Vaccine Development for Toxoplasmosis

A special issue of Vaccines (ISSN 2076-393X). This special issue belongs to the section "Vaccines against (re)emerging and Tropical Infections Diseases".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 5140

Special Issue Editor


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Guest Editor
UCIBIO/REQUIMTE, Departamento de Ciências Biológicas, Faculdade de Farmácia, Universidade do Porto, Porto, Portugal
Interests: toxoplasmosis; immunopathology; drug discovery; vaccines; maternal-fetal
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Special Issue Information

Dear Colleagues,

Toxoplasmosis is a disease caused by Toxoplasma gondii, an obligate intracellular protozoan, exerting a high impact on human health worldwide. This disease may result in serious complications for the fetus, newborn, and immunocompromised individuals. T. gondii infection affects immunocompromised individuals (cancer patients, HIV-seropositive persons and transplanted individuals) causing serious health issues such as encephalitis, pneumonia and even death. When primo infection occurs during the first trimester of pregnancy, diverse clinical manifestations may occur, such as abortion, stillbirth or premature birth. If transmission occurs at later stages of pregnancy, the risk of congenital disease is increased leading to neonatal malformations that are severe enough to ultimately result in blindness, chorioretinitis, mental retardation, heart and brain defects, permanent neurological damage, and even death. Recent data suggest an association between congenital infection and the development of neurological and psychiatric disorders later in life, including schizophrenia, Alzheimer’s disease, bipolar disease, and even suicidal tendencies. 

Current treatment options are old, limited, and possess toxic side effects. Furthermore, pre-natal and post-natal treatment reduces the possibility of congenital transmission and sequela but does not avoid it. Long treatment durations are required since current therapeutic drugs lack efficiency against T. gondii tissue cysts, promoting the establishment of latent infection. At present, no vaccine exists to prevent human disease caused by T. gondii, thus demand for a vaccine presenting complete and lasting protection against toxoplasmosis is urgent. 

This research topic will include contributions that highlight advances and challenges regarding the development of a novel prophylactic vaccine for toxoplasmosis. Research areas in this field may include (but are not limited to) the following: nanotechnology application to nanovaccines development; establishment of in vitro and/or in vivo study models for testing new vaccine formulations; immune responses induced to experimental vaccines; nasal immunization; identification of immune mechanisms induced by vaccination and related to protection against infection; vaccines in congenital toxoplasmosis.

I am pleased to invite you to contribute with original research articles or reviews. 

I look forward to receiving your contributions.

Dr. Margarida Borges
Guest Editor

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Keywords

  • toxoplasmosis
  • vaccines
  • immunotherapy
  • nanotechnology

Published Papers (2 papers)

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Research

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12 pages, 1783 KiB  
Article
Boosting Mouse Defense against Lethal Toxoplasma gondii Infection with Full-Length and Soluble SAG1 Recombinant Protein
by Xiang Li, Wei Yuan, Ting He, Ruiying Guo, Xiuxian Du, Yanhong He, Xuan Li, Saeed El-Ashram, Ebtesam M. Al-Olayan, Na Yang and Xiaoyu Sang
Vaccines 2023, 11(11), 1678; https://doi.org/10.3390/vaccines11111678 - 2 Nov 2023
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Abstract
Toxoplasmosis is a major worldwide protozoan zoonosis. The surface antigen 1 (SAG1) of Toxoplasma gondii (T. gondii) has always been recognized as an ideal vaccine candidate antigen. However, the intact and soluble SAG1 protein is usually difficult to acquire in vitro, [...] Read more.
Toxoplasmosis is a major worldwide protozoan zoonosis. The surface antigen 1 (SAG1) of Toxoplasma gondii (T. gondii) has always been recognized as an ideal vaccine candidate antigen. However, the intact and soluble SAG1 protein is usually difficult to acquire in vitro, which is unfavorable for employing the recombinant protein as a vaccine candidate antigen. In the present study, we obtained the full-length SAG1 recombinant protein in soluble form by Escherichia coli Transetta (DE3) cells under optimized expression conditions. The immunogenicity and protective ability of this recombinant protein against T. gondii acute infection were evaluated in a mouse model. Monitoring changes in serum antibody levels and types, the presence of cytokines, and the rate of lymphocyte proliferation in vaccinated mice were used to assess humoral and cellular immune responses. Additional assessments were performed to determine the protective potency of the recombinant protein in combating T. gondii RH tachyzoites. It was found that the titers of both IgG2a and IgG2b were considerably greater in the immunized mice compared to the titers of IgG1 and IgG3. The levels of Th1-type cytokines (IFN-γ, IL-12p70, IL-2, and TNF-α) and Th2-type cytokines (IL-10) significantly increased when splenocytes from immunological group mice were treated with T. gondii lysate antigen. Compared to the control group, a recombinant protein substantially increased the longevity of infected mice, with an average death time prolonged by 14.50 ± 0.34 days (p < 0.0001). These findings suggest that the full-length and soluble SAG1 recombinant protein produced potent immune responses in mice and could be a preferred subunit vaccine candidate for T. gondii, offering a feasible option for vaccination against acute toxoplasmosis. Full article
(This article belongs to the Special Issue Vaccine Development for Toxoplasmosis)
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Review

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17 pages, 1206 KiB  
Review
Nanoparticles as a Delivery System of Antigens for the Development of an Effective Vaccine against Toxoplasma gondii
by Carina Brito, Camila Lourenço, Joana Magalhães, Salette Reis and Margarida Borges
Vaccines 2023, 11(4), 733; https://doi.org/10.3390/vaccines11040733 - 25 Mar 2023
Cited by 2 | Viewed by 2465
Abstract
Nanoparticles include particles ranging in size from nanometers to micrometers, whose physicochemical characteristics are optimized to make them appropriate delivery vehicles for drugs or immunogens important in the fight and/or prevention of infectious diseases. There has been a rise in the use of [...] Read more.
Nanoparticles include particles ranging in size from nanometers to micrometers, whose physicochemical characteristics are optimized to make them appropriate delivery vehicles for drugs or immunogens important in the fight and/or prevention of infectious diseases. There has been a rise in the use of nanoparticles in preventive vaccine formulations as immunostimulatory adjuvants, and as vehicles for immunogen delivery to target immune cells. Toxoplasma is important worldwide, and may cause human toxoplasmosis. In immunocompetent hosts, infection is usually asymptomatic, but in immunocompromised patients it can cause serious neurological and ocular consequences, such as encephalitis and retinochoroiditis. Primary infection during pregnancy may cause abortion or congenital toxoplasmosis. Currently, there is no effective human vaccine against this disease. Evidence has emerged from several experimental studies testing nanovaccines showing them to be promising tools in the prevention of experimental toxoplasmosis. For the present study, a literature review was carried out on articles published over the last 10 years through the PubMed database, pertaining to in vivo experimental models of T. gondii infection where nanovaccines were tested and protection and immune responses evaluated. This review aims to highlight the way forward in the search for an effective vaccine for toxoplasmosis. Full article
(This article belongs to the Special Issue Vaccine Development for Toxoplasmosis)
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