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Secretory IgA and Mucosal Immune Responses

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Digestive Disease Pathology
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Abstract

Mucosal immunity is charascterized predominantly by a secretory antibody response, involving immunoglobulins of the IgA class. They provide an immunological barrier to foreign matter by preventing absorption of such materials into the mucosal epithelium and penetration into the body. The humoral responses in nonmucosal sites are largely of the IgG class. The cell-mediated immune mechanism is also distinctive in mucosal and nonmucosal lymphoid organs. During the past decade, significant advances have been made in understanding the mucosal immune system. Ontological and physiological relationships between immunocompetent cells in mucosal and nonmucosal sites have been characterized, and the postulation of a common mucosal immune system1,2 involving the intestinal tract, biliary tract, mammary glands, salivary glands, lacrimal glands, and female genital tract has led to new insights.

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References

  1. Bienenstock J.: The physiology of the local immune response and the gastrointestinal tract. In Progress in Immunology 11, vol 4, Brent L, Holborow J. ed. Amsterdam, North-Holland, 1974, p197

    Google Scholar 

  2. McDermott M.R., Bienenstock J.: Evidence for a common mucosal immunologic system. I. Migration of B immunoblasts into intestinal, respiratory, and genital tissues. J Immunol 122: 1892, 1979

    PubMed  CAS  Google Scholar 

  3. Brown W.R.: The central role of the gastrointestinal tract in immunological reactions. Tokai J Exp Clin Med 8: 1, 1983

    PubMed  CAS  Google Scholar 

  4. Stokes C.R.: Induction and control of intestinal immune responses, in Local Immune Responses of the Gut, Newby T.J., Stokes C.R. (eds). Boca Raton, CRC Press, 1984, p97

    Google Scholar 

  5. Hong R., Ammann A.J.: Selective absence of IgA. Autoimmune phenomena and autoimmune disease. Am J Pathol 69: 491, 1972

    PubMed  CAS  Google Scholar 

  6. Morris B., Morris R.: The absorption of 1251-labelled immunoglobulin G by different regions of the gut in young rats. J Physiol (Lond) 241: 761, 1974

    CAS  Google Scholar 

  7. Nagura H., Nakane P.K., Brown W.R.: Breast milk IgA binds to jejuna) epithelium in suckling rats. J Immunol 120: 1333, 1978

    PubMed  CAS  Google Scholar 

  8. Rodewald R., Kraehenbuhl J.P.: Receptor-mediated transport of IgG. J Cell Biol 99: 159s, 1984

    Google Scholar 

  9. Rodewald R.: Intestinal transport of antibodies in the newborn rat. J Cell Biol 58: 189, 1973

    Article  PubMed  CAS  Google Scholar 

  10. Ogra S.S.D., Weintraub D., Ogra P.L.: Immunological aspects of human colostrum and milk. III. Fate and absorption of cellular and soluble components in the gastrointestinal tract of the newborn. J Immunol 119: 245, 1977

    PubMed  CAS  Google Scholar 

  11. Hanson L.A., Ahlstedt S., Andersson B., Carlsson B., Dahlgren U., Lidin-Janson G., Mattsby-Baltzer M., Svanborg-Eden C.: The biologic properties of secretory IgA. J Reticuloendothel Soc 28:!s,1980

    Google Scholar 

  12. Hanson L.A., Winberg J.: Breast milk and defense against infection in the newborn. Arch Dis Child 47: 845, 1972

    Article  PubMed  CAS  Google Scholar 

  13. Walker W.A.: Antigen penetration across the immature gut: effect of immunologic and maturational factors in colostrum. In Immunology of Breast Milk. Ogra P.L., Dayton D. eds. New York, Raven Press, 1979, p227

    Google Scholar 

  14. Diaz-Jouanen E., Williams R.C. Jr.: T and B lymphocytes in human colostrum. Clin Immunol Immunopathol 3: 248, 1974

    Article  PubMed  CAS  Google Scholar 

  15. Reddy V., Bhaskaram C., Raghuramulu N., Jagadeesan V.: Antimicrobial factors in human milk. Acta Paediatr Scand 66: 229, 1977

