Itoh K, Tilden A B, Kumagai K, Balch C M
J Immunol. 1985 Feb;134(2):802-7.
Precursors of activated killer (AK) cells cytotoxic for human noncultured metastatic melanoma and colon carcinoma were characterized. These cells required 3 days incubation with recombinant interleukin 2 (rIL 2) and DNA synthesis for the induction of AK activity. Both negative and positive cell purification methods were used to identify the subpopulation of cells containing AK precursors. By complement-mediated cell depletion studies, AK precursors were largely present in the Leu-11+ fraction, and to a much lesser extent in the Leu-7+ and Leu-2a+ fractions; they were absent in Leu-3a+ and Leu-4+ cells. Lymphocyte subpopulations were then purified with a cell sorter to positively select for the subset containing AK precursors. Leu-11+ cells had the highest level of AK activity and proliferative response when cultured for 3 days with rIL 2 as well as the highest level of NK activity before culture. Leu-7+ cells had neither AK activity nor a proliferative response when cultured with rIL 2, although they still possessed high NK activity. The same levels of AK and NK activity were found in Leu-2a+ and Leu-2a- fractions, but both activities were absent among Leu-4+ and Leu-3a+ cells. Further fractionation with a two-step sorting technique showed that the highest AK activity resided in the Leu-7-Leu-11+ cell fraction. Morphologically, this subfraction was granular lymphocytes. Titration experiments or rIL 2-responsive cells showed that the number of cells required to achieve a comparable level of rIL 2 proliferative response were as follows: 35 X 10(3) cells from unseparated PBL, 10 X 10(3) cells from Leu-11+ cells, 3.3 X 10(3) from Leu-7-Leu-11+ cells, and 640 X 10(3) cells from Leu-7+ cells. These results indicate that the lymphocyte subpopulation that proliferates in the presence of rIL 2 and then develops AK activity was a subpopulation of Leu-11+ granular lymphocytes, which also possessed the highest NK activity. These Leu-11+ cells lacked the antigens defined by the Leu-7, Leu-3a, or Leu-4 antibodies. Although Leu-7+ cells did not respond to rIL 2 by themselves, they may play a role in the induction of AK activity.
对能够杀伤人类非培养转移性黑色素瘤和结肠癌细胞的活化杀伤(AK)细胞的前体细胞进行了特性分析。这些细胞需要与重组白细胞介素2(rIL-2)一起培养3天并进行DNA合成,以诱导AK活性。使用阴性和阳性细胞纯化方法来鉴定含有AK前体细胞的亚群。通过补体介导的细胞清除研究发现,AK前体细胞主要存在于Leu-11+部分,在Leu-7+和Leu-2a+部分中含量较少;在Leu-3a+和Leu-4+细胞中不存在。然后用细胞分选仪纯化淋巴细胞亚群,以阳性选择含有AK前体细胞的亚群。当与rIL-2一起培养3天时,Leu-11+细胞具有最高水平的AK活性和增殖反应,并且在培养前具有最高水平的NK活性。当与rIL-2一起培养时,Leu-7+细胞既没有AK活性也没有增殖反应,尽管它们仍然具有高NK活性。在Leu-2a+和Leu-2a-部分中发现了相同水平的AK和NK活性,但在Leu-4+和Leu-3a+细胞中这两种活性均不存在。用两步分选技术进一步分级分离表明,最高的AK活性存在于Leu-7-Leu-11+细胞部分。从形态学上看,该亚部分是颗粒淋巴细胞。对rIL-2反应性细胞的滴定实验表明,达到可比水平的rIL-2增殖反应所需的细胞数量如下:未分离的外周血淋巴细胞(PBL)中的35×10³个细胞、Leu-11+细胞中的10×10³个细胞、Leu-7-Leu-11+细胞中的3.3×10³个细胞以及Leu-7+细胞中的640×10³个细胞。这些结果表明,在rIL-2存在下增殖然后产生AK活性的淋巴细胞亚群是Leu-11+颗粒淋巴细胞亚群,其也具有最高的NK活性。这些Leu-11+细胞缺乏由Leu-7、Leu-3a或Leu-4抗体定义的抗原。尽管Leu-7+细胞自身对rIL-2没有反应,但它们可能在AK活性的诱导中起作用。