Atomic Layering Thermostable Antigen and Adjuvant (ALTA ® ) platform provides unique antigen delivery system through controlled release to improve immune response to vaccination

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Authors: Keith A. Strand, Heather D’Angelo, Ashley M Gerwing, Isabella R. Walters, Emma Snyder, Alyssa M Ritter, Emily M. Hite, Yalini H. Wijesundara, Annie B Caplan, Daria Leonidovna Ivanova, Isabella Allen, Yu Han
+4 more Lorena R. Antúnez, Antu Dey, Bryan L. Steadman, Sky W. Brubaker
Cited by: 1
References: 18

Abstract

Abstract Prophylactic vaccines are commonly delivered using a multi-dose regimen with the goal of generating potent, durable protection against a specific pathogen. However, the requirement for multiple administrations can impede patient adherence and reduce overall protection. Designing a single-shot vaccine without compromising efficacy could significantly improve vaccine adherence and performance. Previously, it has been shown that atomic-layer deposition (ALD) of alumina (Al 2 O 3 ) can be applied to spray dried, thermostabilized antigen-containing powders to produce alumina-coated vaccine particles that, when compared to a liquid control, elicit improved humoral immunity with response kinetics controlled by ALD-coat thickness. However, previous studies have not defined the particle release/antigen delivery profile of ALD-coated vaccines. The studies in this manuscript were designed to investigate how the kinetics of antigen release from ALD-coated vaccines impacts the timing and magnitude of the immune response relative to single- and multi-dose liquid vaccine regimens using two distinct antigens, Ovalbumin and the HIV-1 envelope trimer, N332-GT5 gp140. By combining longitudinal in vivo imaging and immunological readouts, we demonstrate that ALD-coated vaccines exhibit tunable, variable-rate release and deliver antigen in a unique, prolonged manner that results in an improved immune response to single-shot vaccination for difficult to target pathogens, such as HIV-1. Furthermore, using in vitro analytical methods, we confirmed the ability of our Atomic Layering and Thermostable Antigen and Adjuvant (ALTA ® ) platform to impart thermostability upon the N332-GT5 gp140 antigen, a clinically relevant HIV-1 immunogen, indicating the potential for ALTA ® formulation to generate thermostable, single-dose vaccine products. Highlights – ALTA® microparticles provide sustained antigen delivery with variable release rates, which can be controlled by altering ALD-coat thickness – Sustained antigen release from thermostable, spray-dried ALTA® vaccine products impacts kinetics of humoral and cellular responses, and improves antigen-specific immunogenicity compared to single administration of liquid vaccine – ALTA® formulation imparts vaccine thermostability through spray-drying and ALD-coating to clinically relevant HIV-1 Env antigen, N332-GT5 gp140

Fields of Study & Subjects

Immunotherapy and Immune Responses Advanced Drug Delivery Systems Nanoplatforms for cancer theranostics

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
5 January 2026
Language
EN
Document type
Preprint