Chapter 8 The Role of NKT Cells in Tumor Immunity

自然杀伤性T细胞 免疫系统 CD1D公司 生物 主要组织相容性复合体 CD1型 免疫学 抗原 获得性免疫系统 细胞生物学 细胞毒性T细胞 抗原提呈细胞 CD8型 T细胞 遗传学 体外
作者
Masaki Terabe,Jay A. Berzofsky
出处
期刊:Advances in Cancer Research 卷期号:: 277-348 被引量:299
标识
DOI:10.1016/s0065-230x(08)00408-9
摘要

NKT cells are a relatively newly recognized member of the immune community, with profound effects on the rest of the immune system despite their small numbers. They are true T cells with a T cell receptor (TCR), but unlike conventional T cells that detect peptide antigens presented by conventional major histocompatibility (MHC) molecules, NKT cells recognize lipid antigens presented by CD1d, a nonclassical MHC molecule. As members of both the innate and adaptive immune systems, they bridge the gap between these, and respond rapidly to set the tone for subsequent immune responses. They fill a unique niche in providing the immune system a cellular arm to recognize lipid antigens. They play both effector and regulatory roles in infectious and autoimmune diseases. Furthermore, subsets of NKT cells can play distinct and sometimes opposing roles. In cancer, type I NKT cells, defined by their invariant TCR using Valpha14Jalpha18 in mice and Valpha24Jalpha18 in humans, are mostly protective, by producing interferon-gamma to activate NK and CD8(+) T cells and by activating dendritic cells to make IL-12. In contrast, type II NKT cells, characterized by more diverse TCRs recognizing lipids presented by CD1d, primarily inhibit tumor immunity. Moreover, type I and type II NKT cells counter-regulate each other, forming a new immunoregulatory axis. Because NKT cells respond rapidly, the balance along this axis can greatly influence other immune responses that follow. Therefore, learning to manipulate the balance along the NKT regulatory axis may be critical to devising successful immunotherapies for cancer.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
呀呵发布了新的文献求助10
1秒前
也是难得取个名完成签到 ,获得积分10
2秒前
顾矜应助危机的道天采纳,获得10
2秒前
2秒前
3秒前
脑洞疼应助宇文山柏采纳,获得10
4秒前
Anonymous完成签到,获得积分10
5秒前
5秒前
完美耦合发布了新的文献求助10
6秒前
小星完成签到 ,获得积分10
6秒前
大模型应助杨璨禹采纳,获得10
6秒前
Hello应助影子采纳,获得10
7秒前
南瓜难发布了新的文献求助50
7秒前
hana发布了新的文献求助10
7秒前
8秒前
8秒前
STZHEN发布了新的文献求助10
9秒前
流落尘世发布了新的文献求助10
10秒前
leslie完成签到,获得积分10
13秒前
科研界的一条狗完成签到,获得积分20
14秒前
英姑应助科研小废物采纳,获得10
14秒前
微笑的老头完成签到,获得积分10
14秒前
14秒前
14秒前
早点毕业发布了新的文献求助10
15秒前
15秒前
15秒前
15秒前
aa完成签到,获得积分10
16秒前
17秒前
18秒前
18秒前
18秒前
宇文山柏发布了新的文献求助10
19秒前
19秒前
19秒前
追寻鸵鸟发布了新的文献求助10
19秒前
kkkl发布了新的文献求助10
20秒前
panpan发布了新的文献求助10
22秒前
aa发布了新的文献求助20
22秒前
高分求助中
Evolution 10000
Sustainability in Tides Chemistry 2800
юрские динозавры восточного забайкалья 800
Diagnostic immunohistochemistry : theranostic and genomic applications 6th Edition 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
China's Relations With Japan 1945-83: The Role of Liao Chengzhi 400
Classics in Total Synthesis IV 400
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3149784
求助须知:如何正确求助?哪些是违规求助? 2800775
关于积分的说明 7841901
捐赠科研通 2458351
什么是DOI,文献DOI怎么找? 1308425
科研通“疑难数据库(出版商)”最低求助积分说明 628499
版权声明 601706