Eradication of HIV and Cure of AIDS, Now and How?
Open accessAbstract
Recent studies have highlighted the importance of eradication of human immunodeficiency virus (HIV) and cure of acquired immunodeficiency syndrome (AIDS). However, a pivotal point that the patient immunity controls HIV reactivation after highly active anti-retroviral therapy [HAART or combination anti-retroviral therapy (cART)] remains less well addressed. In spite of the fact that both innate and adaptive immunities are indispensable and numerous cells participate in the anti-HIV immunity, memory CD4 T-cells are indisputably the key cells organizing all immune actions against HIV while being the targets of HIV. Here we present a view and multidisciplinary approaches to HIV/AIDS eradication and cure. We aim at memory CD4 T-cells, utilizing the stem cell properties of these cells to reprogram an anti-HIV memory repertoire to eliminate the viral reservoir, toward achieving an AIDS-free world.
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Engineered nucleases including ZFN, TALEN, and CRISPR Cas9 can disrupt target genes and have raised prospects of selectively deleting HIV-1 proviral DNA integrated into the host genome.
“Advances in the engineered nucleases including zinc finger nuclease (ZFN), transcription activator-like effector nuclease (TALEN), and clustered regularly interspaced short palindromic repeats (CRISPR) associated 9 (Cas9) that can disrupt target genes have raised prospects of selectively deleting HIV-1 proviral DNA integrated into the host genome”
From RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection (2014) · cites this paper as [7]
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Yaşlı Kadınlarda Üreme Sağlığı
Kokanalı, D., & Engin Üstün, Y. (n.d.) · DergiPark (Istanbul University) · Cited by 170,090 · see citing works
Okano, M., Bell, D. W., Haber, D. A., & Li, E. (1999) · Cell · doi:10.1016/s0092-8674(00)81656-6 · Cited by 6,143 · see citing works
(2023) · doi:10.1126/science · Cited by 6,063 · see citing works
(1996) · Institutional Research Information System University of Turin (University of Turin) · doi:10.1111/j · Cited by 5,486 · see citing works
Identification of a reservoir for HIV-1 in patients on highly active antiretroviral therapy
Finzi, D., Hermankova, M., Pierson, T., Carruth, L. M., Buck, C., Chaisson, R. E., Quinn, T. C., Chadwick, K., Margolick, J., Brookmeyer, R., et al. (1997) · Science · doi:10.1126/science.278.5341.1295 · Cited by 3,098 · see citing works
Long-Term Control of HIV by CCR5 Delta32/Delta32 Stem-Cell Transplantation
Hütter, G., Nowak, D., Mossner, M., Ganepola, S., Muessig, A., Allers, K., Schneider, T., Hofmann, J., Kücherer, C., Blau, O., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0802905 · Cited by 1,837 · see citing works
HIV reservoir size and persistence are driven by T cell survival and homeostatic proliferation
Chomont, N., Far, M. E., Ancuța, P., Trautmann, L., Procopio, F. A., Yassine‐Diab, B., Boucher, G., Boulassel, M., Ghattas, G., Brenchley, J. M., et al. (2009) · Nature Medicine · doi:10.1038/nm.1972 · Cited by 1,709 · see citing works
Highly efficient endogenous human gene correction using designed zinc-finger nucleases
Urnov, F. D., Miller, J. C., Lee, Y.-L., Beausejour, C. M., Rock, J. M., Augustus, S., Jamieson, A. C., Porteus, M. H., Gregory, P. D., & Holmes, M. C. (2005) · Nature · doi:10.1038/nature03556 · Cited by 1,642 · see citing works
CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes
Janssen, E. M., Lemmens, E. E., Wolfe, T., Christen, U., von Herrath, M. G., & Schoenberger, S. P. (2003) · Nature · doi:10.1038/nature01441 · Cited by 1,635 · see citing works
Requirement for CD4 T Cell Help in Generating Functional CD8 T Cell Memory
Shedlock, D. J., & Shen, H. (2003) · Science · doi:10.1126/science.1082305 · Cited by 1,450 · see citing works
Defective CD8 T Cell Memory Following Acute Infection Without CD4 T Cell Help
Sun, J. C., & Bevan, M. J. (2003) · Science · doi:10.1126/science.1083317 · Cited by 1,213 · see citing works
CDK inhibitors: Cell cycle regulators and beyond
Besson, A., Dowdy, S. F., & Roberts, J. M. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.013 · Cited by 1,152 · see citing works
Redefining Chronic Viral Infection
Virgin, H. W., Wherry, E. J., & Ahmed, R. (2009) · Cell · doi:10.1016/j.cell.2009.06.036 · Cited by 1,031 · see citing works
Sáez‐Cirión, A., Bacchus, C., Hocqueloux, L., Avettand-Fènoël, V., Girault, I., Lécuroux, C., Potard, V., Versmisse, P., Mélard, A., Prazuck, T., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003211 · Cited by 1,012 · see citing works
The role of the cyclin-dependent kinase inhibitor p21 in apoptosis.
