<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-02T17:10:45Z</responseDate><request verb="GetRecord" identifier="oai:repository.ucc.edu.co:20.500.12494/15978" metadataPrefix="dim">https://repository.ucc.edu.co/server/oai/request</request><GetRecord><record><header><identifier>oai:repository.ucc.edu.co:20.500.12494/15978</identifier><datestamp>2024-08-11T03:42:07Z</datestamp><setSpec>com_20.500.12494_8</setSpec><setSpec>col_20.500.12494_25</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="author">Zapata Builes, Wildeman</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Hernández López, Juan Carlos
</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Lizdany, Florez</dim:field>
   <dim:field mdschema="dc" element="coverage" qualifier="temporal" lang="spa">9</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2020-01-16T13:43:08Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2020-01-16T13:43:08Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2018-10-17</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="issn" lang="spa">16643224</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri" lang="spa">10.3389/fimmu.2018.02290</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/20.500.12494/15978</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="bibliographicCitation" lang="spa">Flórez-Álvarez L, Hernandez JC and Zapata W (2018) NK Cells in HIV-1 Infection: From Basic Science to Vaccine Strategies. Front. Immunol. 9:2290. doi: 10.3389/fimmu.2018.02290</dim:field>
   <dim:field mdschema="dc" element="description" lang="spa">NK cells play a key role in immune response against HIV infection. These cells&#xd;
can destroy infected cells and contribute to adequate and strong adaptive immune&#xd;
responses, by acting on dendritic, T, B, and even epithelial cells. Increased NK cell&#xd;
activity reflected by higher cytotoxic capacity, IFN-g and chemokines (CCL3, CCL4, and&#xd;
CCL5) production, has been associated with resistance to HIV infection and delayed&#xd;
AIDS progression, demonstrating the importance of these cells in the antiviral response.&#xd;
Recently, a subpopulation of NK cells with adaptive characteristics has been described&#xd;
and associated with lower HIV viremia and control of infection. These evidences, together&#xd;
with some degree of protection shown in vaccine trials based on boosting NK cell activity,&#xd;
suggest that these cells can be a feasible option for new treatment and vaccination&#xd;
strategies to overcome limitations that, classical vaccination approaches, might have for&#xd;
this virus. This review is focus on the NK cells role during the immune response against&#xd;
HIV, including all the effector mechanisms associated to these cells; in addition, changes&#xd;
including phenotypic, functional and frequency modifications during HIV infection will be&#xd;
pointed, highlighting opportunities to vaccine development based in NK cells effector&#xd;
functions.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="spa">NK cells play a key role in immune response against HIV infection. These cells&#xd;
can destroy infected cells and contribute to adequate and strong adaptive immune&#xd;
responses, by acting on dendritic, T, B, and even epithelial cells. Increased NK cell&#xd;
activity reflected by higher cytotoxic capacity, IFN-g and chemokines (CCL3, CCL4, and&#xd;
CCL5) production, has been associated with resistance to HIV infection and delayed&#xd;
AIDS progression, demonstrating the importance of these cells in the antiviral response.&#xd;
Recently, a subpopulation of NK cells with adaptive characteristics has been described&#xd;
and associated with lower HIV viremia and control of infection. These evidences, together&#xd;
with some degree of protection shown in vaccine trials based on boosting NK cell activity,&#xd;
suggest that these cells can be a feasible option for new treatment and vaccination&#xd;
strategies to overcome limitations that, classical vaccination approaches, might have for&#xd;
this virus. This review is focus on the NK cells role during the immune response against&#xd;
HIV, including all the effector mechanisms associated to these cells; in addition, changes&#xd;
including phenotypic, functional and frequency modifications during HIV infection will be&#xd;
pointed, highlighting opportunities to vaccine development based in NK cells effector&#xd;
functions.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="cvlac" lang="spa">https://scienti.minciencias.gov.co/cvlac/EnProdArticulo/query.do?cod_producto=73&amp;cod_rh=0000157775</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="orcid" lang="spa">https://orcid.org/0000-0002-7351-8738</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="gruplac" lang="spa">COL0112548</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="email" lang="spa">wildeman.zapatab@campusucc.edu.co</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="gsid" lang="spa">https://scholar.google.com.co/citations?hl=en&amp;user=VLZxl1UAAAAJ</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="spa">13</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="spa">Universidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Medicina, Medellín y Envigado</dim:field>
   <dim:field mdschema="dc" element="publisher" qualifier="program" lang="spa">Medicina</dim:field>