    Article  PubMed  CAS  Google Scholar 

  16. Stephen S., Dolby J.M., Montreuil J., Spik G.: Differences in inhibition of the growth of commensal and enteropathogenic strains of Escherichia coli by lactotransferrin and secretory immunoglobulin A isolated from human milk. Immunology 41: 597, 1980

    Google Scholar 

  17. Watanabe T., Nagura H., Watanabe K., Brown W.R.: The binding of human milk lactoferrin to immunoglobulin A. FEBS Letters 168: 203, 1984

    Article  PubMed  CAS  Google Scholar 

  18. Weaver E.A., Rudloff H.E., Goldblum R.M., Davis C.P., Goldman A.S.: Selection of immunoglobulin A by human milk leukocytes initiated by surface membrane stimuli. J Immunol 132: 684, 1984

    PubMed  CAS  Google Scholar 

  19. Craig S.W., Cebra J.J.: Peyer’s patches: an enriched source of precursors for IgA-producing immunocytes in the rabbit. J Exp Med 134: 188, 1971

    Article  PubMed  CAS  Google Scholar 

  20. Owen R.L., Jones A.L.: Epithelial cell specialization within Peyer’s patches: an ultrastructural study of intestinal lymphoid follicles. Gastroenterology 66: 189, 1974

    PubMed  CAS  Google Scholar 

  21. Owen R.L.: Sequential uptake of horseradish peroxidase by lymphoid follicle epithelium of Peyer’s patches in the normal unobstructed mouse intestine. An ultrastructural study. Gastroenterology 72: 440, 1977

    PubMed  CAS  Google Scholar 

  22. Bockman D.E., Cooper M.D.: Early lymphocpithelial relationship in human appendix. A combined light and electron-microscopic study. Gastroenterology 68: 1160, 1975

    PubMed  CAS  Google Scholar 

  23. Simina T., Plesch B.E.C.: An immunohistochemical study of cells with surface and cytoplasmic immunoglobulins in situ in Peyer’s patches and lamina propria of rat small intestine. Virchow’s Arch B 40: 181, 1982

    Article  Google Scholar 

  24. Mayrhofer G., Pugh C.W., Barclay A.N.: The distribution, ontogeny and origin in the rat of la positive cells with dendritic morphology and Ia antigen in epithelia, with special reference to the intestine. Eur J Immunol 13: 112, 1983

    Article  PubMed  CAS  Google Scholar 

  25. Howard J.C., Hunt S.V., Gowans J.L.: Identification of marrow-derived and thymus-derived small lymphocytes in the lymphoid tissue and thoracic duct lymph of normal rats. J Exp Med 135: 200, 1972

    Article  PubMed  CAS  Google Scholar 

  26. Meuwissen H.J., Kaplan G.T., Percy D.Y., Good R.A.: Role of rabbit gut-associated lymphoid tissue in cell replication. The follicular cortex as a primary germinative site. Proc Soc Exp Biol Med 130: 300, 1969

    PubMed  CAS  Google Scholar 

  27. Cooper G.N., Thonard J.C., Crosby R.L., Dalbow M.H.: Immunological responses in rats following antigenic stimulation of Peyer’s patches. II. Histological changes in germ-free animals. Aust J Exp Biol Med Sci 46: 407, 1968

    Article  PubMed  CAS  Google Scholar 

  28. Pollard M., Sharon N.: Responses of the Peyer’s patches in germ-free mice to antigenic stimulation. Infect Immun 2: 96, 1970

    PubMed  CAS  Google Scholar 

  29. Sobhan P.: The light and electron microscopic studies of Peyer’s patches in non-germfree adult mice. J Morphol 135: 457, 1971

    Article  Google Scholar 

  30. Moore A.R., Hall J.G.: Evidence for a primary association between immunoblast and small gut. Nature (Lond) 239: 161, 1972

    Article  CAS  Google Scholar 

  31. Nagura H., Kohler P.F., Brown W.R.: Immunocytochemical characterization of the lymphocytes in nodular lymphoid hyperplasia of the bowel. Lab Invest 40: 66, 1979

