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Updated: Jun 25, 2026

Expression and Purification of Virus-like Particles for Vaccination
Published on: June 2, 2016
Vaccine progress
James I Ito1, Joseph M Lyons, Diana Diaz-Arevalo
1Division of Infectious Diseases, City of Hope National Medical Center, 1500 E. Duarte Road, Duarte, CA 91010-3000, USA. jito@coh.org
Abstract:
Despite the recent development of new anti-mould agents, there remains a significant incidence of invasive aspergillosis in the most immunocompromised hosts and the response to these agents is still dismal. There is a need for a different approach: prevention by vaccination. We have demonstrated that a hyphal sonicate of Aspergillus fumigatus was capable of conferring protection against subsequent invasive pulmonary aspergillosis in corticosteroid immunosuppressed mice. Subcutaneous vaccination was superior to nasal vaccination. Mice exposed intranasally to viable conidia were noted to respond serologically to a 19 kDa protein. This protein was identified as the allergen Asp f 3 by mass spectrometry. Vaccination with recombinant Asp f 3 was protective. Truncated forms of Asp f 3 that lacked either one of the two known IgE binding sites were cloned and also demonstrated protection against aspergillosis. Although all of these recombinant proteins required an adjuvant (TiterMax) for efficacy, a particulate preparation of rAsp f 3 was also found to be protective without requiring adjuvant. At least two T-cell epitopes (11-mer and 13-mer) have been identified in Asp f 3. There are homologues of Asp f 3 in other Aspergillus species as well as in other moulds (Coccidioides posadasii, Penicillium citrinum) and yeasts (Candida albicans, C. boidinii, Saccharomyces cerevisiae). Asp f 3, truncated non-allergenic versions of Asp f 3, and T-cells epitopes of Asp f 3 are potential candidates for vaccines potentially capable of protecting immunocompromised hosts against invasive aspergillosis.
Insights
Developing a novel vaccine against invasive aspergillosis is crucial for immunocompromised patients. Research shows that targeting the Aspergillus fumigatus allergen Asp f 3, particularly its T-cell epitopes, offers promising protection.
Area of Science:
- Mycology
- Immunology
- Vaccine Development
Background:
- Invasive aspergillosis remains a threat to immunocompromised individuals, with limited treatment efficacy.
- Current anti-mould agents show dismal responses in high-risk populations.
- Vaccination presents a potential alternative strategy for preventing invasive aspergillosis.
Purpose of the Study:
- To investigate the potential of Aspergillus fumigatus components as vaccine candidates.
- To evaluate the protective efficacy of Asp f 3 and its derivatives against invasive pulmonary aspergillosis.
- To identify potential vaccine targets for protecting immunocompromised hosts.
Main Methods:
- Immunization of corticosteroid-immunosuppressed mice with Aspergillus fumigatus hyphal sonicate and recombinant Asp f 3.
- Mass spectrometry to identify serologically recognized proteins.
- Cloning and testing of truncated Asp f 3 variants and T-cell epitopes.
- Evaluation of adjuvant requirements and particulate vaccine formulations.
Main Results:
- Subcutaneous vaccination with hyphal sonicate conferred protection against invasive pulmonary aspergillosis.
- The 19 kDa protein, identified as Asp f 3, was a key target for serological response.
- Recombinant Asp f 3, including truncated non-allergenic forms and T-cell epitopes, demonstrated protective efficacy, with particulate rAsp f 3 being effective without adjuvant.
- Homologues of Asp f 3 exist in other fungal species.
Conclusions:
- Asp f 3 and its modified forms (truncated, T-cell epitopes) are promising vaccine candidates.
- Vaccination strategies targeting Asp f 3 could protect immunocompromised hosts from invasive aspergillosis.
- Further development of Asp f 3-based vaccines may offer a new preventative approach.
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