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Loss-of-function MAVS mutation causes antiviral immunodeficiency: unveiling a novel mechanism linking viral infection to generalized pustular psoriasis in children
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Yanan SUN1, Jiahong ZHOU1, Yaqin LIU1, Juan YANG1, Shasha MENG1, Hongmei LI2, Weihui ZHOU1
Journal of Army Medical University | 2025, 47(23) : 2953 - 2962
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Journal of Army Medical University | 2025, 47(23): 2953-2962
• Clinical Medicine •
Loss-of-function MAVS mutation causes antiviral immunodeficiency: unveiling a novel mechanism linking viral infection to generalized pustular psoriasis in children
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Yanan SUN1, Jiahong ZHOU1, Yaqin LIU1, Juan YANG1, Shasha MENG1, Hongmei LI2, Weihui ZHOU1
Affiliations
  • 1Department of Pediatric Research Institute,Children’s Hospital of Chongqing Medical University,National Clinical Research Center for Child Health and Disorders,Ministry of Education Key Laboratory of Child Development and Disorders,Chongqing
  • 2Department of Dermatology,Children’s Hospital of Chongqing Medical University,Chongqing,China
Published: 2025-12-15 doi: 10.16016/j.2097-0927.202509092
Outline
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Objective

To investigate the role of mitochondrial antiviral signaling protein (MAVS) in viral infection-triggered generalized pustular psoriasis (GPP) in children.

Methods

This retrospective case-control study enrolled 80 GPP patients aged 0~18 years from Children’s Hospital of Chongqing Medical University (from October 2013 to April 2019). Whole-exome sequencing identified rare MAVS variants associated with GPP. Pathogenicity of variants was predicted using Mutation Taster, Disease Association, SIFT, and CADD bioinformatics tools. Sanger sequencing validated variants, followed by construction of wild-type (WT) and mutant MAVS expression plasmids transfected into HEK 293 cells. Protein expression was assessed by Western blot. Dual-luciferase reporter gene assays measured IFNB1 and NF-κB transcriptional activity. Genotype distribution of the MAVS c.171dupT/p.H57fs variant was analyzed using Fisher’s exact test.

Results

This study enrolled 80 pediatric GPP patients (aged 0~18 years). Whole-exome sequencing identified five rare MAVS variants, with bioinformatics analyses predicting deleterious effects on protein stability and function. Western blot demonstrated that the c.171dupT mutation in GPP patients significantly reduced full-length MAVS expression (P<0.001); dual-luciferase assays further revealed this variant impaired MAVS-mediated IFNB1 transcriptional activation by 85% (P<0.001), abrogated NF-κB signaling pathway activation (P<0.001), but exhibited no dominant-negative effect on wild-type MAVS function(P>0.05).

Conclusion

The MAVS c.171dupT frameshift variant may contribute to infection-triggered GPP in children, suggesting its potential as a genetic biomarker for GPP susceptibility.

psoriasis  /  mitochondrial antiviral signaling protein  /  infections  /  inflammation
孙亚楠, 周家红, 刘雅琴, 杨涓, 孟莎莎, 李红梅, 周卫辉. MAVS功能丧失性突变导致抗病毒免疫缺陷:揭示病毒感染触发儿童泛发性脓疱性银屑病的新机制. 陆军军医大学学报, 2025 , 47 (23) : 2953 -2962 . DOI: 10.16016/j.2097-0927.202509092
Yanan SUN, Jiahong ZHOU, Yaqin LIU, Juan YANG, Shasha MENG, Hongmei LI, Weihui ZHOU. Loss-of-function MAVS mutation causes antiviral immunodeficiency: unveiling a novel mechanism linking viral infection to generalized pustular psoriasis in children[J]. Journal of Army Medical University, 2025 , 47 (23) : 2953 -2962 . DOI: 10.16016/j.2097-0927.202509092
Year 2025 volume 47 Issue 23
23
8
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Article Info
doi: 10.16016/j.2097-0927.202509092
  • Receive Date:2025-09-27
  • Online Date:2026-10-30
  • Published:2025-12-15
Article Data
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History
  • Received:2025-09-27
  • Revised:2025-11-14
Affiliations
    1Department of Pediatric Research Institute,Children’s Hospital of Chongqing Medical University,National Clinical Research Center for Child Health and Disorders,Ministry of Education Key Laboratory of Child Development and Disorders,Chongqing
    2Department of Dermatology,Children’s Hospital of Chongqing Medical University,Chongqing,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
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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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