Elite and posttreatment controllers, two facets of HIV control.


Journal

Current opinion in HIV and AIDS
ISSN: 1746-6318
Titre abrégé: Curr Opin HIV AIDS
Pays: United States
ID NLM: 101264945

Informations de publication

Date de publication:
01 09 2022
Historique:
entrez: 8 8 2022
pubmed: 9 8 2022
medline: 10 8 2022
Statut: ppublish

Résumé

The quest for HIV-1 cure could take advantage of the study of rare individuals that control viral replication spontaneously (elite controllers) or after an initial course of antiretroviral therapy (posttreatment controllers, PTCs). In this review, we will compare back-to-back the immunological and virological features underlying viral suppression in elite controllers and PTCs, and explore their possible contributions to the HIV-1 cure research. HIV-1 control in elite controllers shows hallmarks of an effective antiviral response, favored by genetic background and possibly associated to residual immune activation. The immune pressure in elite controllers might select against actively transcribing intact proviruses, allowing the persistence of a small and poorly inducible reservoir. Evidence on PTCs is less abundant but preliminary data suggest that antiviral immune responses may be less pronounced. Therefore, these patients may rely on distinct mechanisms, not completely elucidated to date, suppressing HIV-1 transcription and replication. PTCs and elite controllers may control HIV replication using distinct pathways, the elucidation of which may contribute to design future interventional strategies aiming to achieve a functional cure.

Identifiants

pubmed: 35938466
doi: 10.1097/COH.0000000000000751
pii: 01222929-202209000-00011
pmc: PMC10004771
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

325-332

Informations de copyright

Copyright © 2022 Wolters Kluwer Health, Inc. All rights reserved.

