scholarly journals Pseudotyped SARS-CoV-2 Omicron variant exhibits significant escape from neutralization induced by a third booster dose of vaccination

Author(s):  
Xiaoqi Yu ◽  
Dong Wei ◽  
Wenxin Xu ◽  
Yulong Li ◽  
Xinxin Li ◽  
...  

The Omicron Variant of concern (B.1.1.529) has spread internationally and is raising serious concerns about the reduced vaccine efficacy and the increased risk of reinfection. Here we assessed the serum neutralizing activity using a pseudovirus-based neutralization assay in 292 healthcare workers who had administered a third homologous boosting vaccination 8 to 9 months after completion of the priming two-dose inactivated vaccination to investigate whether the newly identified Omicron variant could escape serum antibody neutralization elicited by the booster vaccination. The third booster dose with BBIBP-CorV lead to a significant rebound in neutralizing immune response against SARS-CoV-2, and the neutralization GMT on day 28 after the third booster dose was 6.1 times higher than the GMT on day 28 after the second dose. The Omicron variant did cause significantly lower neutralization sensitivity compared to the wild-type strain of the booster elicited serum, with about 20.1-fold reduction. Our study demonstrated that a third booster dose of BBIBP-CorV lead to a significant rebound in neutralizing immune response against SARS-CoV-2, while the Omicron variant showed extensive but incomplete escape of the booster elicited neutralization.

2021 ◽  
Author(s):  
Maria Elena Romero-Ibarguengoitia ◽  
Diego Rivera-Salinas ◽  
Yodira Guadalupe Hernandez-Ruiz ◽  
Ana Gabriela Armendariz-Vazquez ◽  
Arnulfo Gonzalez-Cantu ◽  
...  

Background: Vaccination is our main strategy to control SARS-CoV-2 infection. Given a decrease in the quantitative SARS-CoV-2 spike 1-2 IgG antibody titers three months following the second BNT162b2 dose, healthcare workers got a third booster dose after six months of completing the original scheme. This study aimed to analyze quantitative SARS-CoV-2 spike 1-2 IgG antibody titers and safety of the third dose. Material and methods: A prospective longitudinal cohort study included healthcare workers who received a third booster dose after six months of the complete BNT162b2 regimen. We assessed the quantitative SARS-CoV-2 spike 1-2 IgG antibody titers 21-28 days after the first and second dose, three months after the complete scheme, 1-7 days following the third dose, and 21-28 days after the boost. Results: The cohort comprised 168 non-immunocompromised participants of 41(10) years old, 67% being women. The third dose was associated with increasing the quantitative antibody titers, regardless of previous SARS-CoV-2 history. In negative SARS-CoV-2 history, the median (IQR) antibody titers increased from 379 (645.4) to 2960 (2010), while in positive SARS-CoV-2 history, from 590 (1262) to 3090 (2080). The third dose had less number of total side effects compared to the other two shots. The most common side effect after the third BNT162b2 shot was pain at the injection site (n=82, 84.5%), followed by tiredness (n=45, 46.4%), with a mild severity (n=36, 37.1%). Tiredness, myalgias, arthralgias, fever, and adenopathy were proportionally higher following the third dose than the two-dose regimen (p<0.05). Conclusion: The third dose applied after six months of the original BNT162b2 regimen provided a good humoral immune response by elevating the quantitative SARS-CoV-2 spike 1-2 IgG antibody titers. The booster dose was well tolerated with no severe side effects after the additional BNT162b2 dose.


Author(s):  
Jessica A. Breznik ◽  
Ali Zhang ◽  
Angela Huynh ◽  
Matthew S. Miller ◽  
Ishac Nazy ◽  
...  

AbstractNursing home residents often fail to mount robust responses to vaccinations and recent reports of breakthrough infections, particularly from variants of concern, raise questions about whether vaccination regimens elicit a sufficient humoral immune response or if booster doses are warranted. We examined SARS-CoV-2 antibody levels and neutralizing capacity in nursing home residents 3-5 months after 2 doses of mRNA-1273 or BNT163b2 vaccination as per recommended schedules.Nursing home residents were recruited from eight long-term care homes in Ontario, Canada, between March and July 2021. Antibody levels and neutralization capacity from a previously published convalescent cohort were used as a comparator. Serum SARS-CoV-2 IgA/G/M against spike (S) protein and its receptor-binding domain (RBD) were measured by validated ELISA, with assay cut-off at the mean and 3 standard deviations of a pre-COVID-19 population from the same geographic region. Antibody neutralization was measured against the wild-type strain of SARS-CoV-2 and the beta variant of concern (B.1.351).No neutralizing antibodies were detected in ∼20% of residents to the wild-type virus (30/155; 19%) or beta variant (27/134; 20%). Residents that received BNT163b2 had a ∼4-fold reduction in neutralization to the wild-type strain, and a ∼2-fold reduction in neutralization to the beta variant relative to those who received mRNA-1273.Current mRNA SARS-CoV-2 vaccine regimens may not have equivalent efficacy in nursing home residents. Our findings imply that differences in the humoral immune response may contribute to breakthrough infections, and suggest that consideration of the type of vaccine administered to older adults will have a positive impact on the generation of protective immunity.


