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辅助抗肿瘤Lyt-2+细胞毒性T淋巴细胞生成的L3T4+辅助性T细胞的激活:Ia阳性抗原呈递细胞处理和呈递肿瘤抗原的必要性。

The activation of L3T4+ helper T cells assisting the generation of anti-tumor Lyt-2+ cytotoxic T lymphocytes: requirement of Ia-positive antigen-presenting cells for processing and presentation of tumor antigens.

作者信息

Kosugi A, Yoshioka T, Suda T, Sano H, Takahama Y, Fujiwara H, Hamaoka T

机构信息

Department of Oncogenesis, Osaka University Medical School, Japan.

出版信息

J Leukoc Biol. 1987 Dec;42(6):632-41. doi: 10.1002/jlb.42.6.632.

DOI:10.1002/jlb.42.6.632
PMID:2960766
Abstract

The present study investigates the mechanisms of the recognition of tumor antigens by L3T4+ helper T cells responsible for the generation of Lyt-2+ cytotoxic T lymphocytes (CTL) against a major histocompatibility complex (MHC) Class II (Ia) antigen-negative syngeneic X5563 plasmacytoma. Treatment of X5563-immunized spleen cells with anti-L3T4 antibody plus complement (C) diminished the generation of Lyt-2+ anti-X5563 CTL. Since the contribution of L3T4+ cells was completely replaced by the addition of exogenous lymphokines, it was demonstrated that L3T4+ cells functioned as helper T cells assisting the generation of anti-X5563 CTL responses. Elimination of Ia-positive accessory cells (AC) from X5563-immunized spleen cells resulted in the abrogation of CTL generation, whereas the addition of exogenous lymphokines to AC-depleted X5563 immunized spleen cells restored the CTL response. The addition of anti-self Ia antibody to the culture also eliminated CTL responses. These observations demonstrated the requirement of Ia-positive AC for and the involvement of self Ia antigens in the activation of helper T cells. Moreover, use of tumor cells pretreated with paraformaldehyde to cultures of X5563-immunized spleen cells or adding back of AC pretreated with chloroquine to cultures of AC-depleted immune spleen cells failed to generate CTL responses. Finally, the addition of exogenous lymphokines to the above cultures resulted in appreciable restoration of CTL responses. Taken collectively, these results indicate that L3T4+ helper T cells are activated with tumor antigens processed and presented by Ia-positive AC.

摘要

本研究探讨了负责产生针对主要组织相容性复合体(MHC)II类(Ia)抗原阴性的同基因X5563浆细胞瘤的Lyt-2+细胞毒性T淋巴细胞(CTL)的L3T4+辅助性T细胞识别肿瘤抗原的机制。用抗L3T4抗体加补体(C)处理经X5563免疫的脾细胞,可减少Lyt-2+抗X5563 CTL的产生。由于添加外源性淋巴因子可完全替代L3T4+细胞的作用,因此证明L3T4+细胞作为辅助性T细胞发挥作用,协助产生抗X5563 CTL反应。从经X5563免疫的脾细胞中去除Ia阳性辅助细胞(AC)会导致CTL产生的废除,而向AC耗尽的经X5563免疫的脾细胞中添加外源性淋巴因子可恢复CTL反应。向培养物中添加抗自身Ia抗体也可消除CTL反应。这些观察结果证明了Ia阳性AC对于辅助性T细胞激活的必要性以及自身Ia抗原在其中的参与。此外,将用多聚甲醛预处理的肿瘤细胞用于经X5563免疫的脾细胞培养,或向AC耗尽的免疫脾细胞培养物中回加用氯喹预处理的AC,均未能产生CTL反应。最后,向上述培养物中添加外源性淋巴因子可使CTL反应得到明显恢复。总体而言,这些结果表明L3T4+辅助性T细胞是由Ia阳性AC加工和呈递的肿瘤抗原激活的。

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