   <dim:field mdschema="dc" element="publisher" qualifier="place" lang="spa">Medellín</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="isversionof" lang="spa">https://www.frontiersin.org/articles/10.3389/fimmu.2018.02290/full</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="ispartofjournal" lang="spa">Frontiers in Immunology</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">1. Montaldo E, Del Zotto G, Della Chiesa M, Mingari MC, Moretta A, De Maria A, et al. Human NK cell receptors/markers: a tool to analyze NK cell development, subsets and function. Cytom A (2013) 83:702–13. doi: 10.1002/cyto.a.22302</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">2. Fauriat C, Long EO, Ljunggren HG, Bryceson YT. Regulation of human NKcell cytokine and chemokine production by target cell recognition. Blood (2010) 115:2167–76. doi: 10.1182/blood-2009-08-238469</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">3. Roda JM, Parihar R, Magro C, Nuovo GJ, Tridandapani S, Carson WE. Natural killer cells produce T cell–recruiting chemokines in response to antibody-coated tumor cells. Cancer Res. (2006) 66:517–26. doi: 10.1158/0008-5472.CAN-05-2429</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">4. Herberman RB, NunnME, Lavrin DH. Natural cytotoxic reactivity of mouse lymphoid cells against syngeneic acid allogeneic tumors. I. Distribution of reactivity and specificity. Int J Cancer (1975) 16:216–29.</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">5. Bukowski JF, Woda BA, Habu S, Okumura K, Welsh RM. Natural killer cell depletion enhances virus synthesis and virus-induced hepatitis in vivo. J Immunol. (1983) 131:1531–8.</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">6. Lee SH, Miyagi T, Biron CA. Keeping NK cells in highly regulated antiviral warfare. Trends Immunol. (2007) 28:252–9. doi: 10.1016/j.it.2007.04.001</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">7. Raulet DH. Roles of the NKG2D immunoreceptor and its ligands. Nat Rev Immunol. (2003) 3:781–90. doi: 10.1038/nri1199</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">8. Lanier LL. Evolutionary struggles between NK cells and viruses. Nat Rev Immunol. (2008) 8:259–68. doi: 10.1038/nri2276</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">9. Khakoo SI, Carrington M. KIR and disease: a model system or system of models? Immunol Rev. (2006) 214:186–201. doi: 10.1111/j.1600-065X.2006.00459.x</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">10. Jamieson AM, Diefenbach A, McMahon CW, Xiong N, Carlyle JR, Raulet DH. The role of the NKG2D immunoreceptor in immune cell activation and natural killing. Immunity (2002) 17:19–29. doi: 10.1016/S1074-7613(02)00333-3</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">11. Sivori S, Falco M, Chiesa MD, Carlomagno S, Vitale M, Moretta L, et al. CpG and double-stranded RNA trigger human NK cells by Tolllike receptors: Induction of cytokine release and cytotoxicity against tumors and dendritic cells. Proc Natl Acad Sci USA. (2004) 101:10116–21. doi: 10.1073/pnas.0403744101</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">12. Diefenbach A, Jamieson AM, Liu SD, Shastri N, Raulet DH. Ligands for the murine NKG2D receptor: expression by tumor cells and activation of NK cells and macrophages. Nat Immunol. (2000) 1:119–26. doi: 10.1038/77793</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">13. Salih HR, Antropius H, Gieseke F, Lutz SZ, Kanz L, Rammensee HG, et al. Functional expression and release of ligands for the activating immunoreceptor NKG2D in leukemia. Blood (2003) 102:1389–96. doi: 10.1182/blood-2003-01-0019</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">14. Watson FS, Spendlove I, Madjd Z, McGilvray R, Green AR, Ellis IO, et al. Expression of the stress-related MHC class I chain-related protein MICA is an indicator of good prognosis in colorectal cancer patients. Int J Cancer (2006) 118:1445–52. doi: 10.1002/ijc.21510</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">15. Robbins SH, Bessou G, Cornillon A, Zucchini N, Rupp B, Ruzsics Z,et al. Natural killer cells promote early CD8 T cell responses against cytomegalovirus. PLoS Pathog. (2007) 3:e123. doi: 10.1371/journal.ppat.0030123</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">16. Crome SQ, Lang PA, Lang KS, Ohashi PS. Natural killer cells regulate diverse T cell responses Trends Immunol. (2013) 34:342–9. doi: 10.1016/j.it.2013. 03.002</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">17. Campbell KS, Hasegawa J. Natural killer cell biology: an update and future directions. J Allergy Clin Immunol. (2013) 132:536–44. doi: 10.1016/j.jaci.2013.07.006</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">18. Quillay H, El Costa H, Durie M, Marlin R, Cannou C, Madec Y, et al. NK cells control HIV-1 infection of macrophages through soluble factors and cellular contacts in the human decidua. Retrovirology (2016) 13:39. doi: 10.1186/s12977-016-0271-z</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">19. Quaranta MG, Napolitano A, Sanchez M, Giordani L, Mattioli B, Viora M. HIV-1 Nef impairs the dynamic of DC/NK crosstalk: different outcome of CD56(dim) and CD56(bright) NK cell subsets. FASEB J. (2007) 21:2323–34. doi: 10.1096/fj.06-7883com</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">20. Rydyznski C, Daniels KA, Karmele EP, Brooks TR, Mahl SE, Moran MT, et al. Generation of cellular immune memory and B-cell