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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2658-6533-2025-11-1-0-6</article-id><article-id pub-id-type="publisher-id">3685</article-id><article-categories><subj-group subj-group-type="heading"><subject>Pharmacology</subject></subj-group></article-categories><title-group><article-title>&lt;strong&gt;Bioactivity of Vitamin D and &lt;em&gt;Tinospora cordifolia&lt;/em&gt; Extract in Increasing Cathelicidin Synthesis and Regulating TNF Alpha Production in CD66a Cells &lt;/strong&gt;</article-title><trans-title-group xml:lang="en"><trans-title>&lt;strong&gt;Bioactivity of Vitamin D and &lt;em&gt;Tinospora cordifolia&lt;/em&gt; Extract in Increasing Cathelicidin Synthesis and Regulating TNF Alpha Production in CD66a Cells &lt;/strong&gt;</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Jamil</surname><given-names>Ahmad S.</given-names></name><name xml:lang="en"><surname>Jamil</surname><given-names>Ahmad S.</given-names></name></name-alternatives><email>shobrun@umm.ac.id</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Widyarti</surname><given-names>Sri</given-names></name><name xml:lang="en"><surname>Widyarti</surname><given-names>Sri</given-names></name></name-alternatives><email>swid@ub.ac.id</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Setiawan</surname><given-names>Meddy</given-names></name><name xml:lang="en"><surname>Setiawan</surname><given-names>Meddy</given-names></name></name-alternatives><email>meddy_umm@yahoo.com</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Rifa’i</surname><given-names>Muhaimin</given-names></name><name xml:lang="en"><surname>Rifa’i</surname><given-names>Muhaimin</given-names></name></name-alternatives><email>immunobiology@ub.ac.id</email></contrib></contrib-group><pub-date pub-type="epub"><year>2025</year></pub-date><volume>11</volume><issue>1</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2025/1/Биомед-112-120.pdf" /><abstract xml:lang="ru"><p>Background: Cathelicidin is an antimicrobial peptide that plays an important function in the innate immune system as the first line of defense against infections. There is still not a lot of information on the compounds that keep the body&amp;#39;s cathelicidin production going. The aim of the study: To observe the effect of vitamin D and Tinospora cordifolia Extract (TCE) for 28 days on the production of cathelicidin and (Tumor necrosis Factor) TNF alpha in CD66a cells shortly after the mice were infected with E. coli. Materials and methods: We conducted a study with five treatment groups using BALB/c mice. Normal Group (NG): standard diet without treatment, Infected Group (IG): standard diet and infected on day 29, Vitamin D Group (VDG): standard diet + Vitamin D 100 micrograms/kg body weight and infected on day 29, Tinospora cordifolia Group (TCG): standard diet + TCE 100 mg/kg body weight and infected on day 29, and Combination group (CG): standard diet+ Vitamin D 100 micrograms/kg body weight + TCE 100 mg/kg body weight and infected on day 29. On day 29, the spleen was isolated at the end of treatment, and the production of cathelicidin and TNF alpha in CD66a cells was evaluated using flow cytometry and analyzed using one-way ANOVA (p &amp;lt; 0.05). Results: Our findings show that vitamin D significantly increases cathelicidin synthesis, suggesting that it can potentially&amp;nbsp;improve innate immunity. While Vitamin D and TC combined increased cathelicidin production slightly, the effect was not statistically significant. Interestingly, neither vitamin D nor TC substantially affected&amp;nbsp;TNF alpha production. The combination of vitamin D and TC, on the other hand, resulted in a considerable drop in TNF alpha levels, indicating a synergistic anti-inflammatory action. Conclusion: These findings suggest&amp;nbsp;a possible avenue for exploiting vitamin D and TC&amp;#39;s combined effects in enhancing immunological responses, particularly in cathelicidin production</p></abstract><trans-abstract xml:lang="en"><p>Background: Cathelicidin is an antimicrobial peptide that plays an important