Koren H S, Williams M S
J Immunol. 1978 Nov;121(5):1956-60.
Natural killing (NK) in humans, as well as in other species, has been shown to be specific for antigenic determinants present on the surfaces of a variety of tumor cells. Physical separation of NK cells from K cells, which mediate antibody-dependent cellular cytotoxicity (ADCC), has not been successful; however, there is indirect evidence suggesting that these activities are distinct. To further study the relationship between NK and K cells, competitive inhibition techniques were employed. NK cells can be blocked via two mechanisms: 1) by direct inhibition with NK-sensitive tumor cells binding to NK receptor sites present on the effector cells and 2) by steric inhibition resulting from the binding of antibody-coated cells to the FcR on the effector cells. K cells, however, lack the NK receptor site(s) but are FcR+, and can therefore be blocked only by antibody-coated cells. We therefore postulate that NK and K cells are two separate lymphoid populations. NK cells bear receptor site(s) for NK determinants and FcR, whereas K cells bear only FcR.
在人类以及其他物种中,自然杀伤(NK)作用已被证明对多种肿瘤细胞表面存在的抗原决定簇具有特异性。将NK细胞与介导抗体依赖性细胞毒性(ADCC)的K细胞进行物理分离尚未成功;然而,有间接证据表明这些活性是不同的。为了进一步研究NK细胞与K细胞之间的关系,采用了竞争性抑制技术。NK细胞可通过两种机制被阻断:1)通过NK敏感肿瘤细胞与效应细胞上存在的NK受体位点结合进行直接抑制,以及2)通过抗体包被细胞与效应细胞上的FcR结合导致的空间位阻抑制。然而,K细胞缺乏NK受体位点,但具有FcR,因此只能被抗体包被细胞阻断。因此,我们推测NK细胞和K细胞是两个独立的淋巴细胞群体。NK细胞带有NK决定簇的受体位点和FcR,而K细胞仅带有FcR。