4.7 Article

Quantitative features and clinical significance of two subpopulations of AChR-specific CD4+T cells in patients with myasthenia gravis

期刊

CLINICAL IMMUNOLOGY
卷 216, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2020.108462

关键词

Myasthenia gravis; AChR-specific T cells; Th1 cells; Th17 cells

资金

  1. National Natural Science Foundation of China [81620108010, 81873772, 81371386, 81773660, 81971754]
  2. Clinical Study of 5010 Planned Project from Sun Yat-sen University in China [2010003]
  3. Guangdong Province Foundation
  4. Guangdong Science and Technology Department [CANSci (2017)1935]
  5. Pearl River Talents Scheme Fund from Human Resources and Social Security Department of Guangdong Province [CANHum (2017)3]
  6. Southern China International Cooperation Base for Early Intervention and Functional Rehabilitation of Neurological Diseases [2015B050501003]
  7. Guangdong Provincial Engineering Center For Major Neurological Disease Treatment
  8. Guangdong Provincial Translational Medicine Innovation Platform for Diagnosis and Treatment of Major Neurological Disease
  9. Guangdong Provincial Clinical Research Center for Neurological Diseases

向作者/读者索取更多资源

Acetylcholine receptor (AChR)-specific CD4+ T cells play a driving role in myasthenia gravis (MG) by regulating the production of autoantibodies. However, the quantitative features of AChR-specific T cells and their clinical significance in MG are unclear. In this study, we adopted standard and cultured enzyme-linked immunosorbent spot (ELISPOT) assays to quantify subpopulations of AChR-specific CD4+ T cells in MG patients, and evaluate their correlation with clinical characteristics. The results showed that Th1- and Th17-AChR-specific CD4+ T cells were detectable by standard and cultured ELISPOT assay respectively, with higher levels observed in MG patients comparing with healthy controls. The number of Th17-AChR-specific CD4+ T cells was positively correlated with anti-AChR antibody titer and quantitative MG score and may have latent capacity to reflect responses to immunosuppressants. These results highlight the differences in quantitative features of AChR-specific CD4+ T cells and imply Th17-AChR-specific CD4+ T cells can serve as a biomarker in MG.

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