Innate immunity of the bovine mammary gland.

Understanding the immune defenses of the mammary gland is instrumental in devising and developing measures to control mastitis, the major illness of dairy ruminants. Innate immunity is an extremely broad field for investigation, and despite decades of research, our present knowledge of the innate defenses of the udder is incomplete. Yet, information is being gained on the recognition of pathogens by the mammary gland, and on several locally inducible defenses. The contribution of mammary epithelial cells to local defenses and to the mobilization of leucocytes is under growing scrutiny. Interactions of mastitis-causing bacteria such as Escherichia coli or Staphylococcus aureus and the mammary gland represents a suitable model for studies on innate immunity at an epithelium frontier. Powerful new research tools are radically modifying the prospects for the understanding of the interplay between the mammary gland innate defenses and mastitis-causing bacteria: genetic dissection of the immune response, microarray gene technology, transcriptomic methodologies and gene silencing by RNA interference will make possible the discovery of several of the key defense mechanisms which govern the susceptibility/resistance to mastitis at the molecular and genetic levels. It should then be possible to enhance the resistance of dairy ruminants to mastitis through immunomodulation and genetic improvement.

[1]  F. Ceciliani,et al.  Identification of the bovine α1-acid glycoprotein in colostrum and milk , 2005 .

[2]  G. Pighetti,et al.  Impaired Neutrophil Migration Associated with Specific Bovine CXCR2 Genotypes , 2005, Infection and Immunity.

[3]  T. Vuocolo,et al.  Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells. , 2005, Cytokine.

[4]  R. van Dorp,et al.  Gene expression signatures in neutrophils exposed to glucocorticoids: a new paradigm to help explain "neutrophil dysfunction" in parturient dairy cows. , 2005, Veterinary immunology and immunopathology.

[5]  C. Haley,et al.  The genetic dissection of immune response using gene-expression studies and genome mapping. , 2005, Veterinary Immunology and Immunopathology.

[6]  D. Gianola,et al.  Genetic association between susceptibility to clinical mastitis and protein yield in norwegian dairy cattle. , 2005, Journal of dairy science.

[7]  Molecular characterization of a saposin-like protein family member isolated from bovine lymphocytes. , 2005, Journal of dairy science.

[8]  P. Hiemstra,et al.  Interactions between neutrophil‐derived antimicrobial peptides and airway epithelial cells , 2005, Journal of leukocyte biology.

[9]  P. Rainard Tackling mastitis in dairy cows , 2005, Nature Biotechnology.

[10]  M. Paape,et al.  Genetically enhanced cows resist intramammary Staphylococcus aureus infection , 2005, Nature Biotechnology.

[11]  D. Davidson,et al.  Impact of LL‐37 on anti‐infective immunity , 2005, Journal of leukocyte biology.

[12]  S. Jacobsen,et al.  Kinetics of local and systemic isoforms of serum amyloid A in bovine mastitic milk. , 2005, Veterinary immunology and immunopathology.

[13]  K. Persson Waller,et al.  Haptoglobin and serum amyloid A in milk from dairy cows with chronic sub-clinical mastitis. , 2005, Veterinary research.

[14]  S. Mabjeesh,et al.  Expression of albumin in nonhepatic tissues and its synthesis by the bovine mammary gland. , 2005, Journal of dairy science.

[15]  Robert E W Hancock,et al.  A re-evaluation of the role of host defence peptides in mammalian immunity. , 2005, Current protein & peptide science.

[16]  P. V. Berkel,et al.  Structure and biological actions of lactoferrin , 1996, Journal of Mammary Gland Biology and Neoplasia.

[17]  R. van Dorp,et al.  Immunorelevant gene expression in LPS-challenged bovine mammary epithelial cells. , 2005, Journal of applied genetics.

[18]  L. Herzenberg,et al.  Inherent specificities in natural antibodies: a key to immune defense against pathogen invasion , 2005, Springer Seminars in Immunopathology.

[19]  B. Malissen,et al.  Innate and adaptive immunity: specificities and signaling hierarchies revisited , 2004, Nature Immunology.

[20]  L. Duchateau,et al.  Viability of milk neutrophils and severity of bovine coliform mastitis. , 2004, Journal of dairy science.

[21]  S. Davis,et al.  Expression of a β-Defensin mRNA, Lingual Antimicrobial Peptide, in Bovine Mammary Epithelial Tissue Is Induced by Mastitis , 2004, Infection and Immunity.

[22]  M. Paape,et al.  Increase of Escherichia coli inoculum doses induces faster innate immune response in primiparous cows. , 2004, Journal of dairy science.

[23]  A. Alluwaimi The cytokines of bovine mammary gland: prospects for diagnosis and therapy. , 2004, Research in veterinary science.

[24]  M. Paape,et al.  Innate immune response to intramammary infection with Serratia marcescens and Streptococcus uberis. , 2004, Veterinary research.

