Zika virus infection suppresses CYP24A1 and CAMP expression in human monocytes.
Journal
Archives of virology
ISSN: 1432-8798
Titre abrégé: Arch Virol
Pays: Austria
ID NLM: 7506870
Informations de publication
Date de publication:
06 Jun 2024
06 Jun 2024
Historique:
received:
23
11
2023
accepted:
27
03
2024
medline:
6
6
2024
pubmed:
6
6
2024
entrez:
5
6
2024
Statut:
epublish
Résumé
Monocytes are the primary targets of Zika virus (ZIKV) and are associated with ZIKV pathogenesis. Currently, there is no effective treatment for ZIKV infection. It is known that 1,25-dihydroxy vitamin D
Identifiants
pubmed: 38839691
doi: 10.1007/s00705-024-06050-2
pii: 10.1007/s00705-024-06050-2
doi:
Substances chimiques
Vitamin D3 24-Hydroxylase
EC 1.14.15.16
Cathelicidins
0
CYP24A1 protein, human
EC 1.14.15.16
Cytokines
0
Antimicrobial Cationic Peptides
0
Receptors, Calcitriol
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
135Subventions
Organisme : Minciencias/Colciencias
ID : 111584467188
Organisme : Minciencias/Colciencias
ID : contrato No. 455-2019
Organisme : Universidad de Antioquia-CODI
ID : 2017-16389
Informations de copyright
© 2024. The Author(s).
Références
Lessler J, Chaisson LH, Kucirka LM, Bi Q, Grantz K, Salje H, et al (2016) Assessing the global threat from Zika virus. Science (80). 353(6300). https://doi.org/10.1126/science.aaf8160
Chambers TJ, Hahn CS, Galler R, Rice CM (1990) Flavivirus genome organization, expression, and replication. Annu Rev Microbiol. 44(1):649–88. https://doi.org/10.1146/annurev.mi.44.100190.003245
doi: 10.1146/annurev.mi.44.100190.003245
pubmed: 2174669
Magnus MM, Espósito DLA, da Costa VA, de Melo PS, Costa-Lima C, da Fonseca BAL et al (2018) Risk of Zika virus transmission by blood donations in Brazil. Hematol Transfus Cell Ther. 40(3):250–4. https://doi.org/10.1016/j.htct.2018.01.011
doi: 10.1016/j.htct.2018.01.011
pubmed: 30128434
pmcid: 6098187
Miner JJ, Diamond MS (2017) Zika Virus Pathogenesis and Tissue Tropism. Cell Host Microbe. 21(2):134–42. https://doi.org/10.1016/j.chom.2017.01.004
doi: 10.1016/j.chom.2017.01.004
pubmed: 28182948
pmcid: 5328190
Hamel R, Dejarnac O, Wichit S, Ekchariyawat P, Neyret A, Luplertlop N, et al. Biology of Zika Virus Infection in Human Skin Cells. Diamond MS, editor. J Virol. 89(17):8880–96. Available from: https://jvi.asm.org/content/89/17/8880
Faria NR, Azevedo R do S da S, Kraemer MUG, Souza R, Cunha MS, Hill SC, et al. Zika virus in the Americas: Early epidemiological and genetic findings. Science (80- ) [Internet]. 2016 Apr 15;352(6283):345–9. Available from: https://doi.org/10.1126/science.aaf5036
Sabogal-Roman JA, Murillo-García DR, Yepes-Echeverri MC, Restrepo-Mejia JD, Granados-Álvarez S, Paniz-Mondolfi AE, et al (2016) Healthcare students and workers’ knowledge about transmission, epidemiology and symptoms of Zika fever in four cities of Colombia. Travel Med Infect Dis. 14(1):52–4. Available from: https://linkinghub.elsevier.com/retrieve/pii/S1477893915002045
Paniz-Mondolfi AE, Giraldo J, Rodríguez-Morales AJ, Pacheco O, Lombó-Lucero GY, Plaza JD et al (2018) Alice in Wonderland syndrome: a novel neurological presentation of Zika virus infection. J Neurovirol. 24(5):660–3. https://doi.org/10.1007/s13365-018-0645-1
doi: 10.1007/s13365-018-0645-1
pubmed: 30105501
Azevedo RSS, de Sousa JR, Araujo MTF, Martins Filho AJ, de Alcantara BN, Araujo FMC et al (2018) In situ immune response and mechanisms of cell damage in central nervous system of fatal cases microcephaly by Zika virus. Sci Rep 8(1):1
