• MeSH
• buněčná imunita účinky léků   MeSH
• COVID-19 * mortalita   prevence a kontrola   MeSH
• dezinformace MeSH
• karanténa MeSH
• lidé MeSH
• mRNA vakcíny MeSH
• vakcíny proti COVID-19 MeSH
• všeobecná preventivní opatření metody   MeSH
• Check Tag
• lidé MeSH
• Geografické názvy
• Česká republika MeSH
• Evropa MeSH

OBJECTIVES: We prospectively compared the postvaccination immunity to messenger ribonucleic acid BNT162b2 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine of our pediatric patients over 12 years old with inflammatory bowel disease (IBD) to that of healthy controls and looked for predictors of its robustness. METHODS: Anti-receptor binding domain, anti-spike S2, and anti-nucleocapsid immunoglobin-G (IgG) and immunoglobin-A levels were measured in 139 pediatric patients with IBD [65 fully vaccinated (2 doses), median age 16.3, interquartile range (IQR) 15.2-17.8 years, median time from vaccination (IQR) 61.0 (42.0-80.0) days] and 1744 controls (46, 37-57 years) using microblot array. RESULTS: All IBD and control patients developed positive anti-receptor binding domain IgG antibodies at comparable titers. The proportion of observations with positive anti-spike S2 IgG was higher in patients with IBD than in controls [63% vs 21%, odds ratio 2.99 (1.51-5.90)], as was its titer [median (IQR) 485 (92-922) vs 79 [33-180] IU/mL]. Anti-receptor binding domain and anti-spike S2 IgG levels were associated with IBD status. We found an association between anti-spike S2 IgG levels and time since vaccination (β -4.85, 95% CI -7.14 to 2.71, P = 0.0001), history of SARS-CoV-2 polymerase chain reaction positivity (206.76, 95% CI 39.93-374.05, P = 0.0213), and anti-tumor necrosis factor treatment (-239.68, 95% CI -396.44-83.55, P = 0.0047). Forty-three percent of patients reported vaccination side effects (mostly mild). Forty-six percent of observations with positive anti-nucleocapsid IgG had a history of SARS-CoV-2 infection. CONCLUSIONS: Patients with IBD produced higher levels of postvaccination anti-spike S2 antibodies than controls. Previous SARS-CoV-2 infection is associated with higher production of postvaccination antibodies and anti-tumor necrosis factor treatment with lower production.

• MeSH
• COVID-19 * prevence a kontrola   MeSH
• dospělí MeSH
• idiopatické střevní záněty * MeSH
• imunoglobulin G MeSH
• lidé středního věku MeSH
• lidé MeSH
• mladiství MeSH
• nekróza MeSH
• protilátky virové MeSH
• SARS-CoV-2 MeSH
• TNF-alfa MeSH
• vakcína BNT162 MeSH
• vakcinace MeSH
• vakcíny proti COVID-19 MeSH
• Check Tag
• dospělí MeSH
• lidé středního věku MeSH
• lidé MeSH
• mladiství MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

BACKGROUND: Common variable immunodeficiency (CVID) is characterized by an impaired postvaccination response, high susceptibility to respiratory tract infections, and a broad spectrum of noninfectious complications. Thus, patients with CVID may be at high risk for COVID-19, and vaccination's role in prevention is questionable. OBJECTIVE: We evaluated the clinical outcomes, safety, and dynamics of humoral and T-cell immune responses induced by the mRNA vaccine BNT162b2 in CVID. METHODS: This prospective observational cohort study focused on the clinical outcomes (proportion of infected patients and disease severity), safety (incidences of adverse events and changes in laboratory parameters), and dynamics of humoral (specific postvaccination and virus-neutralizing antibody assessment) and T-cell immune responses (anti-SARS-CoV-2-specific T-cell detection) in 21 patients with CVID after a two-dose administration of BNT162b2. The patients were observed for 6 months. RESULTS: Humoral response was observed in 52% of patients (11 of 21) at month 1 after vaccination but continuously decreased to 33.3% at month 6 (five of 15). Nevertheless, they had a remarkably lower anti-SARS-CoV-2 neutralizing antibody titer compared with healthy controls. The T-cell response was measurable in 46% of patients with CVID (six of 13) at month 1 and persisted over the study period. Mild infection occurred in three patients within the follow-up period (14.3%). The vaccine also exhibited a favorable safety profile. CONCLUSIONS: The BNT162b2 vaccine elicited a measurable antibody response in a high proportion of patients, but it was limited by low titer of virus-neutralizing antibodies and rapid waning of anti-receptor-binding domain SARS-CoV-2-specific antibodies. T-cell response was detected in one-third of patients and remained stable within the follow-up period. Vaccination has favorable safety and clinical-related outcomes in preventing severe COVID-19.

