Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes
Introduction Mucosal immune activation, in the context of sexual transmission of HIV-1 infection, is crucial, as the increased presence of activated T cells enhance susceptibility to infection. In this regard, it has been proposed that immunomodulatory compounds capable of modulating immune activati...
- Autores:
-
Zapata Builes, Wildeman
González, Sandra Milena
Aguilar Jiménez, Wbeimar
Trujillo Gil, Edison
Ruey Chyi, Su
Rugeles López, María Teresa
T. Blake, Ball
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2019
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/15801
- Acceso en línea:
- https://doi.org/10.1371/journal.pone.0222878
https://hdl.handle.net/20.500.12494/15801
- Palabra clave:
- HIV-1
VitD
Calcitriol
HIV-1
Seronegative individuals
HIV-1
VitD
Calcitriol
HIV-1
Seronegative individuals
- Rights
- openAccess
- License
- Atribución
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dc.title.spa.fl_str_mv |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
title |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
spellingShingle |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes HIV-1 VitD Calcitriol HIV-1 Seronegative individuals HIV-1 VitD Calcitriol HIV-1 Seronegative individuals |
title_short |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
title_full |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
title_fullStr |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
title_full_unstemmed |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
title_sort |
Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes |
dc.creator.fl_str_mv |
Zapata Builes, Wildeman González, Sandra Milena Aguilar Jiménez, Wbeimar Trujillo Gil, Edison Ruey Chyi, Su Rugeles López, María Teresa T. Blake, Ball |
dc.contributor.author.none.fl_str_mv |
Zapata Builes, Wildeman González, Sandra Milena Aguilar Jiménez, Wbeimar Trujillo Gil, Edison Ruey Chyi, Su Rugeles López, María Teresa T. Blake, Ball |
dc.subject.spa.fl_str_mv |
HIV-1 VitD Calcitriol HIV-1 Seronegative individuals |
topic |
HIV-1 VitD Calcitriol HIV-1 Seronegative individuals HIV-1 VitD Calcitriol HIV-1 Seronegative individuals |
dc.subject.other.spa.fl_str_mv |
HIV-1 VitD Calcitriol HIV-1 Seronegative individuals |
description |
Introduction Mucosal immune activation, in the context of sexual transmission of HIV-1 infection, is crucial, as the increased presence of activated T cells enhance susceptibility to infection. In this regard, it has been proposed that immunomodulatory compounds capable of modulating immune activation, such as Vitamin D (VitD) may reduce HIV-1 transmission and might be used as a safe and cost-effective strategy for prevention. Considering this, we examined the in vitro effect of the treatment of peripheral blood mononuclear cells (PBMCs) with the active form of VitD, calcitriol, on cellular activation, function and susceptibility of CD4+ T cells to HIV-1 infection. Methods We treated PBMCs from healthy HIV unexposed individuals (Co-HC) and frequently exposed, HIV-1 seronegative individuals (HESNs) from Colombia and from healthy nonexposed individuals from Canada (Ca-HC) with calcitriol and performed in vitro HIV-1 infection assays using X4- and R5-tropic HIV-1 strains respectively. In addition, we evaluated the activation and function of T cells and the expression of viral co-receptors, and select antiviral genes following calcitriol treatment. Results Calcitriol reduced the frequency of infected CD4+ T cells and the number of viral particles per cell, for both, X4- and