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CSF2 / GM-CSF:免疫調(diào)節(jié)與疾病治療的關(guān)鍵分子

日期:2025-02-14 17:17:07

近年來(lái),CSF2(粒細(xì)胞-巨噬細(xì)胞集落刺激因子,GM-CSF)在生物醫(yī)學(xué)領(lǐng)域的研究備受矚目。CSF2在免疫調(diào)節(jié)、炎癥反應(yīng)和腫瘤進(jìn)展等過(guò)程中扮演著關(guān)鍵角色,這使其在多種疾病的治療中展現(xiàn)出潛在的臨床應(yīng)用價(jià)值 [1]。2023年的一項(xiàng)研究揭示,CSF2在胃癌進(jìn)展過(guò)程中,通過(guò)促進(jìn)間充質(zhì)干細(xì)胞(MSC)重編程發(fā)揮作用,為胃癌的治療提供了全新的靶點(diǎn) [1]。與此同時(shí),CSF2在急性腎損傷中的保護(hù)作用也引起了科研人員的濃厚興趣,相關(guān)臨床試驗(yàn)正在積極探索其在腎損傷治療方面的應(yīng)用 [2]。接下來(lái),本文將深入探討CSF2在藥物研究中的臨床意義與應(yīng)用前景。


1. CSF2概述

CSF2,又被稱(chēng)為粒細(xì)胞-巨噬細(xì)胞集落刺激因子(GM-CSF),是一種由多種細(xì)胞分泌產(chǎn)生的細(xì)胞因子,這些細(xì)胞包括T細(xì)胞、B細(xì)胞、巨噬細(xì)胞和成纖維細(xì)胞等 [3]。CSF2主要通過(guò)與靶細(xì)胞表面的受體相結(jié)合,從而對(duì)細(xì)胞的增殖、分化以及功能發(fā)揮調(diào)節(jié)作用。CSF2受體由α鏈和β鏈構(gòu)成,其中β鏈承擔(dān)著信號(hào)轉(zhuǎn)導(dǎo)的重要功能 [4]。在免疫系統(tǒng)中,CSF2具有不可或缺的調(diào)節(jié)作用,它能夠促進(jìn)粒細(xì)胞和巨噬細(xì)胞的生成,并增強(qiáng)免疫細(xì)胞的活性。


2. CSF2的結(jié)構(gòu)與功能

CSF2的分子結(jié)構(gòu)包含多個(gè)功能域,其中N端結(jié)構(gòu)域負(fù)責(zé)與受體的α鏈結(jié)合,而C端結(jié)構(gòu)域則參與信號(hào)傳導(dǎo)過(guò)程 [5]。當(dāng)CSF2與受體結(jié)合后,會(huì)激活JAK-STAT信號(hào)通路,進(jìn)而調(diào)控下游基因的表達(dá) [6]。除此之外,CSF2還可以通過(guò)PI3K-Akt和MAPK等信號(hào)通路,對(duì)細(xì)胞的增殖和分化產(chǎn)生影響 [7]。在免疫系統(tǒng)內(nèi),CSF2能夠促進(jìn)巨噬細(xì)胞的活化,增強(qiáng)其吞噬和殺菌能力 [8]。同時(shí),CSF2還能調(diào)節(jié)T細(xì)胞的分化和功能,維持免疫應(yīng)答的平衡 [9]。


3. CSF2的作用機(jī)制

3.1 炎癥反應(yīng)

在炎癥反應(yīng)過(guò)程中,CSF2發(fā)揮著促進(jìn)炎癥細(xì)胞募集和活化的作用,進(jìn)而加劇炎癥反應(yīng) [10]。具體來(lái)說(shuō),CSF2與受體結(jié)合后,激活JAK-STAT信號(hào)通路,促使炎癥因子如IL-6和TNF-α釋放 [11]。這些炎癥因子會(huì)進(jìn)一步活化和增殖炎癥細(xì)胞,形成正反饋機(jī)制,導(dǎo)致炎癥反應(yīng)不斷加劇。此外,CSF2還可以通過(guò)PI3K-Akt信號(hào)通路,促進(jìn)炎癥細(xì)胞的存活和增殖 [12]。

