超越传统治疗:针对全身性红血性狼的新型细胞疗法
Zeinab Zarei-Behjani1, Arghavan Hosseinpouri1,2, Maryam Fotoohi1,2
1Department of Tissue Engineering and Applied Cell Sciences, School of Advanced Medical Sciences and Technologies, Shiraz University of Medical Sciences, Shiraz, Iran.
Journal of translational autoimmunity
|September 22, 2025
概括
基于细胞的新型疗法对治疗全身性红斑狼 (SLE) 是有前途的,提供潜在的长期疾病控制或治愈. 本综述探讨了SLE管理的临床前和临床试验中的新兴细胞疗法.
科学领域:
- 免疫学 免疫学 免疫学
- 类风湿病学 类风湿病学
- 细胞生物学 细胞生物学
背景情况:
- 系统性红斑狼 (SLE) 是一种复杂的自身免疫性疾病,具有影响多个器官的多种临床表现.
- 目前用于SLE的治疗方法,包括抗疟疾药物,葡萄皮质类药物和生物药物,由于副作用和持续的不良结果而存在局限性.
- 由于SLE的异质性和不可预测性,需要创新的治疗策略.
研究的目的:
- 审查SLE基于细胞的治疗方法最近的进展.
- 突出已经达到临床前或临床试验阶段的细胞疗法.
- 讨论用于SLE管理的基于细胞的治疗的潜力.
主要方法:
- 对SLE基于细胞治疗的最新研究的文献综述.
- 专注于进入临床前和临床试验阶段的研究.
- 分析新兴细胞类型及其在SLE中的治疗潜力.
主要成果:
- 几种细胞类型正在作为SLE的潜在治疗方法进行研究.
- 有前途的基于细胞的疗法已经进入临床前和临床试验阶段.
- 基于细胞的疗法有可能在SLE中长期抑制或缓解疾病.
结论:
- 基于细胞的疗法代表了SLE治疗的前沿.
- 进一步的研究和临床试验对于验证这些新的方法至关重要.
- 这些疗法有可能为SLE患者提供改善的结果,并可能治愈SLE患者.
相关概念视频
iPS Cell Differentiation
3.0K
The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
3.0K
Tumor Immunotherapy
1.8K
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
1.8K
Mesenchymal Stem Cells
5.5K
Mesenchymal stem cells (MSCs) are adult stem cells that can differentiate into most connective tissue cell types, except for hematopoietic cells, depending upon the source of MSCs. For example, bone-marrow-derived MSCs (BM-MSCs) can differentiate into osteocytes, hepatocytes, and pancreatic and neuronal cells. MSCs can be isolated from various sources such as bone marrow, placenta, adipose tissue, teeth, and Wharton’s jelly, a gelatinous substance in the umbilical cord. The ease of their...
5.5K
EPS and iPS Cells in Disease Research
3.4K
Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...
3.4K
Autoimmune Disorders
1.5K
Autoimmune diseases are a group of disorders in which the body's immune system mistakenly attacks its own cells, tissues, and organs. This results from an overactive immune response against substances and tissues normally present in the body. Let's delve into the concept and mechanism of autoimmune diseases from an immune system point of view, explore different causes and examples of such diseases, and discuss potential solutions.
Concept and Mechanism of Autoimmune Diseases
The immune...
Concept and Mechanism of Autoimmune Diseases
The immune...
1.5K
Nephrotic Syndrome II : Assessment and Medical Management
203
IntroductionNephrotic syndrome is a kidney disorder marked by excessive protein loss in the urine, leading to various systemic complications. This condition often results from damage to the glomeruli—the kidney's filtering units—causing proteinuria, low blood protein levels, and fluid retention. Understanding the assessment, diagnosis, and management of nephrotic syndrome is essential for effective treatment and prevention of further kidney damage.AssessmentPatient History: Document...
203


