Towards a Cure: Will It Ever Be Truly Achievable?
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Charting a Path Along the Continuum of PMTCT of HIV-1, to Elimination, and Finally to Eradication
EDITORIAL Charting a path along the continuum of PMTCT of HIV-1, to elimination, and finally to eradication In this editorial we traverse the continuum of We stress that much of the hard scientific data on prevention transmission of HIV-1 from mothers to children to and elimination are already available; what is required are health highlight the biomedical history of this problem. service refinements. Eradication demands many more basic science Treatment has progressed from prevention with experiments to confirm the results indicating ‘cure’ in the Mississippi antiretrovirals (ARVs) through to a broader set of baby, and to increase our understanding of the biology of latency interventions, including various breastfeeding options and other health and destruction of the replicative capacity of the virus. We need system improvements, that have increased the possibility of eliminating more information on the cellular and molecular environment of mother-to-child-transmission (MTCT) of HIV. At the far end of the the CD4+ memory cells, and specific sites that harbour the virus. continuum, the spectacular findings in the case of the Mississippi Among the prerequisites for eradication are public health studies ‘cured’ baby indicate that eradication is possible. to enable SA to scale up facilities and personnel for very early HIV infections in children are overwhelmingly due to MTCT,[1] intra- diagnosis and treatment. uterine infections accounting for 10 - 25% of cases and intrapartum infections and those through breastfeeding for 35 - 40%. High- and Prevention middle-income countries have had considerable success in preventing Numerous reviews of trials undertaken to prevent MTCT have new HIV infections in children. -
Are We Standing in Our Own Way on the Path to a Cure for HIV/AIDS
PROFILE Are we standing in our own way on the path to a cure for HIV/AIDS lthough there are many reasons to celebrate the life-extending benefits from antiretroviral Atherapeutics (ART) for HIV/AIDS and the ability to chronically manage patients’ disease for decades, the majority of people around the world living with the virus do not have access to ART and those that do, have over decades developed life-threatening side effects. Our inability to identify a cure to HIV lies not only in the as-of- yet failure of the medical research community to identify and develop appropriate means of ridding the body of the virus but also government and industrial policies that promote public opinion exclusively focused on chronic management scenarios instead of broadly exploring innovation for cure. “An inconvenient truth” (Davis Guggenheim) mates of the magnitude of the global forced government policy for early epidemic. As the majority of Ameri - and expanded access to experimental There are approximately 37 million cans are not rountinely tested for HIV, drugs, the medical community and people living with HIV and 39 million the virus can go years without being society are struggling with the fact have died of AIDS-related diseases diagnosed in an HIV positive person. that we are barely managing the HIV since the start of the epidemic in 1981. With these statistics it is no wonder epidemic and AIDS crisis. For years we As of March 2015, only 15 million that every day an estimated 5,600 have been locked into thinking of people have access to treatments for people globally become newly infected solutions in terms of a chronic disease HIV. -
Pathways to an HIV Cure: Tools for Community and Clinicians AIDS 2020: Virtual Pre-Conference 1 – 3 July
