Literature DB >> 6224616

Gastric mucosal lymphocyte subpopulations in pernicious anemia and in normal stomach.

M D Kaye, P J Whorwell, R Wright.   

Abstract

Gastric mucosal lymphocyte subpopulations were determined by an indirect immunoperoxidase method applied to cryostat sections of gastric biopsies obtained from 12 patients with pernicious anemia (PA group) and from 12 patients whose stomachs were endoscopically and histologically normal (comparison group). T-Cell populations were identified by means of monoclonal antibodies directed against all T cells (UCHT1), T suppressor cells (anti-Leu-2a), and T helper cells (anti-Leu-3a). Non-T cell numbers were estimated indirectly. Concentrations of all T cells, T suppressor cells, T helper cells, and non-T cells were all significantly greater in the PA than in the comparison group. The most striking difference was in non-T cell numbers, which showed an approximately sixfold increase in the PA group. Mean T/non-T cell ratios in PA and comparison groups were significantly different (0.49 and 1.50, respectively). T suppressor/T helper cell ratios were similar in the two groups. There were highly significant positive correlations between numbers of non-T and T helper cells, and non-T and T suppressor cells in PA, but not in comparison groups. If, as seems likely, the majority of non-T cells in these gastritic stomachs were in fact cells of B lineage, these results would be consistent with the hypothesis that gastric mucosal damage in pernicious anemia is mediated primarily by a humoral mechanism, which may involve cytotoxic autoantibodies.

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Year:  1983        PMID: 6224616     DOI: 10.1016/0090-1229(83)90110-1

Source DB:  PubMed          Journal:  Clin Immunol Immunopathol        ISSN: 0090-1229


  13 in total

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Review 2.  Gastritis.

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3.  Major parietal cell antigen in autoimmune gastritis with pernicious anemia is the acid-producing H+,K+-adenosine triphosphatase of the stomach.

Authors:  F A Karlsson; P Burman; L Lööf; S Mårdh
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4.  Vitamin B12 deficiency and gastric histopathology in older patients.

Authors:  K-R Dholakia; T-S Dharmarajan; D Yadav; S Oiseth; E-P Norkus; C-S Pitchumoni
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5.  Lymphocyte subpopulations in patients with hydroxocobalamin responsive megaloblastic anaemia.

Authors:  M A Wodzinski; M J Forrest; D Barnett; A C Lawrence
Journal:  J Clin Pathol       Date:  1985-05       Impact factor: 3.411

6.  Longitudinal study of circulating gastric antibodies in pernicious anaemia.

Authors:  R J Davidson; H I Atrah; H F Sewell
Journal:  J Clin Pathol       Date:  1989-10       Impact factor: 3.411

7.  Serum from patients with pernicious anaemia blocks gastrin stimulation of acid secretion by parietal cells.

Authors:  H J de Aizpurua; B Ungar; B H Toh
Journal:  Clin Exp Immunol       Date:  1985-08       Impact factor: 4.330

8.  A novel and effective approach of developing aggressive experimental autoimmune gastritis in neonatal thymectomized BALB/c mouse by polyinosinic:polycytidylic acid.

Authors:  Y Kobayashi; H Murakami; S M F Akbar; H Matsui; M Onji
Journal:  Clin Exp Immunol       Date:  2004-06       Impact factor: 4.330

9.  Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability.

Authors:  Deanne L V Greenwood; Patricia Crock; Stephen Braye; Patricia Davidson; John W Sentry
Journal:  Eur J Pediatr       Date:  2008-01-24       Impact factor: 3.183

10.  Involvement of the H+/K(+)-ATPase alpha subunit as a major antigenic protein in autoimmune gastritis induced by neonatal thymectomy in mice.

Authors:  K Kontani; O Taguchi; T Takahashi
Journal:  Clin Exp Immunol       Date:  1992-07       Impact factor: 4.330

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