Innate immunity to mycobacteria: vitamin D and autophagy

AKT/PKB signaling: navigating downstream

Manning, B. D., & Cantley, L. C. (2007) · Cell · doi:10.1016/j.cell.2007.06.009 · Cited by 6,115 · see citing works

Toll-Like Receptor Triggering of a Vitamin D-Mediated Human Antimicrobial Response

Liu, P. T., Stenger, S., Li, H., Wenzel, L., Tan, B. H., Krutzik, S. R., Ochoa, M. T., Schauber, J., Wu, K., Meinken, C., et al. (2006) · Science · doi:10.1126/science.1123933 · Cited by 3,924 · see citing works

Autophagy Is a Defense Mechanism Inhibiting BCG and Mycobacterium tuberculosis Survival in Infected Macrophages

Gutierrez, M. G., Master, S. S., Singh, S. B., Taylor, G. A., Colombo, M. I., & Deretic, V. (2004) · Cell · doi:10.1016/j.cell.2004.11.038 · Cited by 2,252 · see citing works

Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1β production

Saitoh, T., Fujita, N., Jang, M. H., Uematsu, S., Yang, B., Satoh, T., Omori, H., Noda, T., Yamamoto, N., Komatsu, M., et al. (2008) · Nature · doi:10.1038/nature07383 · Cited by 2,020 · see citing works

Vitamin effects on the immune system: Vitamins A and D take centre stage

Mora, J. R., Iwata, M., & von Andrian, U. H. (2008) · Nature Reviews Immunology · doi:10.1038/nri2378 · Cited by 1,559 · see citing works

Toll-like receptor signalling in macrophages links the autophagy pathway to phagocytosis

Sanjuan, M. A., Dillon, C. P., Tait, S. W. G., Moshiach, S., Dorsey, F., Connell, S., Komatsu, M., Tanaka, K., Cleveland, J. L., Withoff, S., et al. (2007) · Nature · doi:10.1038/nature06421 · Cited by 1,347 · see citing works

Nod1 and Nod2 direct autophagy by recruiting ATG16L1 to the plasma membrane at the site of bacterial entry

Travassos, L. H., Carneiro, L. A. M., Ramjeet, M., Hussey, S., Kim, Y.-G., Magalhães, J. G., Yuan, L., Soares, F., Chea, E., Le Bourhis, L., et al. (2010) · Nature Immunology · doi:10.1038/ni.1823 · Cited by 1,306 · see citing works

A Role for Ubiquitin in Selective Autophagy

Kirkin, V., McEwan, D. G., Novak, I., & Đikić, I. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.04.026 · Cited by 1,227 · see citing works

Control of Macroautophagy by Calcium, Calmodulin-Dependent Kinase Kinase-β, and Bcl-2

Høyer-Hansen, M., Bastholm, L., Szyniarowski, P., Campanella, M., Szabadkai, G., Farkas, T., Bianchi, K., Fehrenbacher, N., Elling, F., Rizzuto, R., et al. (2007) · Molecular Cell · doi:10.1016/j.molcel.2006.12.009 · Cited by 1,072 · see citing works

LL-37, the only human member of the cathelicidin family of antimicrobial peptides

Dürr, U. H. N., Sudheendra, U. S., & Ramamoorthy, A. (2006) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2006.03.030 · Cited by 1,049 · see citing works

Cathelicidins, multifunctional peptides of the innate immunity

Zanetti, M. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.0403147 · Cited by 988 · see citing works

Human IRGM Induces Autophagy to Eliminate Intracellular Mycobacteria

Singh, S. B., Davis, A. S., Taylor, G. A., & Deretic, V. (2006) · Science · doi:10.1126/science.1129577 · Cited by 915 · see citing works

Ubiquitin and ubiquitin-like proteins as multifunctional signals

Welchman, R., Gordon, C., & Mayer, R. (2005) · Nature reviews. Molecular cell biology · doi:10.1038/nrm1700 · Cited by 881 · see citing works

Toll-like Receptor 4 Is a Sensor for Autophagy Associated with Innate Immunity

Xu, Y., Jagannath, C., Liu, X.-D., Sharafkhaneh, A., Kolodziejska, K. E., & Eissa, N. T. (2007) · Immunity · doi:10.1016/j.immuni.2007.05.022 · Cited by 880 · see citing works