doi: 10.1038/s41598-017-17765-5
pubmed: 29311619
pmcid: 5758755
de Oliveira WK, de França GVA, Carmo EH, Duncan BB, de Souza KR, Schmidt MI (2017) Infection-related microcephaly after the 2015 and 2016 Zika virus outbreaks in Brazil: a surveillance-based analysis. Lancet 390(10097):861–870
doi: 10.1016/S0140-6736(17)31368-5
pubmed: 28647172
Shuaib W, Stanazai H, Abazid AG, Mattar AA (2016) Re-Emergence of Zika Virus: A Review on Pathogenesis, Clinical Manifestations, Diagnosis, Treatment, and Prevention. Am J Med. 129(8):879.e7-879.e12. https://doi.org/10.1016/j.amjmed.2016.02.027
doi: 10.1016/j.amjmed.2016.02.027
pubmed: 26994509
da Silva MHM, Moises RNC, Alves BEB, Pereira HWB, de Paiva AAP, Morais IC et al (2019) Innate immune response in patients with acute Zika virus infection. Med Microbiol Immunol. 208(6):703–14. https://doi.org/10.1007/s00430-019-00588-8
doi: 10.1007/s00430-019-00588-8
pubmed: 30879197
Kam Y-W, Leite JA, Lum F-M, Tan JJL, Lee B, Judice CC, et al (2017) Specific Biomarkers Associated With Neurological Complications and Congenital Central Nervous System Abnormalities From Zika Virus–Infected Patients in Brazil. J Infect Dis. 216(2):172–81. https://academic.oup.com/jid/article/216/2/172/3858563
Tappe D, Pérez-Girón JV, Zammarchi L, Rissland J, Ferreira DF, Jaenisch T et al (2016) Cytokine kinetics of Zika virus-infected patients from acute to reconvalescent phase. Med Microbiol Immunol. 205(3):269–73. https://doi.org/10.1007/s00430-015-0445-7
doi: 10.1007/s00430-015-0445-7
pubmed: 26702627
Michlmayr D, Andrade P, Gonzalez K, Balmaseda A, Harris E (2017) CD14+CD16+ monocytes are the main target of Zika virus infection in peripheral blood mononuclear cells in a paediatric study in Nicaragua. Nat Microbiol. 2(11):1462–70. https://www.nature.com/articles/s41564-017-0035-0
Jurado KA, Iwasaki A (2017) Zika virus targets blood monocytes. Nat Microbiol. 2(11):1460–1. Available from: https://www.nature.com/articles/s41564-017-0049-7
Ayala-Nunez NV, Follain G, Delalande F, Hirschler A, Partiot E, Hale GL et al (2019) Zika virus enhances monocyte adhesion and transmigration favoring viral dissemination to neural cells. Nat Commun. 10(1):4430. https://doi.org/10.1038/s41467-019-12408-x
doi: 10.1038/s41467-019-12408-x
pubmed: 31562326
pmcid: 6764950
Peluso R, Haase A, Stowring L, Edwards M, Ventura P (1985) A Trojan Horse mechanism for the spread of visna virus in monocytes. Virology. 147(1):231–6. Available from: https://linkinghub.elsevier.com/retrieve/pii/0042682285902466
Michlmayr D, Andrade P, Gonzalez K, Balmaseda A, Harris E (2017) CD14+CD16+ monocytes are the main target of Zika virus infection in peripheral blood mononuclear cells in a paediatric study in Nicaragua. Nat Microbiol. 2(11):1462–70. Available from: http://www.nature.com/articles/s41564-017-0035-0
Semenza JC, Rocklöv J, Ebi KL (2022) Climate Change and Cascading Risks from Infectious Disease. Infect Dis Ther. 11(4):1371–90. https://doi.org/10.1007/s40121-022-00647-3
doi: 10.1007/s40121-022-00647-3
pubmed: 35585385
pmcid: 9334478
Kazmi SS, Ali W, Bibi N, Nouroz F (2020) A review on Zika virus outbreak, epidemiology, transmission and infection dynamics. J Biol Res 27(1):5
Siddiqui M, Manansala JS, Abdulrahman HA, Nasrallah GK, Smatti MK, Younes N, et al (2020) Immune Modulatory Effects of Vitamin D on Viral Infections. Nutrients. 12(9):2879. Available from: https://www.mdpi.com/2072-6643/12/9/2879
