WO2021216569A1 - Engineering broadly reactive coronavirus vaccines and related designs and uses - Google Patents
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- C12N2770/00011—Details
- C12N2770/20011—Coronaviridae
- C12N2770/20071—Demonstrated in vivo effect
Definitions
- the disclosure relates to a vaccine platform for developing coronavirus vaccines, and more particularly vaccines to protect mammals from infection from b-coronaviruses.
- the disclosure relates to methods for developing coronavirus vaccines using identified group genetic sequences.
- Coronaviruses are classified into four genera: alpha-, beta-, gamma- and delta- coronaviruses.
- b -CoVs are enveloped, positive-strand RNA viruses capable of infecting mammals, generally bats and rodents, though many b-CoVs are known to infect humans as well. Infections with CoVs in humans and animals commonly produce mild to moderate upper- respiratory tract illnesses of short duration. Exceptions are the Severe Acute Respirator Syndrome (SARS-1), the Middle East Respiratory Syndrome (MERS) and the Wuhan- originating SARS-CoV-2 (SARS-2) (also referred to as COVID-19) that are characterized by severe and often lethal symptoms.
- SARS-1 Severe Acute Respirator Syndrome
- MERS Middle East Respiratory Syndrome
- SARS-2 Wuhan- originating SARS-CoV-2
- SARS-2 The first cases of SARS-2 infections were seen in December 2019. As of April 16, 2020, there were an estimated 632,000 cases reported and an estimated 31,000 deaths in the United States alone, as reported by the Center for Disease Control (CDC), resulting in a 4.9% lethality. SARS-2 is highly infectious to humans. The World Health Organization (WHO) declared the SARS-2 worldwide pandemic a Global Health Emergency on January 30, 2020. [0004] Specific treatments for SARS-2 are not available but under investigation. The best approach to prevent further spread of the disease is the development of specific vaccines. Herd immunity against SARS-2 is better achieved with immunization with a benign vaccine rather than by the natural infection with the active SARS-2 virus.
- WHO World Health Organization
- SARS-related b-CoVs SARS-related b-CoVs
- SARS-2 (COVID-19) is the third lethal b-CoV that has jumped from animal hosts to humans. Considering that 1,800 SARSrs have already been identified in animals, some of which may eventually infect humans, it is desirable to also create group-specific SARSr vaccines to avert future pandemics.
- viral vectors including viral vectors based on the adenovirus
- Such “ad vectors” repeatedly demonstrate higher and more sustained immunogenicity in comparisons to other vaccine systems.
- One problem with using ad vectors in vaccination programs is the strong immune response triggered against the adenovirus itself, as opposed to the target virus.
- ad vectors fully deleted (fd) of all endogenous adenovirus genes were developed.
- the packing information for fd adenovirus genomes was originally delivered with second viral constructs - a hybrid baculovirus-adenovirus or a helper virus. Unfortunately this led to contaminations of the replication component of the ad vector or helper viruses. It is desirable to develop an ad vector vaccine system which avoids these problems with existing ad vector vaccines.
- a vaccine for preventing b-CoV infection comprises at least one viral vector comprising a b-CoV DNA sequence which codes the S protein for the b-CoV.
- the vector is an adenovirus vector. In another embodiment, the vector is a fully deleted adenovirus vector free of all endogenous genes.
- the b-CoV DNA sequence is a SARS-2 b-CoV DNA sequence. In a further embodiment, the SARS-2 b-CoV DNA sequence is the entire sequence coding the S protein. In yet a further embodiment, the SARS-2 b-CoV DNA sequence is a partial sequence coding the S protein. In another embodiment, the SARS-2 b-CoV DNA sequence is a partial sequence coding the S protein from which the receptor binding domain has been removed.
- the SARS-2 b-CoV DNA sequence is a partial sequence coding the S protein in which the receptor binding domain sequences have been replaced by DNA coding for a peptide linker.
- the vaccine further comprises a packaging plasmid based on an adenovirus selected from the group consisting of the Ad2, Ad5, Ad6 and Ad35 serotypes and combinations thereof.
- the at least one viral vector is contained in a packaging cell.
- the packaging cell is encapsidated in a capsid selected from the group consisting of the Ad2, Ad5, Ad6 and Ad35 serotypes, and combinations thereof.
