- Initiative objectives: deliver tens of millions of efficacious and safe COVID-19 vaccines approved/authorized by the FDA for the U.S. population by end of 2020 and/or early 2021.

Initiative

OWS chose candidates based on the following criteria:
- Robust preclinical data or early-stage clinical trial data to support their potential
- Potential (with support from OWS) to enter large phase 3 field efficacy trials July-November 2020
- Deliver outcomes by end of 2020 or first half of 2021
- Candidates had to be based on vaccine-platform technologies permitting fast/effective manufacturing and large-scale abilities
- Use one of four vaccine-platform technologies: mRNA, replication-defective live-vector, recombinant-subunit-adjuvanted protein, attenuated replicating live-vector

Candidate Criteria

- Build a diverse project portfolio with two vaccine candidates based on each of 4 platform technologies
- Accelerate vaccine program development while maintaining safety, efficacy, quality
- Heavy up-front investment
- Partnership of NIAID, Coronavirus Prevention Network, OWS, and sponsor companies

Strategy

- Initiative
- Candidate requirements
- Strategy

University of California, Davis

So far, vaccines consist of either inactivated or weakened versions of antigens or virions. Many pharmaceutical companies like Pfizer and Moderna are developing inactivated antigens in the form of mRNA, DNA, and proteins from the viral envelope or capsid that are often fragmented. 

Vaccine Candidates, Immunogenicity, and Adaptive Immunity

Moncef Slaoui, Ph.D., and Matthew Hepburn, M.D. August 26, 2020 DOI: 10.1056/NEJMp2027405

Developing Safe and Effective Covid Vaccines — Operation Warp Speed’s Strategy and Approach

Moderna was one of the earliest companies to propose potential vaccines after having screen through more than 120 mRNA-based molecules. Among them, they identified mRNA-1273 that is capable of triggering the adaptive immune response. This mRNA essentially codes for the viral spike (S) glycoprotein that is involved in receptor recognition with ACE2 receptors in host cells. In the pre-clinical trial experiments with Rhesus macaque, administration of either 10 or 100 micrograms of the mRNA-1273 showed successful induction of type 1 helper T-cells (Th1) and no detectable viral antigens over the course of the next few days. Immunohistochemistry results detected higher levels of IL-21 cytokines. These non-human primates over the course of 2 weeks also showed regression of upper and lower airway infection. 
In the study, there was elevated antibody-binding activity through ELISA detection as well as neutralization activity in vaccinated primates. mRNA-1273 lead to higher suppression of ACE2 binding recognition with spike protein. mRNA-1273 nucleoside modifications and purification were optimized to stimulate the innate immune system in order to enhance translation and duration. One remaining concern was the half-life of antibodies against spike protein. Recent human data shows a reduction of antibodies over time after initial infection. 


Moderna mRNA-1273

In the phase 1 and 2 clinical studies with BNT162b1, healthy participants from 18 to 55 years old will receive either the lipid nanoparticle-delivered vaccine at (10µg, 30µg, and 100µg) or placebo. The nucleoside-modified mRNA sequence codes for the spike glycoprotein that is trimerized. IgG antibody binding and spike protein neutralization was dosage dependent. The mRNA vaccine was relatively safe as it would not integrate into host genome and would be translated to produce spike antigen to trigger immune response. One particular enhancement was to add 1-methyl pseudouridine to increase translation efficiency while triggering innate immune response. 
The receptor binding domain (RBD) of BNT162b1 was further modified by the addition of a phage T4 fibritin-derived trimerization domain to increase its immunogenicity before being encapsulated in lipid nanoparticles administered through intramuscular injection. Around 7 days into vaccination, both the BNT162b1 and placebo recipients experienced mild to moderate levels of fatigue and headache, with more frequencies from the BNT162b1 participants. For the most part, no fatal symptoms seem to occur. Persistent follow up will need to be continued for up to half a year while immunogenicity will need to be taken for up to 2 years. Adults over 65 years old are also beginning to enroll in this clinical trial. 


Pfizer BNT162b1

The application of synthetic DNA medicine (INO-4800) in blocking the infection pathway of SARS-CoV-2 have already passed phase 1 of clinical trial on a positive note at Inovio as they now look forward to add participants of older age. Unlike RNA-based vaccine candidates, synthetic DNAs are much easier to design and amplify. They are also more temperature-stable and resistant to nucleases. Previous works done on the MERS-CoV vaccine with INO-4700 as well as Zika virus with GLS-5700 were quite successful in halting infections. These experiences show that INOVIO could potentially apply similar strategies to drive neutralizing antibody responses for long-term protection from COVID-19.
	In general, induction of INO-4800 to African green monkey fibroblast (COS-7) and human kidney (HEK-293T) cell lines both showed substantial levels of antibodies in serum. It is capable of activating cellular and humeral responses within several days post immunization. The receptor binding domain sequence of the spike protein was cloned into pGX9501 and pGX9503 vectors that are transfected into COS-7 and HEK-293T cells showed high levels of RNA levels upon detection by RT-qPCR. Spike protein expression was measured by Western blot to be consistently high and further confirmed qualitatively through immunofluorescence staining. INO-4800 seemed to exhibit competitive inhibition against ACE2 receptor and was also detected in the lungs that halted Lower Respiratory Disease (LRD).


