Humoral and cellular factors of maternal immunity in swine

Developmental and Comparative Immunology

Volumn 33, Issue 3, 2009, Pages 384-393

  Salmon, Henri ^a   Berri, Mustapha ^a   Gerdts, Volker ^b   Meurens, François ^a  

^a Institut national de la recherche agronomique   (France)

^b UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

Antibody transfer; CCL25; CCL28; Gut; Lymphocyte homing; MAdCAM 1; Mammary gland; Neonate; VCAM 1

Indexed keywords

ADDRESSIN; CHEMOKINE; FC RECEPTOR; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; IMMUNOGLOBULIN RECEPTOR; MATERNAL ANTIBODY; SECRETORY IMMUNOGLOBULIN;

ANIMAL TISSUE; ARTICLE; CELL MIGRATION; CELLULAR IMMUNITY; COLOSTRUM; EPITHELIUM; HORMONAL REGULATION; HUMORAL IMMUNITY; IMMUNOGLOBULIN PRODUCTION; IMMUNOMODULATION; IMMUNOSTIMULATION; INTESTINE; LACTATION; MAMMARY GLAND; MATERNAL WELFARE; MILK; MILK PRODUCTION; MUCOSAL IMMUNITY; NONHUMAN; PRIORITY JOURNAL; PROTECTION; SWINE; UPPER RESPIRATORY TRACT;

SUIDAE;

EID: 57149121074     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dci.2008.07.007     Document Type: Article

References (162)

1. Kim Y.B. Developmental immunity in the piglet. Birth Defects Orig Artic Ser 11 (1975) 549-557
2. Binns R.M. Bone marrow and lymphoid cell injection of the pig foetus resulting in transplantation tolerance or immunity, and immunoglobulin production. Nature 214 (1967) 179-180
3. Redman D.R., Bohl E.H., and Cross R.F. Intrafetal inoculation of swine with transmissible gastroenteritis virus. Am J Vet Res 39 (1978) 907-911
4. Bianchi A.T., Scholten J.W., Moonen Leusen B.H., and Boersma W.J. Development of the natural response of immunoglobulin secreting cells in the pig as a function of organ, age and housing. Dev Comp Immunol 23 (1999) 511-520
5. Hammerberg C., Schurig G.G., and Ochs D.L. Immunodeficiency in young pigs. Am J Vet Res 50 (1989) 868-874
6. Moughan P.J., Birtles M.J., Cranwell P.D., Smith W.C., and Pedraza M. The piglet as a model animal for studying aspects of digestion and absorption in milk-fed human infants. World Rev Nutr Diet 67 (1992) 40-113
7. Haelterman E.O. Immunity of the transmissible gastroenteritis. Vet Med Small Anim Clin 70 (1975) 715-717
8. Bohl E.H., Gupta R.K., Olquin M.V., and Saif L.J. Antibody responses in serum, colostrum, and milk of swine after infection or vaccination with transmissible gastroenteritis virus. Infect Immun 6 (1972) 289-301
9. Bohl E.H., and Saif L.J. Passive immunity in transmissible gastroenteritis of swine: immunoglobulin characteristics of antibodies in milk after inoculating virus by different routes. Infect Immun 11 (1975) 23-32
10. Saif L.J., van Cott J.L., and Brim T.A. Immunity to transmissible gastroenteritis virus and porcine respiratory coronavirus infections in swine. Vet Immunol Immunopathol 43 (1994) 89-97
11. Evans P.A., Newby T.J., Stokes C.R., Patel D., and Bourne F.J. Antibody response of the lactating sow to oral immunization with Escherichia coli. Scand J Immunol 11 (1980) 419-429
12. Hanson L.A., Carlsson B., Dahlgren U., Mellander L., and Svanborg Eden C. The secretory IgA system in the neonatal period. Ciba Found Symp (1979) 187-204
13. Kleinman R.E., and Walker W.A. The enteromammary immune system: an important new concept in breast milk host defense. Dig Dis Sci 24 (1979) 876-882
14. Lanza I., Shoup D.I., and Saif L.J. Lactogenic immunity and milk antibody isotypes to transmissible gastroenteritis virus in sows exposed to porcine respiratory coronavirus during pregnancy. Am J Vet Res 56 (1995) 739-748
15. Goldblum R.M., Ahlstedt S., Carlsson B., Hanson L.A., Jodal U., Lidin-Janson G., et al. Antibody-forming cells in human colostrum after oral immunisation. Nature 257 (1975) 797-798
16. Saif L.J., and Bohl E.H. Passive immunity in transmissible gastroenteritis of swine: immunoglobulin classes of milk antibodies after oral-intranasal inoculation of sows with a live low cell culture-passaged virus. Am J Vet Res 40 (1979) 115-117
17. Tanneau G.M., Hibrand-Saint Oyant L., Chevaleyre C.C., and Salmon H.P. Differential recruitment of T- and IgA B-lymphocytes in the developing mammary gland in relation to homing receptors and vascular addressins. J Histochem Cytochem 47 (1999) 1581-1592