- the b-CoV DNA sequence is a SARS-2 b-CoV DNA sequence
- the viral vector comprises at least a second b-CoV DNA sequence from a SARSr virus, wherein the second b-CoV DNA sequence codes the S protein for the SARSr virus.
- a vaccine for preventing SARS-2 infection comprises at least one viral vector comprising a SARS-2 b-CoVDNA sequence which codes the S protein for the SARS-2 b-CoV and at least one packing plasmid based on an adenovirus selected from the group consisting of the Ad2, Ad5, Ad6 and Ad36 serotypes and combinations thereof, wherein the at least one viral vector and at least one packing plasmid are contained in a packaging cell, and wherein the packaging cell is encapsidated in a capsid selected from the group consisting of the Ad2, Ad5, Ad6 and Ad35 serotypes and combinations thereof.
- the SARS-2 b-CoV DNA sequence codes for a partial S protein of the SARS-2 virus.
- the disclosure provides a vaccine for preventing b-CoV infection.
- a vaccine for preventing b-CoV infection comprises at least one b-CoV RNA sequence which codes the S protein for the b-CoV.
- the RNA is mRNA.
- the b-CoV RNA sequence is a SARS-2 b-RNA sequence.
- the SARS-2 b-CoV RNA sequence is the entire sequence coding the S protein.
- the SARS-2 b-CoV RNA sequence is a partial sequence coding the S protein.
- the SARS-2 b-CoV RNA sequence is a partial sequence coding the S protein, from which the receptor binding domain has been removed.
- the SARS-2 b- CoV RNA sequence is a partial sequence coding the S protein, in which the receptor binding domain sequences have been replaced by RNA coding for a peptide linker.
- the vaccine further comprises an expression vector that delivers the genetic information for the b-CoV RNA.
- the expression vector is an engineered viral vector.
- the disclosure provides a vaccine for preventing b-CoV infection.
- a vaccine for preventing b-CoV infection comprises at least one viral vector comprising a b-CoV protein sequence which codes the S protein for the b-CoV.
- the b-CoV RNA sequence is a SARS-2 b-CoV protein sequence.
- the SARS-2 b-CoV protein sequence is the entire sequence coding the S protein.
- the SARS-2 b-CoV protein sequence is a partial sequence coding the S protein.
- the SARS-2 b-CoV protein sequence is a partial S protein sequence, from which the receptor binding domain has been removed.
- the SARS-2 b-CoV protein sequence is a partial S protein sequence, in which the receptor binding domain sequences have been replaced by a peptide linker.
- the disclosure provides a method of vaccinating a mammal subject against infection from at least one group of . b-CoV.
- a method of vaccinating a mammal subj ect against infection from at least one group of b-CoV comprises separating a broad group of b-CoV into homology groups based on similarities in the b-CoV RNA sequences which code for their S proteins; identifying at least one consensus sequence for each homology group which have a sequence identity in excess of 60% to all other members of the homology group; and preparing a viral vector including at least a portion of the consensus sequence from at least one homology group.
- the consensus sequence is selected from the group consisting of DNA sequences, RNA sequences, protein sequences and combinations thereof.
- the step of preparing of the viral vector comprising including at least a portion of a consensus sequence from two or more homology groups.
- the method further comprises injecting the vaccine into the mammal subject.
- the disclosure provides a method of vaccinating a mammal subject against infection from at least one group of b-CoV.
- a method of vaccinating a mammal subject against infection from at least one group of b-CoV comprises separating a broad group of b-CoV into homology groups based on similarities in the b-CoV DNA, RNA or protein sequences which code for their S proteins; identifying at least a portion of the b-CoV protein sequences for each homology group which have a sequence identity in excess of 60% to all other members of the homology group; and preparing a DNA, RNA or protein vaccine including at least a portion of the b-CoV protein sequence from at least one homology group.
- the method further comprises injecting the vaccine into the mammal subject.
- FIG. l is a schematic showing functional portions of a SARS-2 b-CoV RNA segment which encodes the S protein, along with the portions of greatest variability and portions eliciting the greatest immune responses, in accordance with embodiments of the present disclosure.
- FIG. 2 illustrates the components of a vaccine in accordance with embodiments of the present disclosure.