Vitamin D3 Induces Autophagy in Human Monocytes/Macrophages via Cathelicidin

Yuk, J., Shin, D., Lee, H., Yang, C., Jin, H. S., Kim, K., Lee, Z., Lee, S.-H., Kim, J., & Jo, E. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.08.004 · Cited by 787 · see citing works

Vitamin D: its role and uses in immunology 1

DeLuca, H. F., & Cantorna, M. T. (2001) · The FASEB Journal · doi:10.1096/fj.01-0433rev · Cited by 784 · see citing works

Cutting Edge: Vitamin D-Mediated Human Antimicrobial Activity against Mycobacterium tuberculosis Is Dependent on the Induction of Cathelicidin

Liu, P. T., Stenger, S., Tang, D. H., & Modlin, R. L. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.4.2060 · Cited by 773 · see citing works

Toll‐like receptors control autophagy

Delgado, M. A., Elmaoued, R. A., Davis, A. S., Kyei, G., & Deretic, V. (2008) · The EMBO Journal · doi:10.1038/emboj.2008.31 · Cited by 744 · see citing works

Cathelicidins: a novel protein family with a common proregion and a variable C‐terminal antimicrobial domain

Zanetti, M., Gennaro, R., & Romeo, D. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)01050-o · Cited by 708 · see citing works

The Adaptor Protein p62/SQSTM1 Targets Invading Bacteria to the Autophagy Pathway

Zheng, Y. T., Shahnazari, S., Brech, A., Lamark, T., Johansen, T., & Brumell, J. H. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0900441 · Cited by 581 · see citing works

Activation of antibacterial autophagy by NADPH oxidases

Huang, J., Canadien, V., Lam, G. Y., Steinberg, B. E., Dinauer, M. C., Magalhaes, M. A. O., Glogauer, M., Grinstein, S., & Brumell, J. H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811045106 · Cited by 556 · see citing works

Mechanism of phagolysosome biogenesis block by viable Mycobacterium tuberculosis

Vergne, I., Chua, J., Lee, H.-H., Lucas, M., Belisle, J. T., & Deretic, V. P. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409716102 · Cited by 537 · see citing works

Vitamin D3, gamma interferon, and control of proliferation of Mycobacterium tuberculosis by human monocytes.

Rook, G. A. W., Steele, J. K., Fraher, L. J., Barker, S. C., Karmali, R., O'Riordan, J. L. H., & Stanford, J. L. (1986) · PubMed Central · Cited by 529 · see citing works

Host Innate Immune Receptors and Beyond: Making Sense of Microbial Infections

Ishii, K. J., Koyama, S., Nakagawa, A., Coban, C., & Akira, S. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.05.003 · Cited by 501 · see citing works

T helper 2 cytokines inhibit autophagic control of intracellular Mycobacterium tuberculosis.

Harris, J., Haro, S. A. D., Master, S. S., Keane, J., Roberts, E. A., Delgado, M. A., & Deretic, V. (2007) · Immunity · doi:10.1016/j.immuni.2007.07.022 · Cited by 497 · see citing works

Autophagy enhances the efficacy of BCG vaccine by increasing peptide presentation in mouse dendritic cells

Jagannath, C., Lindsey, D. R., Dhandayuthapani, S., Xu, Y., Hunter, R. L., & Eissa, N. T. (2009) · Nature Medicine · doi:10.1038/nm.1928 · Cited by 486 · see citing works

NF-κB Activation Represses Tumor Necrosis Factor-α-induced Autophagy

Djavaheri‐Mergny, M., Amelotti, M., Mathieu, J., Besançon, F., Bauvy, C., Souquère, S., Pierron, G., & Codogno, P. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m602097200 · Cited by 467 · see citing works

NBR1 and p62 as cargo receptors for selective autophagy of ubiquitinated targets

Lamark, T., Kirkin, V., Dikic, I., & Johansen, T. (2009) · Cell Cycle · doi:10.4161/cc.8.13.8892 · Cited by 464 · see citing works

Mycobacterium tuberculosis Prevents Inflammasome Activation

Master, S. S., Rampini, S. K., Davis, A. S., Keller, C., Ehlers, S., Springer, B., Timmins, G. S., Sander, P., & Deretic, V. P. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.03.003 · Cited by 421 · see citing works