18. Geyer H., Giese L., and Bentivoglio F. Comparative observation on the development of the mammary gland in the swine and goat. Berl Munch Tierarztl Wochenschr 99 (1986) 176-180
19. Ji F., Hurley W.L., and Kim S.W. Characterization of mammary gland development in pregnant gilts. J Anim Sci 84 (2006) 579-587
20. Salmon H., and Delouis C. Kinetics of lymphocyte sub-populations and plasma cells in the mammary gland of primiparous sows in relation to gestation and lactation. Ann Rech Vet 13 (1982) 41-49
21. Eldridge-White R., Easter R.A., Heaton D.M., O'Day M.B., Petersen G.C., Shanks R.D., et al. Hormonal control of the cervix in pregnant gilts. I. Changes in the physical properties of the cervix correlate temporally with elevated serum levels of estrogen and relaxin. Endocrinology 125 (1989) 2996-3003
22. Kensinger R.S., Collier R.J., Bazer F.W., and Kraeling R.R. Effect of number of conceptuses on maternal hormone concentrations in the pig. J Anim Sci 62 (1986) 1666-1674
23. Willcox D.L., Arthur P.G., Hartmann P.E., and Whitely J.L. Perinatal changes in plasma oestradiol-17 beta, cortisol and progesterone and the initiation of lactation in sows. Aust J Biol Sci 36 (1983) 173-181
24. Farmer C. The role of prolactin for mammogenesis and galactopoiesis in swine. Livestock Prod Sci 70 (2001) 105-113
25. Berthon P., Tanneau G., and Salmon H. Immune factors of mammary secretions. In: Martinet J., and Houdebine L.M. (Eds). Biology of lactation (2000), INRA, Paris
26. Bourne F.J., and Curtis J. The transfer of immunoglobins IgG, IgA and IgM from serum to colostrum and milk in the sow. Immunology 24 (1973) 157-162
27. Schnulle P.M., and Hurley W.L. Sequence and expression of the FcRn in the porcine mammary gland. Vet Immunol Immunopathol 91 (2003) 227-231
28. Butler J.E., Sun J., Wertz N., and Sinkora M. Antibody repertoire development in swine. Dev Comp Immunol 30 (2006) 199-221
29. Vaerman J.P., Langendries A., Pabst R., and Rothkotter H.J. Contribution of serum IgA to intestinal lymph IgA, and vice versa, in minipigs. Vet Immunol Immunopathol 58 (1997) 301-308
30. Kumura B.H., Sone T., Shimazaki K., and Kobayashi E. Sequence analysis of porcine polymeric immunoglobulin receptor from mammary epithelial cells present in colostrum. J Dairy Res 67 (2000) 631-636
31. Le Jan C. Secretory component and IgA expression by epithelial cells in sow mammary gland and mammary secretions. Res Vet Sci 55 (1993) 265-270
32. De Groot N., Van Kuik-Romeijn P., Lee S.H., and De Boer H.A. Increased immunoglobulin A levels in milk by over-expressing the murine polymeric immunoglobulin receptor gene in the mammary gland epithelial cells of transgenic mice. Immunology 101 (2000) 218-224
33. Badolato R., Johnston J.A., Wang J.M., McVicar D., Xu L.L., Oppenheim J.J., et al. Serum amyloid A induces calcium mobilization and chemotaxis of human monocytes by activating a pertussis toxin-sensitive signaling pathway. J Immunol 155 (1995) 4004-4010
34. Brandtzaeg P. Mucosal immunity: integration between mother and the breast-fed infant. Vaccine 21 (2003) 3382-3388
35. Halsey J.F., Mitchell C., Meyer R., and Cebra J.J. Metabolism of immunoglobulin A in lactating mice: origins of immunoglobulin A in milk. Eur J Immunol 12 (1982) 107-112
36. Stirling C.M., Charleston B., Takamatsu H., Claypool S., Lencer W., Blumberg R.S., et al. Characterization of the porcine neonatal Fc receptor-potential use for trans-epithelial protein delivery. Immunology 114 (2005) 542-553
37. Danielsen M., Thymann T., Jensen B.B., Jensen O.N., Sangild P.T., and Bendixen E. Proteome profiles of mucosal immunoglobulin uptake in inflamed porcine gut. Proteomics 6 (2006) 6588-6596
38. Jensen A.R., Elnif J., Burrin D.G., and Sangild P.T. Development of intestinal immunoglobulin absorption and enzyme activities in neonatal pigs is diet dependent. J Nutr 131 (2001) 3259-3265
39. Bradley P.A., Bourne F.J., and Brown P.J. The respiratory tract immune system in the pig. I. Distribution of immunoglobulin-containing cells in the respiratory tract mucosa. II. Associated lymphoid tissues. Vet Pathol 13 (1990) 2-89