Gartel, A. L., & Tyner, A. L. (2002) · PubMed · Cited by 924 · see citing works
Asymmetric T Lymphocyte Division in the Initiation of Adaptive Immune Responses
Chang, J. T., Palanivel, V., Kinjyo, I., Schambach, F., Intlekofer, A. M., Banerjee, A., Longworth, S. A., Vinup, K. E., Mrass, P., Oliaro, J., et al. (2007) · Science · doi:10.1126/science.1139393 · Cited by 845 · see citing works
Daar, E. S., Moudgil, T. L., Meyer, R. D., & Ho, D. D. (1991) · New England Journal of Medicine · doi:10.1056/nejm199104043241405 · Cited by 834 · see citing works
High Titers of Cytopathic Virus in Plasma of Patients with Symptomatic Primary HIV-1 Infection
Clark, S. J., Saag, M. S., Decker, W. D., et al. (1991) · New England Journal of Medicine · doi:10.1056/nejm199104043241404 · Cited by 694 · see citing works
CD4+ T-cell help controls CD8+ T-cell memory via TRAIL-mediated activation-induced cell death
Janssen, E. M., Droin, N. M., Lemmens, E. E., Pinkoski, M. J., Bensinger, S. J., Ehst, B. D., Griffith, T. S., Green, D. R., & Schoenberger, S. P. (2005) · Nature · doi:10.1038/nature03337 · Cited by 619 · see citing works
Lint, C. M. V., Emiliani, S., Ott, M., & Verdin, E. M. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00449.x · Cited by 579 · see citing works
Different patterns of peripheral migration by memory CD4+ and CD8+ T cells
Gebhardt, T., Whitney, P. G., Zaid, A., Mackay, L. K., Brööks, A. G., Heath, W. R., Carbone, F. R., & Mueller, S. N. (2011) · Nature · doi:10.1038/nature10339 · Cited by 529 · see citing works
HIV LatencyPreprint
Siliciano, R. F., & Greene, W. C. (2011) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a007096 · Cited by 509 · see citing works
INFECTIOUS COMPLICATIONS IN PATIENTS WITH ACUTE PROMYELOCITIC LEUKEMIA TREATED WITH THE AIDA REGIMEN
C, G., M, B., La Tagliata, R., Spadea, A., D'Andrea, M., P, M., Lo‐Coco, F., Gentile, G., Micozzi, A., Alimena, G., et al. (2003) · IRIS Research product catalog (Sapienza University of Rome) · doi:10.1038/sj · Cited by 508 · see citing works
Clearing the Dead: Apoptotic Cell Sensing, Recognition, Engulfment, and Digestion
Hochreiter-Hufford, A., & Ravichandran, K. S. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008748 · Cited by 503 · see citing works
Th17 cells are long lived and retain a stem cell-like molecular signature
Muranski, P., Borman, Z. A., Kerkar, S. P., Klebanoff, C. A., Ji, Y., Sanchez-Perez, L., Sukumar, M., Reger, R. N., Yu, Z., Kern, S. J., et al. (2011) · Immunity · doi:10.1016/j.immuni.2011.09.019 · Cited by 443 · see citing works
DNA methylation and the regulation of globin gene expression
Busslinger, M., Hurst, J., & Flavell, R. A. (1983) · Cell · doi:10.1016/0092-8674(83)90150-2 · Cited by 443 · see citing works
Virus-specific CD4(+) memory-phenotype T cells are abundant in unexposed adults
Su, L. F., Kidd, B. A., Han, A., Kotzin, J. J., & Davis, M. M. (2013) · Immunity · doi:10.1016/j.immuni.2012.10.021 · Cited by 429 · cited 1× · see citing works
“Of note, recent studies reveal that memory CD4 T-cells preferentially reside and rest in the bone marrow, and virus-specific memory CD4 T-cells are abundant in unexposed adults (67, 68).”
