Role of dectin-2 for host defense against systemic infection with Candida glabrata

A Controlled Trial of Fluconazole to Prevent Fungal Infections in Patients Undergoing Bone Marrow Transplantation

Goodman, J. L., Winston, D. J., Greenfield, R. A., Chandrasekar, P. H., Fox, B. C., Kaizer, H., Shadduck, R. K., Shea, T. C., Stiff, P. J., Friedman, D. J., et al. (1992) · New England Journal of Medicine · doi:10.1056/nejm199203263261301 · Cited by 1,168 · see citing works

Dectin-1 is required for β-glucan recognition and control of fungal infection

Taylor, P. R., Tsoni, S. V., Willment, J. A., Dennehy, K. M., Rosas, M., Findon, H., Haynes, K., Steele, C. H., Botto, M., Gordon, S., et al. (2006) · Nature Immunology · doi:10.1038/ni1408 · Cited by 1,155 · see citing works

<i>Candida glabrata</i> : Review of Epidemiology, Pathogenesis, and Clinical Disease with Comparison to <i>C. albicans</i>

Fidel, P. L., Vazquez, J. A., & Sobel, J. D. (1999) · Clinical Microbiology Reviews · doi:10.1128/cmr.12.1.80 · Cited by 953 · see citing works

An integrated model of the recognition of Candida albicans by the innate immune system

Netea, M. G., Brown, G. D., Kullberg, B. J., & Gow, N. A. R. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1815 · Cited by 946 · see citing works

The Epidemiology of Hematogenous Candidiasis Caused by Different Candida Species

Abi‐Said, D., Anaissie, E., Uzun, O., Raad, I., Pinzcowski, H., & Vartivarian, S. (1997) · Clinical Infectious Diseases · doi:10.1086/513663 · Cited by 755 · see citing works

Dectin-2 Recognition of α-Mannans and Induction of Th17 Cell Differentiation Is Essential for Host Defense against Candida albicans

Saijo, S., Ikeda, S., Yamabe, K., Kakuta, S., Ishigame, H., Akitsu, A., Fujikado, N., Kusaka, T., Kubo, S., Chung, S.-H., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.05.001 · Cited by 735 · see citing works

STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis

van de Veerdonk, F. L., Plantinga, T. S., Hoischen, A., Smeekens, S. P., Joosten, L. A. B., Gilissen, C., Arts, P., Rosentul, D. C., Carmichael, A., der Graaf, C. A. A. S.-V., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1100102 · Cited by 665 · see citing works

Incidence of Bloodstream Infections Due to <i>Candida</i> Species and In Vitro Susceptibilities of Isolates Collected from 1998 to 2000 in a Population-Based Active Surveillance Program

Hajjeh, R. A., Sofair, A. N., Harrison, L. H., Lyon, G. M., Arthington-Skaggs, B. A., Mirza, S. A., Phelan, M., Morgan, J., Lee-Yang, W., Ciblak, M. A., et al. (2004) · Journal of Clinical Microbiology · doi:10.1128/jcm.42.4.1519-1527.2004 · Cited by 649 · see citing works

Prospective Multicenter Surveillance Study of Funguria in Hospitalized Patients

Kauffman, C. A., Vazquez, J. A., Sobel, J. D., Gallis, H. A., McKinsey, D. S., Karchmer, A. W., Sugar, A. M., Sharkey, P. K., Wise, G. J., Mangi, R., et al. (2000) · Clinical Infectious Diseases · doi:10.1086/313583 · Cited by 483 · see citing works

Dectin-2 is a Syk-coupled pattern recognition receptor crucial for Th17 responses to fungal infection

Robinson, M. J., Osorio, F., Rosas, M., Freitas, R. P., Schweighoffer, E., Groß, O., Verbeek, J. S., Ruland, J., Tybulewicz, V. L. J., Brown, G. D., et al. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20082818 · Cited by 464 · see citing works

Dectin-2 Is a Pattern Recognition Receptor for Fungi That Couples with the Fc Receptor γ Chain to Induce Innate Immune Responses

Sato, K., Yang, X.-L., Yudate, T., Chung, J., Wu, J., Luby‐Phelps, K., Kimberly, R. P., Underhill, D. M., Cruz, P. D., & Ariizumi, K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m606542200 · Cited by 458 · see citing works

Phagosome Extrusion and Host-Cell Survival after Cryptococcus neoformans Phagocytosis by Macrophages

Alvarez, M., & Casadevall, A. (2006) · Current Biology · doi:10.1016/j.cub.2006.09.061 · Cited by 414 · see citing works

The carbohydrate-recognition domain of Dectin-2 is a C-type lectin with specificity for high mannose

McGreal, E. P., Rosas, M., Brown, G. D., ZAMZE, S. E., Wong, S. Y. C., Gordon, S., Martínez‐Pomares, L., & Taylor, P. R. (2006) · Glycobiology · doi:10.1093/glycob/cwj077 · Cited by 380 · see citing works

C-Type Lectin Receptors Dectin-3 and Dectin-2 Form a Heterodimeric Pattern-Recognition Receptor for Host Defense against Fungal Infection

Zhu, L., Zhao, X.-Q., Jiang, C., You, Y., Chen, X., Jiang, Y.-Y., Jia, X., & Lin, X. (2013) · Immunity · doi:10.1016/j.immuni.2013.05.017 · Cited by 340 · see citing works

Organ-Specific Innate Immune Responses in a Mouse Model of Invasive Candidiasis

Lionakis, M. S., Lim, J. K., Lee, C.-C. R., & Murphy, P. M. (2011) · Journal of Innate Immunity · doi:10.1159/000321157 · Cited by 302 · see citing works

Syk Kinase-Coupled C-type Lectin Receptors Engage Protein Kinase C-δ to Elicit Card9 Adaptor-Mediated Innate Immunity

