【摘 要】
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Objective To investigate CTLA4-Ig’s potential role in therapy for allergic asthma by blocking B7/CD28 interactions with cytotoxic T lymphocyte antigen 4-Ig (C
【机 构】
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Department of Respiratory Medicine, Ruijin Hospital, Shanghai Second Medical University, Shanghai 20
【出 处】
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Chinese Medical Journal
论文部分内容阅读
Objective To investigate CTLA4-Ig’s potential role in therapy for allergic asthma by blocking B7/CD28 interactions with cytotoxic T lymphocyte antigen 4-Ig (CTLA4-Ig). Methods We divided BALB/C mice into the three groups: Sham/Sham (control), ovalbumin (OVA)/OVA and mCTLA4-Ig. Blood, bronchoalveolar lavage, histology and determination of cytokines were performed 24 hours after airway challenge. Results In the OVA/OVA group, the number of cells, the percentage of inflamed cells and the level of IL-4 in BALF were increased. Airways in our murine model for allergic asthma underwent pathological changes, which were significantly reduced after treatment with mCTLA4-Ig. Conclusion Blockage of co-stimulation with mCTLA4-Ig can inhibit allergy-specific response of T cells, and asthmatic response as well.
Objective To investigate CTLA4-Ig’s potential role in therapy for allergic asthma by blocking B7 / CD28 interactions with cytotoxic T lymphocyte antigen 4-Ig (CTLA4-Ig). Methods We divided BALB / C mice into the three groups: Sham / Sham ), ovalbumin (OVA) / OVA and mCTLA4-Ig. Blood, bronchoalveolar lavage, histology and determination of cytokines were performed 24 hours after airway challenge. Results In the OVA / OVA group, the number of cells, the percentage of inflamed cells and The levels of IL-4 in BALF were increased. Airways in our murine model for allergic asthma underwent pathological changes, which were significantly reduced after treatment with mCTLA4-Ig. Conclusion Blockage of co-stimulation with mCTLA4-Ig can inhibit allergy-specific response of T cells, and asthmatic response as well.
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