Autoantibodies Targeting G-Protein-Coupled Receptors and RAS-Related Molecules in Post-Acute COVID Vaccination Syndrome: A Retrospective Case Series Study DOI Creative Commons
Mauro Mantovani, Paolo Bellavite, Sergio Fazio

et al.

Biomedicines, Journal Year: 2024, Volume and Issue: 12(12), P. 2852 - 2852

Published: Dec. 15, 2024

Background/Objectives: While post-acute COVID-19 syndrome is well known and extensively studied, the COVID vaccination (PACVS) a more recent nosological entity that poorly defined at immunopathological level, although it shares many symptoms with sequelae of viral infections. Methods: This single-center retrospective study reports case series 17 subjects vaccinated mRNA or adenoviral vector vaccines who were healthy before had never been infected SARS-CoV-2 but presented similar to PACVS for median time 20 months (min 4, max 32). The medical records all patients referred our outpatient clinic over one-year period retrospectively analyzed. Results: In this group, serological tests showed that, in addition positivity anti-spike protein antibodies, high percentage positive antibodies against G protein-coupled receptors molecules involved response SARS-CoV-2. panel 16 autoantibodies tested, few positively associated some reported by patients: anti-ATR1 lymphadenopathy and/or tonsillitis; anti-ACE2 skin such as ecchymosis, oedema, rash; anti-MAS1 widespread burning sensation; anti-STAB1 oedema rash. Anti-ADRA2A negatively memory loss mental fog. ACE2 correlated serum levels anti-S supporting hypothesis an anti-idiotype mechanism immunopathogenesis PACVS. Conclusions: exploratory analysis suggests directed ACE2, probably also MAS1 STAB1, may serve biomarkers

Language: Английский

Evidence for Molecular Mimicry between SARS‐CoV‐2 and Human Antigens: Implications for Autoimmunity in COVID‐19 DOI Creative Commons
Andrea Arévalo‐Cortes, Daniel Rodríguez‐Pinto,

Leonardo Aguilar-Ayala

et al.

Autoimmune Diseases, Journal Year: 2024, Volume and Issue: 2024(1)

Published: Jan. 1, 2024

As for other viral diseases, the mechanisms behind apparent relationship between COVID‐19 and autoimmunity are yet to be clearly defined. Molecular mimicry, existence of sequence and/or conformational homology human antigens, could an important contributing factor. Here, we review accumulated evidence supporting occurrence mimicry SARS‐CoV‐2 proteins. Both bioinformatic approaches antibody cross‐reactions have yielded a significant magnitude events, far more common than expected happen by chance. The clinical implication this phenomenon is ample since many identified antigens may participate in pathophysiology or targets autoimmune diseases. Thus, related partially explained molecular further research designed specifically address possibility needed.

Language: Английский

Citations

4

Post-COVID-19 Small Fiber Neuropathy as a New Emerging Quality of Life-Threatening Disease: A Systematic Review DOI Creative Commons
Francesca Bandinelli, Marco Di Carlo,

Virginia Alba Colantuono

et al.

Microorganisms, Journal Year: 2025, Volume and Issue: 13(2), P. 328 - 328

Published: Feb. 2, 2025

Post-acute sequelae of COVID-19 (PASC) syndrome is considered an emergent and diffuse multidisciplinary problem. Compelling evidence suggests that increases symptoms pre-existent small fiber neuropathy (SFN) might trigger de novo onset SFN. In this systematic review, for the first time, we provide a comprehensive overview clinical diagnostic features PASC-SFN, including accompanying disorders, disease evolution, possible treatments, described in recent literature. Following infection, many patients reported wide range complications, not self-limiting independent from previous infection severity. SFN begins more frequently with distal limb burning pain numbness, which accompany other dysautonomia, cognitive, visual, osteoarticular disorders involving multiple organ systems. initial suspicion, some tests be useful as complementary examinations, such nerve quantitative sensory testing, electromyography, optic tomography. Otherwise, definite diagnosis reached skin biopsy gold standard, along corneal vivo microscopy when ocular discomfort present. Being long-term condition, dissimilar symptomatic disease-modifying drugs were employed treatment condition achievement partial results, steroids, pregabalin, gabapentin, duloxetine, vitamins, homotaurine phosphatidylserine, alpha lipoic acid, immunosuppressants, intravenous immunoglobulin therapy. PASC-SFN complex emerging extremely challenging physicians. At present, only feasible management represented by tailored approach, future definitive protocols deemed essential.

