Alternate mucosal immune system: Organized Peyer's patches are not required for IgA responses in the gastrointestinal tract

被引:128
作者
Yamamoto, M
Rennert, P
McGhee, JR
Kweon, MN
Yamamoto, S
Dohi, T
Otake, S
Bluethmann, H
Fujihashi, K
Kiyono, H
机构
[1] Nihon Univ, Sch Dent, Dept Clin Pathol, Matsudo, Chiba 2718587, Japan
[2] Biogen Inst, Cambridge, MA 02142 USA
[3] Univ Alabama, Med Ctr, Immunobiol Vaccine Ctr, Birmingham, AL 35294 USA
[4] Univ Alabama, Med Ctr, Dept Oral Biol, Birmingham, AL 35294 USA
[5] Univ Alabama, Med Ctr, Dept Microbiol, Birmingham, AL 35294 USA
[6] Osaka Univ, Dept Mucosal Immunol, Microbial Dis Res Inst, Osaka, Japan
[7] F Hoffmann La Roche & Co Ltd, CH-4002 Basel, Switzerland
关键词
D O I
10.4049/jimmunol.164.10.5184
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The progeny of mice treated with lymphotoxin (LT)-beta receptor (LT beta R) and Ig (LT beta R-Ig) lack Peyer's patches but not mesenteric lymph nodes (MLN), In this study, we used this approach to determine the importance of Peyer's patches for induction of mucosal IgA Ab responses in the murine gastrointestinal tract. Immunohistochemical analysis revealed that LT beta R-Ig-treated, Peyer's patch null (PP null) mice possessed significant numbers of IgA-positive (IgA(+)) plasma cells in the intestinal lamina propria, Further, oral immunization of PP null mice with OVA plus cholera toxin as mucosal adjuvant resulted in Ag-specific mucosal IgA and serum IgG Ab responses. OVA-specific CD4(+) T cells of the Th2 type were induced in MLN and spleen of PP null mice. In contrast, when TNF and LT-alpha double knockout (TNF/LT-alpha(-/-)) mice, which lack both Peyer's patches and MLN, were orally immunized with OVA plus cholera toxin, neither mucosal IgA nor serum IgG anti-OVA Abs were induced. On the other hand, LT beta R-Ig- and TNF receptor 55-Ig-treated normal adult mice elicited OVA- and cholera toxin B subunit-specific mucosal IgA responses, indicating that both LT-alpha beta and TNF/LT-alpha pathways do not contribute for class switching for IgA Ab responses. These results show that the MLN plays a more important role than had been appreciated until now for the induction of both mucosal and systemic Ab responses after oral immunization. Further, organized Peyer's patches are not a strict requirement for induction of mucosal IgA Ab responses in the gastrointestinal tract.
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收藏
页码:5184 / 5191
页数:8
相关论文
共 48 条
[1]   Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice [J].
Alimzhanov, MB ;
Kuprash, DV ;
KoscoVilbois, MH ;
Luz, A ;
Turetskaya, RL ;
Tarakhovsky, A ;
Rajewsky, K ;
Nedospasov, SA ;
Pfeffer, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9302-9307
[2]  
BANKS TA, 1995, J IMMUNOL, V155, P1685
[3]  
BEFUS AD, 1978, IMMUNOLOGY, V35, P901
[4]   ORGAN SPECIFICITY OF LYMPHOCYTE MIGRATION - MEDIATION BY HIGHLY SELECTIVE LYMPHOCYTE INTERACTION WITH ORGAN-SPECIFIC DETERMINANTS ON HIGH ENDOTHELIAL VENULES [J].
BUTCHER, EC ;
SCOLLAY, RG ;
WEISSMAN, IL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1980, 10 (07) :556-561
[5]   Lymphocyte homing and homeostasis [J].
Butcher, EC ;
Picker, LJ .
SCIENCE, 1996, 272 (5258) :60-66
[6]  
BUTCHER EC, 1999, MUCOSAL IMMUNOLOGY, P507
[7]   PEYERS PATCHES - ENRICHED SOURCE OF PRECURSORS FOR IGA-PRODUCING IMMUNOCYTES IN RABBIT [J].
CRAIG, SW ;
CEBRA, JJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1971, 134 (01) :188-&
[8]   A SOLID-PHASE ENZYME-LINKED IMMUNOSPOT (ELISPOT) ASSAY FOR ENUMERATION OF SPECIFIC ANTIBODY-SECRETING CELLS [J].
CZERKINSKY, CC ;
NILSSON, LA ;
NYGREN, H ;
OUCHTERLONY, O ;
TARKOWSKI, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 65 (1-2) :109-121
[9]   Abnormal Development of Peripheral Lymphoid Organs in Mice Deficient in Lymphotoxin [J].
De Togni, Pietro ;
Goellner, Josphe ;
Ruddle, Nancy H. ;
Streeter, Philip R. ;
Fick, Andrea ;
Mariathasan, Sanjeev ;
Smith, Stacy C. ;
Carison, Rebecca ;
Shonnick, Laurie P. ;
strauss-Schoenberger, Jena ;
Russell, John H. ;
Karr, Robert ;
Chaplin, David D. .
JOURNAL OF IMMUNOLOGY, 2014, 192 (05) :2010-2014
[10]   Disrupted splenic architecture, but normal lymph node development in mice expressing a soluble lymphotoxin-beta receptor-IgG1 fusion protein [J].
Ettinger, R ;
Browning, JL ;
Michie, SA ;
vanEwijk, W ;
McDevitt, HO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) :13102-13107