chemically defined media. Vet Res Commun 1991, 15: 1-6 [PubMed].
  72. Ward PN, Field TR, Ditcham WG, Maguin E, Leigh JA. Identification and disruption of two discrete loci encoding hyaluronic acid capsule biosynthesis genes hasA, hasB, and hasC in Streptococcus uberis. Infect Immun 2001, 69: 392-399 [CrossRef] [PubMed].
  73. Brownlie J, Howard CJ, Gourlay RN. The effect of an intramammary infusion of endotoxin on experimentally induced mycoplasmal mastitis. J Hyg (Lond) 1979, 83: 501-505.
  74. Schuberth HJ, Krueger C, Zerbe H, Bleckmann E, Leibold W. Characterization of leukocytotoxic and superantigen-like factors produced by Staphylococcus aureus isolates from milk of cows with mastitis. Vet Microbiol 2001, 82: 187-199 [CrossRef] [PubMed].
  75. Loeffler DA, Schat KA, Norcross NL. Use of 51Cr release to measure the cytotoxic effects of staphylococcal leukocidin and toxin neutralization on bovine leukocytes. J Clin Microbiol 1986, 23: 416-420.
  76. Grootenhuis G. Mastitis prevention by selection of sires. Vet Rec 1981, 108: 258-260.
  77. Grootenhuis G. The difference in hereditary susceptibility to three mastitis agents between two daughter groups. Tijdschr Diergeneeskd 1976, 101: 779-786.
  78. Smith JA. Neutrophils, host defense, and inflammation: a double-edged sword. J Leukoc Biol 1994, 56: 672-686 [PubMed].
  79. Leijh PC, van den Barselaar MT, van Zwet TL, Dubbeldeman-Rempt I, van Furth R. Kinetics ofphagocytosis of Staphylococcus aureus and Escherichia coli by human granulocytes. Immunology 1979, 37: 453-465 [PubMed].
  80. Brown EJ. The role of extracellular matrix proteins in the control of phagocytosis. J Leukoc Biol 1986, 39: 579-591.
  81. Lee DA, Hoidal JR, Clawson CC, Quie PG, Peterson PK. Phagocytosis by polymorphonuclear leukocytes of Staphylococcus aureus and Pseudomonas aeruginosa adherent to plastic, agar, or glass. J Immunol Methods 1983, 63: 103-114 [CrossRef] [PubMed].
  82. Rainard P. Assessment by a fluorochrome microassay of phagocytic killing of group B streptococci adherent to glass. J Immunol Methods 1986, 94: 113-118.
  83. Rainard P. Involvement of locomotion of granulocytes in the phagocytosis of glass-adherent group B streptococci in the absence of opsonins. FEMS Microbiol Lett 1988, 49: 309-315.
  84. Hensen SM, Pavicic MJ, Lohuis JA, de Hoog JA, Poutrel B. Location of Staphylococcus aureus within the experimentally infected bovine udder and the expression of capsular polysaccharide type 5 in situ. J Dairy Sci 2000, 83: 1966-1975 [PubMed].
  85. Hallett MB, Lloyds D. Neutrophil priming: the cellular signals that say `amber' but not `green'. Immunol Today 1995, 16: 264-268.
  86. Steinbeck MJ, Roth JA. Neutrophil activation by recombinant cytokines. Rev Infect Dis 1989, 11: 549-568.
  87. Daley MJ, Coyle PA, Williams TJ, Furda G, Dougherty R,HayesPW. Staphylococcus aureus mastitis: pathogenesis and treatment with bovine interleukin-1 beta and interleukin-2. J Dairy Sci 1991, 74: 4413-4424 [PubMed].
  88. Leigh JA, Field TR. Streptococcus uberis resists the bactericidal action of bovine neutrophils despite the presence of bound immunoglobulin. Infect Immun 1994, 62: 1854-1859 [PubMed].
  89. Persson K, Sandgren CH, Rodriguez-Martinez H. Studies of endotoxin-induced neutrophil migration in bovine teat tissues, using indium-111- labeled neutrophils and biopsies. Am J Vet Res 1992, 53: 2235-2240 [PubMed].
  90. McCormick B, Gewirtz AT, Madara JL. Epithelial crosstalk with bacteria and immune cells. Curr Opin Gastroenterol 1998, 14: 492-497.
  91. Eckmann L, Kagnoff MF, Fierer J. Epithelial cells secrete the chemokine interleukin-8 in response to bacterial entry. Infect Immun 1993, 61: 4569-4574.