[25]  S. Pyörälä,et al.  Serum amyloid A and TNF alpha in serum and milk during experimental endotoxin mastitis. , 2004, Veterinary research.

[26]  D. Kerr,et al.  Cryopreserved bovine mammary cells to model epithelial response to infection. , 2004, Veterinary immunology and immunopathology.

[27]  C. Looft,et al.  Bovine β-defensins: Identification and characterization of novel bovine β-defensin genes and their expression in mammarygland tissue , 2004, Mammalian Genome.

[28]  M. Paape,et al.  The production and characterization of anti-bovine CD14 monoclonal antibodies. , 2004, Veterinary research.

[29]  S. Oliver,et al.  Association of CXCR2 polymorphisms with subclinical and clinical mastitis in dairy cattle. , 2004, Journal of dairy science.

[30]  M. Paape,et al.  Characterization of the bovine innate immune response to intramammary infection with Klebsiella pneumoniae. , 2004, Journal of dairy science.

[31]  V. Rutten,et al.  Bacterial growth during the early phase of infection determines the severity of experimental Escherichia coli mastitis in dairy cows. , 2004, Veterinary microbiology.

[32]  Robert E. W. Hancock,et al.  Can innate immunity be enhanced to treat microbial infections? , 2004, Nature Reviews Microbiology.

[33]  D. Legrand,et al.  Lactoferrin and host defence: an overview of its immuno-modulating and anti-inflammatory properties , 2004, Biometals.

[34]  N. Orsi,et al.  The antimicrobial activity of lactoferrin: Current status and perspectives , 2004, Biometals.

[35]  M. Paape,et al.  Escherichia coli and Staphylococcus aureus Elicit Differential Innate Immune Responses following Intramammary Infection , 2004, Clinical Diagnostic Laboratory Immunology.

[36]  M. Netea,et al.  Toll‐like receptors and the host defense against microbial pathogens: bringing specificity to the innate‐immune system , 2004, Journal of leukocyte biology.

[37]  P. Andersen,et al.  Acute phase protein concentrations in serum and milk from healthy cows, cows with clinical mastitis and cows with extramammary inflammatory conditions , 2004, Veterinary Record.

[38]  Leif Andersson,et al.  Domestic-animal genomics: deciphering the genetics of complex traits , 2004, Nature Reviews Genetics.

[39]  R. Bruckmaier,et al.  Short-term changes of mRNA expression of various inflammatory factors and milk proteins in mammary tissue during LPS-induced mastitis. , 2004, Domestic animal endocrinology.

[40]  B. Beutler Innate immunity: an overview. , 2004, Molecular immunology.

[41]  E. Veerman,et al.  Lactoferrampin: a novel antimicrobial peptide in the N1-domain of bovine lactoferrin , 2004, Peptides.

[42]  T. Goldammer,et al.  Mastitis Increases Mammary mRNA Abundance of β-Defensin 5, Toll-Like-Receptor 2 (TLR2), and TLR4 but Not TLR9 in Cattle , 2004, Clinical Diagnostic Laboratory Immunology.

[43]  J. Kobayashi,et al.  Induction of Nitric Oxide Production Mediated by Tumor Necrosis Factor Alpha on Staphylococcal Enterotoxin C-Stimulated Bovine Mammary Gland Cells , 2004, Clinical Diagnostic Laboratory Immunology.

[44]  M. Paape,et al.  Defense of the Bovine Mammary Gland by Polymorphonuclear Neutrophil Leukocytes , 2002, Journal of Mammary Gland Biology and Neoplasia.

[45]  A. Kolb Engineering Immunity in the Mammary Gland , 2002, Journal of Mammary Gland Biology and Neoplasia.

[46]  L. Sordillo,et al.  Mammary Gland Immunity and Mastitis Susceptibility , 2002, Journal of Mammary Gland Biology and Neoplasia.

[47]  M. Ollivier-Bousquet,et al.  Transferrin and Prolactin Transcytosis in the Lactating Mammary Epithelial Cell , 1998, Journal of Mammary Gland Biology and Neoplasia.

[48]  M. Neville,et al.  Tight Junction Regulation in the Mammary Gland , 1998, Journal of Mammary Gland Biology and Neoplasia.

[49]  C. Looft,et al.  Bovine beta-defensins: identification and characterization of novel bovine beta-defensin genes and their expression in mammary gland tissue. , 2004, Mammalian genome : official journal of the International Mammalian Genome Society.

[50]  R. Almeida,et al.  Dynamics of leukocytes and cytokines during experimentally induced Streptococcus uberis mastitis. , 2003, Veterinary immunology and immunopathology.

[51]  R. Bhatnagar,et al.  RNA Interference: Biology, Mechanism, and Applications , 2003, Microbiology and Molecular Biology Reviews.

[52]  P. Eckersall,et al.  Haptoglobin and serum amyloid A in milk and serum during acute and chronic experimentally induced Staphylococcus aureus mastitis , 2003, Journal of Dairy Research.

