tetano
Editor, Senior Moderator
Vaccine. 2019 Aug 2. pii: S0264-410X(19)30247-6. doi: 10.1016/j.vaccine.2019.02.040. [Epub ahead of print]
[h=1]Recombinant hemagglutinin produced from Chinese Hamster Ovary (CHO) stable cell clones and a PELC/CpG combination adjuvant for H7N9 subunit vaccine development.[/h] Chen TH[SUP]1[/SUP], Liu WC[SUP]1[/SUP], Chen IC[SUP]1[/SUP], Liu CC[SUP]2[/SUP], Huang MH[SUP]2[/SUP], Jan JT[SUP]3[/SUP], Wu SC[SUP]4[/SUP].
[h=3]Author information[/h] 1 Institute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan. 2 National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan. 3 Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan. 4 Institute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan; Department of Medical Science, National Tsing Hua University, Hsinchu 30013, Taiwan. Electronic address: scwu@mx.nthu.edu.tw.
[h=3]Abstract[/h] The novel H7N9 avian influenza A virus has caused human infections in China since 2013; some isolates from the fifth wave of infections have emerged as highly pathogenic avian influenza viruses. Recombinant hemagglutinin proteins of H7N9 viruses can be rapidly and efficiently produced with low-level biocontainment facilities. In this study, recombinant H7 antigen was obtained from engineered stable clones of Chinese Hamster Ovary (CHO) cells for subsequent large-scale production. The stable CHO cell clones were also adapted to grow in serum-free suspension cultures. To improve the immunogenicity of the recombinant H7 antigens, we evaluated the use of a novel combination adjuvant of PELC and CpG (PELC/CpG) to augment the anti-H7N9 immune responses in mice. We compared the effects with other adjuvants such as alum, AddaVax (MF59-like), and several Toll-like receptor ligands such as R848, CpG, and poly (I:C). With the PELC/CpG combination adjuvant, CHO cell-expressed rH7 antigens containing terminally sialylated complex type N-glycans were able to induce high titers of neutralizing antibodies in sera and conferred protection following live virus challenges. These data indicate that the CHO cell-expressed recombinant H7 antigens and a PELC/CpG combination adjuvant can be used for H7N9 subunit vaccine development.
Copyright ? 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.
[h=4]KEYWORDS:[/h] CHO cells; H7N9 vaccine; Hemagglutinin; PELC/CpG adjuvant
PMID: 31383491 DOI: 10.1016/j.vaccine.2019.02.040
[h=1]Recombinant hemagglutinin produced from Chinese Hamster Ovary (CHO) stable cell clones and a PELC/CpG combination adjuvant for H7N9 subunit vaccine development.[/h] Chen TH[SUP]1[/SUP], Liu WC[SUP]1[/SUP], Chen IC[SUP]1[/SUP], Liu CC[SUP]2[/SUP], Huang MH[SUP]2[/SUP], Jan JT[SUP]3[/SUP], Wu SC[SUP]4[/SUP].
[h=3]Author information[/h] 1 Institute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan. 2 National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Zhunan, Taiwan. 3 Genomics Research Center, Academia Sinica, Taipei 11529, Taiwan. 4 Institute of Biotechnology, National Tsing Hua University, Hsinchu 30013, Taiwan; Department of Medical Science, National Tsing Hua University, Hsinchu 30013, Taiwan. Electronic address: scwu@mx.nthu.edu.tw.
[h=3]Abstract[/h] The novel H7N9 avian influenza A virus has caused human infections in China since 2013; some isolates from the fifth wave of infections have emerged as highly pathogenic avian influenza viruses. Recombinant hemagglutinin proteins of H7N9 viruses can be rapidly and efficiently produced with low-level biocontainment facilities. In this study, recombinant H7 antigen was obtained from engineered stable clones of Chinese Hamster Ovary (CHO) cells for subsequent large-scale production. The stable CHO cell clones were also adapted to grow in serum-free suspension cultures. To improve the immunogenicity of the recombinant H7 antigens, we evaluated the use of a novel combination adjuvant of PELC and CpG (PELC/CpG) to augment the anti-H7N9 immune responses in mice. We compared the effects with other adjuvants such as alum, AddaVax (MF59-like), and several Toll-like receptor ligands such as R848, CpG, and poly (I:C). With the PELC/CpG combination adjuvant, CHO cell-expressed rH7 antigens containing terminally sialylated complex type N-glycans were able to induce high titers of neutralizing antibodies in sera and conferred protection following live virus challenges. These data indicate that the CHO cell-expressed recombinant H7 antigens and a PELC/CpG combination adjuvant can be used for H7N9 subunit vaccine development.
Copyright ? 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.
[h=4]KEYWORDS:[/h] CHO cells; H7N9 vaccine; Hemagglutinin; PELC/CpG adjuvant
PMID: 31383491 DOI: 10.1016/j.vaccine.2019.02.040