首页> 外文会议>Optical Methods for Tumor Treatment and Detection: Mechanisms and Techniques in Photodynamic Therapy V >Modulation of tumor response to photodynamic therapy in severe combined immunodeficient (SCID) mice by adoptively transferred lymphoid cells
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Modulation of tumor response to photodynamic therapy in severe combined immunodeficient (SCID) mice by adoptively transferred lymphoid cells

机译:过继转移淋巴样细胞对重度联合免疫缺陷(SCID)小鼠对光动力疗法的肿瘤反应的调节

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Abstract: Photodynamic treatment, consisting of intravenous injection of Photofrin$+R$/ (10 mg/kg) followed by exposure to 110 J/cm$+2$/ of 630 plus or minus 10 nm light 24 hours later, cured 100% of EMT6 tumors (murine mammary sarcoma) growing in syngeneic immunocompetent BALB/C mice. In contrast, the same treatment produced no cures of EMT6 tumors growing in either nude or SCID mice (immunodeficient strains). EMT6 tumors growing in BALB/C and SCID mice showed no difference in either the level of Photofrin$+R$/ accumulated per gram of tumor tissue, or the extent of tumor cell killing during the first 24 hours post photodynamic therapy (PDT). In an attempt to improve the sensitivity to PDT of EMT6 tumors growing in SCID mice, these hosts were given either splenic T lymphocytes or whole bone marrow from BALB/C mice. The adoptive transfer of lymphocytes 9 days before PDT was successful in delaying tumor recurrence but produced no cures. A better improvement in PDT response was obtained with tumors growing in SCID mice reconstituted with BALB/C bone marrow (tumor cure rate of 63%). The results of this study demonstrate that, at least with the EMT6 tumor model, antitumor immune activity mediated by lymphoid cell populations makes an important contribution to the curative effect of PDT. !11
机译:摘要:光动力治疗,包括静脉内注射Photofrin $ + R $ /(10 mg / kg),然后在24小时后暴露于110 J / cm $ + 2 $ /的630正负10 nm光中,治愈100%同基因免疫功能的BALB / C小鼠中生长的EMT6肿瘤(鼠乳腺肉瘤)的分布。相比之下,相同的治疗方法无法治愈裸鼠或SCID小鼠(免疫缺陷病毒株)中生长的EMT6肿瘤。在BALB / C和SCID小鼠中生长的EMT6肿瘤在每克肿瘤组织中累积的Photofrin $ + R $ /水平或光动力疗法(PDT)后的最初24小时内杀死肿瘤细胞的程度均无差异。为了提高在SCID小鼠中生长的EMT6肿瘤对PDT的敏感性,对这些宿主给予了BALB / C小鼠的脾脏T淋巴细胞或整个骨髓。在PDT前9天,过继转移淋巴细胞成功延迟了肿瘤的复发,但没有治愈方法。在用BALB / C骨髓重建的SCID小鼠中生长的肿瘤中,PDT反应得到了更好的改善(肿瘤治愈率为63%)。这项研究的结果表明,至少在EMT6肿瘤模型中,淋巴样细胞群体介导的抗肿瘤免疫活性对PDT的疗效起着重要作用。 !11

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