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Cell-type differential targeting of TLR5 and TLR7 agonists and their synergistic effect as nasal mucosal adjuvants
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Kexing ZHUO1, Zihang ZENG1, Shasha WANG2, Sijian HUANG1, 3, Shijia QIU1, Maohua ZHONG1, Piao ZOU1, Jingyi YANG2, Yuan CAO1
Journal of Army Medical University | 2026, 48(8) : 1042 - 1053
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Journal of Army Medical University | 2026, 48(8): 1042-1053
• Monographic Reports •
Cell-type differential targeting of TLR5 and TLR7 agonists and their synergistic effect as nasal mucosal adjuvants
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Kexing ZHUO1, Zihang ZENG1, Shasha WANG2, Sijian HUANG1, 3, Shijia QIU1, Maohua ZHONG1, Piao ZOU1, Jingyi YANG2, Yuan CAO1
Affiliations
  • 1Institute of Infection, Immunology and Tumor Microenvironment, Hubei Provincial Key Laboratory of Occupational Hazard Identification and Control, School of Medicine, Wuhan University of Science and Technology, Wuhan, Hubei
  • 2Shanghai Public Health Clinical Center, Fudan University, Shanghai
  • 3Institute for Clinical Research, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
Published: 2026-04-30 doi: 10.16016/j.2097-0927.202512106
Outline
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Objective

To compare the differential activation characteristics of Toll-like receptor 5 (TLR5) agonist KFD and Toll-like receptor 7 (TLR7) agonist R837 on nasal epithelial cells (NECs) and bone marrow-derived dendritic cells (BMDCs), and to determine whether their combination produces synergistic enhancement as nasal mucosal adjuvants.

Methods

Mouse NECs and BMDCs were stimulated with 200 ng/mL KFD or R837 alone or in combination (n=3). At 3 h after stimulation, transcriptome sequencing was performed to analyze gene expression profiles, with key gene expression validated by qPCR. IL-6 levels in the supernatants were measured by ELISA at 12 h post-stimulation. Female C57BL/6 mice (6 to 8 weeks old, weighing 18 to 20 g) were randomly divided into negative control (normal saline), KFD alone (2 μg) group, R837 alone (2 μg) group, and KFD+R837 combination (2 μg KFD+2 μg R837) groups (n=5). At 18 h after intranasal administration, nasal lavage fluid (NALF) and bronchoalveolar lavage fluid (BALF) were collected to detect IL-6 levels, and the expression of costimulatory molecules CD80/CD86 on dendritic cells (DCs) in cervical lymph nodes (CLNs) was analyzed by flow cytometry. Using ovalbumin (OVA) as a model antigen for intranasal immunization, mice were randomly divided into normal saline (negative control), OVA alone (25 μg), OVA+KFD (25 μg OVA+2 μg KFD), OVA+R837 (25 μg OVA+2 μg R837), and OVA+combination adjuvant (25 μg OVA+1 μg KFD+1 μg R837) groups (n=5). Mice were immunized intranasally at weeks 0, 4, and 8. Serum and saliva samples were collected at 2 weeks after the final immunization, and OVA-specific IgG/IgA antibody levels were detected by ELISA.

Results

Transcriptomic analysis revealed that KFD primarily activated NECs, with differentially expressed genes enriched in innate immune pathways such as TNF and NF-κB. In contrast, R837 potently activated BMDCs, with differentially expressed genes involved in TNF and IL-17 signaling pathways. In vitro BMDC experiments confirmed that R837 upregulated Tnf and Cxcl10 mRNA levels more strongly than KFD (P<0.01). The combination synergistically enhanced the expression of Tnf, Cxcl10, and Cd40 (P<0.001) and IL-6 secretion (KFD+R837 combination vs single agent, P<0.000 1). After intranasal administration, both KFD and R837 significantly upregulated CD80/CD86 expression on CLN DCs, with the combination group showing the most significant CD80 upregulation (KFD+R837 combination vs single agent, P<0.05). KFD alone significantly elevated IL-6 levels in NALF, which was not further enhanced by the combination. In the OVA immunization model, the combination adjuvant group exhibited significantly higher levels of serum OVA-specific IgG and salivary OVA-specific IgA than the OVA group (P<0.000 1), which were superior to either single adjuvant (serum IgG: OVA+ combined adjuvants vs OVA+R837, P<0.05; salivary IgA: OVA+ combined adjuvants vs OVA+KFD, OVA+ combined adjuvants vs OVA+R837, both P<0.05).

Conclusion

TLR5 and TLR7 agonists differentially activate NECs and DCs. Their combination synergistically activates DCs and significantly enhances both systemic and local antigen-specific immune responses to mucosal vaccines.

mucosal adjuvants  /  TLR5 agonist  /  TLR7 agonist  /  epithelial cells  /  dendritic cells  /  synergistic effect
卓可星, 曾子航, 汪莎莎, 黄思剑, 裘诗佳, 钟茂华, 邹飘, 杨菁毅, 操媛. TLR5与TLR7激动剂的细胞靶向差异及其鼻腔黏膜佐剂协同效应. 陆军军医大学学报, 2026 , 48 (8) : 1042 -1053 . DOI: 10.16016/j.2097-0927.202512106
Kexing ZHUO, Zihang ZENG, Shasha WANG, Sijian HUANG, Shijia QIU, Maohua ZHONG, Piao ZOU, Jingyi YANG, Yuan CAO. Cell-type differential targeting of TLR5 and TLR7 agonists and their synergistic effect as nasal mucosal adjuvants[J]. Journal of Army Medical University, 2026 , 48 (8) : 1042 -1053 . DOI: 10.16016/j.2097-0927.202512106
Year 2026 volume 48 Issue 8
70
30
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doi: 10.16016/j.2097-0927.202512106
  • Receive Date:2025-12-19
  • Online Date:2026-10-23
  • Published:2026-04-30
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History
  • Received:2025-12-19
  • Revised:2026-03-20
Affiliations
    1Institute of Infection, Immunology and Tumor Microenvironment, Hubei Provincial Key Laboratory of Occupational Hazard Identification and Control, School of Medicine, Wuhan University of Science and Technology, Wuhan, Hubei
    2Shanghai Public Health Clinical Center, Fudan University, Shanghai
    3Institute for Clinical Research, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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