40. Ogra P.L., Sinks L.F., and Karzon D.T. Poliovirus antibody response in patients with acute leukemia. J Pediatr 79 (1971) 444-449
41. Ward L.A., Rich E.D., and Besser T.E. Role of maternally derived circulating antibodies in protection of neonatal swine against porcine group A rotavirus. J Infect Dis 174 (1996) 276-282
42. Klobasa F., Werhahn E., and Butler J.E. Regulation of humoral immunity in the piglet by immunoglobulins of maternal origin. Res Vet Sci 31 (1981) 195-206
43. Jaeger L.A., Lamar C.H., Bottoms G.D., and Cline T.R. Growth-stimulating substances in porcine milk. Am J Vet Res 48 (1987) 1531-1533
44. Xu R., Doan Q.C., and Regester G.O. Detection and characterisation of transforming growth factor-beta in porcine colostrum. Biol Neonate 75 (1999) 59-64
45. Jin Y., Cox D.A., Knecht R., Raschdorf F., and Cerletti N. Separation, purification, and sequence identification of TGF-beta 1 and TGF-beta 2 from bovine milk. J Protein Chem 10 (1991) 565-575
46. Miettinen P.J., Perheentupa J., Otonkoski T., Lahteenmaki A., and Panula P. EGF- and TGF-alpha-like peptides in human fetal gut. Pediatr Res 26 (1989) 25-30
47. Nguyen T.V., Yuan L., Azevedo M.S., Jeong K.I., Gonzalez A.M., and Saif L.J. Transfer of maternal cytokines to suckling piglets: in vivo and in vitro models with implications for immunomodulation of neonatal immunity. Vet Immunol Immunopathol 117 (2007) 236-248
48. Mora J.R., and von Andrian U.H. Retinoic acid: an educational "vitamin elixir" for gut-seeking T cells. Immunity 21 (2004) 458-460
49. Saurer L., McCullough K.C., and Summerfield A. In vitro induction of mucosa-type dendritic cells by all-trans retinoic acid. J Immunol 179 (2007) 3504-3514
50. Hakansson J., Hakkarainen J., and Lundeheim N. Variation in vitamin E, glutathione peroxidase and retinol concentrations in blood plasma of primiparous sows and their piglets, and in vitamin E, selenium and retinol contents in sows' milk. Acta Agric Scand A Anim Sci (2001) 51
51. Magnusson U., Rodriguez-Martinez H., and Einarsson S. A simple, rapid method for differential cell counts in porcine mammary secretions. Vet Rec 129 (1991) 485-490
52. Evans P.A., Newby T.J., Stokes C.R., and Bourne F.J. A study of cells in the mammary secretions of sows. Vet Immunol Immunopathol 3 (1982) 515-527
53. Schollenberger A., Degorski A., Frymus T., and Schollenberger A. Cells of sow mammary secretions. I. Morphology and differential counts during lactation. Zentralbl Veterinarmed A 33 (1986) 31-38
54. Schollenberger A., Frymus T., Degorski A., and Schollenberger A. Cells of sow mammary secretions. II. Characterization of lymphocyte populations. Zentralbl Veterinarmed A 33 (1986) 39-46
55. Tuboly S., Bernath S., Glavits R., and Medveczky I. Intestinal absorption of colostral lymphoid cells in newborn piglets. Vet Immunol Immunopathol 20 (1988) 75-85
56. Tuboly S., and Bernath S. Intestinal absorption of colostral lymphoid cells in newborn animals. Adv Exp Med Biol 503 (2002) 107-114
57. Williams P.P. Immunomodulating effects of intestinal absorbed maternal colostral leukocytes by neonatal pigs. Can J Vet Res 57 (1993) 1-8
58. Cepica A., and Derbyshire J.B. The effect of adoptive transfer of mononuclear leukocytes from an adult donor on spontaneous cell-mediated cytotoxicity and resistance to transmissible gastroenteritis in neonatal piglets. Can J Comp Med 48 (1984) 360-364
59. Kohl S., Pickering L.K., Cleary T.G., Steinmetz K.D., and Loo L.S. Human colostral cytotoxicity. II. Relative defects in colostral leukocyte cytotoxicity and inhibition of peripheral blood leukocyte cytotoxicity by colostrums. J Infect Dis 142 (1980) 884-891
60. Leece J.G. Effect of dietary regimen on cessation of uptake of macromolecules by piglet intestinal epithelium (closure) and transport to the blood. J Nutr 103 (1973) 751-756
61. Corthesy B. Roundtrip ticket for secretory IgA: role in mucosal homeostasis?. J Immunol 178 (2007) 27-32
62. Kadaoui K.A., and Corthesy B. Secretory IgA mediates bacterial translocation to dendritic cells in mouse Peyer's patches with restriction to mucosal compartment. J Immunol 179 (2007) 7751-7757
