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A novel pre-fusion conformation-specific neutralizing epitope on the respiratory syncytial virus fusion protein

Nature Microbiology volume 2, Article number: 16271 (2017) | Download Citation


Respiratory syncytial virus (RSV) remains a major human pathogen, infecting the majority of infants before age two and causing re-infection throughout life. Despite decades of RSV research, there is no licensed RSV vaccine. Most candidate vaccines studied to date have incorporated the RSV fusion (F) surface glycoprotein, because the sequence of F is highly conserved among strains of RSV. To better define the human B cell response to RSV F, we isolated from a single donor 13 new neutralizing human monoclonal antibodies (mAbs) that recognize the RSV F protein in the pre-fusion conformation. Epitope binning studies showed that the majority of neutralizing mAbs targeted a new antigenic site on the globular head domain of F, designated here antigenic site VIII, which occupies an intermediate position between the previously defined major antigenic sites II and site Ø. Antibodies to site VIII competed for binding with antibodies to both of those adjacent neutralizing sites. The new mAbs exhibited unusual breadth for pre-fusion F-specific antibodies, cross-reacting with F proteins from both RSV subgroups A and B viruses. We solved the X-ray crystal structure of one site VIII mAb, hRSV90, in complex with pre-fusion RSV F protein. The structure revealed a large footprint of interaction for hRSV90 on RSV F, in which the heavy chain and light chain both have specific interactions mediating binding to site VIII, the heavy chain overlaps with site Ø, and the light chain interacts partially with site II.

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The authors thank members of the Crowe Laboratory, especially R. Bombardi, N. Murphy and G. Sapparapu, for technical assistance. A portion of the experiments described here used the Vanderbilt robotic crystallization facility, which was supported by NIH grant S10 RR026915. J.J.M. was supported by T32 AI 07474, NIAID and National Institutes of Health (NIH). The described project was supported by CTSA award no. UL1TR000445 from the National Center for Advancing Translational Sciences. Its contents are solely the responsibility of the authors and do not necessarily represent official views of the National Center for Advancing Translational Sciences or the NIH.

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  1. Vanderbilt Vaccine Center, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA

    • Jarrod J. Mousa
    • , Nurgun Kose
    • , Pranathi Matta
    • , Pavlo Gilchuk
    •  & James E. Crowe Jr
  2. Department of Pathology, Microbiology and Immunology, Vanderbilt University, Nashville, Tennessee 37232, USA

    • James E. Crowe Jr
  3. Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA

    • James E. Crowe Jr


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J.J.M. and J.E.C. designed the experiments and interpreted the data. J.J.M. expressed, purified, crystallized, collected data and solved the crystal structure of the hRSV-90-RSV F SC-TM complex. J.J.M. and N.K. generated hybridomas by electrofusion. P.M. expanded hybridoma cell cultures. J.J.M. and P.M. performed neutralization experiments and J.J.M. performed competition-binding and ELISA binding studies. P.G. performed self-reactivity assays. J.J.M. and J.E.C. wrote the manuscript. All authors reviewed and edited the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to James E. Crowe Jr.

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