| Literature DB >> 26307915 |
Jessica J O'Konek1, Paul E Makidon1,2, Jeffrey J Landers1, Zhengyi Cao1, Carrie-Anne Malinczak3, Jessie Pannu3, Jennifer Sun3, Vira Bitko3, Susan Ciotti3, Tarek Hamouda3, Zbigniew W Wojcinski4, Nicholas W Lukacs5, Ali Fattom3, James R Baker1.
Abstract
Respiratory Syncytial Virus is a leading cause of bronchiolitis and pneumonia in infants, the elderly and individuals with compromised immune systems. Despite decades of research, there is currently no available vaccine for RSV. Our group has previously demonstrated that intranasal immunization of mice with RSV inactivated by and adjuvanted with W805EC nanoemulsion elicits robust humoral and cellular immune responses, resulting in protection against RSV infection. This protection was achieved without the induction of airway hyper-reactivity or a Th2-skewed immune response. The cotton rat Sigmodon hispidus has been used for years as an excellent small animal model of RSV disease. Thus, we extended these rodent studies to the more permissive cotton rat model. Intranasal immunization of the nanoemulsion-adjuvanted RSV vaccines induced high antibody titers and a robust Th1-skewed cellular response. Importantly, vaccination provided sterilizing cross-protective immunity against a heterologous RSV challenge and did not induce marked or severe histological effects or eosinophilia in the lung after viral challenge. Overall, these data demonstrate that nanoemulsion-formulated whole RSV vaccines are both safe and effective for immunization in multiple animal models.Entities:
Keywords: RSV; adjuvant; immunogenicity; intranasal vaccination; nanoemulsion; vaccine
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Year: 2015 PMID: 26307915 PMCID: PMC5054793 DOI: 10.1080/21645515.2015.1075680
Source DB: PubMed Journal: Hum Vaccin Immunother ISSN: 2164-5515 Impact factor: 3.452