Mucosal Immunity
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Mucosal Immunity
The largest immune tissue in the body
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An intranasal live-attenuated SARS-CoV-2 vaccine limits virus transmission | Nature Communications

An intranasal live-attenuated SARS-CoV-2 vaccine limits virus transmission | Nature Communications | Mucosal Immunity | Scoop.it
The development of effective SARS-CoV-2 vaccines has been essential to control COVID-19, but significant challenges remain. One problem is intramuscular administration, which does not induce robust mucosal immune responses in the upper airways—the primary site of infection and virus shedding. Here we compare the efficacy of a mucosal, replication-competent yet fully attenuated virus vaccine, sCPD9-ΔFCS, and the monovalent mRNA vaccine BNT162b2 in preventing transmission of SARS-CoV-2 variants B.1 and Omicron BA.5 in two scenarios. Firstly, we assessed the protective efficacy of the vaccines by exposing vaccinated male Syrian hamsters to infected counterparts. Secondly, we evaluated transmission of the challenge virus from vaccinated and subsequently challenged male hamsters to naïve contacts. Our findings demonstrate that the live-attenuated vaccine (LAV) sCPD9-ΔFCS significantly outperformed the mRNA vaccine in preventing virus transmission in both scenarios. Our results provide evidence for the advantages of locally administered LAVs over intramuscularly administered mRNA vaccines in preventing infection and reducing virus transmission. In this study, the authors evaluated the protective capacity of a mucosal, live-attenuated SARS-CoV-2 vaccine and show that it induces systemic and mucosal humoral immunity, protects from clinical disease symptoms, and prevents virus transmission in hamsters more efficiently than an intramuscular mRNA vaccine.
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A novel dry powder inhaled vaccine platform

A novel dry powder inhaled vaccine platform | Mucosal Immunity | Scoop.it
Scientists proposed a new nano-micro composite delivery concept for vaccines- combines biodegradable microspheres with protein nanoparticles.
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Oral vaccination of wildlife using a vaccinia–rabies-glycoprotein recombinant virus vaccine (RABORAL V-RG ® ): a global review

Oral vaccination of wildlife using a vaccinia–rabies-glycoprotein recombinant virus vaccine (RABORAL V-RG ® ): a global review | Mucosal Immunity | Scoop.it
RABORAL V-RG® is an oral rabies vaccine bait that contains an attenuated (“modified-live”) recombinant vaccinia virus vector vaccine expressing the rabies virus glycoprotein gene (V-RG). Approximately 250 million doses have been distributed globally since 1987 without any reports of adverse reactions in wildlife or domestic animals since the first licensed recombinant oral rabies vaccine (ORV) was released into the environment to immunize wildlife populations against rabies. V-RG is genetically stable, is not detected in the oral cavity beyond 48 h after ingestion, is not shed by vaccinates into the environment, and has been tested for thermostability under a range of laboratory and field conditions. Safety of V-RG has been evaluated in over 50 vertebrate species, including non-human primates, with no adverse effects observed regardless of route or dose. Immunogenicity and efficacy have been demonstrated under laboratory and field conditions in multiple target species (including fox, raccoon, coyote, skunk, raccoon dog, and jackal). The liquid vaccine is packaged inside edible baits (i.e., RABORAL V-RG, the vaccine-bait product) which are distributed into wildlife habitats for consumption by target species. Field application of RABORAL V-RG has contributed to the elimination of wildlife rabies from three European countries (Belgium, France and Luxembourg) and of the dog/coyote rabies virus variant from the United States of America (USA). An oral rabies vaccination program in west-central Texas has essentially eliminated the gray fox rabies virus variant from Texas with the last case reported in a cow during 2009. A long-term ORV barrier program in the USA using RABORAL V-RG is preventing substantial geographic expansion of the raccoon rabies virus variant. RABORAL V-RG has also been used to control wildlife rabies in Israel for more than a decade. This paper: (1) reviews the development and historical use of RABORAL V-RG; (2) highlights wildlife rabies control programs using the vaccine in multiple species and countries; and (3) discusses current and future challenges faced by programs seeking to control or eliminate wildlife rabies.
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Antibody Secreting Cell Responses following Vaccination with Bivalent Oral Cholera Vaccine among Haitian Adults. - PubMed - NCBI

PLoS Negl Trop Dis. 2016 Jun 16;10(6):e0004753. doi: 10.1371/journal.pntd.0004753. eCollection 2016. Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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Mucosal Vaccine Development Based on Liposome Technology

Mucosal Vaccine Development Based on Liposome Technology | Mucosal Immunity | Scoop.it
Immune protection against infectious diseases is most effective if located at the portal of entry of the pathogen. Hence, there is an increasing demand for vaccine formulations that can induce strong protective immunity following oral, respiratory, or genital tract administration. At present, only few mucosal vaccines are found on the market, but recent technological advancements and a better understanding of the principles that govern priming of mucosal immune responses have contributed to a more optimistic view on the future of mucosal vaccines. Compared to live attenuated vaccines, subcomponent vaccines, most often protein-based, are considered safer, more stable, and less complicated to manufacture, but they require the addition of nontoxic and clinically safe adjuvants to be effective. In addition, another limiting factor is the large antigen dose that usually is required for mucosal vaccines. Therefore, the combination ofmucosal adjuvantswith the recent progress in nanoparticle technology provides an attractive solution to these problems. In particular, the liposome technology is ideal for combining protein antigen and adjuvant into an effective mucosal vaccine. Here, we describe and discuss recent progress in nanoparticle formulations using various types of liposomes that convey strong promise for the successful development of the next generation of mucosal vaccines.
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Mucosal Immunity

is the most recent part of Immunology!