ResultClass II-Independent Generation of CD4 Memory T Cells from Effectors
Swain, S. L., Hu, H., & Huston, G. E. (1999) · Science · doi:10.1126/science.286.5443.1381 · Cited by 413 · see citing works
Cellular immunity to HIV activated by CD4 fused to T cell or Fc receptor polypeptides
Romeo, C., & Seed, B. (1991) · Cell · doi:10.1016/0092-8674(91)90327-u · Cited by 396 · see citing works
Epigenetic Regulation of HIV-1 Latency by Cytosine Methylation
Kauder, S. E., Bosque, A., Lindkvist, A., Planelles, V., & Verdin, E. M. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000495 · Cited by 371 · see citing works
Professional Memory CD4+ T Lymphocytes Preferentially Reside and Rest in the Bone Marrow
Tokoyoda, K., Zehentmeier, S., Hegazy, A. N., Albrecht, I., Grün, J. R., Löhning, M., & Radbruch, A. (2009) · Immunity · doi:10.1016/j.immuni.2009.03.015 · Cited by 352 · see citing works
Naïve and Memory CD4 + T Cell Survival Controlled by Clonal Abundance
Hataye, J. M., Moon, J. J., Khoruts, A., Reilly, C., & Jenkins, M. K. (2006) · Science · doi:10.1126/science.1124228 · Cited by 351 · see citing works
Hale, J. S., Youngblood, B., Latner, D. R., Mohammed, A. U. R., Ye, L., Akondy, R. S., Wu, T., Iyer, S. S., & Ahmed, R. (2013) · Immunity · doi:10.1016/j.immuni.2013.02.020 · Cited by 330 · see citing works
Pearson, R., Kim, Y. K., Hokello, J. F., Lassen, K. G., Friedman, J. H., Tyagi, M., & Karn, J. (2008) · Journal of Virology · doi:10.1128/jvi.01383-08 · Cited by 299 · see citing works
Memory CD4 T cells emerge from effector T-cell progenitors
Harrington, L., Janowski, K., Oliver, J., Zajac, A., & Weaver, C. (2008) · Nature · doi:10.1038/nature06672 · Cited by 290 · see citing works
Requirement for T-bet in the aberrant differentiation of unhelped memory CD8+ T cells
Intlekofer, A. M., Takemoto, N., Kao, C., Banerjee, A., Schambach, F., Northrop, J. K., Shen, H., Wherry, E. J., & Reiner, S. L. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070841 · Cited by 288 · see citing works
HIV-Specific Cytolytic CD4 T Cell Responses During Acute HIV Infection Predict Disease Outcome
Soghoian, D. Z., Jessen, H. K., Flanders, M., Sierra-Davidson, K., Cutler, S., Pertel, T., Ranasinghe, S., Lindqvist, M., Davis, I., Lane, K., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003165 · Cited by 277 · see citing works
The Detection of Acute HIV Infection
Cohen, M. S., Gay, C. L., Busch, M. P., et al. (2010) · The Journal of Infectious Diseases · doi:10.1086/655651 · Cited by 277 · see citing works
The split personality of regulatory T cells in HIV infection
Chevalier, M. F., & Weiss, L. (2012) · Blood · doi:10.1182/blood-2012-07-409755 · Cited by 223 · see citing works
Yu, P., Lübben, W., Slomka, H., Gebler, J., Konert, M., Cai, C., Neubrandt, L., Prazeres da Costa, O., Paul, S., Dehnert, S., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.07.018 · Cited by 192 · see citing works
De novo DNA methylation of endogenous retroviruses is shaped by KRAB-ZFPs/KAP1 and ESET
Rowe, H. M., Friedli, M., Offner, S., Verp, S., Mesnard, D., Marquis, J., Aktaş, T., & Trono, D. (2013) · Development · doi:10.1242/dev.087585 · Cited by 189 · see citing works
CD4+ T cells from elite controllers resist HIV-1 infection by selective upregulation of p21