IFN-γ- and TNF-Independent Vitamin D-Inducible Human Suppression of Mycobacteria: The Role of Cathelicidin LL-37

Martineau, A. R., Wilkinson, K. A., Newton, S. M., Floto, R. A., Norman, A. W., Skolimowska, K., Davidson, R. N., Sørensen, O. E., Kampmann, B., Griffiths, C. J., et al. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.11.7190 · Cited by 410 · see citing works

Vitamin D as Supplementary Treatment for Tuberculosis

Wejse, C. M., Gomes, V. F., Rabna, P., Gustafson, P., Aaby, P., Lisse, I. M., Andersen, P. L., Glerup, H., & Sodemann, M. (2009) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200804-567oc · Cited by 396 · see citing works

MyD88 and Trif Target Beclin 1 to Trigger Autophagy in Macrophages

Shi, C.-S., & Kehrl, J. H. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m804478200 · Cited by 395 · see citing works

Neutrophil-mediated innate immune resistance to mycobacteria

Martineau, A. R., Newton, S. M., Wilkinson, K. A., Kampmann, B., Hall, B. M., Nawroly, N., Packe, G. E., Davidson, R. N., Griffiths, C. J., & Wilkinson, R. J. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31097 · Cited by 394 · see citing works

The role of TOR in autophagy regulation from yeast to plants and mammals

Díaz‐Troya, S., Pérez‐Pérez, M. E., Florencio, F. J., & Crespo, J. L. (2008) · Autophagy · doi:10.4161/auto.6555 · Cited by 394 · see citing works

Genome-wide Analysis of the Host Intracellular Network that Regulates Survival of Mycobacterium tuberculosis

Kumar, D., Nath, L., Kamal, M. A., Varshney, A., Jain, A., Singh, S., & Rao, K. V. S. (2010) · Cell · doi:10.1016/j.cell.2010.02.012 · Cited by 345 · see citing works

The vitamin D hormone and its nuclear receptor: molecular actions and disease states

Haussler, M. R., Haussler, C. A., Jurutka, P. W., Thompson, P. D., Hsieh, J., Remus, L. S., Selznick, S. H., & Whitfield, G. K. (1997) · Journal of Endocrinology · doi:10.1677/joe.0.154s057 · Cited by 333 · see citing works

Intracellular signalling cascades regulating innate immune responses to Mycobacteria: branching out from Toll-like receptors

Jo, E., Yang, C., Choi, C. H., & Harding, C. V. (2007) · Cellular Microbiology · doi:10.1111/j.1462-5822.2007.00914.x · Cited by 331 · see citing works

Shigella Phagocytic Vacuolar Membrane Remnants Participate in the Cellular Response to Pathogen Invasion and Are Regulated by Autophagy

Dupont, N., Lacas‐Gervais, S., Bertout, J., Paz, I., Frêche, B., Nhieu, G. T. V., van der Goot, F. G., Sansonetti, P. J., & Lafont, F. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.07.005 · Cited by 322 · see citing works

Lysosomal killing of <i>Mycobacterium</i> mediated by ubiquitin-derived peptides is enhanced by autophagy

Alonso, S., Pethe, K., Russell, D. G., & Purdy, G. E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700036104 · Cited by 318 · see citing works

Delivery of Cytosolic Components by Autophagic Adaptor Protein p62 Endows Autophagosomes with Unique Antimicrobial Properties

Ponpuak, M., Davis, A. S., Roberts, E. A., Delgado, M. A., Dinkins, C., Zhao, Z., Virgin, H. W., Kyei, G. B., Johansen, T., Vergne, I., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.02.009 · Cited by 308 · see citing works

Mycobacterium tuberculosis inhibition of phagolysosome biogenesis and autophagy as a host defence mechanism

Deretic, V. P., Singh, S., Master, S. S., Harris, J., Roberts, E. A., Kyei, G. B., Davis, A., Haro, S. A. D., Naylor, J., Lee, H.-H., et al. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00705.x · Cited by 306 · see citing works

Convergence of IL-1β and VDR Activation Pathways in Human TLR2/1-Induced Antimicrobial Responses