- FIG. 3 shows the activities of an avian influenza vaccine utilizing a viral vector of the present disclosure. Specifically, FIG. 3 A shows the subject groups survival rates, FIG. 3B shows the subject groups body weights, FIG. 3C shows the serum antibody titers, and FIG. 3D shows the lung virus titers.
- FIG. 4 shows the activity of a MERS-CoV vaccine.
- any subrange between any two explicit values is included (e.g., the range 1- 7 above includes subranges 1 to 2; 2 to 6; 5 to 7; 3 to 7; 5 to 6, etc.).
- ranges containing values which are less than one or containing fractional numbers greater than one e.g., 1.1, 1.5, etc.
- one unit is considered to be 0.0001, 0.001, 0.01 or 0.1, as appropriate.
- ranges containing single digit numbers less than ten e.g., 1 to 5
- one unit is typically considered to be 0.1.
- Spatial terms such as “beneath,” “below,” “lower,” “above,” “upper,” and the like, may be used herein for ease of description to describe one element’s or feature’s relationship to another element(s) or feature(s) as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations depending on the orientation in use or illustration. For example, if a device in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, the exemplary term “below” can encompass both an orientation of above and below. A device may be otherwise oriented (rotated 90° or at other orientations) and the spatially relative descriptors used herein interpreted accordingly.
- the term “and/or” includes any and all combinations of one or more of the associated listed items.
- the phrase “and/or” is intended to include both A and B; A or B; A (alone); and B (alone).
- the term “and/or” as used in a phrase such as “A, B and/or C” is intended to encompass each of the following embodiments” A, B and C; A, B, or C; A or C; A or B; B or C; A and C; A and B; B and C; A (alone); B (alone); and C (alone).
- the present disclosure provides a method for preparing a vaccine for preventing at least one b-CoV infection in a subject, particularly a mammal subject, and more specifically a human subject.
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises identifying at least one b-CoV from an animal host, particularly a mammal host.
- the method for preparing a vaccine for preventing at least one b-CoV infection in a subject, particularly a mammal subject, and more specifically a human subj ect comprises identifying at least one b-CoV from a mammal host selected from the group consisting of a bat, a rat, a human, and combinations thereof.
- the at least one b-CoV comprises at least one SARSr.
- the at least one b-CoV comprises at least one SARS-2 b-CoV.
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises separating identified b-CoVs, such as those identified from an animal host, into homology groups based on similarities in genetic sequence and preparing at least one consensus sequence for each homology group.
- the homology groups can be based on similarities in the entirety of the b-CoVs’ genetic sequences, multiple portions of the b-CoVs’ genetic sequences, or a single portion of the b-CoVs’ genetic sequences.
- the genetic sequences are selected from the group consisting of DNA sequences, RNA sequences, protein sequences, and combinations thereof. It will be understood that if a single b-CoV is identified, it is the sole member of a single homology group.
- the b-CoVs comprise a plurality of SARSrs, and the plurality of SARSrs are separated into 1, or at least 2, or at least 3, or at least 4, or at least 5 homology groups.
- the homology groups are based on at least a portion, or at least two or more portions, or all, of the genetic sequence associated with the spike protein, the SARS receptor binding domain (RBD), an envelope protein, a nucleoprotein, and combinations thereof.
- RBD SARS receptor binding domain
- at least one SARS-2 b-CoV is identified and separated into at least one homology group.
- the genetic sequences within each homology group, have a sequence identity greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%, or greater than or equal to 95%, or greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99% to all other members in the homology group.
- the genetic sequences within each homology group, have a sequence identity from greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85% to 90%, or 95%, or 96%, or 97%, or 98%, or 99%, or less than 100% to all other members in the homology group.
- the genetic sequences for each homology group define a distinct protein sequence for the homology group.
- the distinct protein is selected from the group consisting of the S protein, an envelope protein, a nucleoprotein, and combinations thereof. In a further embodiment, the distinct protein is the S protein.
- a plurality of SARSrs are analyzed and separated into 5 homology groups, wherein, within each homology group, the genetic sequences have a sequence identify from greater than 65% to 99%.
- the SARS-2 b-CoV has a positive-sense, single-stranded RNA genome of about 30kb and four structural proteins.
- One of the structural proteins is the spike (S) peplomer. These S proteins are found on the surface of the SARS-2 b-CoV and mediate cell receptor binding, and therefore determine the host tropism o the virus.
