Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder
IntroductionOne rare type of autoimmune disease is called neuromyelitis optica spectrum disorder (NMOSD) and the peripheral immune characteristics of NMOSD remain unclear.MethodsHere, single-cell RNA sequencing (scRNA-seq) is used to characterize peripheral blood mononuclear cells from individuals w...
Main Authors: | , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2024-02-01
|
Series: | Frontiers in Immunology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2024.1322125/full |
_version_ | 1827347446983819264 |
---|---|
author | Yushu Jiang Shuhua Dai Rui Pang Lingzhi Qin Milan Zhang Huiqin Liu Xiaojuan Wang Jiewen Zhang Gongxin Peng Yongchao Wang Wei Li |
author_facet | Yushu Jiang Shuhua Dai Rui Pang Lingzhi Qin Milan Zhang Huiqin Liu Xiaojuan Wang Jiewen Zhang Gongxin Peng Yongchao Wang Wei Li |
author_sort | Yushu Jiang |
collection | DOAJ |
description | IntroductionOne rare type of autoimmune disease is called neuromyelitis optica spectrum disorder (NMOSD) and the peripheral immune characteristics of NMOSD remain unclear.MethodsHere, single-cell RNA sequencing (scRNA-seq) is used to characterize peripheral blood mononuclear cells from individuals with NMOSD.ResultsThe differentiation and activation of lymphocytes, expansion of myeloid cells, and an excessive inflammatory response in innate immunity are observed. Flow cytometry analyses confirm a significant increase in the percentage of plasma cells among B cells in NMOSD. NMOSD patients exhibit an elevated percentage of CD8+ T cells within the T cell population. Oligoclonal expansions of B cell receptors are observed after therapy. Additionally, individuals with NMOSD exhibit elevated expression of CXCL8, IL7, IL18, TNFSF13, IFNG, and NLRP3.DiscussionPeripheral immune response high-dimensional single-cell profiling identifies immune cell subsets specific to a certain disease and identifies possible new targets for NMOSD. |
first_indexed | 2024-03-07T23:50:44Z |
format | Article |
id | doaj.art-0e922aa0018244cba6661d37b1306321 |
institution | Directory Open Access Journal |
issn | 1664-3224 |
language | English |
last_indexed | 2024-03-07T23:50:44Z |
publishDate | 2024-02-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Immunology |
spelling | doaj.art-0e922aa0018244cba6661d37b13063212024-02-19T04:51:55ZengFrontiers Media S.A.Frontiers in Immunology1664-32242024-02-011510.3389/fimmu.2024.13221251322125Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorderYushu Jiang0Shuhua Dai1Rui Pang2Lingzhi Qin3Milan Zhang4Huiqin Liu5Xiaojuan Wang6Jiewen Zhang7Gongxin Peng8Yongchao Wang9Wei Li10Department of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaDepartment of Neurology, Zhoukou Central Hospital, Zhoukou, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaCenter for Bioinformatics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & School of Basic Medicine, Peking Union Medical College, Beijing, ChinaDepartment of Neurology, People’s Hospital of Yexian, Pingdingshan, Henan, ChinaDepartment of Neurology, Henan Joint International Research Laboratory Of Accurate Diagnosis, Treatment, Research And Development, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, Henan, ChinaIntroductionOne rare type of autoimmune disease is called neuromyelitis optica spectrum disorder (NMOSD) and the peripheral immune characteristics of NMOSD remain unclear.MethodsHere, single-cell RNA sequencing (scRNA-seq) is used to characterize peripheral blood mononuclear cells from individuals with NMOSD.ResultsThe differentiation and activation of lymphocytes, expansion of myeloid cells, and an excessive inflammatory response in innate immunity are observed. Flow cytometry analyses confirm a significant increase in the percentage of plasma cells among B cells in NMOSD. NMOSD patients exhibit an elevated percentage of CD8+ T cells within the T cell population. Oligoclonal expansions of B cell receptors are observed after therapy. Additionally, individuals with NMOSD exhibit elevated expression of CXCL8, IL7, IL18, TNFSF13, IFNG, and NLRP3.DiscussionPeripheral immune response high-dimensional single-cell profiling identifies immune cell subsets specific to a certain disease and identifies possible new targets for NMOSD.https://www.frontiersin.org/articles/10.3389/fimmu.2024.1322125/fullneuromyelitis optica spectrum disorderperipheral blood mononuclear cellsingle-cell RNA sequencingB cellT cellmyeloid cell |
spellingShingle | Yushu Jiang Shuhua Dai Rui Pang Lingzhi Qin Milan Zhang Huiqin Liu Xiaojuan Wang Jiewen Zhang Gongxin Peng Yongchao Wang Wei Li Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder Frontiers in Immunology neuromyelitis optica spectrum disorder peripheral blood mononuclear cell single-cell RNA sequencing B cell T cell myeloid cell |
title | Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder |
title_full | Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder |
title_fullStr | Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder |
title_full_unstemmed | Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder |
title_short | Single-cell RNA sequencing reveals cell type-specific immune regulation associated with human neuromyelitis optica spectrum disorder |
title_sort | single cell rna sequencing reveals cell type specific immune regulation associated with human neuromyelitis optica spectrum disorder |
topic | neuromyelitis optica spectrum disorder peripheral blood mononuclear cell single-cell RNA sequencing B cell T cell myeloid cell |
url | https://www.frontiersin.org/articles/10.3389/fimmu.2024.1322125/full |
work_keys_str_mv | AT yushujiang singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT shuhuadai singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT ruipang singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT lingzhiqin singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT milanzhang singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT huiqinliu singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT xiaojuanwang singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT jiewenzhang singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT gongxinpeng singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT yongchaowang singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder AT weili singlecellrnasequencingrevealscelltypespecificimmuneregulationassociatedwithhumanneuromyelitisopticaspectrumdisorder |