ArboledaAlzate JF, Rodenhuis-Zybert IA, Hernández JC, Smit JM, Urcuqui-Inchima S (2017) Human macrophages differentiated in the presence of vitamin D3 restrict dengue virus infection and innate responses by downregulating mannose receptor expression. de Silva AM, editor. PLoS Negl Trop Dis. 11(10):e0005904. https://doi.org/10.1371/journal.pntd.0005904
doi: 10.1371/journal.pntd.0005904
Giraldo DM, Cardona A, Urcuqui-Inchima S (2018) High-dose of vitamin D supplement is associated with reduced susceptibility of monocyte-derived macrophages to dengue virus infection and pro-inflammatory cytokine production: An exploratory study. Clin Chim Acta. 478:140–51. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0009898117305442
Martínez-Moreno J, Hernandez JC, Urcuqui-Inchima S (2020) Effect of high doses of vitamin D supplementation on dengue virus replication, Toll-like receptor expression, and cytokine profiles on dendritic cells. Mol Cell Biochem. 464(1–2):169–80. https://doi.org/10.1007/s11010-019-03658-w
doi: 10.1007/s11010-019-03658-w
pubmed: 31758375
van Helmond N, Brobyn TL, LaRiccia PJ, Cafaro T, Hunter K, Roy S, et al (2022) Vitamin D3 Supplementation at 5000 IU Daily for the Prevention of Influenza-like Illness in Healthcare Workers: A Pragmatic Randomized Clinical Trial. Nutrients. 15(1):180. Available from: https://www.mdpi.com/2072-6643/15/1/180
Hansdottir S, Monick MM, Lovan N, Powers L, Gerke A, Hunninghake GW (2010) Vitamin D Decreases Respiratory Syncytial Virus Induction of NF-κB–Linked Chemokines and Cytokines in Airway Epithelium While Maintaining the Antiviral State. J Immunol. 184(2):965–74. Available from: https://journals.aai.org/jimmunol/article/184/2/965/111822/Vitamin-D-Decreases-Respiratory-Syncytial-Virus
Watkins RR, Lemonovich TL, Salata RA (2015) An update on the association of vitamin D deficiency with common infectious diseases. Can J Physiol Pharmacol. 93(5):363–8. https://doi.org/10.1139/cjpp-2014-0352
doi: 10.1139/cjpp-2014-0352
pubmed: 25741906
Borella E, Nesher G, Israeli E, Shoenfeld Y (2014) Vitamin D: a new anti-infective agent? Ann N Y Acad Sci. 1317(1):76–83. https://doi.org/10.1111/nyas.12321
doi: 10.1111/nyas.12321
pubmed: 24593793
Alvarez N, Aguilar-Jimenez W, Rugeles MT (2019) The Potential Protective Role of Vitamin D Supplementation on HIV-1 Infection. Front Immunol. 10. https://doi.org/10.3389/fimmu.2019.02291/full
Hafezi S, Saheb Sharif-Askari F, Saheb Sharif-Askari N, Ali Hussain Alsayed H, Alsafar H, Al Anouti F, et al (2022) Vitamin D enhances type I IFN signaling in COVID-19 patients. Sci Rep. 12(1):17778. Available from: https://www.nature.com/articles/s41598-022-22307-9
Zurita-Cruz J, Fonseca-Tenorio J, Villasís-Keever M, López-Alarcón M, Parra-Ortega I, López-Martínez B, et al (2022) Efficacy and safety of vitamin D supplementation in hospitalized COVID-19 pediatric patients: A randomized controlled trial. Front Pediatr. 10. https://doi.org/10.3389/fped.2022.943529/full
Baxter BA, Ryan MG, LaVergne SM, Stromberg S, Berry K, Tipton M, et al (2022) Correlation between 25-hydroxyvitamin D/D3 Deficiency and COVID-19 Disease Severity in Adults from Northern Colorado. Nutrients. 14(24):5204. Available from: https://www.mdpi.com/2072-6643/14/24/5204
Mirza WA, Zhang K, Zhang R, Duan G, Khan MSN, Ni P (2022) Vitamin D deficiency in dengue fever patients’ coinfected with H. pylori in Pakistan. A case-control study. Front Public Heal. 10. https://doi.org/10.3389/fpubh.2022.1035560/full