2013 ◽  
Vol 9 (2) ◽  
pp. 127-131
Author(s):  
MS Parvin ◽  
MP Siddique ◽  
MT Islam

Fowl cholera is a highly contagious and economically important disease of poultry worldwide. Control of fowl cholera depends mainly on vaccination throughout the world including Bangladesh. Therefore, the objective of the study was to determine the antibody titre following vaccination with fowl cholera vaccine in different breeds of commercial birds including Aseel and its F1 crosses. The study was conducted at Bangladesh Agricultural University Poultry Farm during the period from March to December 2011. A total of 37 birds of four types of breeds (Synthetic - 10, White Rock - 10, Aseel - 7 and Aseel×Rhode Island Red - 10) of both sex and 17 weeks old were used in this trial. Primary and booster vaccination were done in all the birds of four groups with fowl cholera vaccine (BAU-FCV) @ 0.5 ml/bird IM at 20 weeks and 26 weeks of age, respectively. Blood samples were collected at different occasions of vaccination. The immune responses (serum antibody titre) were determined by using passive haemagglutination assay (PHA). All the four groups of vaccinated birds induced significantly higher humoral immune response after primary and booster vaccination. However, no significant differences were observed in antibody titres between breeds on different occasions of vaccination. Of the four groups, antibody titres were slightly higher in breeds of Aseel×RIR and White Rock birds than other two breeds. It appears from the study that breed variation has no significant effect on immune response to fowl cholera vaccine.DOI: http://dx.doi.org/10.3329/bjvm.v9i2.13453


BMJ Open ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. e042711
Author(s):  
Fayssal Farahat ◽  
Abdulhakeem Althaqafi ◽  
Abdulfattah Al-Amri ◽  
Asim Alsaedi ◽  
Mohammad Abouremsh ◽  
...  

ObjectivesThe present study was conducted to estimate the seroprevalence of antibody to pertussis toxin among adult populations in western Saudi Arabia.DesignA cross-sectional study.SettingKing Abdulaziz Medical City, Jeddah, western Saudi Arabia. A tertiary care teaching hospital.ParticipantsA total of 1200 participants (400 healthcare workers, 400 military recruits and 400 blood donors) were included. The majority were male (79.3%), and the mean (±SD) age was 27.2 (±6.7) years old.InterventionsThe study included the analysis of serum blood samples using commercial ELISA. A consecutive sampling technique was applied.Primary outcome measuresSeropositivity of antipertussis toxin immunoglobulin G (anti-PT IgG) ≥62.5 IU/mL.ResultsAntibody titres ≥62.5 IU/mL, indicating exposure to Bordetella pertussis infection within the last year, were identified in 12.0% (95% CI 10.2% to 14.0%) of the participants. Titres ≥125 IU/mL, suggesting recent infection, were detected in 3.5% (95% CI 2.5% to 4.7%). Seroprevalence of positive IgG antibody titres (≥62.5 IU/mL) was highest among the healthcare workers (HCWs) (14%), then the military recruits (13.5%) and blood donors (8.5%; p=0.03). The multivariate regression analysis showed association between participants group (HCWs and military), male gender and younger age (<25 years old) and higher antibody to pertussis toxin.ConclusionsHigh pertussis seropositivity was associated with participants’ occupation (ie, healthcare workers and military recruits), and anti-PT IgG titre was negatively correlated with age. A substantial deficiency in pertussis reporting in Saudi Arabia has been suggested, with potential increased risk to the most vulnerable populations (ie, infants and elderly). Enhancing the booster dose of pertussis vaccine for adolescents and adults is crucial to minimise the burden of pertussis.


Vaccines ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 309
Author(s):  
Perrine Parize ◽  
Jérémie Sommé ◽  
Laura Schaeffer ◽  
Florence Ribadeau-Dumas ◽  
Sheherazade Benabdelkader ◽  
...  

Pre-exposure rabies prophylaxis (PrEP) is recommended for people at frequent or increased risk of professional exposure to lyssavirus (including rabies virus). PrEP provides protection against unrecognized exposure. After the primary vaccination, one’s immune response against rabies may decline over time. We aimed to evaluate the immune response to rabies in individuals immunized for occupational reasons before and after a booster dose of the rabies vaccine. With this aim, we retrospectively documented factors associated with an inadequate response in individuals vaccinated for occupational purposes. Our findings analyzed data from 498 vaccinated individuals and found that 17.2% of participants had an inadequate antibody titration documented after their primary vaccination without the booster, while inadequate response after an additional booster of the vaccine was evidenced in 0.5% of tested participants. This study showed that a single booster dose of vaccine after PrEP conferred a high and long-term immune response in nearly all individuals except for rare, low responders. A systematic rabies booster after primary vaccination may result in alleviating the monitoring strategy of post-PrEP antibody titers among exposed professionals.