Chen, H., Li, C., Huang, J., Cung, T. D. H., Seiss, K., Beamon, J., Carrington, M. N., Porter, L. C., Burke, P. S., Yang, Y., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci44539 · Cited by 174 · see citing works
Infectivity and methylation of retroviral genomes is correlated with expression in the animal
Stuhlmann, H., Jähner, D., & Jaenisch, R. (1981) · Cell · doi:10.1016/0092-8674(81)90305-6 · Cited by 166 · see citing works
Sainz, T., Villar, S. S., Díaz, L., Tomé, M. I. G., Gurbindo, M. D., de José, M. I., Mellado, M. J., Ramos, J. T., Zamora, J., Moreno, S., et al. (2013) · AIDS · doi:10.1097/qad.0b013e32835faa72 · Cited by 160 · see citing works
Archin, N. M., Cheema, M., Parker, D., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009390 · Cited by 154 · see citing works
Gratz, I. K., Truong, H.-A., Yang, S. H.-Y., Maurano, M. M., Lee, K., Abbas, A. K., & Rosenblum, M. D. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300212 · Cited by 151 · see citing works
Overcoming pharmacologic sanctuaries
Cory, T. J., Schacker, T. W., Stevenson, M., et al. (2013) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e32835fc68a · Cited by 146 · see citing works
Developing and maintaining protective CD8+ memory T cells
Williams, M. A., Holmes, B., Sun, J. C.-Y., & Bevan, M. J. (2006) · Immunological Reviews · doi:10.1111/j.0105-2896.2006.00389.x · Cited by 142 · see citing works
Regulatory T cells control NK cells in an insulitic lesion by depriving them of IL-2
Sitrin, J., Ring, A. M., García, K. C., Benoist, C. O., & Mathis, D. J. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20122248 · Cited by 138 · see citing works
Brenchley, J. M., Vinton, C. L., Tabb, B., Hao, X., Connick, E., Paiardini, M., Lifson, J. D., Silvestri, G., & Estes, J. D. (2012) · Blood · doi:10.1182/blood-2012-06-437608 · Cited by 130 · see citing works
HIV infection and HERV expression: a review
van der Kuyl, A. C. (2012) · Retrovirology · doi:10.1186/1742-4690-9-6 · Cited by 129 · see citing works
Restriction of HIV-1 replication in macrophages and CD4+ T cells from HIV controllers
Sáez‐Cirión, A., Hamimi, C., Bergamaschi, A., David, A., Versmisse, P., Mélard, A., Boufassa, F., Barré‐Sinoussi, F., Lambotte, O., Rouzioux, C., et al. (2011) · Blood · doi:10.1182/blood-2010-12-327106 · Cited by 126 · see citing works
Primitive hematopoietic cells resist HIV-1 infection via p21Waf1/Cip1/Sdi1
Zhang, J., Scadden, D. T., & Crumpacker, C. S. (2007) · Journal of Clinical Investigation · doi:10.1172/jci28971 · Cited by 125 · see citing works
Self-citationKim, C. J., McKinnon, L. R., Kovacs, C. M., Kandel, G. P., Huibner, S., Chege, D., Shahabi, K., Benko, E., Loutfy, M. R., Ostrowski, M., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300829 · Cited by 123 · see citing works
Durand, C. M., Ghiaur, G., Siliciano, J. D., Rabi, S. A., Eisele, E. E., Salgado, M., Liang, S., Lai, J., Zhang, H., Margolick, J. B., et al. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jir884 · Cited by 120 · see citing works
Cellular and molecular mechanisms involved in the establishment of HIV-1 latency
Donahue, D. A., & Wainberg, M. A. (2013) · Retrovirology · doi:10.1186/1742-4690-10-11 · Cited by 110 · see citing works
