Mitani M, Matsumoto T, Mori K, Miake S, Himeno K, Nomoto K
J Clin Lab Immunol. 1985 Oct;18(2):97-101.
A high degree of cytostatic activity was detected in peritoneal exudate cells (PEC) from BALB/c mice immunized with mitomycin C-treated Meth A cells (MMC-MA) given intraperitoneally (i.p.) While this cytostatic activity was not detected in a nonadherent fraction of immune PEC, the addition of starch-induced PEC to the nonadherent immune cells led to a cytostatic activity. Treatment of these nonadherent cells with anti-Thy-1 X 2 or anti-Lyt-1 X 2 antibody plus complement abolished the restored cytostatic activity. Normal PEC were also rendered cytostatic after addition of the culture supernate of a nonadherent fraction of immune PEC mixed with MMC-MA. These findings suggest that macrophages are rendered cytostatic by immunization with tumor antigen and that these cytostatic macrophages evolve after activation of sensitized Lyt-1 positive T lymphocytes.
在用丝裂霉素C处理的Meth A细胞(MMC-MA)腹腔注射免疫的BALB/c小鼠的腹腔渗出细胞(PEC)中检测到高度的细胞抑制活性。虽然在免疫PEC的非黏附部分未检测到这种细胞抑制活性,但将淀粉诱导的PEC添加到非黏附免疫细胞中会产生细胞抑制活性。用抗Thy-1 X 2或抗Lyt-1 X 2抗体加补体处理这些非黏附细胞可消除恢复的细胞抑制活性。在添加与MMC-MA混合的免疫PEC非黏附部分的培养上清液后,正常PEC也具有细胞抑制作用。这些发现表明,巨噬细胞通过肿瘤抗原免疫而具有细胞抑制作用,并且这些细胞抑制性巨噬细胞在致敏的Lyt-1阳性T淋巴细胞激活后产生。