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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Impact of Periodontal Host-Modulation Therapies on Oral-Gut Microbiome Axis in Periodontitis Patients with Hematological Diseases: A Narrative Review.
Impact of Periodontal Host-Modulation Therapies on Oral-Gut Microbiome Axis in Periodontitis Patients with Hematological Diseases: A Narrative Review.
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宿主调节疗法和口腔微生物组靶向策略正成为牙周病治疗的新选择,对接受血液系统恶性肿瘤免疫治疗的患者尤其重要。免疫检查点抑制剂或CAR-T 细胞治疗引起的免疫失调可能加重牙周炎症,并改变口腔微生物群组成和功能。
此外,血液系统恶性肿瘤常用的其他免疫调节治疗——包括单克隆抗体(如利妥昔单抗、达雷妥尤单抗)、免疫调节药物(如来那度胺、沙利度胺)、细胞因子治疗(如干扰素)以及靶向小分子抑制剂(如BTK抑制剂、JAK抑制剂)——也可能通过改变中性粒细胞功能、细胞因子谱和黏膜免疫监视,影响牙周稳态和口腔微生态。口腔微生物群通过口腔—肠道轴与肠道微生物生态系统在功能上相连;牙周病原体可能定植肠道并调节全身免疫应答,进而影响免疫治疗的疗效与安全性。本叙述性综述探讨宿主调节疗法的机制和临床适用性,包括亚抗菌剂量多西环素、ω-3脂肪酸,以及针对微生物组的干预措施(如口腔益生菌、益生元及其他抗微生物制剂),对象为接受免疫治疗的患者。
Host-modulating therapies and oral microbiome-targeted approaches are emerging options in periodontal care and are especially relevant for patients undergoing immunotherapy for hematologic malignancies. Immune dysregulation induced by immune checkpoint inhibitors or CAR-T cell therapy may worsen periodontal inflammation and alter the composition and functions of the oral microbiota. Beyond these, other immunomodulatory treatments commonly employed in hematologic malignancies-including monoclonal antibodies (e. g. , rituximab, daratumumab), immunomodulatory drugs (e. g. , lenalidomide, thalidomide), cytokine-based therapies (e. g. , interferon- ), and targeted small-molecule inhibitors (e. g.
, BTK inhibitors, JAK inhibitors) may also influence periodontal homeostasis and oral microbial ecology by altering neutrophil function, cytokine profiles, and mucosal immune surveillance. The oral microbiota is functionally connected with the intestinal microbial ecosystem through the oral-gut axis, by periodontal pathogens may colonize the gut and modulate systemic immune responses, with potential repercussions on the efficacy and safety of immunotherapy.
This narrative review examines the mechanisms and clinical applicability of host-modulating therapies, including subantimicrobial-dose doxycycline, omega-3 fatty acids, and microbiome-targeted interventions, such as oral probiotics, prebiotics and other antimicrobials in patients treated with immunotherapy.
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