2010
DOI: 10.1016/j.vaccine.2010.03.018
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Corrigendum to “The member of the cyclic di-nucleotide family bis-(3′,5′)-cyclic dimeric inosine monophosphate exerts potent activity as mucosal adjuvant” [Vaccine 28 (2010) 2249–2258]

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Cited by 4 publications
(9 citation statements)
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“…312 Guzman and colleagues extensively explored the immunological profiles of CDN-based adjuvants and vaccines. [313][314][315][316][317] In 2007, the c-di-GMP adjuvant, for the first time, demonstrated its capability in producing both cellular and humoral immune responses against antigens. 313 Intranasal administration of c-di-GMP and OVA induced antigen-specific CTLs and CD4 + T cells as well as mucosal IgA responses in lungs and vaginas.…”
Section: Adjuvants Targeting the Sting Pathwaymentioning
confidence: 99%
“…312 Guzman and colleagues extensively explored the immunological profiles of CDN-based adjuvants and vaccines. [313][314][315][316][317] In 2007, the c-di-GMP adjuvant, for the first time, demonstrated its capability in producing both cellular and humoral immune responses against antigens. 313 Intranasal administration of c-di-GMP and OVA induced antigen-specific CTLs and CD4 + T cells as well as mucosal IgA responses in lungs and vaginas.…”
Section: Adjuvants Targeting the Sting Pathwaymentioning
confidence: 99%
“…They are reported to interact with the transmembrane protein stimulator of interferon genes (STING), which then increases the production of type I interferons and further drives the adaptive immune response (Ishikawa et al, 2009 ; Burdette et al, 2011 ; Shaw et al, 2013 ). Studies of intranasal delivery of model protein antigens such as recombinant influenza nucleoprotein (rNP), β-Gal and OVA together with the adjuvant c-di-AMP/IMP in mice suggest them as potent mucosal adjuvants, especially when cellular immunity is desired (Ebensen et al, 2007 ; Libanova et al, 2010 ; Ebensen et al, 2011 ; Sanchez et al, 2014 ). C-di-GMP can enhance the immune response in mice for H5N1 virosomes after sublingual, intranasal and intramuscular administrations (Pedersen et al, 2011 ).…”
Section: Adjuvants For Mucosal Vaccines With Protein Antigensmentioning
confidence: 99%
“…127 c-di-IMP (4) has been prepared enzymatically from c-di-AMP (2) by use of adenosine-deaminase. 25,26…”
Section: C-di-ampmentioning
confidence: 99%
“…However, in vitro studies have evidenced that retroviral integrases can generate cyclic deoxydinucleotides during the 3′-end processing of viral DNA. Such release seriously supports the possibility of their natural occurrence and has triggered the search of cyclic dinucleotides as new drugs acting by inhibition of viral integrases. Additionally, c-di-IMP ( 4 ), the synthetic inosine-containing analogue of c-di-GMP, displays adjuvant properties promising for development of mucosal vaccination strategies. , …”
Section: Introductionmentioning
confidence: 99%
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