[53]  M. Paape,et al.  Increased levels of LPS-binding protein in bovine blood and milk following bacterial lipopolysaccharide challenge. , 2003, Journal of dairy science.

[54]  M. Paape,et al.  The bovine neutrophil: Structure and function in blood and milk. , 2003, Veterinary research.

[55]  B. Heringstad,et al.  Selection responses for clinical mastitis and protein yield in two Norwegian dairy cattle selection experiments. , 2003, Journal of dairy science.

[56]  L. Duchateau,et al.  Severity of E. coli mastitis is mainly determined by cow factors. , 2003, Veterinary research.

[57]  D. Boichard,et al.  Genetics of resistance to mastitis in dairy cattle. , 2003, Veterinary research.

[58]  P. Rainard The complement in milk and defense of the bovine mammary gland against infections. , 2003, Veterinary research.

[59]  P. Rainard,et al.  Mobilization of neutrophils and defense of the bovine mammary gland. , 2003, Reproduction, nutrition, development.

[60]  Johan Kuiper,et al.  Receptors, Mediators, and Mechanisms Involved in Bacterial Sepsis and Septic Shock , 2003, Clinical Microbiology Reviews.

[61]  M. Paape,et al.  Recombinant Soluble CD14 Reduces Severity of Intramammary Infection by Escherichia coli , 2003, Infection and Immunity.

[62]  M. Paape,et al.  Elevated milk soluble CD14 in bovine mammary glands challenged with Escherichia coli lipopolysaccharide. , 2003, Journal of dairy science.

[63]  R. Erskine,et al.  Immunity and mastitis. Some new ideas for an old disease. , 2003, The Veterinary clinics of North America. Food animal practice.

[64]  D. Kerr,et al.  Mammary expression of new genes to combat mastitis , 2003, Journal of animal science.

[65]  C. Burvenich,et al.  Differential leukocyte count method for bovine low somatic cell count milk. , 2003, Journal of dairy science.

[66]  G. Leitner,et al.  Immune cell differentiation in mammary gland tissues and milk of cows chronically infected with Staphylococcus aureus. , 2003, Journal of veterinary medicine. B, Infectious diseases and veterinary public health.

[67]  B. Heringstad,et al.  Reduced levels of total leukocytes and neutrophils in Norwegian cattle selected for decreased mastitis incidence. , 2002, Journal of dairy science.

[68]  Andreas Peschel,et al.  Chemokines Meet Defensins: the Merging Concepts of Chemoattractants and Antimicrobial Peptides in Host Defense , 2002, Infection and Immunity.

[69]  L. Duchateau,et al.  Blood and milk neutrophil chemiluminescence and viability in primiparous and pluriparous dairy cows during late pregnancy, around parturition and early lactation. , 2002, Journal of dairy science.

[70]  C. Burvenich,et al.  Composition and milk cell characteristics in quarter milk fractions of dairy cows with low cell count. , 2002, Veterinary journal.

[71]  R. Cherry,et al.  Antimicrobial Properties of Milk: Dependence on Presence of Xanthine Oxidase and Nitrite , 2002, Antimicrobial Agents and Chemotherapy.

[72]  J. Detilleux Genetic factors affecting susceptibility of dairy cows to udder pathogens. , 2002, Veterinary immunology and immunopathology.

[73]  S. Pyörälä,et al.  New strategies to prevent mastitis. , 2002, Reproduction in domestic animals = Zuchthygiene.

[74]  M. Paape,et al.  Recombinant bovine soluble CD14 sensitizes the mammary gland to lipopolysaccharide. , 2002, Veterinary immunology and immunopathology.

[75]  E. Pauwels,et al.  Large scale production of recombinant human lactoferrin in the milk of transgenic cows , 2002, Nature Biotechnology.

[76]  H. Kitamura,et al.  Lactoferrin Stimulates A Staphylococcus aureus Killing Activity of Bovine Phagocytes in the Mammary Gland , 2002, Microbiology and immunology.

[77]  R. Almeida,et al.  Identification of lactoferrin-binding proteins in Streptococcus dysgalactiae subsp. dysgalactiae and Streptococcus agalactiae isolated from cows with mastitis. , 2002, FEMS microbiology letters.

[78]  K. P. Waller Mammary Gland Immunology Around Parturition , 2002 .

[79]  M. Kehrli,et al.  Immunity in the mammary gland. , 2001, The Veterinary clinics of North America. Food animal practice.

[80]  A. E. Freeman,et al.  Genetic control of disease resistance and immunoresponsiveness. , 2001, The Veterinary clinics of North America. Food animal practice.

[81]  J. Mehrzad,et al.  Effect of milk sampling techniques on milk composition, bacterial contamination, viability and functions of resident cells in milk. , 2001, Veterinary research.

[82]  M. Ackermann,et al.  Cell adhesion molecules, leukocyte trafficking, and strategies to reduce leukocyte infiltration. , 2001, Journal of veterinary internal medicine.

