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CD24:火熱在研新藥EXO-CD24,“搭載”外泌體,抵抗COVID-19?

日期:2021-12-21 09:57:27

2021年7月18日,WHO COVID-19 Database更新了以色列COVID-19在研新藥EXO-CD24的II期臨床數(shù)據(jù),初步結(jié)果顯示,在30名中度至重度患者中,約29名患者在接受治療幾天內(nèi)康復(fù)。90%接受治療的患者在5天內(nèi)出院(點(diǎn)擊閱讀相關(guān)信息)。目前該臨床數(shù)據(jù)暫未在Clinical Trial網(wǎng)站更新,但這一消息在以色列發(fā)行量最大的報(bào)刊《耶路撒冷郵報(bào)》上報(bào)道后,引起了海內(nèi)外的關(guān)注。EXO-CD24是一種以外泌體為載體,內(nèi)含CD24蛋白的試驗(yàn)性藥物。它可通過囊泡外泌體將藥物CD24遞送至體內(nèi),調(diào)節(jié)細(xì)胞因子風(fēng)暴,從而抵抗COVID-19。靶點(diǎn)CD24不僅聯(lián)合外泌體,CD24-Fc融合蛋白也曾因治療COVID-19在臨床試驗(yàn)獲得積極效果而大放異彩。如果說EXO-CD24證明安全、有效。那么,EXO作為配角,CD24將為最重要的主角!

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熱穩(wěn)定抗原-CD24

CD24是一種熱穩(wěn)定抗原,屬于糖基磷脂酰肌醇(GPI)錨定的細(xì)胞表面蛋白。CD24最初被認(rèn)為是B細(xì)胞的標(biāo)記物,在B細(xì)胞分化早期階段表達(dá),同時(shí)對(duì)淋巴細(xì)胞成熟、神經(jīng)系統(tǒng)發(fā)育及生理狀態(tài)下的組織更新起到重要的作用。CD24主要表達(dá)于造血系統(tǒng)的細(xì)胞、神經(jīng)組織以及一些特定的上皮細(xì)胞,同時(shí)也見于大多實(shí)體腫瘤、炎癥組織以及自身免疫性疾病的某些細(xì)胞。眾多研究發(fā)現(xiàn),CD24在生理與病理狀態(tài)下具有完全相反的作用——在生理狀態(tài)下,CD24可抑制組織生長;但在病理狀態(tài)下,CD24卻促進(jìn)細(xì)胞增殖。這些生理特性使得CD24在自身免疫性疾病、炎癥、腫瘤等疾病的治療研究中受到關(guān)注。

“別吃我”信號(hào)蛋白-CD24

眾所周知,癌細(xì)胞會(huì)通過表達(dá)“別吃我”信號(hào)蛋白,來避免被免疫細(xì)胞殺傷或清除,從而導(dǎo)致腫瘤免疫逃逸。這種信號(hào)蛋白被形象的稱為“別吃我”信號(hào)蛋白。早期,大多數(shù)研究人員發(fā)現(xiàn)CD24在多種實(shí)體瘤腫瘤細(xì)胞中高表達(dá),但其生物學(xué)功能不清楚。2019年,一項(xiàng)研究揭示了CD24/Siglec-10信號(hào)通路在卵巢癌和乳腺癌腫瘤中發(fā)揮的重大作用,表明CD24與巨噬細(xì)胞上的Siglec-10(sialic-acid-binding Ig-like lectin10)互相作用,可抑制巨噬細(xì)胞對(duì)腫瘤細(xì)胞的吞噬,敲除CD24或Siglec-10,將促進(jìn)巨噬細(xì)胞對(duì)腫瘤細(xì)胞的殺傷作用(圖1)。因此,CD24被認(rèn)為是一種新型腫瘤免疫靶點(diǎn),與明星分子CD47一樣,也是一種腫瘤細(xì)胞“別吃我”信號(hào)蛋白。(點(diǎn)擊可查看CD47相關(guān)文章

CD24/Siglec-10信號(hào)通路

圖1. CD24/Siglec-10信號(hào)通路

CD24為何成為COVID-19重要靶點(diǎn)?