• MeSH
• běžná variabilní imunodeficience * MeSH
• COVID-19 * prevence a kontrola   MeSH
• lidé MeSH
• neutralizující protilátky MeSH
• primární imunodeficience * MeSH
• prospektivní studie MeSH
• protilátky blokující MeSH
• protilátky virové MeSH
• SARS-CoV-2 MeSH
• vakcína BNT162 MeSH
• vakcíny * MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• pozorovací studie MeSH
• práce podpořená grantem MeSH

Ciele: Prvotným cieľom nášho monitorovania bolo zistiť dĺžku pretrvávania hladín protilátok po podaní mRNA vakcíny Comirnaty (Pfizer/BioNTech). Druhým cieľom bola analýza vplyvu vybraných faktorov na hladinu protilátok. Metódy: Súbor pozostával z 250 zamestnancov laboratórií Medirex, a. s. Na kvantitatívne stanovenie špecifických protilátok IgG anti-S1 a anti-S2 proti SARS-CoV-2 bola použitá chemiluminiscenčná imunoanalýza. Z analýzy bolo vyradených 29 osôb pre extrémne hodnoty hladín protilátok v jednotlivých meraniach. Analyzoval sa vplyv pohlavia, veku, BMI, pridružených ochorení a nežiadúcich účinkov po vakcinácii mRNA vakcínou Comirnaty (Pfizer/BioNTech) na hladinu protilátok. Porovnanie sa vykonalo na piatich odberoch v rozmedzí od 2 týždňov od podania 1. dávky po 36 týždňov od podania 2. dávky mRNA vakcíny. Po piatom odbere sa súbor rozdelil na dve skupiny. Prvá skupina sa očkovala 3. dávkou a druhá skupina ostala ako kontrolný súbor. Posledný (šiesty) odber sme vykonali v skupine s boostrom 3. dávky vakcíny 2 týždne po podaní boostra a v kontrolnej skupine v 11. mesiaci od podania 2. dávky vakcíny. Medzi 8. až 10. mesiacom od podania 2. dávky sme vykonali test bunkovej imunity. Výsledky: Pozitívnu hladinu protilátok malo v 36. týždni 99,6 % účastníkov. V kontrolnej skupine boli prítomné protilátky aj v 11. mesiaci od podania 2. dávky. Signifikantne vyššie hladiny protilátok boli u ženského pohlavia, mladších jedincov a pri vybraných nežiadúcich účinkoch. Reaktívne špecifické T lymfocyty boli prítomné u 65,6 % testovaných medzi 36. až 44. týždňom. Záver: Protilátková odpoveď klesá s časom od podania 2. dávky, avšak v kontrolnej skupine bola aj v 48. týždni stále prítomná. Efekt podania boostra na hladinu protilátok bol jednoznačne preukázaný. Súvislosť bunkovej imunity s hladinou protilátok ani s prítomnými protilátkami sme nepotvrdili.

Aims: The primary aim of our monitoring was to determine the duration of persistence of antibody levels following administration of the Comirnaty (Pfizer/BioNTech) mRNA vaccine. The second aim was to analyse the effect of selected factors on the level of antibodies. Methods: The study cohort consisted of 250 employees of the Medirex JSC laboratories. For the quantitative determination of specific IgG anti-S1 and anti-S2 antibodies to SARS-CoV-2, chemiluminescence immunoassay was used. Twenty-nine subjects were excluded from the analysis due to extreme values of antibody levels in individual measurements. The effect of gender, age, BMI, comorbidity, and adverse reactions after vaccination with the Comirnaty (Pfizer/BioNTech) mRNA vaccine on antibody levels was analysed. Comparisons were made for five samples collected from two weeks after the 1st dose to 36 weeks after the 2nd dose of the mRNA vaccine. After the fifth sampling, the cohort was divided into two groups. Group 1 received the 3rd dose, and Group 2 were controls. We performed the last (sixth) sample collection two weeks after booster administration in Group 1and 11 months after the 2nd dose of the vaccine in controls. Between months 8 and 10 after the 2nd dose, we performed a cellular immunity test. Results: Altogether 99.6% of the participants had a positive antibody level at week 36. Antibodies were still present in controls at month 11 after the 2nd dose. Significantly higher antibody levels were found in females, younger subjects, and those with selected adverse reactions. Reactive specific T lymphocytes were present in 65.6% of the subjects between weeks 36 and 44. Conslusion: The antibody response decreased with the time since the 2nd dose but was still present in the control group at week 48. The effect of booster on antibody levels was clearly demonstrated. We have not confirmed an association of cellular immunity with the level of antibodies or with the antibodies present.