Références

Buchbinder SP, Katz MH, Hessol NA, et al. Long-term HIV-1 infection without immunologic progression. AIDS 1994; 8:1123–1128.
Deeks SG, Walker BD. Human immunodeficiency virus controllers: mechanisms of durable virus control in the absence of antiretroviral therapy. Immunity 2007; 27:406–416.
Goujard C, Girault I, Rouzioux C, et al. HIV-1 control after transient antiretroviral treatment initiated in primary infection: role of patient characteristics and effect of therapy. Antivir Ther 2012; 17:1001–1009.
Lisziewicz J, Rosenberg E, Lieberman J, et al. Control of HIV despite the discontinuation of antiretroviral therapy. N Engl J Med 1999; 340:1683–1684.
Sáez-Cirión A, Bacchus C, Hocqueloux L, et al. Post-treatment HIV-1 controllers with a long-term virological remission after the Interruption of Early Initiated Antiretroviral Therapy ANRS VISCONTI Study. PLoS Pathog 2013; 9:e1003211.
Davey RT, Bhat N, Yoder C, et al. HIV-1 and T cell dynamics after interruption of highly active antiretroviral therapy (HAART) in patients with a history of sustained viral suppression. Proc Natl Acad Sci U S A 1999; 96:15109–15114.
Hubert JB, Burgard M, Dussaix E, et al. Natural history of serum HIV-1 RNA levels in 330 patients with a known date of infection. The SEROCO Study Group. AIDS 2000; 14:123–131.
Okulicz JF, Marconi VC, Landrum ML, et al. Clinical outcomes of elite controllers, viremic controllers, and long-term nonprogressors in the US Department of Defense HIV Natural History Study. J Infect Dis 2009; 200:1714–1723.
Olson AD, Meyer L, Prins M, et al. An evaluation of HIV elite controller definitions within a large seroconverter cohort collaboration. PLoS One 2014; 9:e86719.
Yang OO, Cumberland WG, Escobar R, et al. Demographics and natural history of HIV-1-infected spontaneous controllers of viremia. AIDS 2017; 31:1091–1098.
Sajadi MM, Constantine NT, Mann DL, et al. Epidemiologic characteristics and natural history of HIV-1 natural viral suppressors. J Acquir Immune Defic Syndr 2009; 50:403–408.
Berg MG, Olivo A, Harris BJ, et al. A high prevalence of potential HIV elite controllers identified over 30 years in Democratic Republic of Congo. eBioMedicine 2021; 65.
Okulicz JF, Lambotte O. Epidemiology and clinical characteristics of elite controllers. Curr Opin HIV AIDS 2011; 6:163–168.
Madec Y, Boufassa F, Porter K, et al. Natural history of HIV-control since seroconversion. AIDS 2013; 27:2451–2460.
Goujard C, Chaix M-L, Lambotte O, et al. Spontaneous control of viral replication during primary HIV infection: when is ‘HIV controller’ status established? Clin Infect Dis 2009; 49:982–986.
Leon A, Perez I, Ruiz-Mateos E, et al. Rate and predictors of progression in elite and viremic HIV-1 controllers. AIDS 2016; 30:1209–1220.
Borrell M, Fernández I, Etcheverrry F, et al. High rates of long-term progression in HIV-1-positive elite controllers. J Int AIDS Soc 2021; 24:e25675.
Hunt PW, Brenchley J, Sinclair E, et al. Relationship between T cell activation and CD4+ T cell count in HIV-seropositive individuals with undetectable plasma HIV RNA levels in the absence of therapy. J Infect Dis 2008; 197:126–133.
Krishnan S, Wilson EMP, Sheikh V, et al. Evidence for innate immune system activation in HIV type 1–infected elite controllers. J Infect Dis 2014; 209:931–939.
Brusca RM, Hanna DB, Wada NI, et al. Subclinical cardiovascular disease in HIV controller and long-term non-progressor populations. HIV Med 2020; 21:217–227.
Pereyra F, Lo J, Triant VA, et al. Increased coronary atherosclerosis and immune activation in HIV-1 elite controllers. AIDS 2012; 26:2409–2412.
Li JZ, Segal FP, Bosch RJ, et al. Antiretroviral therapy reduces T-cell activation and immune exhaustion markers in human immunodeficiency virus controllers. Clin Infect Dis 2020; 70:1636–1642.
Plaçais L, Boufassa F, Lécuroux C, et al. Antiretroviral therapy for HIV controllers: reasons for initiation and outcomes in the French ANRS-CO21 CODEX cohort. eClinicalMedicine 2021; 37:100963.
Initiation of Antiretroviral Therapy | NIH HIV Guidelines. Available at: https://clinicalinfo.hiv.gov/en/guidelines/adult-and-adolescent-arv/initiation-antiretroviral-therapy . Accessed 13 May 2022