[83]  W. Klee,et al.  The relationship between milk yield and the incidence of some diseases in dairy cows. , 2001, Journal of dairy science.

[84]  B. Britigan,et al.  Lactoferrin Binds CpG-Containing Oligonucleotides and Inhibits Their Immunostimulatory Effects on Human B Cells1 , 2001, The Journal of Immunology.

[85]  P. Lacasse,et al.  Induction of nitric oxide production by bovine mammary epithelial cells and blood leukocytes. , 2001, Journal of dairy science.

[86]  P. Rainard,et al.  Cell subpopulations and cytokine expression in cow milk in response to chronic Staphylococcus aureus infection. , 2001, Journal of dairy science.

[87]  P. Eckersall,et al.  Acute phase proteins in serum and milk from dairy cows with clinical mastitis , 2001, Veterinary Record.

[88]  Jai-Wei Lee,et al.  RECOMBINANT HUMAN INTERLEUKIN‐8, BUT NOT HUMAN INTERLEUKIN‐1β, INDUCES BOVINE NEUTROPHIL MIGRATION IN AN IN VITRO CO‐CULTURE SYSTEM , 2000 .

[89]  R. Bruckmaier,et al.  Tumor necrosis factor-alpha and nitrite/nitrate responses during acute mastitis induced by Escherichia coli infection and endotoxin in dairy cows. , 2000, Domestic animal endocrinology.

[90]  X. Zhao,et al.  Bovine interleukin-1 expression by cultured mammary epithelial cells (MAC-T) and its involvement in the release of MAC-T derived interleukin-8. , 2000, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[91]  G. Leitner,et al.  Milk leucocyte population patterns in bovine udder infection of different aetiology. , 2000, Journal of veterinary medicine. B, Infectious diseases and veterinary public health.

[92]  M. Paape,et al.  Phagocytosis and killing of Staphylococcus aureus by bovine neutrophils after priming by tumor necrosis factor-alpha and the des-arginine derivative of C5a. , 2000, American journal of veterinary research.

[93]  M. Affolter,et al.  Innate Recognition of Bacteria in Human Milk Is Mediated by a Milk-Derived Highly Expressed Pattern Recognition Receptor, Soluble Cd14 , 2000, The Journal of experimental medicine.

[94]  P. Rainard,et al.  Generation of complement fragment C5a in milk is variable among cows. , 2000, Journal of dairy science.

[95]  L. Tatarczuch,et al.  Leucocyte phenotypes in involuting and fully involuted mammary glandular tissues and secretions of sheep , 2000, Journal of anatomy.

[96]  P. Rainard,et al.  Differential Induction of Complement Fragment C5a and Inflammatory Cytokines during Intramammary Infections withEscherichia coli and Staphylococcus aureus , 2000, Clinical Diagnostic Laboratory Immunology.

[97]  E. Wouters,et al.  Production of the acute-phase protein lipopolysaccharide-binding protein by respiratory type II epithelial cells: implications for local defense to bacterial endotoxins. , 2000, American journal of respiratory cell and molecular biology.

[98]  P. Moroni,et al.  Relationship between teat tissue immune defences and intramammary infections. , 2000, Advances in experimental medicine and biology.

[99]  K. P. Waller Mammary gland immunology around parturition. Influence of stress, nutrition and genetics. , 2000, Advances in experimental medicine and biology.

[100]  P. Lacasse,et al.  Nitric oxide production during endotoxin-induced mastitis in the cow. , 1999, Journal of dairy science.

[101]  M. Quinn,et al.  Selective Recruitment of T-Cell Subsets to the Udder during Staphylococcal and Streptococcal Mastitis: Analysis of Lymphocyte Subsets and Adhesion Molecule Expression , 1999, Infection and Immunity.

[102]  L. Hinckley,et al.  Inducible and Constitutive In Vitro Neutrophil Chemokine Expression by Mammary Epithelial and Myoepithelial Cells , 1999, Clinical Diagnostic Laboratory Immunology.

[103]  A. Whitehead,et al.  Serum amyloid A, the major vertebrate acute-phase reactant. , 1999, European journal of biochemistry.

[104]  M. Selsted,et al.  Cloning and expression of bovine neutrophil beta-defensins. Biosynthetic profile during neutrophilic maturation and localization of mature peptide to novel cytoplasmic dense granules. , 1999, The Journal of biological chemistry.

[105]  M. Willcox,et al.  Elucidation of the antistaphylococcal action of lactoferrin and lysozyme. , 1999, Journal of medical microbiology.

[106]  R. Jacobs,et al.  Exceptionally long CDR3H region with multiple cysteine residues in functional bovine IgM antibodies , 1999, European journal of immunology.

[107]  M. Brčić,et al.  Differential induction of NO synthesis by gram-positive and gram-negative bacteria and their components in bovine monocyte-derived macrophages. , 1999, Microbial pathogenesis.

