Specific Ag-guiding nano-vaccines attenuate neutrophil-dominant allergic asthma. (January 2021)

• Record Type: Journal Article
• Authors: Zhao, Mei-Zhen; Li, Yan; Han, Hai-Yang; Mo, Li-Hua; Yang, Gui; Liu, Zhi-Qiang; Ma, Chang; Yang, Ping-Chang; Liu, Shuwen
• Is Part Of: Molecular immunology. Volume 129(2021)
• Page Start: 103
• Page End: 111
• Publication Date: 2021-01
• Subjects: Asthma -- Allergy -- Neutrophil -- Exosome -- Immunotherapy; Immunochemistry -- Periodicals; Molecular biology -- Periodicals; Immunochemistry -- Periodicals; Allergy and Immunology -- Periodicals; Molecular Biology -- Periodicals; Immunochimie -- Périodiques; Biologie moléculaire -- Périodiques; Immunochemistry; Molecular biology; Periodicals; Electronic journals; 571.96
• DOI: 10.1016/j.molimm.2020.11.005
• Languages: English
• ISSNs: 0161-5890

Abstract

Highlights: Profound neutrophil infiltration was found in bronchoalveolar lavage fluids of immunized mice. Antigen-specific IgG form a complex with CD64 to sensitize neutrophils. Specific antigens bind the IgG/CD64 complexes to activate sensitized neutrophils. Exposure to tExos induced Ag-specific PMNs apoptosis. Administration of tExos efficiently suppressed experimental asthma. Abstract: Polymorphonuclear neutrophils (PMN) are one fraction of the major inflammatory cells in allergic asthma (asthma, in short); the role of PMN in the asthma pathogenesis is not fully understood yet. This study aims to investigate the effects of specific Ag-guiding exosomes on suppressing the neutrophil-dominant airway inflammation. In this study, BALB/c mice were immunized with ovalbumin plus complete Freund adjuvant to induce an asthma model featured with neutrophil-dominant lung inflammation. The Ag specific PMN (sPMN)-targeting exosomes (tExo), that were exosomes carrying a complex of specific Ag/anti-CD64 Ab and Fas ligand, were constructed to be used to alleviate neutrophilic asthma in mice. We found that sPMNs were the major cellular component in bronchoalveolar lavage fluid (BALF) in asthma mice, while less than 3% PMNs in naive control mice. The sPMNs expressed higher levels of CD64, which formed complexes with Ag-specific IgG (sIgG). The sIgG/CD64 complex-carrying PMNs could be activated upon exposing to specific Ags. Exposure to tExos induced Ag-specific PMNs apoptosis. Administration of tExos efficiently suppressed experimental asthma. We conclude that a fraction of sPMN was identified in the airway of asthma mice. The sPMNs could be activated upon exposure to specific Ags. tExos could induce sPMNs apoptosis, that show the translational potential in the treatment of asthma.