Language: Английский

Citations

0

Post-COVID-19 and Post-COVID-19 Vaccine Arthritis, Polymyalgia Rheumatica and Horton’s Arteritis: A Single-Center Assessment of Clinical, Serological, Genetic, and Ultrasonographic Biomarkers DOI Open Access
Francesca Bandinelli, Mario Pagano, Maria Sole Vallecoccia

et al.

Journal of Clinical Medicine, Journal Year: 2023, Volume and Issue: 12(24), P. 7563 - 7563

Published: Dec. 8, 2023

The potential role of the COVID-19 vaccine and infection to induce autoimmunity is currently underestimated despite literature emphasizing arthralgia as a common adverse event. We aimed study impact rheumatological complications post-COVID-19 (PC) (PCV), comparing undifferentiated arthritis (UA) Polymyalgia Rheumatica, Horton's Arteritis (PMR-HA) isolated UA with "connective-like" accompanying symptoms. retrospectively included 109 patients at least 6 months follow-up, analyzing serum biomarkers, joint ultrasound (US), lung HRCT, DLCO, HLA haplotypes. There were 87 showing increased gastrointestinal involvement (p = 0.021 p 0.012), higher anti-spike protein IgG levels 0.003), anti-SARS-CoV-2 positivity 0.003). Among them, 66 cases progressed ACR-EULAR 2010 early after 3 months, whereas PMR-HA more commonly PCV (81.8%, 0.008), demonstrating CRP 0.007) ESR 0.006) levels, lower rate ANA 0.005), remission six 0.050). In patients, prevalent was DRB1*11 C*07 (36.8% 42.1%). Serum calprotectin, interleukin-6, 0.021, 0.041, 0.018) seemed specific for UA. Conversely, showed poorer DLCO 0.041) frequent US synovitis 0.041). conclusion, PC complication may persist over time when compared PMR-HA.

Language: Английский

Citations

7

New-onset Immune-mediated Necrotizing Myopathy and Trigeminal Neuropathy after SARS-CoV-2 mRNA Vaccination in a Patient with Rheumatoid Arthritis and Sjögren's Syndrome DOI Open Access
Takuma Tsuzuki Wada, Kazuhiro Yokota,

Fumito Inayoshi

et al.

Internal Medicine, Journal Year: 2023, Volume and Issue: 62(24), P. 3699 - 3706

Published: Oct. 12, 2023

We present the case of a 42-year-old woman with rheumatoid arthritis and Sjögren's syndrome treated adalimumab who developed immune-mediated necrotizing myopathy (IMNM) trigeminal neuropathy after SARS-CoV-2 mRNA vaccination. Trigeminal neuralgia elevated serum creatine kinase levels emerged 12 days post-vaccination, followed by myalgia in femoral muscles. IMNM was histologically diagnosed. The pathogenesis may involve molecular mimicry between spike glycoprotein autologous tissues triggered This emphasizes association vaccination, tumor necrosis factor inhibitor, IMNM, neuropathy, as well importance monitoring adverse events following vaccination patients autoimmune disease.

Language: Английский

Citations

6

Hypocortisolemic ASIA: a vaccine- and chronic infection-induced syndrome behind the origin of long COVID and myalgic encephalomyelitis DOI Creative Commons
Manuel Ruiz-Pablos, Bruno Paiva, Aintzane Zabaleta

et al.