63. Robinson J.K., Blanchard T.G., Levine A.D., Emancipator S.N., and Lamm M.E. A mucosal IgA-mediated excretory immune system in vivo. J Immunol 166 (2001) 3688-3692
64. Butler J.E., Klobasa F., and Werhahn E. The differential localization of IgA. IgM and IgG in the gut of suckled neonatal piglets. Vet Immunol Immunopathol 2 (1981) 53-65
65. Salmon H. The mammary gland and neonate mucosal immunity. Vet Immunol Immunopathol 72 (1999) 143-155
66. Chabaudie N., Le Jan C., Olivier M., and Salmon H. Lymphocyte subsets in the mammary gland of sows. Res Vet Sci 55 (1993) 351-355
67. Weisz-Carrington P., Roux M.E., and Lamm M.E. Plasma cells and epithelial immunoglobulins in the mouse mammary gland during pregnancy and lactation. J Immunol 119 (1977) 1306-1307
68. Lee C.G., Ladds P.W., and Watson D.L. Immunocyte populations in the mammary gland of the rat at different stages of pregnancy and lactation. Res Vet Sci 24 (1978) 322-327
69. Brandtzaeg P. The secretory immune system of lactating human mammary glands compared with other exocrine organs. Ann N Y Acad Sci 409 (1983) 353-382
70. Newby T.J., and Bourne J. The nature of the local immune system of the bovine mammary gland. J Immunol 118 (1977) 461-465
71. Welsh J.K., and May J.T. Anti-infective properties of breast milk. J Pediatr 94 (1979) 1-9
72. Rumbo M., Chirdo F.G., Anon, and Fossati C.A. Detection and characterization of antibodies specific to food antigens (gliadin, ovalbumin and beta-lactoglobulin) in human serum, saliva, colostrum and milk. Clin Exp Immunol 112 (1998) 453-458
73. Macpherson A.J., Gatto D., Sainsbury E., Harriman G.R., Hengartner H., and Zinkernagel R.M. A primitive T cell-independent mechanism of intestinal mucosal IgA responses to commensal bacteria. Science 288 (2000) 2222-2226
74. Bouvet J.P., and Dighiero G. From natural polyreactive autoantibodies to a la carte monoreactive antibodies to infectious agents: is it a small world after all?. Infect Immun 66 (1998) 1-4
75. Harris N.L., Spoerri I., Schopfer J.F., Nembrini C., Merky P., Massacand J., et al. Mechanisms of neonatal mucosal antibody protection. J Immunol 177 (2006) 6256-6262
76. Inoue R., Otsuka M., and Ushida K. Development of intestinal microbiota in mice and its possible interaction with the evolution of luminal IgA in the intestine. Exp Anim 54 (2005) 437-445
77. Telemo E., Bailey M., Miller B.G., Stokes C.R., and Bourne F.J. Dietary antigen handling by mother and offspring. Scand J Immunol 34 (1991) 689-696
78. Verhasselt V., Milcent V., Cazareth J., Kanda A., Fleury S., Dombrowicz D., et al. Breast milk-mediated transfer of an antigen induces tolerance and protection from allergic asthma. Nat Med (2008)
79. Kemeny L.J., and Woods R.D. Quantitative transmissible gastroenteritis virus shedding patterns in lactating sows. Am J Vet Res 38 (1977) 307-310
80. Wagstrom E.A., Chang C.C., Yoon K.J., and Zimmerman J.J. Shedding of porcine reproductive and respiratory syndrome virus in mammary gland secretions of sows. Am J Vet Res 62 (2001) 1876-1880
81. Labeta M.O., Vidal K., Nores J.E., Arias M., Vita N., Morgan B.P., et al. Innate recognition of bacteria in human milk is mediated by a milk-derived highly expressed pattern recognition receptor, soluble CD14. J Exp Med 191 (2000) 1807-1812
82. LeBouder E., Rey-Nores J.E., Rushmere N.K., Grigorov M., Lawn S.D., Affolter M., et al. Soluble forms of Toll-like receptor (TLR)2 capable of modulating TLR2 signaling are present in human plasma and breast milk. J Immunol 171 (2003) 6680-6689
83. Rumbo M., and Schiffrin E.J. Ontogeny of intestinal epithelium immune functions: developmental and environmental regulation. Cell Mol Life Sci 62 (2005) 1288-1296
84. Donovan S.M., McNeil L.K., Jimenez-Flores R., and Odle J. Insulin-like growth factors and insulin-like growth factor binding proteins in porcine serum and milk throughout lactation. Pediatr Res 36 (1994) 159-168
85. Odle J., Zijlstra R.T., and Donovan S.M. Intestinal effects of milkborne growth factors in neonates of agricultural importance. J Anim Sci 74 (1996) 2509-2522
