A novel HBc-S230 protein chimeric VLPs induced robust immune responses against SARS-CoV-2 DOI Creative Commons

Weixu Feng,

Zhuo Chen,

Lianpeng Wu

и другие.

International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113362 - 113362

Опубликована: Окт. 18, 2024

Here, we report that four functional fragments of the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) spike protein including receptor binding motif (RBM), fusion peptide (FP), heptad repeat 1 (HR1) and 2 (HR2) were chosen to develop a recombinant S subunit vaccine. This consisting S230 amino acids (aa) (S230) bound specifically antibody from COVID-19-patients serum, which showed very strong antigenicity. The was then engineered present on surface Hepatitis B core (HBc) virus-like particles (VLPs) HBc-S230 chimeric VLPs Both vaccines induced humoral cellular immune responses in mice, however, elicited significantly higher immunogenicity than S230. promoted generate not only dramatically levels S230-specific serum antibodies, but also marked CD4+/CD8 + T cells ratio substantially yields IFN-γ IL-6. Furthermore, antibodies could effectively neutralize infection with three SARS-CoV-2 pseudoviruses (Wild type, Delta Omicron). Our results demonstrated immunization conveyed immunity, lasted longer six months. Clearly, enhanced S230, provide potent durable protection against infection, indicating possessed great potential for developing highly immunogenic SARS-CoV-2.

Язык: Английский

Recent developments in the immunopathology of COVID‐19 DOI Creative Commons
Huanping Zhang,

Yuanli Sun,

Yanfen Wang

и другие.

Allergy, Год журнала: 2022, Номер 78(2), С. 369 - 388

Опубликована: Ноя. 24, 2022

Abstract There has been an important change in the clinical characteristics and immune profile of Coronavirus disease 2019 (COVID‐19) patients during pandemic thanks to extensive vaccination programs. Here, we highlight recent studies on COVID‐19, from immunological protective risk factors for severity mortality COVID‐19. The efficacy COVID‐19 vaccines potential allergic reactions after administration are also discussed. occurrence new variants concerns such as Omicron BA.2, BA.4, BA.5 global have changed scenario Multisystem inflammatory syndrome children (MIS‐C) may cause severe heterogeneous but with a lower rate. Perturbations immunity T cells, B mast well autoantibodies metabolic reprogramming contribute long‐term symptoms is conflicting evidence about whether atopic diseases, asthma rhinitis, associated susceptibility better outcomes At beginning pandemic, European Academy Allergy Clinical Immunology (EAACI) developed guidelines that provided timely information management diseases preventive measures reduce transmission clinics. distribution emerging acute respiratory coronavirus 2 (SARS‐CoV‐2) reduced pathogenic dramatically decreased morbidity, severity, Nevertheless, breakthrough infection remains challenge control. Hypersensitivity (HSR) low compared other vaccines, these were addressed EAACI statements indications reactions, including anaphylaxis vaccines. We gained depth knowledge experience over years since start yet full eradication SARS‐CoV‐2 not horizon. Novel strategies warranted prevent high‐risk groups, development MIS‐C long

Язык: Английский

Процитировано

77

Differential decline of SARS‐CoV‐2‐specific antibody levels, innate and adaptive immune cells, and shift of Th1/inflammatory to Th2 serum cytokine levels long after first COVID‐19 DOI Creative Commons
Bernhard Kratzer, Pia Gattinger,

Doris Trapin

и другие.

Allergy, Год журнала: 2024, Номер 79(9), С. 2482 - 2501

Опубликована: Июль 14, 2024

SARS-CoV-2 has triggered a pandemic and contributes to long-lasting morbidity. Several studies have investigated immediate cellular humoral immune responses during acute infection. However, little is known about long-term effects of COVID-19 on the system.

Язык: Английский

Процитировано

13

Enhanced SARS-CoV-2 breakthrough infections in patients with hematologic and solid cancers due to Omicron DOI Creative Commons
Maximilian J. Mair, Manfred Mitterer, Pia Gattinger

и другие.

Cancer Cell, Год журнала: 2022, Номер 40(5), С. 444 - 446

Опубликована: Апрель 12, 2022

Язык: Английский

Процитировано

35

Importance, Applications and Features of Assays Measuring SARS-CoV-2 Neutralizing Antibodies DOI Open Access
Pia Gattinger, Anna Ohradanova‐Repic, Rudolf Valenta

и другие.

