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1
A 71-kD heat shock protein (hsp) from Mycobacterium tuberculosis has modulatory effects on experimental rat arthritis.来自结核分枝杆菌的一种71-kD热休克蛋白(hsp)对实验性大鼠关节炎具有调节作用。
Clin Exp Immunol. 1996 Jan;103(1):77-82. doi: 10.1046/j.1365-2249.1996.929628.x.
2
Inhibition of adjuvant-induced arthritis by DNA vaccination with the 70-kd or the 90-kd human heat-shock protein: immune cross-regulation with the 60-kd heat-shock protein.用70kd或90kd人热休克蛋白进行DNA疫苗接种对佐剂诱导性关节炎的抑制作用:与60kd热休克蛋白的免疫交叉调节
Arthritis Rheum. 2004 Nov;50(11):3712-20. doi: 10.1002/art.20635.
3
A conserved mycobacterial heat shock protein (hsp) 70 sequence prevents adjuvant arthritis upon nasal administration and induces IL-10-producing T cells that cross-react with the mammalian self-hsp70 homologue.一种保守的分枝杆菌热休克蛋白(hsp)70序列经鼻腔给药可预防佐剂性关节炎,并诱导产生与哺乳动物自身hsp70同源物发生交叉反应的分泌白细胞介素-10的T细胞。
J Immunol. 2000 Mar 1;164(5):2711-7. doi: 10.4049/jimmunol.164.5.2711.
4
A mycobacterial 65-kD heat shock protein induces antigen-specific suppression of adjuvant arthritis, but is not itself arthritogenic.一种分枝杆菌65-kD热休克蛋白可诱导佐剂性关节炎的抗原特异性抑制,但它本身并不致关节炎。
J Exp Med. 1990 Jan 1;171(1):339-44. doi: 10.1084/jem.171.1.339.
5
A synthetic 10-kD heat shock protein (hsp10) from Mycobacterium tuberculosis modulates adjuvant arthritis.来自结核分枝杆菌的一种合成10千道尔顿热休克蛋白(hsp10)可调节佐剂性关节炎。
Clin Exp Immunol. 1996 Mar;103(3):384-90. doi: 10.1111/j.1365-2249.1996.tb08291.x.
6
Activation of T cells recognizing self 60-kD heat shock protein can protect against experimental arthritis.识别自身60-kD热休克蛋白的T细胞激活可预防实验性关节炎。
J Exp Med. 1995 Mar 1;181(3):943-52. doi: 10.1084/jem.181.3.943.
7
Differential mycobacterial 65-kDa heat shock protein T cell epitope recognition after adjuvant arthritis-inducing or protective immunization protocols.佐剂性关节炎诱导或保护性免疫方案后分枝杆菌65 kDa热休克蛋白T细胞表位的差异性识别
J Immunol. 1994 Apr 1;152(7):3656-64.
8
Natural antibodies to 65 kD mycobacterial heat shock protein in rats do not correlate with susceptibility for Mycobacterium tuberculosis induced adjuvant arthritis.大鼠体内针对65kD分枝杆菌热休克蛋白的天然抗体与结核分枝杆菌诱导的佐剂性关节炎易感性无关。
Immunobiology. 1991 Mar;182(2):127-34. doi: 10.1016/S0171-2985(11)80196-8.
9
T cell reactivity to an epitope of the mycobacterial 65-kDa heat-shock protein (hsp 65) corresponds with arthritis susceptibility in rats and is regulated by hsp 65-specific cellular responses.T细胞对分枝杆菌65-kDa热休克蛋白(hsp 65)表位的反应性与大鼠关节炎易感性相关,并受hsp 65特异性细胞反应调控。
Eur J Immunol. 1991 May;21(5):1289-96. doi: 10.1002/eji.1830210529.
10
Induction of IL-10 and inhibition of experimental arthritis are specific features of microbial heat shock proteins that are absent for other evolutionarily conserved immunodominant proteins.诱导白细胞介素-10及抑制实验性关节炎是微生物热休克蛋白的特异性特征,而其他进化上保守的免疫显性蛋白则不具备这些特征。
J Immunol. 2001 Oct 15;167(8):4147-53. doi: 10.4049/jimmunol.167.8.4147.