immunity is impaired by natural killer cells. Nat Commun. (2015) 6:6375. doi: 10.1038/ ncomms7375</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">21. Horton RE,McLaren PJ, Fowke K, Kimani J, Ball TB. Cohorts for the Study of HIV-1–exposed but uninfected individuals: benefits and limitations. J Infect Dis. (2010) 202:S377–81. doi: 10.1086/655971</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">22. Johansson SE, Rollman E, Chung AW, Center RJ, Hejdeman B, Stratov I, et al. NK cell function and antibodies mediating ADCC in HIV-1- infected viremic and controller patients. Viral Immunol. (2011) 24:359–68. doi: 10.1089/vim.2011.0025</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">23. Taborda NA, Hernández JC, Lajoie J, Juno JA, Kimani J, Rugeles MT, et al. Short communication: low expression of activation and inhibitory molecules on NK cells and CD4(+) T cells is associated with viral control. AIDS Res Hum Retroviruses. (2015) 31:636–40. doi: 10.1089/AID. 2014.0325</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">24. Lohman-Payne B, Slyker JA, Moore S, Maleche-Obimbo E, Wamalwa DC, Richardson BA, et al. Breast milk cellular HIV-specific interferon g responses are associated with protection from peripartum HIV transmission. AIDS (2012) 26:2007–16. doi: 10.1097/QAD.0b013e328 359b7e0</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">25. Scott-Algara D, Truong LX, Versmisse P, David A, Luong TT, Nguyen VN,et al. Cutting edge: increased NK cell activity in HIV-1-exposed but uninfected Vietnamese intravascular drug users. J Immunol. (2003) 171:5663–7. doi: 10.4049/jimmunol.171.11.5663</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">26. Montoya CJ, Velilla PA, Chougnet C, Landay AL, Rugeles MT. Increased IFN-gamma production by NK and CD3+/CD56+ cells in sexually HIV- 1-exposed but uninfected individuals. Clin Immunol. (2006) 120:138–46. doi: 10.1016/j.clim.2006.02.008</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">27. Alter G, Altfeld M. Mutiny or scrutiny: NK cell modulation of DC function in HIV-1 infection. Trends Immunol. (2011) 32:219–24. doi: 10.1016/j.it.2011.02.003</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">28. Osborn L, Kunkel S, Nabel GJ. Tumor necrosis factor alpha and interleukin 1 stimulate the human immunodeficiency virus enhancer by activation of the nuclear factor kappa B. Proc Natl Acad Sci USA. (1989) 86:2336–40.</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">29. Wada NI, Jacobson LP, Margolick JB, Breen EC, Macatangay B, Penugonda S,et al. The effect of HAART-induced HIV suppression on circulating markers of inflammation and immune activation. AIDS (2015) 29:463–71. doi: 10.1097/QAD.0000000000000545</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">30. Kumar A, Abbas W, Herbein G. TNF and TNF receptor superfamily members in HIV infection: new cellular targets for therapy? Mediators Inflamm. (2013) 2013:484378. doi: 10.1155/2013/ 484378</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">31. Gallitano SM, McDermott L, Brar K, Lowenstein E. Use of tumor necrosis factor (TNF) inhibitors in patients with HIV/AIDS. J Am Acad Dermatol. (2016) 74:974–80. doi: 10.1016/j.jaad.2015.11.043</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">32. Roff SR, Noon-Song EN, Yamamoto JK, Johnson HM. The significance of interferon-g in HIV-1 pathogenesis, therapy, and prophylaxis. Front Immunol. (2014) 4:498. doi: 10.3389/fimmu.2013.00498</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">33. Oliva A, Kinter AL, Vaccarezza M, Rubbert A, Catanzaro A, Moir S, et al. Natural killer cells from human immunodeficiency virus (HIV)- infected individuals are an important source of CC-chemokines and suppress HIV-1 entry and replication in vitro. J Clin Invest. (1998) 102:223–31. doi: 10.1172/JCI2323</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">34. WalkerWE, Kurscheid S, Joshi S, Lopez CA, Goh G, ChoiM, et al. Increased levels of macrophage inflammatory proteins result in resistance to R5- tropic HIV-1 in a subset of elite controllers. J Virol. (2015) 89:5502–14. doi: 10.1128/jvi.00118-15</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">35. Vega JA, Villegas-Ospina S, Aguilar-Jiménez W, Rugeles MT, Bedoya G, ZapataW, et al. Haplotypes in CCR5-CCR2, CCL3, and CCL5 are associated with natural resistance to HIV-1 infection in a Colombian cohort. Biomédica (2017) 37:267–73. doi: 10.7705/biomedica.v37i3.3237</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">36. Zapata W, Aguilar-Jiménez W, Pineda-Trujillo N, Rojas W, Estrada H, Rugeles MT. Influence of CCR5 and CCR2 genetic variants in the resistance/susceptibility to HIV in serodiscordant couples from Colombia. AIDS Res Hum Retroviruses. (2013) 29:1594–603. doi: 10.1089/aid. 2012.0299</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">37. Cella M, Fuchs A, Vermi W, Facchetti F, Otero KJ, Lennerz KM, et al. A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity. Nature (2009) 457:722–5. doi: 10.1038/nature07537</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">38. Zenewicz LA, Flavell RA. Recent advances in IL-22 biology. Int Immunol. (2011) 23:159–63. doi: 10.1093/intimm/dxr001</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">39. Xu X, Weiss ID, Zhang HH, Singh SP, Wynn TA, Wilson MS, et al. Conventional NK cells can produce IL-22 and promote host defense in