Strasser, D., Neumann, K., Bergmann, H., Marakalala, M. J., Guler, R., Rojowska, A., Hopfner, K., Brombacher, F., Urlaub, H., Baier, G., et al. (2012) · Immunity · doi:10.1016/j.immuni.2011.11.015 · Cited by 287 · see citing works

A family of glycosylphosphatidylinositol-linked aspartyl proteases is required for virulence of <i>Candida glabrata</i>

Kaur, R., Ma, B., & Cormack, B. P. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611195104 · Cited by 284 · see citing works

Invasive fungal infection and impaired neutrophil killing in human CARD9 deficiency

Drewniak, A., Gazendam, R. P., Tool, A. T. J., van Houdt, M., Jansen, M. H., van Hamme, J. L., van Leeuwen, E. M. M., Roos, D., Scalais, E., de Beaufort, C. E., et al. (2013) · Blood · doi:10.1182/blood-2012-08-450551 · Cited by 276 · see citing works

Candida bloodstream infections: comparison of species distribution and resistance to echinocandin and azole antifungal agents in intensive care unit (ICU) and non-ICU settings in the SENTRY antimicrobial surveillance program (2008–2009)

Pfaller, M. A., Messer, S. A., Moet, G. J., Jones, R. N., & Castanheira, M. (2011) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2011.02.016 · Cited by 274 · see citing works

Contribution of <i>Candida albicans</i> Cell Wall Components to Recognition by and Escape from Murine Macrophages

McKenzie, C. G. J., Koser, U., Lewis, L. E., Bain, J. M., Mora-Montes, H. M., Barker, R. N., Gow, N. A. R., & Erwig, L. P. (2010) · Infection and Immunity · doi:10.1128/iai.00001-10 · Cited by 250 · see citing works

Dectin-2 Recognition of House Dust Mite Triggers Cysteinyl Leukotriene Generation by Dendritic Cells

Barrett, N. A., Maekawa, A., Rahman, O. M., Austen, K. F., & Kanaoka, Y. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.2.1119 · Cited by 247 · see citing works

Dendritic Cell Interaction with Candida albicans Critically Depends on N-Linked Mannan

Cambi, A., Netea, M. G., Mora-Montes, H. M., Gow, N. A. R., Hato, S. V., Lowman, D. W., Kullberg, B. J., Torensma, R., Williams, D. L., & Figdor, C. G. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709334200 · Cited by 247 · see citing works

Mice with Disseminated Candidiasis Die of Progressive Sepsis

Spellberg, B., Ibrahim, A. S., Edwards Jr., J. E., & Filler, S. G. (2005) · The Journal of Infectious Diseases · doi:10.1086/430952 · Cited by 230 · see citing works

The role of Syk/CARD9 coupled C-type lectins in antifungal immunity

Drummond, R. A., Saijo, S., Iwakura, Y., & Brown, G. D. (2011) · European Journal of Immunology · doi:10.1002/eji.201041252 · Cited by 221 · see citing works

The Facultative Intracellular Pathogen <i>Candida glabrata</i> Subverts Macrophage Cytokine Production and Phagolysosome Maturation

Seider, K., Brunke, S., Schild, L., Jablonowski, N., Wilson, D., Majer, O., Barz, D., Haas, A., Kuchler, K., Schaller, M., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1003730 · Cited by 220 · see citing works

IL-12 prevents mortality in mice infected with Histoplasma capsulatum through induction of IFN-γ

Zhou, P., Sieve, M. C., Bennett, J. E., Kwon-Chung, K. J., Tewari, R. P., Gazzinelli, R. T., Sher, A., & Seder, R. A. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.155.2.785 · Cited by 215 · see citing works

Fluconazole versus Amphotericin B in the treatment of Hematogenous Candidiasis: A matched cohort study

Anaissie, E. J., Vartivarian, S. E., Abi-Said, D., Uzun, Ö., Pinczowski, H., Kontoyiannis, D. P., Khoury, P. N., Papadakis, K., Gardner, A., RAAD, I. I., et al. (1996) · The American Journal of Medicine · doi:10.1016/s0002-9343(96)80072-6 · Cited by 186 · see citing works

Cloning of a Second Dendritic Cell-associated C-type Lectin (Dectin-2) and Its Alternatively Spliced Isoforms

Ariizumi, K., Shen, G.-L., Shikano, S., Ritter, R., Zukas, P. K., Edelbaum, D., Morita, A., & Takashima, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.16.11957 · Cited by 164 · see citing works

Candida albicans cell wall glycans, host receptors and responses: elements for a decisive crosstalk

Poulain, D., & Jouault, T. (2004) · Current Opinion in Microbiology · doi:10.1016/j.mib.2004.06.011 · Cited by 153 · see citing works

Recombinant Interferon- Enhances Resistance to Acute Disseminated Candida albicans Infection in Mice

Kullberg, B. J., Wout, J. W. V. ’., Hoogstraten, C., & van Furth, R. (1993) · The Journal of Infectious Diseases · doi:10.1093/infdis/168.2.436 · Cited by 148 · see citing works

Inflammatory Monocytes Mediate Early and Organ-Specific Innate Defense During Systemic Candidiasis

Ngo, L. Y., Kasahara, S., Kumasaka, D. K., Knoblaugh, S. E., Jhingran, A., & Hohl, T. M. (2013) · The Journal of Infectious Diseases · doi:10.1093/infdis/jit413 · Cited by 135 · see citing works

CARD9 Mediates Dectin-2-induced IκBα Kinase Ubiquitination Leading to Activation of NF-κB in Response to Stimulation by the Hyphal Form of Candida albicans

Bi, L., Gojestani, S., Wu, W., Hsu, Y.-M. S., Zhu, J., Ariizumi, K., & Lin, X. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.131300 · Cited by 126 · see citing works