Salazar-Gonzalez, J. F., Moody, D. J., Giorgi, J. V., Martínez-Maza, O., Mitsuyasu, R. T., & Fahey, J. L. (1985) · The Journal of Immunology · doi:10.4049/jimmunol.135.3.1778 · Cited by 106 · see citing works
Stem Cell Based Cancer Gene Therapy
Cihova, M., Altanerová, V., & Altaner, Č. (2011) · Molecular Pharmaceutics · doi:10.1021/mp200151a · Cited by 101 · see citing works
Ndhlovu, Z., Proudfoot, J., Cesa, K., Alvino, D., McMullen, A., Vine, S. M., Stampouloglou, E., Piechocka-Trocha, A., Walker, B., & Pereyra, F. (2012) · Journal of Virology · doi:10.1128/jvi.00531-12 · Cited by 101 · see citing works
Blazkova, J., Chun, T., Belay, B. W., et al. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis412 · Cited by 97 · see citing works
Rapid default transition of CD4 T cell effectors to functional memory cells
McKinstry, K. K., Golech, S., Lee, W.-H., Huston, G. E., Weng, N., & Swain, S. L. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070041 · Cited by 96 · see citing works
T cell regulation of natural killer cells
Kerdiles, Y. M., Ugolini, S., & Vivier, É. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20130960 · Cited by 93 · see citing works
Josefsson, L., Eriksson, S., Sinclair, E., et al. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis301 · Cited by 92 · see citing works
HERV-K–specific T cells eliminate diverse HIV-1/2 and SIV primary isolates
Jones, R. B., Garrison, K. E., Mujib, S., Mihajlovic, V., Aidarus, N., Hunter, D. V., Martin, E., John, V. M., Zhan, W., Faruk, N. F., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci64560 · Cited by 91 · see citing works
Developing strategies for HIV-1 eradication
Durand, C. M., Blankson, J. N., & Siliciano, R. F. (2012) · Trends in Immunology · doi:10.1016/j.it.2012.07.001 · Cited by 90 · see citing works
ACE inhibitors and tissue binding: Originally published as Volume 336, Issue 8724
Jeremy, J. Y., Gill, J., Fonseca, V, et al. (1990) · University of Groningen research database (University of Groningen / Centre for Information Technology) · doi:10.1016/0140-6736 · Cited by 90 · see citing works
Desirable cell death during anticancer chemotherapy
Locher, C., Conforti, R., Aymeric, L., Ma, Y., Yamazaki, T., Rusakiewicz, S., Tesnière, A., Ghiringhelli, F., Apétoh, L., Morel, Y., et al. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05763.x · Cited by 81 · see citing works
Loss and Dysregulation of Th17 Cells during HIV Infection
Bixler, S. L., & Mattapallil, J. J. (2013) · Clinical and Developmental Immunology · doi:10.1155/2013/852418 · Cited by 77 · see citing works
Glässner, A., Eisenhardt, M., Kokordelis, P., Krämer, B., Wolter, F., Nischalke, H. D., Boesecke, C., Sauerbruch, T., Rockstroh, J. K., Spengler, U., et al. (2013) · Journal of Hepatology · doi:10.1016/j.jhep.2013.04.029 · Cited by 75 · see citing works
Bergamaschi, A., David, A., Rouzic, E. L., Nisole, S., Barré‐Sinoussi, F., & Pancino, G. (2009) · Journal of Virology · doi:10.1128/jvi.01395-09 · Cited by 70 · see citing works
The search for an HIV cure: tackling latent infection
Kent, S. J., Reece, J. C., Petravic, J., Martyushev, A., Kramski, M., Rose, R. D., Cooper, D. A., Kelleher, A. D., Emery, S., Cameron, P. U., et al. (2013) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(13)70043-4 · Cited by 70 · see citing works
