Báo cáo sinh học: Biochemical prevention and treatment of viral infections – A new paradigm in medicine for infectious diseases
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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành hóa học dành cho các bạn yêu hóa học tham khảo đề tài: Biochemical prevention and treatment of viral infections – A new paradigm in medicine for infectious diseases
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Báo cáo sinh học: " Biochemical prevention and treatment of viral infections – A new paradigm in medicine for infectious diseases"Virology Journal BioMed Central Open AccessReviewBiochemical prevention and treatment of viral infections – A newparadigm in medicine for infectious diseasesHervé Le Calvez*1, Mang Yu2 and Fang Fang2Address: 1Abgent, Inc. 6310 Nancy Ridge Drive, Suite 106, San Diego, CA 92121 USA and 2NexBio, Inc. 6330 Nancy Ridge Drive, Suite 105, SanDiego, CA 92121 USAEmail: Hervé Le Calvez* - lecalvez@abgent.com; Mang Yu - myu@nexbio.com; Fang Fang - ffang@nexbio.com* Corresponding authorPublished: 23 November 2004 Received: 10 November 2004 Accepted: 23 November 2004Virology Journal 2004, 1:12 doi:10.1186/1743-422X-1-12This article is available from: http://www.virologyj.com/content/1/1/12© 2004 Le Calvez et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.viral mRNAanti-sense oligonucleotideribozymeRNA interferenceviral infectious diseaseblocking antibodysoluble receptorrhinovirus Abstract For two centuries, vaccination has been the dominating approach to develop prophylaxis against viral infections through immunological prevention. However, vaccines are not always possible to make, are ineffective for many viral infections, and also carry certain risk for a small, yet significant portion of the population. In the recent years, FDAs approval and subsequent market acceptance of Synagis, a monoclonal antibody indicated for prevention and treatment of respiratory syncytial virus (RSV) has heralded a new era for viral infection prevention and treatment. This emerging paradigm, herein designated Biochemical Prevention and Treatment, currently involves two aspects: (1) preventing viral entry via passive transfer of specific protein-based anti-viral molecules or host cell receptor blockers; (2) inhibiting viral amplification by targeting the viral mRNA with anti-sense DNA, ribozyme, or RNA interference (RNAi). This article summarizes the current status of this field. system, we refer the new antiviral approaches as Bio-IntroductionA landmark in the battle against viral infectious diseases chemical Prevention and Treatment (see figure 1). Bio-was made in 1798 when Jenner first inoculated humans chemical Prevention and Treatment, as an alternative toagainst smallpox with the less virulent cowpox. For about vaccines and chemical compound based antiviral drugs,two centuries since then, humans relied almost exclu- may prove to be particularly valuable in the areas wheresively on vaccines for protection against viruses. Only in vaccines and/or chemical drugs can not be generated orthe recent years, new strategies for controlling viral infec- have not been successful in human, including diseasestious diseases have emerged, which have so far led to a caused by some common pathogenic viruses, such as HIV,couple of viral prophylaxis/therapeutics on the market. hepatitis C virus (HCV), RSV and human rhinovirusThese strategies are fundamentally different from vaccines (HRV). In this review, we will discuss various molecularin that they attempt to directly interrupt viral infectious intervention approaches.life cycle at molecular level by using proteins or oligonu-cleotides. To differentiate them from the conventionalvaccines that prevent viral infection by boosting immune Page 1 of 6 (page number not for citation purposes)Virology Journal 2004, 1:12 http://www.virologyj.com/content/1/1/12 ...
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Báo cáo sinh học: " Biochemical prevention and treatment of viral infections – A new paradigm in medicine for infectious diseases"Virology Journal BioMed Central Open AccessReviewBiochemical prevention and treatment of viral infections – A newparadigm in medicine for infectious diseasesHervé Le Calvez*1, Mang Yu2 and Fang Fang2Address: 1Abgent, Inc. 6310 Nancy Ridge Drive, Suite 106, San Diego, CA 92121 USA and 2NexBio, Inc. 6330 Nancy Ridge Drive, Suite 105, SanDiego, CA 92121 USAEmail: Hervé Le Calvez* - lecalvez@abgent.com; Mang Yu - myu@nexbio.com; Fang Fang - ffang@nexbio.com* Corresponding authorPublished: 23 November 2004 Received: 10 November 2004 Accepted: 23 November 2004Virology Journal 2004, 1:12 doi:10.1186/1743-422X-1-12This article is available from: http://www.virologyj.com/content/1/1/12© 2004 Le Calvez et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.viral mRNAanti-sense oligonucleotideribozymeRNA interferenceviral infectious diseaseblocking antibodysoluble receptorrhinovirus Abstract For two centuries, vaccination has been the dominating approach to develop prophylaxis against viral infections through immunological prevention. However, vaccines are not always possible to make, are ineffective for many viral infections, and also carry certain risk for a small, yet significant portion of the population. In the recent years, FDAs approval and subsequent market acceptance of Synagis, a monoclonal antibody indicated for prevention and treatment of respiratory syncytial virus (RSV) has heralded a new era for viral infection prevention and treatment. This emerging paradigm, herein designated Biochemical Prevention and Treatment, currently involves two aspects: (1) preventing viral entry via passive transfer of specific protein-based anti-viral molecules or host cell receptor blockers; (2) inhibiting viral amplification by targeting the viral mRNA with anti-sense DNA, ribozyme, or RNA interference (RNAi). This article summarizes the current status of this field. system, we refer the new antiviral approaches as Bio-IntroductionA landmark in the battle against viral infectious diseases chemical Prevention and Treatment (see figure 1). Bio-was made in 1798 when Jenner first inoculated humans chemical Prevention and Treatment, as an alternative toagainst smallpox with the less virulent cowpox. For about vaccines and chemical compound based antiviral drugs,two centuries since then, humans relied almost exclu- may prove to be particularly valuable in the areas wheresively on vaccines for protection against viruses. Only in vaccines and/or chemical drugs can not be generated orthe recent years, new strategies for controlling viral infec- have not been successful in human, including diseasestious diseases have emerged, which have so far led to a caused by some common pathogenic viruses, such as HIV,couple of viral prophylaxis/therapeutics on the market. hepatitis C virus (HCV), RSV and human rhinovirusThese strategies are fundamentally different from vaccines (HRV). In this review, we will discuss various molecularin that they attempt to directly interrupt viral infectious intervention approaches.life cycle at molecular level by using proteins or oligonu-cleotides. To differentiate them from the conventionalvaccines that prevent viral infection by boosting immune Page 1 of 6 (page number not for citation purposes)Virology Journal 2004, 1:12 http://www.virologyj.com/content/1/1/12 ...
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