Klebsiella pneumoniae Pneumonia. J Immunol. (2014) 192:1778–86. doi: 10.4049/jimmunol.1300039</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">40. Colonna M. Interleukin-22-producing natural killer cells and lymphoid tissue inducer-like cells in mucosal immunity. Immunity (2009) 31:15–23. doi: 10.1016/j.immuni.2009.06.008</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">41. Wolk K, Kunz S, Witte E, Friedrich M, Asadullah K, Sabat R. IL-22 increases the innate immunity of tissues. Immunity (2004) 21:241–54. doi: 10.1016/j.immuni.2004.07.007</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">42. Wolk K, Sabat R. Interleukin-22: a novel T- and NK-cell derived cytokine that regulates the biology of tissue cells. Cytokine Growth Factor Rev. (2006) 17:367–80. doi: 10.1016/j.cytogfr.2006.09.001</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">43. Zheng Y, Valdez PA, Danilenko DM, Hu Y, Sa SM, Gong Q, et al. Interleukin- 22 mediates early host defense against attaching and effacing bacterial pathogens. Nat Med. (2008) 14:282–9. doi: 10.1038/nm1720</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">44. Zapata W, Rodriguez B, Weber J, Estrada H, Quinones-Mateu M, Zimermman P, et al. Increased levels of human beta-defensins mRNA in sexually HIV-1 exposed but uninfected individuals. Curr HIV Res. (2008) 6:531–8. doi: 10.2174/157016208786501463</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">45. Zapata W, Aguilar-Jiménez W, Feng Z, Weinberg A, Russo A, Potenza N, et al. Identification of innate immune antiretroviral factors during in vivo and in vitro exposure to HIV-1. Microbes Infect. (2016) 18:211–9. doi: 10.1016/j.micinf.2015.10.009</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">46. Wang W, Wu F, Cong Z, Liu K, Qin C, Wei Q. The secretion of IL-22 from mucosal NKp44 + NK cells is associated with microbial translocation and virus infection in SIV/SHIV-infected Chinese macaques. J Immunol Res. (2014) 2014:1–13. doi: 10.1155/2014/387950</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">47. Missé D, Yssel H, Trabattoni D, Oblet C, Lo Caputo S, Mazzotta F, et al. IL-22 Participates in an innate anti-HIV-1 host-resistance network through acute-phase protein induction. J Immunol. (2006) 178:407–15. doi: 10.4049/jimmunol.178.1.407</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">48. Topham NJ, Hewitt EW. Natural killer cell cytotoxicity: how do they pull the trigger? Immunology (2009) 128:7–15. doi: 10.1111/j.1365-2567.2009.03123.x</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">49. Elliott JM, Yokoyama WM. Unifying concepts of MHC-dependent natural killer cell education. Trends Immunol. (2011) 32:364–72. doi: 10.1016/j.it.2011.06.001</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">50. Martin MP, Qi Y, Gao X, Yamada E, Martin JN, Pereyra F, et al. Innate partnership of HLA-B and KIR3DL1 subtypes against HIV-1. Nat Genet. (2007) 39:733–40. doi: 10.1038/ng2035</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">51. Richard J, Sindhu S, Pham NQ, Belzile JP, Cohen EA. HIV-1 Vpr up-regulates expression of ligands for the activating NKG2D receptor and promotes NK cell-mediated killing. Blood (2010) 115:1354–63. doi: 10.1182/blood-2009-08-237370</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">52. Bernard NF, Kiani Z, Tremblay-McLean A, Kant SA, Leeks CE, Dupuy FP. Natural Killer (NK) cell education differentially influences HIV antibodydependent NK cell activation and antibody-dependent cellular cytotoxicity. Front Immunol. (2017) 8:1033. doi: 10.3389/fimmu.2017.01033</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">53. Barouch DH, Alter G, Broge T, Linde C, Ackerman ME, Brown EP, et al. Protective efficacy of adenovirus/protein vaccines against SIV challenges in rhesus monkeys. Science (2015) 349:320–4. doi: 10.1126/science.aab3886</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">54. Bournazos S, Klein F, Pietzsch J, Seaman MS, Nussenzweig MC, Ravetch JV. Broadly Neutralizing anti-HIV-1 antibodies require Fc effector functions for in vivo activity. Cell (2014) 158:1243–53. doi: 10.1016/j.cell.2014.08.023</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">55. DiLillo DJ, Tan GS, Palese P, V Ravetch J. Broadly neutralizing hemagglutinin stalk–specific antibodies require FcgR interactions for protection against influenza virus in vivo. Nat Med. (2014) 20:143–51. doi: 10.1038/ nm.3443</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">56. Chung AW, Kumar MP, Arnold KB, Yu WH, Schoen MK, Dunphy LJ, et al. Dissecting polyclonal vaccine-induced humoral immunity against hiv using systems serology. Cell (2015) 163:988–98. doi: 10.1016/j.cell.2015.10.027 57. Ackerman ME, Mikhailova A, Brown EP, Dowell KG, Walker BD, Bailey-</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">57. Ackerman ME, Mikhailova A, Brown EP, Dowell KG, Walker BD, Bailey- Kellogg C, et al. Polyfunctional HIV-specific antibody responses are associated with spontaneous HIV control. PLOS Pathog. (2016) 12:e1005315. doi: 10.1371/journal.ppat.1005315</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">58. Giese S,MarshM. Tetherin can restrict cell-free and cell-cell transmission of HIV fromprimary macrophages to T Cells. PLoS Pathog (2014) 10:e1004189. doi: 10.1371/journal.ppat.1004189</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">59. Arias JF, Heyer