[108]  S. Oliver,et al.  Identification of lactoferrin-binding proteins in bovine mastitis-causing Streptococcus uberis. , 1999, FEMS microbiology letters.

[109]  R. Hancock,et al.  Salt-Resistant Alpha-Helical Cationic Antimicrobial Peptides , 1999, Antimicrobial Agents and Chemotherapy.

[110]  C. Burvenich,et al.  Diapedesis across mammary epithelium reduces phagocytic and oxidative burst of bovine neutrophils. , 1999, Veterinary immunology and immunopathology.

[111]  T. Rosol,et al.  Effects of lipopolysaccharide on production of interleukin-1 and interleukin-6 by bovine mammary epithelial cells in vitro. , 1999, The Journal of veterinary medical science.

[112]  Ø. Rekdal,et al.  Initial binding sites of antimicrobial peptides in Staphylococcus aureus and Escherichia coli. , 1999, Scandinavian journal of infectious diseases.

[113]  X. Li,et al.  Interleukin 8 response by bovine mammary epithelial cells to lipopolysaccharide stimulation. , 1998, American journal of veterinary research.

[114]  M. Onoda,et al.  Localization of Nitric Oxide Synthases and Nitric Oxide Production in the Rat Mammary Gland , 1998, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[115]  G. Dighiero,et al.  From Natural Polyreactive Autoantibodies to À La Carte Monoreactive Antibodies to Infectious Agents: Is It a Small World after All? , 1998, Infection and Immunity.

[116]  T. J. Yang,et al.  Chemotactic Activities in Nonmastitic and Mastitic Mammary Secretions: Presence of Interleukin-8 in Mastitic but Not Nonmastitic Secretions , 1998, Clinical Diagnostic Laboratory Immunology.

[117]  M. Paape,et al.  Quantification of C5a/C5a(desArg) in bovine plasma, serum and milk. , 1998, Veterinary research.

[118]  M. Ackermann,et al.  Epithelial antibiotic induced in states of disease. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[119]  M. Paape,et al.  Complement fragment C5a and inflammatory cytokines in neutrophil recruitment during intramammary infection with Escherichia coli , 1997, Infection and immunity.

[120]  L. Sordillo,et al.  Immunobiology of the mammary gland. , 1997, Journal of dairy science.

[121]  T. Rosol,et al.  Detection of interleukin-1 and interleukin-6 on cryopreserved bovine mammary epithelial cells in vitro. , 1997, The Journal of veterinary medical science.

[122]  Drapier Jc Nitric oxide and macrophages , 1997 .

[123]  C. Nathan,et al.  Nitric oxide and macrophage function. , 1997, Annual review of immunology.

[124]  Y. Schukken,et al.  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. , 1997, Journal of dairy science.

[125]  J. Rosen,et al.  Production of active bovine tracheal antimicrobial peptide in milk of transgenic mice. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[126]  L. Ek,et al.  Bacterial growth, inflammatory cytokine production, and neutrophil recruitment during coliform mastitis in cows within ten days after calving, compared with cows at midlactation. , 1996 .

[127]  M. Paape,et al.  Cell culture system for studying bovine neutrophil diapedesis. , 1996, Journal of dairy science.

[128]  I. Mattsby‐Baltzer,et al.  Lactoferrin or a Fragment Thereof Inhibits the Endotoxin-Induced Interleukin-6 Response in Human Monocytic Cells , 1996, Pediatric Research.

[129]  Wayne L. Smith,et al.  Purification, primary structures, and antibacterial activities of β-defensins, a new family of antimicrobial peptides from bovine neutrophils. , 1996, The Journal of Biological Chemistry.

[130]  R. Wilkins,et al.  Elevation of lactoferrin gene expression in developing, ductal, resting, and regressing parenchymal epithelium of the ruminant mammary gland. , 1996, Journal of dairy science.

[131]  M. Paape,et al.  Intramammary defense against infections induced by Escherichia coli in cows. , 1996, American journal of veterinary research.

[132]  F. Bastida-Corcuera,et al.  Effect of staphylococcal β toxin on the cytotoxicity, proliferation and adherence of Staphylococcus aureus to bovine mammary epithelial cells , 1996 .

[133]  D. Shuster,et al.  Bacterial growth, inflammatory cytokine production, and neutrophil recruitment during coliform mastitis in cows within ten days after calving, compared with cows at midlactation. , 1996, American journal of veterinary research.

[134]  F. Bastida-Corcuera,et al.  Effect of staphylococcal beta toxin on the cytotoxicity, proliferation and adherence of Staphylococcus aureus to bovine mammary epithelial cells. , 1996, Veterinary microbiology.

[135]  P. Rainard,et al.  Deposition of complement components on Streptococcus agalactiae in bovine milk in the absence of inflammation , 1995, Infection and immunity.

[136]  W. Parks,et al.  Cellular expression of the C5a anaphylatoxin receptor (C5aR): demonstration of C5aR on nonmyeloid cells of the liver and lung. , 1995, Journal of immunology.