R5-tropic viruses tested in the Co-HC and the Ca-HC, respectively, but not in HESNs. Furthermore, in the Co-HC, calcitriol reduced the frequency of polyclonally activated T cells expressing the activation markers HLA-DR and CD38, and those HLA-DR+CD38-, whereas increased the subpopulation HLA-DR-CD38+. Calcitriol treatment also decreased production of granzyme, IL-2 and MIP-1β by T cells and increased the transcriptional expression of the inhibitor of NF-kB and the antiviral genes cathelicidin (CAMP) and APOBEC3G in PBMCs from Co-HC. Conclusion Our in vitro findings suggest that VitD treatment could reduce HIV-1 transmission through a specific modulation of the activation levels and function of T cells, and the production of antiviral factors. In conclusion, VitD remains as an interesting potential strategy to prevent HIV- 1 transmission that should be further explored. |
publishDate |
2019 |
dc.date.accessioned.none.fl_str_mv |
2019-12-17T17:08:03Z |
dc.date.available.none.fl_str_mv |
2019-12-17T17:08:03Z |
dc.date.issued.none.fl_str_mv |
2019-09-24 |
dc.type.none.fl_str_mv |
Artículo |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.coarversion.none.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_6501 |
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publishedVersion |
dc.identifier.issn.spa.fl_str_mv |
1932-6203 |
dc.identifier.uri.spa.fl_str_mv |
https://doi.org/10.1371/journal.pone.0222878 |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12494/15801 |
dc.identifier.bibliographicCitation.spa.fl_str_mv |
Gonzalez S. M., Aguilar Jimenez W., Trujillo Gil E., Zapata W., Su R-C, Ball T. B., et al. (2019) Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes. PLoS ONE 14(9): e0222878. https://doi.org/10.1371/journal.pone.0222878. Recuperado de: |
identifier_str_mv |
1932-6203 Gonzalez S. M., Aguilar Jimenez W., Trujillo Gil E., Zapata W., Su R-C, Ball T. B., et al. (2019) Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes. PLoS ONE 14(9): e0222878. https://doi.org/10.1371/journal.pone.0222878. Recuperado de: |
url |
https://doi.org/10.1371/journal.pone.0222878 https://hdl.handle.net/20.500.12494/15801 |
dc.relation.isversionof.spa.fl_str_mv |
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0222878 |
dc.relation.ispartofjournal.spa.fl_str_mv |
PLOS ONE |
dc.relation.references.spa.fl_str_mv |
1. Shapira-Nahor O, Kalinkovich A, Weisman Z, Greenberg Z, Nahmias J, Shapiro M, et al. Increased susceptibility to HIV-1 infection of peripheral blood mononuclear cells from chronically immune-activated individuals. AIDS. 1998; 12(13):1731–3. PMID: 9764802 2. Zhang Z, Schuler T, Zupancic M, Wietgrefe S, Staskus KA, Reimann KA, et al. Sexual transmission and propagation of SIV and HIV in resting and activated CD4+ T cells. Science. 1999; 286(5443):1353–7. https://doi.org/10.1126/science.286.5443.1353 PMID: 10558989 3. Lawn SD, Butera ST, Folks TM. Contribution of Immune Activation to the Pathogenesis and Transmission of Human Immunodeficiency Virus Type 1 Infection. Clin Microbiol Rev. 2001; 14(4):753–77. https://doi.org/10.1128/CMR.14.4.753-777.2001 PMID: 11585784 4. Aguilar-Jimenez W, Villegas-Ospina S, Gonzalez S, Zapata W, Saulle I, Garziano M, et al. Precursor Forms of Vitamin D Reduce HIV-1 Infection In Vitro. 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Antiviral molecules correlate with vitamin D pathway genes and are associated with natural resistance to HIV-1 infection. Microbes Infect. 