  92. McCormick BA, Colgan SP, Delp-Archer C, Miller SI, Madara JL. Salmonella typhimurium attachment to human intestinal epithelial monolayers: transcellular signalling to subepithelial neutrophils. J Cell Biol 1993, 123: 895-907 [PubMed].
  93. McCormick BA, Hofman PM, Kim J, Carnes DK, Miller SI, Madara JL. Surface attachment of Salmonella typhimurium to intestinal epithelia imprints the subepithelial matrix with gradients chemotactic for neutrophils. J Cell Biol 1995, 131: 1599-1608 [PubMed].
  94. Hogg N. A model of leukocyte adhesion to vascular endothelium. Curr TopMicrobiol Immunol 1993, 184: 79-86.
  95. Jung HC, Eckmann L, Yang SK, Panja A, Fierer J, Morzycka-Wroblewska E,KagnoffMF.Adistinct array of proinflammatory cytokines is expressed in human colon epithelial cells in response to bacterial invasion. J Clin Invest 1995, 95: 55-65 [PubMed].
  96. Boudjellab N, Chan-Tang HS, Li X, Zhao X. Interleukin 8 response by bovine mammary epithelial cells to lipopolysaccharide stimulation. Am J Vet Res 1998, 59: 1563-1567.
  97. Nickerson SC, Heald CW. Cells in local reaction to experimental Staphylococcus aureus infection in bovine mammary gland. J Dairy Sci 1982, 65: 105-116 [PubMed].
  98. Jain NC, Schalm OW, Carroll EJ, Lasmanis J. Experimental mastitis in leukopenic cows: immunologically induced neutropenia and response to intramammary inoculation of Aerobacter aerogenes. Am J Vet Res 1968, 29: 2089-2097 [PubMed].
  99. Cassatella MA. The production of cytokines by polymorphonuclear neutrophils. Immunol Today 1995, 16: 21-26.
  100. Jain NC, Schalm OW, Carroll EJ, Lasmanis J. Leukocytes and tissue factors in the pathogenesis of bovine mastitis. Am J Vet Res 1972, 33: 1137-1145.
  101. Carroll EJ, Mueller R, Panico L. Chemotactic factors for bovine leukocytes. Am J Vet Res 1982, 43: 1661-1664.
  102. Gray GD, Knight KA, Nelson RD, Herron MJ. Chemotactic requirements of bovine leukocytes. Am J Vet Res 1982, 43: 757-759.
  103. Issekutz AC. Effect of vasoactive agents on polymorphonuclear leukocyte emigration in vivo. Lab Invest 1981, 45: 234-240.
  104. Giri SN, Chen Z, Carroll EJ, Mueller R, Schiedt MJ, Panico L. Role of prostaglandins in pathogenesis of bovine mastitis induced by Escherichia coli endotoxin. Am J Vet Res 1984, 45: 586-591 [PubMed].
  105. Rose DM, Giri SN,Wood SJ, Cullor JS. Role of leukotriene B4 in the pathogenesis of Klebsiella pneumoniae-induced bovine mastitis. Am J Vet Res 1989, 50: 915-918 [PubMed].
  106. Craven N. Chemotactic factors for bovine neutrophils in relation to mastitis. Comp Immunol Microbiol Infect Dis 1986, 9: 29-36.
  107. Persson K, Larsson I, Hallen SC. Effects of certain inflammatory mediators on bovine neutrophil migration in vivo and in vitro. Vet Immunol Immunopathol 1993, 37: 99-112.
  108. Persson K, Colditz IG, Flapper P, Franklin NA, Seow HF. Cytokine-induced inflammation in the ovine teat and udder. Vet Immunol Immunopathol 1996, 53: 73-85.
  109. Colditz IG, Maas PJ. The inflammatory activity of activated complement in ovine and bovine mammary glands. Immunol Cell Biol 1987, 65: 433-436.
  110. Rainard P. Bovine milk fat globules do not inhibit C5a chemotactic activity. Vet Res 2002, 33: 413-419.
  111. Shuster DE, Kehrli ME Jr, Rainard P, Paape M. Complement fragment C5a and inflammatory cytokines in neutrophil recruitment during intramammary infection with Escherichia coli. Infect Immun 1997, 65: 3286-3292 [PubMed].
