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PLoS One

Publication date: 2013-12-01
Publisher: Public Library of Sciene

Author:

De Vooght, Vanessa
Carlier, Vincent ; Devos, Fien ; Haenen, Steven ; Verbeken, Erik ; Nemery, Benoit ; Hoet, Peter ; Vanoirbeek, Jeroen

Keywords:

Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, IMMUNOLOGICAL DETERMINANTS, DERMAL SENSITIZATION, CELL SUBSETS, MURINE MODEL, MOUSE MODEL, EFFECTOR, RESPONSES, EXPOSURE, LONG, CD19, Animals, Asthma, B-Lymphocyte Subsets, B7-1 Antigen, B7-2 Antigen, Bronchoconstrictor Agents, CD40 Antigens, Disease Models, Animal, Immunoglobulin E, Male, Methacholine Chloride, Mice, Mice, Inbred BALB C, Mice, Knockout, Mice, SCID, Toluene 2,4-Diisocyanate, General Science & Technology

Abstract:

T-lymphocytes and B-lymphocytes are key players in allergic asthma, with B-lymphocytes producing antigen-specific immunoglobulins E (IgE). We used a mouse model of chemical-induced asthma and transferred B-lymphocytes from sensitized animals into naïve wild type mice, B-lymphocyte knock-out (B-KO) mice or severe combined immunodeficiency (SCID) mice. On days 1 and 8, BALB/c mice were dermally sensitized with 0.3% toluene diisocyanate (TDI) (20μl/ear). On day 15, mice were euthanized and the auricular lymph nodes isolated. B-lymphocytes (CD19+) were separated from the whole cell suspension and 175,000 cells were injected in the tail vein of naïve wild type, B-KO or SCID mice. Three days later, the mice received a single oropharyngeal challenge with 0.01% TDI (20μl) or vehicle (acetone/olive oil (AOO)) (controls). Airway reactivity to methacholine and total and differential cell counts in the bronchoalveolar lavage (BAL) fluid were measured 24 hours after challenge. B-lymphocytes of AOO or TDI-sensitized mice were characterized for the expression of surface markers and production of cytokines. We found that transfer of B-cells obtained from mice dermally sensitized to toluene diisocyanate (TDI) into naïve wild type mice, B-KO mice or SCID mice led, within three days, to an acute asthma-like phenotype after an airway challenge with TDI. This response was specific and independent of IgE. These B-lymphocytes showed antigen presenting capacities (CD80/CD86 and CD40) and consisted of B effector (Be)2- (IL-4) and Be1-lymphocytes (IFN-γ). The transferred B-lymphocytes were visualized near large airways, 24 hours after TDI challenge. Thus, B-lymphocytes can provoke an asthmatic response without the action of T-lymphocytes and without major involvement of IgE.