Department of Pediatrics, Virginia Commonwealth University, Richmond, VA 23298-0225, USA.
J Clin Immunol. 2012 Feb;32(1):150-60. doi: 10.1007/s10875-011-9605-8. Epub 2011 Oct 19.
Desensitization is a clinical procedure whereby incremental doses of a drug are administered over several hours to a sensitive patient until a therapeutic dose and clinical tolerance are achieved. Clinical tolerance may occur in part by attenuating the mast cell response. In the present study, primary human skin mast cells were used to establish and characterize an in vitro model of desensitization. Mast cells in culture were armed with allergen-specific (4-hydroxy-3-nitrophenylacety and Der p2) and non-specific IgE antibodies, and then desensitized by incremental exposures to 4-hydroxy-3-nitrophenylacety-BSA. This desensitization procedure abrogated the subsequent degranulation response to the desensitizing allergen, to an unrelated allergen, and to IgG anti-FcεRI, but not to C5a, substance P, compound 48/80, and calcium ionophore. Desensitized cells regained their FcεRI-dependent degranulation capability by 24-48 h after free allergen had been removed. Therefore, sensitized human skin mast cells are reversibly desensitized in vitro by exposure to incremental doses of that allergen, which also cross-desensitizes them to an unrelated allergen.
脱敏是一种临床程序,通过在数小时内给敏感患者递增剂量的药物,直到达到治疗剂量和临床耐受。临床耐受可能部分通过减弱肥大细胞反应来实现。在本研究中,使用原代人皮肤肥大细胞建立并表征了体外脱敏模型。在培养的肥大细胞中武装有过敏原特异性(4-羟基-3-硝基苯乙酰基和 Der p2)和非特异性 IgE 抗体,然后通过递增暴露于 4-羟基-3-硝基苯乙酰基-BSA 进行脱敏。这种脱敏程序消除了随后对脱敏过敏原、无关过敏原和 IgG 抗 FcεRI 的脱颗粒反应,但对 C5a、P 物质、化合物 48/80 和钙离子载体没有影响。脱敏细胞在游离过敏原去除后 24-48 小时恢复其 FcεRI 依赖性脱颗粒能力。因此,致敏的人皮肤肥大细胞可通过暴露于递增剂量的该过敏原在体外可逆地脱敏,这也使它们对无关过敏原产生交叉脱敏。