Frontiers in Immunology, Journal Year: 2024, Volume and Issue: 15

Published: July 9, 2024

Myalgic encephalomyelitis or chronic fatigue syndrome (ME/CFS), long COVID (LC) and post-COVID-19 vaccine show similarities in their pathophysiology clinical manifestations. These disorders are related to viral adjuvant persistence, immunological alterations, autoimmune diseases hormonal imbalances. A developmental model is postulated that involves the interaction between immune hyperactivation, hypophysitis pituitary hypophysitis, depletion. This process might begin with a deficient CD4 T-cell response infections genetically predisposed individuals (HLA-DRB1), followed by an uncontrolled CD8 hyperactivation elevated antibody production, some of which may be directed against autoantigens, can trigger direct damage pituitary, resulting decreased production hormones, such as ACTH. As disease progresses, prolonged exposure antigens lead exhaustion system, exacerbating symptoms pathology. It suggested these could included autoimmune/adjuvant-induced inflammatory (ASIA) because similar manifestations possible relationship genetic factors, polymorphisms HLA-DRB1 gene. In addition, it proposed treatment antivirals, corticosteroids/ginseng, antioxidants, metabolic precursors improve modulating response, function, inflammation oxidative stress. Therefore, purpose this review suggest origin adenohypophysis improvement after corticosteroid replacement therapy.

Language: Английский

Citations

1

Small Fiber Neuropathy Associated with Post-COVID-19 and Post-COVID-19 Vaccination Arthritis: A Rare Post-Infective Syndrome or a New-Onset Disease? DOI Open Access
Francesca Bandinelli, Romina Nassini,

Eleonora Gherardi

et al.

Journal of Personalized Medicine, Journal Year: 2024, Volume and Issue: 14(8), P. 789 - 789

Published: July 25, 2024

Post-COVID-19 (PC) and post-COVID-19 vaccination (PCV) syndromes are considered emergent multidisciplinary disorders. PC/PCV small fiber neuropathy (SFN) was rarely described its association with undifferentiated arthritis (UA) never defined. We aimed to evaluate PC/PCV-UA associated the recent onset of severe lower limb paresthesia, compare SFN positive (+) negative (-) patients, changes in biomarkers SFN+ during treatments. Nineteen PC/PCV-UA-patients possible underwent skin biopsy at Usl Tuscany Center (Florence) early outpatient clinic from September 2021 March 2024. Eight selected were compared ten SFN- patients. In baseline joint ultrasound (US), electromyography (EMG), optical coherence tomography (OCT), repeated six months. Moreover, patients clinically assessed by a 0-10 numeric rating scale for neurological symptoms DAS28/ESR up 12 months follow-up. showed intraepidermal nerve density histopathological examination biopsies higher frequency OCT EMG abnormalities comparison US significantly improved, while did not change six-month Fatigue, motor impairment, burning pain, brain fog, sensitivity disorders decreased long-term follow-up (12 months).

Language: Английский

Citations

1

Vogt-Koyanagi-Harada Disease and COVID DOI Open Access
Priscilla Manni,

Maria Carmela Saturno,

Massimo Accorinti

et al.

Journal of Clinical Medicine, Journal Year: 2023, Volume and Issue: 12(19), P. 6242 - 6242

Published: Sept. 27, 2023

Vogt–Koyanagi–Harada (VKH) is a rare multisystem inflammatory disease affecting the eyes, ears, brain, skin, and hair. The Coronavirus Disease 2019 (COVID-19) new contagious infection that might trigger onset of VKH disease, as previously proposed for other viruses. Moreover, after mass vaccination against SARS-CoV-2 worldwide, cases associated with COVID-19 have been reported. We present an overview comprehensive literature revision all described vaccination, adding our experience. No differences found considering epidemiology clinical findings compared to those reported in no-COVID era. All patients promptly responded systemic local corticosteroid therapy good final visual prognosis. Different possible pathogenetic mechanisms underlying are discussed, while presence HLA DR4 antigen genetic predisposition proposed. one most frequently uveitic entities but response should not discourage vaccination. Nevertheless, ophthalmologists be alerted possibility occurrence or relapse especially genetically predisposed subjects.