- the protein portion of the RNA which codes the S protein is divided into an SI chain and an S2 chain, with the SI chain 10 and the S2 chain 20 separated by a furan cut site 25, as shown in FIG. 1.
- the RBD 30 is located in the SI chain 10.
- the membrane fusion section 40 is located in the S2 chain 20. Further shown in FIG. 1 are the heptapeptides HR1 and HR2, the transmembrane TM and the cytoplasmic domain of the S protein.
- the S protein of the SARS-2 b-CoV is not enzymatically cleaved during virus assembly.
- the SARS-2 b-CoV S protein is pre-activated by proprotein convertase furin. Therefore, its dependence on target cell proteases on cell entry is reduced.
- the SARS-2 b-CoV S protein is split into the SI chain 10 and the S2 chain 20. Conformational changes in the S2 chain 20 lead to the fusion of the virus within the host cell. In combination with the S protein-encoding RNA sequence including the RBD, this makes the S protein-encoding RNA sequence a significant candidate for use in an anti-SARS-2 b-CoV vaccine regimen.
- FIG. 1 also shows the S protein portions of the SARS-2 b-CoV which elicit greater immune responses (60).
- portion 60b overlaps with the RBD 30 and is a sizable portion, meaning there is significant immune response associated with the RBD 30.
- Portions 60d and 60e, while overlapping with the less-variable membrane fusion section 40, are smaller and therefore do not elicit as strong of an immune response.
- b-CoVs such as SARS-CoV-1 and MERS-CoV
- aligning the S protein-encoding sequences of RNA from various SARSrs shows significant divergence throughout the gene (50).
- a vaccine based on present SARS-2 b-CoV RNA may therefore fail to efficiently protect against infections caused by other SARSrs.
- the SARSrs can be separated into homology groups, as shown in Table 1.
- SARS-CoV group 1130 sequences from GenBank and ViPR covering the original SARS-CoV-1 were analyzed. A couple of the sequences contained random inserts which are likely responsible for the gaps, but the small variants have all maintained antibody binding.
- SARS-CoV 2 group greater than 3000 sequences were analyzed, includingnew clades 20H, 201, and 20 J (corresponding to the South African, California and UK variants, respectively).
- WIV-1 is a prominent SARSr in bats, but shown to replicate in human cells. 56 WIV-1 strains, including the RaTG13 strain thought to have given rise to SARS-2 b-CoV, were analyzed. Only 16 of the strains had complete CDS.
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises identifying at least one consensus sequence for each homology group.
- a consensus sequence is a DNA, RNA or protein sequence developed for a group containing the statistically most frequent residue at each position in the sequence.
- the consensus sequence for a homology group has at least 65%, or at least 70%, or at least 75%, or at least 80%, or at least 85%, or at least 90%, or at least 95%, or at least 99% commonality with each member of the corresponding homology group.
- a consensus sequence is a DNA sequence having a sequence identity greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%, or greater than or equal to 95%, or greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99% to all other members in the corresponding homology group.
- a consensus sequence is an RNA sequence having a sequence identity greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%, or greater than or equal to 95%, or greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99% to all other members in the corresponding homology group.
- a consensus sequence is a protein sequence having a sequence identity greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%, or greater than or equal to 95%, or greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99% to all other members in the corresponding homology group.
- the consensus sequences are edited to remove variable domains.
- An exemplary variable domain is shown as the sequence at 324 to 533 in FIG. 1.
- the deleted sequence is replaced by a smaller linker peptide designed to bridge the gap created by the deletion.
- the consensus sequence for each homology group is selected from the group consisting of a DNA sequence, an RNA sequence, a protein sequence, and combinations thereof.
- the consensus sequence for at least one of the homology groups is RNA.
- the RNA is mRNA.
- the b-CoVs analyzed are SARSrs.
- the S ARSrs include at least one SARS-2 b-CoV separated into at least one homology group, and the consensus sequence of the at least one homology group is a DNA sequence, an RNA sequence, or a protein sequence.
- a consensus sequence may be a DNA sequence, RNA sequence or protein sequence will have 100% commonality with the SARSr.