[137]  J. Stabel,et al.  Study of immunological dysfunction in periparturient Holstein cattle selected for high and average milk production. , 1995, Veterinary immunology and immunopathology.

[138]  R. Horst,et al.  Regulation of L‐selectin and CD18 on bovine neutrophils by glucocorticoids: effects of cortisol and dexamethasone , 1995, Journal of leukocyte biology.

[139]  R. Cook,et al.  Pathologic findings of experimentally induced Streptococcus uberis infection in the mammary gland of cows. , 1994, American journal of veterinary research.

[140]  K. Koehler,et al.  Immunological parameters of periparturient Holstein cattle: genetic variation. , 1994, Journal of dairy science.

[141]  J. Cullor,et al.  Bovine milk lymphocytes display the phenotype of memory T cells and are predominantly CD8+. , 1994, Cellular immunology.

[142]  M. Paape,et al.  Role of the neutrophil leucocyte in the local and systemic reactions during experimentally induced E. coli mastitis in cows immediately after calving. , 1994, The Veterinary quarterly.

[143]  R. Goodman,et al.  Bovine mammary lactoferrin: implications from messenger ribonucleic acid (mRNA) sequence and regulation contrary to other milk proteins. , 1993, Journal of dairy science.

[144]  P. Rainard Activation of the classical pathway of complement by binding of bovine lactoferrin to unencapsulated Streptococcus agalactiae. , 1993, Immunology.

[145]  I. Larsson,et al.  Effects of certain inflammatory mediators on bovine neutrophil migration in vivo and in vitro. , 1993, Veterinary immunology and immunopathology.

[146]  D. Taub,et al.  Review of the chemokine meeting the Third International Symposium of Chemotactic Cytokines. , 1993, Cytokine.

[147]  M. Daley,et al.  Prevention and treatment of Staphylococcus aureus infections with recombinant cytokines. , 1993, Cytokine.

[148]  A. Guidry,et al.  Opsonization of Staphylococcus aureus by bovine immunoglobulin isotypes. , 1993, Journal of dairy science.

[149]  R. Gilbert,et al.  Effect of parity on periparturient neutrophil function in dairy cows. , 1993, Veterinary immunology and immunopathology.

[150]  D. Shuster,et al.  Cytokine production during endotoxin-induced mastitis in lactating dairy cows. , 1993, American journal of veterinary research.

[151]  M. Selsted,et al.  Purification, primary structures, and antibacterial activities of beta-defensins, a new family of antimicrobial peptides from bovine neutrophils. , 1993, The Journal of biological chemistry.

[152]  P. Rainard Binding of bovine lactoferrin to Streptococcus agalactiae. , 1992, FEMS microbiology letters.

[153]  R. Gilbert,et al.  Identification and prevalence of a genetic defect that causes leukocyte adhesion deficiency in Holstein cattle. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[154]  Miguel Calvo Rebollar,et al.  Synthesis of lactoferrin and transport of transferrin in the lactating mammary gland of sheep. , 1992, Journal of dairy science.

[155]  L. Fox,et al.  Bovine mononuclear leukocyte subpopulations in peripheral blood and mammary gland secretions during lactation. , 1992, Journal of dairy science.

[156]  J. Cullor,et al.  Immunobiology of hematopoietic colony-stimulating factors: potential application to disease prevention in the bovine. , 1991, Journal of dairy science.

[157]  L. Babiuk,et al.  Pathological changes in bovine mammary glands following intramammary infusion of recombinant interleukin-2. , 1991, Journal of dairy science.

[158]  M. Daley,et al.  Staphylococcus aureus mastitis: pathogenesis and treatment with bovine interleukin-1 beta and interleukin-2. , 1991, Journal of dairy science.

[159]  H. Huynh,et al.  Establishment of bovine mammary epithelial cells (MAC-T): an in vitro model for bovine lactation. , 1991, Experimental cell research.

[160]  L. Babiuk,et al.  Antibacterial activity of bovine mammary gland lymphocytes following treatment with interleukin-2. , 1991, Journal of dairy science.

[161]  I. Politis,et al.  Examination of chemotactic properties of bovine mammary macrophages. , 1991, Canadian journal of veterinary research = Revue canadienne de recherche veterinaire.

[162]  J. Goff,et al.  Effects of granulocyte colony-stimulating factor administration to periparturient cows on neutrophils and bacterial shedding. , 1991, Journal of dairy science.

[163]  I. Politis,et al.  Secretion of interleukin-1 by bovine milk macrophages. , 1991, American journal of veterinary research.

[164]  M. Zasloff,et al.  Tracheal antimicrobial peptide, a cysteine-rich peptide from mammalian tracheal mucosa: peptide isolation and cloning of a cDNA. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[165]  A. Forsgren,et al.  Bovine lactoferrin receptors in Staphylococcus aureus isolated from bovine mastitis. , 1991, Journal of dairy science.

