{"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. 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":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Innate Immunity","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1177/17534259221116799","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
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
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.