Validation of a gastrointestinal explant system for measurement of mucosal antibody production

被引:10
作者
Losonsky, GA
Fantry, GT
Reymann, M
Lim, Y
机构
[1] Univ Maryland, Sch Med, Ctr Vaccine Dev,Dept Med, Hlth Sci Facil,Div Infect Dis & Trop Pediat, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Med, Div Geog Med, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Med, Div Gastroenterol, Baltimore, MD 21201 USA
关键词
D O I
10.1128/CDLI.6.6.803-807.1999
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 mu g/ml/10 mg of antral and duodenal biopsy tissues, respectively, while the cumulative geometric mean IgG levels were 1.54 and 2.92 mu g/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.
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收藏
页码:803 / 807
页数:5
相关论文
共 17 条
[1]  
Brandtzaeg P, 1986, Monogr Allergy, V20, P179
[2]   Impairment of the mucosal immune system: IgA and IgM cleavage detected in vaginal washings of a subgroup of patients with bacterial vaginosis [J].
Cauci, S ;
Monte, R ;
Driussi, S ;
Lanzafame, P ;
Quadrifoglio, F .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (06) :1698-1706
[3]   AN ORGAN FRAGMENT CULTURE MODEL TO STUDY LYMPHOCYTE-ACTIVATION IN HUMAN LYMPHOID-TISSUE [J].
FERRO, LM ;
WEEDON, HM ;
FLEGO, LR ;
BEROUKAS, D ;
ZOLA, H .
IMMUNOBIOLOGY, 1993, 188 (1-2) :51-61
[4]  
KAGNOFF MF, 1972, GASTROENTEROLOGY, V63, P541
[5]   DIFFERENT PROFILES OF THE HUMAN IMMUNE-RESPONSE TO PRIMARY AND SECONDARY IMMUNIZATION WITH AN ORAL SALMONELLA-TYPHI TY21A VACCINE [J].
KANTELE, A ;
MAKELA, PH .
VACCINE, 1991, 9 (06) :423-427
[6]   DEFENSE-MECHANISMS INVOLVING FC-DEPENDENT FUNCTIONS OF IMMUNOGLOBULIN-A AND THEIR SUBVERSION BY BACTERIAL IMMUNOGLOBULIN-A PROTEASES [J].
KILIAN, M ;
MESTECKY, J ;
RUSSELL, MW .
MICROBIOLOGICAL REVIEWS, 1988, 52 (02) :296-303
[7]   USE OF PEYER PATCH AND LYMPH-NODE FRAGMENT CULTURES TO COMPARE LOCAL IMMUNE-RESPONSES TO MORGANELLA-MORGANII [J].
LOGAN, AC ;
CHOW, KPN ;
GEORGE, A ;
WEINSTEIN, PD ;
CEBRA, JJ .
INFECTION AND IMMUNITY, 1991, 59 (03) :1024-1031
[8]   SECONDARY VIBRIO-CHOLERAE-SPECIFIC CELLULAR ANTIBODY-RESPONSES FOLLOWING WILD-TYPE HOMOLOGOUS CHALLENGE IN PEOPLE VACCINATED WITH CVD 103-HGR LIVE ORAL CHOLERA VACCINE - CHANGES WITH TIME AND LACK OF CORRELATION WITH PROTECTION [J].
LOSONSKY, GA ;
TACKET, CO ;
WASSERMAN, SS ;
KAPER, JB ;
LEVINE, MM .
INFECTION AND IMMUNITY, 1993, 61 (02) :729-733
[9]   PRODUCTION OF ANTIBODIES TO GLIADIN IN INTESTINAL-MUCOSA OF PATIENTS WITH CELIAC-DISEASE - A STUDY AT THE SINGLE CELL LEVEL [J].
LYCKE, N ;
KILANDER, A ;
NILSSON, LA ;
TARKOWSKI, A ;
WERNER, N .
GUT, 1989, 30 (01) :72-77
[10]   ROLE OF LOCAL IGA ANTITOXIN-PRODUCING CELLS FOR INTESTINAL PROTECTION AGAINST CHOLERA-TOXIN CHALLENGE [J].
LYCKE, N ;
BROMANDER, AK ;
HOLMGREN, J .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1989, 88 (03) :273-279