Literature DB >> 9354677

Preferential dissemination of B-cell gastric mucosa-associated lymphoid tissue (MALT) lymphoma to the splenic marginal zone.

M Q Du1, H Z Peng, A Dogan, T C Diss, H Liu, L X Pan, R P Moseley, M J Briskin, J K Chan, P G Isaacson.   

Abstract

The tendency for gastric mucosa-associated lymphoid tissue (MALT) lymphoma cells preferentially to localize around reactive B-cell follicles, both in the mucosa and regional lymph nodes, coupled with their immunophenotype, has led to the proposal that the normal cell counterpart of this lymphoma is the marginal zone B cell. In keeping with this proposition, lymphocytes expressing the lymphoma idiotype have been detected in the splenic marginal zone in a single case of gastric MALT lymphoma. To confirm that this truly represented preferential homing of MALT lymphoma to the splenic marginal zone, we have now re-examined this case, together with 17 other cases, using both immunohistochemical and molecular methods in an attempt to establish clonal identity between the gastric lymphoma and cells in the splenic marginal zone. In three cases, the spleen was characterized by marked expansion of marginal zones by cells showing the same pattern of Ig light chain restriction as the gastric lymphoma. None of the remaining 15 cases showed histologic evidence of lymphomatous infiltration. Analysis of the Ig genes by polymerase chain reaction (PCR), cloning, and sequencing confirmed clonal identity between the splenic marginal zone infiltrates and the gastric lymphoma in the histologically involved cases. Amplifiable DNA could be extracted from only 5 of the remaining 15 cases. In 3 of these cases, including the case previously studied using an anti-idiotype, involvement of the splenic marginal zone could be confirmed using microdissection and clone-specific PCR. No involvement could be detected in the remaining 2 cases. In addition, we have shown that mucosal addressin cell adhesion molecule-1 (MAdCAM-1), the primary homing receptor of gut-mucosa for lymphocytes, was strongly expressed by the sinus lining cells of the splenic marginal zone. These results provide strong evidence for preferential involvement of the marginal zone when gastric MALT lymphomas disseminate to the spleen, which is in keeping with the notion that the marginal zone B cells are the normal counterparts of MALT lymphoma cells.

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Year:  1997        PMID: 9354677

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  7 in total

Review 1.  Molecular subtyping of gastric MALT lymphomas: implications for prognosis and management.

Authors:  M-Q Du; J C Atherton
Journal:  Gut       Date:  2006-06       Impact factor: 23.059

2.  Stage IV intramucosal gastric marginal zone B cell lymphoma of mucosa-associated lymphoid tissue type.

Authors:  Masahiko Ohtaka; Tadashi Sato; Shouji Kobayashi; Ryouta Sueki; Tatsuya Yamaguchi; Tomoyoshi Uetake; Hiroyuki Ohtsuka; Noriaki Iwao; Keita Kirito; Nobuyuki Enomoto
Journal:  Clin J Gastroenterol       Date:  2013-03-20

3.  Detection of two cell populations corresponding to distinct maturation stages in API-2/MLT-positive mucosa-associated lymphoid tissue lymphoma cells proliferating in pleural effusion.

Authors:  Yuya Kunisaki; Tsuyoshi Muta; Yujiro Yamano; Yukio Kobayashi
Journal:  Int J Hematol       Date:  2003-11       Impact factor: 2.490

Review 4.  Chronic inflammatory disease, lymphoid tissue neogenesis and extranodal marginal zone B-cell lymphomas.

Authors:  Richard J Bende; Febe van Maldegem; Carel J M van Noesel
Journal:  Haematologica       Date:  2009-07-16       Impact factor: 9.941

Review 5.  Mucosa-associated lymphoid tissue lymphomas.

Authors:  M Gospodarowicz; R Tsang
Journal:  Curr Oncol Rep       Date:  2000-03       Impact factor: 5.945

6.  Splenic marginal zone lymphoma: a literature review of diagnostic and therapeutic challenges.

Authors:  Tayse Silva Dos Santos; Renato Sampaio Tavares; Danielle Leão Cordeiro de Farias
Journal:  Rev Bras Hematol Hemoter       Date:  2016-12-22

7.  A role for gut-associated lymphoid tissue in shaping the human B cell repertoire.

Authors:  Anna Vossenkämper; Paul A Blair; Niloufar Safinia; Louise D Fraser; Lisa Das; Theodore J Sanders; Andrew J Stagg; Jeremy D Sanderson; Kirstin Taylor; Fuju Chang; Lee M Choong; David P D'Cruz; Thomas T Macdonald; Giovanna Lombardi; Jo Spencer
Journal:  J Exp Med       Date:  2013-08-12       Impact factor: 14.307

  7 in total

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