    PubMed  CAS  Google Scholar 

  32. Kawanishi H., Saltzman L.E., Strober W.: Mechanisms regulating IgA class-specific immunoglobulin production in murine gut-associated lymphoid tissues. I. T cells derived from Peyer’s patches that switch slgM B cells to sIgA B cells in vitro. J Exp Med 157: 433, 1983

    Article  PubMed  CAS  Google Scholar 

  33. Simina T., Janse E.M., Wilders M.M.: Antigen-trapping cells in Peyer’s patches of the rat. Scand J Immunol 16: 481, 1982

    Article  Google Scholar 

  34. Nagura H., Tsutsumi Y., Shimamura K., Shioda Y., Hasegawa H., Tamaoki K.: Immunohistochemical observation of human solitary lymphoid follicles. Digestive Organ and Immunology 12: 89, 1984

    Google Scholar 

  35. Shioda Y., Nagura H., Tsutsumi Y., Shimamura K., Tamaoki N.: Distribution of Leu7 (HNK-1) antigen in human digestive organs: an immunohistochemical study with monoclonal antibody. Histochem J 16: 843, 1984

    Article  PubMed  CAS  Google Scholar 

  36. Gowans J.L., Knight E.J.: The route of recirculation of lymphocytes in the rat. Proc Roy Soc Lond Ser B 159: 257, 1964

    Article  CAS  Google Scholar 

  37. Barclay A.N.: Different reticular elements in rat lymphoid tissue identified by localization of Ia, Thy-1 and MRC OX2 antigens. Immunology 44: 727, 1981

    PubMed  CAS  Google Scholar 

  38. Bhalla D.K., Murakami T., Owen R.L.: Microcirculation of intestinal lymphoid follicles in rat Peyer’s patches. Gastroenterology 81: 481, 1981

    PubMed  CAS  Google Scholar 

  39. Keren D.F.: Immunology and Immunopathology of the Gastrointestinal Tract. Chicago, American Soci clonal antibodies: a distinct subset of monocytes conety of Clinical Pathologists, 1980, pl0 tains the cells capable of including the autologous

    Google Scholar 

  40. Ferguson A.: Intraepithelial lymphocytes of the small intestine. Gut 18: 921, 1977

    Article  PubMed  CAS  Google Scholar 

  41. Cerf-Bensussan N., Schneeberger E.E., Bhan A.K.: Immunohistologic and immunoelectron microscopic characterization of the mucosal lymphocytes of tibodies. J Immunol 130: 2615, 1983

    PubMed  CAS  Google Scholar 

  42. Sprent J.: Fate of H2-activated T-lymphocytes in syn geneic host. I. Fate in lymphoid tissues and intestines traced with 3H-thymidine, 1251-dcoxyuridine and 51chromium. Cell Immunol 21: 278, 1976

    Article  PubMed  CAS  Google Scholar 

  43. Selby W.S., Janossy G., Goldstein G., Jewell D.P.: T lymphocyte subsets in human intestinal mucosa: the distribution and relationship to MHC-derived anti gens. Clin Exp Immunol 44: 453, 1981

    PubMed  CAS  Google Scholar 

  44. Shioda Y., Nagura H., Tsutsumi Y., Saito H., Tama-oki K.: Immunohistochemical analysis of intraepithe lial lymphocytes of human intestine. Digestive Organ and Immunology 10: 149, 1983

    Google Scholar 

  45. Flexman J.P., Shellam G.R., Mayrhofer G.: Naturalcytotoxicity, responsiveness to interferon and mor-phology of intraepithelial lymphocytes from the small intestine of the rat. Immunology 48: 733, 1983

    PubMed  CAS  Google Scholar 

  46. Crabbe P.A., Nash D.R., Bazin H., Eyssen H., Heremans J.F.: Immunohistochemical observations on lymphoid tissue from conventional and germ-free mice. Lab Invest 22: 448, 1970

    PubMed  CAS  Google Scholar 

  47. Nagura H., Hasegawa H., Yoshimura S., Aihara K., Watanabe K., Ozawa A.: Comparative studies on se-conventional and germfree rat intestinal mucosa: with special reference to microbial flora and secretory IgA; in Recent Advances in Germfree Research. Sa- cretory component (SC) on the surface of human in-saki S., Ozawa A., Hashimoto K. (eds). Tokyo, Tokai Univ Press, 1982, p511