Chemokine Receptor Ccr1 Drives Neutrophil-Mediated Kidney Immunopathology and Mortality in Invasive Candidiasis

Lionakis, M. S., Fischer, B. G., Lim, J. K., Swamydas, M., Wan, W., Richard Lee, C.-C., Cohen, J. I., Scheinberg, P., Gao, J.-L., & Murphy, P. M. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002865 · Cited by 118 · see citing works

Role of granulocytes in increased host resistance to Candida albicans induced by recombinant interleukin-1

Kullberg, B. J., van 't Wout, J. W., & van Furth, R. (1990) · Infection and Immunity · doi:10.1128/iai.58.10.3319-3324.1990 · Cited by 105 · see citing works

Cre recombinase-mediated inversion using lox66 and lox71: method to introduce conditional point mutations into the CREB-binding protein

Zhang, Z. (2002) · Nucleic Acids Research · doi:10.1093/nar/gnf089 · Cited by 104 · see citing works

Phenotypic switching and filamentation in Candida glabrata

Lachke, S. A., Joly, S., Daniels, K., & Soll, D. R. (2002) · Microbiology · doi:10.1099/00221287-148-9-2661 · Cited by 103 · see citing works

Non-lytic expulsion/exocytosis of Candida albicans from macrophages

Bain, J. M., Lewis, L. E., Okai, B., Quinn, J., Gow, N. A. R., & Erwig, L. (2012) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2012.01.008 · Cited by 100 · see citing works

Protective Role of Naturally Occurring Interleukin-17A-Producing γδ T Cells in the Lung at the Early Stage of Systemic Candidiasis in Mice

Dejima, T., Shibata, K., Yamada, H., Hara, H., Iwakura, Y., Naito, S., & Yoshikai, Y. (2011) · Infection and Immunity · doi:10.1128/iai.05799-11 · Cited by 85 · see citing works

The complete mitochondrial genome sequence of the pathogenic yeast Candida (Torulopsis) glabrata

Koszul, R., Malpertuy, A., Frangeul, L., Bouchier, C., Wincker, P., Thierry, A., Duthoy, S., Ferris, S., Hennequin, C., & Dujon, B. (2002) · FEBS Letters · doi:10.1016/s0014-5793(02)03749-3 · Cited by 76 · see citing works

Phospholipase Cγ2 (PLCγ2) Is Key Component in Dectin-2 Signaling Pathway, Mediating Anti-fungal Innate Immune Responses

Gorjestani, S., Yu, M., Tang, B., Zhang, D., Wang, D., & Lin, X. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.307389 · Cited by 52 · see citing works

Identification and expression profiling of a human C‐type lectin, structurally homologous to mouse dectin‐2

Gavino, A. C. P., Chung, J., Sato, K., Ariizumi, K., & Cruz, P. D. (2005) · Experimental Dermatology · doi:10.1111/j.0906-6705.2005.00312.x · Cited by 52 · see citing works

Mice lacking both G-CSF and IL-6 are more susceptible toCandida albicansinfection: Critical role of neutrophils in defense againstCandida albicans

Basu, S., Quilici, C., Zhang, H., Grail, D., & Dunn, A. R. (2008) · Growth Factors · doi:10.1080/08977190801987513 · Cited by 40 · see citing works

Tumor Necrosis Factor Receptor-associated Factor 6 (TRAF6) and TGFβ-activated Kinase 1 (TAK1) Play Essential Roles in the C-type Lectin Receptor Signaling in Response to Candida albicans Infection

Gorjestani, S., Darnay, B. G., & Lin, X. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.414276 · Cited by 28 · see citing works

In Vitro Susceptibilities of Invasive Isolates of Candida Species: Rapid Increase in Rates of Fluconazole Susceptible-Dose Dependent Candida glabrata Isolates

Ruan, S., Chu, C., & Hsueh, P. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00323-08 · Cited by 28 · see citing works

Immune function and leukocyte sequestration under the influence of parenteral lipid emulsions in healthy humans: a placebo-controlled crossover study

Versleijen, M. W. J., Oyen, W. J. G., Roelofs, H. M. J., Vries, S. E. V. E., Willems, P. H. G. M., Jansen, J. B. �. �., & Wanten, G. J. A. (2008) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/87.3.539 · Cited by 27 · see citing works

Live-cell Video Microscopy of Fungal Pathogen Phagocytosis

Lewis, L. E., Bain, J. M., Okai, B., Gow, N. A. R., & Erwig, L. P. (2013) · Journal of Visualized Experiments · doi:10.3791/50196 · Cited by 22 · see citing works

Invasive candidiasis

Pappas, P. G., Lionakis, M. S., Arendrup, M. C., Ostrosky-Zeichner, L., & Kullberg, B. J. (2018) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2018.26 · Cited by 1,636 · see citing works

Immune defence against Candida fungal infections

Netea, M. G., Joosten, L. A. B., van der Meer, J. W. M., Kullberg, B.-J., & van de Veerdonk, F. L. (2015) · Nature Reviews Immunology · doi:10.1038/nri3897 · Cited by 642 · see citing works

C-type lectins in immunity: recent developments

Dambuza, I. M., & Brown, G. D. (2015) · Current Opinion in Immunology · doi:10.1016/j.coi.2014.12.002 · Cited by 482 · see citing works

C-type lectins: their network and roles in pathogen recognition and immunity

Mayer, S., Raulf, M., & Lepenies, B. (2016) · Histochemistry and Cell Biology · doi:10.1007/s00418-016-1523-7 · Cited by 257 · see citing works

Pattern recognition receptors in fungal immunity

Patin, E. C., Thompson, A., & Orr, S. J. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.03.003 · Cited by 228 · see citing works

