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通过接种疫苗靶向皮肤驻留记忆 T 细胞来对抗金黄色葡萄球菌感染。

Targeting Skin-Resident Memory T Cells via Vaccination to Combat Staphylococcus aureus Infections.

机构信息

Host Pathogen Interactions Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland; GlaxoSmithKline, Siena, Italy.

GlaxoSmithKline, Siena, Italy.

出版信息

Trends Immunol. 2021 Jan;42(1):6-17. doi: 10.1016/j.it.2020.11.005. Epub 2020 Dec 9.

Abstract

Tissue-resident memory T cells are important in adaptive immunity against many infections, rendering these cells attractive potential targets in vaccine development. Genetic and experimental evidence highlights the importance of cellular immunity in protection from Staphylococcus aureus skin infections, yet skin-resident memory T cells are, thus far, an untested component of immunity during such infections. Novel methods of generating and sampling vaccine-induced skin memory T cells are paralleled by discoveries of global, skin-wide immunosurveillance. We propose skin-resident memory CD4 T cells as a potential missing link in the search for correlates of protection during S. aureus infections. A better appreciation of their phenotypes and functions could accelerate the development of preventive vaccines against this highly virulent and antibiotic-resistant pathogen.

摘要

组织驻留记忆 T 细胞在针对许多感染的适应性免疫中很重要,这使得这些细胞成为疫苗开发的有吸引力的潜在靶点。遗传和实验证据强调了细胞免疫在预防金黄色葡萄球菌皮肤感染中的重要性,但迄今为止,皮肤驻留记忆 T 细胞是这种感染期间免疫的一个未经测试的组成部分。新型生成和采样疫苗诱导的皮肤记忆 T 细胞的方法与全身性、广泛的皮肤免疫监视的发现相平行。我们提出皮肤驻留记忆 CD4 T 细胞作为在金黄色葡萄球菌感染期间寻找保护相关因素的潜在缺失环节。更好地了解它们的表型和功能可以加速针对这种高度毒力和抗药性病原体的预防性疫苗的开发。

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