Liu, P. T., Schenk, M., Walker, V. P., Dempsey, P. W., Kanchanapoomi, M., Wheelwright, M., Vazirnia, A., Zhang, X., Steinmeyer, A., Zügel, U., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005810 · Cited by 298 · see citing works

Activation of Toll-Like Receptor 2 on Human Tracheobronchial Epithelial Cells Induces the Antimicrobial Peptide Human β Defensin-2

Hertz, C. J., Wu, Q., Porter, E. M., Zhang, Y. J., Weismüller, K., Godowski, P. J., Ganz, T., Randell, S. H., & Modlin, R. L. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.12.6820 · Cited by 285 · see citing works

Macrophage-derived IL-1β stimulates Wnt signaling and growth of colon cancer cells: a crosstalk interrupted by vitamin D3

Kaler, P., Augenlicht, L. H., & Klampfer, L. (2009) · Oncogene · doi:10.1038/onc.2009.247 · Cited by 272 · see citing works

Vitamin D analog EB1089 triggers dramatic lysosomal changes and Beclin 1-mediated autophagic cell death

Høyer-Hansen, M. H., Bastholm, L., Mathiasen, I. S., Elling, F., & Jäättelä, M. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401651 · Cited by 252 · see citing works

Expression of Cathelicidin LL-37 duringMycobacterium tuberculosisInfection in Human Alveolar Macrophages, Monocytes, Neutrophils, and Epithelial Cells

Rivas-Santiago, B. T., Hernández‐Pando, R., Carranza, C., Juárez, E., Contreras, J. L., Aguilar‐León, D., Torres, M., & Sada, E. (2007) · Infection and Immunity · doi:10.1128/iai.01218-07 · Cited by 250 · see citing works

Autophagy in Innate and Adaptive Immunity

Xu, Y., & Eissa, N. T. (2010) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200909-103js · Cited by 242 · see citing works

1α,25-Dihydroxyvitamin D3-induced Monocyte Antimycobacterial Activity Is Regulated by Phosphatidylinositol 3-Kinase and Mediated by the NADPH-dependent Phagocyte Oxidase

Sly, L. M., Lopez, M., Nauseef, W. M., & Reiner, N. E. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102876200 · Cited by 238 · see citing works

Genomic mechanisms involved in the pleiotropic actions of 1,25-dihydroxyvitamin D3

Christakos, S., Raval-Pandya, M., Wernyj, R. P., & Yang, W. (1996) · Biochemical Journal · doi:10.1042/bj3160361 · Cited by 231 · see citing works

Autophagy Gene Variant IRGM −261T Contributes to Protection from Tuberculosis Caused by Mycobacterium tuberculosis but Not by M. africanum Strains

Intemann, C. D., Thye, T., Niemann, S., Browne, E. N. L., Chinbuah, M. A., Enimil, A. K., Gyapong, J. O., Osei, I., Owusu‐Dabo, E., Helm, S., et al. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000577 · Cited by 226 · see citing works

IL-15 Links TLR2/1-Induced Macrophage Differentiation to the Vitamin D-Dependent Antimicrobial Pathway

Krutzik, S. R., Hewison, M., Liu, P. T., Robles, J. A., Stenger, S., Adams, J. S., & Modlin, R. L. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.10.7115 · Cited by 226 · see citing works

The role of gamma-interferon, vitamin D3 metabolites and tumour necrosis factor in the pathogenesis of tuberculosis.

Rook, G. A. W., Taverne, J., Leveton, C., & Steele, J. K. (1987) · PubMed Central · Cited by 213 · see citing works

Divergence of Macrophage Phagocytic and Antimicrobial Programs in Leprosy

Montoya, D. J., Cruz, D., Teles, R. M. B., Lee, D. J., Ochoa, M. T., Krutzik, S. R., Chun, R. F., Schenk, M., Zhang, X., Ferguson, B. G., et al. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.09.002 · Cited by 197 · see citing works

1α,25-Dihydroxyvitamin D3–Induced Myeloid Cell Differentiation Is Regulated by a Vitamin D Receptor–Phosphatidylinositol 3-Kinase Signaling Complex

Hmama, Z., Nandan, D., Sly, L. M., Knutson, K. L., Herrera-Velit, P., & Reiner, N. E. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.190.11.1583 · Cited by 176 · see citing works