引用本文的文献

1
Extracellular cell stress (heat shock) proteins-immune responses and disease: an overview.细胞外应激(热休克)蛋白与免疫反应和疾病:概述。
Philos Trans R Soc Lond B Biol Sci. 2018 Jan 19;373(1738). doi: 10.1098/rstb.2016.0522.
2
Heat shock proteins (HSPs) in the homeostasis of regulatory T cells (Tregs).热休克蛋白在调节性T细胞(Tregs)稳态中的作用
Cent Eur J Immunol. 2016;41(3):317-323. doi: 10.5114/ceji.2016.63133. Epub 2016 Oct 25.
3
Exosomal Hsp70 mediates immunosuppressive activity of the myeloid-derived suppressor cells via phosphorylation of Stat3.外泌体热休克蛋白70通过信号转导和转录激活因子3的磷酸化介导髓源性抑制细胞的免疫抑制活性。
Med Oncol. 2015 Feb;32(2):453. doi: 10.1007/s12032-014-0453-2. Epub 2015 Jan 21.
4
Mycobacterial and mouse HSP70 have immuno-modulatory effects on dendritic cells.分枝杆菌和小鼠 HSP70 对树突状细胞具有免疫调节作用。
Cell Stress Chaperones. 2013 Jul;18(4):439-46. doi: 10.1007/s12192-012-0397-4. Epub 2012 Dec 27.
5
PLGA, PLGA-TMC and TMC-TPP nanoparticles differentially modulate the outcome of nasal vaccination by inducing tolerance or enhancing humoral immunity.PLGA、PLGA-TMC 和 TMC-TPP 纳米粒通过诱导耐受或增强体液免疫来差异化调节鼻内疫苗接种的结果。
PLoS One. 2011;6(11):e26684. doi: 10.1371/journal.pone.0026684. Epub 2011 Nov 2.
6
The gene expression profile of preclinical autoimmune arthritis and its modulation by a tolerogenic disease-protective antigenic challenge.临床前自身免疫性关节炎的基因表达谱及其对耐受原性疾病保护抗原挑战的调节。
Arthritis Res Ther. 2011;13(5):R143. doi: 10.1186/ar3457. Epub 2011 Sep 13.
7
Serum heat shock protein 60 can predict remission of flare-up in juvenile idiopathic arthritis.血清热休克蛋白 60 可预测幼年特发性关节炎发作缓解。
Clin Rheumatol. 2011 Jul;30(7):959-65. doi: 10.1007/s10067-011-1709-2. Epub 2011 Feb 22.
8
Prolonged survival of allografts induced by mycobacterial Hsp70 is dependent on CD4+CD25+ regulatory T cells.由分枝杆菌 Hsp70 诱导的同种异体移植物的长期存活依赖于 CD4+CD25+调节性 T 细胞。
PLoS One. 2010 Dec 8;5(12):e14264. doi: 10.1371/journal.pone.0014264.
9
Expression of Mycobacterium leprae HSP65 in tobacco and its effectiveness as an oral treatment in adjuvant-induced arthritis.麻风分枝杆菌 HSP65 在烟草中的表达及其作为佐剂性关节炎口服治疗药物的效果。
Transgenic Res. 2011 Apr;20(2):221-9. doi: 10.1007/s11248-010-9404-7. Epub 2010 Jun 6.
10
Membrane-associated Hsp72 from tumor-derived exosomes mediates STAT3-dependent immunosuppressive function of mouse and human myeloid-derived suppressor cells.肿瘤来源的外泌体中膜相关的 HSP72 通过 STAT3 介导小鼠和人源髓系来源抑制细胞的免疫抑制功能。
J Clin Invest. 2010 Feb;120(2):457-71. doi: 10.1172/JCI40483. Epub 2010 Jan 19.

来自结核分枝杆菌的一种71-kD热休克蛋白(hsp)对实验性大鼠关节炎具有调节作用。

A 71-kD heat shock protein (hsp) from Mycobacterium tuberculosis has modulatory effects on experimental rat arthritis.

作者信息

Kingston A E, Hicks C A, Colston M J, Billingham M E

机构信息

Lilly Research Centre Ltd., Eli Lilly and Company, Windlesham, Surrey, UK.

出版信息

Clin Exp Immunol. 1996 Jan;103(1):77-82. doi: 10.1046/j.1365-2249.1996.929628.x.

DOI:10.1046/j.1365-2249.1996.929628.x
PMID:8565291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2200306/
Abstract

The effects of a mycobacterial 71-kD hsp antigen have been investigated for its ability to modulate arthritis in rats. Subcutaneous injection (base of tail) of increasing amounts of hsp71 from Mycobacterium tuberculosis (MTB) produced dose-dependent differential inhibitory effects on induction of arthritis by MTB and CP20961 in rats. As little as 1 microgram of the hsp71 produced a reduction in MTB arthritis, whereas complete protection was observed when 50 micrograms were administered. When 71-kD-treated rats were challenged with CP20961, all developed reduced symptoms of arthritis compared with control rats, but in this model no complete protection was observed over the dose range studied. The effects of 71-kD pretreatment on collagen II arthritis were not significant, but in general symptoms of arthritis were milder than in the control group. The same pattern of results was observed previously when hsp65 was used in the different models. These results show that the modulatory effects of hsp on adjuvant arthritis are not restricted to the hsp65 series, but are also mediated by a member of the hsp70 family.

摘要

已对一种分枝杆菌71-kD热休克蛋白抗原调节大鼠关节炎的能力进行了研究。从结核分枝杆菌(MTB)中皮下注射(尾基部)递增剂量的hsp71,对MTB和CP20961诱导的大鼠关节炎产生了剂量依赖性的差异抑制作用。低至1微克的hsp71就能减轻MTB诱导的关节炎,而给予50微克时则观察到完全保护作用。当用CP20961攻击经71-kD处理的大鼠时,与对照大鼠相比,所有大鼠的关节炎症状都有所减轻,但在该模型中,在所研究的剂量范围内未观察到完全保护作用。71-kD预处理对Ⅱ型胶原诱导的关节炎的影响不显著,但总体而言,关节炎症状比对照组轻。以前在不同模型中使用hsp65时也观察到了相同的结果模式。这些结果表明,hsp对佐剂性关节炎的调节作用不仅限于hsp65系列,还可由hsp70家族的一个成员介导。