Candida albicans and Candida glabrata : global priority pathogens

Katsipoulaki, M., Stappers, M. H. T., Malavia, D., Brunke, S., Hube, B., & Gow, N. A. R. (2024) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00021-23 · Cited by 174 · see citing works

Regulation of phagocytosis by Rho GTPases

Mao, Y., & Finnemann, S. C. (2015) · Small GTPases · doi:10.4161/21541248.2014.989785 · Cited by 163 · see citing works

Immunity against fungi

Lionakis, M. S., Iliev, I. D., & Hohl, T. M. (2017) · JCI Insight · doi:10.1172/jci.insight.93156 · Cited by 153 · see citing works

How neutrophils kill fungi

Gazendam, R. P., van de Geer, A., Roos, D., van den Berg, T. K., & Kuijpers, T. W. (2016) · Immunological Reviews · doi:10.1111/imr.12454 · Cited by 146 · see citing works

The Interaction of Human Pathogenic Fungi With C-Type Lectin Receptors

Goyal, S., Castrillón-Betancur, J. C., Klaile, E., & Slevogt, H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01261 · Cited by 142 · see citing works

Immune Interactions with Pathogenic and Commensal Fungi: A Two-Way Street

Underhill, D. M., & Pearlman, E. (2015) · Immunity · doi:10.1016/j.immuni.2015.10.023 · Cited by 130 · see citing works

Crossing Kingdoms: How the Mycobiota and Fungal-Bacterial Interactions Impact Host Health and Disease

Santus, W., Devlin, J. R., & Behnsen, J. (2021) · Infection and Immunity · doi:10.1128/iai.00648-20 · Cited by 132 · see citing works

Candida glabrata: A Lot More Than Meets the Eye

Kumar, K., Askari, F., Sahu, M. S., & Kaur, R. (2019) · Microorganisms · doi:10.3390/microorganisms7020039 · Cited by 128 · see citing works

Immunity to Commensal Fungi: Detente and Disease

Wheeler, M. L., Limon, J. J., & Underhill, D. M. (2017) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathol-052016-100342 · Cited by 123 · see citing works

The Role of IL-17 in Protection against Mucosal Candida Infections

Mengesha, B., & Conti, H. R. (2017) · Journal of Fungi · doi:10.3390/jof3040052 · Cited by 124 · see citing works

The innate immune receptor Dectin-2 mediates the phagocytosis of cancer cells by Kupffer cells for the suppression of liver metastasis

Kimura, Y., Inoue, A., Hangai, S., Saijo, S., Negishi, H., Nishio, J., Yamasaki, S., Iwakura, Y., Yanai, H., & Taniguchi, T. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617903113 · Cited by 121 · see citing works

Intracellular survival ofCandida glabratain macrophages: immune evasion and persistence

Kasper, L., Seider, K., & Hube, B. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov042 · Cited by 115 · see citing works

Microbial Phagocytic Receptors and Their Potential Involvement in Cytokine Induction in Macrophages

Fu, Y., & Harrison, R. E. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.662063 · Cited by 109 · see citing works

Divergent Approaches to Virulence in C. albicans and C. glabrata: Two Sides of the Same Coin

Galocha, M., Pais, P., Cavalheiro, M., Pereira, D., Viana, R., & Teixeira, M. C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20092345 · Cited by 105 · see citing works

Immune Recognition of Fungal Polysaccharides

Snarr, B. D., Qureshi, S. T., & Sheppard, D. C. (2017) · Journal of Fungi · doi:10.3390/jof3030047 · Cited by 96 · see citing works

Anti-Immune Strategies of Pathogenic Fungi

Marcos, C. M., de Oliveira, H. C., Melo, W., da Silva, J. D. F., Assato, P. A., Scorzoni, L., Rossi, S. A., Silva, A. C. A. D. P. E., Mendes‐Giannini, M. J. S., & Fusco‐Almeida, A. M. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00142 · Cited by 94 · see citing works

Candida albicans triggers NADPH oxidase-independent neutrophil extracellular traps through dectin-2

Wu, S.-Y., Weng, C.-L., Jheng, M.-J., Kan, H., Hsieh, S., Liu, F., & Wu‐Hsieh, B. A. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1008096 · Cited by 91 · see citing works

Mechanism of pathogen recognition by human dectin-2

Feinberg, H., Jégouzo, S. A. F., Rex, M. J., Drickamer, K., Weis, W. I., & Taylor, M. E. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.799080 · Cited by 90 · see citing works

Innate Immunity against Cryptococcus, from Recognition to Elimination

Campuzano, A., & Wormley, F. L. (2018) · Journal of Fungi · doi:10.3390/jof4010033 · Cited by 88 · see citing works

Antifungal innate immunity: recognition and inflammatory networks

Becker, K. L., Ifrim, D. C., Quintin, J., Netea, M. G., & van de Veerdonk, F. L. (2015) · Seminars in Immunopathology · doi:10.1007/s00281-014-0467-z · Cited by 86 · see citing works

Remembering Pathogen Dose: Long-Term Adaptation in Innate Immunity

Bauer, M. W., Weis, S., Netea, M. G., & Wetzker, R. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.04.001 · Cited by 83 · see citing works

Contact, Collaboration, and Conflict: Signal Integration of Syk-Coupled C-Type Lectin Receptors

Ostrop, J., & Lang, R. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601665 · Cited by 80 · see citing works

Role of Protein Glycosylation in Candida parapsilosis Cell Wall Integrity and Host Interaction

Pérez-García, L. A., Csonka, K., Flores-Carreón, A., Estrada-Mata, E., Mellado‐Mojica, E., Németh, T., López-Ramírez, L. A., Tóth, R., López, M. G., Vízler, C., et al. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00306 · Cited by 76 · see citing works

Dectin-2 Deficiency Promotes Th2 Response and Mucin Production in the Lungs after Pulmonary Infection with Cryptococcus neoformans