    Google Scholar 

  48. Gustafsson B.E., Laurell C.B.: Gamma-globulins in germ-free rats. J Exp Med 108: 251, 1958

    Article  PubMed  CAS  Google Scholar 

  49. Miyakawa M., Iijima S., Kobayashi R., Tajima M.: Observations on the lymphoid tissue of the germ-free guinea pig. Acta Pathol Jpn 7: 183, 1957

    Google Scholar 

  50. Wastmann B.S.: Recent studies on the serum proteins of germfree animals. Ann NY Acad Sci 94: 272, 1961

    Article  Google Scholar 

  51. Hummel K.P.: The structure and development of the lymphatic tissue in the intestine of the albino rat. Am J Anat 57: 907, 1972

    Google Scholar 

  52. Spalding D.M., Williamson S.I., Koopman W.J., McGhee J.R.: Preferential induction of polyclonal IgA secretion by murine Peyer’s patch dendritic cell-T cell mixture. J Exp Med 160: 941, 1984

    Article  PubMed  CAS  Google Scholar 

  53. Nagura H., Watanabe K.: Mucosal immune system and immune responses in the intestine. In Gastroin testinal Function Regulation and Disturbances, vol.2, Kasuya Y., Tsuchiya M., Nagao F., Matsuo Y. eds. Amsterdam, Excerpta Medica, 1984, p147

    Google Scholar 

  54. Butcher E.C., Stevens S.K., Reichert R.A., Scollay R.G., Weissman I.L.: Lymphocyte-endothelial cell recognition in lymphocyte migration and the segre gation of mucosal and nonmucosal immunity. In Re cent Advances in Mucosal Immunity, Strober W., Hanson L.A., Sell K.W. eds, New York, Raven Press, 1982, p3

    Google Scholar 

  55. Parrott D.M., Ferguson A.: Selective migration of lymphocytes within the mouse small intestine. Im munology 26: 571, 1974

    CAS  Google Scholar 

  56. Nagura H., Koshikawa T.: Immunocytochemical analysis of the structure and function of Peyer’s 80: 623, 1981

    Google Scholar 

  57. Shen H.H., Talle M.A., Goldstein G., Chess L.: Funetional subsets of human monocytes defined by mono-mixed lymphocyte culture. J Immunol 130: 698, 1983

    PubMed  CAS  Google Scholar 

  58. Ahnen D.J., Brown W.R., Kloppel T.M.: Secretory component: the polymeric immunoglobulin receptor. What’s in it for the gastroenterologist and hepatolo-human small intestine by the use of monoclonal angist? Gastroenterology 89: 667, 1985

    PubMed  CAS  Google Scholar 

  59. Nagura H., Brandtzaeg P., Nakane P.K., Brown W.R.: Ultrastructural localization of J chain in human intestinal mucosa. J Immunol 123: 1044, 1979

    CAS  Google Scholar 

  60. Nagura H., Tsutsumi Y., Hasegawa H., Watanabe K., Nakane P.K., Brown W.R.: IgA plasma cells in biliary mucosa: a likely source of locally synthesized IgA in human hepatic bile. Clin Exp Immunol 54: 671, 1983

    PubMed  CAS  Google Scholar 

  61. Halsey J.F., Johnson B.H., Cebra J.J.: Transport of immunoglobulin from scrum into colostrum. J Exp Med 151: 767, 1980

    Article  PubMed  CAS  Google Scholar 

  62. Nagura H., Smith P.D., Nakane P.K., Brown W.R.: IgA in human bile and liver. J Immunol 126:587, 1981

    Google Scholar 

  63. Heremans J.F.: Immunoglobulin A. In The Antigens, vol II, Sela Med, New York, Academic Press, 1974, p365

    Google Scholar 

  64. Nagura H., Tsutsumi Y., Shioda Y., Watanabe K.: Immunohistochemistry of gastric carcinomas and as-sociated diseases: novel distribution of carcinoem-bryonic antigen and secretory component on the surface of gastric cancer cells. J Histochem Cytochem 31: 193, 1983