BHIVA guidelines on antiretroviral treatment for adults living with HIV-1 2022. Available at: https://www.bhiva.org/treatment-guidelines-consultation . Accessed 13 May 2022
Prise en charge du VIH – Recommandations du groupe d’experts. Available at: https://cns.sante.fr/actualites/prise-en-charge-du-vih-recommandations-dugroupe-dexperts/ . Accessed 13 May 2022
Deacon NJ, Tsykin A, Solomon A, et al. Genomic structure of an attenuated quasi species of HIV-1 from a blood transfusion donor and recipients. Science 1995; 270:988–991.
Zaunders J, Dyer WB, Churchill M, et al. Possible clearance of transfusion-acquired nef/LTR-deleted attenuated HIV-1 infection by an elite controller with CCR5Δ32 heterozygous and HLA-B57 genotype. J Virus Erad 2019; 5:73–83.
Ali A, Ng HL, Blankson JN, et al. Highly attenuated infection with a Vpr-deleted molecular clone of human immunodeficiency virus-1. J Infect Dis 2018; 218:1447–1452.
Miura T, Brumme ZL, Brockman MA, et al. Impaired replication capacity of acute/early viruses in persons who become HIV controllers. J Virol 2010; 84:7581–7591.
Miura T, Brockman MA, Schneidewind A, et al. HLA-B57/B∗5801 human immunodeficiency virus type 1 elite controllers select for rare gag variants associated with reduced viral replication capacity and strong cytotoxic T-lymphocyte recognition. J Virol 2009; 83:2743–2755.
Blankson JN, Bailey JR, Thayil S, et al. Isolation and characterization of replication-competent human immunodeficiency virus type 1 from a subset of elite suppressors. J Virol 2007; 81:2508–2518.
Jiang C, Lian X, Gao C, et al. Distinct viral reservoirs in individuals with spontaneous control of HIV-1. Nature 2020; 585:261–267.
Hatano H, Delwart EL, Norris PJ, et al. Evidence for persistent low-level viremia in individuals who control human immunodeficiency virus in the absence of antiretroviral therapy. J Virol 2009; 83:329–335.
O’Connell KA, Brennan TP, Bailey JR, et al. Control of HIV-1 in elite suppressors despite ongoing replication and evolution in plasma virus. J Virol 2010; 84:7018–7028.
Mens H, Kearney M, Wiegand A, et al. HIV-1 continues to replicate and evolve in patients with natural control of HIV infection. J Virol 2010; 84:12971–12981.
Fukazawa Y, Lum R, Okoye AA, et al. B cell follicle sanctuary permits persistent productive simian immunodeficiency virus infection in elite controllers. Nat Med 2015; 21:132–139.
Boritz EA, Darko S, Swaszek L, et al. Multiple origins of virus persistence during natural control of HIV infection. Cell 2016; 166:1004–1015.
Kiepiela P, Leslie AJ, Honeyborne I, et al. Dominant influence of HLA-B in mediating the potential co-evolution of HIV and HLA. Nature 2004; 432:769–775.
Goulder PJR, Walker BD. HIV and HLA class I: an evolving relationship. Immunity 2012; 37:426–440.
Costello C, Tang J, Rivers C, et al. HLA-B∗5703 independently associated with slower HIV-1 disease progression in Rwandan women. AIDS 1999; 13:1990–1991.
Migueles SA, Sabbaghian MS, Shupert WL, et al. HLA B∗5701 is highly associated with restriction of virus replication in a subgroup of HIV-infected long term nonprogressors. Proc Natl Acad Sci U S A 2000; 97:2709–2714.
Pereyra F, Jia S X, et al. International HIV Controllers Study. The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. Science 2010; 330:1551–1557.
Kaseke C, Park RJ, Singh NK, et al. HLA class-I-peptide stability mediates CD8+ T cell immunodominance hierarchies and facilitates HLA-associated immune control of HIV. Cell Rep 2021; 36:109378.
Altfeld M, Allen TM, Yu XG, et al. HIV-1 superinfection despite broad CD8+ T-cell responses containing replication of the primary virus. Nature 2002; 420:434–439.
Caetano DG, Côrtes FH, Bello G, et al. A case report of HIV-1 superinfection in an HIV controller leading to loss of viremia control: a retrospective of 10 years of follow-up. BMC Infect Dis 2019; 19:588.
Clerc O, Colombo S, Yerly S, et al. HIV-1 elite controllers: beware of super-infections. J Clin Virol 2010; 47:376–378.
Gaiha GD, Rossin EJ, Urbach J, et al. Structural topology defines protective CD8+ T cell epitopes in the HIV proteome. Science 2019; 364:480–484.
Betts MR, Nason MC, West SM, et al. HIV nonprogressors preferentially maintain highly functional HIV-specific CD8+ T cells. Blood 2006; 107:4781–4789.
