British Journal of Dermatology

<jats:p>We report promising clinical outcomes using ustekinumab as a first-line therapy in bullous pemphigoid (BP) when combined with a short, 8-week regimen of super-potent topical corticosteroids. Furthermore, the CD40L/IL-4 ratio emerged as a potential predictive biomarker of treatment response, possibly reflecting a Th1-skewed immune environment that favors ustekinumab’s mechanism of action.</jats:p>

Ustekinumab as a potential therapeutic agent in Bullous Pemphigoid: a biological and clinical proof-of-concept study.

Ustekinumab as a potential therapeutic agent in Bullous Pemphigoid: a biological and clinical proof-of-concept study

JAMA Dermatology

<jats:sec id="ab-doi240049-4"><jats:title>Importance</jats:title><jats:p>Few studies have investigated the association between COVID-19 and autoimmune and autoinflammatory connective tissue disorders; however, research with long-term observation remains insufficient.</jats:p></jats:sec><jats:sec id="ab-doi240049-5"><jats:title>Objective</jats:title><jats:p>To investigate the long-term risk of autoimmune and autoinflammatory diseases after COVID-19 over an extended observation period.</jats:p></jats:sec><jats:sec id="ab-doi240049-6"><jats:title>Design, Setting, and Participants</jats:title><jats:p>This retrospective nationwide population-based study investigated the Korea Disease Control and Prevention Agency–COVID-19–National Health Insurance Service (K-COV-N) cohort. Individuals with confirmed COVID-19 from October 8, 2020, to December 31, 2022, and controls identified among individuals who participated in the general health examination in 2018 were included in the analysis.</jats:p></jats:sec><jats:sec id="ab-doi240049-7"><jats:title>Exposures</jats:title><jats:p>Confirmed COVID-19.</jats:p></jats:sec><jats:sec id="ab-doi240049-8"><jats:title>Main Outcomes and Measures</jats:title><jats:p>Incidence and risk of autoimmune and autoinflammatory connective tissue disorders in patients after COVID-19. Various covariates, such as demographic characteristics, general health data, socioeconomic status, and comorbidity profiles, were balanced using inverse probability weighting.</jats:p></jats:sec><jats:sec id="ab-doi240049-9"><jats:title>Results</jats:title><jats:p>A total of 6 912 427 participants (53.6% male; mean [SD] age, 53.39 [20.13] years) consisting of 3 145 388 with COVID-19 and 3 767 039 controls with an observational period of more than 180 days were included. Alopecia areata (adjusted hazard ratio [AHR], 1.11 [95% CI, 1.07-1.15]), alopecia totalis (AHR, 1.24 [95% CI, 1.09-1.42]), vitiligo (AHR, 1.11 [95% CI, 1.04-1.19]), Behçet disease (AHR, 1.45 [95% CI, 1.20-1.74]), Crohn disease (AHR, 1.35 [95% CI, 1.14-1.60]), ulcerative colitis (AHR, 1.15 [95% CI, 1.04-1.28]), rheumatoid arthritis (AHR, 1.09 [95% CI, 1.06-1.12]), systemic lupus erythematosus (AHR, 1.14 [95% CI, 1.01-1.28]), Sjögren syndrome (AHR, 1.13 [95% CI, 1.03-1.25]), ankylosing spondylitis (AHR, 1.11 [95% CI, 1.02-1.20]), and bullous pemphigoid (AHR, 1.62 [95% CI, 1.07-2.45]) were associated with higher risk in the COVID-19 group. Subgroup analyses revealed that demographic factors, including male and female sex, age younger than 40 years, and age 40 years and older, exhibited diverse associations with the risk of autoimmune and autoinflammatory outcomes. In addition, severe COVID-19 infection requiring intensive care unit admission, the Delta period, and not being vaccinated were associated with higher risk.</jats:p></jats:sec><jats:sec id="ab-doi240049-10"><jats:title>Conclusions and Relevance</jats:title><jats:p>This retrospective cohort study with an extended follow-up period found associations between COVID-19 and the long-term risk of various autoimmune and autoinflammatory connective tissue disorders. Long-term monitoring and care of patients is crucial after COVID-19, considering demographic factors, disease severity, and vaccination status, to mitigate these risks.</jats:p></jats:sec>

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Molecular mimicry, bystander activation, or viral persistence: infections and autoimmune disease.

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New onset systemic lupus erythematosus after COVID-19 infection: a case report.

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New-onset vitiligo following COVID-19 disease.

Skin Health Dis

Vitiligo following COVID-19: a case report and review of pathophysiology.

Vitiligo pathogenesis and emerging treatments.

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COVID-19 and oxidative stress.

Biochemistry (Mosc)

New-onset bullous pemphigoid in a COVID-19 patient.

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Few studies have investigated the association between COVID-19 and autoimmune and autoinflammatory connective tissue disorders; however, research with long-term observation remains insufficient.
To investigate the long-term risk of autoimmune and autoinflammatory diseases after COVID-19 over an extended observation period.
This retrospective nationwide population-based study investigated the Korea Disease Control and Prevention Agency-COVID-19-National Health Insurance Service (K-COV-N) cohort. Individuals with confirmed COVID-19 from October 8, 2020, to December 31, 2022, and controls identified among individuals who participated in the general health examination in 2018 were included in the analysis.
Confirmed COVID-19.
Incidence and risk of autoimmune and autoinflammatory connective tissue disorders in patients after COVID-19. Various covariates, such as demographic characteristics, general health data, socioeconomic status, and comorbidity profiles, were balanced using inverse probability weighting.
A total of 6 912 427 participants (53.6% male; mean [SD] age, 53.39 [20.13] years) consisting of 3 145 388 with COVID-19 and 3 767 039 controls with an observational period of more than 180 days were included. Alopecia areata (adjusted hazard ratio [AHR], 1.11 [95% CI, 1.07-1.15]), alopecia totalis (AHR, 1.24 [95% CI, 1.09-1.42]), vitiligo (AHR, 1.11 [95% CI, 1.04-1.19]), Behçet disease (AHR, 1.45 [95% CI, 1.20-1.74]), Crohn disease (AHR, 1.35 [95% CI, 1.14-1.60]), ulcerative colitis (AHR, 1.15 [95% CI, 1.04-1.28]), rheumatoid arthritis (AHR, 1.09 [95% CI, 1.06-1.12]), systemic lupus erythematosus (AHR, 1.14 [95% CI, 1.01-1.28]), Sjögren syndrome (AHR, 1.13 [95% CI, 1.03-1.25]), ankylosing spondylitis (AHR, 1.11 [95% CI, 1.02-1.20]), and bullous pemphigoid (AHR, 1.62 [95% CI, 1.07-2.45]) were associated with higher risk in the COVID-19 group. Subgroup analyses revealed that demographic factors, including male and female sex, age younger than 40 years, and age 40 years and older, exhibited diverse associations with the risk of autoimmune and autoinflammatory outcomes. In addition, severe COVID-19 infection requiring intensive care unit admission, the Delta period, and not being vaccinated were associated with higher risk.
This retrospective cohort study with an extended follow-up period found associations between COVID-19 and the long-term risk of various autoimmune and autoinflammatory connective tissue disorders. Long-term monitoring and care of patients is crucial after COVID-19, considering demographic factors, disease severity, and vaccination status, to mitigate these risks.

Long-Term Risk of Autoimmune and Autoinflammatory Connective Tissue Disorders Following COVID-19.

Long-Term Risk of Autoimmune and Autoinflammatory Connective Tissue Disorders Following COVID-19

Papers