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Robust neutralizing antibodies elicited by HIV-1 JRFL envelope glycoprotein trimers in nonhuman primates.

Publication ,  Journal Article
Chakrabarti, BK; Feng, Y; Sharma, SK; McKee, K; Karlsson Hedestam, GB; Labranche, CC; Montefiori, DC; Mascola, JR; Wyatt, RT
Published in: J Virol
December 2013

Host cell-mediated proteolytic cleavage of the human immunodeficiency virus type 1 (HIV-1) gp160 precursor glycoprotein into gp120 and gp41 subunits is required to generate fusion-competent envelope glycoprotein (Env) spikes. The gp120-directed broadly neutralizing monoclonal antibodies (bNabs) isolated from HIV-infected individuals efficiently recognize fully cleaved JRFL Env spikes; however, nonneutralizing gp120-directed monoclonal antibodies isolated from infected or vaccinated subjects recognize only uncleaved JRFL spikes. Therefore, as an immunogen, cleaved spikes that selectively present desired neutralizing epitopes to B cells may elicit cross-reactive neutralizing antibodies. Accordingly, we inoculated nonhuman primates (NHPs) with plasmid DNA encoding transmembrane-anchored, cleaved JRFL Env or by electroporation (EP). Priming with DNA expressing soluble, uncleaved gp140 trimers was included as a comparative experimental group of NHPs. DNA inoculation was followed by boosts with soluble JRFL gp140 trimers, and control NHPs were inoculated with soluble JRFL protein trimers without DNA priming. In the TZM-bl assay, elicitation of neutralizing antibodies against HIV-1 tier 1 isolates was robust following the protein boost. Neutralization of tier 2 isolates was detected, but only in animals primed with plasmid DNA and boosted with trimeric protein. Using the more sensitive A3R5 assay, consistent neutralization of both clade B and C tier 2 isolates was detected from all regimens assessed in the current study, exceeding levels achieved by our previous vaccine regimens in primates. Together, these data suggest a potential advantage of B cell priming followed by a rest interval and protein boosting to present JRFL Env spikes to the immune system to better generate HIV-1 cross-clade neutralizing antibodies.

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Published In

J Virol

DOI

EISSN

1098-5514

Publication Date

December 2013

Volume

87

Issue

24

Start / End Page

13239 / 13251

Location

United States

Related Subject Headings

  • Virology
  • Protein Multimerization
  • Macaca mulatta
  • Humans
  • HIV-1
  • HIV Infections
  • HIV Envelope Protein gp120
  • HIV Antibodies
  • B-Lymphocytes
  • Antibodies, Neutralizing
 

Citation

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MLA
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Chakrabarti, B. K., Feng, Y., Sharma, S. K., McKee, K., Karlsson Hedestam, G. B., Labranche, C. C., … Wyatt, R. T. (2013). Robust neutralizing antibodies elicited by HIV-1 JRFL envelope glycoprotein trimers in nonhuman primates. J Virol, 87(24), 13239–13251. https://doi.org/10.1128/JVI.01247-13
Chakrabarti, Bimal K., Yu Feng, Shailendra Kumar Sharma, Krisha McKee, Gunilla B. Karlsson Hedestam, Celia C. Labranche, David C. Montefiori, John R. Mascola, and Richard T. Wyatt. “Robust neutralizing antibodies elicited by HIV-1 JRFL envelope glycoprotein trimers in nonhuman primates.J Virol 87, no. 24 (December 2013): 13239–51. https://doi.org/10.1128/JVI.01247-13.
Chakrabarti BK, Feng Y, Sharma SK, McKee K, Karlsson Hedestam GB, Labranche CC, et al. Robust neutralizing antibodies elicited by HIV-1 JRFL envelope glycoprotein trimers in nonhuman primates. J Virol. 2013 Dec;87(24):13239–51.
Chakrabarti, Bimal K., et al. “Robust neutralizing antibodies elicited by HIV-1 JRFL envelope glycoprotein trimers in nonhuman primates.J Virol, vol. 87, no. 24, Dec. 2013, pp. 13239–51. Pubmed, doi:10.1128/JVI.01247-13.
Chakrabarti BK, Feng Y, Sharma SK, McKee K, Karlsson Hedestam GB, Labranche CC, Montefiori DC, Mascola JR, Wyatt RT. Robust neutralizing antibodies elicited by HIV-1 JRFL envelope glycoprotein trimers in nonhuman primates. J Virol. 2013 Dec;87(24):13239–13251.

Published In

J Virol

DOI

EISSN

1098-5514

Publication Date

December 2013

Volume

87

Issue

24

Start / End Page

13239 / 13251

Location

United States

Related Subject Headings

  • Virology
  • Protein Multimerization
  • Macaca mulatta
  • Humans
  • HIV-1
  • HIV Infections
  • HIV Envelope Protein gp120
  • HIV Antibodies
  • B-Lymphocytes
  • Antibodies, Neutralizing