Koofhethile CK, Ndhlovu ZM, Thobakgale-Tshabalala C, et al. CD8+ T cell breadth and ex vivo virus inhibition capacity distinguish between viremic controllers with and without protective HLA class I alleles. J Virol 2016; 90:6818–6831.
Pereyra F, Addo MM, Kaufmann DE, et al. Genetic and immunologic heterogeneity among persons who control HIV infection in the absence of therapy. J Infect Dis 2008; 197:563–571.
Sáez-Cirión A, Sinet M, Shin SY, et al. Heterogeneity in HIV suppression by CD8 T cells from HIV controllers: association with Gag-specific CD8 T cell responses. J Immunol 2009; 182:7828–7837.
Gea-Banacloche JC, Migueles SA, Martino L, et al. Maintenance of large numbers of virus-specific CD8+ T cells in HIV-infected progressors and long-term nonprogressors. J Immunol 2000; 165:1082–1092.
Migueles SA, Laborico AC, Shupert WL, et al. HIV-specific CD8+ T cell proliferation is coupled to perforin expression and is maintained in nonprogressors. Nat Immunol 2002; 3:1061–1068.
Sáez-Cirión A, Lacabaratz C, Lambotte O, et al. HIV controllers exhibit potent CD8 T cell capacity to suppress HIV infection ex vivo and peculiar cytotoxic T lymphocyte activation phenotype. Proc Natl Acad Sci USA 2007; 104:6776–6781.
Perdomo-Celis F, Passaes C, Monceaux V, et al. Reprogramming dysfunctional CD8+ T cells to promote properties associated with natural HIV control. J Clin Invest 2022; 132:e157549.
Rutishauser RL, Deguit CDT, Hiatt J, et al. TCF-1 regulates HIV-specific CD8+ T cell expansion capacity. JCI Insight 2021; 6:e136648.
Nguyen S, Deleage C, Darko S, et al. Elite control of HIV is associated with distinct functional and transcriptional signatures in lymphoid tissue CD8 + T cells. Sci Transl Med 2019; 11:eaax4077.
Kaufmann DE, Kavanagh DG, Pereyra F, et al. Upregulation of CTLA-4 by HIV-specific CD4+ T cells correlates with disease progression and defines a reversible immune dysfunction. Nat Immunol 2007; 8:1246–1254.
Ferre AL, Hunt PW, McConnell DH, et al. HIV controllers with HLA-DRB1∗13 and HLA-DQB1∗06 alleles have strong, polyfunctional mucosal CD4 + T-cell responses. J Virol 2010; 84:11020–11029.
Buranapraditkun S, Pissani F, Teigler JE, et al. Preservation of peripheral T follicular helper cell function in HIV controllers. J Virol 2017; 91:e00497–e517.
Claireaux M, Galperin M, Benati D, et al. A high frequency of HIV-specific circulating follicular helper T cells is associated with preserved memory B cell responses in HIV controllers. mBio 2018; 9:e00317–e00318.
Benati D, Galperin M, Lambotte O, et al. Public T cell receptors confer high-avidity CD4 responses to HIV controllers. J Clin Investig 2016; 126:2093–2108.
Soghoian DZ, Jessen H, Flanders M, et al. HIV-specific cytolytic CD4 T cell responses during acute HIV infection predict disease outcome. Sci Transl Med 2012; 4:123ra25–123ra25.
Alter G, Dowell KG, Brown EP, et al. High-resolution definition of humoral immune response correlates of effective immunity against HIV. Mol Syst Biol 2018; 14:e7881.
Ackerman ME, Mikhailova A, Brown EP, et al. Polyfunctional HIV-specific antibody responses are associated with spontaneous HIV control. PLoS Pathog 2016; 12:e1005315.
Marras F, Nicco E, Bozzano F, et al. Natural killer cells in HIV controller patients express an activated effector phenotype and do not up-regulate NKp44 on IL-2 stimulation. Proc Natl Acad Sci U S A 2013; 110:11970–11975.
Martin MP, Naranbhai V, Shea PR, et al. Killer cell immunoglobulin-like receptor 3DL1 variation modifies HLA-B∗57 protection against HIV-1. J Clin Invest 2018; 128:1903–1912.
Alter G, Martin MP, Teigen N, et al. Differential natural killer cell-mediated inhibition of HIV-1 replication based on distinct KIR/HLA subtypes. J Exp Med 2007; 204:3027–3036.
Martin-Gayo E, Buzon MJ, Ouyang Z, et al. Potent cell-intrinsic immune responses in dendritic cells facilitate HIV-1-specific T cell immunity in HIV-1 elite controllers. PLoS Pathog 2015; 11:e1004930.
Hartana CA, Rassadkina Y, Gao C, et al. Long noncoding RNA MIR4435-2HG enhances metabolic function of myeloid dendritic cells from HIV-1 elite controllers. J Clin Invest 2021; 131:146136.
Nishimura Y, Gautam R, Chun T-W, et al. Early antibody therapy can induce long-lasting immunity to SHIV. Nature 2017; 543:559–563.
