Related Experiment Video
Updated: Jul 16, 2026

11:12
Interrogating Individual Autoreactive Germinal Centers by Photoactivation in a Mixed Chimeric Model of Autoimmunity
Published on: April 11, 2019
BCMA-CD19 CAR T Cells in Systemic Lupus Erythematosus: Humoral Reset or Antigen-Specific Tolerance?
Amir Muhammad1,2, Qiongjing Yuan1,3,4, Ling Yuan2
1Department of Nephrology, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China.
Arthritis & Rheumatology (Hoboken, N.J.)
|July 15, 2026
Abstract
No abstract available in PubMed .
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The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
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T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
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The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...

