{"title":"讣告:路易斯·塞利姆·切迪德博士是名誉终身会员","authors":"J. Cavaillon","doi":"10.1177/17534259221116799","DOIUrl":null,"url":null,"abstract":"Louis Selim Chedid was born in Cairo (Egypt) in June 1922 anddied inParis inMarch2021at the ageof98.After obtaining his bachelor’s degree in Cairo, he started hismedical studies in Beirut and completed them in Paris, defending his medical thesis on artificial estrogen in 1947. After being trained in Egypt and the United States, he joined the laboratory of Robert Courrier at the College de France (1946). In 1952, he was recruited by the CNRS (National Center for Scientific Research, France). In 1955, he defended his PhD on hormones and infection and started working at the Institut Pasteur (Paris) in the laboratory of Therapeutic Chemistry under André Lamensans.He joined the Institut Pasteur in 1961 andwas promoted to Professor in 1972. In 1973, he became the head of the Experimental Immunotherapy laboratory. In 1986, he moved to the H. Lee Moffit Cancer Center and Research Institute at the Universiy of South Florida, Tampa where he founded a startup working on vaccine adjuvants (VacSyn). Louis Chedid was the co-author of 26 patents. He investigated immune mechanisms with the goal of boosting the defense against infections. Among his main contributions is the identification with Edgar Lederer (1908–1988) of the muramyl dipeptide (MDP), the smallest active part of the peptidoglycan of mycobacteria present in complete Freund adjuvant. He then devoted part of his career to study homologs of MDP and their bioactivities, synthetic vaccines, and adjuvants. He also performed numerous investigations on endotoxins including investigations on enhanced resistance to infection by endotoxins, LPS-induced abortion, production of interleukin-1 and tumor necrosis factor in response to endotoxins, the synergy between MDP and LPS, prevention of endotoxin-induced lethality, the influence of endotoxin on bone marrow cells, endotoxin tolerance, polyclonal activation, LPS-induced radioresistance, localization of injected Cr-labeled LPS, and studies on alkalyl detoxified endotoxins. He offered the basis for an universal anti-endotoxin antibody: “Thereafter, the presence of a few types of “R’ (rough) antibodies or of serum factors reacting with rough antigens have the capability of coping, like masterkeys, with a wide range of infection due to serologically unrelated organisms”. He collaborated with eminent US scientists including JJ Oppenheim, HS Warren, CA Dinarello, SM Wolff, and JM Krueger. With the latter three, he investigated the links between slow wave sleep and IL-1, his most cited paper (462 citations), and addressed the links between sleep and MDP. A Romanian scientist, Constantin Bona (1934–2015) worked for a while in his laboratory on so-called nonspecific immunity before joining the Mount Sinaï Hospital in New York, working on idiotypes and neonatal immunity. They are co-authors of 17 papers including reports on a Nocardia water soluble mitogen. Claude Leclerc started her bright career on vaccines and cancer at Institut Pasteur in his laboratory. Based on an idea of Agnès Ullman, she used the adenylate cyclase toxin from Bordetella pertussis to deliver antigen into the cytosol of the antigen presenting cell. Her work was a continuation of the work on synthetic vaccines pioneered by Louis Chedid and Michael Sela (Weizman Institute), using peptides corresponding to fragments of diphtheria toxin. In 1984, Claude Leclerc showed that intracellular delivery of MDP with the help of antibodies increased its adjuvanticity 10,000-fold. With Chedid, they hypothesized that the MDP receptor was intracellular: “Specific receptors for MDP exist inside the macrophage [...]