Coussens AK, Naude CE, Goliath R, Chaplin G, Wilkinson RJ, Jablonski NG (2015) High-dose vitamin D 3 reduces deficiency caused by low UVB exposure and limits HIV-1 replication in urban Southern Africans. Proc Natl Acad Sci. 112(26):8052–7. https://doi.org/10.1073/pnas.1500909112
doi: 10.1073/pnas.1500909112
pubmed: 26080414
pmcid: 4491791
Den Bout-Van Van, Den Beukel CJP, Fievez L, Michels M, Sweep FCGJ, Hermus ARMM, Bosch MEW et al (2008) Vitamin D Deficiency among HIV Type 1-Infected Individuals in the Netherlands: Effects of Antiretroviral Therapy. AIDS Res Hum Retroviruses. 24(11):1375–82. https://doi.org/10.1089/aid.2008.0058
doi: 10.1089/aid.2008.0058
Tuohimaa P (2008) Vitamin D, aging, and cancer. Nutr Rev. 66:S147–52. https://doi.org/10.1111/j.1753-4887.2008.00095.x
Pineda-Lancheros LE, Gálvez-Navas JM, Rojo-Tolosa S, Membrive-Jiménez C, Valverde-Merino MI, Martínez-Martínez F, et al (2023) Polymorphisms in VDR, CYP27B1, CYP2R1, GC and CYP24A1 Genes as Biomarkers of Survival in Non-Small Cell Lung Cancer: A Systematic Review. Nutrients. 15(6):1525. Available from: https://www.mdpi.com/2072-6643/15/6/1525
DeLuca HF (2014) History of the discovery of vitamin D and its active metabolites. Bonekey Rep. 3. Available from: http://www.portico.org/Portico/article?article=pgk2ph97rtf
Nurminen V, Seuter S, Carlberg C (2019) Primary Vitamin D Target Genes of Human Monocytes. Front Physiol. 10. https://doi.org/10.3389/fphys.2019.00194/full
Bhalla AK, Amento EP, Clemens TL, Holick MF, Krane SM (1983) Specific high-affinity receptors for 1,25-dihydroxyvitamin D3 in human peripheral blood mononuclear cells: presence in monocytes and induction in T lymphocytes following activation. J Clin Endocrinol Metab. 57(6):1308–10. https://doi.org/10.1210/jcem-57-6-1308
doi: 10.1210/jcem-57-6-1308
pubmed: 6313738
Baeke F, Takiishi T, Korf H, Gysemans C, Mathieu C (2010) Vitamin D: modulator of the immune system. Curr Opin Pharmacol 10(4):482–96. https://doi.org/10.1016/j.coph.2010.04.001
doi: 10.1016/j.coph.2010.04.001
pubmed: 20427238
Cantorna MT, Arora J. Two lineages of immune cells that differentially express the vitamin D receptor. J Steroid Biochem Mol Biol. 2023 Apr;228:106253. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0960076023000080
Yuk J-M, Shin D-M, Lee H-M, Yang C-S, Jin HS, Kim K-K, et al (2009) Vitamin D3 Induces Autophagy in Human Monocytes/Macrophages via Cathelicidin. Cell Host Microbe [Internet]. 6(3):231–43. Available from: https://linkinghub.elsevier.com/retrieve/pii/S1931312809002832
Hernández-Sarmiento LJ, Valdés-López JF, Urcuqui-Inchima S (2023) American-Asian- and African lineages of Zika virus induce differential pro-inflammatory and Interleukin 27-dependent antiviral responses in human monocytes. Virus Res. 325:199040. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0168170223000023
Tamayo-Molina YS, Velilla PA, Hernández-Sarmiento LJ, Urcuqui-Inchima S (2023) Multitranscript analysis reveals an effect of 2-deoxy-d-glucose on gene expression linked to unfolded protein response and integrated stress response in primary human monocytes and monocyte-derived macrophages. Biochim Biophys Acta - Gen Subj 1867(9):130397
doi: 10.1016/j.bbagen.2023.130397
pubmed: 37290716
Valdés-López JF, Velilla PA, Urcuqui Inchima S (2020) Chikungunya virus infection induces differential inflammatory and antiviral responses in human monocytes and monocyte-derived macrophages. Acta Trop. 211.
