Genetically stable recombinant modified vaccinia ankara (rMVA) vaccines and methods of preparation thereof
AssigneeCity of Hope
InventorsDon Diamond, Zhongde Wang
Life of this patent
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AssigneeCity of Hope
InventorsDon Diamond, Zhongde Wang
Estimating the term…
A vaccine comprising an immunologically effective amount of recombinant modified vaccinia Ankara (rMVA) virus which is genetically stable after serial passage and produced by a) constructing a transfer plasmid vector comprising a modified H5 (mH5) promoter operably linked to a DNA sequence encoding a heterologous foreign protein antigen, wherein the expression of said DNA sequence is under the control of the mH5 promoter; b) generating rMVA virus by transfecting one or more plasmid vectors obtained from step a) into wild type MVA virus; c) identifying rMVA virus expressing one or more heterologous foreign protein antigens using one or more selection methods for serial passage; d) conducting serial passage; e) expanding an rMVA virus strain identified by step d); and f) purifying the rMVA viruses from step e) to form the vaccine. One embodiment is directed to a fusion cytomegalovirus (CMV) protein antigen comprising a nucleotide sequence encoding two or more antigenic portions of Immediate-Early Gene-1 or Immediate-Early Gene-2 (IEfusion), wherein the antigenic portions elicit an immune response when expressed by a vaccine.
A fusion nucleotide sequence which encodes an IEfusion cytomegalovirus (CMV) protein antigen, said fusion nucleotide sequence comprising a nucleotide sequence encoding an-Immediate-Early Gene-1 (IE1) antigenic portion directly fused to a nucleotide sequence encoding an Immediate-Early Gene-2 (IE2) antigenic portion,
A fusion nucleotide sequence which encodes an IEfusion cytomegalovirus (CMV) protein antigen, said fusion nucleotide sequence comprising a nucleotide sequence encoding an-Immediate-Early Gene-1 (IE1) antigenic portion directly fused to a nucleotide sequence encoding an Immediate-Early Gene-2 (IE2) antigenic portion,
An rMVA virus comprising a fusion nucleotide sequence which encodes an IEfusion cytomegalovirus (CMV) protein antigen, said fusion nucleotide sequence comprising a nucleotide sequence encoding an-Immediate-Early Gene-1 (IE1) antigenic portion directly fused to a nucleotide sequence encoding an Immediate-Early Gene-2 (IE2) antigenic portion, wherein
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