86. Berri M., Meurens F., Lefevre F., Chevaleyre C., Zanello G., Gerdts V., et al. Molecular cloning and functional characterization of porcine CCL28: possible involvement in homing of IgA antibody secreting cells into the mammary gland. Mol Immunol 45 (2008) 271-277
87. Hieshima K., Ohtani H., Shibano M., Izawa D., Nakayama T., Kawasaki Y., et al. CCL28 has dual roles in mucosal immunity as a chemokine with broad-spectrum antimicrobial activity. J Immunol 170 (2003) 1452-1461
88. Takahata Y., Takada H., Nomura A., Nakayama H., Ohshima K., and Hara T. Detection of interferon-gamma-inducible chemokines in human milk. Acta Paediatr 92 (2003) 659-665
89. Zhu Y., Berg M., Fossum C., and Magnusson U. Proinflammatory cytokine mRNA expression in mammary tissue of sows following intramammary inoculation with Escherichia coli. Vet Immunol Immunopathol 116 (2007) 98-103
90. Maheshwari A., Christensen R.D., and Calhoun D.A. ELR+ CXC chemokines in human milk. Cytokine 24 (2003) 91-102
91. Srivastava M.D., Srivastava A., Brouhard B., Saneto R., Groh-Wargo S., and Kubit J. Cytokines in human milk. Res Commun Mol Pathol Pharmacol 93 (1996) 263-287
92. Lee C.S., McCauley I., and Hartmann P.E. Light and electron microscopy of cells in pig colostrum, milk and involution secretion. Acta Anat (Basel) 116 (1983) 126-135
93. Bertotto A., Gerli R., Fabietti G., Crupi S., Arcangeli C., Scalise F., et al. Human breast milk T lymphocytes display the phenotype and functional characteristics of memory T cells. Eur J Immunol 20 (1990) 1877-1880
94. Campbell D.J., and Butcher E.C. Rapid acquisition of tissue-specific homing phenotypes by CD4(+) T cells activated in cutaneous or mucosal lymphoid tissues. J Exp Med 195 (2002) 135-141
95. Masopust D., Vezys V., Marzo A.L., and Lefrancois L. Preferential localization of effector memory cells in nonlymphoid tissue. Science 291 (2001) 2413-2417
96. Kunkel E.J., Campbell J.J., Haraldsen G., Pan J., Boisvert J., Roberts A.I., et al. Lymphocyte CC chemokine receptor 9 and epithelial thymus-expressed chemokine (TECK) expression distinguish the small intestinal immune compartment: epithelial expression of tissue-specific chemokines as an organizing principle in regional immunity. J Exp Med 192 (2000) 761-768
97. Salmon H. The intestinal and mammary immune system in pigs. Vet Immunol Immunopathol 17 (1987) 367-388
98. Magnusson U. Longitudinal study of lymphocyte subsets and major histocompatibility complex-class II expressing cells in mammary glands of sows. Am J Vet Res 60 (1999) 546-548
99. Picker L.J., and Butcher E.C. Physiological and molecular mechanisms of lymphocyte homing. Annu Rev Immunol 10 (1992) 561-591
100. Salmi M., and Jalkanen S. How do lymphocytes know where to go: current concepts and enigmas of lymphocyte homing. Adv Immunol 64 (1997) 139-218
101. Chao C.C., Jensen R., and Dailey M.O. Mechanisms of l-selectin regulation by activated T cells. J Immunol 159 (1997) 1686-1694
102. Mackay C.R., Marston W.L., Dudler L., Spertini O., Tedder T.F., and Hein W.R. Tissue-specific migration pathways by phenotypically distinct subpopulations of memory T cells. Eur J Immunol 22 (1992) 887-895
103. Nishimura T., Koike R., and Miyasaka M. Mammary glands of Aly mice: developmental changes and lactation-related expression of specific proteins, alpha-casein, GLyCAM-1 and MAdCAM-1. Am J Reprod Immunol 43 (2000) 351-358
104. Bourges D., Wang C.H., Chevaleyre C., and Salmon H. T and IgA B lymphocytes of the pharyngeal and palatine tonsils: differential expression of adhesion molecules and chemokines. Scand J Immunol 60 (2004) 338-350
105. Bourges D., Meurens F., Berri M., Chevaleyre C., Zanello G., Levast B., et al. New insights into the dual recruitment of IgA(+) B cells in the developing mammary gland. Mol Immunol 45 (2008) 3354-3362
106. Roux M.E., McWilliams M., Phillips-Quagliata J.M., Weisz-Carrington P., and Lamm M.E. Origin of IgA-secreting plasma cells in the mammary gland. J Exp Med 146 (1977) 1311-1322
107. Salmon H. Mammary gland immunology and neonate protection in pigs. Homing of lymphocytes into the MG. Adv Exp Med Biol 480 (2000) 279-286