Language: Английский

Citations

3

A Comprehensive Review on the Intricate Interplay between COVID-19 Immunization and the New Onset of Pemphigus Foliaceus DOI Creative Commons
Beatrice Bălăceanu-Gurău, Adrian Dumitrascu, Călin Giurcăneanu

et al.

Vaccines, Journal Year: 2024, Volume and Issue: 12(8), P. 857 - 857

Published: July 30, 2024

Autoimmune bullous diseases (AIBDs) are characterized by the formation of vesicles, lesions, and mucosal erosions. The autoantibodies target cellular anchoring structures from surface epidermal keratinocyte named desmosomes, leading to a loss cohesion acantholysis. AIBDs classified into intraepidermal or subepidermal types based on clinical features, histological characteristics, immunofluorescence patterns. Pemphigus foliaceus (PF) is an acquired, rare, autoimmune skin condition associated with that specifically desmoglein-1, presentation delicate cutaneous blisters, typically sparing mucous membranes. Several factors, including genetic predisposition, environmental triggers, malignancies, medication use, vaccination (for influenza, hepatitis B, rabies, tetanus, more recently, severe acute respiratory syndrome Coronavirus 2 known as SARS-CoV-2), can potentially trigger onset pemphigus. With advent vaccines playing pivotal role in combatting 2019 coronavirus disease (COVID-19), extensive research has been conducted globally ascertain their efficacy potential adverse effects. While reports post-COVID-19 exist medical literature, instances PF following have less commonly reported worldwide. disease's pathophysiology likely attributed resemblance between ribonucleic acid (RNA) antigen present these nuclear matter. protein produced BNT-162b2 messenger (mRNA) vaccine includes immunogenic epitopes could phenomena predisposed individuals through several mechanisms, molecular mimicry, activation pattern recognition receptors, polyclonal stimulation B cells, type I interferon production, autoinflammation. In this review, we comprehensive examination existing literature regarding relationship COVID-19 PF, delving intricate interactions. This exploration improves understanding both pemphigus mRNA highlighting importance close monitoring for post-immunization.

Language: Английский

Citations

0

Autoantibodies Targeting G-Protein-Coupled Receptors and RAS-Related Molecules in Post-Acute COVID Vaccination Syndrome: A Retrospective Case Series Study DOI Creative Commons
Mauro Mantovani, Paolo Bellavite, Sergio Fazio

et al.

Biomedicines, Journal Year: 2024, Volume and Issue: 12(12), P. 2852 - 2852

Published: Dec. 15, 2024

Background/Objectives: While post-acute COVID-19 syndrome is well known and extensively studied, the COVID vaccination (PACVS) a more recent nosological entity that poorly defined at immunopathological level, although it shares many symptoms with sequelae of viral infections. Methods: This single-center retrospective study reports case series 17 subjects vaccinated mRNA or adenoviral vector vaccines who were healthy before had never been infected SARS-CoV-2 but presented similar to PACVS for median time 20 months (min 4, max 32). The medical records all patients referred our outpatient clinic over one-year period retrospectively analyzed. Results: In this group, serological tests showed that, in addition positivity anti-spike protein antibodies, high percentage positive antibodies against G protein-coupled receptors molecules involved response SARS-CoV-2. panel 16 autoantibodies tested, few positively associated some reported by patients: anti-ATR1 lymphadenopathy and/or tonsillitis; anti-ACE2 skin such as ecchymosis, oedema, rash; anti-MAS1 widespread burning sensation; anti-STAB1 oedema rash. Anti-ADRA2A negatively memory loss mental fog. ACE2 correlated serum levels anti-S supporting hypothesis an anti-idiotype mechanism immunopathogenesis PACVS. Conclusions: exploratory analysis suggests directed ACE2, probably also MAS1 STAB1, may serve biomarkers

Language: Английский

Citations

0