Tannic Acid, as a Structural Moiety Coupled to a Protein Antigen, Exhibiting a Molecular-structure Adjuvant Activity for Antibody Specificity Enhancement

抗原 佐剂 牛血清白蛋白 免疫原性 单宁酸 抗体 免疫系统 体液免疫 化学 抗体效价 分子生物学 生物 生物化学 免疫学 效价 有机化学
作者
Brenda Molina-Ramírez,Nidia Cabral-Hipólito,Irais Castillo‐Maldonado,Dealmy Delgadillo‐Guzmán,Rocío Meza-Velázquez,Agustina Ramírez‐Moreno,Erika Flores‐Loyola,Pablo Ruíz-Flores,Jorge Haro-Santa Cruz,Perla-Karina Espino-Silva,Joaquín Ávalos-Soto,Miguel-Ángel Téllez-López,Rubén Daniel Arellano Pérez Vertti,Manuel-Gerardo Rosales-González,David Pedroza‐Escobar
出处
期刊:Protein and Peptide Letters [Bentham Science]
卷期号:29 (11): 925-936 被引量:3
标识
DOI:10.2174/0929866529666220902152147
摘要

An antigen is a small foreign substance, such as a microorganism structural protein, that may trigger an immune response once inside the body. Antigens are preferentially used rather than completely attenuated microorganisms to develop safe vaccines. Unfortunately, not all antigens are able to induce an immune response. Thus, new adjuvants to enhance the antigen's ability to stimulate immunity must be developed.Therefore, this work aimed to evaluate the molecular-structure adjuvant activity of tannic acid (TA) coupled to a protein antigen in Balb/c mice.Bovine serum albumin (BSA) was used as an antigen. The coupling of BSA and TA was mediated by carbodiimide crosslinking, and verified by SDS-PAGE. Forty-two Balb/c mice were divided into seven groups, including two controls without antigen, an antigen control, an adjuvant control, and two treatment groups. An additional group was used for macrophages isolation. A 30-day scheme was used to immunize the mice. The analysis of humoral immunity included immunoglobulin quantification, isotyping and antigen-antibody precipitation. The analysis of cell-mediated immunity included the quantification of nitric oxide from peritoneal macrophages and splenocytes' proliferation assay after treatment stimulation.No differences were found in the antibodies' concentration or isotypes induced with the conjugate or the pure BSA. However, an immunogenicity improvement (p < 0.05) was observed through the specific anti-BSA antibody titers in mice immunized with the conjugate. Besides, macrophage activation (p < 0.05) was detected when stimulated with the treatments containing TA.Tannic acid exhibited macrophages' activation properties. Moreover, when TA was incorporated into the structure of a protein antigen, such as BSA, an antibody specificity enhancement was observed. This was a consequence of antigen processing by activated antigen-presenting cells. These results showed the use of tannic acid as a novel candidate for vaccine molecular-structure adjuvant.
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