108. Czarneski J., Berguer P., Bekinschtein P., Kim D.C., Hakimpour P., Wagner N., et al. Neonatal infection with a milk-borne virus is independent of beta7 integrin- and l-selectin-expressing lymphocytes. Eur J Immunol 32 (2002) 945-956
109. Middleton J., Neil S., Wintle J., Clark-Lewis I., Moore H., Lam C., et al. Transcytosis and surface presentation of IL-8 by venular endothelial cells. Cell 91 (1997) 385-395
110. Czinn S.J., and Lamm M.E. Selective chemotaxis of subsets of B lymphocytes from gut-associated lymphoid tissue and its implications for the recruitment of mucosal plasma cells. J Immunol 136 (1986) 3607-3611
111. Fronteau D., Tanneau G.M., Henry G., Chevaleyre C., Leonil J., and Salmon H. Activités chimiotactiques de lait d'artyodactyle sur les lymphocytes porcins. J Rech Porcine 30 (1998) 363-367
112. Meurens F., Berri M., Whale J., Dybvig T., Strom S., Thompson D., et al. Expression of TECK/CCL25 and MEC/CCL28 chemokines and their respective receptors CCR9 and CCR10 in porcine mucosal tissues. Vet Immunol Immunopathol 113 (2006) 313-327
113. Mickanin C.S., Bhatia U., and Labow M. Identification of a novel beta-chemokine, MEC, down-regulated in primary breast tumors. Int J Oncol 18 (2001) 939-944
114. Wang W., Soto H., Oldham E.R., Buchanan M.E., Homey B., Catron D., et al. Identification of a novel chemokine (CCL28), which binds CCR10 (GPR2). J Biol Chem 275 (2000) 22313-22323
115. Lazarus N.H., Kunkel E.J., Johnston B., Wilson E., Youngman K.R., and Butcher E.C. A common mucosal chemokine (mucosae-associated epithelial chemokine/CCL28) selectively attracts IgA plasmablasts. J Immunol 170 (2003) 3799-3805
116. Wilson E., and Butcher E.C. CCL28 controls immunoglobulin (Ig)A plasma cell accumulation in the lactating mammary gland and IgA antibody transfer to the neonate. J Exp Med 200 (2004) 805-809
117. Hodgkinson A.J., Carpenter E.A., Smith C.S., Molan P.C., and Prosser C.G. Adhesion molecule expression in the bovine mammary gland. Vet Immunol Immunopathol 115 (2007) 205-215
118. Harp J.A., Waters T.E., and Goff J.P. Adhesion molecule and homing receptor expression on blood and milk polymorphonuclear leukocytes during the periparturient period of dairy cattle. Vet Immunol Immunopathol 104 (2005) 99-103
119. Meurens F., Whale J., Brownlie R., Dybvig T., Thompson D.R., and Gerdts V. Expression of mucosal chemokines TECK/CCL25 and MEC/CCL28 during fetal development of the ovine mucosal immune system. Immunology 120 (2007) 544-555
120. Kaetzel C.S. The polymeric immunoglobulin receptor: bridging innate and adaptive immune responses at mucosal surfaces. Immunol Rev 206 (2005) 83-99
121. Phillips J.O., Everson M.P., Moldoveanu Z., Lue C., and Mestecky J. Synergistic effect of IL-4 and IFN-gamma on the expression of polymeric Ig receptor (secretory component) and IgA binding by human epithelial cells. J Immunol 145 (1990) 1740-1744
122. Martin M.G., Wang J., Li T.W., Lam J.T., Gutierrez E.M., Solorzano-Vargas R.S., et al. Characterization of the 5′-flanking region of the murine polymeric IgA receptor gene. Am J Physiol 275 (1998) G778-G788
123. Weisz-Carrington P., Emancipator S., and Lamm M.E. Binding and uptake of immunoglobulins by mouse mammary gland epithelial cells in hormone-treated cultures. J Reprod Immunol 6 (1984) 63-75
124. Weisz-Carrington P., Roux M.E., McWilliams M., Phillips-Quagliata J.M., and Lamm M.E. Hormonal induction of the secretory immune system in the mammary gland. Proc Natl Acad Sci USA 75 (1978) 2928-2932
125. Sampaio S.O., Li X., Takeuchi M., Mei C., Francke U., Butcher E.C., et al. Organization, regulatory sequences, and alternatively spliced transcripts of the mucosal addressin cell adhesion molecule-1 (MAdCAM-1) gene. J Immunol 155 (1995) 2477-2486
126. Fagarasan S., and Honjo T. Intestinal IgA synthesis: regulation of front-line body defences. Nat Rev Immunol 3 (2003) 63-72
127. Husband A.J., Kramer D.R., Bao S., Sutherland R.M., and Beagley K.W. Regulation of mucosal IgA responses in vivo: cytokines and adjuvants. Vet Immunol Immunopathol 54 (1996) 179-186
128. Siegrist C.A. Mechanisms by which maternal antibodies influence infant vaccine responses: review of hypotheses and definition of main determinants. Vaccine 21 (2003) 3406-3412
