| Journal of Neuroinflammation | 卷:19 |
| Elevated proportion of TLR2- and TLR4-expressing Th17-like cells and activated memory B cells was associated with clinical activity of cerebral cavernous malformations | |
| Lana M. Lopes1  Camilla Castro1  Marcos Octávio S. D. Cafasso1  Hugo A. A. Oyamada1  Cleonice A. M. Bento1  Priscila M. Sacramento1  Joana Hygino1  Clarice Monteiro1  Jorge Paes Barreto Marcondes de Souza2  Soniza Vieira Alves-Leon2  Gustavo da Fontoura Galvão3  | |
| [1] Department of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro; | |
| [2] Post-Graduate Program in Neurology, University of the State of Rio de Janeiro; | |
| [3] Service of Neurosurgery, University Hospital of the Federal University of Rio de Janeiro; | |
| 关键词: Cerebral cavernous malformations; T cells; Th17 cells; TLR; Cytokines; B cells; | |
| DOI : 10.1186/s12974-022-02385-2 | |
| 来源: DOAJ | |
【 摘 要 】
Abstract Background Recent evidences have suggested the involvement of toll-like receptor (TLR)-4 in the pathogenesis of cerebral cavernous malformations (CCM). Elevated frequency of TLR+T-cells has been associated with neurological inflammatory disorders. As T-cells and B-cells are found in CCM lesions, the objective of the present study was to evaluate the cytokine profile of T-cells expressing TLR2 and TLR4, as well as B-cell subsets, in asymptomatic (CCMAsympt) and symptomatic (CCMSympt) patients. Methods For our study, the cytokine profile from TLR2+ and TLR4+ T-cell and B-cell subsets in CCMAsympt and CCMSympt patients was investigated using flow cytometry and ELISA. T-cells were stimulated in vitro with anti-CD3/anti-CD28 beads or TLR2 (Pam3C) and TLR4 (LPS) ligands. Results CCMSymptc patients presented a higher frequency of TLR4+(CD4+ and CD8+) T-cells and greater density of TLR4 expression on these cells. With regard to the cytokine profile, the percentage of TLR2+ and TLR4+ Th17 cells was higher in CCMSympt patients. In addition, an elevated proportion of TLR4+ Tc-1 cells, as well as Tc-17 and Th17.1 cells expressing TLR2 and TLR4, was observed in the symptomatic patients. By contrast, the percentage of TLR4+ IL-10+CD4+ T cells was higher in the CCMAsympt group. Both Pam3C and LPS were more able to elevate the frequency of IL-6+CD4+T cells and Th17.1 cells in CCMSympt cell cultures. Furthermore, in comparison with asymptomatic patients, purified T-cells from the CCMSympt group released higher levels of Th17-related cytokines in response to Pam3C and, mainly, LPS, as well as after activation via TCR/CD28. Concerning the B-cell subsets, a higher frequency of memory and memory activated B-cells was observed in CCMSympt patients. Conclusions Our findings reveal an increase in circulating Th17/Tc-17 cell subsets expressing functional TLR2 and, mainly, TLR4 molecules, associated with an increase in memory B-cell subsets in CCM patients with clinical activity of the disease.
【 授权许可】
Unknown