LN, von Bredow B,Weisgrau KL, Moldt B, Burton DR, et al. Tetherin antagonism by Vpu protects HIV-infected cells from antibodydependent cell-mediated cytotoxicity, Proc Natl Acad Sci USA. (2014) 111:6425–30. doi: 10.1073/pnas.1321507111</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">60. Borg C, Jalil A, Laderach D, Maruyama K, Wakasugi H, Charrier S, et al. NK cell activation by dendritic cells (DCs) requires the formation of a synapse leading to IL-12 polarization in DCs, Blood (2004) 104:3267–75. doi: 10.1182/blood-2004-01-0380</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">61. Gerosa F, Baldani-Guerra B, Nisii C, Marchesini V, Carra G, Trinchieri G. Reciprocal activating interaction between natural killer cells and dendritic cells. J Exp Med. (2002) 195:327–33. doi: 10.1084/jem.20010938</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">62. Ferlazzo G, TsangML,Moretta L,Melioli G, Steinman RM,Münz C. Human dendritic cells activate resting natural killer (NK) cells and are recognized via the NKp30 receptor by activated NK cells. J ExpMed. (2002) 195:343–51. doi: 10.1084/JEM.20011149</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">63. Ferlazzo G, Moretta L. Dendritic cell editing by natural killer cells. Crit Rev Oncog. (2014) 19:67–75. doi: 10.1615/CritRevOncog.2014010827</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">64. Wilder JA, Koh CY, Yuan D. The role of NK cells during in vivo antigenspecific antibody responses. J Immunol. (1996) 156:146–52.</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">65. Krebs P, Barnes MJ, Lampe K, Whitley K, Bahjat KS, Beutler B, et al. NK cell-mediated killing of target cells triggers robust antigen-specific T cell-mediated and humoral responses. Blood (2009) 113:6593–602. doi: 10.1182/blood-2009-01-201467</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">66. Perreau M, Savoye AL, De Crignis E, Corpataux JM, Cubas R, Haddad EK, et al. Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production. J Exp Med. (2013) 210:143–56. doi: 10.1084/jem.20121932</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">67. Huot N, Jacquelin B, Garcia-Tellez T, Rascle P, Ploquin MJ, Madec Y, et al. Natural killer cells migrate into and control simian immunodeficiency virus replication in lymph node follicles in African green monkeys. Nat Med. (2017) 23:1277–86. doi: 10.1038/nm.4421</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">68. Huot N, Bosinger SE, Paiardini M, Reeves RK, Müller-Trutwin M. Lymph node cellular and viral dynamics in natural hosts and impact for HIV cure strategies. Front Immunol. (2018) 9:780. doi: 10.3389/fimmu.2018.00780</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">69. Scully E, Alter G. NK Cells in HIV Disease. Curr HIV/AIDS Rep. (2016) 13:85–94. doi: 10.1007/s11904-016-0310-3</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">70. Michel T, Poli A, Cuapio A, Briquemont B, Iserentant G, Ollert M, et al. Human CD56bright NK cells: an update. J Immunol. (2016) 196:2923–31. doi: 10.4049/jimmunol.1502570</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">71. Taborda NA, Hernández JC, Montoya CJ, Rugeles MT. Las células natural killer y su papel en la respuesta inmunitaria durante la infección por el virus de la inmunodeficiencia humana tipo-1. Inmunología (2014) 33:11–20. doi: 10.1016/j.inmuno.2013.11.002</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">72. Moretta A, Marcenaro E, Parolini S, Ferlazzo G, Moretta L. NK cells at the interface between innate and adaptive immunity. Cell Death Differ. (2008) 15:226–33. doi: 10.1038/sj.cdd.4402170</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">73. Moretta L. Dissecting CD56dim human NK cells. Blood (2010) 116:3689–91. doi: 10.1182/blood-2010-09-303057</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">74. Alter G, Teigen N, Davis BT, Addo MM, Suscovich TJ, Waring MT, et al. Sequential deregulation of NK cell subset distribution and function starting in acute HIV-1 infection. Blood (2005) 106:3366–9. doi: 10.1182/blood-2005-03-1100</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">75. Hong HS, Ahmad F, Eberhard JM, Bhatnagar N, Bollmann BA, Keudel P, Ballmaier M, et al. Loss of CCR7 Expression on CD56bright NK Cells Is associated with a CD56dimCD16+ NK cell-like phenotype and correlates with HIV viral load. PLoS ONE (2012) 7:e44820. doi: 10.1371/journal.pone.0044820</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">76. Bhardwaj S, Ahmad F, Wedemeyer H, Cornberg M, Schulze zur Wiesch J, van Lunzen J, et al. Increased CD56bright NK cells in HIV-HCV co-infection and HCV mono-infection are associated with distinctive alterations of their phenotype. Virol J. (2016) 13:67. doi: 10.1186/s12985-016-0507-5</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">77. Hong HS, Eberhard JM, Keudel P, Bollmann BA, Ballmaier M, Bhatnagar N, et al. HIV infection is associated with a preferential decline in lessdifferentiated CD56dim CD16+ NK cells. J. Virol. (2010) 84:1183–8. doi: 10.1128/JVI.01675-09</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">78. Lopez-Vergès S, Milush JM, Pandey S, York VA, Arakawa-Hoyt J, Pircher H, et al. CD57 defines a functionally distinct population of mature NK cells in the human CD56dimCD16+ NK-cell subset. Blood (2010) 116:3865–74. doi: 10.1182/blood-2010-04-282301</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">79. Milush