    Article  PubMed  CAS  Google Scholar 

  65. Brandtzaeg, P.: Transport models for secretory IgA and IgM. Clin Exp Immunol 44: 221, 1981

    PubMed  CAS  Google Scholar 

  66. Brandtzaeg P.: Polymeric IgA is complexed with cretory component (SC) on the surface of human in testinal epithelial cells. Scand J Immunol 8: 39, 1978

    Article  PubMed  CAS  Google Scholar 

  67. Nagura H., Nakane P.K., Brown W.R.: Translocation of dimeric IgA through neoplastic colon cells in vitro. J Immunol 123: 2359, 1979

    PubMed  CAS  Google Scholar 

  68. Koshland M.E.: Structure and function of the J chain. Adv Immunol 20: 41, 1975

    Article  CAS  Google Scholar 

  69. Mostov K.E., Kraehenbuhl J.P., Brobel F.: Receptor-mediated transcellular transport of immunoglobulin: synthesis of secretory component as multiple and larger transmembrane forms. Proc Natl Acad Sci USA 77: 7257, 1980

    Article  PubMed  CAS  Google Scholar 

  70. Lemaitre-Coelho I., Jackson G.D.F., Vaerman J-P.: Rat bile as a convenient source of secretory IgA and free secretory component. EurJ Immunol 8: 588, 1977

    Article  Google Scholar 

  71. Vaerman J-P., Lemaitre-Coelho, I.M., Limet J.N., Delacroix D.L.: Hepatic transfer of polymeric IgA from plasma to bile in rats and other mammals: a sur-vey. In Recent Advances in Mucosal Immunity. Strober W, Hanson LA, Sell KW eds. New York,Raven Press, 1982, p233

    Google Scholar 

  72. Takahashi I., Nakane P.K., Brown W.R.: Ultrastruc-tural events in the translocation of polymeric IgA by rat hepatocytes. J Immunol 128: 1181, 1982

    PubMed  CAS  Google Scholar 

  73. Chandy K.G., Hubscher S.G., Elias E., Berg J., Khan M., Burnett D.: Dual role of the liver in regulating circulating polymeric IgA in man: studies on patients with liver disease. Clin Exp Immunol 52: 207, 1983

    PubMed  CAS  Google Scholar 

  74. Brown T.A., Russell M.W., Mestecky J.: Hepatobiliary transport of IgA immune complexes: molecular and cellular aspects. J Immunol 128: 2183, 1982

    PubMed  CAS  Google Scholar 

  75. Peppard J., Orlans E., Payne A.W.R., Andrew E.: The elimination of circulating complexes containing polymeric IgA by excretion in the bile. Immunology 42: 83, 1981

    PubMed  CAS  Google Scholar 

  76. Kraft S.C.: The liver as an “IgA pump.” Gastroenterpatches. Jap J Gastroenterol 82: 2312, 1985

    Google Scholar 

  77. Hall R.P., Lawley T.J., Heck J.A.: IgA-containing cir-ology culating immune complexes in dermatitis herpetiformis, Henoch-Schoenlein purpura, systemic lupus erythematosus and other diseases. Clin Exp Immunol 40: 431, 1980

    PubMed  CAS  Google Scholar 

  78. Kater L., Jobsis A.C., de la Faille-Kuyper E.H.B., Vogten A.J.M., Grijm R.: Alcoholic hepatic disease. Specificity of IgA deposits in liver. Am J Clin Pathol 71: 51, 1979

    Google Scholar 

  79. Nagura H., Tsutsumi Y., Watanabe K., Hasegawa H., Kobayashi K.: Studies on the relationships of IgA in human liver. Digestive Organ and Immunology 8: 315, 1982

    Google Scholar 

  80. Delacroix D.L., Reymaert M., Pauwels S., Geubel A.P., Vaerman J.P.: High serum levels of secretory IgA in liver disease. Possible liver origin of the circulating secretory component. Dig Dis Sci 27: 333, 1982