Author(s):  
B.L. Meena ◽  
Nikhil Gandhi ◽  
M.P. Sharma

Background: Aim of our study was to evaluate the immune response after hepatitis B vaccination and to determine the duration of protective levels of HBsAb titre in doctors. From our study we concluded that hepatitis-B vaccine gives protection for more than 10 years after primary vaccination and booster dose of Hepatitis-B vaccine is not required in immunocompetent persons after primary vaccination. Method: In this study total 100 doctors of our institution were included who were vaccinated against hepatitis B. Data were obtained regarding age, sex, weight, height, BMI and duration of vaccination period. Doctors with no prior vaccination or incomplete vaccination or those who took booster vaccination were excluded from this study. Results: The mean titre was observed to be higher in 30 to 34 years of age group (584.42±4.03.21) as compared to age group of less than 25 and greater than 40 years. Moreover, males were observed to have higher mean titre as compared to females. (411.64± 417.27 vs 333.66± 431.49) but not statistically significant.  Similar with age and sex, duration of vaccination status was also not statistically significant. When we compared the  duration of vaccination status with  age group , mean titre was more in ≥30 years of age group as compared to <30 years (younger age groups) but statistically significant relation was observed only with the 1 month to <5 years of duration. Conclusion: From our study we concluded that hepatitis-B vaccinegives protection for more than 10 years after primary vaccination and booster dose of Hepatitis-B vaccine is not required inimmuno-competent persons after primary vaccination. Keywords: HbsAg titre , HepatitsB vaccine , seroprotection rate.


2021 ◽  
Author(s):  
Judit Gervain ◽  
Katalin B Szabo ◽  
Erika H Baki ◽  
Lidia Kadlecsik ◽  
Attila Gyenesei ◽  
...  

Abstract Introduction SARS-CoV-2 infections have very different clinical manifestations and anti-SARS-CoV-2 immunisation may also trigger very different levels and length of protection. While (re)infection after previous COVID-19 illness or following vaccination are known, their impact and the optimal timing of any booster vaccination is currently debated. International evidence about potential underlying immune response differences remains limited and is currently not available in Hungary. Methods We prospectively investigated the magnitude of immune responses to infection or immunisation, their over-time changes and the occurrence of new infections through anti-SARS-CoV-2 IgG levels and the association with selected individual and clinical parameters in two voluntary cohorts of healthcare workers at a public teaching hospital in a real-world longitudinal cohort study in Hungary. In the first cohort, the anti-nucleocapsid IgG levels of 42 health care workers (female: 100%) with SARS-CoV-2 infection were followed-up over 8 months between June 2020 and February 2021. Beyond the change in immune response, associations with age, selected existing chronic conditions, blood type and severity of symptoms were investigated. In the immunised cohort, anti-spike-RBD protein IgG levels of 49 health care workers (female: 73%) with no prior COVID-19 infection were monitored up to 4 months following initial immunisation with BNT162b2 vaccine between December 2020 and April 2021. Statistical analyses included median analysis, linear regression, ANCOVA, Kruskal-Wallis test and Skillings-Mack test for block designs as relevant. Results Within the infected cohort, the median time of anti-SARS-CoV-2 IgG level reduction below the positive test cut-off was 6 months. First month IgG levels were on average the highest among those in illness severity category 4, but the difference to less severe categories was not statistically significant. Higher age was associated with higher IgG levels. Within the immunised cohort, the anti-SARS-CoV-2 spike-RBD protein IgG levels increased 25-fold between the first and second immunisations, significantly decreased to 33% of the peak level after 90 days, and had an overall negative tendency with older age and male sex. IgG monitoring revealed 17% (7/42) and 14% (7/49) new infections in the infected and the immunised cohorts, respectively, all symptomless. Discussion Our study is the first to investigate the level, change and associations of anti-SARS-CoV-2 IgG immune response in infected or immunised healthcare workers in Hungary. It provides further evidence about the significantly declining IgG protection through initial infection beyond 6 months. While immunisation with mRNA vaccination shows a similar pattern of reduction in protection, IgG levels remained within the positive range at 4 months. The observed rate of 15% new, asymptomatic infections and their potential broader impacts call for further investigations. Overall, our findings are confirmative of the effectiveness of vaccination to prevent illness, recent considerations for booster vaccination beyond 6 months, and indicate the potential benefit of anti-SARS-CoV-2 IgG monitoring for optimisation.


2020 ◽  
pp. 49-57
Author(s):  
S. V. Orlova ◽  
E. A. Nikitina ◽  
L. I. Karushina ◽  
Yu. A. Pigaryova ◽  
O. E. Pronina

Vitamin A (retinol) is one of the key elements for regulating the immune response and controls the division and differentiation of epithelial cells of the mucous membranes of the bronchopulmonary system, gastrointestinal tract, urinary tract, eyes, etc. Its significance in the context of the COVID‑19 pandemic is difficult to overestimate. However, a number of studies conducted in the past have associated the additional intake of vitamin A with an increased risk of developing cancer, as a result of which vitamin A was practically excluded from therapeutic practice in developed countries. Our review highlights the role of vitamin A in maintaining human health and the latest data on its effect on the development mechanisms of somatic pathology.


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