Novel mucosal vaccine against HSV-2 based on the LysM-BLP system as carrier and antigen adjuvant
Revista Bioquímica y Patología Clínica (ByPC) 
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Keywords

mucosal vaccines
bacterium-like particles
antigen presentation
adjuvants
adaptive immune response

How to Cite

Novel mucosal vaccine against HSV-2 based on the LysM-BLP system as carrier and antigen adjuvant. (2024). Biochemistry and Clinical Pathology Journal, 88(2), 41-50. https://doi.org/10.62073/bypc.v88i2.278

Abstract

Introduction: The development of a vaccine against herpes simplex virus type 2 (HSV-2), which causes a lifelong sexually transmitted infection, would be a great step to improve sexual and reproductive health worldwide. Objectives: To study the mucosal and systemic immune responses induced by an experimental vaccine consisting of bacterium-like particles (BLP) derived from lactobacilli, which retain their peptidoglycan matrix and expose the HSV-2 gD antigen on their surface thanks to its fusion with LysM domains. Materials and methods: Six-week-old BALB/c mice were nasally immunized with the His-AcglugD- BLP027 complex on days 0, 14, and 28. As a control, His-Acglu-gD was administered intranasally or His-gD with complete Freund’s adjuvant peritoneally. The levels of specific immunoglobulins in serum and in bronchoalveolar lavage (BAL), as well as the production of cytokines by splenocytes after the antigenic restimulation, were evaluated. Results: The experimental vaccine induced higher levels of IgA in BAL than in mice immunized with Freund’s adjuvant. Conclusions: This new antigen presentation system could be a useful tool for the development of mucosal vaccines that stimulate local and distant immunity.

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