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Volume 4, Issue 4(Suppl)

J Infect Dis Ther 2016

ISSN: 2332-0877, JIDT an open access journal

Infectious Diseases 2016

August 24-26, 2016

Page 27

Notes:

conference

series

.com

August 24-26, 2016 Philadelphia, USA

&

Infectious Diseases

Joint Event on

2

nd

World Congress on

Pediatric Care & Pediatric Infectious Diseases

International Conference on

Rachel Groppo, J Infect Dis Ther 2016, 4:4(Suppl)

http://dx.doi.org/10.4172/2332-0877.C1.007

Characterization of RSV F prefusion and postfusion specific neutralizing antibody response in animal models

V

iral entry of

respiratory syncytial virus

(RSV) is mediated by the fusion glycoprotein protein (F), which exists in two

forms; metastable prefusion and stable postfusion. These two forms of F share a common structural region containing

several antigenic sites. The prefusion form also contains unique antigenic sites to which potent neutralizing antibodies bind,

such as site Ø. Humans repeatedly infected with RSV possess high serum neutralizing antibody titers that are predominantly

prefusion specific. To better understand animal models for RSV vaccine evaluation, we assessed whether mice, cotton rats

and primates could mount primarily a prefusion specific neutralizing antibody response after infection. To show prefusion

specific antibody could be induced in an animal model system, mice were intramuscularly vaccinated with 10 µg recombinant

stabilized prefusion or postfusion F protein. Mice immunized with stabilized prefusion protein showed a high neutralizing

response with the majority of this activity generated against prefusion specific antigenic sites. Immunization with postfusion F

induced a lower neutralizing titer with the majority of neutralizing antibody against antigenic sites common to both prefusion

and postfusion F. Mice intranasally immunized twice with RSV mounted a predominant prefusion specific serum neutralizing

antibody response. A similar pattern was also seen in cotton rats. Furthermore, African green monkeys intranasally immunized

multiple times with RSV showed a robust serum neutralizing response with the majority of this activity specific to prefusion

antigenic sites. Thus, animal models of RSV infection mimic the human response in that multiple exposures can induce anF

prefusion dominant serum neutralizing response.

Biography

Rachel Groppo has completed her PhD in the laboratory of Dr. Ann Palmenberg at the University of Wisconsin, USA. After completing her Post doctorate at the

University of Massachusetts Medical School, she has joined Sanofi Pasteur. Currently she is a Virology Manager at Sanofi Pasteur North American Research.

Rachel.groppo@sanofipasteur.com

Rachel Groppo

Sanofi Pasteur, USA