[166]  L. Babiuk,et al.  Modulation of bovine mammary neutrophil function during the periparturient period following in vitro exposure to recombinant bovine interferon gamma. , 1991, Veterinary immunology and immunopathology.

[167]  A. E. Freeman,et al.  Bovine sire effects on daughters' in vitro blood neutrophil functions, lymphocyte blastogenesis, serum complement and conglutinin levels. , 1991, Veterinary immunology and immunopathology.

[168]  C. Czuprynski,et al.  Priming and Stimulation of Bovine Neutrophils by Recombinant Human interleukin‐1 Alpha and Tumor Necrosis Factor Alpha , 1991, Journal of leukocyte biology.

[169]  R. Ulevitch,et al.  CD14, a receptor for complexes of lipopolysaccharide (LPS) and LPS binding protein. , 1990, Science.

[170]  E. Berg,et al.  Neutrophil Mac-1 and MEL-14 adhesion proteins inversely regulated by chemotactic factors. , 1989, Science.

[171]  J. Madara,et al.  Interferon-gamma directly affects barrier function of cultured intestinal epithelial monolayers. , 1989, The Journal of clinical investigation.

[172]  Miguel Calvo Rebollar,et al.  Concentration of lactoferrin and transferrin throughout lactation in cow's colostrum and milk. , 1988, Biological chemistry Hoppe-Seyler.

[173]  K. Sletten,et al.  Characterization of Bovine Amyloid Proteins SAA and AA , 1988, Scandinavian journal of immunology.

[174]  S. Oliver,et al.  Growth inhibition of Escherichia coli and Klebsiella pneumoniae during involution of the bovine mammary gland: relation to secretion composition. , 1987, American journal of veterinary research.

[175]  L. Sordillo,et al.  Secretion composition during bovine mammary involution and the relationship with mastitis. , 1987, The International journal of biochemistry.

[176]  C. Concha Cell types and their immunological functions in bovine mammary tissues and secretions--a review of the literature. , 1986, Nordisk veterinaermedicin.

[177]  R. Collins,et al.  Antibody-containing cells and specialised epithelial cells in the bovine teat. , 1986, Research in veterinary science.

[178]  P. Rainard Bacteriostatic activity of bovine milk lactoferrin against mastitic bacteria. , 1986, Veterinary microbiology.

[179]  N. Craven,et al.  Local cellular reaction and release of neutrophil chemotaxin from abraded polyethylene devices implanted in bovine udders. , 1986, The British veterinary journal.

[180]  P. Rainard Bacteriostasis of Escherichia coli by bovine lactoferrin, transferrin and immunoglobulins (IgG1, IgG2, IgM) acting alone or in combination. , 1986, Veterinary microbiology.

[181]  N. Craven Chemotactic factors for bovine neutrophils in relation to mastitis. , 1986, Comparative immunology, microbiology and infectious diseases.

[182]  M. Williams,et al.  Defences of the bovine mammary gland against infection and prospects for their enhancement. , 1985, Veterinary immunology and immunopathology.

[183]  Loeffler Da,et al.  Enzyme-linked immunosorbent assay for detection of milk immunoglobulins to leukocidin toxin of Staphylococcus aureus. , 1985 .

[184]  K. Nguyen,et al.  Phagocytic and bactericidal properties of bovine macrophages from non-lactating mammary glands. , 1985, Research in veterinary science.

[185]  D. Loeffler,et al.  Enzyme-linked immunosorbent assay for detection of milk immunoglobulins to leukocidin toxin of Staphylococcus aureus. , 1985, American journal of veterinary research.

[186]  M. Williams,et al.  Further studies on the variation among cows, bulls and calves in the ability of their blood polymorphonuclear leucocytes to kill Staphylococcus aureus. , 1984, The British veterinary journal.

[187]  S. C. Nickerson,et al.  Distribution, location, and ultrastructure of plasma cells in the uninfected, lactating bovine mammary gland , 1984, Journal of Dairy Research.

[188]  Schultze Wd,et al.  Changes in penetrability of bovine papillary duct to endotoxin after milking. , 1983 .

[189]  N. Craven Generation of neutrophil chemoattractants by phagocytosing bovine mammary macrophages. , 1983, Research in veterinary science.

[190]  N. Sc,et al.  Cytologic observations of the bovine teat end. , 1983 .

[191]  M. Williams,et al.  The opsonic activity of bovine milk whey for the phagocytosis and killing by neutrophils of encapsulated and non-encapsulated Escherichia coli. , 1983, Veterinary microbiology.

[192]  W. Schultze,et al.  Changes in penetrability of bovine papillary duct to endotoxin after milking. , 1983, American journal of veterinary research.

[193]  S. C. Nickerson,et al.  Cytologic observations of the bovine teat end. , 1983, American journal of veterinary research.

[194]  P. Rainard Experimental mastitis with Escherichia coli: kinetics of bacteriostatic and bactericidal activities. , 1983, Annales de recherches veterinaires. Annals of veterinary research.