. To be active, MDP has to be present inside the cells in sufficient concentration.” before Dana Philpott’s and Gabriel Nuñez’ teams later identified the NOD1 & NOD2 cytoplasmic pattern recognition receptors in 2001/ 2002. In 1964, he obtained French citizenship. He received the Bouchard Prize Laureate of the Society of Biology (1954), and the Claude Bernard Prize of the City of","PeriodicalId":13676,"journal":{"name":"Innate Immunity","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"ObituaryLouis Selim Chedid, MD PhDIEIIS honorary life member\",\"authors\":\"J. Cavaillon\",\"doi\":\"10.1177/17534259221116799\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Louis Selim Chedid was born in Cairo (Egypt) in June 1922 anddied inParis inMarch2021at the ageof98.After obtaining his bachelor’s degree in Cairo, he started hismedical studies in Beirut and completed them in Paris, defending his medical thesis on artificial estrogen in 1947. After being trained in Egypt and the United States, he joined the laboratory of Robert Courrier at the College de France (1946). In 1952, he was recruited by the CNRS (National Center for Scientific Research, France). In 1955, he defended his PhD on hormones and infection and started working at the Institut Pasteur (Paris) in the laboratory of Therapeutic Chemistry under André Lamensans.He joined the Institut Pasteur in 1961 andwas promoted to Professor in 1972. In 1973, he became the head of the Experimental Immunotherapy laboratory. In 1986, he moved to the H. Lee Moffit Cancer Center and Research Institute at the Universiy of South Florida, Tampa where he founded a startup working on vaccine adjuvants (VacSyn). Louis Chedid was the co-author of 26 patents. He investigated immune mechanisms with the goal of boosting the defense against infections. Among his main contributions is the identification with Edgar Lederer (1908–1988) of the muramyl dipeptide (MDP), the smallest active part of the peptidoglycan of mycobacteria present in complete Freund adjuvant. He then devoted part of his career to study homologs of MDP and their bioactivities, synthetic vaccines, and adjuvants. He also performed numerous investigations on endotoxins including investigations on enhanced resistance to infection by endotoxins, LPS-induced abortion, production of interleukin-1 and tumor necrosis factor in response to endotoxins, the synergy between MDP and LPS, prevention of endotoxin-induced lethality, the influence of endotoxin on bone marrow cells, endotoxin tolerance, polyclonal activation, LPS-induced radioresistance, localization of injected Cr-labeled LPS, and studies on alkalyl detoxified endotoxins. He offered the basis for an universal anti-endotoxin antibody: “Thereafter, the presence of a few types of “R’ (rough) antibodies or of serum factors reacting with rough antigens have the capability of coping, like masterkeys, with a wide range of infection due to serologically unrelated organisms”. He collaborated with eminent US scientists including JJ Oppenheim, HS Warren, CA Dinarello, SM Wolff, and JM Krueger. With the latter three, he investigated the links between slow wave sleep and IL-1, his most cited paper (462 citations), and addressed the links between sleep and MDP. A Romanian scientist, Constantin Bona (1934–2015) worked for a while in his laboratory on so-called nonspecific immunity before joining the Mount Sinaï Hospital in New York, working on idiotypes and neonatal immunity. They are co-authors of 17 papers including reports on a Nocardia water soluble mitogen. Claude Leclerc started her bright career on vaccines and cancer at Institut Pasteur in his laboratory. Based