Northern Blood Research Laboratory, Kolling Institute of Medical Research, Royal North Shore Hospital and the Sydney Medical School, University of Sydney, Sydney, Australia.
Immunology Laboratory, New South Wales Health Pathology, Royal North Shore Hospital, Sydney, Australia.
Hum Vaccin Immunother. 2023 Dec 31;19(1):2182527. doi: 10.1080/21645515.2023.2182527. Epub 2023 Mar 13.
Coronavirus (COVID-19) vaccines have proved to be effective in the pandemic response but can cause adverse events such as delayed hypersensitivity reactions (DHRs). Delayed-reading intradermal tests (IDT) to vaccines are limited by false-positive results and may reflect a cell-mediated rather than IgE-mediated immune response. Lymphocyte transformation test (LTT), which has been utilized in the diagnosis of drug allergy, may be helpful in suspected COVID-19 vaccine and/or its excipient-related DHRs. To investigate the use of LTT in two suspected cases of COVID-19 vaccine-induced DHRs, two patients with suspected DHRs to COVID-19 vaccination were tested by delayed-reading IDT and LTT against vaccines and their excipients. A 47-year-old man developed acute mixed-pattern hepatitis after the second dose of ChAdOx1 vaccine. LTT performed at 2 months post-vaccination revealed reactivity to the ChAdOx1 vaccine, polysorbate 80 and mildly to PEG 2050 but not BNT162b2 vaccine. Delayed-reading IDT returned negative to both vaccines and excipients. He tolerated BNT162b2 vaccination with no adverse events. A 36-year-old woman presented with subacute morbilliform eruption and hepatitis after the first dose of BNT162b2 vaccine. LTT performed 3 months later revealed reactivity to the BNT162b2 but not PEG 2050. Repeat LTT following subsequent natural Severe Acute Respiratory Coronavirus-2 (SARS-CoV-2) infection revealed reactivity to ChAdOx1 and NVX-CoV2373 vaccines but not polysorbate 80. Delayed-reading IDT remained negative. She proceeded with NVX-CoV2373 vaccination with no symptom recurrence. LTT may be a useful tool in suspected COVID-19 vaccine-related DHRs. Further evaluation with a larger patient cohort is required.
新型冠状病毒(COVID-19)疫苗已被证明在大流行应对中有效,但会引起迟发性超敏反应(DHR)等不良反应。疫苗的延迟读数皮内试验(IDT)受到假阳性结果的限制,并且可能反映细胞介导而不是 IgE 介导的免疫反应。淋巴细胞转化试验(LTT)已用于药物过敏的诊断,对于疑似 COVID-19 疫苗及其赋形剂相关 DHR 可能会有所帮助。为了研究 LTT 在两例疑似 COVID-19 疫苗诱导的 DHR 中的应用,对两例疑似 DHR 的 COVID-19 疫苗接种患者进行了延迟读数 IDT 和 LTT 检测,以检测疫苗及其赋形剂。一名 47 岁男性在接种第二剂 ChAdOx1 疫苗后出现急性混合模式肝炎。接种后 2 个月进行的 LTT 显示对 ChAdOx1 疫苗、聚山梨醇酯 80 具有反应性,对 PEG 2050 轻度反应,但对 BNT162b2 疫苗无反应。延迟读数 IDT 对两种疫苗和赋形剂均呈阴性。他接种 BNT162b2 疫苗后无不良反应。一名 36 岁女性在接种 BNT162b2 疫苗第一剂后出现亚急性麻疹样皮疹和肝炎。3 个月后进行的 LTT 显示对 BNT162b2 有反应,但对 PEG 2050 无反应。随后自然感染 SARS-CoV-2 后重复 LTT 显示对 ChAdOx1 和 NVX-CoV2373 疫苗有反应,但对聚山梨醇酯 80 无反应。延迟读数 IDT 仍呈阴性。她接种了 NVX-CoV2373 疫苗,没有症状复发。LTT 可能是疑似 COVID-19 疫苗相关 DHR 的有用工具。需要进一步评估更大的患者队列。