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Journal Abstract Search

408 related items for PubMed ID: 30868152

  • 1. Distinct roles for Peyer's patch B cells for induction of antigen-specific IgA antibody responses in mice administered oral recombinant Salmonella.
    Hashizume-Takizawa T, Shibata N, Kurashima Y, Kiyono H, Kurita-Ochiai T, Fujihashi K.
    Int Immunol; 2019 Jul 30; 31(8):531-541. PubMed ID: 30868152
    [Abstract] [Full Text] [Related]

  • 2. Peyer's patches are required for intestinal immunoglobulin A responses to Salmonella spp.
    Hashizume T, Togawa A, Nochi T, Igarashi O, Kweon MN, Kiyono H, Yamamoto M.
    Infect Immun; 2008 Mar 30; 76(3):927-34. PubMed ID: 18086815
    [Abstract] [Full Text] [Related]

  • 3. Toll-like receptor 5 is not essential for the promotion of secretory immunoglobulin A antibody responses to flagellated bacteria.
    Hashizume-Takizawa T, Yamamoto M.
    Microbiol Immunol; 2015 Dec 30; 59(12):716-23. PubMed ID: 26564803
    [Abstract] [Full Text] [Related]

  • 4. CCR7-deficient mice exhibit a delayed antigen-specific mucosal IgA antibody response to an oral recombinant Salmonella strain.
    Hashizume-Takizawa T, Kobayashi R, Tsuzukibashi O, Saito M, Kurita-Ochiai T.
    Pathog Dis; 2019 Apr 01; 77(3):. PubMed ID: 31065695
    [Abstract] [Full Text] [Related]

  • 5. Helper T cell subsets for immunoglobulin A responses: oral immunization with tetanus toxoid and cholera toxin as adjuvant selectively induces Th2 cells in mucosa associated tissues.
    Xu-Amano J, Kiyono H, Jackson RJ, Staats HF, Fujihashi K, Burrows PD, Elson CO, Pillai S, McGhee JR.
    J Exp Med; 1993 Oct 01; 178(4):1309-20. PubMed ID: 8376936
    [Abstract] [Full Text] [Related]

  • 6. Alternate mucosal immune system: organized Peyer's patches are not required for IgA responses in the gastrointestinal tract.
    Yamamoto M, Rennert P, McGhee JR, Kweon MN, Yamamoto S, Dohi T, Otake S, Bluethmann H, Fujihashi K, Kiyono H.
    J Immunol; 2000 May 15; 164(10):5184-91. PubMed ID: 10799877
    [Abstract] [Full Text] [Related]

  • 7. Mechanisms regulating IgA class-specific immunoglobulin production in murine gut-associated lymphoid tissues. I. T cells derived from Peyer's patches that switch sIgM B cells to sIgA B cells in vitro.
    Kawanishi H, Saltzman LE, Strober W.
    J Exp Med; 1983 Feb 01; 157(2):433-50. PubMed ID: 6185611
    [Abstract] [Full Text] [Related]

  • 8. Oral immunization of interleukin-4 (IL-4) knockout mice with a recombinant Salmonella strain or cholera toxin reveals that CD4+ Th2 cells producing IL-6 and IL-10 are associated with mucosal immunoglobulin A responses.
    Okahashi N, Yamamoto M, Vancott JL, Chatfield SN, Roberts M, Bluethmann H, Hiroi T, Kiyono H, McGhee JR.
    Infect Immun; 1996 May 01; 64(5):1516-25. PubMed ID: 8613355
    [Abstract] [Full Text] [Related]

  • 9. IgA responses in xid mice: oral antigen primes Peyer's patch cells for in vitro immune responses and secretory antibody production.
    Kiyono H, Mosteller LM, Eldridge JH, Michalek SM, McGhee JR.
    J Immunol; 1983 Dec 01; 131(6):2616-22. PubMed ID: 6227659
    [Abstract] [Full Text] [Related]

  • 10. Mechanisms regulating IgA class-specific immunoglobulin production in murine gut-associated lymphoid tissues. II. Terminal differentiation of postswitch sIgA-bearing Peyer's patch B cells.
    Kawanishi H, Saltzman L, Strober W.
    J Exp Med; 1983 Sep 01; 158(3):649-69. PubMed ID: 6604126
    [Abstract] [Full Text] [Related]

