CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Adaptive natural killer cell expression in response to cytomegalovirus infection in blood and solid cancer.
Adaptive natural killer cell expression in response to cytomegalovirus infection in blood and solid cancer.
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自然杀伤(NK)细胞传统上被认为是固有免疫中一个恒定不变的部分。然而,在NK细胞的一个特定亚群中,近期数据表明其在免疫监视和免疫应答中的“职责”有所扩展,在持久性和细胞毒性方面具有适应性免疫的特征。这些细胞被称为适应性或记忆样NK细胞,其中人巨细胞病毒(HCMV)感染已被证明可驱动适应性NKG2C+ NK细胞的扩增。HCMV是一种普遍存在的病原体,其流行率在全球范围内因国家的社会经济状况而异。适应性NK细胞亚群通常以NKG2C、CD16和CD2表达上调,以及NKG2A、FCεRγ和杀伤细胞免疫球蛋白样受体(KIR)表达受限为特征,尽管这些表型在不同疾病组中可能有所不同。这些受体分布的重新配置与表观遗传因素有关。
因此,本综述试图评估报道HCMV感染后与适应性或记忆样NK细胞相关标志物的文献,并将其与实体癌和血液系统恶性肿瘤相关联。分离并经过离体修饰的适应性NK细胞具有增强抗肿瘤应答的潜力,这可能成为过继性免疫治疗的一种有前景的策略。
Natural Killer (NK) cells are conventionally thought to be an indefinite part of innate immunity.
However, in a specific subset of NK cells, recent data signify an extension of their "duties" in immune surveillance and response, having characteristics of adaptive immunity, in terms of persistence and cytotoxicity. These cells are known as the adaptive or memory-like NK cells, where human cytomegalovirus (HCMV) infection has been shown to drive the expansion of adaptive NKG2C+ NK cells. HCMV is a ubiquitous pathogen whose prevalence differs worldwide with respect to the socioeconomic status of countries.
The adaptive NK cell subpopulation is often characterized by the upregulated expression of NKG2C, CD16, and CD2, and restricted expression of NKG2A, FCεRγ and killer immunoglobulin-like receptors (KIR), although these phenotypes may differ in different disease groups. The reconfiguration of these receptor distributions has been linked to epigenetic factors.
Hence, this review attempts to appraise literature reporting markers associated with adaptive or memory-like NK cells post-HCMV infection, in relation to solid cancers and hematological malignancies. Adaptive NK cells, isolated and subjected to ex vivo modifications, have the potential to enhance anti-tumor response which can be a promising strategy for adoptive immunotherapy.
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