Nakamura, Y., Sato, K., Yamamoto, H., Matsumura, K., Matsumoto, I., Nomura, T., Miyasaka, T., Ishii, K., Kanno, E., Tachi, M., et al. (2014) · Infection and Immunity · doi:10.1128/iai.02835-14 · Cited by 69 · see citing works

Lectin Receptors Expressed on Myeloid Cells

Brown, G. D., & Crocker, P. R. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0036-2016 · Cited by 66 · see citing works

C-Type Lectin Receptors in Phagocytosis

Li, K., & Underhill, D. M. (2020) · Current topics in microbiology and immunology · doi:10.1007/82_2020_198 · Cited by 64 · see citing works

C-type lectin receptors in anti-fungal immunity

Shiokawa, M., Yamasaki, S., & Saijo, S. (2017) · Current Opinion in Microbiology · doi:10.1016/j.mib.2017.11.004 · Cited by 65 · see citing works

Non-albicans Candida Species: Immune Response, Evasion Mechanisms, and New Plant-Derived Alternative Therapies

Gómez-Gaviria, M., Ramírez-Sotelo, U., & Mora-Montes, H. M. (2022) · Journal of Fungi · doi:10.3390/jof9010011 · Cited by 68 · see citing works

Identification of Candida glabrata Genes Involved in pH Modulation and Modification of the Phagosomal Environment in Macrophages

Kasper, L., Seider, K., Gerwien, F., Allert, S., Brunke, S., Schwarzmüller, T., Ames, L., Zubiria-Barrera, C., Mansour, M. K., Becken, U., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096015 · Cited by 59 · see citing works

The Role of Dectin-2 for Host Defense Against Disseminated Candidiasis

Ifrim, D. C., Quintin, J., Courjol, F., Verschueren, I., van Krieken, J. H., Köentgen, F., Fradin, C., Gow, N. A. R., Joosten, L. A. B., van der Meer, J. W. M., et al. (2016) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2015.0040 · Cited by 59 · see citing works

Dectin-2 is a primary receptor for NLRP3 inflammasome activation in dendritic cell response to Histoplasma capsulatum

Chang, T.-H., Huang, J.-H., Lin, H.-C., Chen, W.-Y., Lee, Y.-H., Hsu, L.-C., Netea, M. G., Ting, J. P. ‐., & Wu‐Hsieh, B. A. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006485 · Cited by 57 · see citing works

Beyond Candida albicans: Mechanisms of immunity to non-albicans Candida species

Whibley, N., & Gaffen, S. L. (2015) · Cytokine · doi:10.1016/j.cyto.2015.07.025 · Cited by 57 · see citing works

International Union of Basic and Clinical Pharmacology. XCVI. Pattern Recognition Receptors in Health and Disease

Bryant, C. E., Orr, S. J., Ferguson, B. J., Symmons, M. F., Boyle, J. P., & Monie, T. P. (2015) · Pharmacological Reviews · doi:10.1124/pr.114.009928 · Cited by 53 · see citing works

The Interaction of Pneumocystis with the C-Type Lectin Receptor Mincle Exerts a Significant Role in Host Defense against Infection

Kottom, T. J., Hebrink, D. M., Jenson, P. E., Nandakumar, V., Wüthrich, M., Wang, H., Klein, B. S., Yamasaki, S., Lepenies, B., & LIMPER, A. H. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1600744 · Cited by 53 · see citing works

Disruption of Protein Mannosylation Affects Candida guilliermondii Cell Wall, Immune Sensing, and Virulence

Navarro-Arias, M. J., Defosse, T. A., Dementhon, K., Csonka, K., Mellado‐Mojica, E., Valério, A. D., González-Hernández, R. J., Courdavault, V., Clastre, M., Hernández, N. V., et al. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01951 · Cited by 51 · see citing works

Aspartyl proteases in Candida glabrata are required for suppression of the host innate immune response

Rasheed, M., Battu, A., & Kaur, R. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.813741 · Cited by 51 · see citing works

NLRX1 Facilitates Histoplasma capsulatum-Induced LC3-Associated Phagocytosis for Cytokine Production in Macrophages

Huang, J.-H., Liu, C.-Y., Wu, S.-Y., Chen, W., Chang, T.-H., Kan, H., Hsieh, S., Ting, J. P. ‐., & Wu‐Hsieh, B. A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.02761 · Cited by 52 · see citing works

Delinking CARD9 and IL-17: CARD9 Protects against Candida tropicalis Infection through a TNF-α–Dependent, IL-17–Independent Mechanism

Whibley, N., Jaycox, J. R., Reid, D. M., Garg, A. V., Taylor, J. A., Clancy, C. J., Nguyen, M. H., Biswas, P. S., McGeachy, M. J., Brown, G. D., et al. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500870 · Cited by 49 · see citing works

Dectin-1 plays an important role in host defense against systemicCandida glabratainfection

Chen, S. M., Shen, H., Zhang, T., Huang, X., Liu, X. Q., Guo, S. Y., Zhao, J. J., Wang, C. F., Yan, L., Xu, G. T., et al. (2017) · Virulence · doi:10.1080/21505594.2017.1346756 · Cited by 49 · see citing works

Vaccine immunity against fungal infections

Nanjappa, S. G., & Klein, B. S. (2014) · Current Opinion in Immunology · doi:10.1016/j.coi.2014.01.014 · Cited by 47 · see citing works

C-Type Lectin Receptors in Antifungal Immunity

Nikolakopoulou, C., Willment, J. A., & Brown, G. D. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-1580-4_1 · Cited by 43 · see citing works

Ligation of Dectin-2 with a novel microbial ligand promotes adjuvant activity for vaccination

Wang, H., Lee, T.-J., Fites, J. S., Merkhofer, R. M., Żarnowski, R., Brandhorst, T. T., Galles, K., Klein, B. S., & Wüthrich, M. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006568 · Cited by 39 · see citing works

