Tveita Anders, Fauskanger Marte, Bogen Bjarne, Haabeth Ole Audun Werner
Centre for Immune Regulation, Department of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
KG Jebsen Centre for Research on Influenza Vaccines, Institute of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Oncotarget. 2016 Oct 11;7(41):67175-67182. doi: 10.18632/oncotarget.11946.
CD4+ T cells have been shown to reject tumor cells with no detectable expression of major histocompatibility complex class II (MHC II). However, under certain circumstances, induction of ectopic MHC II expression on tumor cells has been reported.To confirm that CD4+ T cell-mediated anti-tumor immunity can be successful in the complete absence of antigen display on the tumor cells themselves, we eliminated MHC II on tumor cells using CRISPR/Cas9. Our results demonstrate that ablation of the relevant MHC II (I-Ed) in multiple myeloma cells (MOPC315) does not hinder rejection by tumor-specific CD4+ T cells. These findings provide conclusive evidence that CD4+ T cells specific for tumor antigens can eliminate malignant cells in the absence of endogenous MHC class II expression on the tumor cells. This occurs through antigen uptake and indirect presentation on tumor-infiltrating macrophages.
已证明CD4+ T细胞能够排斥主要组织相容性复合体II类(MHC II)无可检测表达的肿瘤细胞。然而,在某些情况下,有报道称肿瘤细胞上会诱导异位MHC II表达。为了证实CD4+ T细胞介导的抗肿瘤免疫在肿瘤细胞自身完全不存在抗原呈递的情况下也能成功,我们使用CRISPR/Cas9消除了肿瘤细胞上的MHC II。我们的结果表明,多发性骨髓瘤细胞(MOPC315)中相关MHC II(I-Ed)的缺失并不妨碍肿瘤特异性CD4+ T细胞的排斥作用。这些发现提供了确凿证据,即肿瘤抗原特异性的CD4+ T细胞能够在肿瘤细胞上不存在内源性MHC II表达的情况下消除恶性细胞。这是通过抗原摄取以及在肿瘤浸润巨噬细胞上的间接呈递实现的。