    Article  PubMed  CAS  Google Scholar 

  81. Fukuda Y., Imoto M., Hayakawa T.: Serum levels of secretory immunoglobulin A in liver diseases. Am J Gastroenterol 80: 237, 1985

    PubMed  CAS  Google Scholar 

  82. Fukuda Y., Nagura H., Asai J., Satake T.: Possible mechanisms of elevation of serum immunoglobulin A in liver diseases. Am J Gastroenterol 81: 315, 1986

    PubMed  CAS  Google Scholar 

  83. Kleinman R.E., Harmatz P.R., Walker W.A.: The liver: an integral part of the enteric mucosal immune system. Hepatology 2: 379, 1982

    Article  PubMed  CAS  Google Scholar 

  84. Nagura H., Koshikawa T., Fukuda Y., Asai J.: Hepatic vascular endothelial cells heterogeneously express surface antigens associated with monocytes, macrophages and T lymphocytes. Virchows Arch A 409: 407, 1985

    Article  Google Scholar 

  85. Berzofsky J.A., Richman L.K., Strober W.: Determinant-specific antigen presentation by liver Kupffer cells under control of H-2-linked Ir genes. In Recent Advances in Mucosal Immunity. Strober W., Hanson L.A., Sell K.W. eds, New York, Raven Press, 1982, p215

    Google Scholar 

  86. Praaning-van Dalen D.P., Brouwer A., Knook D.L.: Clearance capacity of rat liver Kupffer, endothelial, and parenchymal cells. Gastroenterology 81: 1036, 1981

    Google Scholar 

  87. Souhami R.L.: The effect of colloidal carbon on the organ distribution of sheep red blood cells and the immune response. Immunology 22: 685, 1972

    PubMed  CAS  Google Scholar 

  88. Richman L.K., Klingenstein R.J., Richman J.A., Strober W., Berzofsky J.A.: The murine Kupffer cell. I. Characterization of the cell serving accessory function in antigen-specific T cell proliferation. J Immunol 123: 2602, 1980

    Google Scholar 

  89. Strober W., Richman L.K., Elson C.O.: The regulation of gastrointestinal immune responses. Immunology Today, August: 156, 1981

    Google Scholar 

  90. Richman L.K., GraeffA.S., Yarchoan R., Strobcr W.: Simultaneous induction of antigen-specific IgA helper T cells and IgG suppressor T cells in the murine Peycr’s patch after protein feeding. J Immunol 126: 2079, 1981

    PubMed  CAS  Google Scholar 

  91. Andre C., Lambert R., Bazin H.: Interference of oral immunization with the intestinal absorption of heterologous albumin. Eur J Immunol 4: 701, 1974

    Article  PubMed  CAS  Google Scholar 

  92. Stokes C.R., Swarbrick E.T., Soothill J.F.: Immune elimination and enhanced antibody responses: functions of circulating IgA. Immunology 40: 455, 1980

    PubMed  CAS  Google Scholar 

  93. Cunningham-Rundles C., Brandeis W.E., Good R.A., Day N.K.: Bovine antigens and the formation of circulating immune complexes in selective immunoglobulin A deficiency. J Clin Invest 64: 272, 1979

    Article  PubMed  CAS  Google Scholar 

  94. Thomas H.C., Derilliers D., Potter B.J., Hodgson H., Jain S., Jewell D.P., Sherlock S.: Immune complexes in acute and chronic liver disease. Clin Exp Immunol 31: 150, 1978

    PubMed  CAS  Google Scholar 

  95. Triger D.R., Alp M.H., Wright R.: Bacterial and dietary antibodies in liver disease. Lancet 1: 60, 1972

    Article  PubMed  CAS  Google Scholar 

  96. Cantor H.M., Dumont A.H.: Hepatic suppression of sensitization to antigen absorbed into the portal system. Nature (London) 215: 744, 1967

    Article  CAS  Google Scholar 

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Nagura, H., Sumi, Y. (1988). Secretory IgA and Mucosal Immune Responses. In: Watanabe, S., Wolff, M., Sommers, S.C. (eds) Digestive Disease Pathology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-11562-6_9

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