International Journal of Molecular Sciences, Год журнала: 2023, Номер 24(6), С. 5352 - 5352

Опубликована: Март 10, 2023

More than three years ago, the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) caused unforeseen COVID-19 pandemic with millions of deaths. In meantime, SARS-CoV-2 has become endemic and is now part repertoire viruses causing seasonal severe respiratory infections. Due to several factors, among them development immunity through natural infection, vaccination current dominance seemingly less pathogenic strains belonging omicron lineage, situation stabilized. However, challenges remain possible new occurrence highly variants remains a threat. Here we review development, features importance assays measuring neutralizing antibodies (NAbs). particular focus on in vitro infection molecular interaction studying binding receptor domain (RBD) its cognate cellular ACE2. These assays, but not measurement SARS-CoV-2-specific per se, can inform us whether produced by convalescent or vaccinated subjects may protect against thus have potential predict risk becoming newly infected. This information extremely important given fact that considerable number subjects, vulnerable persons, respond poorly production antibodies. Furthermore, these allow determine evaluate virus-neutralizing capacity induced vaccines administration plasma-, immunoglobulin preparations, monoclonal antibodies, ACE2 synthetic compounds be used for therapy assist preclinical evaluation vaccines. Both types relatively quickly adapted emerging virus about magnitude cross-neutralization, which even estimate infected appearing variants. Given paramount discuss their specific features, advantages disadvantages, technical aspects yet fully resolved issues, such as cut-off levels predicting degree vivo protection.

Язык: Английский

Процитировано

21

Advances in SARS-CoV-2 receptor-binding domain-based COVID-19 vaccines DOI Creative Commons
Xiao‐Qing Guan, Yang Yang, Lanying Du

и другие.

Expert Review of Vaccines, Год журнала: 2023, Номер 22(1), С. 422 - 439

Опубликована: Май 10, 2023

Introduction The Coronavirus Disease 2019 (COVID-19) pandemic has caused devastating human and economic costs. Vaccination is an important step in controlling the pandemic. Severe acute respiratory coronavirus-2 (SARS-CoV-2), causative agent of COVID-19, infects cells by binding a cellular receptor through receptor-binding domain (RBD) within S1 subunit spike (S) protein. Viral entry membrane fusion are mediated S2 subunit.Areas covered SARS-CoV-2 S protein, particularly RBD, serves as target for vaccines. Here we review structure function protein its summarize current COVID-19 vaccines targeting outline potential strategies improving RBD-based Overall, this provides information that will facilitate rational design development safer more effective vaccines.Expert opinion harbors numerous mutations, mostly resulting multiple variant strains. Although many RBD original virus strain (and previous variants) can prevent infection these strains, their ability against recent dominant variants, Omicron offspring, significantly reduced. Collective efforts needed to develop broad-spectrum control future variants have potential.

Язык: Английский

Процитировано

20

Vaccine based on folded receptor binding domain‐PreS fusion protein with potential to induce sterilizing immunity to SARS‐CoV‐2 variants DOI Creative Commons
Pia Gattinger, Bernhard Kratzer, Inna Tulaeva

и другие.

Allergy, Год журнала: 2022, Номер 77(8), С. 2431 - 2445

Опубликована: Март 31, 2022

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the ongoing global COVID-19 pandemic. One possibility to control pandemic induce sterilizing immunity through induction and maintenance of neutralizing antibodies preventing SARS-CoV-2 from entering human cells replicate in.

Язык: Английский

Процитировано

26

Broad immunity to SARS-CoV-2 variants of concern mediated by a SARS-CoV-2 receptor-binding domain protein vaccine DOI Creative Commons
Georgia Deliyannis, Nicholas A. Gherardin,

Chinn Yi Wong

и другие.

EBioMedicine, Год журнала: 2023, Номер 92, С. 104574 - 104574

Опубликована: Май 4, 2023

The SARS-CoV-2 global pandemic has fuelled the generation of vaccines at an unprecedented pace and scale. However, many challenges remain, including: emergence vaccine-resistant mutant viruses, vaccine stability during storage transport, waning vaccine-induced immunity, concerns about infrequent adverse events associated with existing vaccines.We report on a protein subunit comprising receptor-binding domain (RBD) ancestral spike protein, dimerised immunoglobulin IgG1 Fc domain. These were tested in conjunction three different adjuvants: TLR2 agonist R4-Pam2Cys, NKT cell glycolipid α-Galactosylceramide, or MF59® squalene oil-in-water adjuvant, using mice, rats hamsters. We also developed RBD-human RBD sequence immuno-evasive beta variant (N501Y, E484K, K417N). as heterologous third dose booster following priming whole vaccine.Each formulation RBD-Fc drove strong neutralising antibody (nAb) responses provided durable highly protective immunity against lower upper airway infection mouse models COVID-19. 'beta variant' vaccine, combined induced protection mice strain well strain. Furthermore, when used booster, increased titres nAb other variants including alpha, delta, delta+, gamma, lambda, mu, omicron BA.1, BA.2 BA.5.These results demonstrated that subunit/MF59® adjuvanted can induce high levels broadly reactive nAbs, prior immunisation ancestral-strain vaccines. This platform offers potential approach to augment some currently approved face emerging concern, it now entered phase I clinical trial.This work was supported by grants from Medical Research Future Fund (MRFF) (2005846), Jack Ma Foundation, National Health Council Australia (NHMRC; 1113293) Singapore (MOH-COVID19RF-003). Individual researchers NHMRC Senior Principal Fellowship (1117766), Investigator Awards (2008913 1173871), Australian Discovery Early Career Award (ARC DECRA; DE210100705) philanthropic awards IFM investors A2 Milk Company.

