Live-Attenuated Respiratory Syncytial Virus Vaccine Candidate With Deletion of RNA Synthesis Regulatory Protein M2-2 is Highly Immunogenic in Children. (2nd March 2018)
- Record Type:
- Journal Article
- Title:
- Live-Attenuated Respiratory Syncytial Virus Vaccine Candidate With Deletion of RNA Synthesis Regulatory Protein M2-2 is Highly Immunogenic in Children. (2nd March 2018)
- Main Title:
- Live-Attenuated Respiratory Syncytial Virus Vaccine Candidate With Deletion of RNA Synthesis Regulatory Protein M2-2 is Highly Immunogenic in Children
- Authors:
- McFarland, Elizabeth J
Karron, Ruth A
Muresan, Petronella
Cunningham, Coleen K
Valentine, Megan E
Perlowski, Charlotte
Thumar, Bhagvanji
Gnanashanmugam, Devasena
Siberry, George K
Schappell, Elizabeth
Barr, Emily
Rexroad, Vivian
Yogev, Ram
Spector, Stephen A
Aziz, Mariam
Patel, Nehali
Cielo, Mikhaela
Luongo, Cindy
Collins, Peter L
Buchholz, Ursula J - Abstract:
- Abstract: Background: Live respiratory syncytial virus (RSV) candidate vaccine LIDΔM2-2 is attenuated by deletion of the RSV RNA regulatory protein M2-2, resulting in upregulated viral gene transcription and antigen expression but reduced RNA replication. Methods: RSV-seronegative children ages 6–24 months received a single intranasal dose of 10 5 plaque forming units (PFU) of LIDΔM2-2 (n = 20) or placebo (n = 9) (NCT02237209, NCT02040831). RSV serum antibodies, vaccine infectivity, and reactogenicity were assessed. During the following RSV season, participants were monitored for respiratory illness and pre- and post-RSV season serum antibodies. Results: Vaccine virus was shed by 95% of vaccinees (median peak titers of 3.8 log10 PFU/mL by quantitative culture and 6.3 log10 copies/mL by PCR); 90% had ≥4-fold rise in serum neutralizing antibodies. Respiratory symptoms and fever were common in vaccine (95%) and placebo (78%). One vaccinee had grade 2 rhonchi concurrent with vaccine shedding, rhinovirus, and enterovirus. Eight of 19 vaccinees versus 2 of 9 placebo recipients had substantially increased RSV antibody titers after the RSV season without medically attended RSV disease, indicating anamnestic vaccine responses to wild-type RSV without significant illness. Conclusion: LIDΔM2-2 had excellent infectivity and immunogenicity, encouraging further study of vaccine candidates attenuated by M2-2 deletion. Clinical Trials Registration: NCT02237209, NCT02040831. Abstract : TheAbstract: Background: Live respiratory syncytial virus (RSV) candidate vaccine LIDΔM2-2 is attenuated by deletion of the RSV RNA regulatory protein M2-2, resulting in upregulated viral gene transcription and antigen expression but reduced RNA replication. Methods: RSV-seronegative children ages 6–24 months received a single intranasal dose of 10 5 plaque forming units (PFU) of LIDΔM2-2 (n = 20) or placebo (n = 9) (NCT02237209, NCT02040831). RSV serum antibodies, vaccine infectivity, and reactogenicity were assessed. During the following RSV season, participants were monitored for respiratory illness and pre- and post-RSV season serum antibodies. Results: Vaccine virus was shed by 95% of vaccinees (median peak titers of 3.8 log10 PFU/mL by quantitative culture and 6.3 log10 copies/mL by PCR); 90% had ≥4-fold rise in serum neutralizing antibodies. Respiratory symptoms and fever were common in vaccine (95%) and placebo (78%). One vaccinee had grade 2 rhonchi concurrent with vaccine shedding, rhinovirus, and enterovirus. Eight of 19 vaccinees versus 2 of 9 placebo recipients had substantially increased RSV antibody titers after the RSV season without medically attended RSV disease, indicating anamnestic vaccine responses to wild-type RSV without significant illness. Conclusion: LIDΔM2-2 had excellent infectivity and immunogenicity, encouraging further study of vaccine candidates attenuated by M2-2 deletion. Clinical Trials Registration: NCT02237209, NCT02040831. Abstract : The live respiratory syncytial virus (RSV) vaccine LIDΔM2-2, attenuated by deletion of the RNA regulatory protein M2-2, had excellent infectivity and immunogenicity in RSV seronegative 6–24-month old children, encouraging further study of vaccine candidates attenuated by M2-2 deletion. … (more)
- Is Part Of:
- Journal of infectious diseases. Volume 217:Number 9(2018)
- Journal:
- Journal of infectious diseases
- Issue:
- Volume 217:Number 9(2018)
- Issue Display:
- Volume 217, Issue 9 (2018)
- Year:
- 2018
- Volume:
- 217
- Issue:
- 9
- Issue Sort Value:
- 2018-0217-0009-0000
- Page Start:
- 1347
- Page End:
- 1355
- Publication Date:
- 2018-03-02
- Subjects:
- respiratory syncytial virus -- live attenuated viral vaccine -- pediatric RSV vaccine -- neutralizing antibodies -- immunogenicity -- RNA regulatory protein M2-2
Communicable diseases -- Periodicals
Diseases -- Causes and theories of causation -- Periodicals
Medicine -- Periodicals
Communicable Diseases -- Periodicals
Electronic journals
616.9 - Journal URLs:
- http://jid.oxfordjournals.org/content/by/year ↗
http://www.journals.uchicago.edu/JID/journal/ ↗
http://www.jstor.org/journals/00221899.html ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/infdis/jiy040 ↗
- Languages:
- English
- ISSNs:
- 0022-1899
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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