• MeSH
• lidé MeSH
• protilátky virové analýza   farmakologie   imunologie   krev   MeSH
• SARS-CoV-2 imunologie   izolace a purifikace   MeSH
• sérologické testování na COVID-19 * klasifikace   metody   statistika a číselné údaje   MeSH
• vakcína BNT162 aplikace a dávkování   farmakologie   imunologie   MeSH
• vakcíny proti COVID-19 analýza   farmakologie   klasifikace   krev   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• klinická studie MeSH
• práce podpořená grantem MeSH
• Geografické názvy
• Slovenská republika MeSH

Although vaccines against COVID-19 are effective tools in preventing severe disease, recent studies have shown enhanced protection after vaccine boosters. The aim of our study was to examine the dynamics and duration of both humoral and cellular immune responses following a three-dose regimen of the BNT162b2 mRNA vaccine. In a longitudinal prospective study we enrolled 86 adults who received the BNT162b2 vaccine, 35 unvaccinated individuals with a history of mild COVID-19 and a control group of 30 healthy SARS-CoV-2 seronegative persons. We assessed the SARS-CoV-2-specific T cell responses and IgG production up to 12 months post the third BNT162b2 dose in 24 subjects. The vaccinated group had significantly higher IgG antibody levels after two doses compared to the convalescent group (p<0.001). After the third dose, IgG levels surged beyond those detected after the second dose (p<0.001). Notably, these elevated IgG levels were maintained 12 months post the third dose. After two doses, specific T cell responses were detected in 87.5% of the vaccinated group. Additionally, there was a significant decrease before the third dose. However, post the third dose, specific T cell responses surged and remained stable up to the 12-month period. Our findings indicate that the BNT162b2 vaccine induces potent and enduring humoral and cellular responses, which are notably enhanced by the third dose and remain persistant without a significant decline a year after the booster. Further research is essential to understand the potential need for subsequent boosters.

• MeSH
• COVID-19 * prevence a kontrola   MeSH
• dospělí MeSH
• imunita MeSH
• imunoglobulin G MeSH
• lidé MeSH
• messenger RNA MeSH
• prospektivní studie MeSH
• SARS-CoV-2 MeSH
• vakcína BNT162 MeSH
• vakcinace MeSH
• vakcíny proti COVID-19 MeSH
• Check Tag
• dospělí MeSH
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

• MeSH
• lidé MeSH
• mRNA vakcíny * MeSH
• objevování léků MeSH
• vakcíny proti COVID-19 MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• novinové články MeSH
• zprávy MeSH

BACKGROUND: Kidney transplant recipients are at risk for a severe course of COVID-19 with a high mortality rate. A considerable number of patients remains without a satisfactory serological response after the baseline and adjuvant SARS-CoV-2 vaccination schedule. METHODS: In this prospective, randomized study, we evaluated the efficacy and safety of one and two booster doses of mRNA vaccines (either mRNA-1273 or BNT162b2) in 125 COVID-19 naive, adult kidney transplant recipients who showed an insufficient humoral response (SARS-CoV-2 IgG <10 AU/ml) to the previous 2-dose vaccination schedule. The primary outcome was the difference in the rate of a positive antibody response (SARS-CoV-2 IgG ≥10 AU/ml) between one and two booster doses at 1 month after the final booster dose. RESULTS: A positive humoral response was observed in 36 (62%) patients receiving two booster doses and in 28 (44%) patients receiving one booster dose (odds ratio [OR], 2.10, 95% confidence interval [CI], 1.02-4.34, p = .043). Moreover, median SARS-CoV-2 IgG levels were higher with two booster doses (p = .009). The number of patients with positive virus neutralizing antibody (VNA) levels was numerically higher with two booster doses compared to one booster dose, but without statistical significance (66% vs. 50%, p = .084). There was no significant difference in positive seroconversions rate and antibody levels between mRNA-1273 and BNT162b2. CONCLUSION: A higher number of kidney transplant recipients achieved a positive antibody response after two booster doses compared to one booster dose.

