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Development of Acquired Immunity Following Repeated Respiratory Syncytial Virus Infections in Cotton Rats

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Journal PLoS One
Date 2016 May 26
PMID 27224021
Citations 10
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Abstract

Respiratory syncytial virus (RSV) infections occur every year worldwide. Most infants are infected with RSV by one year of age and are reinfected because immune responses after the first infection are too weak to protect against subsequent infections. In the present study, immune responses against RSV were investigated in order to obtain a better understanding of repetitive RSV infections in cotton rats. No detectable neutralizing antibody (NT) was developed after the first infection, and the second infection was not prevented. The results of histological examinations revealed severe inflammation, viral antigens were detected around bronchial epithelial cells, and infectious viruses were recovered from lung homogenates. Following the second infection neutralizing antibodies were significantly elevated, and CD8+ cells were activated in response to RSV-F253-265. No viral antigens was detected thereafter in lung tissues and infectious viruses were not recovered. Similar results were obtained in the present study using the subgroups A and B. These results support the induction of humoral and cellular immune responses following repetitive infections with RSV; however, these responses were insufficient to eliminate viruses in the first and second infections.

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References
1.
Prince G, Horswood R, Chanock R . Quantitative aspects of passive immunity to respiratory syncytial virus infection in infant cotton rats. J Virol. 1985; 55(3):517-20. PMC: 254995. DOI: 10.1128/JVI.55.3.517-520.1985. View

2.
Yamaji Y, Nakayama T . Recombinant measles viruses expressing respiratory syncytial virus proteins induced virus-specific CTL responses in cotton rats. Vaccine. 2014; 32(35):4529-4536. DOI: 10.1016/j.vaccine.2014.06.024. View

3.
Zomer-Kooijker K, van der Ent C, Ermers M, Uiterwaal C, Rovers M, Bont L . Increased risk of wheeze and decreased lung function after respiratory syncytial virus infection. PLoS One. 2014; 9(1):e87162. PMC: 3909049. DOI: 10.1371/journal.pone.0087162. View

4.
Shaw C, Galarneau J, Bowenkamp K, Swanson K, Palmer G, Palladino G . The role of non-viral antigens in the cotton rat model of respiratory syncytial virus vaccine-enhanced disease. Vaccine. 2012; 31(2):306-12. DOI: 10.1016/j.vaccine.2012.11.006. View

5.
RAMMENSEE H, Bachmann J, Emmerich N, Bachor O, Stevanovic S . SYFPEITHI: database for MHC ligands and peptide motifs. Immunogenetics. 1999; 50(3-4):213-9. DOI: 10.1007/s002510050595. View