JM, López-Vergès S, York VA, Deeks SG, Martin JN, Hecht FM, et al. CD56negCD16+ NK cells are activated mature NK cells with impaired effector function during HIV-1 infection Retrovirology (2013) 10:158. doi: 10.1186/1742-4690-10-158</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">80. Gonzalez VD, Falconer K, Bjorkstrom NK, Blom KG, Weiland O, Ljunggren G, et al. Expansion of functionally skewed CD56-negative NK cells in chronic hepatitis c virus infection: correlation with outcome of pegylated IFN- and ribavirin treatment. J Immunol. (2009) 183:6612–8. doi: 10.4049/jimmunol.0901437</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">81. Shao JY, Yin WW, Zhang QF, Liu Q, Peng ML, Hu HD,et al. Siglec- 7 defines a highly functional natural killer cell subset and inhibits cellmediated activities. Scand J Immunol. (2016) 84:182–90. doi: 10.1111/sji. 12455</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">82. Brunetta E, Fogli M, Varchetta S, Bozzo L, Hudspeth KL, Marcenaro E, Moretta A, et al. The decreased expression of Siglec-7 represents an early marker of dysfunctional natural killer-cell subsets associated with high levels of HIV-1 viremia. Blood (2009) 114:3822–30. doi: 10.1182/blood-2009-06-226332</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">83. Ndhlovu LC, Lopez-Verges S, Barbour JD, Jones RB, Jha AR, Long BR, et al. Tim-3 marks human natural killer cell maturation and suppresses cell-mediated cytotoxicity. Blood (2012) 119:3734–43. doi: 10.1182/blood-2011-11-392951</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">84. Jost S, Moreno-Nieves U, Garcia-Beltran W, Rands K. Dysregulated Tim-3 expression on natural killer cells is associated with increased Galectin-9 levels in HIV-1 infection. Retrovirology (2013) 10:74. doi: 10.1186/1742-4690-10-74</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">85. Schafer JL, Li H, Evans TI, Estes JD, Reeves RK. Accumulation of cytotoxic CD16+ NK cells in simian immunodeficiency virus-infected lymph nodes associated with in situ differentiation and functional anergy. J Virol. (2015) 89:6887–94. doi: 10.1128/JVI.00660-15</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">86. Reeves RK, Rajakumar PA, Evans TI, Connole M, Gillis J, Wong FE, et al. Gut inflammation and indoleamine deoxygenase inhibit IL-17 production and promote cytotoxic potential in NKp44+ mucosal NK cells during SIV infection. Blood (2011)118:3321–30. doi: 10.1182/blood-2011-04- 347260</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">87. Xu H, Wang X, Liu DX, Moroney-Rasmussen T, Lackner AA, Veazey RS. IL-17-producing innate lymphoid cells are restricted to mucosal tissues and are depleted in SIV-infected macaques. Mucosal Immunol. (2012) 5:658–69. doi: 10.1038/mi.2012.39</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">88. Körner C, Altfeld M. Role of KIR3DS1 in human diseases. Front Immunol. (2012) 3:326. doi: 10.3389/fimmu.2012.00326</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">89. Habegger de Sorrentino A, Sinchi JL, Marinic K, López R, Iliovich E. KIRHLA- A and B alleles of the Bw4 epitope against HIV infection in discordant heterosexual couples in Chaco Argentina. Immunology (2013) 140:273–9. doi: 10.1111/imm.12137</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">90. Jackson E, Zhang CX, Kiani Z, Lisovsky I, Tallon B, Del Corpo A, et al. HIV exposed seronegative (HESN) compared to HIV infected individuals have higher frequencies of telomeric Killer Immunoglobulinlike Receptor (KIR) B motifs; Contribution of KIR B motif encoded genes to NK cell responsiveness. PLoS ONE (2017) 12:e0185160. doi: 10.1371/journal.pone.0185160</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">91. Carr WH, Rosen DB, Arase H, Nixon DF, Michaelsson J, Lanier LL. Cutting edge: KIR3DS1, a gene implicated in resistance to progression to AIDS, encodes a DAP12-associated receptor expressed on NK cells that triggers NK cell activation 1. J Immunol. (2007) 178:647–51. doi: 10.4049/jimmunol.178.2.647</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">92. Martin MP, Gao X, Lee JH, Nelson GW, Detels R, Goedert JJ, et al. Epistatic interaction between KIR3DS1 and HLA-B delays the progression to AIDS. Nat Genet. (2002) 31:429–34. doi: 10.1038/ng934</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">93. Lisovsky I, Isitman G, Song R, DaFonseca S, Tremblay-McLean A, Lebouché B, et al. A higher frequency ofNKG2A + than ofNKG2A − NK cells responds to autologous HIV-infected CD4 cells irrespective of whether or not they coexpress KIR3DL1. J Virol. (2015) 89:9909–19. doi: 10.1128/JVI.01546-15</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">94. O’Leary JG, Goodarzi M, Drayton DL, von Andrian UH. T cell– and B cell–independent adaptive immunity mediated by natural killer cells. Nat Immunol. (2006) 7:507–16. doi: 10.1038/ni1332</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">95. Björkström NK, Riese P, Heuts F, Andersson S, Fauriat C, Ivarsson MA, et al. Expression patterns of NKG2A, KIR, and CD57 define a process of CD56dim NK-cell differentiation uncoupled from NK-cell education. Blood (2010) 116:3853–64. doi: 10.1182/blood-2010-04-281675</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">96. Holder K, Comeau E, Grant M. Origins of natural killer cell memory: special creation or adaptive evolution. Immunology (2018) 