function in the innate immune system as the first line of defense against infections. There is still not a lot of information on the compounds that keep the body&amp;#39;s cathelicidin production going. The aim of the study: To observe the effect of vitamin D and Tinospora cordifolia Extract (TCE) for 28 days on the production of cathelicidin and (Tumor necrosis Factor) TNF alpha in CD66a cells shortly after the mice were infected with E. coli. Materials and methods: We conducted a study with five treatment groups using BALB/c mice. Normal Group (NG): standard diet without treatment, Infected Group (IG): standard diet and infected on day 29, Vitamin D Group (VDG): standard diet + Vitamin D 100 micrograms/kg body weight and infected on day 29, Tinospora cordifolia Group (TCG): standard diet + TCE 100 mg/kg body weight and infected on day 29, and Combination group (CG): standard diet+ Vitamin D 100 micrograms/kg body weight + TCE 100 mg/kg body weight and infected on day 29. On day 29, the spleen was isolated at the end of treatment, and the production of cathelicidin and TNF alpha in CD66a cells was evaluated using flow cytometry and analyzed using one-way ANOVA (p &amp;lt; 0.05). Results: Our findings show that vitamin D significantly increases cathelicidin synthesis, suggesting that it can potentially&amp;nbsp;improve innate immunity. While Vitamin D and TC combined increased cathelicidin production slightly, the effect was not statistically significant. Interestingly, neither vitamin D nor TC substantially affected&amp;nbsp;TNF alpha production. The combination of vitamin D and TC, on the other hand, resulted in a considerable drop in TNF alpha levels, indicating a synergistic anti-inflammatory action. Conclusion: These findings suggest&amp;nbsp;a possible avenue for exploiting vitamin D and TC&amp;#39;s combined effects in enhancing immunological responses, particularly in cathelicidin production</p></trans-abstract><kwd-group xml:lang="ru"><kwd>Cathelicidin</kwd><kwd>CD66a</kwd><kwd>Tinospora</kwd><kwd>TNF alpha</kwd><kwd>vitamin D</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Cathelicidin</kwd><kwd>CD66a</kwd><kwd>Tinospora</kwd><kwd>TNF alpha</kwd><kwd>vitamin D</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Alford MA, Baquir B, Santana FL, et al. Cathelicidin Host Defense Peptides and Inflammatory Signaling: Striking a Balance. Frontiers in Microbiology. 2020;11:1-18. DOI: https://doi.org/10.3389/fmicb.2020.01902</mixed-citation></ref><ref id="B2"><mixed-citation>Mookherjee N, Brown KL, Hancock REW. Cathelicidins [Internet]. Second Edi. Handb. Biol. Act. Pept. Elsevier Inc.; 2013. Available from: http://dx.doi.org/10.1016/B978-0-12-385095-9.00015-4. DOI: https://doi.org/10.1016/B978-0-12-385095-9.00015-4</mixed-citation></ref><ref id="B3"><mixed-citation>van Harten RM, van Woudenbergh E, van Dijk A, Haagsman HP. Cathelicidins: Immunomodulatory antimicrobials. Vaccines. 2018;6(3):63. DOI: https://doi.org/10.3390/vaccines6030063</mixed-citation></ref><ref id="B4"><mixed-citation>Lee WJ, Cha HW, Sohn MY, et al. Vitamin D increases expression of cathelicidin in cultured sebocytes. Archives of Dermatological Research. 2012;304:627-632. DOI: https://doi.org/10.1007/s00403-012-1255-z</mixed-citation></ref><ref id="B5"><mixed-citation>Chung C, Silwal P, Kim I, et al. Vitamin D-cathelicidin axis: At the crossroads between protective immunity and pathological inflammation during infection. Immune Network. 2020;20:1-26. DOI: http://dx.doi.org/10.4110/in.2020.20.e12</mixed-citation></ref><ref id="B6"><mixed-citation>Grabulosa CC, Manfredi SR, Canziani ME, et al. Chronic kidney disease induces inflammation by increasing Toll-like receptor-4, cytokine and cathelicidin expression in neutrophils and monocytes. Experimental Cell Research. 2018;365(2):157-162. DOI: https://doi.org/10.1016/j.yexcr.2018.02.022</mixed-citation></ref><ref id="B7"><mixed-citation>Reddi KK, Tetali SD. Dry leaf extracts of Tinospora cordifolia (Willd.) Miers attenuate oxidative stress and inflammatory condition in human monocytic (THP-1) cells. Phytomedicine. 