3.2 腫瘤微環(huán)境

在腫瘤微環(huán)境中,CSF2通過(guò)影響腫瘤相關(guān)巨噬細(xì)胞(TAM)的極化,對(duì)腫瘤的進(jìn)展產(chǎn)生作用 [13]。CSF2能夠誘導(dǎo)TAM向M2型巨噬細(xì)胞極化,增強(qiáng)其免疫抑制功能 [14]。M2型巨噬細(xì)胞會(huì)分泌抗炎因子,如IL-10和TGF-β,這些因子能夠抑制T細(xì)胞的活化和增殖,從而助力腫瘤細(xì)胞實(shí)現(xiàn)免疫逃逸 [15]。另外,CSF2還可以通過(guò)MAPK信號(hào)通路,影響腫瘤細(xì)胞的增殖和遷移 [16]。

3.3 組織修復(fù)與再生

在組織修復(fù)和再生過(guò)程中,CSF2能夠促進(jìn)巨噬細(xì)胞的活化,增強(qiáng)其清除壞死組織和促進(jìn)組織修復(fù)的能力 [17]。CSF2激活JAK-STAT信號(hào)通路后,會(huì)促使巨噬細(xì)胞分泌生長(zhǎng)因子,例如VEGF和HGF,這些生長(zhǎng)因子能夠促進(jìn)血管生成和組織修復(fù) [18]。此外,CSF2通過(guò)PI3K-Akt信號(hào)通路,還可以提升巨噬細(xì)胞的存活能力和功能,強(qiáng)化其在組織修復(fù)中的作用 [19]。


4. 相關(guān)信號(hào)通路

CSF2主要借助JAK-STAT信號(hào)通路發(fā)揮作用。當(dāng)CSF2與受體結(jié)合后,JAK2被激活,進(jìn)而使STAT5磷酸化,促進(jìn)其發(fā)生二聚化并轉(zhuǎn)位至細(xì)胞核內(nèi),最終調(diào)節(jié)下游基因的表達(dá) [20]。具體而言,CSF2通過(guò)JAK2-STAT5信號(hào)通路,促進(jìn)炎癥因子的釋放以及炎癥細(xì)胞的活化 [21]。同時(shí),CSF2還能夠通過(guò)PI3K-Akt信號(hào)通路,促進(jìn)細(xì)胞的存活和增殖 [22]。在某些特定的細(xì)胞類(lèi)型中,CSF2還可以激活MAPK信號(hào)通路,對(duì)細(xì)胞的分化和功能產(chǎn)生影響。這些信號(hào)通路的激活,使得CSF2在免疫調(diào)節(jié)、炎癥反應(yīng)和腫瘤進(jìn)展等過(guò)程中發(fā)揮著至關(guān)重要的作用。


5. 相關(guān)疾病

5.1 炎癥性疾病

在炎癥性疾病中,CSF2能夠促進(jìn)炎癥細(xì)胞的募集和活化,增強(qiáng)炎癥反應(yīng) [23]。以類(lèi)風(fēng)濕性關(guān)節(jié)炎為例,CSF2會(huì)促使炎癥細(xì)胞活化和增殖,加劇關(guān)節(jié)炎癥和破壞程度 [24]。在炎癥性腸病中,CSF2通過(guò)促進(jìn)炎癥細(xì)胞的活化,進(jìn)一步加重腸道的炎癥反應(yīng) [25]

5.2 腫瘤進(jìn)展

在腫瘤的發(fā)展過(guò)程中,CSF2通過(guò)促進(jìn)腫瘤相關(guān)巨噬細(xì)胞的極化,影響腫瘤的生長(zhǎng)和轉(zhuǎn)移 [26]。比如在胃癌中,CSF2通過(guò)促進(jìn)MSC的重編程,增強(qiáng)腫瘤的侵襲和轉(zhuǎn)移能力 [1]。在乳腺癌中,CSF2通過(guò)促進(jìn)巨噬細(xì)胞的極化,助力腫瘤細(xì)胞實(shí)現(xiàn)免疫逃逸,推動(dòng)腫瘤的進(jìn)展 [27]

