2016
DOI: 10.1016/j.vaccine.2016.04.001
|View full text |Cite
|
Sign up to set email alerts
|

Intranasal hydroxypropyl-β-cyclodextrin-adjuvanted influenza vaccine protects against sub-heterologous virus infection

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
23
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 29 publications
(24 citation statements)
references
References 35 publications
1
23
0
Order By: Relevance
“…For example, it has been established that methylated beta-cyclodextrin can reduce influenza A virus and coronavirus infectivity by sequestering cholesterol from viral particles or depleting it from the host cell membranes [51]. Hydroxypropyl-β-cyclodextrin was used as a vaccine adjuvant providing protection against the H1N1 influenza virus in the cynomolgus monkey model [52,53]. One point to emphasize is that for natural CDs, the intramolecular hydrogen bond with the CD molecule decreases their hydrogen bond formation with the surrounding water molecules [54].…”
Section: Cyclodextrinsmentioning
confidence: 99%
“…For example, it has been established that methylated beta-cyclodextrin can reduce influenza A virus and coronavirus infectivity by sequestering cholesterol from viral particles or depleting it from the host cell membranes [51]. Hydroxypropyl-β-cyclodextrin was used as a vaccine adjuvant providing protection against the H1N1 influenza virus in the cynomolgus monkey model [52,53]. One point to emphasize is that for natural CDs, the intramolecular hydrogen bond with the CD molecule decreases their hydrogen bond formation with the surrounding water molecules [54].…”
Section: Cyclodextrinsmentioning
confidence: 99%
“…The synergic effect of HPβCD with immunoglobulins was proven by several previous in vivo studies with mice and macaques, which demonstrated that HPβCD brings a 30% increase in the production of antibodies and that it further induces the production of a subclass of immune cells responsible for long-term immune 'memory'; that is, long-term immunization against the virus [44,45]. It was also demonstrated that the effect of immunization occurs not only at the nasal mucosa, the site of administration, but that it is systemic, spreading throughout the entire body to convey strong immunity to the virus [46]. The vaccine is undergoing phase I clinical studies, which started in October 2017 and continue until the present day [47].…”
Section: Influenza Treatment and Preventionmentioning
confidence: 95%
“…Forty-one compounds showed protective efficacy similar or superior to that of alum on the basis of survival rates (Table 2). These 41 hit compounds comprised 18 totally novel adjuvant candidates, 15 novel adjuvant candidates for the influenza vaccine with previously reported adjuvant effects for other antigens but not for the influenza vaccine, and 8 previously reported adjuvant candidates for the influenza vaccine (Tables 1 and 2), namely β-cyclodextrin [30,31], poly-L-γ-glutamic acid sodium salt [32,33], polyvinylpyrrolidone (MW 3,600,000) [34], pullulan [35], riboflavin [36], saponin [37][38][39], sepiolite [40], and sodium alginate 80-120 [41] (Table 1, Figure 1, and Table S1). a Six-week-old BALB/c mice were intramuscularly immunized with the indicated immunogens (100 µL) twice at a two-week interval.…”
Section: Identification Of 41 Compounds That Enhance the Protective Ementioning
confidence: 99%