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CD8 T 细胞非细胞毒性抗病毒反应。

The CD8 T Cell Noncytotoxic Antiviral Responses.

机构信息

Division of Hematology/Oncology, Department of Medicine, University of California, San Francisco, San Francisco, California, USA.

Versatope Therapeutics Inc., Lowell, Massachusetts, USA.

出版信息

Microbiol Mol Biol Rev. 2021 May 12;85(2). doi: 10.1128/MMBR.00155-20. Print 2021 May 19.

Abstract

The CD8 T cell noncytotoxic antiviral response (CNAR) was discovered during studies of asymptomatic HIV-infected subjects more than 30 years ago. In contrast to CD8 T cell cytotoxic lymphocyte (CTL) activity, CNAR suppresses HIV replication without target cell killing. This activity has characteristics of innate immunity: it acts on all retroviruses and thus is neither epitope specific nor HLA restricted. The HIV-associated CNAR does not affect other virus families. It is mediated, at least in part, by a CD8 T cell antiviral factor (CAF) that blocks HIV transcription. A variety of assays used to measure CNAR/CAF and the effects on other retrovirus infections are described. Notably, CD8 T cell noncytotoxic antiviral responses have now been observed with other virus families but are mediated by different cytokines. Characterizing the protein structure of CAF has been challenging despite many biologic, immunologic, and molecular studies. It represents a low-abundance protein that may be identified by future next-generation sequencing approaches. Since CNAR/CAF is a natural noncytotoxic activity, it could provide promising strategies for HIV/AIDS therapy, cure, and prevention.

摘要

CD8 T 细胞非细胞毒性抗病毒反应 (CNAR) 是在 30 多年前对无症状 HIV 感染者的研究中发现的。与 CD8 T 细胞细胞毒性淋巴细胞 (CTL) 活性相反,CNAR 在不杀伤靶细胞的情况下抑制 HIV 复制。这种活性具有先天免疫的特征:它作用于所有逆转录病毒,因此既不是表位特异性的,也不是 HLA 受限的。与 HIV 相关的 CNAR 不影响其他病毒家族。它至少部分是由一种 CD8 T 细胞抗病毒因子 (CAF) 介导的,该因子阻止 HIV 转录。描述了用于测量 CNAR/CAF 及其对其他逆转录病毒感染影响的各种检测方法。值得注意的是,现在已经在其他病毒家族中观察到 CD8 T 细胞非细胞毒性抗病毒反应,但由不同的细胞因子介导。尽管进行了许多生物学、免疫学和分子研究,但 CAF 的蛋白结构特征仍具有挑战性。它代表一种低丰度的蛋白质,可能通过未来的下一代测序方法来鉴定。由于 CNAR/CAF 是一种天然的非细胞毒性活性,它可能为 HIV/AIDS 的治疗、治愈和预防提供有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e98/8139528/a0b80d0ae409/MMBR.00155-20-f001.jpg

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