- the consensus sequence is a SARS-2 b-CoVDNA sequence, wherein the SARS-2 b-CoV DNA sequence is at least a portion of the S protein-encoding sequences. In a further embodiment, the consensus sequence is a SARS-2 b-CoV DNA comprising the entire S protein-encoding sequence.
- the consensus sequence is a SARS-2 b-CoV RNA sequence, wherein the SARS-2 b-CoV RNA sequence is at least a portion of the S protein-encoding sequence.
- the consensus sequence is a SARS-2 b-CoV protein sequence, wherein the SARS-2 b-CoV protein sequence is at least a portion of the S protein.
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises inserting the at least one consensus sequence into a viral vector.
- the viral vector is an adenovirus vector component.
- all endogenous genes have been deleted from the viral vector component, which is an adenovirus vector component. That is, in an embodiment, the viral vector component is a fully deleted (fd) adenovirus vector.
- the adenovirus vector 70 is capable of receiving gene constructs of up to 33 kb and carry inverted terminal repeat sequences (ITRs) 72, 72 and a packaging signal (Y) 73, as shown in FIG. 2.
- ITRs inverted terminal repeat sequences
- Y packaging signal
- the deleted endogenous genes are replaced with size-compensating stuffers 75.
- these stuffers 75 are prepared from fragments of the human gene 5-aminoimidazole-4-carboxamide ribonucleotide formyltrans-ferase gene (ATIC).
- ATIC 5-aminoimidazole-4-carboxamide ribonucleotide formyltrans-ferase gene
- other stuffer sequences such as, but not limited to, human hypoxanthine-guanine phosphoribosyltransferase, can be used.
- consensus sequences 80a, 80b, 80c, 80d, 80e are received by the viral vector, or adenovirus vector, or fd adenovirus vector.
- a viral vector may contain more or fewer consensus sequences.
- a consensus sequence is in accordance with any embodiment or combination of embodiments provided herein.
- consensus sequence 80a is a SARS-2 b-CoV RNA sequence derived from a homology group containing only SARS-2 b- CoVs.
- the SARS-2 b-CoV RNA sequence is the only consensus sequence contained in the viral vector, the resulting vaccine is intended to provide specific protection from infection by SARS-2 b-CoV.
- the consensus sequence may be derived from a homology group containing a broader collection of SARS-2 b-CoVs.
- the viral vector may contain additional consensus sequences, as shown in FIG. 2, derived from different homology groups. In such embodiments, the resulting vaccine may provide broader protection for viruses of the different homology groups.
- the viral vector may be a viral vector configured to deliver transgenes, such as DNA transgenes.
- exemplary viral vectors configured to deliver transgenes include, but are not limited to Adenovirus Associated Vector and vaccinia virus vector.
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises providing at least one packaging plasmid.
- an exemplary plasmid 82 used in the present disclosure contains a plurality of genes, such as late genes and early genes.
- the plasmid 82 includes a plurality of late genes, and preferably the late regions 1, 2, 3, 4 and 6 as shown in FIG.2.
- the plasmid 82 used in the present disclosure contains a plurality of early genes, and preferably the early regions 2 and 4 shown in FIG. 2.
- the late genes and early genes are provided in trans.
- the plasmid 82 further includes a major late promotor (MLP) and a right ITR.
- MLP major late promotor
- the capsid used in the present disclosure is, however, void of the left ITR, the early genes El and E3, its packing signal, and its protein IX genes.
- the plasmid consists essentially of (i) late regions 1, 2, 3, 4, 5, (ii) early regions 2 and 4, (iii) an MLP, and (iv) a right ITR.
- the plasmid is wholly void of a left ITF, the early genes El and E3, the packing signal, and the protein IX genes.
- the plasmid 82 is based on an adenovirus. In a further embodiment, the plasmid 82 is based on an adenovirus selected from the group consisting of the Ad2, Ad5, Ad6 and Ad35 serotypes and combinations thereof, wherein the adenoviral capsids of the human serotype Ad2 are coded with pPaC2, Ad5 with pPaC5, Ad6 with pPaC6 and Ad35 with pPaB35. Transfection
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises transfecting a packaging cell with the viral vector(s) and packing plasmid.
- a packaging cell may contain one or more viral vectors and one or more plasmids.
- a packaging cell comprises at least one, preferably two or more, and more preferably three or more viral vectors and one packing plasmid.
