98%
921
2 minutes
20
Avian colibacillosis, mainly caused by avian pathogenic Escherichia coli (APEC), is one of the most prominent diseases in the poultry industry. Inactivated vaccines are crucial for preventing and controlling APEC infection, with adjuvants playing a key role in ensuring their effectiveness. However, traditional oil-emulsion inactivated vaccines often cause severe adverse reactions in animals. Based on the serogroups of 343 clinically isolated APEC strains from many provinces of China, O36, O78 and O109 were identified as the predominant serogroups currently circulating in these regions, with O36 and O109 being rarely noticed before. Consequently, we further screened these three dominant serogroups for their promising immunogenicity to develop effective inactivated vaccines. The immune side effects of 7 adjuvants including water-in-oil emulsions (Marc-52, ISA 71 VG, and ISA 78 VG), water-in-oil-in-water emulsions (ADJ 501 and HMT 13), oil-in-water emulsion (ADJ 2052), and aluminum hydroxide gels were evaluated and compared. The results showed that the vaccine formulated with HMT 13 as an adjuvant exhibited sufficient protective efficacy against homotypic APEC infection while effectively stimulating humoral and cellular immune responses. Moreover, inactivated vaccines containing HMT 13 could be easily absorbed at the inoculation site without interfering with chicken growth; they also possessed favorable emulsification properties facilitating storage. Therefore, HMT 13 represents an excellent adjuvant for developing an inactivated vaccine against chicken colibacillosis. This study presents a novel multivalent inactivated vaccine against chicken colibacillosis based on the use of HMT13 as an adjuvant, which offers a new approach for the prevention and control of APEC currently prevalent in most of China.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12008629 | PMC |
http://dx.doi.org/10.1016/j.psj.2025.105097 | DOI Listing |
Int J Dermatol
September 2025
Pfizer S.L.U, Madrid, Spain.
Atopic dermatitis therapy has undergone a revolutionary change with the introduction of Janus kinase (JAK) inhibitors. Despite their general safety profile, these immunomodulatory drugs require special precautions with respect to infection risk and vaccine administration. This document aims to provide dermatologists and other healthcare practitioners with comprehensive practical vaccination recommendations for adults and adolescent patients with atopic dermatitis who are receiving or are about to receive treatment with JAK inhibitors.
View Article and Find Full Text PDFEur Heart J Open
September 2025
Department of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, Copenhagen, Gentofte Hospitalsvej 8, 2900 Hellerup, Denmark.
Aims: Atrial fibrillation (AF) may be associated with adverse influenza-related outcomes. We assessed the relative vaccine effectiveness (rVE) of high-dose (HD-IIV) vs. standard-dose (SD-IIV) inactivated influenza vaccination against cardiovascular and all-cause hospitalizations and all-cause mortality according to history of AF.
View Article and Find Full Text PDFJ Biomed Sci
September 2025
Virology and Vaccine Immunology, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Background: Enteroviruses, including Coxsackie B (CVB) viruses, can cause severe diseases such as myocarditis, pancreatitis, and meningitis. Vaccines can prevent these complications, but conserved non-neutralizing epitopes in the viral capsid may limit their effectiveness. The immunodominant PALXAXETG motif, located in the VP1 N-terminus, is a highly conserved region in enteroviruses that elicits non-neutralizing antibody responses.
View Article and Find Full Text PDFFront Vet Sci
August 2025
College of Veterinary Medicine, China Agricultural University, Beijing, China.
Introduction: This study investigated the mucosal immunoadjuvant effects of Gynostemma Pentaphyllum Extract (Gynostemma P.E), the bioactive constituents of , against porcine epidemic diarrhea virus (PEDV).
Methods: Twenty-four mice were randomly divided into four groups: a negative control group (intranasal administration of antigen only), a Gynostemma P.
Front Immunol
September 2025
Bacterial Scientific Area, GSK Vaccine, Siena, Italy.
Background: Protein-polysaccharide conjugate vaccines rely on the induction of T-cell-dependent responses that support germinal center (GC) reactions to potentiate the expansion of antigen-specific memory B-cell (MBC) populations and high-avidity antibody responses. The effects of adjuvants on B-cell and antibody responses are well described for protein antigens but remain largely unexplored for conjugated polysaccharidic antigens.
Methods: We assessed the effects of five adjuvants present in licensed vaccines (AS01, AS03, AS04, and aluminum hydroxide [Alum]) or under clinical evaluation (AS37) on the magnitude and quality of antigen-specific antibody responses and local/systemic B-cell responses.