  • 11. Mucosal immunoregulation: environmental lipopolysaccharide and GALT T lymphocytes regulate the IgA response.
    McGhee JR, Michalek SM, Kiyono H, Eldridge JH, Colwell DE, Williamson SI, Wannemuehler MJ, Jirillo E, Mosteller LM, Spalding DM.
    Microbiol Immunol; 1984 Sep 01; 28(3):261-80. PubMed ID: 6234450
    [Abstract] [Full Text] [Related]

  • 12. Sphingosine 1-phosphate regulates the egress of IgA plasmablasts from Peyer's patches for intestinal IgA responses.
    Gohda M, Kunisawa J, Miura F, Kagiyama Y, Kurashima Y, Higuchi M, Ishikawa I, Ogahara I, Kiyono H.
    J Immunol; 2008 Apr 15; 180(8):5335-43. PubMed ID: 18390715
    [Abstract] [Full Text] [Related]

  • 13. Lack of antigen-specific immune responses in anti-IL-7 receptor alpha chain antibody-treated Peyer's patch-null mice following intestinal immunization with microencapsulated antigen.
    Kunisawa J, Takahashi I, Okudaira A, Hiroi T, Katayama K, Ariyama T, Tsutsumi Y, Nakagawa S, Kiyono H, Mayumi T.
    Eur J Immunol; 2002 Aug 15; 32(8):2347-55. PubMed ID: 12209648
    [Abstract] [Full Text] [Related]

  • 14. In vivo immune response to a T-cell-dependent antigen by cultures of disassociated murine Peyer's patch.
    Kiyono H, McGhee JR, Wannemuehler MJ, Frangakis MV, Spalding DM, Michalek SM, Koopman WJ.
    Proc Natl Acad Sci U S A; 1982 Jan 15; 79(2):596-600. PubMed ID: 6979042
    [Abstract] [Full Text] [Related]

  • 15. Comparison of murine nasal-associated lymphoid tissue and Peyer's patches.
    Heritage PL, Underdown BJ, Arsenault AL, Snider DP, McDermott MR.
    Am J Respir Crit Care Med; 1997 Oct 15; 156(4 Pt 1):1256-62. PubMed ID: 9351630
    [Abstract] [Full Text] [Related]

  • 16. Immunosuppression caused by antigen feeding II. Suppressor T cells mask Peyer's patch B cell priming to orally administered antigen.
    MacDonald TT.
    Eur J Immunol; 1983 Feb 15; 13(2):138-42. PubMed ID: 6219883
    [Abstract] [Full Text] [Related]

  • 17. Optimizing oral vaccines: induction of systemic and mucosal B-cell and antibody responses to tetanus toxoid by use of cholera toxin as an adjuvant.
    Jackson RJ, Fujihashi K, Xu-Amano J, Kiyono H, Elson CO, McGhee JR.
    Infect Immun; 1993 Oct 15; 61(10):4272-9. PubMed ID: 8406816
    [Abstract] [Full Text] [Related]

  • 18. CD19-deficient mice exhibit poor responsiveness to oral immunization despite evidence of unaltered total IgA levels, germinal centers and IgA-isotype switching in Peyer's patches.
    Gärdby E, Lycke NY.
    Eur J Immunol; 2000 Jul 15; 30(7):1861-71. PubMed ID: 10940875
    [Abstract] [Full Text] [Related]

  • 19. The preference for switching to IgA expression by Peyer's patch germinal center B cells is likely due to the intrinsic influence of their microenvironment.
    Weinstein PD, Cebra JJ.
    J Immunol; 1991 Dec 15; 147(12):4126-35. PubMed ID: 1753088
    [Abstract] [Full Text] [Related]

  • 20. Oral vaccine models: multiple delivery systems employing tetanus toxoid.
    Jackson RJ, Staats HF, Xu-Amano J, Takahashi I, Kiyono H, Hudson ME, Gilley RM, Chatfield SN, McGhee JR.
    Ann N Y Acad Sci; 1994 Aug 15; 730():217-34. PubMed ID: 8080173
    [Abstract] [Full Text] [Related]

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