[195]  Schwartz Lw,et al.  Bovine peripheral blood polymorphonuclear neutrophil chemotactic response to Pasteurella haemolytica or zymosan-activated serum. , 1982 .

[196]  E. J. Carroll,et al.  Chemotactic factors for bovine leukocytes. , 1982, American journal of veterinary research.

[197]  M. Williams,et al.  A role for IgM in the in vitro opsonisation of Staphylococcus aureus and Escherichia coli by bovine polymorphonuclear leucocytes. , 1982, Research in veterinary science.

[198]  Harmon Rj,et al.  Migration of polymorphonuclear leukocytes into the bovine mammary gland during experimentally induced Staphylococcus aureus mastitis. , 1982 .

[199]  R. Nelson,et al.  Chemotactic requirements of bovine leukocytes. , 1982, American journal of veterinary research.

[200]  L. Schwartz,et al.  Bovine peripheral blood polymorphonuclear neutrophil chemotactic response to Pasteurella haemolytica or zymosan-activated serum. , 1982, American journal of veterinary research.

[201]  R. Harmon,et al.  Migration of polymorphonuclear leukocytes into the bovine mammary gland during experimentally induced Staphylococcus aureus mastitis. , 1982, American journal of veterinary research.

[202]  P. Rainard,et al.  Lactoferrin and transferrin in bovine milk in relation to certain physiological and pathological factors. , 1982, Annales de recherches veterinaires. Annals of veterinary research.

[203]  Anderson Aj,et al.  Total and differential somatic cell counts in secretions from noninfected bovine mammary glands: the peripartum period. , 1981 .

[204]  Anderson Aj,et al.  Total and differential somatic cell counts in secretions from noninfected bovine mammary glands: the early nonlactating period. , 1981 .

[205]  Jensen Dl,et al.  Total and differential cell counts in secretions of the nonlactating bovine mammary gland. , 1981 .

[206]  D. Jensen,et al.  Total and differential cell counts in secretions of the nonlactating bovine mammary gland. , 1981, American journal of veterinary research.

[207]  Butler Je A concept of humoral immunity among ruminants and an approach to its investigation. , 1981 .

[208]  J. Mcdonald,et al.  Total and differential somatic cell counts in secretions from noninfected bovine mammary glands: the peripartum period. , 1981, American journal of veterinary research.

[209]  J. Mcdonald,et al.  Total and differential somatic cell counts in secretions from noninfected bovine mammary glands: the early nonlactating period. , 1981, American journal of veterinary research.

[210]  J. Butler A concept of humoral immunity among ruminants and an approach to its investigation. , 1981, Advances in experimental medicine and biology.

[211]  B. Brooker,et al.  The early pathogenesis of bovine mastitis due to Escherichia coli , 1980, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[212]  C. S. Lee,et al.  Identification, properties, and differential counts of cell populations using electron microscopy of dry cows secretions, colostrum and milk from normal cows , 1980, Journal of Dairy Research.

[213]  S. G. Campbell,et al.  Bovine mammary gland macrophage: isolation, morphologic features, and cytophilic immunoglobulins. , 1980 .

[214]  R. Harmon,et al.  Neutrophil leukocyte as a source of lactoferrin in bovine milk. , 1980 .

[215]  R. van Furth,et al.  Kinetics of phagocytosis of Staphylococcus aureus and Escherichia coli by human granulocytes. , 1979, Immunology.

[216]  M. Paape,et al.  Effect of Fat and Casein on Intracellular Killing of Staphylococcus aureus by Milk Leukocytes , 1977, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[217]  Smith Kl,et al.  Lactoferrin as a factor of resistance to infection of the bovine mammary gland. , 1977 .

[218]  K. Smith,et al.  Lactoferrin as a factor of resistance to infection of the bovine mammary gland. , 1977, Journal of the American Veterinary Medical Association.

[219]  R. Harmon,et al.  Changes in lactoferrin, immunoglobulin G, bovine serum albumin, and alpha-lactalbumin during acute experimental and natural coliform mastitis in cows , 1976, Infection and immunity.

[220]  M. Paape,et al.  Measurement of phagocytosis of 32P-labeled Staphylococcus aureus by bovine leukocytes: lysostaphin digestion and inhibitory effect of cream. , 1975, American journal of veterinary research.

[221]  Jensen Dl,et al.  Macrophages in bovine milk. , 1975 .

[222]  D. Jensen,et al.  Macrophages in bovine milk. , 1975, American journal of veterinary research.

[223]  J. Derbyshire,et al.  Isolation of milk leucocytes and their nuclei. , 1969, Journal of dairy science.

[224]  A. Gall,et al.  OBSERVATIONS SUR LA CROISSANCE DES STAPHYLOCOQUES ET LA RÉACTION LEUCOCYTAIRE AU COURS DES PREMIÈRES HEURES DE LA MAMMITE EXPÉRIMENTALE DE LA BREBIS , 1965 .