Lim Xin Rong, Leung Bernard Pui, Ng Carol Yee Leng, Tan Justina Wei Lynn, Chan Grace Yin Lai, Loh Chien Mei, Tan Gwendolyn Li Xuan, Goh Valerie Hui Hian, Wong Lok To, Chua Chong Rui, Tan Sze Chin, Lee Samuel Shang Ming, Howe Hwee Siew, Thong Bernard Yu Hor, Leong Khai Pang
Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, 11 Jalan Tan Tock Seng, Singapore 308433, Singapore.
Health and Social Sciences, Singapore Institute of Technology, Singapore 138683, Singapore.
Vaccines (Basel). 2021 Aug 31;9(9):974. doi: 10.3390/vaccines9090974.
Anaphylactic reactions were observed after Singapore's national coronavirus disease 2019 (COVID-19) vaccination programme started in December 2020. We report the clinical and laboratory features of three patients in our institution who developed anaphylactic reactions after receiving the Pifzer BNT162b2 vaccine. IgM and IgG antibodies, but not IgE antibodies to the Pfizer BNT162b2 vaccine, were detected in all subjects. Similarly, mild to high elevated levels of anti-polyethylene glycol (PEG) IgG (1035-19709 U/mL, vs. vaccine-naive < 265 U/mL, vaccine-tolerant < 785 U/mL) and IgM (1682-5310 U/mL, vs. vaccine-naive < 1011 U/mL, vaccine-tolerant < 1007 U/mL) were detected in two out of three patients via commercial ELISA. High levels of serum anaphylatoxin C3a (79.0 ± 6.3 μg/mL, mean ± SD, vs. normal < 10 μg/mL) were observed in all three patients during the acute phase of the reaction, while tryptase levels, a marker of mast cell activation, were not elevated. Finally, one patient with the highest levels of anti-PEG IgG, IgM, and anti-Pfizer BNT162b2 IgG and IgM exhibited an enhanced Th2 cytokine serum profile during an acute reaction, with high levels of IL-4 (45.7 pg/mL, vs. vaccine-naive/tolerant < 2.30 pg/mL), IL-33 (86.4 pg/mL, vs. vaccine-naive/tolerant < 5.51 pg/mL) and IL-10 (22.9 pg/mL, vs. vaccine-naive/tolerant < 12.49 pg/mL) diminishing over time following corticosteroid treatment. Taken together, we propose these cases of anaphylaxis described are driven by a complement activation-related pseudoallergy (CAPRA), rather than classical IgE-mediated mechanisms.
自2020年12月新加坡启动国家2019冠状病毒病(COVID-19)疫苗接种计划后,观察到了过敏反应。我们报告了本院3例接种辉瑞BNT162b2疫苗后发生过敏反应患者的临床和实验室特征。在所有受试者中均检测到针对辉瑞BNT162b2疫苗的IgM和IgG抗体,但未检测到IgE抗体。同样,通过商业ELISA在3例患者中的2例中检测到轻度至高度升高的抗聚乙二醇(PEG)IgG(1035 - 19709 U/mL,未接种疫苗者<265 U/mL,耐受疫苗者<785 U/mL)和IgM(1682 - 5310 U/mL,未接种疫苗者<1011 U/mL,耐受疫苗者<1007 U/mL)。在反应急性期,所有3例患者均观察到高水平的血清过敏毒素C3a(79.0±6.3μg/mL,平均值±标准差,正常<10μg/mL),而肥大细胞活化标志物类胰蛋白酶水平未升高。最后,1例抗PEG IgG、IgM以及抗辉瑞BNT162b2 IgG和IgM水平最高的患者在急性反应期间表现出增强的Th2细胞因子血清谱,高水平的IL-4(45.7 pg/mL,未接种疫苗/耐受疫苗者<2.30 pg/mL)、IL-33(86.4 pg/mL,未接种疫苗/耐受疫苗者<5.51 pg/mL)和IL-10(22.9 pg/mL,未接种疫苗/耐受疫苗者<12.49 pg/mL)在皮质类固醇治疗后随时间逐渐降低。综上所述,我们认为所描述的这些过敏反应病例是由补体激活相关假过敏(CAPRA)驱动的,而非经典的IgE介导机制。