Lessons from the Cerebrospinal Fluid Analysis of HTLV-1-Infected Individuals: Biomarkers of Inflammation for HAM/TSP Development

被引:9
|
作者
Freitas, Nicole Lardini [1 ]
Pinheiro Gomes, Yago Cortes [1 ,2 ]
Souza, Flavia dos Santos [1 ]
Torres, Rafael Carvalho [3 ,4 ]
Echevarria-Lima, Juliana [5 ]
Celestino Bezerra Leite, Ana Claudia [1 ]
Sales Dantas Lima, Marco Antonio [1 ]
Campos Araujo, Abelardo Queiroz [1 ]
Teixeira Silva, Marcus Tulius [1 ]
Espindola, Otavio de Melo [1 ]
机构
[1] Fundacao Oswaldo Cruz FIOCRUZ, Inst Nacl Infectol Evandro Chagas INI, BR-21040900 Rio De Janeiro, Brazil
[2] Fundacao Oswaldo Cruz FIOCRUZ, Inst Oswaldo Cruz IOC, BR-21040900 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro UFRJ, Inst Biofis Carlos Chagas Filho IBCCF, BR-21941902 Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro UFRJ, Inst Puericultura & Pediat Martagao Gesteira, BR-21941912 Rio De Janeiro, Brazil
[5] Univ Fed Rio de Janeiro UFRJ, Inst Microbiol Paulo Goes, BR-21941902 Rio De Janeiro, Brazil
来源
VIRUSES-BASEL | 2022年 / 14卷 / 10期
关键词
HTLV-1; HAM; TSP; biomarkers; cerebrospinal fluid; neurodegeneration; inflammasome; IL-18; NERVE GROWTH-FACTOR; SYSTEMIC-LUPUS-ERYTHEMATOSUS; CELL-SURFACE RECEPTOR; SPINAL-CORD LESIONS; SPASTIC PARAPARESIS; MULTIPLE-SCLEROSIS; SOLUBLE TREM-2; VIRUS; EXPRESSION; HTLV-1;
D O I
10.3390/v14102146
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a neurodegenerative disease that leads to motor impairment due to a chronic inflammatory process in the central nervous system (CNS). However, the HAM/TSP pathogenesis is not completely clear, and biomarkers to define the disease prognosis are still necessary. Thus, we aimed to identify biomarkers for HAM/TSP and potential mechanisms involved in disease development. To that end, the concentrations of VILIP-1, BDNF, VEGF, beta-NGF, TGF-beta 1, fractalkine/CX3CL1, IL-6, IL-18, and TNF-alpha, and the soluble forms of TREM-1, TREM-2, and RAGE, were assessed using a multiplex bead-based immunoassay in paired cerebrospinal fluid (CSF) and serum samples from HAM/TSP patients (n = 20), asymptomatic HTLV-1 carriers (AC) (n = 13), and HTLV-1-seronegative individuals (n = 9), with the results analyzed according to the speed of HAM/TSP progression. HAM/TSP patients had elevated fractalkine in the serum but not in the CSF, particularly those with low neuroinflammatory activity (CSF/serum ratio of neopterin <1 and of CXCL10 < 2). HAM/TSP patients with normal CSF levels of neurofilament light chain (NfL) showed elevated beta-NGF in serum, and serum BDNF levels were increased in HTLV-1-infected individuals, particularly in HTLV-1 AC. Both HTLV-1 AC and HAM/TSP patients had lower TGF-beta 1 levels in CSF compared to uninfected individuals, and HAM/TSP patients with active CNS inflammation showed higher CSF levels of IL-18, which correlated with markers of inflammation, neuronal death, and blood-brain-barrier permeability. Although none of the factors evaluated were associated with the speed of HAM/TSP progression, reduced TGF-beta 1 levels in CSF suggest that suppressive responses to control subclinical and/or active neurodegeneration are impaired, while increased CSF IL-18 indicates the involvement of inflammasome-mediated mechanisms in HAM/TSP development.
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页数:18
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