Collins DR, Urbach JM, Racenet ZJ, et al. Functional impairment of HIV-specific CD8+ T cells precedes aborted spontaneous control of viremia. Immunity 2021; 54:2372.e7–2384.e7.
Pernas M, Tarancón-Diez L, Rodríguez-Gallego E, et al. Factors leading to the loss of natural elite control of HIV-1 infection. J Virol 2018; 92:e01805–e01817.
Rosás-Umbert M, Llano A, Bellido R, et al. Mechanisms of abrupt loss of virus control in a cohort of previous HIV controllers. J Virol 2019; 93:e01436–e01518.
Lodi S, Meyer L, Kelleher AD, et al. Immunovirologic control 24 months after interruption of antiretroviral therapy initiated close to HIV seroconversion. Arch Intern Med 2012; 172:1252–1255.
Martin GE, Gossez M, Williams JP, et al. Posttreatment control or treated controllers? Viral remission in treated and untreated primary HIV infection. AIDS 2017; 31:477–484.
The SPARTAC Trial Investigators. Short-course antiretroviral therapy in primary HIV infection. New Engl J Med 2013; 368:207–217.
Namazi G, Fajnzylber JM, Aga E, et al. The Control of HIV After Antiretroviral Medication Pause (CHAMP) study: posttreatment controllers identified from 14 clinical studies. J Infect Dis 2018; 218:1954–1963.
Etemad B, Esmaeilzadeh E, Li JZ. Learning from the exceptions: HIV remission in posttreatment controllers. Front Immunol 2019; 10:1749.
Ananworanich J, Chomont N, Eller LA, et al. HIV DNA set point is rapidly established in acute HIV infection and dramatically reduced by early ART. EBioMedicine 2016; 11:68–72.
Schuetz A, Deleage C, Sereti I, et al. Initiation of ART during early acute HIV infection preserves mucosal Th17 function and reverses HIV-related immune activation. PLoS Pathog 2014; 10:e1004543.
Henrich TJ, Hatano H, Bacon O, et al. HIV-1 persistence following extremely early initiation of antiretroviral therapy (ART) during acute HIV-1 infection: an observational study. PLoS Med 2017; 14:e1002417.
Luzuriaga K, Gay H, Ziemniak C, et al. Viremic relapse after HIV-1 remission in a perinatally infected child. N Engl J Med 2015; 372:786–788.
Violari A, Cotton MF, Kuhn L, et al. A child with perinatal HIV infection and long-term sustained virological control following antiretroviral treatment cessation. Nat Commun 2019; 10:412.
Colby DJ, Trautmann L, Pinyakorn S, et al. Rapid HIV RNA rebound after antiretroviral treatment interruption in persons durably suppressed in Fiebig I acute HIV infection. Nat Med 2018; 24:923–926.
Maggiolo F, Di Filippo E, Comi L, et al. Posttreatment controllers after treatment interruption in chronically HIV-infected patients. AIDS 2018; 32:623–628.
Gulck EV, Bracke L, Heyndrickx L, et al. Immune and viral correlates of ‘secondary viral control’ after treatment interruption in chronically HIV-1 infected patients. PLoS One 2012; 7:e37792.
Blazkova J, Gao F, Marichannegowda MH, et al. Distinct mechanisms of long-term virologic control in two HIV-infected individuals after treatment interruption of antiretroviral therapy. Nat Med 2021; 27:1893–1898.
Veenhuis RT, Kwaa AK, Garliss CC, et al. Long-term remission despite clonal expansion of replication-competent HIV-1 isolates. JCI Insight 2018; 3:e122795.
Molinos-Albert LM, Lorin V, Monceaux V, et al. Transient viral exposure drives functionally-coordinated humoral immune responses in HIV-1 posttreatment controllers. Nat Commun 2022; 13:1944.
Uruena A, Cassetti I, Kashyap N, et al. Prolonged posttreatment virologic control and complete seroreversion after advanced human immunodeficiency virus-1 infection. Open Forum Infect Dis 2021; 8:ofaa613.
Li JZ, Etemad B, Ahmed H, et al. The size of the expressed HIV reservoir predicts timing of viral rebound after treatment interruption. AIDS 2016; 30:343–353.
Assoumou L, Weiss L, Piketty C, et al. A low HIV-DNA level in peripheral blood mononuclear cells at antiretroviral treatment interruption predicts a higher probability of maintaining viral control. AIDS 2015; 29:2003–2007.
Pasternak AO, Grijsen ML, Wit FW, et al. Cell-associated HIV-1 RNA predicts viral rebound and disease progression after discontinuation of temporary early ART. JCI Insight 2020; 5:e134196.