Pathways to an HIV cure: tools for community and clinicians AIDS 2020: Virtual Pre-Conference 1 – 3 July WEDNESDAY 1 JULY 2020 7am PDT/ 10am EDT/ 4pm CEST & SAST/ 10pm CST/ midnight AEST 45’ Opening Welcome and Introduction Session Semi live Sharon Lewin, The Doherty Institute, The University of Melbourne, Australia Steve Deeks, UCSF, United States Keynote HIV cure strategies relevant to resource-limited settings Thumbi Ndung’u, Africa Health Research Institute, South Africa Community A glass half full: changing attitudes and values to achieve opening an HIV cure Michael Louella, defeatHIV CAB, United States 7.45am PDT/ 10.45am EDT/ 4.45pm CEST & SAST/ 10.45pm CST/ 00.45am AEST (+1d) 45’ Session 1 Advancing the HIV cure field and debunking myths and misconceptions On demand Chair Jessica Salzwedel, AVAC, United States Invited Top 5 myths and misconceptions speakers Advocacy-for-Cure grantees: Philister Adhiambo, Kenya Medical Research Institute, Kenya Owen Mulenga, Treatment Advocacy and Literacy Campaign, Zambia Josephine Nabukenya, MUJHU, Uganda Top 10 advances in laboratory research Lillian Cohn, Chan Zuckerberg Biohub, United States Top 10 advances in clinical research and social sciences Katharine J. Bar, Penn Centre for AIDS Research, United States THURSDAY 2 JULY 2020 6am PDT/ 9am EDT/ 3pm CEST & SAST/ 9pm CST/ 11pm AEST 45’ Session 2 Challenges of clinical trials in cure Semi live Moderator Richard Jefferys, TAG, United States Panelists Analytical Treatment Interruptions in HIV Cure clinical trials - community and clinician perspectives -
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WHAT ABOUT CONDOMS? CONFERENCE UPDATE: T HE CROI REPORT WHY I RIDE: Ou T AND OPEN IN THE RIDE FOR AIDS CHICAGO POSITIVELY AWARE THE HIV TREATMENT JOURNAL OF TEST POSITIVE AWARE NETWORK MAY+JUNE 2015 T HE BIGGES CHANGES IN 20 YEARS ARE COMING REIn THINK NG HIV NEW APPROACHES TO TREATMENT n CHASING THE CURE n 3D animation OF HIV Client Name: GSK/Triumeq Healthcare This advertisement prepared by: Product: Triumeq Havas Worldwide Job Number: 200 Hudson Street 65013 Filename 65013_58522_M02_DTR045R0_CouchSpread_ Last Modified 1-14-2015 12:41 PM User / PrevUs- Derrick.Edwin / Aileen.Boyce Client GSK Triumeq Art Director M. Culbreth Bleed 16.25” x 10.75” Path Premedia:Volumes:Premedia:Pre- CMYK press:65013_58522:Final:Pre- 0000065013_0000058522_M02_DTR045R0_FCAD – Positively Aware New York, New York 10013 Create 1-14-2015 10:42 AM Artist Kerry Trim 16” x 10.5” press:65013_58522_M02_DTR045R0_ CouchSpread_FCAD-for PREPRESS. Proof Caption: “I have the courage to start HIV…” (Man on Couch) 3 Traffic R. Rodriguez Saftey 15” x 10” indd Fonts Helvetica Neue LT Std (75 Bold, 77 Bold Condensed, 57 Condensed, 55 Roman, 47 Light Condensed, 67 Medium Condensed, 47 Light Condensed Oblique; OpenType), Minion Pro (Regular; OpenType), TT Slug Media: 4/C Magazine Spread + PBW +PBW + ½ PBW AD: M. Culbreth OTF (Regular; OpenType) PAR # DTR045R0 AE: M. Halle Art TRIU_58522_01_CeasarCouchAd_SW_V6_HR.tif (Premedia:Prepress:65013_58522:Original:1.14.15:0000065013_0000058522_M02_DTR045R0_CouchSpread_FCAD Folder:Links:TRIU_58522_01_CeasarCouch- Ad_SW_V6_HR.tif), ViiVHCcmyk.ai (Premedia:Prepress:65013_58522:Original:1.14.15:0000065013_0000058522_M02_DTR045R0_CouchSpread_FCAD Folder:Links:ViiVHCcmyk.ai), Triumeq_US_CMYK_Reg_NEW. Prod: I. Waugh ai (Premedia:Prepress:65013_58522:Original:1.14.15:0000065013_0000058522_M02_DTR045R0_CouchSpread_FCAD Folder:Links:Triumeq_US_CMYK_Reg_NEW.ai), TRIU_58522_02_ItsTimeLogo_SW_V1_130_ B: 16.25” x 10.75” T: 16” x 10.5” Bill Studio Labor OOP to: 0000065013 S: 15” x 10” Gutter Safety = 1” B:16.25” T:16” S:15” TRIUMEQ is a once-a-day pill used to treat HIV-1. -
HIV/AIDS and Cancer Cure: Is It the Same Battle?
