tetano
Editor, Senior Moderator
J Nanobiotechnology. 2017 Oct 5;15(1):69. doi: 10.1186/s12951-017-0305-2.
[h=1]Nanodiamond enhances immune responses in mice against recombinant HA/H7N9 protein.[/h] Pham NB[SUP]1,[/SUP][SUP]2[/SUP], Ho TT[SUP]1[/SUP], Nguyen GT[SUP]1[/SUP], Le TT[SUP]1[/SUP], Le NT[SUP]1[/SUP], Chang HC[SUP]3[/SUP], Pham MD[SUP]1,[/SUP][SUP]3[/SUP], Conrad U[SUP]4[/SUP], Chu HH[SUP]5,[/SUP][SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] [h=4]BACKGROUND:[/h] The continuing spread of the newly emerged H7N9 virus among poultry in China, as well as the possibility of human-to-human transmission, has attracted numerous efforts to develop an effective vaccine against H7N9. The use of nanoparticles in vaccinology is inspired by the fact that most pathogens have a dimension within the nano-size range and therefore can be processed efficiently by the immune system, which leads to a potent immune response. Herein, we report a facile approach to increase antigen size to achieve not only fast but also effective responses against the recombinant HA/H7N9 protein via a simple conjugation of the protein onto the surface of nanodiamond particles.
[h=4]RESULTS:[/h] In this study, trimeric Haemagglutinin (H7) that is transiently expressed in N. benthamiana was purified using affinity chromatography, and its trimeric state was revealed successfully by the cross-linking reaction. The trimeric H7 solution was subsequently mixed with a nanodiamond suspension in different ratios. The successful conjugation of the trimeric H7 onto the surface of nanodiamond particles was demonstrated by the changes in size and Zeta-potential of the particles before and after protein coating, Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and Western-blot analysis. Next, biofunction of the protein-nanodiamond conjugates was screened using a haemagglutination assay. A mixture containing 5 ?g of trimeric H7 and 60 ?g of nanodiamond corresponds to a ratio of 1:12 (w/w) of agglutinated chicken red blood cells at HA titer of 1024, which is 512-fold higher than the HA titer of free trimeric H7. After the 2nd and 3rd immunization in mice, ELISA and Western blot analyses demonstrated that the physical mixture of trimeric H7 protein and nanodiamond (1:12, w/w) elicited statistically significant stronger H7-specific-IgG response demonstrated by higher amounts of H7N9-specific IgG (over 15.4-fold with P < 0.05 after the second immunization).
[h=4]CONCLUSIONS:[/h] These results indicated a potential effect inherent to nanodiamond towards modulating immune systems, which should be further evaluated and broadly applied in nanovaccine development.
[h=4]KEYWORDS:[/h] Influenza virus A/H7N9; Nanodiamond; Plant-derived protein; Recombinant H7 haemagglutinin; Synthetic virus-like particles
PMID: 28982373 DOI: 10.1186/s12951-017-0305-2
[h=1]Nanodiamond enhances immune responses in mice against recombinant HA/H7N9 protein.[/h] Pham NB[SUP]1,[/SUP][SUP]2[/SUP], Ho TT[SUP]1[/SUP], Nguyen GT[SUP]1[/SUP], Le TT[SUP]1[/SUP], Le NT[SUP]1[/SUP], Chang HC[SUP]3[/SUP], Pham MD[SUP]1,[/SUP][SUP]3[/SUP], Conrad U[SUP]4[/SUP], Chu HH[SUP]5,[/SUP][SUP]6[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] [h=4]BACKGROUND:[/h] The continuing spread of the newly emerged H7N9 virus among poultry in China, as well as the possibility of human-to-human transmission, has attracted numerous efforts to develop an effective vaccine against H7N9. The use of nanoparticles in vaccinology is inspired by the fact that most pathogens have a dimension within the nano-size range and therefore can be processed efficiently by the immune system, which leads to a potent immune response. Herein, we report a facile approach to increase antigen size to achieve not only fast but also effective responses against the recombinant HA/H7N9 protein via a simple conjugation of the protein onto the surface of nanodiamond particles.
[h=4]RESULTS:[/h] In this study, trimeric Haemagglutinin (H7) that is transiently expressed in N. benthamiana was purified using affinity chromatography, and its trimeric state was revealed successfully by the cross-linking reaction. The trimeric H7 solution was subsequently mixed with a nanodiamond suspension in different ratios. The successful conjugation of the trimeric H7 onto the surface of nanodiamond particles was demonstrated by the changes in size and Zeta-potential of the particles before and after protein coating, Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and Western-blot analysis. Next, biofunction of the protein-nanodiamond conjugates was screened using a haemagglutination assay. A mixture containing 5 ?g of trimeric H7 and 60 ?g of nanodiamond corresponds to a ratio of 1:12 (w/w) of agglutinated chicken red blood cells at HA titer of 1024, which is 512-fold higher than the HA titer of free trimeric H7. After the 2nd and 3rd immunization in mice, ELISA and Western blot analyses demonstrated that the physical mixture of trimeric H7 protein and nanodiamond (1:12, w/w) elicited statistically significant stronger H7-specific-IgG response demonstrated by higher amounts of H7N9-specific IgG (over 15.4-fold with P < 0.05 after the second immunization).
[h=4]CONCLUSIONS:[/h] These results indicated a potential effect inherent to nanodiamond towards modulating immune systems, which should be further evaluated and broadly applied in nanovaccine development.
[h=4]KEYWORDS:[/h] Influenza virus A/H7N9; Nanodiamond; Plant-derived protein; Recombinant H7 haemagglutinin; Synthetic virus-like particles
PMID: 28982373 DOI: 10.1186/s12951-017-0305-2