LC3-Associated Phagocytosis Is Required for Dendritic Cell Inflammatory Cytokine Response to Gut Commensal Yeast Saccharomyces cerevisiae

Lamprinaki, D., Beasy, G., Zhekova, A., Wittmann, A., James, S. A., Dicks, J. L., Iwakura, Y., Saijo, S., Wang, X., Chow, C., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01397 · Cited by 40 · see citing works

Multi-facets of neutrophil extracellular trap in infectious diseases: Moving beyond immunity

Tabrizi, Z. A., Khosrojerdi, A., Aslani, S., Hemmatzadeh, M., Babaie, F., Bairami, A., Shomali, N., Hosseinzadeh, R., Safari, R., & Mohammadi, H. (2021) · Microbial Pathogenesis · doi:10.1016/j.micpath.2021.105066 · Cited by 39 · see citing works

Candida glabrata’s Genome Plasticity Confers a Unique Pattern of Expressed Cell Wall Proteins

López-Fuentes, E., Gutiérrez-Escobedo, G., Timmermans, B., Van Dijck, P., De Las Peñas, A., & Castaño, I. (2018) · Journal of Fungi · doi:10.3390/jof4020067 · Cited by 35 · see citing works

Characterizing the Mechanisms of Nonopsonic Uptake of Cryptococci by Macrophages

Lim, J., Coates, C. J., Seoane, P. I., Garelnabi, M., Taylor-Smith, L. M., Monteith, P., Macleod, C. L., Escaron, C. J., Brown, G. D., Hall, R. A., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1700790 · Cited by 35 · see citing works

The pattern recognition receptors dectin-2, mincle, and FcRγ impact the dynamics of phagocytosis of Candida, Saccharomyces, Malassezia, and Mucor species

Haider, M. J. A., Dambuza, I. M., Asamaphan, P., Stappers, M. H. T., Reid, D. M., Yamasaki, S., Brown, G. D., Gow, N. A. R., & Erwig, L. P. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220867 · Cited by 35 · see citing works

Dectin-2 polymorphism associated with pulmonary cryptococcosis in HIV-uninfected Chinese patients

Hu, X., Wang, R., Wang, X., Cao, Y., Chen, Y., Zhao, H., Wu, J., Weng, X., Gao, X.-H., Sun, R., et al. (2015) · Medical Mycology · doi:10.1093/mmy/myv043 · Cited by 34 · see citing works

Differential Regulation of Myeloid-Derived Suppressor Cells by Candida Species

Singh, A., Lelis, F., Braig, S., Schäfer, I., Hartl, D., & Rieber, N. P. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01624 · Cited by 32 · see citing works

Dependence on Dectin-1 Varies With Multiple Candida Species

Thompson, A., Griffiths, J. S., Walker, L. A., da Fonseca, D. M., Lee, K. K., Taylor, P. R., Gow, N. A. R., & Orr, S. J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01800 · Cited by 30 · see citing works

Role of Dectin-2 in the Phagocytosis of Cryptococcus neoformans by Dendritic Cells

Kitai, Y., Sato, K., Tanno, D., Yuan, X., Umeki, A., Kasamatsu, J., Kanno, E., Tanno, H., Hara, H., Yamasaki, S., et al. (2021) · Infection and Immunity · doi:10.1128/iai.00330-21 · Cited by 31 · see citing works

Specific pathways mediating inflammasome activation by Candida parapsilosis

Tóth, A., Zajta, E., Csonka, K., Vágvölgyi, C., Netea, M. G., & Gácser, A. (2017) · Scientific Reports · doi:10.1038/srep43129 · Cited by 30 · see citing works

<i>Candida</i>Immunity

Naglik, J. R. (2014) · New Journal of Science · doi:10.1155/2014/390241 · Cited by 29 · see citing works

Host–pathogen interaction inCandida glabratainfection: current knowledge and implications for antifungal therapy

Rasheed, M., Battu, A., & Kaur, R. (2020) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2020.1792773 · Cited by 30 · see citing works

Molecular association of Candida albicans and vulvovaginal candidiasis: focusing on a solution

David, H., & Solomon, A. P. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1245808 · Cited by 29 · see citing works

Candida glabrata is a successful pathogen: An artist manipulating the immune response

Castrejón-Jiménez, N. S., Castillo-Cruz, J., Baltierra‐Uribe, S. L., Hernández-González, J. C., & Estela, G.-P. B. (2022) · Microbiological Research · doi:10.1016/j.micres.2022.127038 · Cited by 28 · see citing works

Exopolysaccharides from Aspergillus terreus: Production, chemical elucidation and immunoactivity

Costa, C. R. L. D. M., Menolli, R. A., Osaku, É. F., Tramontina, R., de Melo, R. H., do Amaral, A. E., Duarte, P. A. D., de Carvalho, M. M., Smiderle, F. R., Silva, J. L. D. C., et al. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.08.039 · Cited by 25 · see citing works

Progranulin aggravates lethal Candida albicans sepsis by regulating inflammatory response and antifungal immunity

Liu, J., Lai, X., Yu, R., Ding, H., Bai, H., Yang, Z., Yin, Y., Xu, F., & Cao, J. (2022) · PLoS Pathogens · doi:10.1371/journal.ppat.1010873 · Cited by 24 · see citing works

Eicosanoid biosynthesis influences the virulence of Candida parapsilosis

Chakraborty, T., Thuer, E., Heijink, M., Tóth, R., Bodai, L., Vágvölgyi, C., Giera, M. A., Gabaldón, T., & Gácser, A. (2018) · Virulence · doi:10.1080/21505594.2018.1475797 · Cited by 24 · see citing works

Histone Acetylation Regulator Gcn5 Mediates Drug Resistance and Virulence of Candida glabrata