on an idea of Agnès Ullman, she used the adenylate cyclase toxin from Bordetella pertussis to deliver antigen into the cytosol of the antigen presenting cell. Her work was a continuation of the work on synthetic vaccines pioneered by Louis Chedid and Michael Sela (Weizman Institute), using peptides corresponding to fragments of diphtheria toxin. In 1984, Claude Leclerc showed that intracellular delivery of MDP with the help of antibodies increased its adjuvanticity 10,000-fold. With Chedid, they hypothesized that the MDP receptor was intracellular: “Specific receptors for MDP exist inside the macrophage [...]. To be active, MDP has to be present inside the cells in sufficient concentration.” before Dana Philpott’s and Gabriel Nuñez’ teams later identified the NOD1 & NOD2 cytoplasmic pattern recognition receptors in 2001/ 2002. In 1964, he obtained French citizenship. 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引用次数: 0
摘要
路易·塞利姆·谢迪德1922年6月出生于埃及开罗,2021年3月在巴黎去世,享年98岁。在开罗获得学士学位后,他在贝鲁特开始医学学习,并在巴黎完成学业,1947年为他关于人工雌激素的医学论文辩护。在埃及和美国接受训练后,他于1946年加入了法兰西学院罗伯特·库里尔的实验室。1952年,他被法国国家科学研究中心录用。1955年,他为自己的激素和感染博士学位辩护,并开始在巴黎巴斯德研究所(Institut Pasteur)的治疗化学实验室工作,导师是安德烈·拉曼桑(andr Lamensans)。1961年加入巴斯德研究所,1972年晋升为教授。1973年,他成为实验免疫疗法实验室的负责人。1986年,他搬到坦帕南佛罗里达大学的H. Lee Moffit癌症中心和研究所,在那里他创立了一家致力于疫苗佐剂(VacSyn)的初创公司。路易斯·切迪德是26项专利的共同作者。他研究了免疫机制,目的是增强对感染的防御。他的主要贡献之一是与Edgar Lederer(1908-1988)鉴定了muramyl二肽(MDP),这是存在于完全弗氏佐剂中的分枝杆菌肽聚糖中最小的活性部分。随后,他将部分职业生涯用于研究MDP的同源物及其生物活性、合成疫苗和佐剂。他还对内毒素进行了大量的研究,包括对内毒素感染的增强抵抗,LPS诱导的流产,内毒素反应中白细胞介素-1和肿瘤坏死因子的产生,MDP和LPS之间的协同作用,内毒素诱导的致死性的预防,内毒素对骨髓细胞的影响,内毒素耐受性,多克隆活化,LPS诱导的辐射抗性,注射cr标记的LPS的定位,以及碱解毒内毒素的研究。他为通用抗内毒素抗体提供了基础:“此后,几种‘R’(粗糙)抗体或与粗糙抗原反应的血清因子的存在,就像万能钥匙一样,具有应对由血清学无关的生物体引起的广泛感染的能力。”他与美国著名科学家合作,包括JJ Oppenheim, HS Warren, CA Dinarello, SM Wolff和JM Krueger。通过后三篇论文,他研究了慢波睡眠和被引用次数最多的论文IL-1(462次)之间的联系,并阐述了睡眠和MDP之间的联系。罗马尼亚科学家康斯坦丁·博纳(Constantin Bona, 1934-2015)在加入纽约Sinaï山医院(Mount Hospital)之前,曾在自己的实验室从事过一段时间的所谓非特异性免疫研究,研究独特型和新生儿免疫。他们是17篇论文的合著者,其中包括关于诺卡菌水溶性丝裂原的报告。克劳德·勒克莱尔在巴斯德研究所的实验室开始了她在疫苗和癌症方面的辉煌事业。基于agn Ullman的想法,她使用百日咳博德泰拉的腺苷酸环化酶毒素将抗原传递到抗原提呈细胞的细胞质中。她的工作是Louis Chedid和Michael Sela (Weizman研究所)开创的合成疫苗工作的延续,使用与白喉毒素片段相对应的肽。1984年,Claude Leclerc研究表明,在抗体的帮助下,细胞内递送MDP可使其佐剂性提高10,000倍。通过Chedid,他们假设MDP受体在细胞内:“MDP的特异性受体存在于巨噬细胞内[…]。为了保持活性,MDP必须在细胞内以足够的浓度存在。之后Dana Philpott和Gabriel Nuñez的团队在2001/ 2002年发现了NOD1和NOD2细胞质模式识别受体。1964年,他获得法国国籍。他获得了生物学会的布沙尔奖(1954年)和伦敦市的克劳德·伯纳德奖
ObituaryLouis Selim Chedid, MD PhDIEIIS honorary life member
Louis Selim Chedid was born in Cairo (Egypt) in June 1922 anddied inParis inMarch2021at the ageof98.After obtaining his bachelor’s degree in Cairo, he started hismedical studies in Beirut and completed them in Paris, defending his medical thesis on artificial estrogen in 1947. After being trained in Egypt and the United States, he joined the laboratory of Robert Courrier at the College de France (1946). In 1952, he was recruited by the CNRS (National Center for Scientific Research, France). In 1955, he defended his PhD on hormones and infection and started working at the Institut Pasteur (Paris) in the laboratory of Therapeutic Chemistry under André Lamensans.He joined the Institut Pasteur in 1961 andwas promoted to Professor in 1972. In 1973, he became the head of the Experimental Immunotherapy laboratory. In 1986, he moved to the H. Lee Moffit Cancer Center and Research Institute at the Universiy of South Florida, Tampa where he founded a startup working on vaccine adjuvants (VacSyn). Louis Chedid was the co-author of 26 patents. He investigated immune mechanisms with the goal of boosting the defense against infections. Among his main contributions is the identification with Edgar Lederer (1908–1988) of the muramyl dipeptide (MDP), the smallest