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从自然杀伤细胞受体的发现到原发性免疫缺陷中自然杀伤细胞缺陷的表征。

From Natural Killer Cell Receptor Discovery to Characterization of Natural Killer Cell Defects in Primary Immunodeficiencies.

机构信息

Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.

Laboratory of Host Defenses, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.

出版信息

Front Immunol. 2019 Jul 24;10:1757. doi: 10.3389/fimmu.2019.01757. eCollection 2019.

Abstract

Alessandro Moretta was Professor of Histology at University of Brescia from 1994 to 1997. It was in that period that we met and started a collaboration that continued in the years to follow. He immediately involved us in the production of monoclonal antibodies (mAbs) that allowed the identification and fine characterization of novel receptor molecules that were able to activate or inhibit human Natural Killer cell function, including several antibodies specific for Natural Cytotoxicity Receptor (NCR) and Killer-cell Immunoglobulin-like Receptor (KIR) molecules. These reagents, generated in our laboratory in Brescia, contributed to complete the studies aimed to characterize innate lymphoid NK cells, that had been initiated by Alessandro and his brother Lorenzo in Genoa. Soon, we identified an anti-KIR3DL2 that was subsequently shown to be helpful for the diagnosis and treatment of various forms of cutaneous T cell lymphoma. While in Brescia, Alessandro established a partnership with those of us who were working in the Department of Pediatrics; together, in short time we tackled the goal of studying the role of NK cells in patients with primary immunodeficiencies. This collaboration led to novel discoveries that shed light on the critical role played by NK cells in the immune response against virus and tumors in humans, as best exemplified by our characterization of the molecular mechanisms of impaired control of Epstein-Barr Virus (EBV) infection in patients with X-linked lymphoproliferative (XLP) disease. After Alessandro left Brescia to return to Genoa, our collaboration continued with the same enthusiasm, and even from a distance he remained an extraordinary example of an inspirational and generous mentor. This review is a sign of our gratitude to a mentor and a friend whom we deeply miss.

摘要

亚历山德罗·莫雷塔(Alessandro Moretta)于 1994 年至 1997 年在布雷西亚大学担任组织学教授。正是在那段时间里,我们相识并开始了合作,这种合作一直持续到后来的几年。他立即让我们参与生产单克隆抗体(mAbs),这些抗体能够识别和精细描述能够激活或抑制人类自然杀伤细胞功能的新型受体分子,包括几种针对自然细胞毒性受体(NCR)和杀伤细胞免疫球蛋白样受体(KIR)分子的特异性抗体。这些在我们布雷西亚实验室产生的试剂,有助于完成旨在表征先天淋巴细胞 NK 细胞的研究,这些研究是由亚历山德罗和他在热那亚的哥哥洛伦佐(Lorenzo)发起的。很快,我们鉴定出一种抗 KIR3DL2,随后证明它有助于诊断和治疗各种形式的皮肤 T 细胞淋巴瘤。在布雷西亚期间,亚历山德罗与我们在儿科学系工作的人建立了伙伴关系;在一起,我们在短时间内解决了研究 NK 细胞在原发性免疫缺陷患者中的作用的目标。这种合作带来了新的发现,揭示了 NK 细胞在人类针对病毒和肿瘤的免疫反应中所起的关键作用,我们对 X 连锁淋巴组织增生性疾病(XLP)患者中 EBV 感染失控的分子机制的特征描述就是最好的例证。亚历山德罗离开布雷西亚回到热那亚后,我们的合作继续保持着同样的热情,即使相隔甚远,他仍然是一位鼓舞人心和慷慨大方的导师的杰出典范。这篇综述是我们对一位导师和朋友的感激之情的体现,我们深深地怀念他。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6bb/6668486/6a6963284d36/fimmu-10-01757-g0001.jpg

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