我們先回到這個(gè)新藥:EXO-CD24。首先,EXO-CD24 并不是一個(gè)抗病毒的藥物,而是作為一款尚在試驗(yàn)當(dāng)中的免疫治療藥物。這個(gè)藥的本質(zhì)是一種包裹著CD24的外泌體。外泌體(exosomes)是一種細(xì)胞分泌的微小膜泡,廣泛分布于各種體液中,外泌體可以攜帶多種蛋白質(zhì)、脂類、DNA和RNA等信息,形成一種細(xì)胞-細(xì)胞間的信號(hào)傳遞。真正起效的還是CD24,它可以通過多種機(jī)制調(diào)節(jié)人體的免疫反應(yīng)。CD24正是憑借其良好的抑制免疫風(fēng)暴的能力,被用于治療中至重癥新冠患者。這并非CD24第一次因抑制免疫風(fēng)暴而用于新冠治療的藥物,在此之前還有CD24-Fc。

2020年11月,默沙東(Merck)宣布以4.25億美元的預(yù)付款收購美國公司昂科免疫(OncoImmune)藥物CD24-Fc,但考慮到新的試驗(yàn)及相應(yīng)規(guī)模的生產(chǎn),至少到2022年上半年才能完成。2021年4月15日,默沙東宣布暫停CD24-Fc治療新冠住院患者的臨床研究,但 CD24-Fc其他適應(yīng)癥不受影響。早在去年,昂科免疫公布了III臨床中期數(shù)據(jù),203例患者接受CD24-Fc治療,降低死亡率超過50%。

因抑制免疫風(fēng)暴而用于新冠治療的藥物,還有妥珠單抗和激素類藥物。但對(duì)于靶向單一細(xì)胞因子通路的妥珠單抗,重癥患者的臨床益處目前不是很明朗。從機(jī)制上來看,CD24比IL-6/IL-6R等單一細(xì)胞因子作為靶點(diǎn)的潛力更大,但不管是CD24-Fc或EXO-C24治療COVID-19,其具體臨床益處仍需繼續(xù)臨床驗(yàn)證。

CD24最新臨床研究進(jìn)展

來自Clinical Trials的數(shù)據(jù)表明,針對(duì)CD24的臨床藥物已有4款在研項(xiàng)目,適應(yīng)癥主要為COVID-19。來自藥渡的數(shù)據(jù)表明,其中2款已處于臨床階段,分別是CD24-Fc,EXO-CD24。除了用于COVID-19,藥物CD24-Fc還用于骨髓增生異常綜合征,急性淋巴細(xì)胞白血病,白血病等多種免疫類型疾病治療。因此,CD24作為新型的免疫調(diào)節(jié)分子,不僅僅是作用于COVID-19,大量研究已表明CD24在惡心腫瘤細(xì)胞中高表達(dá),參與調(diào)節(jié)細(xì)胞免疫應(yīng)答,提示CD24有望作為抗腫瘤治療的潛力靶標(biāo)。同樣,我們期待更多基于CD24靶向藥能在COVID-19的臨床研究中有更重要的突破,這將使得CD24這個(gè)靶點(diǎn)再次大放異彩。

