tetano
Editor, Senior Moderator
Front Immunol
. 2022 Sep 29;13:967972.
doi: 10.3389/fimmu.2022.967972. eCollection 2022.
Case report: Bilateral panuveitis resembling Vogt-Koyanagi-Harada disease after second dose of BNT162b2 mRNA COVID-19 vaccine
Tomohito Sato[SUP] 1 [/SUP], Ryotaro Nihei[SUP] 1 [/SUP], Daisuke Sora[SUP] 1 [/SUP], Yoshiaki Nishio[SUP] 1 [/SUP], Masaru Takeuchi[SUP] 1 [/SUP]
Affiliations
Abstract
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a serious pandemic. COVID-19 vaccination is urgent needed for limiting SARS-CoV-2 outbreaks by herd immunity. Simultaneously, post-marketing surveillance to assess vaccine safety is important, and collection of vaccine-related adverse events has been in progress. Vision-threatening ophthalmic adverse events of COVID-19 vaccines are rare but are a matter of concern. We report a 45-year-old Japanese male with positive for HLA-DR4/HLA-DRB1*0405, who developed bilateral panuveitis resembling Vogt-Koyanagi-Harada (VKH) disease after the second dose of Pfizer-BioNTech COVID-19 mRNA (BNT162b2) vaccine. Glucocorticosteroid (GC) therapy combined with cyclosporine A (CsA) readily improved the panuveitis. The immune profile at the time of onset was analyzed using CyTOF technology, which revealed activations of innate immunity mainly consisting of natural killer cells, and acquired immunity predominantly composed of B cells and CD8[SUP]+[/SUP] T cells. On the other hand, the immune profile in the remission phase was altered by GC therapy with CsA to a profile composed primarily of CD4[SUP]+[/SUP] cells, which was considerably similar to that of the healthy control before the vaccination. Our results indicate that BNT162b2 vaccine may trigger an accidental immune cross-reactivity to melanocyte epitopes in the choroid, resulting in the onset of panuveitis resembling VKH disease.
Keywords: BNT162b2 vaccine; Vogt-Koyanagi-Harada disease; covid-19 mRNA vaccines; cyTOF; heat map; multiplex bead analysis; uveitis.
. 2022 Sep 29;13:967972.
doi: 10.3389/fimmu.2022.967972. eCollection 2022.
Case report: Bilateral panuveitis resembling Vogt-Koyanagi-Harada disease after second dose of BNT162b2 mRNA COVID-19 vaccine
Tomohito Sato[SUP] 1 [/SUP], Ryotaro Nihei[SUP] 1 [/SUP], Daisuke Sora[SUP] 1 [/SUP], Yoshiaki Nishio[SUP] 1 [/SUP], Masaru Takeuchi[SUP] 1 [/SUP]
Affiliations
- PMID: 36248859
- PMCID: PMC9556971
- DOI: 10.3389/fimmu.2022.967972
Abstract
Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a serious pandemic. COVID-19 vaccination is urgent needed for limiting SARS-CoV-2 outbreaks by herd immunity. Simultaneously, post-marketing surveillance to assess vaccine safety is important, and collection of vaccine-related adverse events has been in progress. Vision-threatening ophthalmic adverse events of COVID-19 vaccines are rare but are a matter of concern. We report a 45-year-old Japanese male with positive for HLA-DR4/HLA-DRB1*0405, who developed bilateral panuveitis resembling Vogt-Koyanagi-Harada (VKH) disease after the second dose of Pfizer-BioNTech COVID-19 mRNA (BNT162b2) vaccine. Glucocorticosteroid (GC) therapy combined with cyclosporine A (CsA) readily improved the panuveitis. The immune profile at the time of onset was analyzed using CyTOF technology, which revealed activations of innate immunity mainly consisting of natural killer cells, and acquired immunity predominantly composed of B cells and CD8[SUP]+[/SUP] T cells. On the other hand, the immune profile in the remission phase was altered by GC therapy with CsA to a profile composed primarily of CD4[SUP]+[/SUP] cells, which was considerably similar to that of the healthy control before the vaccination. Our results indicate that BNT162b2 vaccine may trigger an accidental immune cross-reactivity to melanocyte epitopes in the choroid, resulting in the onset of panuveitis resembling VKH disease.
Keywords: BNT162b2 vaccine; Vogt-Koyanagi-Harada disease; covid-19 mRNA vaccines; cyTOF; heat map; multiplex bead analysis; uveitis.