• MeSH
• COVID-19 * prevence a kontrola   MeSH
• dospělí MeSH
• imunoglobulin G MeSH
• lidé MeSH
• mRNA vakcíny MeSH
• příjemce transplantátu MeSH
• protilátky virové MeSH
• SARS-CoV-2 MeSH
• transplantace ledvin * škodlivé účinky   MeSH
• vakcína BNT162 MeSH
• vakcína firmy Moderna proti COVID-19 MeSH
• vakcíny proti COVID-19 škodlivé účinky   MeSH
• Check Tag
• dospělí MeSH
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• randomizované kontrolované studie MeSH

Pandémia ochorenia COVID-19 (COronaVIrus Disease 2019) spôsobená koronavírusom SARS -CoV-2 (severe acute respiratory syndrome coronavirus 2) zapríčinila milióny úmrtí a mnoho pacientov má po prekonaní akútneho stavu chronické následky. V snahe o zastavenie šírenia vírusu boli vyvinuté viaceré očkovacie látky, ktoré však majú potenciálne vážne nežiaduce účinky. Prezentujeme kazuistiku pacienta s akútnymi (myokarditída, exacerbácia bronchiálnej astmy) aj dlhodobými (syn- dróm posturálnej ortostatickej tachykardie − POTS) komplikáciami po očkovaní druhou dávkou mRNA vakcíny BNT162b2 (Comirnaty®). Liečba pozostáva z režimových opatrení, početnej farmakoterapie (metoprolol, ivabradín, kortikosteroidy, antihistaminiká, antiflogistiká, bronchodilatanciá) a viacerých nutraceutík (extrakt z borovice prímorskej, kvercetín, vitamíny, horčík, fosfatidylcholín). V diskusii analyzujeme povakcinačné poškodenie a prinášame krátky prehľad z aktuálnej literatúry.

The pandemic of the disease COVID-19 (COronaVIrus Disease 2019) caused by the SARS-CoV-2 coronavirus (severe acute respiratory syndrome coronavirus 2) resulted in millions of deaths and many patients have chronic consequences after overcoming the acute condition. Several vaccines have been developed in an effort to stop the spread of the virus, but they have potentially serious adverse effects. We present a case report of a patient with acute (myocarditis, exacerbation of bronchial asthma) and long-term (postural orthostatic tachycardia syndrome - POTS) complications after vaccination with the second dose of mRNA vaccine BNT162b2 (Comirnaty®). Treatment consists of regimen measures, numerous pharmacotherapy (metoprolol, ivabradine, corticosteroids, antihistamines, antiphlogistics, bronchodilators) and several nutraceuticals (maritime pine bark extract, quercetin, vitamins, magnesium, phosphatidylcholine). In the discussion, we analyze post-vaccination injury and present a short review of the current literature.

• MeSH
• bronchiální astma farmakoterapie   patologie   MeSH
• dospělí MeSH
• kardiovaskulární látky aplikace a dávkování   MeSH
• lidé MeSH
• mRNA vakcíny * škodlivé účinky   MeSH
• myokarditida chemicky indukované   diagnostické zobrazování   farmakoterapie   krev   patologie   MeSH
• postakutní syndrom COVID-19 farmakoterapie   patologie   MeSH
• potravní doplňky MeSH
• prednison aplikace a dávkování   MeSH
• progrese nemoci MeSH
• syndrom posturální ortostatické tachykardie chemicky indukované   patologie   MeSH
• vakcíny proti COVID-19 * škodlivé účinky   MeSH
• Check Tag
• dospělí MeSH
• lidé MeSH
• Publikační typ
• kazuistiky MeSH