Giraldo DM, Hernandez JC, Velilla P, Urcuqui-Inchima S (2016) HIV-1–neutrophil interactions trigger neutrophil activation and Toll-like receptor expression. Immunol Res. 64(1):93–103. https://doi.org/10.1007/s12026-015-8691-8
doi: 10.1007/s12026-015-8691-8
pubmed: 26350266
Valdés-López JF, Velilla P, Urcuqui-Inchima S (2022) Vitamin D modulates the expression of Toll-like receptors and pro-inflammatory cytokines without affecting Chikungunya virus replication, in monocytes and macrophages. Acta Trop 232:106497
doi: 10.1016/j.actatropica.2022.106497
pubmed: 35508271
Vanwalscappel B, Tada T, Landau NR (2018) Toll-like receptor agonist R848 blocks Zika virus replication by inducing the antiviral protein viperin. Virology. 522:199–208. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0042682218302162
Luo H, Winkelmann ER, Fernandez-Salas I, Li L, Mayer SV, Danis-Lozano R et al (2018) Zika, dengue and yellow fever viruses induce differential anti-viral immune responses in human monocytic and first trimester trophoblast cells. Antiviral Res 151(1):55–62
doi: 10.1016/j.antiviral.2018.01.003
pubmed: 29331320
pmcid: 5844857
Foo S-S, Chen W, Chan Y, Bowman JW, Chang L-C, Choi Y, et al (2017) Asian Zika virus strains target CD14+ blood monocytes and induce M2-skewed immunosuppression during pregnancy. Nat Microbiol. 2(11):1558–70. Available from: https://www.nature.com/articles/s41564-017-0016-3
Dang J, Tiwari SK, Lichinchi G, Qin Y, Patil VS, Eroshkin AM, et al (2016) Zika Virus Depletes Neural Progenitors in Human Cerebral Organoids through Activation of the Innate Immune Receptor TLR3. Cell Stem Cell. 19(2):258–65. Available from: https://linkinghub.elsevier.com/retrieve/pii/S1934590916300571
Faizan MI, Abdullah M, Ali S, Naqvi IH, Ahmed A, Parveen S (2017) Zika Virus-Induced Microcephaly and Its Possible Molecular Mechanism. Intervirol S Karger AG 59:152–8
doi: 10.1159/000452950
Rossi SL, Tesh RB, Azar SR, Muruato AE, Hanley KA, Auguste AJ et al (2016) Characterization of a Novel Murine Model to Study Zika Virus. Am J Trop Med Hyg. 94(6):1362–9. https://doi.org/10.4269/ajtmh.16-0111
doi: 10.4269/ajtmh.16-0111
pubmed: 27022155
pmcid: 4889758
Ahluwalia S, Choudhary D, Tyagi P, Kumar V, Vivekanandan P (2021) Vitamin D signaling inhibits HBV activity by directly targeting the HBV core promoter. J Biol Chem. 297(4):101233. Available from: https://linkinghub.elsevier.com/retrieve/pii/S002192582101036X
Ravid A, Rapaport N, Issachar A, Erman A, Bachmetov L, Tur-Kaspa R, et al (2019) 25-Hydroxyvitamin D Inhibits Hepatitis C Virus Production in Hepatocellular Carcinoma Cell Line by a Vitamin D Receptor-Independent Mechanism. Int J Mol Sci. 20(9):2367. Available from: https://www.mdpi.com/1422-0067/20/9/2367
Telcian AG, Zdrenghea MT, Edwards MR, Laza-Stanca V, Mallia P, Johnston SL, et al (2017) Vitamin D increases the antiviral activity of bronchial epithelial cells in vitro. Antiviral Res. 137:93–101. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0166354216303692
Wei D, Wang L, Zuo X, Bresalier RS (2021) Vitamin D: Promises on the Horizon and Challenges Ahead for Fighting Pancreatic Cancer. Cancers (Basel). 13(11):2716. Available from: https://www.mdpi.com/2072-6694/13/11/2716
