We have isolated subsets of cells from human PBL and have investigated their abilities to mediate lysis targeted by bispecific antibodies. Targeted cytotoxic cells were divided into two distinct types based on buoyant density. The low buoyant density fraction contained all of the targetable cytotoxic activity in unstimulated PBL, including both T and K cells targeted with anti-CD3 and anti-Fc gamma RIII (CD16) containing bispecific antibodies, respectively. Both types of targetable cytotoxic cells required IL-2 for maintenance of cytotoxic activity, expressed the CD56 (NKH1) marker, and mediated MHC-unrestricted lysis. The targetable T cells in low density PBL were exclusively CD8+ and represented only about 2% of the total PBL. The high buoyant density lymphocytes, depleted of NK cells, had no targetable activity, but were able to generate over several days, targetable T cell activity in the presence of a TCR cross-linking signal plus IL-2. Unlike the low-density cells, the activated high buoyant density effector T cells did not express CD56, consisted of both CD4+ and CD8+ cells, and did not mediate MHC-unrestricted lysis. These cells proliferated more rapidly and generated more total lytic activity than the low-density fraction. Our studies show that targetable cytotoxic activity in human PBL is mediated by several subsets of cells with different activation requirements. Presumably all of these activities could be directed against unwanted cells in clinical or preclinical studies involving targeted cytotoxic cells.

译文

:我们已经从人PBL中分离出细胞子集,并研究了它们介导双特异性抗体靶向裂解的能力。根据浮力密度,靶向的细胞毒性细胞分为两种不同的类型。低浮力密度部分包含未刺激的PBL中所有可靶向的细胞毒活性,包括分别用含双特异性抗体的抗CD3和抗FcγRIII(CD16)靶向的T细胞和K细胞。两种类型的可靶向细胞毒性细胞都需要IL-2来维持细胞毒性活性,表达CD56(NKH1)标记,并介导MHC不受限制的裂解。低密度PBL中的可靶向T细胞仅是CD8,仅占总PBL的约2%。耗尽NK细胞的高浮力密度淋巴细胞没有可靶向的活性,但在存在TCR交联信号加IL-2的情况下,能够在几天内产生可靶向的T细胞活性。与低密度细胞不同,活化的高浮力效应T细胞不表达CD56,由CD4和CD8细胞组成,并且不介导MHC不受限制的裂解。与低密度级分相比,这些细胞增殖更快并产生更多的总裂解活性。我们的研究表明,人PBL中可靶向的细胞毒活性是由具有不同激活要求的细胞的几个子集介导的。在涉及靶细胞毒性细胞的临床或临床前研究中,推测所有这些活性都可以针对不需要的细胞。

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