Grant: Project Grant
University of Alberta
$956,250.00
Studies on a broadly-protective novel lipopeptides-based intranasal vaccine for SARS-CoV2
FY 2024-25
Summary
Severe acute respiratory syndrome virus-2 (SARS-CoV-2), the causative agent of the COVID-19 pandemic, has led to multiple (4-6) waves of infections worldwide during the past two years. As of August 2023, there are >774M confirmed cases of COVID-19 and >7M deaths related to COVID-19 globally. The development of vaccines against SARS-CoV-2 has led to successful mass immunizations worldwide, mitigating the worldwide pandemic-related mortality to a great extent. Yet the evolution and rapid spread of new variants has prolonged the pandemic and highlighted a need to develop a universal vaccine which can prevent infections from all virulent and emerging SARS-CoV-2 strains. The current vaccines have a common spike antigen-based design from the Wuhan isolate, which is intended to elicit antibody responses against the SARS-CoV-2 spike protein. However, emerging SARS-CoV-2 variants, from alpha to omicron, result in the reduction of vaccine efficacy due to alterations in S protein. In addition, vaccine-induced immunity seems to be short-lived and declines in a short period. Therefore, there is a critical need for a new generation of vaccine, which can provide sustained protection against heterologous SARS-CoV-2 variants.
Recently, we have discovered novel modified peptides from conserved epitopes of SARS-CoV-2 antigens, which induce multiple arms of protective immunity (cellular and humoral), as a universal vaccine candidate against SARS-CoV-2 variants. In the proposed work, we will investigate the protective immunity induced by the designed multi-epitopes containing modified-peptides, their nanoparticle formulation and a prime boost strategy with current vaccines. These studies will contribute significantly to the investigation of new vaccine approaches, will facilitate and accelerate the clinical development of an effective broadly-protective vaccine candidate for SARS-CoV-2 and its variants, and will have a major impact on the health of Canadians and people worldwide.
Department
Program
Project Grant
Recipient
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
507422
Name
Agrawal Babita
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Pharmaceutical Sciences
Projecttitle
Studies on a broadly-protective novel lipopeptides-based intranasal vaccine for SARS-CoV2
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$956,250
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Broadly-Protective Coronavirus Vaccine; In Vitro And In Vivo Studies; Nanoparticles; Pharmaceuticals; Vaccine
Abstract
Severe acute respiratory syndrome virus-2 (SARS-CoV-2), the causative agent of the COVID-19 pandemic, has led to multiple (4-6) waves of infections worldwide during the past two years. As of August 2023, there are >774M confirmed cases of COVID-19 and >7M deaths related to COVID-19 globally. The development of vaccines against SARS-CoV-2 has led to successful mass immunizations worldwide, mitigating the worldwide pandemic-related mortality to a great extent. Yet the evolution and rapid spread of new variants has prolonged the pandemic and highlighted a need to develop a universal vaccine which can prevent infections from all virulent and emerging SARS-CoV-2 strains. The current vaccines have a common spike antigen-based design from the Wuhan isolate, which is intended to elicit antibody responses against the SARS-CoV-2 spike protein. However, emerging SARS-CoV-2 variants, from alpha to omicron, result in the reduction of vaccine efficacy due to alterations in S protein. In addition, vaccine-induced immunity seems to be short-lived and declines in a short period. Therefore, there is a critical need for a new generation of vaccine, which can provide sustained protection against heterologous SARS-CoV-2 variants.
Recently, we have discovered novel modified peptides from conserved epitopes of SARS-CoV-2 antigens, which induce multiple arms of protective immunity (cellular and humoral), as a universal vaccine candidate against SARS-CoV-2 variants. In the proposed work, we will investigate the protective immunity induced by the designed multi-epitopes containing modified-peptides, their nanoparticle formulation and a prime boost strategy with current vaccines. These studies will contribute significantly to the investigation of new vaccine approaches, will facilitate and accelerate the clinical development of an effective broadly-protective vaccine candidate for SARS-CoV-2 and its variants, and will have a major impact on the health of Canadians and people worldwide.
Competitiondate
202409
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Agrawal, Babita
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $956,250~ $0~