Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only

Novel adjuvants present a concern for adverse effects, generating a need for alternatives. Rotavirus inner capsid VP6 protein could be considered a potential candidate, due to its ability to self-assemble into highly immunogenic nanospheres and nanotubes. These nanostructures exhibit immunostimulato...

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Main Authors: Suvi Heinimäki, Kirsi Tamminen, Vesa P. Hytönen, Maria Malm, Vesna Blazevic
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/8/3/365
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author Suvi Heinimäki
Kirsi Tamminen
Vesa P. Hytönen
Maria Malm
Vesna Blazevic
author_facet Suvi Heinimäki
Kirsi Tamminen
Vesa P. Hytönen
Maria Malm
Vesna Blazevic
author_sort Suvi Heinimäki
collection DOAJ
description Novel adjuvants present a concern for adverse effects, generating a need for alternatives. Rotavirus inner capsid VP6 protein could be considered a potential candidate, due to its ability to self-assemble into highly immunogenic nanospheres and nanotubes. These nanostructures exhibit immunostimulatory properties, which resemble those of traditional adjuvants, promoting the uptake and immunogenicity of the co-administered antigens. We have previously elucidated an adjuvant effect of VP6 on co-delivered norovirus and coxsackievirus B1 virus-like particles, increasing humoral and cellular responses and sparing the dose of co-delivered antigens. This study explored an immunostimulatory effect of VP6 nanospheres on smaller antigens, P particles formed by protruding domain of a norovirus capsid protein and a short peptide, extracellular matrix protein (M2e) of influenza A virus. VP6 exhibited a notable improving impact on immune responses induced by P particles in immunized mice, including systemic and mucosal antibody and T cell responses. The adjuvant effect of VP6 nanospheres was comparable to the effect of alum, except for induction of superior mucosal and T cell responses when P particles were co-administered with VP6. However, unlike alum, VP6 did not influence M2e-specific immune responses, suggesting that the adjuvant effect of VP6 is dependent on the particulate nature of the co-administered antigen.
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spelling doaj.art-c80a5462ef0e4bab93b087dc49dbcc9e2023-11-20T06:05:22ZengMDPI AGVaccines2076-393X2020-07-018336510.3390/vaccines8030365Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens OnlySuvi Heinimäki0Kirsi Tamminen1Vesa P. Hytönen2Maria Malm3Vesna Blazevic4Vaccine Development and Immunology/Vaccine Research Center, Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, FinlandVaccine Development and Immunology/Vaccine Research Center, Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, FinlandProtein Dynamics Group, Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, FinlandVaccine Development and Immunology/Vaccine Research Center, Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, FinlandVaccine Development and Immunology/Vaccine Research Center, Faculty of Medicine and Health Technology, Tampere University, 33520 Tampere, FinlandNovel adjuvants present a concern for adverse effects, generating a need for alternatives. Rotavirus inner capsid VP6 protein could be considered a potential candidate, due to its ability to self-assemble into highly immunogenic nanospheres and nanotubes. These nanostructures exhibit immunostimulatory properties, which resemble those of traditional adjuvants, promoting the uptake and immunogenicity of the co-administered antigens. We have previously elucidated an adjuvant effect of VP6 on co-delivered norovirus and coxsackievirus B1 virus-like particles, increasing humoral and cellular responses and sparing the dose of co-delivered antigens. This study explored an immunostimulatory effect of VP6 nanospheres on smaller antigens, P particles formed by protruding domain of a norovirus capsid protein and a short peptide, extracellular matrix protein (M2e) of influenza A virus. VP6 exhibited a notable improving impact on immune responses induced by P particles in immunized mice, including systemic and mucosal antibody and T cell responses. The adjuvant effect of VP6 nanospheres was comparable to the effect of alum, except for induction of superior mucosal and T cell responses when P particles were co-administered with VP6. However, unlike alum, VP6 did not influence M2e-specific immune responses, suggesting that the adjuvant effect of VP6 is dependent on the particulate nature of the co-administered antigen.https://www.mdpi.com/2076-393X/8/3/365adjuvantalumVP6nanostructureP particlepeptide
spellingShingle Suvi Heinimäki
Kirsi Tamminen
Vesa P. Hytönen
Maria Malm
Vesna Blazevic
Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only
Vaccines
adjuvant
alum
VP6
nanostructure
P particle
peptide
title Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only
title_full Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only
title_fullStr Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only
title_full_unstemmed Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only
title_short Rotavirus Inner Capsid VP6 Acts as an Adjuvant in Formulations with Particulate Antigens Only
title_sort rotavirus inner capsid vp6 acts as an adjuvant in formulations with particulate antigens only
topic adjuvant
alum
VP6
nanostructure
P particle
peptide
url https://www.mdpi.com/2076-393X/8/3/365
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