Clinical and Diagnostic Laboratory Immunology, November 1999, p. 803-807, Vol. 6, No. 6
1071-412X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Center for Vaccine Development,
Received 28 May 1999/Returned for modification 24 June
1999/Accepted 11 August 1999
A gastrointestinal explant culture system was developed and
compared to the mononuclear cell extraction and enzyme-linked immunospot assay method for measurement of immunoglobulin A (IgA) and
IgG antibody-secreting cells (ASCs) in gastric antral and duodenal
biopsies of non-Helicobacter pylori-infected volunteers. IgA and IgG were detected in explant supernatants during 6 to 7 days of
culture in all subjects. IgA containing secretory component was also
detected throughout the culture period, although peak production
occurred only in the first 3 days. During 7 days of culture, the
cumulative geometric mean IgA levels produced were 2.2 and 8.02 µg/ml/10 mg of antral and duodenal biopsy tissues, respectively,
while the cumulative geometric mean IgG levels were 1.54 and 2.92 µg/ml/10 mg of antral and duodenal biopsy tissues, respectively.
Cycloheximide treatment resulted in a >90% reduction in both
immunoglobulin classes after 6 days of treatment compared to levels in
untreated controls. The detection of IgA and IgG ASCs extracted from
biopsies on days 1 and 6 of culture confirmed that the antibody
detected was derived from mucosal lamina propria. The IgA and IgG ASC
responses were positively correlated with antibody concentrations
detected in culture supernatants (r = 0.87 and 0.85, respectively). These results validate the potential usefulness of our
gastrointestinal explant system for the evaluation of mucosal effector
B-cell function.
*
Corresponding author. Mailing address: Center for
Vaccine Development, University of Maryland School of Medicine, Health
Science Facility, 685 West Baltimore St., Baltimore, MD 21201. Phone: (410) 706-5328. Fax: (410) 706-6209. E-mail:
glosonsk{at}umppa1.ab.umd.edu.
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