Please use this identifier to cite or link to this item: https://doi.org/10.3390/vaccines11061020
Title: Anaphylatoxin Complement 5a in Pfizer BNT162b2-Induced Immediate-Type Vaccine Hypersensitivity Reactions
Authors: Lim, Xin Rong
Chan, Grace Yin Lai
Tan, Justina Wei Lynn
Ng, Carol Yee Leng
Chua, Choon Guan
Tan, Guat Bee
Chan, Stephrene Seok Wei
Ong, Kiat Hoe 
Tan, Ying Zhi
Tan, Sarah Hui Zhen
Teo, Claire Min Li
Lee, Samuel Shang Ming
Thong, Bernard Yu Hor
Leung, Bernard Pui Lam 
Issue Date: 23-May-2023
Publisher: MDPI AG
Citation: Lim, Xin Rong, Chan, Grace Yin Lai, Tan, Justina Wei Lynn, Ng, Carol Yee Leng, Chua, Choon Guan, Tan, Guat Bee, Chan, Stephrene Seok Wei, Ong, Kiat Hoe, Tan, Ying Zhi, Tan, Sarah Hui Zhen, Teo, Claire Min Li, Lee, Samuel Shang Ming, Thong, Bernard Yu Hor, Leung, Bernard Pui Lam (2023-05-23). Anaphylatoxin Complement 5a in Pfizer BNT162b2-Induced Immediate-Type Vaccine Hypersensitivity Reactions. Vaccines 11 (6) : 1020-1020. ScholarBank@NUS Repository. https://doi.org/10.3390/vaccines11061020
Abstract: The underlying immunological mechanisms of immediate-type hypersensitivity reactions (HSR) to COVID-19 vaccines are poorly understood. We investigate the mechanisms of immediate-type hypersensitivity reactions to the Pfizer BNT162b2 vaccine and the response of antibodies to the polyethylene glycol (PEG)ylated lipid nanoparticle after two doses of vaccination. Sixty-seven participants, median age 35 and 77.3% females who tolerated two doses of the BNT162b2 vaccine (non-reactors), were subjected to various blood-sampling time points. A separate group of vaccine reactors (10 anaphylaxis and 37 anonymised tryptase samples) were recruited for blood sampling. Immunoglobulin (Ig)G, IgM and IgE antibodies to the BNT162b2 vaccine, biomarkers associated with allergic reaction, including tryptase for anaphylaxis, complement 5a(C5a), intercellular adhesion molecule 1 (ICAM-1) for endothelial activation and Interleukin (IL)-4, IL-10, IL-33, tumour necrosis factor (TNF) and monocyte chemoattractant protein (MCP-1), were measured. Basophil activation test (BAT) was performed in BNT162b2-induced anaphylaxis patients by flow cytometry. The majority of patients with immediate-type BNT162b2 vaccine HSR demonstrated raised C5a and Th2-related cytokines but normal tryptase levels during the acute reaction, together with significantly higher levels of IgM antibodies to the BNT162b2 vaccine (IgM 67.2 (median) vs. 23.9 AU/mL, p < 0.001) and ICAM-1 when compared to non-reactor controls. No detectable IgE antibodies to the BNT162b2 vaccine were found in these patients. The basophil activation tests by flow cytometry to the Pfizer vaccine, 1,2-dimyristoyl-rac-glycero-3-methoxypolyethylene glycol (DMG-PEG) and PEG-2000 were negative in four anaphylaxis patients. Acute hypersensitivity reactions post BNT162b2 vaccination suggest pseudo-allergic reactions via the activation of anaphylatoxins C5a and are independent of IgE-mechanisms. Vaccine reactors have significantly higher levels of anti-BNT162b2 IgM although its precise role remains unclear.
Source Title: Vaccines
URI: https://scholarbank.nus.edu.sg/handle/10635/241137
ISSN: 2076-393X
DOI: 10.3390/vaccines11061020
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