- the viral vectors 70 and plasmid 82 are introduced via co transfection into a eukaryotic host cell, or packaging cell 85.
- the viral vectors 70 and plasmid 82 are co-transfected into the packaging cell 85 using an optimized standardized one-week co-transfection protocol.
- the viral vector is an adenovirus vector, particularly a fd adenovirus vector
- the packaging cell is derived from cell lines such as, but not limited to, human embryonic kidney cells (HEK293) and PerC.6 cells.
- the packaging cell necessary to package fd adenovirus vectors must be modified to express the genes coded within the El region of an adenoviral vector.
- the packaging cell is an HEK293 -derived Q7 packaging cell modified to express the genes coded within the El region of an adenoviral vector.
- fd adenoviral vector is initiated by the chemical transfection of the packaging cell with a mixture of the engineered adenoviral genome, the packaging expression plasmid and a chemical transfection reagent.
- a method for preparing a vaccine for preventing at least one b-CoV infection in a subject comprises encapsidating the packaging cell 85, containing the viral vectors 70 and plasmid 82, in a capsid, as shown in FIG. 2.
- the packaging cell 85 containing the viral vectors 70 and plasmid 82, is delivered in capsids of serotypes of the adenovirus which are rare to the mammal being vaccinated.
- the mammal being vaccinated is a human and the viral vector is delivered in capsids of serotypes of the adenovirus which are rare to humans.
- the viral vector is delivered in capsids of the Ad2, Ad5, Ad6 and Ad35 serotypes, and combinations thereof.
- the viral vector is delivered in capsids of the Ad6 serotype.
- the present disclosure provides a composition of a vaccine, and more particularly a vaccine to prevent against infection from b-CoVs, and preferably SARSrs.
- the vaccine includes one or more consensus sequences derived from one or more b-CoVs, and preferably one or more SARSrs, carried on at least one viral vector.
- a consensus sequence may be in accordance with any embodiment or combination of embodiments described herein.
- a viral vector may be in accordance with any embodiment or combination of embodiments described above.
- the one or more consensus sequences is a b-CoV DNA sequence, RNA sequence, protein sequence, or combinations thereof, and preferably a SARSr DNA sequence, RNA sequence, protein sequence, or combinations thereof.
- the one or more consensus sequences comprise at least one SARSr DNA or RNA sequence, or preferably at least one S ARS-2 b-CoV DNA or RNA sequence.
- the SARSr DNA or RNA sequence, or SARS-2 b-CoV DNA or RNA sequence is at least a part of the S protein-encoding sequence.
- one or more of the one or more consensus sequences has a variable region partially or completely removed.
- one or more consensus sequences comprises at least one SARSr DNA or RNA sequences, and preferably at least one SARS-2 b-CoV DNA or RNA sequence, which is at least part of the S protein-encoding sequence, and at least part of the variable region of the S protein-encoding sequences are removed.
- expression of the consensus sequence is driven by a promotor.
- the promotor may be specific to the consensus sequence, animal being vaccinated, and the particular composition of the vaccine.
- a promotor is selected from the group consisting of human cytomegalovirus immediate early promotor/enhancer, a poly-adenylation site derived from the human growth gene, the elongation factor 1 -alpha, the phosphogly cerate kinase, ubiquitin C, beta actin genes, and combinations thereof.
- the promotor’s activity may be influenced by a chemical, such as, but not limited to, an antibiotic. Tetracycline is a nonlimiting example of an antibiotic that influences a promotor’s activity.
- the vaccine is specifically designed to prevent infection from at least SARS-2 b-CoV.
- the one or more consensus sequences includes at least one SARS-2 b-CoV DNA or RNA sequence.
- the SARS-2 b-CoV DNA or RNA sequence is an S protein-encoding DNA or RNA sequence.
- the SARS-2 b-CoV DNA or RNA sequence is an RNA sequence which is an S protein-encoding sequence (in part or in its entirety).
- the SARS-2 b-CoV DNA sequence is human codon-optimized and expression of the specific RNA is driven by a human cytomegalovirus immediate early promotor/enhancer followed by a poly-adenylation site derived from the human growth gene.
- the expression of the SARS-2 b-CoV RNA is driven by other promoters, such as, but not limited to, those derived from the elongation factor 1 -alpha, the phosphoglycerate kinase, ubiquitin C, beta actin genes, and combinations thereof.