154:38–49. doi: 10.1111/imm.12898</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">97. Lopez-Vergès S, Milush JM, Schwartz BS, Pando MJ, Jarjoura J, York VA, et al. Expansion of a unique CD57+NKG2Chi natural killer cell subset during acute human cytomegalovirus infection. Proc Natl Acad Sci USA. (2011) 108:14725–32. doi: 10.1073/pnas.1110900108</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">98. Paust S, Gill HS,Wang Z, Flynn MP, Moseman EA, Senman B, et al. Critical role for the chemokine receptor CXCR6 in NK cell–mediated antigenspecific memory of haptens and viruses. Nat Immunol. (2010) 11:1127–35. doi: 10.1038/ni.1953</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">99. Venkatasubramanian S, Cheekatla S, Paidipally P, Tripathi D, Welch E, Tvinnereim AR, et al. IL-21-dependent expansion of memory-like NK cells enhances protective immune responses againstMycobacteriumtuberculosis. Mucosal Immunol. (2017) 10:1031–42. doi: 10.1038/mi.2016.105</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">100. Reeves RK, Li H, Jost S, Blass E, Li H, Schafer JL, et al. Antigen-specific NK cell memory in rhesus macaques. Nat Immunol. (2015) 16:927–32. doi: 10.1038/ni.3227</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">101. Lima JF, Oliveira MS, Pereira NZ, Mitsunari GE, Duarte JS, Sato MN. Distinct natural killer cells in HIV-exposed seronegative subjects with effector cytotoxic CD56dim and CD56bright cells and memory-like CD57+NKG2C+CD56dim Cells. J Acquir Immune Defic Syndr. (2014) 67:463–71. doi: 10.1097/QAI.0000000000000350</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">102. Gondois-Rey F, Chéret A, Granjeaud S,Mallet F, Bidaut G, Lécuroux C, et al. NKG2C+memory-like NK cells contribute to the control of HIV viremia during primary infection: Optiprim-ANRS 147. Clin Transl Immunol. (2017) 6:e150. doi: 10.1038/cti.2017.22</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">103. Anderson DJ, Politch JA, Nadolski AM, Blaskewicz CD, Pudney J, Mayer KH. Targeting trojan horse leukocytes for HIV prevention. AIDS (2010) 24:163–87. doi: 10.1097/QAD.0b013e32833424c8</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">104. Childs RW, Carlsten M. Therapeutic approaches to enhance natural killer cell cytotoxicity against cancer: the force awakens. Nat Rev Drug Discov. (2015) 14:487–98. doi: 10.1038/nrd4506</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">105. Bergamaschi C, Kulkarni V, Rosati M, Alicea C, Jalah R, Chen S, et al. Intramuscular delivery of heterodimeric IL-15 DNA in macaques produces systemic levels of bioactive cytokine inducing proliferation of NK and T cells. Gene Ther. (2015) 2284:76–86. doi: 10.1038/gt. 2014.84</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">106. Conlon KC, Lugli E, Welles HC, Rosenberg SA, Fojo AT, Morris JC, et al. Redistribution, hyperproliferation, activation of natural killer cells and CD8 T cells, and cytokine production during first-in-human clinical trial of recombinant human interleukin-15 in patients with cancer. J Clin Oncol. (2015) 33:74–82. doi: 10.1200/JCO.2014.57.3329</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">107. Garrido C, Abad-Fernandez M, Tuyishime M, Pollara JJ, Ferrari G, Soriano- Sarabia N, Margolis DM. Interleukin-15-stimulated natural killer cells clear HIV-1-infected cells following latency reversal ex vivo. J Virol. (2018) 92:JVI.00235-18. doi: 10.1128/JVI.00235-18</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">108. Romee R, Rosario M, Berrien-Elliott MM, Wagner JA, Jewell BA, Schappe T, et al. Cytokine-induced memory-like natural killer cells exhibit enhanced responses against myeloid leukemia. Sci Transl Med. (2016) 8:357ra123. doi: 10.1126/scitranslmed.aaf2341</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">109. Cummings JS, Moreno-Nieves UY, Arnold V, Gilbert A, Yarbrough K, Didier C, et al. ANRS HIV Vaccine Network (AHVN), Natural killer cell responses to dendritic cells infected by the ANRS HIV-1 vaccine candidate, MVA HIV. Vaccine (2014) 32:5577–84. doi: 10.1016/j.vaccine.2014. 07.094</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">110. Ahmad R, Sindhu ST, Toma E, Morisset R, Vincelette J, Menezes J, Ahmad A. Evidence for a correlation between antibody-dependent cellular cytotoxicity-mediating anti-HIV-1 antibodies and prognostic predictors of HIV infection. J Clin Immunol. (2001) 21:227–33. doi: 10.1023/A:1011087 132180</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">111. Milligan CB, Richardson AA, John-Stewart G, Nduati R, Overbaugh J, John-Stewart G. Passively Acquired Antibody-Dependent Cellular Cytotoxicity (ADCC) activity in HIV-infected infants is associated with reduced mortality. Cell Host Microbe (2015) 17:500–6. doi: 10.1016/j.chom.2015.03.002</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">112. Lu L, Murakowski DK, Bournazos S, Schoofs T, Sarkar D, Halper- Stromberg A, et al. Enhanced clearance of HIV-1-infected cells by broadly neutralizing antibodies against HIV-1 in vivo. Science (2016) 352:1001–4. doi: 10.1126/science.aaf1279</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">113. Gómez-Román VR, Patterson LJ, Venzon D, Liewehr D, Aldrich K, Florese R, et al. Vaccine-elicited antibodies mediate antibody-dependent cellular cytotoxicity correlated with significantly reduced acute viremia in rhesus macaques challenged with SIVmac251. J Immunol. (2005) 174:2185–9. doi: 10.4049/jimmunol.174.4.2185</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">114. Davis ZB, Lenvik T, Hansen L, Felices M, Cooley S, Vallera D, et al. A Novel HIV envelope Bi-specific killer engager enhances natural killer cell mediated ADCC responses against HIV-infected cells. Blood (2016) 128: 2517.