Norman P S, Ohman J L, Long A A, Creticos P S, Gefter M A, Shaked Z, Wood R A, Eggleston P A, Hafner K B, Rao P, Lichtenstein L M, Jones N H, Nicodemus C F
Johns Hopkins Asthma and Allergy Center, Baltimore, MD 21224-6801, USA.
Am J Respir Crit Care Med. 1996 Dec;154(6 Pt 1):1623-8. doi: 10.1164/ajrccm.154.6.8970345.
We induced in allergic humans the counterpart of murine experimental T-cell tolerance. T-cell lines from cat-allergic humans were used to map T-cell epitopes for the principal allergen of cat dander, Fel d 1. Two peptides of 27 amino acids each were synthesized to contain the dominant epitopes (ALLERVAX CAT). After a safety trial, we carried out a blinded study of the dose required for efficacy. We randomly divided 95 cat-sensitive patients into placebo, 7.5 micrograms, 75 micrograms, and 750 micrograms groups. Patients received a subcutaneous injection weekly for 4 wk. Before and after treatment, patients were exposed in a room inhabited by live cats and scored by nose and lung symptoms. Baseline nasal and lung scores (+/-SEM) were 6.2 +/- 0.56 and 5.4 +/- 0.73 in the 750 micrograms group; 7.8 +/- 0.53 and 4.7 +/- 0.68 in the placebo group. Six weeks after treatment, scores adjusted for baseline differences were reduced in the 750 micrograms group: -2.3 +/- 4.9 and -2.3 +/- 0.59 compared with -0.84 +/- 0.50 and -0.85 +/- 0.62 in the placebo group. The 75 micrograms group showed intermediate effects and the 7.5 micrograms group no effect. Linear trend analysis indicated a significant dose response effect: p = 0.05 for nose and 0.03 for lung symptoms. Allergic side effects occurred an hour or more after the first 750 micrograms dose in 16 of 24 patients but required little or no treatment with one exception. T-cell reactive treatment peptides safely improved allergic responses to cats.
我们在过敏人群中诱导出了与小鼠实验性T细胞耐受性相对应的情况。利用来自对猫过敏人群的T细胞系来定位猫皮屑主要过敏原Fel d 1的T细胞表位。合成了两条各含27个氨基酸的肽段,以包含主要表位(ALLERVAX CAT)。在进行安全性试验后,我们对疗效所需剂量进行了一项双盲研究。我们将95名对猫敏感的患者随机分为安慰剂组、7.5微克组、75微克组和750微克组。患者每周皮下注射一次,共注射4周。治疗前后,让患者在有活猫居住的房间里接触,并根据鼻部和肺部症状进行评分。750微克组的基线鼻部和肺部评分(±标准误)分别为6.2±0.56和5.4±0.73;安慰剂组为7.8±0.53和4.7±0.68。治疗六周后,750微克组经基线差异校正后的评分降低:分别为-2.3±4.9和-2.3±0.59,而安慰剂组为-0.84±0.50和-0.85±0.62。75微克组显示出中等效果,7.5微克组无效果。线性趋势分析表明有显著的剂量反应效应:鼻部症状p = 0.05,肺部症状p = 0.03。24名患者中有16名在首次注射750微克剂量后一小时或更长时间出现过敏副作用,但除一例例外,几乎无需治疗或根本无需治疗。T细胞反应性治疗肽安全地改善了对猫的过敏反应。