A comparison of autologous serum, plasma, and whole blood for intradermal autoreactivity testing in patients with chronic spontaneous urticarial: A cross-sectional study

Rasimah Ismail, A. Jamil, N. Md Nor, M. Bakhtiar
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Abstract

Background: Autologous serum (ASST) and plasma (APST) skin testing confirm autoreactivity in chronic spontaneous urticaria (CSU). Whole blood autohemotherapy has been used. Plasma and even whole blood may be used instead of serum with relatively quicker preparation and cheaper method especially using the latter in centers with limited resources. Purpose: The purpose of the study is to determine if similar intradermal skin reactions can be observed when using either serum, plasma, or whole blood in autologous skin tests and to determine factors associated with positive tests and wheal diameter. Methods: We performed a cross-sectional study of chronic urticaria patients in a dermatology clinic. Tests were performed according to EAACI/GA2 LEN Task Force recommendations. Urticaria Activity Score over 7 days (UAS7) was assessed. Statistical analyses included Chi-square, Mann–Whitney U, Spearman's, and Wilcoxon rank tests. Results: Twenty-six (77%) females and 8 (24%) males mean age 34 (26–42) years participated. ASST, APST and autologous whole blood for skin testing (AWBST) positivity rates were 24%, 29% and 27%, respectively (P = 0.86). 13 (38%) had at least 1 positive test; all tests were negative in 21 (62%). All tests were positive in 7 (21%), 3 (23%) were positive APST alone, 2 (15%) AWBST, 1 (8%) ASST. Pretest UAS7 was higher with those with test positive (P = 0.04). Test results were unaffected by age, gender, disease duration, atopy, anti-nuclear antibody, and thyroid status. Wheal diameter correlated with thyroid-stimulating hormone (P = 0.04). Conclusion: Autoreactivity rates were similar with ASST, APST, and AWBST. Positive tests were associated with severe CSU. Autologous whole blood may be a simpler and less costly alternative to plasma and serum for autoreactivity skin testing in patients with chronic urticaria.
慢性自发性荨麻疹患者皮内自体反应性检测的自体血清、血浆和全血比较:一项横断面研究
背景:自体血清和血浆皮肤试验证实慢性自发性荨麻疹(CSU)的自身反应性。已采用全血自体血液疗法。血浆甚至全血可以代替血清,制备速度较快,方法便宜,特别是在资源有限的中心使用血清。目的:本研究的目的是确定在自体皮肤试验中使用血清、血浆或全血时是否可以观察到类似的皮内皮肤反应,并确定与阳性试验和轮径相关的因素。方法:我们对皮肤科门诊的慢性荨麻疹患者进行了横断面研究。根据EAACI/GA2 LEN工作组的建议进行了测试。评估7天以上荨麻疹活动评分(UAS7)。统计分析包括卡方检验、Mann-Whitney U检验、Spearman’s检验和Wilcoxon秩检验。结果:女性26例(77%),男性8例(24%),平均年龄34岁(26-42岁)。自体全血皮肤试验(AWBST)阳性率分别为24%、29%和27% (P = 0.86)。至少1次阳性检查13例(38%);21例(62%)检测结果均为阴性。所有试验均阳性7例(21%),单APST阳性3例(23%),AWBST阳性2例(15%),asst阳性1例(8%)。试验前UAS7高于试验阳性(P = 0.04)。测试结果不受年龄、性别、病程、特应性、抗核抗体和甲状腺状态的影响。轮径与促甲状腺激素相关(P = 0.04)。结论:自体反应率与自体血清、APST、AWBST相似。阳性结果与严重的CSU相关。自体全血可能是慢性荨麻疹患者自体反应性皮肤试验中较血浆和血清更简单、成本更低的替代方法。
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