  112. Rainard P, Sarradin P, Paape MJ, Poutrel B. Quantification of C5a/C5a(desArg) in bovine plasma, serum and milk. Vet Res 1998, 29: 73-88 [PubMed].
  113. Hisaeda K, Hagiwara K, Eguchi J, Yamanaka H, Kirisawa R, Iwai H. Interferon-gamma and tumor necrosis factor-alpha levels in sera andwhey of cattle with naturally occurring coliformmastitis. J Vet Med Sci 2001, 63: 1009-1011.
  114. Taylor BC, Keefe RG, Dellinger JD, Nakamura Y, Cullor JS, Stott JL. T cell populations and cytokine expression in milk derived from normal and bacteria-infected bovine mammary glands. Cell Immunol 1997, 182: 68-76.
  115. Riollet C, Rainard P, Poutrel B. Differential induction of complement fragment C5a and inflammatory cytokines during intramammary infections with Escherichia coli and Staphylococcus aureus. Clin Diagn Lab Immunol 2000, 7: 161-167 [CrossRef] [PubMed].
  116. Bargatze RF, Kurk S, Butcher EC, Jutila MA. Neutrophils roll on adherent neutrophils bound to cytokine-induced endothelial cells via Lselectin on the rolling cells. J Exp Med 1994, 180: 1785-1792.
  117. Jutila MA, Rott L, Berg EL, Butcher EC. Function and regulation of the neutrophilMEL-14 antigen in vivo: comparisonwith LFA-1 andMAC- 1. J Immunol 1989, 143: 3318-3324.
  118. Kehrli ME Jr, Schmalstieg FC, Anderson DC, Van der Maaten MJ, Hughes BJ, Ackermann MR, Wilhelmsen CL, Brown GB, StevensMG, Whetstone CA. Molecular definition of the bovine granulocytopathy syndrome: identification of deficiency of the Mac-1 (CD11b/CD18) glycoprotein. Am J Vet Res 1990, 51: 1826-1836.
  119. Smits E, Burvenich C, Guidry AJ, Massart-Leen A. Adhesion receptor CD11b/CD18 contributes to neutrophil diapedesis across the bovine blood-milk barrier. Vet Immunol Immunopathol 2000, 73: 255-265.
  120. Gourlay RN, Howard CJ, Brownlie J. Localized immunity in experimental bovine mastitis caused by Mycoplasma dispar. Infect Immun 1975, 12: 947-950 [PubMed].
  121. Targowski SP, Berman DT. Leukocytic response of bovine mammary gland to injection of killed cells and cell walls of Staphylococcus aureus. Am J Vet Res 1975, 36: 1561-1565 [PubMed].
  122. De Cueninck BJ. Expression of cell-mediated hypersensitivity in the lumen of the mammary gland in guinea pigs. Am J Vet Res 1982, 43: 1696-1700.
  123. Targowski SP, Nonnecke BJ. Cell-mediated immune response of the mammary gland in guniea pigs. I. Effect of antigen injection into the vaccinated and unvaccinated glands. Am J Reprod Immunol 1982, 2: 29-38.
  124. Appelberg R. CD4+ T cells are required for antigen- specific recruitment of neutrophils by BCGimmune spleen cells. Immunology 1992, 75: 414-419.
  125. Appelberg R. Mycobacterial infection primes T cells and macrophages for enhanced recruitment of neutrophils. J Leukoc Biol 1992, 51: 472 477.
  126. Ibanez OM, Stiffel C, Ribeiro OG, CabreraWK, Massa S, De Franco M, Sant anna OA, Decreusefond C, Mouton D, SiqueiraM. Genetics of nonspecific immunity. I. Bidirectional selective breeding of lines of mice endowed with maximal or minimal inflammatory responsiveness. Eur J Immunol 1992, 22: 2555-2563.
  127. Araujo LM, Ribeiro OG, SiqueiraM, De Franco M, Starobinas N, Massa S, Cabrera WH, Mouton D, Seman M, Ibanez OM. Innate resistance to infection by intracellular bacterial pathogens differs in mice selected for maximal or minimal acute inflammatory response. Eur J Immunol 1998, 28: 2913-2920.
  128. Vigar ND, Cabrera WH, Araujo LM, Ribeiro OG, Ogata TR, Siqueira M, Ibanez OM, De Franco M. Pristane-induced arthritis in mice selected for maximal or minimal acute inflammatory reaction. Eur J Immunol 2000, 30: 431-437.