129. Kit S., Kit M., McConnell S., and Lawhorn B. Development of active immunity in newborn pigs with colostral antibodies by vaccination with gIII-deleted PRV. Acta Vet Hung 42 (1994) 319-330
130. Kit S., McConnell S., Kit M., and Lawhorn B. Circumvention of maternal antibody interference by immunization of newborn pigs with glycoprotein gIII-deleted marker vaccine. Immunol Cell Biol 71 Pt 5 (1993) 421-430
131. Van Oirschot J.T. Intranasal vaccination of pigs against Aujeszky's disease: comparison with one or two doses of attenuated vaccines in pigs with high maternal antibody titres. Res Vet Sci 42 (1987) 12-16
132. Van Oirschot J.T., and De Leeuw P.W. Intranasal vaccination of pigs against Aujeszky's disease. 4. Comparison with one or two doses of an inactivated vaccine in pigs with moderate maternal antibody titres. Vet Microbiol 10 (1985) 401-408
133. Wittmann G., and Ohlinger V. Aujeszky's disease vaccination and infection of pigs with maternal immunity: effects on cell- and antibody-mediated immunity. Arch Virol 92 (1987) 87-101
134. Boersma W.J., Van Rooij E.M., Scholten J.W., Zwart R.J., Kimman T.G., and Bianchi A. Silent memory induction in maternal immune young animals. Vet Q 20 Suppl. 3 (1998) S89-S92
135. van Oirschot J.T. Vaccination in food animal populations. Vaccine 12 (1994) 415-418
136. Kimman T.G., Oei-Lie N., and van Zaane D. Role of memory B-cell responses in serum and mucosal fluids of swine for protective immunity against pseudorabies virus. Am J Vet Res 53 (1992) 1992-1998
137. Weigel R.M., Lehman J.R., Herr L., and Hahn E.C. Field trial to evaluate immunogenicity of a glycoprotein I (gE)-deleted pseudorabies virus vaccine after its administration in the presence of maternal antibodies. Am J Vet Res 56 (1995) 1155-1162
138. Le Potier M.F., Monteil M., Houdayer C., and Eloit M. Study of the delivery of the gD gene of pseudorabies virus to one-day-old piglets by adenovirus or plasmid DNA as ways to by-pass the inhibition of immune response by colostral antibodies. Vet Microbiol 55 (1997) 75-80
139. Monteil M., Le Pottier M.F., Ristov A.A., Cariolet R., L'Hospitalier R., Klonjkowski B., et al. Single inoculation of replication-defective adenovirus-vectored vaccines at birth in piglets with maternal antibodies induces high level of antibodies and protection against pseudorabies. Vaccine 18 (2000) 1738-1742
140. Monteil M., Le Potier M.F., Cariolet R., Houdayer C., and Eloit M. Effective priming of neonates born to immune dams against the immunogenic pseudorabies virus glycoprotein gD by replication-incompetent adenovirus-mediated gene transfer at birth. J Gen Virol 78 Pt 12 (1997) 3303-3310
141. Brockmeier S.L., Lager K.M., and Mengeling W.L. Vaccination with recombinant vaccinia virus vaccines expressing glycoprotein genes of pseudorabies virus in the presence of maternal immunity. Vet Microbiol 58 (1997) 93-103
142. Monteil M., Le Potier M.F., Guillotin J., Cariolet R., Houdayer C., and Eloit M. Genetic immunization of seronegative one-day-old piglets against pseudorabies induces neutralizing antibodies but not protection and is ineffective in piglets from immune dams. Vet Res 27 (1996) 443-452
143. Fischer L., Barzu S., Andreoni C., Buisson N., Brun A., and Audonnet J.C. DNA vaccination of neonate piglets in the face of maternal immunity induces humoral memory and protection against a virulent pseudorabies virus challenge. Vaccine 21 (2003) 1732-1741
144. van Rooij E.M., Moonen-Leusen H.W., de Visser Y.E., Middel W.G., Boersma W.J., and Bianchi A.T. A DNA vaccine coding for gB and gD of pseudorabies virus (suid herpes type 1) primes the immune system in the presence of maternal immunity more efficiently than conventional vaccines. Vaccine 24 (2006) 1264-1273
145. Loeffen W.L., Heinen P.P., Bianchi A.T., Hunneman W.A., and Verheijden J.H. Effect of maternally derived antibodies on the clinical signs and immune response in pigs after primary and secondary infection with an influenza H1N1 virus. Vet Immunol Immunopathol 92 (2003) 23-35
