Increased Mucosal Production of Monomeric IgA1 but No IgA1 Protease Activity in Helicobacter pylori Gastritis
Immunoglobulin A and IgM are subjected to epithelial transport only when they are produced as polymers with incorporated J chain. Immunocytes containing various Ig isotypes and associated J chain in gastric mucosa, as well as IgA-degrading protease activity in Helicobacter pylori cultures, were exam...
Saved in:
Published in | The American journal of pathology Vol. 155; no. 4; pp. 1097 - 1104 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Elsevier Inc
01.10.1999
ASIP American Society for Investigative Pathology |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Immunoglobulin A and IgM are subjected to epithelial transport only when they are produced as polymers with incorporated J chain. Immunocytes containing various Ig isotypes and associated J chain in gastric mucosa, as well as IgA-degrading protease activity in
Helicobacter pylori
cultures, were examined. Gastric body specimens from 15
H. pylori
-positive and 14
H. pylori
-negative patients were studied by paired immunofluorescence for IgA, IgA1, IgA2, IgG, or IgM and concurrent cellular J chain.
H. pylori
isolates were incubated with IgA1 or secretory IgA and examined by immunoelectrophoresis for cleavage products. A substantial increase of Ig-producing cells occurred in chronic gastritis, particularly in the IgA1 isotype, but
H. pylori
was shown to possess neither IgA1-specific nor nonspecific IgA-degrading protease activity. Regardless of infection status, reduced J chain expression was observed for all immunocyte isotypes (except for IgM) in inflamed compared with normal gastric body mucosa, the median positivity for IgA1 cells being reduced to 58.7%
versus
87.9% (
P
= 0.0002), and for IgA2 cells to 48.9%
versus
87.8% (
P
= 0.0002). This down-regulation of the J chain suggested that a large fraction of IgA monomers is produced in gastritis. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0002-9440 1525-2191 |
DOI: | 10.1016/S0002-9440(10)65212-1 |