NADPH Oxidase 2 Interaction with TLR2 Is Required for Efficient Innate Immune Responses to Mycobacteria via Cathelicidin Expression

Yang, C., Shin, D., Kim, K.-H., Lee, Z.-W., Lee, C., Park, S. G., Bae, Y. S., & Jo, E. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802217 · Cited by 173 · see citing works

ATP-induced autophagy is associated with rapid killing of intracellular mycobacteria within human monocytes/macrophages

Biswas, D., Qureshi, O. S., Lee, W.-Y. J., Croudace, J. E., Mura, M., & Lammas, D. A. (2008) · BMC Immunology · doi:10.1186/1471-2172-9-35 · Cited by 156 · see citing works

1α,25‐dihydroxyvitamin D3 inhibits matrix metalloproteinases induced by Mycobacterium tuberculosis infection

Coussens, A. K., Timms, P. M., Boucher, B. J., Venton, T. R., Ashcroft, A., Skolimowska, K. H., Newton, S. M., Wilkinson, K. A., Davidson, R. N., Griffiths, C., et al. (2008) · Immunology · doi:10.1111/j.1365-2567.2008.03024.x · Cited by 152 · see citing works

The Mycobacterial 38-Kilodalton Glycolipoprotein Antigen Activates the Mitogen-Activated Protein Kinase Pathway and Release of Proinflammatory Cytokines through Toll-Like Receptors 2 and 4 in Human Monocytes

Jung, S.-B., Yang, C., Lee, J., Shin, A.-R., Jung, S. S., Son, J. W., Harding, C. V., Kim, H., Park, J., Paik, T.-H., et al. (2006) · Infection and Immunity · doi:10.1128/iai.74.5.2686-2696.2006 · Cited by 150 · see citing works

Toll-like receptor signaling in the lysosomal pathways

Sanjuan, M. A., Milasta, S., & Green, D. R. (2009) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00732.x · Cited by 137 · see citing works

Structure and Biology of Cathelicidins

Zanetti, M., Gennaro, R., Scocchi, M., & Skerlavaj, B. (2002) · Advances in experimental medicine and biology · doi:10.1007/0-306-46831-x_17 · Cited by 132 · see citing works

Vitamin D3 Induces Autophagy of Human Myeloid Leukemia Cells

Wang, J., Lian, H., Zhao, Y. L., Kauss, M. A., & Spindel, S. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801716200 · Cited by 124 · see citing works

Autophagy and antigen presentation

Münz, C. (2006) · Cellular Microbiology · doi:10.1111/j.1462-5822.2006.00714.x · Cited by 90 · see citing works

Autophagy in innate and adaptive immunity.

Deretic, V. (2005) · Trends in immunology · doi:10.1016/j.it.2005.08.003 · Cited by 89 · see citing works

Viral evasion of autophagy

Orvedahl, A., & Levine, B. (2008) · Autophagy · doi:10.4161/auto.5289 · Cited by 87 · see citing works

Potentiation of radiation sensitivity in breast tumor cells by the vitamin D3 analogue, EB 1089, through promotion of autophagy and interference with proliferative recovery

DeMasters, G. A., Di, X. M., Newsham, I., Shiu, R. P. C., & Gewirtz, D. A. (2006) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-06-0316 · Cited by 83 · see citing works

High IL-13 production by human neonatal T cells: neonate immune system regulator?

Ribeiro-do-Couto, L. M., Boeije, L. C. M., Kroon, J., Hooibrink, B., Breur-Vriesendorp, B. S., Aarden, L. A., & Boog, C. J. P. (2001) · European Journal of Immunology · doi:10.1002/1521-4141(200111)31:11 · Cited by 80 · see citing works

Effect of 1, 25 dihydroxyvitamin D3 on matrix metalloproteinases MMP-7, MMP-9 and the inhibitor TIMP-1 in pulmonary tuberculosis

Anand, S. P., & Selvaraj, P. (2009) · Clinical Immunology · doi:10.1016/j.clim.2009.06.009 · Cited by 77 · see citing works

Autophagy, an Immunologic Magic bullet: Mycobacterium Tuberculosis Phagosome Maturation Block and how to Bypass it

Deretic, V. P. (2008) · Future Microbiology · doi:10.2217/17460913.3.5.517 · Cited by 72 · see citing works