Sakaki T, Kagawa N, Yamamoto K, Inouye K (2005) Metabolism of vitamin D3 by cytochromes P450. Front Biosci. 10(1–3):134. Available from: https://imrpress.com/journal/FBL/10/1/10.2741/1514
Wang J, Dou X, Song J, Lyu Y, Zhu X, Xu L et al (2019) Antimicrobial peptides: Promising alternatives in the post feeding antibiotic era. Med Res Rev. 39(3):831–59. https://doi.org/10.1002/med.21542
doi: 10.1002/med.21542
pubmed: 30353555
Haug C, Müller F, Aukrust P, Frøland SS (1994) Subnormal serum concentration of 1, 25-vitamin d in human immunodeficiency virus infection: Correlation with degree of immune deficiency and survival. J Infect Dis 169(4):889–893
doi: 10.1093/infdis/169.4.889
pubmed: 7907645
Haug CJ, Aukrust P, Haug E, Mørkrid L, Müller F, Frøland SS (1998) Severe Deficiency of 1,25-Dihydroxyvitamin D3 in Human Immunodeficiency Virus Infection: Association with Immunological Hyperactivity and Only Minor Changes in Calcium Homeostasis. J Clin Endocrinol Metab. 83(11):3832–8. Available from: https://academic.oup.com/jcem/article/83/11/3832/2865349
Rieder FJJ, Gröschel C, Kastner M-T, Kosulin K, Laengle J, Zadnikar R, et al (2017) Human cytomegalovirus infection downregulates vitamin-D receptor in mammalian cells. J Steroid Biochem Mol Biol. 165:356–62. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0960076016302175
Wang T, Dabbas B, Laperriere D, Bitton AJ, Soualhine H, Tavera-mendoza LE et al (2010) Direct and Indirect Induction by 1, 25-Dihydroxyvitamin D 3 of the Innate Immune Pathway Defective in Crohn Disease. J Biol Chem 285(4):2227–31
doi: 10.1074/jbc.C109.071225
pubmed: 19948723
Jones G, Prosser DE, Kaufmann M (2012) 25-Hydroxyvitamin D-24-hydroxylase (CYP24A1): Its important role in the degradation of vitamin D. Arch Biochem Biophys 523:9–18
doi: 10.1016/j.abb.2011.11.003
pubmed: 22100522
Yenamandra SP, Lundin A, Arulampalam V, Yurchenko M, Pettersson S, Klein G et al (2009) Expression profile of nuclear receptors upon Epstein - Barr virus induced B cell transformation. Exp Oncol 31(2):92–96
pubmed: 19550398
Gotlieb N, Tachlytski I, Lapidot Y, Sultan M, Safran M, Ben-Ari Z (2018) Hepatitis B virus downregulates vitamin D receptor levels in hepatoma cell lines, thereby preventing vitamin D-dependent inhibition of viral transcription and production. Mol Med 24:53
doi: 10.1186/s10020-018-0055-0
pubmed: 30326825
pmcid: 6192355
Yang J, Chen D, Tian G, Mao X, He J, Zheng P, et al (2022) 1,25-Dihydroxyvitamin D3 Negatively Regulates the Inflammatory Response to Porcine Epidemic Diarrhea Virus Infection by Inhibiting NF-κB and JAK/STAT Signaling Pathway in IPEC-J2 Porcine Epithelial Cells. Int J Mol Sci. 23(18):10603. Available from: https://www.mdpi.com/1422-0067/23/18/10603
Fernandez GJ, Ramírez-Mejía JM, Urcuqui-Inchima S (2022) Transcriptional and post-transcriptional mechanisms that regulate the genetic program in Zika virus-infected macrophages. Int J Biochem Cell Biol. 153:106312. Available from: https://linkinghub.elsevier.com/retrieve/pii/S1357272522001571
Bellamy R, Ruwende C, Corrah T, McAdam KPWJ, Thursz M, Whittle HC et al (1999) Tuberculosis and chronic hepatitis B virus infection in Africans and variation in the vitamin D receptor gene. J Infect Dis 179(3):721–724
doi: 10.1086/314614
pubmed: 9952386
