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Macrophage activation syndrome in a patient with adult-onset Still's disease following first COVID-19 vaccination with BNT162b2.
Muench, Frédéric; Krusche, Martin; Sander, Leif Erik; Rose, Thomas; Burmester, Gerd-Rüdiger; Schneider, Udo.
  • Muench F; Department of Nephrology and Medical Intensive Care, Charité - Universitätsmedizin Berlin, Berlin, Germany. frederic.muench@charite.de.
  • Krusche M; Department of Rheumatology and Immunology, Charité - Universitätsmedizin, Berlin, Germany.
  • Sander LE; Department of Rheumatology and Systemic Inflammatory Diseases, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
  • Rose T; Department of Infectious Diseases and Respiratory Medicine, Charité - Universitätsmedizin, Berlin, Germany.
  • Burmester GR; Department of Rheumatology and Immunology, Charité - Universitätsmedizin, Berlin, Germany.
  • Schneider U; Department of Rheumatology and Immunology, Charité - Universitätsmedizin, Berlin, Germany.
BMC Rheumatol ; 5(1): 60, 2021 Dec 28.
Article in English | MEDLINE | ID: covidwho-1817296
ABSTRACT

BACKGROUND:

Adult-onset Still's disease (AOSD) is an autoinflammatory multi-systemic syndrome. Macrophage activation syndrome (MAS) is a potentially life-threatening complication of AOSD with a mortality rate of 10-20%. Especially viral infection is thought to be a common trigger for development of MAS. On the other hand, the occurrence of MAS following vaccinations is extremely rare and has been described in a few cases after measles or influenza vaccinations and more recently after ChAdOx1 nCoV-19 (COVID-19 viral vector vaccine, Oxford-AZ). CASE PRESENTATION We report the case of a twenty-year-old female with adult-onset Still's disease (AOSD), who developed a MAS six days after receiving her first COVID-19 vaccine dose of BNT162b2 (mRNA vaccine, BioNTech/Pfizer) with ferritin levels of 136,680 µg/l (ref. 13-150 µg/l).

CONCLUSIONS:

To the best of our knowledge, this is the first case report of development of MAS in a patient with preexisting AOSD after vaccination in general, and SARS-CoV-2 vaccination in particular. The new mRNA vaccines have generally shown a reassuring safety profile, but it has been shown that nucleic acids in general, including mRNA can act as pathogen-associated molecular patterns that activate toll-like receptors with extensive production of pro-inflammatory cytokines and further activation of immune cells. Proving an interferon 1 response in our patient directly after vaccination, we think that in this particular case the vaccination might have acted as trigger for the development of MAS. Even if it remains difficult to establish causality in the case of rare adverse events, especially in patients with autoimmune or autoinflammatory conditions, these complications are important to monitor and register, but do not at all diminish the overwhelming positive benefit-risk ratio of licensed COVID-19 vaccines.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Vaccines Language: English Journal: BMC Rheumatol Year: 2021 Document Type: Article Affiliation country: S41927-021-00237-9

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Prognostic study Topics: Vaccines Language: English Journal: BMC Rheumatol Year: 2021 Document Type: Article Affiliation country: S41927-021-00237-9