Histological and immunohistochemical study of the lymphoid tissue in the normal stomach of the gnotobiotic pig

被引:13
作者
Driessen, A
Van Ginneken, C
Creemers, J
Lambrichts, I
Weyns, A
Geboes, K
Ectors, N
机构
[1] Katholieke Univ Leuven Hosp, Dept Pathol, Univ Ziekenhuis St Rafael, B-3000 Louvain, Belgium
[2] Limburgs Univ Ctr, Dept Histol, B-2590 Diepenbeek, Belgium
[3] Univ Antwerp, Dept Morphol Vet Anat Embryol, B-2020 Antwerp, Belgium
关键词
animal model; pig; mucosa-associated lymphoid tissue; Helicobacter pylori; gastritis; stomach;
D O I
10.1007/s00428-002-0651-8
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
Animal models have been developed in which the role of Helicobacter pylori in the pathogenesis of different gastroduodenal diseases can be investigated. The gnotobiotic pig was one of the first animal models used. In this model, Helicobacter pylori infection causes gastritis, which shows some similarities to that in humans, such as the development of mucosa-associated lymphoid tissue (MALT). Hence, this animal model can be used to study the development of MALT in the normal stomach. The aim of our study is to see if lymphoid tissue is present or absent in the normal stomach of gnotobiotic pigs before birth and if so, to investigate its development and composition as a function of gestational age and location in the stomach. Therefore, we studied 82 foetal piglets using routine histology and immunohistochemistry. Our findings show that lymphoid tissue is present at birth. It is composed of lymphoid nodules, a diffuse mononuclear infiltrate and intra-epithelial lymphocytes. The development is a sequential process. The lymphoid tissue in the stomach at birth is composed of the immunohistochemically different immunocompetent cells normally present. In conclusion, MALT is present in normal foetal gnotobiotic pig gastric mucosa, and in this model the stomach is no exception to the rest of the gastrointestinal tract.
引用
收藏
页码:589 / 598
页数:10
相关论文
共 56 条
[1]
Appleyard GD, 1998, CLIN EXP IMMUNOL, V111, P225
[2]
GENERATION OF MEMORY B-CELLS AND PLASMA-CELLS IN-VITRO [J].
ARPIN, C ;
DECHANET, J ;
VANKOOTEN, C ;
MERVILLE, P ;
GROUARD, G ;
BRIERE, F ;
BANCHEREAU, J ;
LIU, YJ .
SCIENCE, 1995, 268 (5211) :720-722
[3]
Lymphocytes in the human gastric mucosa during Helicobacter pylori have a T helper cell 1 phenotype [J].
Bamford, KB ;
Fan, XJ ;
Crowe, SE ;
Leary, JF ;
Gourley, WK ;
Luthra, GK ;
Brooks, EG ;
Graham, DY ;
Reyes, VE ;
Ernst, PB .
GASTROENTEROLOGY, 1998, 114 (03) :482-492
[4]
B-1 and B-2 cell-derived immunoglobulin M antibodies are nonredundant components of the protective response to influenza virus infection [J].
Baumgarth, N ;
Herman, OC ;
Jager, GC ;
Brown, LE ;
Herzenberg, LA ;
Chen, JZ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (02) :271-280
[5]
DIFFERENCE IN EXPRESSION OF HELICOBACTER-PYLORI GASTRITIS IN ANTRUM AND BODY [J].
BAYERDORFFER, E ;
LEHN, N ;
HATZ, R ;
MANNES, GA ;
OERTEL, H ;
SAUERBRUCH, T ;
STOLTE, M .
GASTROENTEROLOGY, 1992, 102 (05) :1575-1582
[6]
DEVELOPMENT OF THE B-CELL AND T-CELL COMPARTMENTS IN PORCINE LYMPHOID ORGANS FROM BIRTH TO ADULT LIFE - AN IMMUNOHISTOLOGICAL APPROACH [J].
BIANCHI, ATJ ;
ZWART, RJ ;
JEURISSEN, SHM ;
MOONENLEUSEN, HWM .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1992, 33 (03) :201-221
[7]
BOFILL M, 1985, J IMMUNOL, V134, P1531
[8]
CHAPMAN HA, 1974, J IMMUNOL, V112, P555
[9]
[10]
Isotype and antibody specificity of spontaneously formed immunoglobulins in pig fetuses and germ-free piglets: Production by CD5(-) B cells [J].
Cukrowska, B ;
Sinkora, J ;
Rehakova, Z ;
Sinkora, M ;
Splichal, I ;
Tuckova, L ;
Avrameas, S ;
Saalmuller, A ;
BarotCiorbaru, R ;
TlaskalovaHogenova, H .
IMMUNOLOGY, 1996, 88 (04) :611-617