南方医科大学学报 ›› 2013, Vol. 33 ›› Issue (11): 1673-.

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MHSP65-TCL抗黑色素瘤疫苗对免疫细胞活性的影响

董博翰,戴广丽,戚之琳,杨光,吕俊,章尧   

  • 出版日期:2013-11-20 发布日期:2013-11-20

Effect of MHSP65-TCL anti-melanoma vaccine on the activity of immunocytes

  • Online:2013-11-20 Published:2013-11-20

摘要: 目的研究B16黑色素瘤来源的MHSP65-TCL疫苗对黑色素瘤的治疗作用,以及该疫苗在疾病治疗过程中对免疫细胞活
性的影响。方法利用反复冻融的方法裂解B16黑色素瘤细胞制备肿瘤细胞裂解物(TCL),将TCL同结核分支杆菌热休克蛋白
65(MHSP65)联用制备MHSP65-TCL。于不同时间点,给B16黑色素瘤荷瘤小鼠免疫MHSP65-TCL疫苗,观察该疫苗抑制黑
色素细细胞瘤的情况。与此同时,为了验证MHSP65-TCL中的TCL对免疫细胞活性的影响,我们将TCL于体外作用于小鼠脾
细胞,然后流式检测脾细胞CD69表达、脾细胞凋亡以及细胞培养上清液中IL-10和IFN-γ的表达情况。结果通过小鼠体内抑
瘤实验发现,B16黑色素瘤来源的MHSP65-TCL疫苗在小鼠体内产生了抑制黑色素细胞瘤的作用。通过体外细胞实验发现,
MHSP65-TCL中的TCL可以显著刺激体外培养的小鼠脾细胞的活化。除此之外,与这种细胞活化作用相反的,发现TCL还可
以诱导一部分体外培养的小鼠脾细胞发生凋亡,并促进脾细胞分泌IL-10,同时抑制IFN-γ的分泌。结论B16黑色素瘤来源的
MHSP65-TCL疫苗对黑色素瘤具有抑制作用。这种抑制作用主要是通过活化免疫细胞产生的。MHSP65-TCL的主要成分
TCL对免疫细胞还有抑制作用。这可能同TCL中存在的一些免疫细胞抑制物质有关。这些物质的明确以及去除将有助于提
高MHSP65-TCL疫苗的抗肿瘤效力。

Abstract: Objective To evaluate the therapeutic effect of MHSP65-TCL on melanoma and its effect on the activity of the
immunocytes. Methods MHSP65-TCL was prepared by mixing MHSP65 with TCL derived from B16 melanoma cell lysate by
repeated freezing and thawing. The MHSP65-TCL vaccine was administered in mice bearing B16 melanoma, and the changes
in melanoma growth was observed. To investigate the influence of TCL in MHSP65-TCL on the activity of the immunocytes,
we co-cultured TCL and mouse spleen cells in vitro, and analyzed CD69 expression on the cells, cell apoptosis, and levels of
IL-10 and IFN-γ in the cell culture supernatant. Results The MHSP65-TCL vaccine showed an anti-melanoma effect in the
tumor-bearing mice. In the in vitro experiment, TCL in MHSP65-TCL strongly stimulated the activation of mouse spleen cells
while causing apoptosis in some of the immunocytes and promoting cellular IL-10 secretion, but not IFN-γ. Conclusions
MHSP65-TCL derived from B16 melanoma cells has an anti-melanoma effect mediated by the activation of immunocytes. TCL
in MHSP65-TCL also has immunosuppressive effect on immunocytes possibly due to the presence of suppressive components
in TCL, and identifying and eliminating these components may potentially improve the anti-tumor actovoty of MSHP65-TCL
vaccine.