It appeared less than 40 years ago, while systemic immunity exploded 60  years ago.

It is still a minor part of Immunology teaching and research, while the mucosal immune system is at the frontline of encounters with germs, antigens... in other words the environment.

 

major keywords:

> 450 posts IgA http://www.scoop.it/t/mucosal-immunity?q=IgA

> 125 posts tolerance http://www.scoop.it/t/mucosal-immunity?q=tolerance

> 400 posts : microbiome http://www.scoop.it/t/mucosal-immunity?q=microbiome

 

july 2015: almost 2100 scoops, >1700 visitors, >3900 views

november 2017 >10K views of >3300 scoops

june 2020 >17.6K views, >5.5K visitors,  >4.5K scoops

may 2024 >22K views, >6.9 visitors,  >5.2 scoops

Gilbert C FAURE's insight:

This topic complements the more general Immunology topic.

 http://www.scoop.it/t/immunology

 

It includes also reproductive immunology (#100posts) searchable on

http://www.scoop.it/t/mucosal-immunity?q=reproductive

https://www.scoop.it/t/mucosal-immunity/?&tag=REPRODUCTION

 

and  also covers lung immunology (>325 posts)

http://www.scoop.it/t/mucosal-immunity?q=lung

 

Covid (>200 posts) can be found on 

https://www.scoop.it/topic/mucosal-immunity?q=covid

 

Vaccines are available on

https://www.scoop.it/topic/mucosal-immunity?q=vaccines

 

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Creating new non-influenza vaccines: an interview with Julie Phillips, CEO of ... - News-Medical.net

Creating new non-influenza vaccines: an interview with Julie Phillips, CEO of ... - News-Medical.net | Mucosal Immunity | Scoop.it
Creating new non-influenza vaccines: an interview with Julie Phillips, CEO of ...News-Medical.netThe intranasal vaccine triggers a rapid immune response in the mucosal lining of nose and the pharynx and systemically in the blood.
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Novel nasal COVID-19 vaccine offers longer, better immunity than jabs

Novel nasal COVID-19 vaccine offers longer, better immunity than jabs | Mucosal Immunity | Scoop.it
Researchers have developed a novel intranasal COVID-19 vaccine that enhances the immune system’s response to the virus, providing longer-lasting, greater protection than vaccine injections, even against new and emerging variants.
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Single-dose vaccine could provide faster protection in cholera epidemics

Single-dose vaccine could provide faster protection in cholera epidemics | Mucosal Immunity | Scoop.it
Each year there are more than three million cases of cholera worldwide, a disease transmitted through contaminated food and water that hits developing countries particularly hard. While the standard regimen for protectin
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Extending The Range Of Diseases Covered By A Rice-Based Vaccine

Extending The Range Of Diseases Covered By A Rice-Based Vaccine | Mucosal Immunity | Scoop.it
Astellas and the Institute of Medical Science at the University of Tokyo are expanding the range of diseases that can be covered by their rice-based oral vaccine, MucoRice.
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Rationalized design of a mucosal vaccine protects against Mycobacterium tuberculosis challenge in mice. - PubMed - NCBI

Rationalized design of a mucosal vaccine protects against Mycobacterium tuberculosis challenge in mice. - PubMed - NCBI | Mucosal Immunity | Scoop.it
J Leukoc Biol. 2017 Mar 3. pii: jlb.4A0616-270R. doi: 10.1189/jlb.4A0616-270R. [Epub ahead of print]
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Frontiers | Sublingual Priming with a HIV gp41-Based Subunit Vaccine Elicits Mucosal Antibodies and Persistent B Memory Responses in Non-Human Primates | Mucosal Immunity

Frontiers | Sublingual Priming with a HIV gp41-Based Subunit Vaccine Elicits Mucosal Antibodies and Persistent B Memory Responses in Non-Human Primates | Mucosal Immunity | Mucosal Immunity | Scoop.it
Persistent B cell responses in mucosal tissues are crucial to control infection against sexually transmitted pathogens like Human Immunodeficiency Virus 1 (HIV-1). The genital tract is a major site of infection by HIV. Sublingual immunization in mice was previously shown to generate HIV-specific B cell immunity that disseminates to the genital tract. We report here the immunogenicity in female cynomolgus macaques of a sublingual vaccine based on a modified gp41 polypeptide coupled to the cholera toxin B subunit designed to expose hidden epitopes and to improve mucosal retention. Combined sublingual/intramuscular immunization with such muco-adhesive gp41-based vaccine elicited mucosal HIV-specific IgG and IgA antibodies more efficiently than intramuscular immunization alone. This strategy increased the number and duration of gp41-specific IgA secreting cells. Importantly, combined immunization improved the generation of functional antibodies three months after vaccination as detected in HIV-neutralizing assays. Therefore, sublingual immunization represents a promising vaccine strategy to block HIV-1 transmission.
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Recent progress in mucosal vaccine development: potential and ...

Nature Reviews Immunology August 2012 Vol 12 No 8 http://www.nature.com/nri/journal/v12/n7/index.html Recent progress in mucosal vaccine development: potential and limitations Nils Lycke p592 | doi:10.1038/nri3251 ...
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