HIV/AIDS and Cancer cure: Is it the same battle? Monsef Benkirane Molecular Virology Laboratory [email protected] IAS HIV Cure & Cancer Forum Paris, France www.iasociety.org Dynamic of imatinib-treated Chronic Myeloid Leukemia Mature cancer cells Highly divinding Cancer Stem cells www.iasociety.org Persistence and resistance are theBarriers to Cure HIV/AIDS Cancer Latent provirus Quiescent / slow-cycling Quiescent/ slow-cycling Long-lived Long-lived Indefinite proliferative potential Non sensitive to ART Enhanced repair capacity Not visible to the immune system highly resistant to DNA HIV-specific CD8 T cell response damage/Tolerance decreases with cART Enhanced checkpoint kinase expression drug efflux transporter Renewed by dedifferentiation of proliferating cancer HIV/AIDS and cancer are Residual diseases Although their molecular bases are different, similar cure strategies are being developed www.iasociety.org which cure and how to achieve it? Two main strategies are being pursued Eradication, which will require a complete elimination of infected cells, for which the Berlin patient represents a proof of concept. Considering the Boston patients, eradication will require elimination of HIV infected cells and replacement with HIV resistant cells. Remission: HIV controllers and the VISCONTI patients suggest that remission is achievable. This strategy should include monitoring of inflammatory and procoagulant indices. – Find and diminish size of the reservoir (LRAs, bNAbs, CAR-T cell) – Reduce seeding of latent pool with early/more ART – Reverse latency (LRAs, TLR7) – Increase HIV-specific immune function (vaccines or anti PD-L1) – Reduce immune activation – Gene therapy targeting the virus and the host – Allogeneic stem cell transplantation Combination therapy may be necessary While proof-of-concepts are there, we still have to gain important knowledge to achieve HIV eradication or remission Strategies to eradicate latent reservoirs. -
Study Protocol
RIVER Protocol Version 5.0 20-Oct-2016 GENERAL INFORMATION This document was constructed using the MRC CTU Protocol Template Version 3.0. The MRC CTU endorses the Standard Protocol Items: Recommendations For Interventional Trials (SPIRIT) initiative. It describes the RIVER trial, co-ordinated by the Medical Research Council (MRC) Clinical Trials Unit at UCL (herein referred to as MRC CTU), and provides information about procedures for entering participants into it. The protocol should not be used as an aide-memoire or guide for the treatment of other participants. Every care has been taken in drafting this protocol, but corrections or amendments may be necessary. These will be circulated to the registered investigators in the trial, but sites entering participants for the first time are advised to contact RIVER Co-ordinating Centre at, MRC CTU, to confirm they have the most up-to-date version. COMPLIANCE The trial will be conducted in compliance with the approved protocol, the Declaration of Helsinki 1996, the principles of Good Clinical Practice (GCP), Commission Directive 2005/28/EC with the implementation in national legislation in the UK by Statutory Instrument 2004/1031 and subsequent amendments, the UK Data Protection Act (DPA number: Z6364106), and the National Health Service (NHS) Research Governance Framework for Health and Social Care (RGF). SPONSOR Imperial College London is the trial sponsor and has delegated responsibility for the overall management of the RIVER trial to the MRC CTU (RIVER Co-ordinating Centre). Queries relating to Imperial sponsorship of this trial should be addressed to the chief investigator via the Imperial Joint Research Compliance Office. -
What Will It Take to Cure HIV?
IAS–USA Topics in Antiviral Medicine Perspective What Will It Take to Cure HIV? Investigational strategies to attempt HIV cure or remission include very detectable virus during 3 years of treat- early initiation of antiretroviral therapy to limit the latent HIV reservoir and ment but exhibited viral rebound 2 preinfection vaccination. In the setting of viral suppression, strategies include weeks to 3 weeks after stopping treat- reactivation of latently infected cells (eg, through “shock” therapy with ment. Similarly, an HIV-infected baby histone deacetylase inhibitors or other agents); use of broadly neutralizing in Milan began antiretroviral treatment antibodies, therapeutic vaccines, immunotoxins, or other immune-based 12 hours after birth and had no detect- therapies to kill latently infected cells; and gene editing to induce target able virus for 3 years while receiving cell resistance (eg, by eliminating the CC chemokine receptor 5 [CCR5] treatment but exhibited viral rebound 2 coreceptor). Improved ability to detect and quantify very low levels of virus weeks to 3 weeks after stopping treat- is needed. This article summarizes a presentation by Jintanat Ananworanich, ment.5-9 MD, PhD, at the IAS–USA continuing education program held in New York, In general, it is believed that earlier New York, in October 2014. initiation of antiretroviral therapy and the longer it is maintained improve the Keywords: HIV, cure, remission, viral reservoir, latent infection chance of limiting the viral reservoir and achieving HIV remission. How- ever, among the infants who eventually HIV cure research currently focuses 7 months, respectively, after receiv- exhibited rebound after stopping anti- on 2 goals: complete eradication of ing bone marrow transplantation with retroviral therapy, time to viral rebound HIV from the body and HIV remission. -
Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection
Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection Developed by the HHS Panel on Antiretroviral Therapy and Medical Management of Children Living with HIV—A Working Group of the Office of AIDS Research Advisory Council (OARAC) How to Cite the Pediatric Guidelines: Panel on Antiretroviral Therapy and Medical Management of Children Living with HIV. Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection. Available at http://aidsinfo.nih.gov/content- files/lvguidelines/pediatricguidelines.pdf. Accessed (insert date) [include page numbers, table number, etc. if applicable] Use of antiretrovirals in pediatric patients is evolving rapidly. These guidelines are updated regularly to provide current information.The most recent information is available at http://aidsinfo.nih.gov. What’s New in the Pediatric Guidelines (Last updated April 14, 2020; last reviewed April 14, 2020) The Panel on Antiretroviral Therapy and Medical Management of Children Living with HIV (the Panel) has reviewed previous versions of the Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection and revised the text and references. Key updates are summarized below. April 14, 2020 When to Initiate Therapy in Antiretroviral-Naive Children • The Panel now recommends rapid initiation of antiretroviral therapy (ART) for all children, not just those aged <1 year. Rapid initiation is defined as initiating therapy immediately or within days of HIV diagnosis. • Because the Panel no longer makes recommendations about when to initiate ART based on a child’s age (either <1 year of age or ≥1 year of age), Table A has been deleted and the data that support rapid initiation have been grouped by outcome (i.e., survival and health benefits, neurodevelopmental benefits, immune benefits, and viral reservoirs and viral suppression). -
(Rftca) Accelerates a Global Cure for Aids with License of Chromocell’S Proprietary Cell Engineering Technology
RESEARCH FOUNDATION TO CURE AIDS (RFTCA) ACCELERATES A GLOBAL CURE FOR AIDS WITH LICENSE OF CHROMOCELL’S PROPRIETARY CELL ENGINEERING TECHNOLOGY • The Chromovertâ Technology platform provides an opportunity to create a scalable cell therapy cure for HIV/AIDS by enabling the purification of sufficient numbers of curative cells following the use of other biotechnologies already demonstrated to engineer cells that mimic natural biological resistance to HIV/AIDS; • With this technology, RFTCA will establish a new and charitable non-for-profit research incubator hub in order to research, develop and commercialize a safe and scalable cure for all those in need, regardless of ability to pay; • Chromovert Technology was invented at The Rockefeller University by Kambiz Shekdar, Ph.D., and is pioneered and owned by Chromocell Corporation, a life sciences company that was spun-out of the university. September 4, 2019 – NEW YORK, NY. – Research Foundation to Cure AIDS (RFTCA) has obtained a worldwide license to biotechnology known as Chromovertâ Technology, to research, develop and commercialize a cure for HIV/AIDS. This is the first and only case of an IRS Code § 501(c)3 not-for-profit organization holding rights to biotechnology with the promise to cure AIDS. RFTCA’s mission is to develop an AIDS cure and to make it available and affordable to all of the 37 million people living with HIV/AIDS worldwide. The emphasis in the medical community, until recently, has been on containing the AIDS epidemic with treatment and prevention alone. But recent advances in stem cell biology and cellular engineering have created new opportunities that could lead to a global cure. -
Get on the Fast-Track — the Life-Cycle Approach To
