Jutel Marek, Bartkowiak-Emeryk Małgorzata, Bręborowicz Anna, Cichocka-Jarosz Ewa, Emeryk Andrzej, Gawlik Radosław, Gonerko Paweł, Rogala Barbara, Nowak-Węgrzyn Anna, Samoliński Bolesław
Wroclaw Medical University, Wrocław, Poland.
Chair of Clinical Immunology, Department of Clinical Immunology, University of Medicine, Lublin, Poland.
Ann Agric Environ Med. 2016 Mar 23;23(1):44-53. doi: 10.5604/12321966.1196851.
SLIT (sublingual immunotherapy,) induces allergen-specific immune tolerance by sublingual administration of a gradually increasing dose of an allergen. The mechanism of SLIT is comparable to those during SCIT (subcutaneous immunotherapy), with the exception of local oral dendritic cells, pre-programmed to elicit tolerance. In the SLIT dose, to achieve the same efficacy as in SCIT, it should be 50-100 times higher with better safety profile. The highest quality evidence supporting the efficacy of SLIT lasting 1-3 years has been provided by the large scale double-blind, placebo-controlled (DBPC) trials for grass pollen extracts, both in children and adults with allergic rhinitis. Current indications for SLIT are allergic rhinitis (and conjunctivitis) in both children and adults sensitized to pollen allergens (trees, grass, Parietaria), house dust mites (Dermatophagoides pteronyssinus, Dermatophagoides farinae), cat fur, as well as mild to moderate controlled atopic asthma in children sensitized to house dust mites. There are positive findings for both asthma and new sensitization prevention. Severe adverse events, including anaphylaxis, are very rare, and no fatalities have been reported. Local adverse reactions develop in up to 70 - 80% of patients. Risk factors for SLIT adverse events have not been clearly identified. Risk factors of non-adherence to treatment might be dependent on the patient, disease treatment, physician-patient relationship, and variables in the health care system organization.
舌下免疫治疗(SLIT)通过舌下给予逐渐增加剂量的变应原诱导变应原特异性免疫耐受。SLIT的机制与皮下免疫治疗(SCIT)期间的机制相当,但局部口腔树突状细胞预先编程以引发耐受的情况除外。在SLIT剂量方面,为达到与SCIT相同的疗效,其剂量应高50 - 100倍,且安全性更好。支持SLIT疗效持续1 - 3年的最高质量证据来自针对草花粉提取物的大规模双盲、安慰剂对照(DBPC)试验,试验对象为患有过敏性鼻炎的儿童和成人。SLIT目前的适应证包括对花粉变应原(树木、草、墙草属)、屋尘螨(粉尘螨、屋尘螨)、猫毛致敏的儿童和成人的过敏性鼻炎(和结膜炎),以及对屋尘螨致敏的儿童轻度至中度控制的特应性哮喘。在哮喘和预防新的致敏方面均有阳性结果。严重不良事件,包括过敏反应,非常罕见,且未报告有死亡病例。高达70 - 80%的患者会出现局部不良反应。SLIT不良事件的危险因素尚未明确确定。不依从治疗的危险因素可能取决于患者、疾病治疗、医患关系以及医疗保健系统组织中的变量。