Induction of mucosal tolerance in Peyer's patch-deficient, ligated small bowel loops

被引:71
作者
Kraus, TA
Brimnes, J
Muong, C
Liu, JH
Moran, TM
Tappenden, KA
Boros, P
Mayer, L
机构
[1] Mt Sinai Sch Med, Immunobiol Ctr, New York, NY 10029 USA
[2] Mt Sinai Sch Med, Dept Liver Transplant, New York, NY 10029 USA
[3] Mt Sinai Sch Med, Dept Microbiol, New York, NY 10029 USA
[4] Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA
[5] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
关键词
D O I
10.1172/JCI19102
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To explore the requirement for M cells and the Peyer's patch (PP) in induction of oral tolerance and address the potential in vivo role of intestinal epithelial cells as nonprofessional APCs, we have attempted to induce tolerance in mice with ligated small bowel loops without M cells and Peyer's patches. A 2-centimeter section of vascularized small bowel was spliced away from the gut without disruption of the mesenteric attachments. We introduced OVA directly into the lumen of the loop prior to footpad immunization. By excising segments of bowel that contain PPs in some mice and segments without patches in others, we could study the necessity of the M cell and the underlying patch versus epithelial cells in induction of mucosal tolerance. We show that OVA-specific T cell proliferation and serum antibody responses are reduced in mice that have previously been given OVA both in PP-containing loops and in loops without patches. Furthermore, both high- and low-dose tolerance could be induced in the absence of PPs. Low-dose tolerance is associated with bystander suppression and requires IL-10, which indicates active suppression and the induction of regulatory cells. These data suggest that there is a critical role for components of the mucosal immune system other than PPs in antigen sampling and induction of oral tolerance.
引用
收藏
页码:2234 / 2243
页数:10
相关论文
共 44 条
[21]   SIGNIFICANCE OF INTESTINAL FOOD PROTEIN-TRANSPORT [J].
HEYMAN, M ;
DESJEUX, JF .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1992, 15 (01) :48-57
[22]  
HUSBY S, 1994, J IMMUNOL, V152, P4663
[23]  
JAIN SL, 1995, ADV EXP MED BIOL, V371, P1245
[24]   Intestinal villous M cells: An antigen entry site in the mucosal epithelium [J].
Jang, MH ;
Kweon, MN ;
Iwatani, K ;
Yamamoto, M ;
Terahara, K ;
Sasakawa, C ;
Suzuki, T ;
Nochi, T ;
Yokota, Y ;
Rennert, PD ;
Hiroi, T ;
Tamagawa, H ;
Iijima, H ;
Kunisawa, J ;
Yuki, Y ;
Kiyono, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (16) :6110-6115
[25]   In vivo depletion of CD11c+ dendritic cells abrogates priming of CD8+ T cells by exogenous cell-associated antigens [J].
Jung, S ;
Unutmaz, D ;
Wong, P ;
Sano, GI ;
De los Santos, K ;
Sparwasser, T ;
Wu, SJ ;
Vuthoori, S ;
Ko, K ;
Zavala, F ;
Pamer, EG ;
Littman, DR ;
Lang, RA .
IMMUNITY, 2002, 17 (02) :211-220
[26]   Conversion by Peyer's patch lymphocytes of human enterocytes into M cells that transport bacteria [J].
Kerneis, S ;
Bogdanova, A ;
Kraehenbuhl, JP ;
Pringault, E .
SCIENCE, 1997, 277 (5328) :949-952
[27]   Hypoxia differentially regulates nutrient transport in rat jejunum regardless of luminal nutrient present [J].
Kles, KA ;
Tappenden, KA .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 283 (06) :G1336-G1342
[28]   Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice [J].
Koni, PA ;
Sacca, R ;
Lawton, P ;
Browning, JL ;
Ruddle, NH ;
Flavell, RA .
IMMUNITY, 1997, 6 (04) :491-500
[29]  
Liu LM, 1999, J IMMUNOL, V163, P2284
[30]   Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin β receptor, and TNF receptor I function [J].
Lorenz, RG ;
Chaplin, DD ;
McDonald, KG ;
McDonough, JS ;
Newderry, RD .
JOURNAL OF IMMUNOLOGY, 2003, 170 (11) :5475-5482