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bcrc 17680 evs caco 2  (ATCC)


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    ATCC bcrc 17680 evs caco 2
    Bcrc 17680 Evs Caco 2, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 15355 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ev/Caco-2/pm42879097-282-0-35
    Average 99 stars, based on 15355 article reviews
    bcrc 17680 evs caco 2 - by Bioz Stars, 2026-10
    99/100 stars

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    Isolation:

    Article Title: Amuc_1473 Links Gut Microbes to Skeletal Homeostasis and Counteracts Multifactorial Osteoporosis.
    Article Snippet: .. Liver and kidney function-related-parameters were measured in serum samples using automated analyzers at Changsha Huancai Streaming Technology Co., Ltd. 5.2 Akk Culture and Akk -EV Isolation Akk (ATCC BAA-835, Manassas, VA) was grown in Brain Heart Infusion (BHI) broth (BD Bioscience, San Jose, USA) with 0.5% porcine mucin (Sigma–Aldrich, St Louis, USA) and 0.05% Lcysteine-HCl (Sigma–Aldrich) as mentioned previously [ 17 ]. ..

    Vaccines:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Comparison:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Expressing:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Animal Model:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    In Vivo:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Cell Culture:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Adjuvant:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Biomarker Discovery:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Virus:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..

    Immunopeptidomics:

    Article Title: Progress in enterovirus D68-neutralizing antibodies and vaccines.
    Article Snippet: .. However, such vaccines still have limitations: heterologous strain protection is limited, and some strains may disrupt key neutralizing epitopes during TABLE 3 Comparison table of core data of different vaccine platforms for EV-D68 Vaccine platform Expression/production system Animal model Cross-neutralization spectrum Protective efficacy in vivo Limitations/future directions Mucosal bivalent inactivated vaccine Vero cell culture, formalin inactivation, ganoderma polysaccharide (PS-G) adjuvant ICR neonatal and adult mice EV-D68 (B1/B3/A2); EV-A71 (multiple subclades) 100% protection in neonates; blocks CNS invasion; mucosal sIgA persists 16–19 weeks Duration of mucosal immunity; pediatric clinical validation needed VLP vaccine (Pichia pastoris) pastoris co-expression of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% survival in neonates (passive and maternal); blocks muscle/spinal cord replication Limited protection vs. B3/D clades; immunization route optimization VLP vaccine (Baculovirus-Insect Cell) Baculovirus/Sf9 co-expres sion of P1 + 3 CD ICR neonatal and adult mice EV-D68 (A/B1/ Fermon) 100% neonatal survival; clears respiratory virus Complex production; immunogenicity in NHPs required Vero-adapted inactivated vaccine Vero cell adaptation, formalin inactivation ± alum adjuvant BALB/c and ICR neonatal mice EV-D68 (A/B1/ Fermon) 100% protection; reduces tissue viral load by 3–6 log Seven adaptive mutations in strain; human dosing studies needed Cotton rat inactivated vaccine HeLa cell culture, live/UV-inactivated virus Sigmodon hispidus (cotton rat) EV-D68 (A1/B1/ATCC prototype) Blocks respiratory replication; reduces lung inflammation; nAbs > 9 weeks Does not induce nAbs; potential immune enhancement risk Rhesus-derived inactivated vaccine Vero cell culture, formalin inactivation, alum adjuvant Rhesus macaque, C57BL/6 neonatal mice EV-D68 (KM/Fermon) 100% neonatal survival via maternal antibodies; prevents paralysis after IC challenge Macaque cohort size; pediatric immunoge nicity validation Month XXXX Volume 0 Issue 0 10.1128/jvi.00123-26 13 D ow nl oa de d fr om h ttp s: //j ou rn al s. as m .o rg /jo ur na l/j vi o n 04 J un e 20 26 b y 21 2. ..



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    Dose-response and fluorescence imaging of antiviral inhibitors with C3SIR biosensor. A Dose-response curves of the C3SIR biosensor for Boceprevir, Telaprevi and Narlaprevir were marked in red. Cell viability (blue) was assessed relative to the solvent (DMSO) control group. IC50 and R-squared values of each inhibitor were estimated via nonlinear regression. B HEK293T cells were transfected with the C3SIR sensor. Culture medium containing inhibitors at concentrations of 50, 20, 10, 5 and 2 μM was added 6 h post-transfection. Fluorescence microscopy images were captured 24 h post-transfection. C Dose-response curves of the C3SIR biosensor for Oseltamivir, Ritonavir and Rupintrivir were marked in red. Cell viability (blue) was assessed relative to the solvent (DMSO) control group. IC50 and R-squared values of each inhibitor were estimated via nonlinear regression. D HEK293T cells were transfected with the C3SIR sensor. Culture medium containing inhibitors at concentrations of 50, 20, 10, 5 and 2 μM was added 6 h post-transfection. Fluorescence microscopy images were captured 24 h post-transfection. IC 50 and R 2 values were estimated via nonlinear regression curve fitting to single experimental data for each inhibitor. All images show the same magnification, scale bar: 1000 μm ( B , D ).

    Journal: Virologica Sinica

    Article Title: A modular APEX biosensor enables sensitive and visualized monitoring of viral protease activity

    doi: 10.1016/j.virs.2026.08.001

    Figure Lengend Snippet: Dose-response and fluorescence imaging of antiviral inhibitors with C3SIR biosensor. A Dose-response curves of the C3SIR biosensor for Boceprevir, Telaprevi and Narlaprevir were marked in red. Cell viability (blue) was assessed relative to the solvent (DMSO) control group. IC50 and R-squared values of each inhibitor were estimated via nonlinear regression. B HEK293T cells were transfected with the C3SIR sensor. Culture medium containing inhibitors at concentrations of 50, 20, 10, 5 and 2 μM was added 6 h post-transfection. Fluorescence microscopy images were captured 24 h post-transfection. C Dose-response curves of the C3SIR biosensor for Oseltamivir, Ritonavir and Rupintrivir were marked in red. Cell viability (blue) was assessed relative to the solvent (DMSO) control group. IC50 and R-squared values of each inhibitor were estimated via nonlinear regression. D HEK293T cells were transfected with the C3SIR sensor. Culture medium containing inhibitors at concentrations of 50, 20, 10, 5 and 2 μM was added 6 h post-transfection. Fluorescence microscopy images were captured 24 h post-transfection. IC 50 and R 2 values were estimated via nonlinear regression curve fitting to single experimental data for each inhibitor. All images show the same magnification, scale bar: 1000 μm ( B , D ).

    Article Snippet: The C3SIR (EV-71) biosensor was validated with Rupintrivir (TargetMOI).

    Techniques: Fluorescence, Imaging, Solvent, Control, Transfection, Microscopy