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Vaccine2000; 19(4-5); 492-497; doi: 10.1016/s0264-410x(00)00187-0

Induction of mucosal and systemic antibody specific for SeMF3 of Streptococcus equi by intranasal vaccination using a sucrose acetate isobutyrate based delivery system.

Abstract: Streptococcus equi causes equine strangles, a highly contagious disease of the upper respiratory tract. The antiphagocytic surface protein SeM is strongly immunogenic and evokes mucosal and systemic antibodies during convalescence. The present study investigated the potential of sucrose acetate isobutyrate (SAIB); a high viscosity excipient that provides controlled release of biologically active substances, to enhance antibody responses following intranasal immunization of horses with a 108 a.a. peptide of SeM (SeMF3). SeMF3-SAIB was administered intranasally to each of the 11 adult horses on days 0 and 28. A second group of seven horses was vaccinated with SeMF3 alone. SAIB enhanced the mucosal and systemic immunogenicity of SeMF3, whereas SeMF3 by itself stimulated only a shortlived mucosal IgA and no systemic response. Moreover, nasal mucosal responses of horses immunized with SeMF3-SAIB were qualitatively and quantitatively similar to those observed in convalescent horses and involved similar linear epitopes of SeM. Epitope analysis also suggested that the nasal response was different from that observed in serum. A booster response was obtained after the second vaccination. These results suggest that SAIB has potential as a vehicle for intranasal immunization of horses with antigenic peptides.
Publication Date: 2000-10-12 PubMed ID: 11027813DOI: 10.1016/s0264-410x(00)00187-0Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research explores how use of a substance called sucrose acetate isobutyrate (SAIB) can enhance the immune response in horses vaccinated against Streptococcus equi, the bacterium causing the respiratory infection equine strangles. The method involves intranasal administration of the vaccine.

Introduction and Background

  • The study is focused on the bacterial disease equine strangles, which affects the upper respiratory tract of horses. It is caused by the bacterium Streptococcus equi. This disease is highly contagious and results in a powerful immune response.
  • One of the surface proteins of the bacteria, SeM, is an important part of this immune response, helping to trigger both mucosal and systemic antibodies – important components of the immune system.

Methodology

  • The research explores the potential of a high viscosity substance called sucrose acetate isobutyrate (SAIB) to improve the antibody response generated by intranasal immunisation with a peptide of the SeM protein, called SeMF3.
  • SAIB works by providing a controlled release of the biologically active substance (in this case, the SeMF3 peptide). This is administered via the nose to 11 horses on two separate occasions (on day 0 and day 28), while a second group of seven horses are given the SeMF3 peptide without SAIB.

Findings

  • The study found that SAIB allowed for a more powerful immune response than just the SeMF3 peptide on its own. SeMF3 by itself only prompted a short-term IgA response in the mucosa (an essential antibody for immune response), and did not stimulate a system-wide immune response.
  • Samples taken from the nasal mucosa of horses vaccinated with SeMF3 and SAIB showed this approach triggered both a quantitative and qualitative response similar to what is seen in horses recovering naturally from the disease. This response included the activation of similar linear epitopes of SeM (regions of the protein which antibodies bind to).
  • Epitope analysis also suggested a difference between the nasal and systemic response, indicating the mucosal response as potentially more targeted.
  • Upon a second vaccination, a booster response was observed, suggesting the intranasal delivery and usage of SAIB elicited a robust immunological response.

Conclusion

  • The study concluded that using SAIB as a delivery system for intranasal immunisation has potential for improving the vaccine’s efficacy against Streptococcus equi. This offers hope for better prevention and control of equine strangles.

Cite This Article

APA
Nally JE, Artiushin S, Sheoran AS, Burns PJ, Simon B, Gilley RM, Gibson J, Sullivan S, Timoney JF. (2000). Induction of mucosal and systemic antibody specific for SeMF3 of Streptococcus equi by intranasal vaccination using a sucrose acetate isobutyrate based delivery system. Vaccine, 19(4-5), 492-497. https://doi.org/10.1016/s0264-410x(00)00187-0

Publication

ISSN: 0264-410X
NlmUniqueID: 8406899
Country: Netherlands
Language: English
Volume: 19
Issue: 4-5
Pages: 492-497

Researcher Affiliations

Nally, J E
  • 108 Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington, KY 40546-0099, USA.
Artiushin, S
    Sheoran, A S
      Burns, P J
        Simon, B
          Gilley, R M
            Gibson, J
              Sullivan, S
                Timoney, J F

                  MeSH Terms

                  • Administration, Intranasal
                  • Amino Acid Sequence
                  • Animals
                  • Antibodies, Bacterial / biosynthesis
                  • Antigens, Bacterial / genetics
                  • Bacterial Proteins / genetics
                  • Bacterial Proteins / immunology
                  • Bacterial Vaccines / administration & dosage
                  • Drug Delivery Systems
                  • Female
                  • Horse Diseases / prevention & control
                  • Horses
                  • Immunity, Mucosal
                  • Immunoglobulin A / biosynthesis
                  • Immunoglobulin G / biosynthesis
                  • Molecular Sequence Data
                  • Streptococcal Infections / prevention & control
                  • Streptococcal Infections / veterinary
                  • Streptococcus equi / immunology
                  • Sucrose / analogs & derivatives
                  • Vaccines, Synthetic / administration & dosage

                  Citations

                  This article has been cited 3 times.
                  1. Haider M, Elsayed I, Ahmed IS, Fares AR. In Situ-Forming Microparticles for Controlled Release of Rivastigmine: In Vitro Optimization and In Vivo Evaluation. Pharmaceuticals (Basel) 2021 Jan 14;14(1).
                    doi: 10.3390/ph14010066pubmed: 33466880google scholar: lookup
                  2. Flock M, Jacobsson K, Frykberg L, Hirst TR, Franklin A, Guss B, Flock JI. Recombinant Streptococcus equi proteins protect mice in challenge experiments and induce immune response in horses. Infect Immun 2004 Jun;72(6):3228-36.
                  3. Bowersock TL. Evolving importance of biologics and novel delivery systems in the face of microbial resistance. AAPS PharmSci 2002;4(4):E33.
                    doi: 10.1208/ps040433pubmed: 12646005google scholar: lookup