2016; 18(7– 8):510–6. https://doi.org/10.1016/j.micinf.2016.03.015 PMID: 27083474 20. Villegas-Ospina S, Aguilar-Jimenez W, Gonzalez SM, Rugeles MT. Vitamin D modulates the expression of HLA-DR and CD38 after in vitro activation of T-cells. Horm Mol Biol Clin Investig. 2017; 29(3):93–103. https://doi.org/10.1515/hmbci-2016-0037 PMID: 28222027 21. Hewison M, Freeman L, Hughes S V., Evans KN, Bland R, Eliopoulos AG, et al. Differential Regulation of Vitamin D Receptor and Its Ligand in Human Monocyte-Derived Dendritic Cells. J Immunol. 2003; 170(11):5382–90. https://doi.org/10.4049/jimmunol.170.11.5382 PMID: 12759412 22. O’Doherty U, Swiggard WJ, Malim MH. Human immunodeficiency virus type 1 spinoculation enhances infection through virus binding. J Virol. 2000; 74(21):10074–80. https://doi.org/10.1128/jvi.74.21.10074- 10080.2000 PMID: 11024136 23. Coussens AK, Naude CE, Goliath R, Chaplin G, Wilkinson RJ, Jablonski NG. High-dose vitamin D3 reduces deficiency caused by low UVB exposure and limits HIV-1 replication in urban Southern Africans. Proc Natl Acad Sci U S A. 2015; 112(26):8052–7. https://doi.org/10.1073/pnas.1500909112 PMID: 26080414 24. Biswas P, Mengozzi M, Mantelli B, Delfanti F, Brambilla A, Vicenzi E, et al. 1,25-Dihydroxyvitamin D3 upregulates functional CXCR4 human immunodeficiency virus type 1 coreceptors in U937 minus clones: NF-kappaB-independent enhancement of viral replication. J Virol. 1998; 72(10):8380–3. PMID: 9733889 25. Pauza CD, Kornbluth R, Emau P, Richman DD, Deftos LJ. Vitamin D3 compounds regulate human immunodeficiency virus type 1 replication in U937 monoblastoid cells and in monocyte-derived macrophages. J Leukoc Biol. 1993; 53(2):157–64. https://doi.org/10.1002/jlb.53.2.157 PMID: 8383166 26. Locardi C, Petrini C, Boccoli G, Testa U, Dieffenbach C, Buttò S, et al. Increased human immunodeficiency virus (HIV) expression in chronically infected U937 cells upon in vitro differentiation by hydroxyvitamin D3: roles of interferon and tumor necrosis factor in regulation of HIV production. J Virol. 1990; 64 (12):5874–82. PMID: 1700829 27. Kuebler PJ, Mehrotra ML, Shaw BI, Leadabrand KS, Milush JM, York VA, et al. Persistent HIV Type 1 Seronegative Status Is Associated With Lower CD8 + T-Cell Activation. J Infect Dis. 2016; 213(4):569– 73. https://doi.org/10.1093/infdis/jiv425 PMID: 26310308 28. Savarino A, Bottarel F, Calosso L, Feito MJ, Bensi T, Bragardo M, et al. Effects of the human CD38 glycoprotein on the early stages of the HIV-1 replication cycle. FASEB J. 1999; 13(15):2265–76. https:// doi.org/10.1096/fasebj.13.15.2265 PMID: 10593874 29. Sandoval-Montes C, Santos-Argumedo L. CD38 is expressed selectively during the activation of a subset of mature T cells with reduced proliferation but improved potential to produce cytokines. 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Sarkar S, Hewison M, Studzinski GP, Li YC, Kalia V. Role of vitamin D in cytotoxic T lymphocyte immunity to pathogens and cancer. Crit Rev Clin Lab Sci. 2016; 53(2):132–45. https://doi.org/10.3109/ 10408363.2015.1094443 PMID: 26479950 34. Matilainen JM, Ra¨sa¨nen A, Gynther P, Va¨isa¨nen S. The genes encoding cytokines IL-2, IL-10 and IL12B are primary 1α,25(OH)2D3 target genes. J Steroid Biochem Mol Biol. 2010; 121(1–2):142–5. https://doi.org/10.1016/j.jsbmb.2010.03.020 PMID: 20236616 35. Ragab D, Soliman D, Samaha D, Yassin A. Vitamin D status and its modulatory effect on interferon gamma and interleukin-10 production by peripheral blood mononuclear cells in culture. Cytokine. 2016; 85:5–10. https://doi.org/10.1016/j.cyto.2016.05.024 PMID: 27269178 36. Giulietti A, van Etten E, Overbergh L, Stoffels K, Bouillon R, Mathieu C. Monocytes from type 2 diabetic patients have a pro-inflammatory profile. Diabetes Res Clin Pract. 