5.3 自身免疫性疾病

在自身免疫性疾病方面,CSF2能夠調(diào)節(jié)免疫細(xì)胞的功能,進(jìn)而影響疾病的發(fā)展進(jìn)程 [28]。例如在系統(tǒng)性紅斑狼瘡中,CSF2會(huì)促進(jìn)免疫細(xì)胞的活化,加劇自身免疫反應(yīng) [29]。在多發(fā)性硬化癥中,CSF2通過(guò)調(diào)節(jié)免疫細(xì)胞的功能,對(duì)疾病的進(jìn)展產(chǎn)生影響 [30]。

5.4 感染性疾病

在感染性疾病中,CSF2能夠增強(qiáng)免疫細(xì)胞的功能,提升機(jī)體的抗感染能力 [31]。在結(jié)核病中,CSF2可以促進(jìn)巨噬細(xì)胞的活化,增強(qiáng)其殺菌能力 [32]。在病毒感染時(shí),CSF2通過(guò)促進(jìn)免疫細(xì)胞的活化,提高機(jī)體的抗病毒能力 [33]。


6. 藥物研發(fā)進(jìn)展

目前,針對(duì)CSF2/GM-CSF的藥物研發(fā)主要聚焦于兩大領(lǐng)域:一是利用GM-CSF的免疫調(diào)節(jié)功能以及刺激骨髓產(chǎn)生白細(xì)胞的能力,來(lái)治療癌癥和其他疾??;二是開(kāi)發(fā)抑制GM-CSF的藥物,以降低炎癥和自身免疫疾病中GM-CSF的水平。

當(dāng)下,GM-CSF類(lèi)藥物有多條研發(fā)管線(xiàn)正在推進(jìn),其適應(yīng)癥涵蓋了多種癌癥,如淋巴瘤、白血病、鼻咽腫瘤等,并且在自身免疫性疾病的治療中也被視作潛在的靶點(diǎn)。部分在研管線(xiàn)整理如下表:

藥物 作用機(jī)制 藥物類(lèi)型 在研適應(yīng)癥(疾病名) 在研機(jī)構(gòu) 最高研發(fā)階段
Lenzilumab GM-CSF抑制劑 單克隆抗體 非霍奇金淋巴瘤 | 急性移植物抗宿主病 | 慢性粒單核細(xì)胞白血病 Humanigen, Inc. 臨床3期
Gimsilumab GM-CSF抑制劑 單克隆抗體 鼻咽腫瘤 Morphotek, Inc. 臨床2期
Granulocyte Macrophage Colony Stimulating Factor(Fundació Sant Joan de Déu) GM-CSF調(diào)節(jié)劑 集落刺激因子 復(fù)發(fā)性神經(jīng)母細(xì)胞瘤 | 難治性神經(jīng)母細(xì)胞瘤 | 軟組織腫瘤 Fundació Sant Joan De Déu 臨床2期
Namilumab GM-CSF抑制劑 單克隆抗體 肺結(jié)節(jié)病 | 銀屑病 | 類(lèi)風(fēng)濕關(guān)節(jié)炎 | 結(jié)節(jié)病 Roivant Sciences Ltd. | Kinevant Sciences GmbH | Izana Bioscience Ltd. | Amgen, Inc. 臨床2期
普那利單抗 GM-CSF抑制劑 單克隆抗體 噬血細(xì)胞性淋巴組織細(xì)胞增多癥 | 巨噬細(xì)胞活化綜合征 | 類(lèi)風(fēng)濕關(guān)節(jié)炎 | 痛風(fēng)性關(guān)節(jié)炎 天境生物科技(杭州)有限公司 | 天境生物科技(上海)有限公司 臨床2期
CD40L-GVAX(University of South Florida) CD40激動(dòng)劑 | CSF-2R刺激劑 | GM-CSF刺激劑 治療性疫苗 非小細(xì)胞肺癌 Cell Genesys, Inc. 臨床1/2期
PDM-608 GM-CSF刺激劑 集落刺激因子 | 抗體融合蛋白 帕金森病 California Institute for Biomedical Research 臨床1期

