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Potential mechanisms of anaphylaxis to COVID-19 mRNA vaccines.
Risma, Kimberly A; Edwards, Kathryn M; Hummell, Donna S; Little, Frederic F; Norton, Allison E; Stallings, Amy; Wood, Robert A; Milner, Joshua D.
  • Risma KA; Cincinnati Children's Hospital Medical Center, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio. Electronic address: Kimberly.Risma@cchmc.org.
  • Edwards KM; Division of Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tenn.
  • Hummell DS; Division of Pediatric Allergy, Immunology, and Pulmonary Medicine, Department of Pediatrics, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Little FF; Division of Pulmonary, Allergy, Sleep and Critical Care Medicine, Department of Pediatrics, Boston University School of Medicine, Boston, Mass.
  • Norton AE; Division of Pediatric Allergy, Immunology, and Pulmonary Medicine, Department of Pediatrics, Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University School of Medicine, Nashville, Tenn.
  • Stallings A; Division of Pediatric Allergy and Immunology, Duke University Medical Center, Durham, NC.
  • Wood RA; Division of Pediatric Allergy and Immunology, Johns Hopkins University School of Medicine, Baltimore, Md.
  • Milner JD; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY.
J Allergy Clin Immunol ; 147(6): 2075-2082.e2, 2021 06.
Article in English | MEDLINE | ID: covidwho-1185028
ABSTRACT
Anaphylaxis to vaccines is historically a rare event. The coronavirus disease 2019 pandemic drove the need for rapid vaccine production applying a novel antigen delivery system messenger RNA vaccines packaged in lipid nanoparticles. Unexpectedly, public vaccine administration led to a small number of severe allergic reactions, with resultant substantial public concern, especially within atopic individuals. We reviewed the constituents of the messenger RNA lipid nanoparticle vaccine and considered several contributors to these reactions (1) contact system activation by nucleic acid, (2) complement recognition of the vaccine-activating allergic effector cells, (3) preexisting antibody recognition of polyethylene glycol, a lipid nanoparticle surface hydrophilic polymer, and (4) direct mast cell activation, coupled with potential genetic or environmental predispositions to hypersensitivity. Unfortunately, measurement of anti-polyethylene glycol antibodies in vitro is not clinically available, and the predictive value of skin testing to polyethylene glycol components as a coronavirus disease 2019 messenger RNA vaccine-specific anaphylaxis marker is unknown. Even less is known regarding the applicability of vaccine use for testing (in vitro/vivo) to ascertain pathogenesis or predict reactivity risk. Expedient and thorough research-based evaluation of patients who have suffered anaphylactic vaccine reactions and prospective clinical trials in putative at-risk individuals are needed to address these concerns during a public health crisis.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Messenger / Drug Hypersensitivity / Nanoparticles / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 / Anaphylaxis / Lipids Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines Limits: Animals / Humans Language: English Journal: J Allergy Clin Immunol Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Messenger / Drug Hypersensitivity / Nanoparticles / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 / Anaphylaxis / Lipids Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines Limits: Animals / Humans Language: English Journal: J Allergy Clin Immunol Year: 2021 Document Type: Article