2007; 77(1):47–57. https://doi.org/ 10.1016/j.diabres.2006.10.007 PMID: 17112620 37. Neve A, Corrado A, Cantatore FP. Immunomodulatory effects of vitamin D in peripheral blood monocyte-derived macrophages from patients with rheumatoid arthritis. Clin Exp Med. 2014; 14(3):275–83. https://doi.org/10.1007/s10238-013-0249-2 PMID: 23824148 38. Khoo A-L, Chai LYA, Koenen HJPM, Sweep FCGJ, Joosten I, Netea MG, et al. Regulation of cytokine responses by seasonality of vitamin D status in healthy individuals. Clin Exp Immunol. 2011; 164(1):72– 9. https://doi.org/10.1111/j.1365-2249.2010.04315.x PMID: 21323660 39. Hansdottir S, Monick MM, Lovan N, Powers L, Gerke A, Hunninghake GW. Vitamin D Decreases Respiratory Syncytial Virus Induction of NF- B-Linked Chemokines and Cytokines in Airway Epithelium While Maintaining the Antiviral State. J Immunol. 2010; 184(2):965–74. https://doi.org/10.4049/jimmunol. 0902840 PMID: 20008294 40. Hansdottir S, Monick MM, Hinde SL, Lovan N, Look DC, Hunninghake GW. Respiratory epithelial cells convert inactive vitamin D to its active form: potential effects on host defense. J Immunol. 2008; 181(10):7090–9. https://doi.org/10.4049/jimmunol.181.10.7090 PMID: 18981129 41. Lachmann R, Bevan MA, Kim S, Patel N, Hawrylowicz C, Vyakarnam A, et al. A comparative phase 1 clinical trial to identify anti-infective mechanisms of vitamin D in people with HIV infection. AIDS. 2015; 29(10):1127–35. https://doi.org/10.1097/QAD.0000000000000666 PMID: 25870995 42. Wu-Wong JR, Nakane M, Chen Y, Qiang W. Different Effects of Calcidiol and Calcitriol on Regulating Vitamin D Receptor Target Gene Expression in Human Vascular Smooth Muscle Cells. Journal of cardiovascular disease research. 2013; 1(2):15–20. 43. Szabo G, Mandrekar P, Girouard L, Catalano D. Regulation of human monocyte functions by acute ethanol treatment: decreased tumor necrosis factor-alpha, interleukin-1 beta and elevated interleukin-10, and transforming growth factor-beta production. Alcohol Clin Exp Res. 1996; 20(5):900–7. https://doi. org/10.1111/j.1530-0277.1996.tb05269.x PMID: 8865966 44. Mandrekar P, Catalano D, White B, Szabo G. Moderate alcohol intake in humans attenuates monocyte inflammatory responses: inhibition of nuclear regulatory factor kappa B and induction of interleukin 10. Alcohol Clin Exp Res. 2006; 30(1):135–9. https://doi.org/10.1111/j.1530-0277.2006.00012.x PMID: 16433741 45. Barr T, Helms C, Grant K, Messaoudi I. Opposing Effects of Alcohol on the Immune System. Prog Neuropsychopharmacol Biol Psychiatry. 2016; 65: 242–251. https://doi.org/10.1016/j.pnpbp.2015.09.001 PMID: 26375241 |
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Zapata Builes, WildemanGonzález, Sandra MilenaAguilar Jiménez, WbeimarTrujillo Gil, EdisonRuey Chyi, SuRugeles López, María TeresaT. Blake, Ball14(9)2019-12-17T17:08:03Z2019-12-17T17:08:03Z2019-09-241932-6203https://doi.org/10.1371/journal.pone.0222878https://hdl.handle.net/20.500.12494/15801Gonzalez S. M., Aguilar Jimenez W., Trujillo Gil E., Zapata W., Su R-C, Ball T. B., et al. (2019) Vitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytes. PLoS ONE 14(9): e0222878. https://doi.org/10.1371/journal.pone.0222878. Recuperado de:Introduction Mucosal immune activation, in the context of sexual transmission of HIV-1 infection, is crucial, as the increased presence of activated T cells enhance susceptibility to infection. In this regard, it has been proposed that immunomodulatory compounds capable of modulating immune activation, such as