146. Kitikoon P., Nilubol D., Erickson B.J., Janke B.H., Hoover T.C., Sornsen S.A., et al. The immune response and maternal antibody interference to a heterologous H1N1 swine influenza virus infection following vaccination. Vet Immunol Immunopathol 112 (2006) 117-128
147. Kono Y., Suzuki S., Mukai T., Okazaki K., Honda E., and Yamashiro T. Detection of specific systemic and local IgG and IgA antibodies of pigs after infection with Bordetella bronchiseptica by ELISA. J Vet Med Sci 56 (1994) 249-253
148. Klinkenberg D., Moormann R.J., de Smit A.J., Bouma A., and de Jong M.C. Influence of maternal antibodies on efficacy of a subunit vaccine: transmission of classical swine fever virus between pigs vaccinated at 2 weeks of age. Vaccine 20 (2002) 3005-3013
149. Vandeputte J., Too H.L., Ng F.K., Chen C., Chai K.K., and Liao G.A. Adsorption of colostral antibodies against classical swine fever, persistence of maternal antibodies, and effect on response to vaccination in baby pigs. Am J Vet Res 62 (2001) 1805-1811
150. Suradhat S., and Damrongwatanapokin S. The influence of maternal immunity on the efficacy of a classical swine fever vaccine against classical swine fever virus, genogroup 2.2, infection. Vet Microbiol 92 (2003) 187-194
151. Opriessnig T., Patterson A.R., Elsener J., Meng X.J., and Halbur P.G. Influence of maternal antibodies on efficacy of porcine circovirus type 2 (PCV2) vaccination to protect pigs from experimental infection with PCV2. Clin Vaccine Immunol 15 (2008) 397-401
152. Hodgins D.C., Kang S.Y., deArriba L., Parreno V., Ward L.A., Yuan L., et al. Effects of maternal antibodies on protection and development of antibody responses to human rotavirus in gnotobiotic pigs. J Virol 73 (1999) 186-197
153. Parreno V., Hodgins D.C., de Arriba L., Kang S.Y., Yuan L., Ward L.A., et al. Serum and intestinal isotype antibody responses to Wa human rotavirus in gnotobiotic pigs are modulated by maternal antibodies. J Gen Virol 80 Pt 6 (1999) 1417-1428
154. Nguyen T.V., Yuan L., Azevedo M.S., Jeong K.I., Gonzalez A.M., Iosef C., Lovgren-Bengtsson K., Morein B., Lewis P., and Saif L.J. Low titer maternal antibodies can both enhance and suppress B cell responses to a combined live attenuated human rotavirus and VLP-ISCOM vaccine. Vaccine 24 (2006) 2302-2316
155. Nguyen T.V., Yuan L., Azevedo M.S., Jeong K.I., Gonzalez A.M., Iosef C., et al. High titers of circulating maternal antibodies suppress effector and memory B-cell responses induced by an attenuated rotavirus priming and rotavirus-like particle-immunostimulating complex boosting vaccine regimen. Clin Vaccine Immunol 13 (2006) 475-485
156. Clarkson R.W., Wayland M.T., Lee J., Freeman T., and Watson C.J. Gene expression profiling of mammary gland development reveals putative roles for death receptors and immune mediators in post-lactational regression. Breast Cancer Res 6 (2004) R92-109
157. Pfaffl M.W., Wittmann S.L., Meyer H.H., and Bruckmaier R.M. Gene expression of immunologically important factors in blood cells, milk cells, and mammary tissue of cows. J Dairy Sci 86 (2003) 538-545
158. Muller A., Homey B., Soto H., Ge N., Catron D., Buchanan M.E., et al. Involvement of chemokine receptors in breast cancer metastasis. Nature 410 (2001) 50-56
159. Sikorski E.E., Hallmann R., Berg E.L., and Butcher E.C. The Peyer's patch high endothelial receptor for lymphocytes, the mucosal vascular addressin, is induced on a murine endothelial cell line by tumor necrosis factor-alpha and IL-1. J Immunol 151 (1993) 5239-5250
160. Fanti P., Nazareth M., Bucelli R., Mineo M., Gibbs K., Kumin M., et al. Estrogen decreases chemokine levels in murine mammary tissue: implications for the regulatory role of MIP-1 alpha and MCP-1/JE in mammary tumor formation. Endocrine 22 (2003) 161-168
161. Janis K., Hoeltke J., Nazareth M., Fanti P., Poppenberg K., and Aronica S.M. Estrogen decreases expression of chemokine receptors, and suppresses chemokine bioactivity in murine monocytes. Am J Reprod Immunol 51 (2004) 22-31
162. Morcol T., Akers R.M., Johnson J.L., Williams B.L., Gwazdauskas F.C., Knight J.W., et al. The porcine mammary gland as a bioreactor for complex proteins. Ann N Y Acad Sci 721 (1994) 218-233