7. 相關(guān)產(chǎn)品推薦

CSF2作為一種重要的細(xì)胞因子,在免疫調(diào)節(jié)、炎癥反應(yīng)和腫瘤進(jìn)展中發(fā)揮著關(guān)鍵作用。通過(guò)深入研究CSF2的作用機(jī)制和相關(guān)信號(hào)通路,可以為多種疾病的治療提供新的靶點(diǎn)和策略。華美生物重磅推出多款高活性的CSF2蛋白產(chǎn)品,并提供CSF2抗體及ELISA試劑盒產(chǎn)品,助力您在CSF2機(jī)制方面的研究或其潛在臨床價(jià)值的探索。

● CSF2 / GM-CSF Recombinant Proteins

● CSF2 / GM-CSF Antibodies

CSB-PA06475A0Rb IHC1 CSB-PA06475A0Rb IHC2

CSF2 Antibody

CSB-PA06475A0Rb

Applications: ELISA, IHC

CSB-PA268599 IHC CSB-PA268599 WB

CSF2 Antibody

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Applications: ELISA, WB, IHC

● CSF2 / GM-CSF ELISA Kits


參考文獻(xiàn):

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[2] Li Y, Zhai P, Zheng Y, et al. Csf2 Attenuated Sepsis-Induced Acute Kidney Injury by Promoting Alternative Macrophage Transition. Frontiers in Immunology, 2020, 11:1415.

[3] Hamilton JA. GM-CSF: from growth factor to central mediator of tissue inflammation. Frontiers in Immunology, 2019, 10:2055.

[4] Kitamura T, Hayashida K, Sakamaki K, et al. Reconstitution of functional receptors for human granulocyte/macrophage colony-stimulating factor (GM-CSF): evidence that the protein encoded by the AIC2B cDNA is a subunit of the murine GM-CSF receptor. Proceedings of the National Academy of Sciences, 1991, 88:5082-5086.

[5] Metcalf D. The biology of granulocyte-macrophage colony-stimulating factor. Blood, 1985, 66:1229-1236.

[6] Shuai K, Liu B, Ziff S, et al. JAK2 is associated with the GM-CSF receptor and is tyrosine phosphorylated and activated following receptor ligation. Cell, 1992, 70:519-529.

[7] Spina D, Zingarelli B, Greter M, et al. GM-CSF controls nonlymphoid tissue dendritic cell homeostasis but is dispensable for the differentiation of inflammatory dendritic cells. Immunity, 2012, 36:1031-1046.

[8] Hamilton JA. GM-CSF: from growth factor to central mediator of tissue inflammation. Frontiers in Immunology, 2019, 10:2055.

[9] Zingarelli B, Helft J, Chow A, et al. GM-CSF controls nonlymphoid tissue dendritic cell homeostasis but is dispensable for the differentiation of inflammatory dendritic cells. Immunity, 2012, 36:1031-1046.

[10] Rousselle A, Sonnemann J, Amann K, et al. CSF2-dependent monocyte education in the pathogenesis of ANCA-induced glomerulonephritis. Annals of the Rheumatic Diseases, 2022, 81:1162-1172.

[11] Ji R, Wu C, Yao J, et al. IGF2BP2-mediated m6A modification of CSF2 reprograms MSC to promote gastric cancer progression. Cell Death and Disease, 2023, 14:693.

[12] Huen SC, Huynh L, Marlier A, et al. GM-CSF promotes macrophage alternative activation after renal ischemia/reperfusion injury. Journal of the American Society of Nephrology, 2015, 26:1334-1345.

[13] Li Y, Zhai P, Zheng Y, et al. Csf2 Attenuated Sepsis-Induced Acute Kidney Injury by Promoting Alternative Macrophage Transition. Frontiers in Immunology, 2020, 11:1415.

[14] Shuai K, Liu B, Ziff S, et al. JAK2 is associated with the GM-CSF receptor and is tyrosine phosphorylated and activated following receptor ligation. Cell, 1992, 70:519-529.

