The long-term efficacy of intra-cervical lymphatic immunotherapy on adults with allergic rhinitis: A randomized controlled study

IF 4.6 2区 医学 Q2 ALLERGY Clinical and Translational Allergy Pub Date : 2024-02-11 DOI:10.1002/clt2.12341
Yang Qin, Weijun Huang, Rui Zheng, Qixing Wang, Qingqing Yu, Yin Li, Kai Wang, Jun Tang
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Abstract

Background

The efficacy and safety of the novel immunotherapy method, intra-cervical lymphatic immunotherapy (ICLIT), need to be investigated. Comparing it with subcutaneous immunotherapy (SCIT), we clarified the long-term efficacy and safety of intra-cervical lymphatic immunotherapy on allergic rhinitis (AR), and investigated the improvement of clinical efficacy of the booster injection at 1 year after ICLIT treatment.

Methods

Ninety adult patients with dust mite allergy were randomly divided into 3 groups: 30 in the SCIT group, 30 in the ILCLIT group, and 30 in ICLIT booster group. Changes in total symptom score (TSS), nasal symptom score (TNSS), ocular symptom score (TOSS) and total medication score (TMS) were evaluated in the three groups. Adverse reactions were recorded, and serum dust mite specific IgE (sIgE) and specific IgG4 were assessed in the ICLIT group and ICLIT booster group.

Results

TSS, TNSS, TOSS, and TMS scores were significantly lower in the three groups at 36 months after treatment (p < 0. 05). And at 36 months the ICLIT-booster group showed results similar to SCIT and superior to ICLIT (p < 0. 05). Serum specific IgE decreased in all three groups at 12 and 36 months after treatment, p < 0.01. The ICLIT group and the ICLIT booster group showed a significant increase in sIgG4, p < 0.01. None of the patients in the three groups had any serious systemic adverse effects during the 3-year follow-up.

Conclusion

The ICLIT treatment is effective and safe on AR. One booster injection of allergens at 1 year can greatly improve its long-term efficacy.

Trial Registry

Clinical trial registration number: ChiCTR1800017130.

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颈内淋巴免疫疗法对成人过敏性鼻炎的长期疗效:随机对照研究
背景 新型免疫疗法--颈内淋巴免疫疗法(ICLIT)的疗效和安全性有待研究。通过与皮下免疫疗法(SCIT)比较,我们明确了颈内淋巴免疫疗法对过敏性鼻炎(AR)的长期疗效和安全性,并研究了颈内淋巴免疫疗法治疗 1 年后加强注射对临床疗效的改善。 方法 将90例成年尘螨过敏患者随机分为3组:SCIT组30例、ILCLIT组30例、ICLIT加强组30例。评估三组患者的症状总分(TSS)、鼻部症状总分(TNSS)、眼部症状总分(TOSS)和用药总分(TMS)的变化。记录不良反应,并评估 ICLIT 组和 ICLIT 强化组的血清尘螨特异性 IgE(sIgE)和特异性 IgG4。 结果 在治疗后 36 个月,三组的 TSS、TNSS、TOSS 和 TMS 评分均显著降低(P < 0.)而在 36 个月时,ICLIT 强化组的结果与 SCIT 相似,优于 ICLIT(p < 0.)在治疗后的 12 个月和 36 个月,所有三组的血清特异性 IgE 都有所下降(p < 0.01)。ICLIT 组和 ICLIT 强化组的 sIgG4 显著增加(p < 0.01)。在为期 3 年的随访中,三组患者均未出现严重的全身不良反应。 结论 ICLIT 治疗对 AR 有效且安全。1 年注射一次过敏原加强剂可大大提高其长期疗效。 试验注册 临床试验注册号:ChiCTR1800017130。
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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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