Get on the Fast-Track The life-cycle approach to HIV Finding solutions for everyone at every stage of life 0 – 14 50+ 1 5 – 24 Key 2 5 – populations 49 UNAIDS | 2016 2 contents 1 Foreword 3 2 Introduction 6 3 Children (0–14) 12 4 Young people (15–24) 28 5 Key populations throughout the life cycle 50 6 Adulthood (25–49) 72 7 Ageing (50+) 90 8 Conclusion 101 9 AIDS by the numbers 105 10 Annex on methods 133 2 foreword The scope of HIV prevention and treatment options has never been wider than it is today. The world now has the scientific knowledge and experience to reach people with HIV options tailored to their lives in the communities in which they live. This life-cycle approach to HIV ensures that we find the best solutions for people throughout their lifetime. And it begins with giving children a healthy start in life free from HIV. The progress made in reducing mother-to-child transmission of HIV is one of the remarkable success stories in global health. Antiretroviral medicines have averted 1.6 million new HIV infections among children since 2000. Even so, intensified efforts are needed to virtually eliminate transmis- sion from mother to child. Adolescence is a turbulent time, and a particularly dangerous time for young women living in sub-Saharan Africa. As they transition to adulthood, their risk of becoming infected with HIV increases dramatically. When women and girls are empowered, they have the means to protect themselves from becoming infected with HIV and to access HIV services. -
Editing a Cure
MILESTONES infection and prompted further research into gene-based therapies to genome editing target HIV. Although genome editing had had been been proven efficient in rendering proven efficient T cells refractory to HIV infection, in rendering it was not until years later, in 2014, T cells that a team led by Pablo Tebas and Carl June at the University of refractory to Pennsylvania in Philadelphia showed HIV infection this could be done in infected Credit: Bloomberg/Rob Waters via Getty Images Getty via Bloomberg/Rob Waters Credit: individuals. The clinical trial enrolled 12 patients who were infused with autologous CD4+ T cells modified at the CCR5 locus by zinc-finger nucleases (ZFNs). The patients who stopped ART after cell transfusion exhibited slow viral rebound and proliferation of the modified T cells, MILESTONE 18 indicating enhanced control of the virus. Moreover, one study participant with no viral rebound Editing a cure during ART interruption was found to harbor a single mutated copy of CCR5 and after transfusion a large Timothy Ray Brown—also known transplantation and interruption of proportion of this patient’s T cells as the ‘Berlin patient’—is the only antiretroviral therapy (ART). were resistant to HIV. person ever to be cured of HIV. His Although at the time of transplant Together, these findings story and the research that followed Brown also carried HIV variants demonstrated that gene-targeting are intimately linked to the discovery, tropic for the CXCR4 chemokine approaches could provide a safer back in 1996, that homozygosity for receptor, Hütter reasoned that their and more practical approach than a CCR5 allele with a 32-base-pair numbers might have been too low to the risky and restrictive HSCT and deletion (delta32/delta32) renders allow reseeding of the new immune opened the door for ZFNs and some individuals resistant to system. -
Enhanced Normalisation of CD4/CD8 Ratio with Earlier Antiretroviral Therapy at Primary HIV Infection
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Spiral - Imperial College Digital Repository JAIDS Journal of Acquired Immune Deficiency Syndromes Publish Ahead of Print DOI: 10.1097/QAI.0000000000001013 Enhanced normalisation of CD4/CD8 ratio with earlier antiretroviral therapy at Primary HIV Infection John Thornhill 1, Jamie Inshaw 2, Pontiano Kaleebu 3, David Cooper 4, Gita Ramjee 5, Mauro Schechter 6, Giuseppe Tambussi 7, Julie Fox 8, Miriam Samuel 8, Jose Maria Miro 9, Jonathan Weber 1, Kholoud Porter 2, Sarah Fidler 1 on behalf of UK Register of HIV Seroconverters and SPARTAC Trial Investigators 1. Imperial College, Department of Medicine, London, United Kingdom; 2. MRC Clinical Trials Unit at UCL, Institute of Clinical Trials & Methodology, London, United Kingdom; 3. Medical Research Council, Uganda Virus Research Institute, Entebbe, Uganda; 4. University of New South Wales, Kirby Institute, Sydney, Australia; 5. Medical Research Council, HIV Prevention Unit, Durban, South Africa; 6. Projeto Praça Onze, Hospital Escola Sao Francisco de Assis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; 7. Ospedale San Raffaele, Division of Infectious Diseases, Milan, Italy; 8. Kings College London, Guys and St Thomas' NHS Trust, London, United Kingdom; 9. University of Barcelona, Hospital Clinic, Barcelona, Spain †Correspondence should be addressed to: John Thornhill, Winston Churchill Wing, St Mary’s Hospital, Praed St. London W2 1NY Email: [email protected] Keywords: Primary HIV Infection, Seroconversion, Acute HIV infection, CD4/CD8 ratio, CD4:CD8, Early Antiretroviral therapy Conflicts of Interest & Source of Funding: The SPARTAC Trial was funded by the Wellcome Trust (Grant Reference Number: 069598).