[15] Spina D, Zingarelli B, Greter M, et al. GM-CSF controls nonlymphoid tissue dendritic cell homeostasis but is dispensable for the differentiation of inflammatory dendritic cells. Immunity, 2012, 36:1031-1046.

[16] Li Y, Zhai P, Zheng Y, et al. Csf2 Attenuated Sepsis-Induced Acute Kidney Injury by Promoting Alternative Macrophage Transition. Frontiers in Immunology, 2020, 11:1415.

[17] Rousselle A, Sonnemann J, Amann K, et al. CSF2-dependent monocyte education in the pathogenesis of ANCA-induced glomerulonephritis. Annals of the Rheumatic Diseases, 2022, 81:1162-1172.

[18] Ji R, Wu C, Yao J, et al. IGF2BP2-mediated m6A modification of CSF2 reprograms MSC to promote gastric cancer progression. Cell Death and Disease, 2023, 14:693.

[19] Hamilton JA. GM-CSF: from growth factor to central mediator of tissue inflammation. Frontiers in Immunology, 2019, 10:2055.

[20] Shuai K, Liu B, Ziff S, et al. JAK2 is associated with the GM-CSF receptor and is tyrosine phosphorylated and activated following receptor ligation. Cell, 1992, 70:519-529.

[21] Spina D, Zingarelli B, Greter M, et al. GM-CSF controls nonlymphoid tissue dendritic cell homeostasis but is dispensable for the differentiation of inflammatory dendritic cells. Immunity, 2012, 36:1031-1046.

[22] Li Y, Zhai P, Zheng Y, et al. Csf2 Attenuated Sepsis-Induced Acute Kidney Injury by Promoting Alternative Macrophage Transition. Frontiers in Immunology, 2020, 11:1415.

[23] Ji R, Wu C, Yao J, et al. IGF2BP2-mediated m6A modification of CSF2 reprograms MSC to promote gastric cancer progression. Cell Death and Disease, 2023, 14:693.

[24] Helft J, Bottcher J, Chakravarty P, et al. GM-CSF mouse bone marrow cultures comprise a heterogeneous population of Cd11c(+)Mhcii(+) macrophages and dendritic cells. Immunity, 2015, 42:1197-1211.

[25] Huen SC, Huynh L, Marlier A, et al. GM-CSF promotes macrophage alternative activation after renal ischemia/reperfusion injury. Journal of the American Society of Nephrology, 2015, 26:1334-1345.

[26] Ji R, Wu C, Yao J, et al. IGF2BP2-mediated m6A modification of CSF2 reprograms MSC to promote gastric cancer progression. Cell Death and Disease, 2023, 14:693.

[27] Liao R, Chen X, Cao Q, et al. HIST1H1B Promotes Basal-Like Breast Cancer Progression by Modulating CSF2 Expression. Frontiers in Oncology, 2021, 11:780094.

[28] Hamilton JA. GM-CSF: from growth factor to central mediator of tissue inflammation. Frontiers in Immunology, 2019, 10:2055.

[29] Meisel C, Schefold JC, Pschowski R, et al. Granulocyte-macrophage colony-stimulating factor to reverse sepsis-associated immunosuppression: a double-blind, randomized, placebo-controlled multicenter trial. American Journal of Respiratory and Critical Care Medicine, 2009, 180:640-648.

[30] Huen SC, Huynh L, Marlier A, et al. GM-CSF promotes macrophage alternative activation after renal ischemia/reperfusion injury. Journal of the American Society of Nephrology, 2015, 26:1334-1345.

[31] Ji R, Wu C, Yao J, et al. IGF2BP2-mediated m6A modification of CSF2 reprograms MSC to promote gastric cancer progression. Cell Death and Disease, 2023, 14:693.

[32] Helft J, Bottcher J, Chakravarty P, et al. GM-CSF mouse bone marrow cultures comprise a heterogeneous population of Cd11c(+)Mhcii(+) macrophages and dendritic cells. Immunity, 2015, 42:1197-1211.

[33] Huen SC, Huynh L, Marlier A, et al. GM-CSF promotes macrophage alternative activation after renal ischemia/reperfusion injury. Journal of the American Society of Nephrology, 2015, 26:1334-1345.