Inovio INO-4800

In a study done by Oxford and Astrazeneca on an adenovirus vector vaccine candidate from chimpanzee (ChAdOx1 nCoV-19) expressing the spike protein, phase 1 and 2 were done on healthy adults from 18 to 55 years old with no prior exposure to COVID-19. ChAdOx1 (AZD1222) consisted of the entire spike sequence linked to a tissue plasminogen activator leader sequence. For placebo, some adults were administered a meningococcal conjugated vaccine (MenACWY) while the other were administered ChAdOx1 all with single intramuscular dosages. MenACWY was used as placebo in order to cover up the effects of receiving AZD1222. Previous clinical studies in Rhesus macaques show promising efficacy in inducing humoral/cellular immune responses as well as resistance toward lower respiratory tract infections.

Oxford-Astrazeneca: ChAdOx1

Operation Warp Speed

Corum, J., Wee, S., & Zimmer, C. (2020). Coronavirus Vaccine Tracker. https://www.nytimes.com/interactive/2020/science/coronavirus-vaccine-tracker.html

Coronavirus Vaccine Tracker

- Novavex, in collaboration with Takeda, recently developed a protein-based vaccine candidate (NVX-CoV2373) that were constructed from the COVID-19 full-length spike protein, transfected into Spodoptera frugiperda (SF9, fall armyworm) cell lines, and purified. 
- A stable inactivated form of premature S-protein was constructed through mutagenesis by mutating the furin cleavage site as well as incorporating 2 proline substitutions that destabilize the central alpha-helix. 
- Administration of NVX-CoV2373 with Matrix-M adjuvant, a synthetic biomolecule consisting of saponins conjugated to cholesterol and phospholipids, compacted into nanoparticles have shown to induce strong immune responses like Th1 B-cell and T-cell responses as well as secretion of neutralizing antibodies in serum.
******
- In preclinical trials, mice were administered in increasing doses of 0.01μg, 0.1μg, 1μg, and 10μg each with 5μg of the Matrix-M. Mice at all dosages exhibit high anti-spike IgG within 3-4 weeks post-initial vaccination. 
- Those vaccinated at 10μg even had complete inhibition of ACE2 receptor binding to spike protein. 
-Even with the smallest dosage, significant amount of inflammatory cytokines like interferon (IFN-γ), tumor necrosis factor (TNF-α), and interleukins (IL-2, IL-4, & IL-5) were secreted from effector memory T-cells. 
- Histopathology of lung tissues showed significant regression of lung tissue inflammation for those administered with NVX-CoV2372 compared to placebo. 
******
Description from Lit Review Draft:

"NVX-CoV2373 is a recombinant nanoparticle vaccine composed of trimetric full-length SARS-CoV2 spike glycoproteins and Matrix M1 adjuvant. A randomized, placebo-control, phase 1-2 trial was conducted on 131 healthy adults.  It has high immunogenicity and high levels of neutralizing antibodies. On September 24, 2020, phase 3 clinical trials began and immunized 10,000 people in the next 4-6 weeks. This took place at the Nucleus Network in Herston, Queensland and Melbourne, Victoria.
This vaccine candidate is a recombinant nanoparticle vaccine constructed from full-length wild-type SARS-CoV-2 spike glycoprotein. It includes Matrix M1 Which is a saponin based adjuvant made by Novavax. The rSARS-CoV-2 and Matrix M1 parts were mixed just before use. This vaccine is favorable because it can be stored between 2°C and 8°C, allowing for easy preservation and, therefore, distribution (Novavax Initiates Phase 3 Efficacy Trial of COVID-19 Vaccine in the United Kingdom | Novavax Inc. - IR Site, n.d.)."

Novavax: NVX-CoV2373

Johnson & Johnson and Janssen Pharmaceuticals, in collaboration with Beth Israel Deaconess Medical Center, developed the Ad26.COV2.S COVID-19 vaccine candidate. It utilizes AdVac technology to engineer adenovirus serotype 26 (Ad26) vectors to express the SARS-CoV-2 spike (S) protein, stimulating neutralizing antibody secretion. Following successful application in the Ad26.ZEBOV Ebola vaccine, the Ad26 vector was tested in preclinical trials with rhesus macaques. Subjects were immunized with spike variants and exposed to SARS-CoV-2, identifying Ad26.COV2.S as the most effective candidate for eliciting strong immune responses.

Learn Before

Related

Learn After