Yu, S., Paderu, P., Lee, A., Eirekat, S., Healey, K., Chen, L., Perlin, D. S., & Zhao, Y. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.00963-22 · Cited by 23 · see citing works

Dependence on Mincle and Dectin-2 Varies With Multiple Candida Species During Systemic Infection

Thompson, A., da Fonseca, D. M., Walker, L. A., Griffiths, J. S., Taylor, P. R., Gow, N. A. R., & Orr, S. J. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.633229 · Cited by 23 · see citing works

Controlling Candida : immune regulation of commensal fungi in the gut

Jensen, O., Trujillo, E. N., Hanson, L., & Ost, K. S. (2024) · Infection and Immunity · doi:10.1128/iai.00516-23 · Cited by 22 · see citing works

Systems Level Dissection of Candida Recognition by Dectins: A Matter of Fungal Morphology and Site of Infection

Rizzetto, L., Weil, T., & Cavalieri, D. (2015) · Pathogens · doi:10.3390/pathogens4030639 · Cited by 21 · see citing works

Role of Protein Mannosylation in the Candida tropicalis-Host Interaction

Hernández-Chávez, M. J., Clavijo-Giraldo, D. M., Novák, Á., Lozoya‐Pérez, N. E., Martínez-Álvarez, J. A., Salinas-Marín, R., Hernández, N. V., Martínez-Duncker, I., Gácser, A., & Mora-Montes, H. M. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02743 · Cited by 22 · see citing works

IL-4 and helminth infection downregulate MINCLE-dependent macrophage response to mycobacteria and Th17 adjuvanticity

Schick, J., Altunay, M., Lacorcia, M., Marschner, N., Westermann, S., Schluckebier, J., Schubart, C., Bodendorfer, B., Christensen, D., Alexander, C., et al. (2023) · eLife · doi:10.7554/elife.72923 · Cited by 22 · see citing works

Advances in Candida albicans

Wang, X. (2021) · Infectious diseases · doi:10.5772/intechopen.87410 · Cited by 22 · see citing works

Different Candida parapsilosis clinical isolates and lipase deficient strain trigger an altered cellular immune response

Tóth, R., Alonso, M. F., Bain, J. M., Vágvölgyi, C., Erwig, L., & Gácser, A. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01102 · Cited by 21 · see citing works

Fluorescent Tracking of Yeast Division Clarifies the Essential Role of Spleen Tyrosine Kinase in the Intracellular Control of Candida glabrata in Macrophages

Dagher, Z., Xu, S., Negoro, P. E., Khan, N. S., Feldman, M. B., Reedy, J. L., Tam, J. M., Sykes, D. B., & Mansour, M. K. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01058 · Cited by 21 · see citing works

The effect of herbal medicine in innate immunity to Candida albicans

Bao, M.-Y., Li, M., Bu, Q., Yang, Y., Song, H., Wang, C., Wang, T.-M., & Li, N. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1096383 · Cited by 19 · see citing works

Signaling C-Type Lectin Receptors in Antifungal Immunity

Höft, M. A., Hoving, J. C., & Brown, G. D. (2020) · Current topics in microbiology and immunology · doi:10.1007/82_2020_224 · Cited by 18 · see citing works

Borrelia- induced cytokine production is mediated by spleen tyrosine kinase (Syk) but is Dectin-1 and Dectin-2 independent

Oosting, M., Buffen, K., Cheng, S., Verschueren, I., Köentgen, F., van de Veerdonk, F. L., Netea, M. G., & Joosten, L. A. B. (2015) · Cytokine · doi:10.1016/j.cyto.2015.08.005 · Cited by 17 · see citing works

Candida glabratasurvives and replicates in human osteoblasts

Muñóz-Duarte, A. R., Castrejón-Jiménez, N. S., Baltierra‐Uribe, S. L., Pérez-Rangel, S. J., Carapia-Minero, N., Castañeda‐Sánchez, J. I., Luna‐Herrera, J., López‐Santiago, R., Rodríguez-Tovar, A. V., & García‐Pérez, B. E. (2016) · Pathogens and Disease · doi:10.1093/femspd/ftw030 · Cited by 16 · see citing works

C-type lectin receptor expression is a hallmark of neutrophils infiltrating the skin in epidermolysis bullosa acquisita

Guerrero‐Juarez, C. F., Schilf, P., Li, J., Zappia, M. P., Bao, L., Patel, P. M., Gieseler-Tillmann, J., Murthy, S., Cole, C., Sverdlov, M. S., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1266359 · Cited by 14 · see citing works

Signaling through Syk or CARD9 Mediates Species-Specific Anti-CandidaProtection in Bone Marrow Chimeric Mice

Zajta, E., Csonka, K., Tóth, A., Tiszlavicz, L., Németh, T., Orosz, A., Novák, Á., Csikós, M., Vágvölgyi, C., Mócsai, A., et al. (2021) · mBio · doi:10.1128/mbio.01608-21 · Cited by 13 · see citing works

Neutrophils require SKAP2 for reactive oxygen species production following C-type lectin and Candida stimulation

Nguyen, G. T., Xu, S., Adams, W., Leong, J. M., Bunnell, S. C., Mansour, M. K., Sykes, D. B., & Mecsas, J. C. (2021) · iScience · doi:10.1016/j.isci.2021.102871 · Cited by 12 · see citing works

β-Glucan-Functionalized Nanoparticles Down-Modulate the Proinflammatory Response of Mononuclear Phagocytes Challenged with Candida albicans

Lima, T., Gunnarsson, S. B., Coelho, E., Evtuguin, D. V., Correia, A., Coimbra, M. A., Cedervall, T., & Vilanova, M. (2022) · Nanomaterials · doi:10.3390/nano12142475 · Cited by 11 · see citing works