active part of the peptidoglycan of mycobacteria present in complete Freund adjuvant. He then devoted part of his career to study homologs of MDP and their bioactivities, synthetic vaccines, and adjuvants. He also performed numerous investigations on endotoxins including investigations on enhanced resistance to infection by endotoxins, LPS-induced abortion, production of interleukin-1 and tumor necrosis factor in response to endotoxins, the synergy between MDP and LPS, prevention of endotoxin-induced lethality, the influence of endotoxin on bone marrow cells, endotoxin tolerance, polyclonal activation, LPS-induced radioresistance, localization of injected Cr-labeled LPS, and studies on alkalyl detoxified endotoxins. He offered the basis for an universal anti-endotoxin antibody: “Thereafter, the presence of a few types of “R’ (rough) antibodies or of serum factors reacting with rough antigens have the capability of coping, like masterkeys, with a wide range of infection due to serologically unrelated organisms”. He collaborated with eminent US scientists including JJ Oppenheim, HS Warren, CA Dinarello, SM Wolff, and JM Krueger. With the latter three, he investigated the links between slow wave sleep and IL-1, his most cited paper (462 citations), and addressed the links between sleep and MDP. A Romanian scientist, Constantin Bona (1934–2015) worked for a while in his laboratory on so-called nonspecific immunity before joining the Mount Sinaï Hospital in New York, working on idiotypes and neonatal immunity. They are co-authors of 17 papers including reports on a Nocardia water soluble mitogen. Claude Leclerc started her bright career on vaccines and cancer at Institut Pasteur in his laboratory. Based on an idea of Agnès Ullman, she used the adenylate cyclase toxin from Bordetella pertussis to deliver antigen into the cytosol of the antigen presenting cell. Her work was a continuation of the work on synthetic vaccines pioneered by Louis Chedid and Michael Sela (Weizman Institute), using peptides corresponding to fragments of diphtheria toxin. In 1984, Claude Leclerc showed that intracellular delivery of MDP with the help of antibodies increased its adjuvanticity 10,000-fold. With Chedid, they hypothesized that the MDP receptor was intracellular: “Specific receptors for MDP exist inside the macrophage [...]. To be active, MDP has to be present inside the cells in sufficient concentration.” before Dana Philpott’s and Gabriel Nuñez’ teams later identified the NOD1 & NOD2 cytoplasmic pattern recognition receptors in 2001/ 2002. In 1964, he obtained French citizenship. He received the Bouchard Prize Laureate of the Society of Biology (1954), and the Claude Bernard Prize of the City of
期刊介绍:
Innate Immunity is a highly ranked, peer-reviewed scholarly journal and is the official journal of the International Endotoxin & Innate Immunity Society (IEIIS). The journal welcomes manuscripts from researchers actively working on all aspects of innate immunity including biologically active bacterial, viral, fungal, parasitic, and plant components, as well as relevant cells, their receptors, signaling pathways, and induced mediators. The aim of the Journal is to provide a single, interdisciplinary forum for the dissemination of new information on innate immunity in humans, animals, and plants to researchers. The Journal creates a vehicle for the publication of articles encompassing all areas of research, basic, applied, and clinical. The subject areas of interest include, but are not limited to, research in biochemistry, biophysics, cell biology, chemistry, clinical medicine, immunology, infectious disease, microbiology, molecular biology, and pharmacology.