2019;61:152831. DOI: https://doi.org/10.1016/j.phymed.2019.152831</mixed-citation></ref><ref id="B8"><mixed-citation>Widodo WT, Widyarti S, Sumitro SB, et al. In silico study of Tyramine-Fe complex in Brotowali (Tinospora crispa) as anti-inflammatory. In: Proceedings of the 11th Annual International Conference on Industrial Engineering and Operations Management Singapore, March 7-11, 2021:3473-3480.</mixed-citation></ref><ref id="B9"><mixed-citation>Jacob J, Babu BM, Mohan MC, et al. Inhibition of proinflammatory pathways by bioactive fraction of Tinospora cordifolia. Inflammopharmacology. 2018;26:531-538. DOI: https://doi.org/10.1007/s10787-017-0319-2</mixed-citation></ref><ref id="B10"><mixed-citation>Philip S, Tom G, Balakrishnan Nair P, et al. Tinospora cordifolia chloroform extract inhibits LPS-induced inflammation via NF-&amp;kappa;B inactivation in THP-1cells and improves survival in sepsis. BMC Complementary Medicine and Therapies. 2021;21:97. DOI: https://doi.org/10.1186/s12906-021-03244-y</mixed-citation></ref><ref id="B11"><mixed-citation>Ismail MM, Zaghloul A, Abdulateef N, et al. Membranous Expression of pan CD66, CD66a, CD66b, and CD66c and their Clinical Impact in Acute Leukemia: Cross Sectional Longitudinal Cohort Study in Saudi Arabia. Journal of Leukemia. 2017;5:1-9. DOI: http://dx.doi.org/10.4172/2329-6917.1000230</mixed-citation></ref><ref id="B12"><mixed-citation>Zhang Y, Wang Y, Wu W, et al. Elevation of neutrophil carcinoembryonic antigen-related cell adhesion molecule 1 associated with multiple inflammatory mediators was related to different clinical stages in ischemic stroke patients. Journal of Clinical Laboratory Analysis. 2022;36(7):e24526. DOI: https://doi.org/10.1002/jcla.24526</mixed-citation></ref><ref id="B13"><mixed-citation>Thirion G, Feliu AA, Coutelier JP. CD 66 a ( CEACAM 1 ) expression by mouse natural killer cells. Immunology. 2008;125:535-540. DOI: https://doi.org/10.1111/j.1365-2567.2008.02867.x</mixed-citation></ref><ref id="B14"><mixed-citation>Koivisto O, Hanel A, Carlberg C. Key vitamin D target genes with functions in the immune system. Nutrients. 2020;12(4):1140. DOI: https://doi.org/10.3390/nu12041140</mixed-citation></ref><ref id="B15"><mixed-citation>Gombart AF, Borregaard N, Koeffler HP. Human cathelicidin antimicrobial peptide (CAMP) gene is a direct target of the vitamin D receptor and is strongly up‐regulated in myeloid cells by 1,25‐dihydroxyvitamin D 3. FASEB Journal. 2005;19(9):1067-1077. DOI: https://doi.org/10.1096/fj.04-3284com</mixed-citation></ref><ref id="B16"><mixed-citation>Al-Jaberi FAH, Crone CG, Lindenstr&amp;oslash;m T, et al. Reduced vitamin D-induced cathelicidin production and killing of Mycobacterium tuberculosis in macrophages from a patient with a non-functional vitamin D receptor: A case report. Frontiers in Immunology. 2022;13:1038960. DOI: https://doi.org/10.3389/fimmu.2022.1038960</mixed-citation></ref><ref id="B17"><mixed-citation>Schr&amp;ouml;der-Heurich B, Springer CJP, von Versen-H&amp;ouml;ynck F. Vitamin d effects on the immune system from periconception through pregnancy. Nutrients. 2020;12(5):1432. DOI: https://doi.org/10.3390/nu12051432</mixed-citation></ref><ref id="B18"><mixed-citation>Svensson D, Nebel D, Nilsson BO. Vitamin D3 modulates the innate immune response through regulation of the hCAP-18/LL-37 gene expression and cytokine production. Inflammation Research. 2016;65:25-32. DOI: https://doi.org/10.1007/s00011-015-0884-z</mixed-citation></ref><ref id="B19"><mixed-citation>M&amp;eacute;ndez-Samperio P, Miranda E, Trejo A. Expression and secretion of cathelicidin LL-37 in human epithelial cells after infection by Mycobacterium bovis bacillus Calmette-Gu&amp;eacute;rin. Clinical and Vaccine Immunology. 2008;15(9):1450-1455. DOI: https://doi.org/10.1128/CVI.00178-08</mixed-citation></ref><ref id="B20"><mixed-citation>Li G, Domenico J, Jia Y, et al. NF-&amp;kappa;B-dependent induction of cathelicidin-related antimicrobial peptide in murine mast cells by lipopolysaccharide. International Archives of Allergy and Immunology. 