- the expression of the SARS-2 b-CoV RNA is driven by a promoter whose activity can be influenced by a chemical, such as, but not limited to, the antibiotic tetracycline.
- the vaccine includes two or more consensus sequences one or more viral vectors.
- one consensus sequence is a SARS-2 b-CoV DNA or RNA sequence
- the vaccine includes at least one additional consensus sequence which is a SARSr DNA, RNA or protein sequence.
- the at least one viral vector is an adenovirus vector, and more preferably an fd adenovirus vector.
- the vaccine is a SARSr vaccine containing viral vectors with the SARS-2 b-CoV RNA sequence, in whole or in part) and at least one other SARSr RNA (in whole or in part) sequence.
- the viral vector likewise carries an expression cassette of the human codon-optimized S protein for each of the SARSr groups represented on the viral vector.
- the human codon-optimized S protein is drive by a CMV immediate early promotor/enhancer followed by a poly-adenylation site derived from the human growth hormone.
- the SARS-2 b-CoV RNA and, if presented the additional SARSr RNA have had the variable region of the S protein-encoding sequences removed completely or partially.
- the vaccine further includes a packing plasmid.
- the packing plasmid may be in accordance with any embodiment or combination of embodiments described herein.
- the at least one consensus sequence is a SARSr DNA or RNA sequence, and particularly a SARSr DNA or RNA sequence which is an S protein-encoding sequence, and the packing plasmid is void of the left ITR, the early genes El and E3, its packing signal, and its protein IX genes.
- the at least one consensus sequence is a SARSr DNA or RNA sequence, and particularly a SARSr DNA or RNA sequence which is an S protein-encoding sequence, contained on a viral vector and the packing plasmid based on an adenovirus selected from the group consisting of the Ad2, Ad5, Ad6 and Ad35 serotypes and combinations thereof, wherein the adenoviral capsids of the human serotype Ad2 are coded with pPaC2, Ad5 with pPaC5, Ad6 with pPaC6 and Ad35 with pPaB35, and the plasmid is void of the left ITR, the early genes El and E3, its packing signal, and its protein IX genes.
- the vaccine includes a packaging cell into which the consensus-containing viral vector(s) and plasmid(s) are co transfected.
- the packaging is in accordance with any embodiment or combination or embodiments disclosed herein.
- the viral vector(s) and plasmid are co-transfected into the packaging cell using an optimized standardized one-week co-transfection protocol using HEK-293 -derived Q7 packaging cell.
- the viral vector contains at least one consensus sequence comprising a SARSr DNA or RNA sequence, and particularly a SARSr DNA or RNA sequence which is an S protein-encoding sequence, and plasmid is based on an adenovirus selected from the group consisting of the Ad2, Ad5, Ad6 and Ad35 serotypes and combinations thereof, wherein the adenoviral capsids of the human serotype Ad2 are coded with pPaC2, Ad5 with pPaC5, Ad6 with pPaC6 and Ad35 with pPaB35, and the viral vector(s) and plasmid are co transfected into the packaging cell using an optimized standardized one-week co-transfection protocol using HEK-293 -derived Q7 packaging cell.
- the vaccine includes a capsid, in which the packaging cell (along with the viral vectors and plasmid) are encapsidated.
- the capsid may be in accordance with any embodiment or combination of embodiments disclosed herein.
- the capsid is of the Ad2, Ad5, Ad6 and Ad35 serotypes, and combinations thereof.
- the disclosure provides a method of vaccinating an animal subject, preferably a mammal subject, and more preferably a human subject against infection from at least one group of b-CoV.
- the method comprises providing a vaccine comprising at least one viral vector comprising at least one b-CoV consensus sequence, preferably at least one SARSr consensus sequence, and more preferably at least one SARS-2 b-CoV consensus sequence and a plasmid, wherein the at least one viral vector and plasmid are transfected into a packaging cell, and the packaging cell is encapsidated into a capsid.
- the at least one b-CoV consensus sequence is in accordance with any embodiment or combination or embodiments described herein.
- the at least one viral vector is in accordance with any embodiment or combination of embodiments described herein.
- the plasmid is in accordance with any embodiment or combination of embodiments described herein.
