Selective Modulation of B-Cell Activation Markers CD86 and I-A on Murine Draining Lymph Node Cells Following Allergen or Irritant Treatment

It is well known that T cells are key effector cells in the development of allergic contact dermatitis. However, we and others have shown that mice exposed to contact allergens show a preferential increase in B lymphocytes in the draining lymph nodes (DLN) as seen by an increase in the percentage of...

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Veröffentlicht in:Toxicology and applied pharmacology 1999-09, Vol.159 (2), p.142-151
Hauptverfasser: Gerberick, G F, Cruse, L W, Miller, C M, Ridder, G M
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Sprache:eng
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Zusammenfassung:It is well known that T cells are key effector cells in the development of allergic contact dermatitis. However, we and others have shown that mice exposed to contact allergens show a preferential increase in B lymphocytes in the draining lymph nodes (DLN) as seen by an increase in the percentage of B220 super(+) or IgG /IgM super(+) cells. The purpose of the present investigation was to determine whether chemical allergens, in contrast to irritants, would modulate B-cell activation markers, CD86 and I-A super(k), on B cells isolated from DLN of treated mice using the local lymph node assay (LLNA) protocol. Mice were treated on the ears for 3 consecutive days with concentrations of allergens (1-chloro-2,4-dinitrobenzene, alpha -hexylcinnamaldehyde, 4-ethoxymethylene-2-phenyl-2-oxazoline-5-one, and trinitrochlorobenzene), or irritants (benzalkonium chloride and sodium lauryl sulfate), which caused an increase in the number of DLN cells. The DLN were excised 72 h following the final chemical treatment, and the cells were prepared for analysis by flow cytometry. In mice treated with allergens an increase in the median intensity of I-A super(K) and CD86 on B220 super(+) or IgG/IgM super(+) B cells was observed compared to mice treated with irritants or vehicles. Mice treated with allergens demonstrated an increase in the median intensity of CD86 on B220 super(+) B cells that was dose dependent and peaked at 72 h following the final allergen treatment. The increase in the median intensity of I-A super(K) also was dose dependent but peaked at 96 h. Finally, T and B cells isolated from both allergen- and irritant-treated mice demonstrated an increase in [ super(3)H]thymidine incorporation compared to vehicle-treated and naive mice at 72 h following the final chemical treatment. The results suggest that B cells isolated from DLN of allergen-treated mice are activated and proliferating. Analysis of B-cell activation markers may be useful in differentiating allergen and irritant responses in the draining lymph nodes of chemically treated mice.
ISSN:0041-008X
DOI:10.1006/taap.1999.8734