Liu PT, Stenger S, Li H, Wenzel L, Tan BH, Krutzik SR et al (2006) Toll-like receptor triggering of a vitamin D-mediated human antimicrobial response. Science. 311(5768):1770–3
doi: 10.1126/science.1123933
pubmed: 16497887
Beutler B, Jiang Z, Georgel P, Crozat K, Croker B, Rutschmann S et al (2006) Genetic analysis of host resistance: Toll-like receptor signaling and immunity at large. Annu Rev Immunol. 24(1):353–89. https://doi.org/10.1146/annurev.immunol.24.021605.090552
doi: 10.1146/annurev.immunol.24.021605.090552
pubmed: 16551253
Yazdanpanah E, Mahmoudi M, Sahebari M, Rezaieyazdi Z, Esmaeili SA, Tabasi N et al (2017) Vitamin D3 Alters the Expression of Toll-like Receptors in Peripheral Blood Mononuclear Cells of Patients With Systemic Lupus Erythematosus. J Cell Biochem 118(12):4831–4835
doi: 10.1002/jcb.26155
pubmed: 28544067
Li B, Baylink DJ, Deb C, Zannetti C, Rajaallah F, Xing W et al (2013) 1,25-Dihydroxyvitamin D3 Suppresses TLR8 Expression and TLR8-Mediated Inflammatory Responses in Monocytes In Vitro and Experimental Autoimmune Encephalomyelitis In Vivo. Nataf S, editor. PLoS One 8(3):e58808. https://doi.org/10.1371/journal.pone.0058808
doi: 10.1371/journal.pone.0058808
pubmed: 23516559
pmcid: 3597563
Martinez Viedma M, Pickett B (2018) Characterizing the Different Effects of Zika Virus Infection in Placenta and Microglia Cells. Viruses. 10(11):649. Available from: http://www.mdpi.com/1999-4915/10/11/649
Campbell GR, Spector SA (2012) Toll-Like Receptor 8 Ligands Activate a Vitamin D Mediated Autophagic Response that Inhibits Human Immunodeficiency Virus Type 1. PLoS Pathog 8(11):e1003017
doi: 10.1371/journal.ppat.1003017
pubmed: 23166493
pmcid: 3499571
Gorden KB, Gorski KS, Gibson SJ, Kedl RM, Kieper WC, Qiu X, et al (2005) Synthetic TLR Agonists Reveal Functional Differences between Human TLR7 and TLR8. J Immunol. 174(3):1259–68. Available from: https://journals.aai.org/jimmunol/article/174/3/1259/72450/Synthetic-TLR-Agonists-Reveal-Functional
Bleakley AS, Licciardi P V, Binks MJ (2021) Vitamin D Modulation of the Innate Immune Response to Paediatric Respiratory Pathogens Associated with Acute Lower Respiratory Infections. Nutrients. 13(1):276. Available from: https://www.mdpi.com/2072-6643/13/1/276
Castillo JA, Urcuqui-Inchima S (2023) Vitamin D modulates inflammatory response of DENV-2-infected macrophages by inhibiting the expression of inflammatory-liked miRNAs. Pathog Glob Health. 117(2):167–80. https://doi.org/10.1080/20477724.2022.2101840
doi: 10.1080/20477724.2022.2101840
pubmed: 35850625
Torres M, Casado G, Vigón L, Rodríguez-Mora S, Mateos E, Ramos-Martín F, et al (2022) Changes in the immune response against SARS-CoV-2 in individuals with severe COVID-19 treated with high dose of vitamin D. Biomed Pharmacother. 150:112965. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0753332222003547
Khare D, Godbole NM, Pawar SD, Mohan V, Pandey G, Gupta S et al (2013) Calcitriol [1, 25[OH]2 D3] pre- and post-treatment suppresses inflammatory response to influenza A (H1N1) infection in human lung A549 epithelial cells. Eur J Nutr 52(4):1405–1415
doi: 10.1007/s00394-012-0449-7
pubmed: 23015061
Mackowiak PA (1998) Concepts of Fever. Arch Intern Med. 158(17):1870. Available from: www.ama-assn.org/internal .