- the packaging cell is in accordance with any embodiment or combination of embodiments described herein.
- the capsid is in accordance with any embodiment or combination of embodiments described herein.
- the method further comprising injecting the viral vector into an animal subject, preferably a mammal subject, such as, for example, a human.
- a single dose is sufficient to provide protection against at least one b-CoV, and more specifically provide protection against any b-CoVs having a sequence identity greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%, or greater than or equal to 95%, or greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99% to at least one of the consensus sequences contained in the vaccine.
- two or more doses may be required to provide protection.
- two, or three, or four doses is sufficient to provide protection against at least one b- CoV, and more particularly against any b-CoVs having a sequence identity greater than or equal to 60%, or greater than or equal to 65%, or greater than or equal to 70%, or greater than or equal to 75%, or greater than or equal to 80%, or greater than or equal to 85%, or greater than or equal to 90%, or greater than or equal to 95%, or greater than or equal to 96%, or greater than or equal to 97%, or greater than or equal to 98%, or greater than or equal to 99% to least one of the consensus sequences contained in the vaccine.
- mice were given varying doses of an A/Vietname/1203/2004 (H5N1) vaccine using a viral vector in accordance with embodiments of the present disclosure and then exposed to the H5N 1 virus. Particularly, there were four groups of ten mice each. A first control group (Cl) is vaccinated with a placebo. A second control group (C2) is not vaccinated.
- H5N1 A/Vietname/1203/2004
- a first experimental group (El) is vaccinated with 3 x 10 8 genome equivalents of the GreFluVie vaccine (containing a viral vector with a consensus sequence having at least 60% commonality with the H5N1 virus) suspended in vector suspension buffer (PBS, MgC12 5 mM, EDTA 01. mM, sucruose 5%).
- a second experimental group (E2) is vaccinated with 3 x 10 7 genome equivalents of the GreFluVie vaccine suspended in vector suspension buffer.
- Groups Cl, El and E2 were boosted at day 24 with the same control or vaccine preparations.
- groups Cl, El and E2 were given a medial lethal dose (LD50), applied intranasally, of H5N1. They groups were observed and their body weights determined daily.
- the mice were bled at day 48 and tested for the presence of antibodies neutralizing infection of MDCK test sells with the H5N1 virus and antibodies inhibiting hemagglutination horse red blood cells.
- the Cl group has a very low survival rate, with all mice dying before 15 days after infection.
- both the El and E2 groups show a significantly improved survival rate, with body weights mimicking the trend of the C2 group.
- the El group shows greater virus neutralization and a lower lung virus titer.
- both the El and E2 groups show significant improvement in ability to fight off the infection after immunization.
- a control group (C3) of five mice are vaccinated with a placebo.
- An experimental group (E3) of five mice are vaccinated with 3 x 10 7 genome equivalents of the GreMERSfl vaccine (containing a viral vector with a consensus sequence having at least 60% commonality with the EMX/2012 MERS-CoV) suspended in a vector suspension buffer (PBS, MgC125 mM, EDTA 0. ImM, sucrose 5%).
- the consensus sequence is, specifically, the full-length spike protein of the MERS-CoV.
- Groups C3 and E3 were boosted at day 17 with the same control or vaccine preparations.
Abstract
Description
Claims
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MX2022013002A MX2022013002A (en) | 2020-04-20 | 2021-04-20 | Engineering broadly reactive coronavirus vaccines and related designs and uses. |
JP2022563395A JP2023522108A (en) | 2020-04-20 | 2021-04-20 | Engineering and related design and use of broadly reactive coronavirus vaccines |
US17/996,727 US20230210979A1 (en) | 2020-04-20 | 2021-04-20 | Engineering broadly reactive coronavirus vaccines and related designs and uses |
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US20070190065A1 (en) * | 2005-06-03 | 2007-08-16 | Ralf Altmeyer | Nucleic acids, polypeptides, methods of expression, and immunogenic compositions associated with SARS corona virus spike protein |
US20100233250A1 (en) * | 2007-06-19 | 2010-09-16 | Benoit Baras | Vaccine |
CN110951756A (en) * | 2020-02-23 | 2020-04-03 | 广州恩宝生物医药科技有限公司 | Nucleic acid sequence for expressing SARS-CoV-2 virus antigen peptide and its application |
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