2009;150(2):122-132. DOI:&amp;nbsp; https://doi.org/10.1159/000218115</mixed-citation></ref><ref id="B21"><mixed-citation>Park K, Elias PM, Oda Y, et al. Regulation of cathelicidin antimicrobial peptide expression by an Endoplasmic Reticulum (ER) stress signaling, vitamin D receptor-independent pathway. Journal of Biological Chemistry. 2011;286(39):34121-34130. DOI: https://doi.org/10.1074/jbc.m111.250431</mixed-citation></ref><ref id="B22"><mixed-citation>Gupta PK, Chakraborty P, Kumar S, et al. G1-4A, a Polysaccharide from Tinospora cordifolia Inhibits the Survival of Mycobacterium tuberculosis by Modulating Host Immune Responses in TLR4 Dependent Manner. PLoS ONE. 2016;11(5):e0154725. DOI: https://doi.org/10.1371/journal.pone.0154725</mixed-citation></ref><ref id="B23"><mixed-citation>Alsuhaibani S, Khan MA. Immune-stimulatory and therapeutic activity of tinospora cordifolia: Double-edged sword against salmonellosis. Journal of Immunology Research. 2017;2017:1787803. DOI: https://doi.org/10.1155/2017/1787803</mixed-citation></ref><ref id="B24"><mixed-citation>Malve H, More D, More A. Effects of two formulations containing Phyllanthus emblica and Tinospora cordifolia with and without Ocimum sanctum in immunocompromised mice. Journal of Ayurveda and Integrative Medicine. 2021;12(4):682-688. DOI: https://doi.org/10.1016/j.jaim.2021.06.021</mixed-citation></ref><ref id="B25"><mixed-citation>G&amp;ouml;nen MS, Alaylıoğlu M, Durcan E, et al. Rapid and effective vitamin d supplementation may present better clinical outcomes in covid-19 (Sars-cov-2) patients by altering serum inos1, il1b, ifng, cathelicidin-ll37, and icam1. Nutrients. 2021;13(11):4047. DOI: https://doi.org/10.3390/nu13114047</mixed-citation></ref><ref id="B26"><mixed-citation>Yates CR, Bruno EJ, Yates MED. Tinospora Cordifolia: A review of its immunomodulatory properties. Journal of Dietary Supplements. 2022;19(2):271-285. DOI: https://doi.org/10.1080/19390211.2021.1873214</mixed-citation></ref><ref id="B27"><mixed-citation>Ghatpande NS, Misar A V, Waghole RJ, et al. Tinospora cordifolia protects against inflammation associated anemia by modulating inflammatory cytokines and hepcidin expression in male Wistar rats. Scientific Reports. 2019;9:10969. DOI: https://doi.org/10.1038/s41598-019-47458-0</mixed-citation></ref><ref id="B28"><mixed-citation>Sannegowda K, Venkatesha S, Moudgil K. Tinospora cordifolia inhibits autoimmune arthritis by regulating key immune mediators of inflammation and bone damage. International Journal of Immunopathology and Pharmacology. 2015;28(4):521-531. DOI: https://doi.org/10.1177/0394632015608248</mixed-citation></ref><ref id="B29"><mixed-citation>Singer BB, Klaile E, Scheffrahn I, et al. CEACAM1 (CD66a) mediates delay of spontaneous and Fas ligand-induced apoptosis in granulocytes. European Journal of Immunology. 2005;35(6):1949-1959. DOI: https://doi.org/10.1002/eji.200425691</mixed-citation></ref><ref id="B30"><mixed-citation>Holani R, Babbar A, Blyth GAD, et al. Cathelicidin-mediated lipopolysaccharide signaling via intracellular TLR4 in colonic epithelial cells evokes CXCL8 production. Gut Microbes. 2020;12(1):1785802. DOI: https://doi.org/10.1080/19490976.2020.1785802</mixed-citation></ref><ref id="B31"><mixed-citation>Febriza A, Natzir R, Hatta M, et al. Curcumin effects in inducing mRNA gene cathelidicin antimicrobial peptidein Balb/c mice infected with Salmonella typhi. Journal of Biological Research. 2020;93:76-80. DOI: https://doi.org/10.4081/jbr.2020.8942</mixed-citation></ref><ref id="B32"><mixed-citation>Zhao L, Tan S, Zhang H, et al. Astragalus polysaccharides exerts anti-infective activity by inducing human cathelicidin antimicrobial peptide LL-37 in respiratory epithelial cells. Phytotherapy Research. 2018;32(8):1521-1529. DOI: https://doi.org/10.1002/ptr.6080</mixed-citation></ref><ref id="B33"><mixed-citation>Guo BJ, Bian ZX, Qiu HC, et al. Biological and clinical implications of herbal medicine and natural products for the treatment of inflammatory bowel disease. Annals of the New York Academy of Sciences. 2017;1401(1):37-48. DOI: https://doi.org/10.1111/nyas.13414</mixed-citation></ref></ref-list></back></article>