{"title":"Therapeutic vaccines and immunotherapy revisited.","authors":"Frances Gotch","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Imunotherapy to induce long-term, non-progressor status in HIV-1-positive persons may be considered in the context of highly active antiretroviral therapy (HAART). The aim of such therapy must be to allow the induction or regeneration of HIV-1-specific immune responses which have the potential to control viraemia, and to alleviate the immunosuppression caused by HIV-1. Trials of therapeutic vaccines and/or cytokines and/or hormones have been conducted and are briefly described. In many cases, potentially beneficial transient HIV-1-specific responses which may translate into clinical advantage have been induced, but these do not persist. Future studies are warranted so that: 1) novel immunogens and other immunotherapeutic agents are further defined and optimised; 2) therapeutic regimens are carefully and rationally designed; and 3) patients are followed for protracted periods of time to observe clinical benefit.</p>","PeriodicalId":81665,"journal":{"name":"Journal of HIV therapy","volume":"10 3","pages":"48-50"},"PeriodicalIF":0.0000,"publicationDate":"2005-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of HIV therapy","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Imunotherapy to induce long-term, non-progressor status in HIV-1-positive persons may be considered in the context of highly active antiretroviral therapy (HAART). The aim of such therapy must be to allow the induction or regeneration of HIV-1-specific immune responses which have the potential to control viraemia, and to alleviate the immunosuppression caused by HIV-1. Trials of therapeutic vaccines and/or cytokines and/or hormones have been conducted and are briefly described. In many cases, potentially beneficial transient HIV-1-specific responses which may translate into clinical advantage have been induced, but these do not persist. Future studies are warranted so that: 1) novel immunogens and other immunotherapeutic agents are further defined and optimised; 2) therapeutic regimens are carefully and rationally designed; and 3) patients are followed for protracted periods of time to observe clinical benefit.