BACKGROUND: Rituximab (RTX) and ocrelizumab (OCR), B cell-depleting therapy targeting CD20 molecules, affect the humoral immune response after vaccination. How these therapies influence T-cell-mediated immune response against SARS-CoV-2 after immunization remains unclear. We aimed to evaluate the humoral and cellular immune response to the COVID-19 vaccine in a cohort of patients with multiple sclerosis (MS), neuromyelitis optica spectrum disorders (NMOSD), and myasthenia gravis (MG). METHODS: Patients with MS (83), NMOSD (19), or MG (7) undergoing RTX (n=47) or OCR (n=62) treatment were vaccinated twice with the mRNA BNT162b2 vaccine. Antibodies were quantified using the SARS-CoV-2 IgG chemiluminescence immunoassay, targeting the spike protein. SARS-CoV-2-specific T cell responses were quantified by interferon γ release assays (IGRA). The responses were evaluated at two different time points (4-8 weeks and 16-20 weeks following the 2nd dose of the vaccine). Immunocompetent vaccinated individuals (n=41) were included as controls. RESULTS: Almost all immunocompetent controls developed antibodies against the SARS-CoV-2 trimeric spike protein, but only 34.09% of the patients, without a COVID-19 history and undergoing anti-CD20 treatment (via RTX or OCR), seroconverted. This antibody response was higher in patients with intervals of longer than 3 weeks between vaccinations. The duration of therapy was significantly shorter in seroconverted patients (median 24 months), than in the non-seroconverted group. There was no correlation between circulating B cells and the levels of antibodies. Even patients with a low proportion of circulating CD19+ B cells (<1%, 71 patients) had detectable SARS-CoV-2 specific antibody responses. SARS-CoV-2 specific T cell response measured by released interferon γ was detected in 94.39% of the patients, independently of a humoral immune response. CONCLUSION: The majority of MS, MG, and NMOSD patients developed a SARS-CoV-2-specific T cell response. The data suggest that vaccination can induce SARS-CoV-2-specific antibodies in a portion of anti-CD20 treated patients. The seroconversion rate was higher in OCR-treated patients compared to those on RTX. The response represented by levels of antibodies was better in individuals, with intervals of longer than 3 weeks between vaccinations.

• MeSH
• autoimunitní nemoci nervového systému * MeSH
• COVID-19 * MeSH
• glykoprotein S, koronavirus MeSH
• humanizované monoklonální protilátky terapeutické užití   MeSH
• lidé MeSH
• myasthenia gravis * MeSH
• protilátky virové MeSH
• rituximab terapeutické užití   MeSH
• roztroušená skleróza * farmakoterapie   MeSH
• SARS-CoV-2 MeSH
• vakcína BNT162 MeSH
• vakcinace MeSH
• vakcíny proti COVID-19 MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

The study was designed to evaluate the medical relevance of Malondialdehyde (MDA) (a marker of oxidative stress) and total antioxidant capacity (TAC) in coronavirus disease 2019 (COVID-19) groups, cured groups, and control groups; before and after taking the vaccine. Blood samples were taken from Oncology Unit in Al-Mahaweel hospital in Hilla city. Sixteen patients, sixteen cured patients, thirty control, sixteen subjects were taken one dose of Pfizer vaccine, sixteen subjects were taken two doses of Pfizer vaccine. We found that significantly increased lipid peroxidation, measured as MDA, was demonstrated in the serum of COVID-19 patients and TAC decreased in patients when compared with the control groups. Inversely, we found the mean MDA levels decrease and increase in TAC levels in cured patients when compare with COVID-19 patients. In addition, it is found that subjects were taken one dose or two doses of the Pfizer vaccine have less MDA levels and more TAC levels than the COVID-19 vaccine for that reason the Pfizer vaccines play the important role in the activity of immune systems.

• MeSH
• angiotensin konvertující enzym 2 metabolismus   MeSH
• antioxidancia analýza   metabolismus   MeSH
• COVID-19 * komplikace   metabolismus   MeSH
• ELISA metody   MeSH
• lidé MeSH
• malondialdehyd analýza   metabolismus   MeSH
• reaktivní formy kyslíku metabolismus   MeSH
• vakcína BNT162 MeSH
• vakcíny proti COVID-19 škodlivé účinky   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• klinické zkoušky kontrolované MeSH
• pozorovací studie MeSH