Anderson J, Do LAH, Toh ZQ, Hoe E, Reitsma A, Mulholland K, et al (2020) Vitamin D Induces Differential Effects on Inflammatory Responses During Bacterial and/or Viral Stimulation of Human Peripheral Blood Mononuclear Cells. Front Immunol. 11. https://doi.org/10.3389/fimmu.2020.00602/full
Mehta V, Verma R, Garg R, Malhotra H, Sharma P, Jain A (2017) Study of interleukin-6 and interleukin-8 levels in patients with neurological manifestations of dengue. J Postgrad Med. 63(1):11. Available from: http://www.jpgmonline.com/text.asp?2017/63/1/11/188545
Antonelli LR, Gollob KJ, Costa PAC, Duarte MM, Caldas S, de Iani FC, M, et al (2016) Dengue Patients with Early Hemorrhagic Manifestations Lose Coordinate Expression of the Anti-Inflammatory Cytokine IL-10 with the Inflammatory Cytokines IL-6 and IL-8. Am J Trop Med Hyg. 95(1):193–200. https://doi.org/10.4269/ajtmh.15-0537
doi: 10.4269/ajtmh.15-0537
pubmed: 27139443
pmcid: 4944688
Gui B, Chen Q, Hu C, Zhu C, He G (2017) Effects of calcitriol (1, 25-dihydroxy-vitamin D3) on the inflammatory response induced by H9N2 influenza virus infection in human lung A549 epithelial cells and in mice. Virol J. 14(1):10. https://doi.org/10.1186/s12985-017-0683-y
doi: 10.1186/s12985-017-0683-y
pubmed: 28114957
pmcid: 5259864
Nascimento-Carvalho GC, Nascimento-Carvalho EC, Ramos CL, Vilas-Boas A-L, Moreno-Carvalho OA, Vinhaes CL, et al (2021) Zika-exposed microcephalic neonates exhibit higher degree of inflammatory imbalance in cerebrospinal fluid. Sci Rep. 11(1):8474. Available from: https://www.nature.com/articles/s41598-021-87895-4
Remick DG (2005) Interleukin-8. Crit Care Med. 33(Suppl):S466–7. Available from: http://journals.lww.com/00003246-200512001-00021
Haberstroh U, Pocock J, Gómez-Guerrero C, Helmchen U, Hamann A, Gutierrez-Ramos JC, et al (2002) Expression of the chemokines MCP-1/CCL2 and RANTES/CCL5 is differentially regulated by infiltrating inflammatory cells. Kidney Int. 62(4):1264–76. Available from: https://linkinghub.elsevier.com/retrieve/pii/S0085253815486685
Sánchez-Arcila JC, Badolato-Correa J, de Souza TMA, Paiva IA, Barbosa LS, Nunes PCG, et al (2020) Clinical, Virological, and Immunological Profiles of DENV, ZIKV, and/or CHIKV-Infected Brazilian Patients. Intervirology. 63(1–6):33–45. Available from: https://www.karger.com/Article/FullText/510223
Chen K, Bao Z, Tang P, Gong W, Yoshimura T, Wang JM (2018) Chemokines in homeostasis and diseases. Cell Mol Immunol. 15(4):324–34. Available from: http://www.nature.com/articles/cmi2017134
Barros JB de S, Silva PAN da, Koga R de CR, Gonzalez-Dias P, Carmo Filho JR, Nagib PRA, et al (2018) Acute Zika Virus Infection in an Endemic Area Shows Modest Proinflammatory Systemic Immunoactivation and Cytokine-Symptom Associations. Front Immunol. 9. https://doi.org/10.3389/fimmu.2018.00821/full
Tsai T-T, Chuang Y-J, Lin Y-S, Wan S-W, Chen C-L, Lin C-F (2013) An emerging role for the anti-inflammatory cytokine interleukin-10 in dengue virus infection. J Biomed Sci 20(1):40
doi: 10.1186/1423-0127-20-40
pubmed: 23800014
pmcid: 3700829
Rojas JM, Avia M, Martín V, Sevilla N (2017) IL-10: A Multifunctional Cytokine in Viral Infections. J Immunol Res. 2017:1–14. Available from: https://www.hindawi.com/journals/jir/2017/6104054/