Vitamin D (VitD) may reduce HIV-1 transmission and might be used as a safe and cost-effective strategy for prevention. Considering this, we examined the in vitro effect of the treatment of peripheral blood mononuclear cells (PBMCs) with the active form of VitD, calcitriol, on cellular activation, function and susceptibility of CD4+ T cells to HIV-1 infection. Methods We treated PBMCs from healthy HIV unexposed individuals (Co-HC) and frequently exposed, HIV-1 seronegative individuals (HESNs) from Colombia and from healthy nonexposed individuals from Canada (Ca-HC) with calcitriol and performed in vitro HIV-1 infection assays using X4- and R5-tropic HIV-1 strains respectively. In addition, we evaluated the activation and function of T cells and the expression of viral co-receptors, and select antiviral genes following calcitriol treatment. Results Calcitriol reduced the frequency of infected CD4+ T cells and the number of viral particles per cell, for both, X4- and R5-tropic viruses tested in the Co-HC and the Ca-HC, respectively, but not in HESNs. Furthermore, in the Co-HC, calcitriol reduced the frequency of polyclonally activated T cells expressing the activation markers HLA-DR and CD38, and those HLA-DR+CD38-, whereas increased the subpopulation HLA-DR-CD38+. Calcitriol treatment also decreased production of granzyme, IL-2 and MIP-1β by T cells and increased the transcriptional expression of the inhibitor of NF-kB and the antiviral genes cathelicidin (CAMP) and APOBEC3G in PBMCs from Co-HC. Conclusion Our in vitro findings suggest that VitD treatment could reduce HIV-1 transmission through a specific modulation of the activation levels and function of T cells, and the production of antiviral factors. In conclusion, VitD remains as an interesting potential strategy to prevent HIV- 1 transmission that should be further explored.https://scienti.minciencias.gov.co/cvlac/EnProdArticulo/query.do?cod_producto=73&cod_rh=0000157775https://orcid.org/0000-0002-7351-8738COL0112548wildeman.zapatab@campusucc.edu.comilena.gonzalez@udea.edu.coedisonetg@gmail.comrueyc.su@canada.caaguilar.wb@gmail.comblake.ball@umanitoba.camaria.rugeles@udea.edu.cohttps://scholar.google.com.co/citations?hl=en&user=VLZxl1UAAAAJ15Grupo Infettare, Facultad de Medicina, Universidad Cooperativa de Colombia, Medellin, ColombiaMedicinaMedellínhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0222878PLOS ONE1. Shapira-Nahor O, Kalinkovich A, Weisman Z, Greenberg Z, Nahmias J, Shapiro M, et al. Increased susceptibility to HIV-1 infection of peripheral blood mononuclear cells from chronically immune-activated individuals. AIDS. 1998; 12(13):1731–3. PMID: 97648022. 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Prog Neuropsychopharmacol Biol Psychiatry. 2016; 65: 242–251. https://doi.org/10.1016/j.pnpbp.2015.09.001 PMID: 26375241HIV-1VitDCalcitriolHIV-1Seronegative individualsHIV-1VitDCalcitriolHIV-1Seronegative individualsVitamin D treatment of peripheral blood mononuclear cells modulated immune activation and reduced susceptibility to HIV-1 infection of CD4+ T lymphocytesArtículohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAtribucióninfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2PublicationORIGINALVitamin D treatment of peripheral blood UCC UdeA 2019.pdfVitamin D treatment of peripheral blood UCC UdeA 2019.pdfArtículoapplication/pdf1047762https://repository.ucc.edu.co/bitstreams/7022d55b-0083-4856-98b8-c0c0cc94cb2a/downloadabf6f434a8d4d8a115ba4e0c3da4bc7fMD51LICENSElicense.txtlicense.txttext/plain; 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