</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">115. Flynn NM, Forthal DN, Harro CD, Judson FN, Mayer KH, Para MF, et al. Placebo-controlled phase 3 trial of a recombinant glycoprotein 120 vaccine to prevent HIV-1 infection. J Infect Dis. (2005) 191:654–65. doi: 10.1086/ 428404</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">116. PitisuttithumP, Gilbert P, GurwithM, HeywardW,MartinM, van Griensven F, et al. Randomized, double-blind, placebo-controlled efficacy trial of a bivalent recombinant glycoprotein 120 HIV-1 vaccine among injection drug users in Bangkok, Thailand. J Infect Dis. (2006) 194:1661–71. doi: 10.1086/508748</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">117. Karnasuta C, Paris RM, Cox JH, Nitayaphan S, Pitisuttithum P, Thongcharoen P, et al. Thai AIDS Vaccine Evaluation Group, Thailand, Antibody-dependent cell-mediated cytotoxic responses in participants enrolled in a phase I/II ALVAC-HIV/AIDSVAXR B/E prime-boost HIV-1 vaccine trial in Thailand. Vaccine (2005) 23:2522–9. doi: 10.1016/j.vaccine.2004.10.028</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">118. Rerks-Ngarm S, Pitisuttithum P, Nitayaphan S, Kaewkungwal J, Chiu J, Paris R, et al. MOPH-TAVEG Investigators, Vaccination with ALVAC and AIDSVAX to Prevent HIV-1 Infection in Thailand. N Engl J Med. (2009) 361:2209–2220. doi: 10.1056/NEJMoa0908492</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">119. Haynes BF, Gilbert PB,McElrathMJ, Zolla-Pazner S, Tomaras GD, AlamSM, et al. Immune-correlates analysis of an HIV-1 vaccine efficacy trial. N Engl J Med. (2012) 366:1275–86. doi: 10.1056/NEJMoa1113425</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">120. Yates NL, Liao HX, Fong Y, DeCamp A, Vandergrift NA, Williams WT. Vaccine-induced Env V1-V2 IgG3 correlates with lower HIV-1 infection risk and declines soon after vaccination. Sci Transl Med. (2014) 6:228ra39. doi: 10.1126/scitranslmed.3007730</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">121. Callaway E. Clues emerge to explain first successful HIV vaccine trial. Nature (2011). doi: 10.1038/news.2011.541</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">122. Bradley T, Pollara J, Santra S, Vandergrift N, Pittala S, Bailey-Kellogg C, et al. Pentavalent HIV-1 vaccine protects against simian-human immunodeficiency virus challenge. Nat Commun. (2017) 8:15711. doi: 10.1038/ncomms15711</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">123. Glienke W, Esser R, Priesner C, Suerth JD, Schambach A, Wels WS, et al. Advantages and applications of CAR-expressing natural killer cells. Front Pharmacol. (2015) 6:21. doi: 10.3389/fphar.2015.00021</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">124. Liu D, Tian S, Zhang K, Xiong W, Michel Lubaki N, Chen Z, et al. Chimeric antigen receptor (CAR)-modified natural killer cell-based immunotherapy and immunological synapse formation in cancer and HIV. Protein Cell (2017) 8:861–77. doi: 10.1007/s13238-017-0415-5</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="references" lang="spa">125. Zhen A, Kamata M, Rezek V, Rick J, Levin B, Kasparian S, et al. HIV-specific immunity derived from chimeric antigen receptor-engineered stem cells. Mol Ther. (2015) 23:1358–67. doi: 10.1038/mt.2015.102</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">natural killer cells</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">HIV-1</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">HIV resistance</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">HIV vaccine</dim:field>
   <dim:field mdschema="dc" element="subject" lang="spa">Memory NK cells</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">natural killer cells</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">HIV-1</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">HIV resistance</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">HIV vaccine</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="other" lang="spa">Memory NK cells</dim:field>
   <dim:field mdschema="dc" element="title" lang="spa">NK Cells in HIV-1 Infection: From Basic Science to Vaccine Strategies</dim:field>
   <dim:field mdschema="dc" element="type">Artículo</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="coar">http://purl.org/coar/resource_type/c_6501</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="coarversion">http://purl.org/coar/version/c_970fb48d4fbd8a85</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="driver">info:eu-repo/semantics/article</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="version">info:eu-repo/semantics/publishedVersion</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="license">Atribución</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="accessrights">info:eu-repo/semantics/openAccess</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="coar">http://purl.org/coar/access_right/c_abf2</dim:field>
   <dim:field mdschema="dspace" element="entity" qualifier="type">Publication</dim:field>restricted</dim:dim></metadata></record></GetRecord></OAI-PMH>