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Cholera toxin enhances alloantigen presentation by cultured intestinal epithelial cells.

Bromander, A K (author)
Kjerrulf, Martin (author)
Holmgren, Jan, 1944 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicinsk mikrobiologi och immunologi,Institute of Medical Microbiology/Immunology
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Lycke, Nils Y, 1954 (author)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk immunologi,Institute of Laboratory Medicine, Dept of Clinical Immunology
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 (creator_code:org_t)
1993
1993
English.
In: Scandinavian journal of immunology. - 0300-9475. ; 37:4, s. 452-8
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • In the present study we show that cholera toxin (CT) strongly potentiates antigen presentation by intestinal epithelial cells, probably by enhancing co-stimulation. This was demonstrated in an allogeneic system using cells from the IEC-17 rat epithelial cell line as antigen presenting cells (APC). These cells were induced by optimal concentrations of IFN-gamma to express good amounts of Ia antigen and cultured for 24-48 h in the presence or absence of CT. Thereafter the cells were thoroughly washed and added to cultures containing MHC-incompatible spleen cells as responder cells. Epithelial cells exposed to CT demonstrated greatly enhanced ability to trigger allogen-specific T-cell proliferation as compared with IEC-17 cells treated with IFN-gamma alone. The mechanism for the enhanced APC function was investigated by analysing CT-treated IEC-17 cells for increased class II MHC antigen expression or enhanced production of cytokines with known co-stimulatory function. We found no significant increase in class II MHC antigen expression. By contrast, CT strongly promoted, in a dose-dependent fashion, the production of both IL-1 and IL-6 cytokines by IEC-17 cells as compared with untreated epithelial cells. This effect of CT was specific and not due to contaminating endotoxin because excess amounts of soluble toxin receptor, ganglioside GM1, added to the IEC-17 cultures completely abrogated the cytokine response to CT. These results together with our previous findings of enhanced antigen presentation by macrophages stimulated by CT suggest that the potent adjuvant function of CT for induction of mucosal immune responses might be attributed to an enhanced co-stimulating ability of several putative APC in the mucosal immune system: macrophages, B cells and epithelial cells.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine (hsv//eng)
NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Keyword

Animals
Antigen-Presenting Cells
drug effects
immunology
B-Lymphocytes
immunology
Cell Line
drug effects
Cholera Toxin
antagonists & inhibitors
pharmacology
Dose-Response Relationship
Drug
Epithelium
immunology
G(M1) Ganglioside
pharmacology
Interleukin-1
secretion
Interleukin-6
secretion
Intestinal Mucosa
drug effects
immunology
Isoantigens
analysis
Macrophages
immunology
Rats
Rats
Sprague-Dawley
Spleen

Publication and Content Type

ref (subject category)
art (subject category)

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Bromander, A K
Kjerrulf, Martin
Holmgren, Jan, 1 ...
Lycke, Nils Y, 1 ...
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MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
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Scandinavian jou ...
By the university
University of Gothenburg

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