Язык: Английский

Процитировано

13

Immunogenicity and In Vivo Protective Effects of Recombinant Nucleocapsid-Based SARS-CoV-2 Vaccine Convacell® DOI Creative Commons
Sevastyan O. Rabdano, Ellina Ruzanova,

Iuliia V. Pletyukhina

и другие.

Vaccines, Год журнала: 2023, Номер 11(4), С. 874 - 874

Опубликована: Апрель 20, 2023

The vast majority of SARS-CoV-2 vaccines which are licensed or under development focus on the spike (S) protein and its receptor binding domain (RBD). However, S shows considerable sequence variations among variants concern. aim this study was to develop characterize a vaccine targeting highly conserved nucleocapsid (N) protein. Recombinant N expressed in Escherichia coli, purified homogeneity by chromatography characterized SDS-PAGE, immunoblotting, mass spectrometry, dynamic light scattering differential scanning calorimetry. vaccine, formulated as squalane-based emulsion, used immunize Balb/c mice NOD SCID gamma (NSG) engrafted with human PBMCs, rabbits marmoset monkeys. Safety immunogenicity assessed via ELISA, cytokine titer assays CFSE dilution assays. protective effect studied SARS-CoV-2-infected Syrian hamsters. Immunization induced sustainable N-specific IgG responses an mixed Th1/Th2 response. In monkeys, CD4+/CD8+ T cell response observed. Vaccinated hamsters showed reduced lung histopathology, lower virus proliferation, weight relative body, faster body recovery. Convacell® thus is shown be effective may augment existing armamentarium against COVID-19.

Язык: Английский

Процитировано

12

Construction by artificial intelligence and immunovalidation of hypoallergenic mite allergen Der f 36 vaccine DOI Creative Commons

Qiaozhi Qin,

Jian Tang, Cai-Yun Wang

и другие.

Frontiers in Immunology, Год журнала: 2024, Номер 15

Опубликована: Март 27, 2024

Background The house dust mite (HDM) is widely recognized as the most prevalent allergen in allergic diseases. Allergen-specific immunotherapy (AIT) has been successfully implemented clinical treatment for HDM. Hypoallergenic B-cell epitope-based vaccine designed by artificial intelligence (AI) represents a significant progression of recombinant hypoallergenic derivatives. Method three-dimensional protein structure Der f 36 was constructed using Alphafold2. AI-based tools were employed to predict epitopes, which subsequently verified through IgE-reaction testing. then synthesized, expressed, and purified. reduced allergenicity assessed enzyme-linked immunosorbent assay (ELISA), immunoblotting, basophil activation test. T-cell response evaluated based on cytokine expression peripheral blood mononuclear cells (PBMCs) patients. immunogenicity compared rabbit immunization with 36, respectively. inhibitory effect blocking IgG antibody specific IgE-binding activity also examined. Results final selected non-allergic epitopes 25–48, 57–67, 107–112, 142–151, 176–184. showed reduction activity. competitive inhibition investigated only 20% could be achieved, greatly when (98%). exhibited low basophil-stimulating ratio similar that negative control, it induce an increasing level IFN‐γ but not Th2 cytokines IL-5 IL-13 PBMCs. vaccine-specific antibodies inhibit patients’ IgE binding stimulation Derf 36. Conclusion This study first application AI strategy facilitate development vaccine, may become promising HDM-allergic patients due its high inducing IgG.

Язык: Английский

Процитировано

4

Safety, immunogenicity, and protective effective of inhaled COVID‐19 vaccines: A systematic review and meta‐analysis DOI Creative Commons
Song Gao,

Rong Li,

Meng-Qun Cheng

и другие.

Journal of Medical Virology, Год журнала: 2024, Номер 96(4)

Опубликована: Апрель 1, 2024

This study aimed to examine the safety, immunogenicity and protective effective of inhaled COVID-19 vaccines (ICVs). Literature research was done through EMBASE, Cochrane, PubMed, Web Science up 10 March 2024. Pooled estimates with corresponding 95% confidence intervals (CI) were computed compared using random effects common model. Of 15 studies, 11 analyzed 13 immunogenicity, 3 effective. The results showed a favorable safety profile ICVs for primary vaccination series, however it does not always seem produce expected immune response Meta-analysis booster vaccinations (BVs) that levels neutralizing antibody Geometric mean titer (nAb-GMT) aerosolised Ad5-nCoV (AAd5-nCoV) all higher than those inactivated vaccine (INA-nCoV) (standard difference (SMD) = 2.32; CI: 1.96-2.69) intramuscular (IMAd5-nCoV) (SMD 0.31; 0.14-0.48) against original strain SARS-CoV-2. Importantly, we also observed similar in omicron variant. In addition, ICV BVs has high mucosal immunity IgA antibodies. risk adverse events comparable or lower AAd5-nCoV INA-nCoV IMAd5-nCoV. Current evidence shows well. dose had (including immunity) provided protection caused by SARS-CoV-2 Further studies are needed investigate long-term intranasal various types ICVs.

Язык: Английский

Процитировано

4