Abstract

Inflammation conditions are associated with autism spectrum disorder (ASD) and cerebral palsy (CP), primarily observed in the peripheral immune system. However, the extent of neuro-inflammation and neuro-immune dysregulation remains poorly studied. In this study, we analyzed the composition of cerebrospinal fluid (CSF) to uncover the inflammatory mediators driving the neuro-immune system in ASD and CP patients. Our findings revealed that ASD patients had elevated levels of four inflammatory cytokines (TNF-α, IL-4, IL-21, and BAFF) compared to controls, while CP patients exhibited increased levels of eight inflammatory cytokines (IFN-γ, GM-CSF, TNF-α, IL-2, IL-4, IL-6, IL-17A and IL-12), one anti-inflammatory cytokine (IL-10), and five growth factors (GFs) (NGF-β, EGF, GDF-15, G-CSF and BMP-9) compared to both controls and ASD patients. Additionally, intrathecal infusion of autologous bone marrow mononuclear cells (BMMNCs) led to a slight decrease in TGF-β and GDF-15 levels in the CSF of ASD and CP patients, respectively. Our study provides new insights into the molecular composition of CSF in ASD and CP patients, with the potential to develop more effective diagnosis methods and improved treatment for these diseases.

Clinical trial registration CSF samples used in this study are from clinical trials NCT03225651, NCT05307536, NCT02569775, NCT03123562, NCT02574923, NCT05472428 and previous reports [7, 9, 17–19].

Details

Title
Inflammatory mediators drive neuroinflammation in autism spectrum disorder and cerebral palsy
Author
Than, Uyen Thi Trang 1 ; Nguyen, Liem Thanh 2 ; Nguyen, Phuong Hoang 3 ; Nguyen, Xuan-Hung 4 ; Trinh, Dong Phuong 5 ; Hoang, Diem Huong 6 ; Nguyen, Phuong Anh Thi 7 ; Dang, Van Duc 8 

 Vinmec Healthcare System, Vinmec Hi-Tech Center and Vinmec-VinUni Institute of Immunology, Hanoi, Vietnam 
 Vinmec Healthcare System, Vinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam (GRID:grid.489359.a) (ISNI:0000 0004 6334 3668); VinUniversity, College of Health Sciences, Hanoi, Vietnam (GRID:grid.507915.f) (ISNI:0000 0004 8341 3037) 
 Vinmec Healthcare System, Vinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam (GRID:grid.489359.a) (ISNI:0000 0004 6334 3668) 
 Vinmec Healthcare System, Vinmec Hi-Tech Center and Vinmec-VinUni Institute of Immunology, Hanoi, Vietnam (GRID:grid.489359.a); Vinmec Healthcare System, Vinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam (GRID:grid.489359.a) (ISNI:0000 0004 6334 3668); VinUniversity, College of Health Sciences, Hanoi, Vietnam (GRID:grid.507915.f) (ISNI:0000 0004 8341 3037) 
 Vietnam National University, Faculty of Biology, VNU University of Science, Hanoi, Vietnam (GRID:grid.267852.c) (ISNI:0000 0004 0637 2083) 
 Vinmec Healthcare System, Vinmec Hi-Tech Center and Vinmec-VinUni Institute of Immunology, Hanoi, Vietnam (GRID:grid.267852.c) 
 Vinmec Healthcare System, Vinmec International Hospital Times City, Hanoi, Vietnam (GRID:grid.489359.a) (ISNI:0000 0004 6334 3668) 
 Vinmec Healthcare System, Vinmec Research Institute of Stem Cell and Gene Technology, Hanoi, Vietnam (GRID:grid.489359.a) (ISNI:0000 0004 6334 3668); Vietnam National University, Faculty of Biology, VNU University of Science, Hanoi, Vietnam (GRID:grid.267852.c) (ISNI:0000 0004 0637 2083); Leibniz Institute, Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany (GRID:grid.418217.9) (ISNI:0000 0000 9323 8675) 
Pages
22587
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2903739676
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.