Hurst J, Hoffmann M, Pace M, et al. Immunological biomarkers predict HIV-1 viral rebound after treatment interruption. Nat Commun 2015; 6:8495.
Giron LB, Papasavvas E, Azzoni L, et al. Plasma and antibody glycomic biomarkers of time to HIV rebound and viral setpoint. AIDS 2020; 34:681–686.
Giron LB, Palmer CS, Liu Q, et al. Noninvasive plasma glycomic and metabolic biomarkers of posttreatment control of HIV. Nat Commun 2021; 12:3922.
Calin R, Hamimi C, Lambert-Niclot S, et al. Treatment interruption in chronically HIV-infected patients with an ultralow HIV reservoir. AIDS 2016; 30:761–769.
Castagna A, Muccini C, Galli L, et al. Analytical treatment interruption in chronic HIV-1 infection: time and magnitude of viral rebound in adults with 10 years of undetectable viral load and low HIV-DNA (APACHE study). J Antimicrob Chemother 2019; 74:2039–2046.
Pannus P, Rutsaert S, De Wit S, et al. Rapid viral rebound after analytical treatment interruption in patients with very small HIV reservoir and minimal on-going viral transcription. J Int AIDS Soc 2020; 23:e25453.
Strongin Z, Micci L, Fromentin R, et al. Virologic and immunologic features of simian immunodeficiency virus control post-ART interruption in rhesus macaques. J Virol 2020; 94:e00338–e420.
Graf EH, Mexas AM, Yu JJ, et al. Elite suppressors harbor low levels of integrated HIV DNA and high levels of 2-LTR circular HIV DNA compared to HIV+ patients on and off HAART. PLoS Pathog 2011; 7:e1001300.
Julg B, Pereyra F, Buzón MJ, et al. Infrequent recovery of HIV from but robust exogenous infection of activated CD4+ T cells in HIV elite controllers. Clin Infect Dis 2010; 51:233–238.
Kwaa AK, Garliss CC, Ritter KD, et al. Elite suppressors have low frequencies of intact HIV-1 proviral DNA. AIDS 2020; 34:641–643.
Lian X, Gao C, Sun X, et al. Signatures of immune selection in intact and defective proviruses distinguish HIV-1 elite controllers. Sci Transl Med 2021; 13:eabl4097.
Noel N, Peña R, David A, et al. Long-term spontaneous control of HIV-1 is related to low frequency of infected cells and inefficient viral reactivation. J Virol 2016; 90:6148–6158.
Sharaf R, Lee GQ, Sun X, et al. HIV-1 proviral landscapes distinguish posttreatment controllers from noncontrollers. J Clin Invest 2018; 128:4074–4085.
Hütter G, Nowak D, Mossner M, et al. Long-term control of HIV by CCR5 Delta32/Delta32 stem-cell transplantation. N Engl J Med 2009; 360:692–698.
Gupta RK, Abdul-Jawad S, McCoy LE, et al. HIV-1 remission following CCR5Δ32/Δ 32 haematopoietic stem-cell transplantation. Nature 2019; 568:244–248.
HIV-1 REMISSION WITH CCR5Δ32ΔHAPLO-CORD TRANSPLANT IN A US WOMAN: IMPAACT P1107. In: CROI Conference 2022 .
LONGITUDINAL DYNAMICS OF INTACT PROVIRAL HIV-1 DNA IN POSTTREATMENT CONTROLLERS. In: CROI Conference 2021.
Lederman MM, Connick E, Landay A, et al. Immunologic responses associated with 12 weeks of combination antiretroviral therapy consisting of zidovudine, lamivudine, and ritonavir: results of AIDS Clinical Trials Group Protocol 315. J Infect Dis 1998; 178:70–79.
Yero A, Shi T, Farnos O, et al. Dynamics and epigenetic signature of regulatory T-cells following antiretroviral therapy initiation in acute HIV infection. EBioMedicine 2021; 71:103570.
Wada NI, Jacobson LP, Margolick JB, et al. The effect of HAART-induced HIV suppression on circulating markers of inflammation and immune activation. AIDS 2015; 29:463–471.
Abrahams M-R, Joseph SB, Garrett N, et al. The replication-competent HIV-1 latent reservoir is primarily established near the time of therapy initiation. Sci Transl Med 2019; 11:eaaw5589.
Brodin J, Zanini F, Thebo L, et al. Establishment and stability of the latent HIV-1 DNA reservoir. eLife 2016; 5:e18889.
Shan L, Deng K, Gao H, et al. Transcriptional reprogramming during effector-to-memory transition renders CD4+ T cells permissive for latent HIV-1 infection. Immunity 2017; 47:766–775.
Post-treatment controllers limit completed and spliced HIV transcripts after ATI. In: CROI Conference 2022 .
Einkauf KB, Osborn MR, Gao C, et al. Parallel analysis of transcription, integration, and sequence of single HIV-1 proviruses. Cell 2022; 185:266.e15–282.e15.

Auteurs

Andrea Mastrangelo (A)

Service of Immunology and Allergy, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH