関連する実験動画
Updated: Nov 1, 2025

09:19
Recombinant Retroviral Production and Infection of B Cells
Published on: February 18, 2011
14.3K
ICOSは,CD40媒介抗体クラスの切り替えにおいて極めて重要です
A J McAdam1, R J Greenwald, M A Levin
1Departments of Pathology, Brigham and Women's Hospital and Harvard Medical School, 221 Longwood Avenue, Boston, Massachusetts 02115, USA.
Nature
|May 9, 2001
まとめ
誘導性共刺激分子 (ICOS) は,T細胞の活性化とB細胞の協力に不可欠です. ICOS欠乏したマウスは,免疫グロブリンクラスの切り替えの障害を示し,免疫応答におけるICOSの役割を強調しています.
科学分野:
- 免疫学 免疫学とは
- 分子生物学は分子生物学である.
背景:
- 同刺激信号は,最適なT細胞活性化に不可欠である.
- 誘導性共刺激分子 (ICOS) は,T細胞の分化に関与するCD28の同型である.
- B7-CD28のような既存の共刺激経路は,T細胞活性化を完全に説明できない.
研究 の 目的:
- 免疫反応におけるICOSの重要な機能を調査する.
- T細胞とB細胞の相互作用におけるICOSの役割を決定する.
主な方法:
- ICOS欠乏した (ICOS-/-) マウスの生成.
- ICOS-/-マウスにおける免疫グロブリン同型クラス交換と生殖中心形成の分析.
- CD40刺激によるクラス・スイッチングの回復の評価.
主要な成果:
- ICOS-/-マウスは,免疫グロブリン同型型のクラス切り替えに重大な欠陥を示した.
- ゲルミナルセンター形成は,ICOS-/-マウスで障害がありました.
- CD40刺激により,ICOS-/-マウスのクラス・スイッチングが回復し,T細胞/B細胞の協働におけるICOSの役割が示された.
結論:
- ICOSは,免疫グロブリンクラスの切り替えと生殖中心の形成において重要な役割を果たします.
- ICOSは,おそらくCD40/CD40L経路を通じて,T細胞/B細胞の協力を促進する.
- ICOSの機能を理解することで,免疫媒介疾患に対する新しい治療法が開発される可能性があります.
関連する概念動画
T Cell Activation and Clonal Selection
12.4K
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.
Naive T cells that have not yet encountered an antigen express two primary CD...
Naive T cells that have not yet encountered an antigen express two primary CD...
12.4K
B Cell Activation and Differentiation
13.5K
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.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...
13.5K
Transcytosis of IgG
3.4K
Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
3.4K
Immunoglobulin-like Cell Adhesion Molecules
3.7K
Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
3.7K
Cytotoxic T Cells-mediated Immune Response
5.4K
Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
5.4K