1,25-Dihydroxyvitamin D3 Stimulates Expression and Translocation of Protein Kinase Cα and Cδ via a Nongenomic Mechanism and Rapidly Induces Phosphorylation of a 33-kDa Protein in Acute Promyelocytic NB4 Cells

Berry, D. M., Antochi, R. M., Bhatia, M., et al. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.27.16090 · Cited by 69 · see citing works

Depressed Interleukin-12 (IL-12), but not IL-18, Production in Response to a 30- or 32-Kilodalton Mycobacterial Antigen in Patients with Active Pulmonary Tuberculosis

Song, C., Kim, H., Park, J., et al. (2000) · Infection and Immunity · doi:10.1128/iai.68.8.4477-4484.2000 · Cited by 69 · see citing works

Xenophagy in herpes simplex virus replication and pathogenesis

Alexander, D., & Leib, D. A. (2008) · Autophagy · doi:10.4161/auto.5222 · Cited by 57 · see citing works

Down-Regulation by Nuclear Factor κB of Human 25-Hydroxyvitamin D3 1α-Hydroxylase Promoter

Ebert, R., Jovanovic, M., Ulmer, M., Schneider, D., Meißner-Weigl, J., Adamski, J., & Jakob, F. J. (2004) · Molecular Endocrinology · doi:10.1210/me.2002-0441 · Cited by 50 · see citing works

Vitamin D resistance

Malloy, P. J., & Feldman, D. I. (1999) · The American Journal of Medicine · doi:10.1016/s0002-9343(98)00419-7 · Cited by 47 · see citing works

Nongenomic signaling by vitamin D

Gniadecki, R. (1998) · Biochemical Pharmacology · doi:10.1016/s0006-2952(98)00182-8 · Cited by 46 · see citing works

A Vitamin for Autophagy

Fabri, M., & Modlin, R. L. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.08.008 · Cited by 31 · see citing works

Differential cytokine levels and immunoreactivities against Mycobacterium tuberculosis antigens between tuberculous and malignant effusions

Yang, C., Lee, J., Lee, H., et al. (2008) · Respiratory Medicine · doi:10.1016/j.rmed.2007.08.016 · Cited by 31 · see citing works

Effect of Vitamin D on Tuberculosis and HIV Replication Depends on Conversion to Calcitriol and Concentration

Eisenhut, M. (2009) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.180.8.795 · Cited by 5 · see citing works

Macrophage defense mechanisms against intracellular bacteria

Weiss, G., & Schaible, U. E. (2015) · Immunological Reviews · doi:10.1111/imr.12266 · Cited by 989 · see citing works

The role of vitamin D in regulating the iron-hepcidin-ferroportin axis in monocytes

Zughaier, S. M., Alvarez, J. A., Sloan, J. H., Konrad, R. J., & Tangpricha, V. (2014) · Journal of Clinical &amp; Translational Endocrinology · doi:10.1016/j.jcte.2014.01.003 · Cited by 174 · see citing works

Cathelicidin Mediates a Protective Role of Vitamin D in Ulcerative Colitis and Human Colonic Epithelial Cells

Gubatan, J. M. B., Mehigan, G. A., Villegas, F., et al. (2020) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izz330 · Cited by 52 · see citing works

Antibacterial Function of the Human Cathelicidin-18 Peptide (LL-37) between Theory and Practice

Iacob, S. A., & Iacob, D. G. (2014) · Protein and Peptide Letters · doi:10.2174/0929866521666140805124855 · Cited by 9 · see citing works

Cod cathelicidin: Isolation of the mature peptide, cleavage site characterisation and developmental expression

Broekman, D. C., Frei, D. M., Gylfason, G. A., et al. (2010) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2010.10.002 · Cited by 60 · see citing works

Cathelicidin is a host defense peptide in controlling Helicobacter pylori survival and infection

Zhang, L., Yu, J. Q., Wu, W. K. K., et al. (2013) · The FASEB Journal · doi:10.1096/fasebj.27.1_supplement.1093.7

Expression of an additional cathelicidin antimicrobial peptide protects against bacterial skin infection

Lee, P. H. A., Ohtake, T., Zaiou, M., Murakami, M., Rudisill, J. A., Lin, K. H., & Gallo, R. L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500268102 · Cited by 131 · see citing works