Zloza, A., Kohlhapp, F. J., Lyons, G. E., Schenkel, J. M., Moore, T. V., Lacek, A. T., O’Sullivan, J. A., Varanasi, V., Williams, J. W., Jagoda, M. C., et al. (2012) · Nature Medicine · doi:10.1038/nm.2683 · Cited by 66 · see citing works
Ex vivo targeting of p21Cip1/Waf1 permits relative expansion of human hematopoietic stem cells
Stier, S., Cheng, T., Forkert, R., Lutz, C., Dombkowski, D., Zhang, J. L., & Scadden, D. T. (2003) · Blood · doi:10.1182/blood-2002-10-3053 · Cited by 65 · see citing works
Self-citationSiliciano, J. D., & Siliciano, R. F. (2013) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e328361eaca · Cited by 64 · see citing works
Palacios, J. A., Pérez-Piñar, T., Toro, C., et al. (2012) · Journal of Virology · doi:10.1128/jvi.01741-12 · Cited by 56 · see citing works
Targeted gene disruption to cure HIV
Stone, D., Kiem, H.-P., & Jerome, K. R. (2013) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e32835f736c · Cited by 55 · see citing works
How to best measure HIV reservoirs?
Rouzioux, C., & Richman, D. D. (2013) · Current Opinion in HIV and AIDS · doi:10.1097/coh.0b013e32835fc619 · Cited by 55 · see citing works
In vivo, in vitro, and in silico analysis of methylation of the HIV-1 provirus
Chávez, L., Kauder, S. E., & Verdin, E. M. (2010) · Methods · doi:10.1016/j.ymeth.2010.05.009 · Cited by 49 · see citing works
Eliminating the latent HIV reservoir by reactivation strategies: Advancing to clinical trials
Rasmussen, T. A., Tolstrup, M., Winckelmann, A. A., Østergaard, L. J., & Søgaard, O. S. (2013) · Human Vaccines & Immunotherapeutics · doi:10.4161/hv.23202 · Cited by 47 · see citing works
Stoye, J. P., & Coffin, J. M. (2000) · Nature · doi:10.1038/35001700 · Cited by 46 · see citing works
Unmet therapeutic needs in the new era of combination antiretroviral therapy for HIV-1
Taiwo, B., Hicks, C. B., & Eron, J. (2010) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkq096 · Cited by 46 · see citing works
Epigenetic Regulation of HIV-1 Transcription
Tripathy, M. K., Abbas, W., & Herbein, G. (2011) · Epigenomics · doi:10.2217/epi.11.61 · Cited by 43 · see citing works
The role of recipient T cells in mesenchymal stem cell-based tissue regeneration
Liu, Y. F., Wang, S., & Shi, S. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.08.003 · Cited by 38 · see citing works
Tite, J. P., Russell, S. M., Dougan, G., et al. (1988) · The Journal of Immunology · doi:10.4049/jimmunol.141.11.3980 · Cited by 36 · see citing works
Zhang, J., Attar, E. C., Cohen, K. S., Crumpacker, C. S., & Scadden, D. T. (2005) · Gene Therapy · doi:10.1038/sj.gt.3302544 · Cited by 36 · see citing works
Self-citationImmune pathogenesis of AIDS and related syndromes
Fahey, J. L., Giorgi, J., Martinez-Maza, O., et al. (1987) · Annales de l Institut Pasteur Immunologie · doi:10.1016/s0769-2625(87)80075-2 · Cited by 36 · see citing works
Control of Innate Immunity by Memory CD4 T Cells
Strutt, T. M., McKinstry, K. K., & Swain, S. L. (2011) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-5632-3_6 · Cited by 35 · see citing works
A sychnological cell penetrating peptide mimic of p21WAF1/CIP1 is pro-apoptogenic