臨床項(xiàng)目 臨床狀態(tài) 適應(yīng)癥 臨床階段 招募數(shù) 研發(fā)公司
CD24Fc (MK-7110) as a Non-antiviral Immunomodulator in COVID-19 Treatment (MK-7110-007) Completed 新型冠狀病毒肺炎(COVID-19);
骨髓增生異常綜合征;
急性淋巴細(xì)胞白血病;
急性髓細(xì)胞樣白血病;
移植物抗宿主病;
造血干細(xì)胞移植;
白血病;
HIV感染;
黑色素瘤;
血脂障礙;
Phase 3 234 OncoImmune, Inc.
A Phase II Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of Exosomes Overexpressing CD24 to Prevent Clinical Deterioration in Patients With Moderate or Severe COVID-19 Infection Active, not recruiting 新型冠狀病毒肺炎(COVID-19) Phase 2 155 Eli Sprecher, MD
Safety and Efficacy of Exosomes Overexpressing CD24 in Two Doses for Patients With Moderate or Severe COVID-19 Recruiting 新型冠狀病毒肺炎(COVID-19) Pre-clinical 90 Athens Medical Society
Evaluation of the Safety of CD24-Exosomes in Patients With COVID-19 Infection Recruiting SARS-CoV-2 Pre-clinical 35 Tel-Aviv Sourasky Medical Center

數(shù)據(jù)來源:Clinical Trials

為鼎力協(xié)助各藥企針對(duì)CD24在新冠COVID-19或免疫疾病領(lǐng)域上的研發(fā),CUSABIO推出CD24活性蛋白產(chǎn)品 Recombinant Human CD24 -Nanoparticle (Active) (Code: CSB-MP004902HU) ,歡迎聯(lián)系我們。

The Validated Data of CD24-Nanoparticle (Active)

High Purity Validated by SDS-PAGE

Purity was greater than 95% as determined by SDS-PAGE. (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.

Excellent Bioactivity Validated by Functional ELISA.

Immobilized human CD24 at 2 μg/ml can bind anti-CD24 recombinant Monoclonal Antibody (CSB-RA004902A0HU). The EC50 is 5.409-8.219 ng/ml.

參考文獻(xiàn):

[1] Sprecher, Eli. "A Phase II Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of Exosomes Overexpressing CD24 to Prevent Clinical Deterioration in Patients With Moderate or Severe COVID-19 Infection."(2021).

[2] Altevogt, Peter, et al. "Novel insights into the function of CD24: A driving force in cancer." International Journal of Cancer 148.3 (2021): 546-559.

[3] Aroldi, Andrea, et al. "CD24/Siglec-10 Don't Eat Me Signal Blockade Is a Potential Immunotherapeutic Target in Mantle-Cell Lymphoma." Blood 138. Supplement 1 (2021): 2276-2276.

[4] Shapira, Shiran, et al. "Integrase-derived peptides together with CD24-targeted lentiviral particles inhibit the growth of CD24-expressing cancer cells." Oncogene 40.22 (2021): 3815-3825.

[5] Wu, Hao, et al. "Prospects of antibodies targeting CD47 or CD24 in the treatment of glioblastoma." CNS Neuroscience & Therapeutics 27.10 (2021): 1105-1117.

[6] Kelley, Shannon M., and Kodi S. Ravichandran. "Putting the brakes on phagocytosis: "don't-eat-me " signaling in physiology and disease." EMBO reports (2021): e52564.

[7] Ghasempour Dabaghi, G., M. Rabiee Rad, and L. Saberian. "Treatment of COVID-19 by CD24FC; a mini-review to the current knowledge. "J Prev Epidemiol 6.1 ( 2021): e04.

[8] Song, No-Joon, et al. "Immunological Insights Into the Therapeutic Roles of CD24Fc Against Severe COVID-19." medRxiv (2021).

[9] Sagiv, Eyal, and Michael A. Portman. "CD24 for Cardiovascular Researchers: a Key Molecule in Cardiac Immunology, Marker of Stem Cells and Target for Drug Development." Journal of Personalized Medicine 11.4 (2021): 260.

[10] Song, No-Joon, et al. "Treatment with Soluble CD24 Attenuates COVID-19-Associated Systemic Immunopathology." medRxiv (2021): 2021-08.

[11] Barkal, Amira A., et al. "CD24 signalling through macrophage Siglec-10 is a target for cancer immunotherapy." Nature 572.7769 (2019): 392-396.