Baker, R. D., Howl, J., & Nicholl, I. D. (2006) · Peptides · doi:10.1016/j.peptides.2006.12.013 · Cited by 29 · see citing works
The Role of Vpr in the Regulation of HIV-1 Gene Expression
Cui, J., Tungaturthi, P. K., Ayyavoo, V., Ghafouri, M., Ariga, H., Khalili, K., Srinivasan, A., Amini, S., & Sawaya, B. E. (2006) · Cell Cycle · doi:10.4161/cc.5.22.3442 · Cited by 28 · see citing works
A peripheral CD4+ T cell precursor for naive, memory, and regulatory T cells
Zhao, C., & Davies, J. D. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20100598 · Cited by 28 · see citing works
Mesenchymal stem cells as a novel vaccine platform
Tomchuck, S. L., Norton, E. B., Garry, R. F., Bunnell, B. A., Morris, C. A., Freytag, L. C., & Clements, J. D. (2012) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2012.00140 · Cited by 27 · see citing works
9-aminoacridine Inhibition of HIV-1 Tat Dependent Transcription
Guendel, I., Carpio, L., Easley, R. L., Duyne, R. V., Coley, W., Agbottah, E. T., Dowd, C. S., Kashanchi, F., & Kehn‐Hall, K. (2009) · Virology Journal · doi:10.1186/1743-422x-6-114 · Cited by 27 · see citing works
Stem-Cell-like Qualities of Immune Memory; CD4+ T Cells Join the Party
Luckey, C. J., & Weaver, C. T. (2012) · Cell stem cell · doi:10.1016/j.stem.2012.01.011 · Cited by 25 · see citing works
Advances in antiretroviral therapy.
Taylor, B., Sk, O., Wilkin, T. J., et al. (2012) · PubMed · Cited by 25 · see citing works
Long-Term Non-Progression and Broad HIV-1-Specific Proliferative T-Cell Responses
Imami, N., Westrop, S. J., Grageda, N., & Herasimtschuk, A. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00058 · Cited by 23 · see citing works
Hu, M., Wang, J., Chen, P., & Reilly, R. M. (2006) · Bioconjugate Chemistry · doi:10.1021/bc060053r · Cited by 22 · see citing works
HIV viraemia and seroconversion
Lu, W., Eme, D., & Andrieu, J. (1993) · The Lancet · doi:10.1016/0140-6736(93)92589-l · Cited by 19 · see citing works
Drug 9AA reactivates p21/Waf1 and Inhibits HIV-1 progeny formation
Wu, W., Kehn‐Hall, K., Pedati, C., Zweier, L., Castro, I., Klase, Z. A., Dowd, C. S., Dubrovsky, L., Bukrinsky, M., & Kashanchi, F. (2008) · Virology Journal · doi:10.1186/1743-422x-5-41 · Cited by 19 · see citing works
Zhang, L., Waters, C. A., NICHOLS, J. C., et al. (1992) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/00126334-199212000-00001 · Cited by 15 · see citing works
Scheuring, U. J., Sabzevari, H., Corbeil, J., & Theofilopoulos, A. N. (1999) · AIDS · doi:10.1097/00002030-199902040-00004 · Cited by 14 · see citing works
Hematopoietic stem and progenitor cells in HIV/AIDS and immune reconstitution
Zhang, J., & Crumpacker, C. S. (2010) · Cell Research · doi:10.1038/cr.2010.85 · Cited by 14 · see citing works
Self-citationGandhi, R. T., Bosch, R. J., Aga, E., et al. (2013) · Antiviral Therapy · doi:10.3851/imp2543 · Cited by 13 · see citing works
Elite control of HIV: p21 (waf-1/cip-1) at its best
Yu, X. G., & Lichterfeld, M. (2011) · Cell Cycle · doi:10.4161/cc.10.19.17051 · Cited by 10 · see citing works
Forbi, J. C., & Agwale, S. M. (2009) · Tanzania journal of health research/Tanzania Journal of Health Research · doi:10.4314/thrb.v11i3.47701 · Cited by 10 · see citing works
CROI 2013: Advances in antiretroviral therapy.
Taylor, B. S., Wilkin, T. J., Shalev, N., et al. (2013) · PubMed · Cited by 9 · see citing works
Park, S. Y., Kim, K.-C., Hong, K., et al. (2013) · Intervirology · doi:10.1159/000350563 · Cited by 8 · see citing works
Persistent immune complexes and abnormal CD4/CD8 ratios in HIV infection.
Roy, S., Morrow, W. J., Christian, C. R., et al. (1990) · PubMed · Cited by 7 · see citing works
A new chimeric protein represses HIV-1 LTR-mediated expression by DNA methylase.
Martinez-Colom, A., Lasarte, S., Fernández-Pineda, A., Relloso, M., & Muñoz-Fernández, M. (2013) · Antiviral Research · doi:10.1016/j.antiviral.2013.04.007 · Cited by 7 · see citing works
Subset of CD4 Cells May Hold Key to Reaching HIV Cure
Cohen, J. D. (2013) · Science · doi:10.1126/science.339.6125.1262 · Cited by 4 · see citing works
Naive and Memory CD4+ T Cells in HIV Eradication and Immunization
Zhang, J., Poznansky, M. C., & Crumpacker, C. S. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis387 · Cited by 4 · see citing works
Self-citationDNA methylation: a new twist in the tail
Kelsey, G. (2011) · Cell Research · doi:10.1038/cr.2011.110 · Cited by 3 · see citing works
Therapeutic imprinting of the immune system: towards a remission of AIDS in primates?
Savarino, A., & Garaci, E. (2012) · Retrovirology · doi:10.1186/1742-4690-9-75 · Cited by 3 · see citing works
Grand Challenges in the Immunology of HIV and AIDS
Miedema, F. F. (2011) · Frontiers in Immunology · doi:10.3389/fimmu.2011.00020 · Cited by 2 · see citing works
Flagged first, then by citations
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Sorted by citations
RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection
Hu, W., Kaminski, R., Yang, F., Zhang, Y., Cosentino, L., Li, F., Luo, B., Alvarez-Carbonell, D., Garcia-Mesa, Y., Karn, J., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405186111 · Cited by 527 · see citing works
- Authors
- Zhang, J., & Crumpacker, C.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- Corresponding author
- Crumpacker, Clyde
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2013
- Volume
- 4
- Pages
- 337-337
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC3799464
- OpenAlex
- W2060076563
- Cited by
- 36
- References
- 113
- Citations by year
- 2026: 2 · 2023: 2 · 2022: 4 · 2021: 1 · 2020: 8 · 2019: 3 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 3 · 2014: 6
- FWCI
- 0.55
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
- Health Sciences › Medicine › Infectious Diseases › HIV/AIDS drug development and treatment
- Keywords
- HIV eradication, HIV reservoir, memory CD4+ T cells, HIV reactivation, highly active antiretroviral therapy, stem cell properties, innate and adaptive immunity
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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