Trichoderma asperelloides Spores Downregulate dectin1/2 and TLR2 Receptors of Mice Macrophages and Decrease Candida parapsilosis Phagocytosis Independent of the M1/M2 Polarization

Santos, A. G., Mendes, É. A., de Oliveira, R. P., Faria, A. M. C., de Sousa, A. O., Pirovani, C. P., de Araújo, F. F., Teixeira‐Carvalho, A., da Costa, M. C., Santos, D. A., et al. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01681 · Cited by 10 · see citing works

Candida tropicalis Affects Candida albicans Virulence by Limiting Its Capacity to Adhere to the Host Intestinal Surface, Leading to Decreased Susceptibility to Colitis in Mice

Roberts, K. D., Ösme, A., Salvo, C. D., Zoli, E., Herrada, J., McCormick, T. S., Ghannoum, M. A., Cominelli, F., & Martino, L. D. (2024) · Journal of Fungi · doi:10.3390/jof10040245 · Cited by 9 · see citing works

Infection and Immunity

Saleki, K., Razi, S., & Rezaei, N. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-818006-8.00007-4 · Cited by 7 · see citing works

Innate Immunity and Inflammation

McKarns, S. C. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.64228-9 · Cited by 6 · see citing works

Dectin-2 is critical for phagocyte function and resistance to Paracoccidioides brasiliensis in mice

Cardoso-Miguel, M. D. R. D., Bürgel, P. H., de Castro, R. J. A., Marina, C. L., de Oliveira, S. A., Albuquerque, P., Silva-Pereira, I., Bocca, A. L., & Tavares, A. H. (2023) · Medical Mycology · doi:10.1093/mmy/myad117 · Cited by 5 · see citing works

Immunity to Fungal Infections

Altmeier, S., & LeibundGut‐Landmann, S. (2017) · Springer eBooks · doi:10.1007/978-3-319-50842-9_2 · Cited by 5 · see citing works

Pathogenicity Mechanism of Candida albicans

Pattnaik, S., Maharana, L., & Sethi, M. (2021) · Infectious diseases · doi:10.5772/intechopen.99737 · Cited by 5 · see citing works

The cell wall as a mediator of the pathogenic activity of fungi of the genus Candida sp.

Enoktaeva, O. V., Николенко, М. В., Trushnikov, D., & Baryshnikova, N. V. (2021) · Immunopathology Allergology Infectology · doi:10.14427/jipai.2021.4.60 · Cited by 5 · see citing works

Mammalian Pattern Recognition Receptors (PRRs) Involved in Recognition of Fungi

Sey, E. A., Willment, J. A., & Brown, G. D. (2024) · The mycota · doi:10.1007/978-3-031-64853-3_8 · Cited by 4 · see citing works

C-Type Lectins and Their Roles in Disease and Immune Homeostasis

Ebbecke, T., Diersing, C., Lindenwald, D. L., Stegmann, F., & Lepenies, B. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819475-1.00063-8 · Cited by 4 · see citing works

Host immune responses to fungal infection

García-Carnero, L. C., Gómez-Gaviria, M., Tamez-Castrellón, A. K., & Mora-Montes, H. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-818619-0.00136-2 · Cited by 3 · see citing works

Lectin Receptors Expressed on Myeloid Cells

Brown, G. D., & Crocker, P. R. (2017) · ASM Press eBooks · doi:10.1128/9781555819194.ch25 · Cited by 3 · see citing works

Differential Transcriptional Responses of Human Granulocytes to Fungal Infection with Candida albicans and Aspergillus fumigatus

Klassert, T. E., Hölzer, M., Zubiría-Barrera, C., Bethge, J., Klaile, E., Müller, M. M., Marz, M., & Slevogt, H. (2023) · Journal of Fungi · doi:10.3390/jof9101014 · Cited by 2 · see citing works

Allergenic Microfungi and Human Health: A Review on Exposure, Sensitization, and Sequencing Allergenic Proteins

Amado, M., & Barnes, C. S. (2016) · Fungal biology · doi:10.1007/978-3-319-29137-6_17 · Cited by 2 · see citing works

Galleria mellonella as a versatile model for investigating Candida glabrata virulence and antifungal resistance

Holt, C. J. D., Williams, C. C., & Usher, J. (2026) · Journal of Medical Microbiology · doi:10.1099/jmm.0.002127 · Cited by 1 · see citing works

Candida glabrata and the host: a neglected affair

Ghosh, M., Raney, M., & Kaur, R. (2026) · Journal of Medical Microbiology · doi:10.1099/jmm.0.002161 · Cited by 1 · see citing works

Association of modulation of pro‐inflammatory responses by dectin‐2 with preterm delivery: An experimental model

Liassidou, A., Renieris, G., Droggiti, D., Gkavogianni, T., Liassides, C., Sabracos, L., Giamarellos‐Bourboulis, E. J., & Siristatidis, C. S. (2019) · American Journal of Reproductive Immunology · doi:10.1111/aji.13216 · Cited by 1 · see citing works

C-Type Lectin (C-Type Lectin Receptor)

Kim, C.-H. (2022) · Springer eBooks · doi:10.1007/978-981-16-9081-5_8 · Cited by 1 · see citing works

Candida tropicalis critically affects Candida albicans virulence by limiting its capacity to adhere to the host intestinal surface leading to decreased susceptibility to colitis in micePreprint

Roberts, K. D., Ösme, A., Salvo, C. D., Zoli, E., Herrada, J., McCormick, T. S., Ghannoum, M. A., Cominelli, F., & Martino, L. D. (2024) · Preprints.org · doi:10.20944/preprints202402.1714.v1 · Cited by 1 · see citing works

Dectin-1 plays an important role in host defense against systemicCandida glabratainfection

Chen, S. M., Shen, H., Zhang, T., Huang, X., Liu, X. Q., Guo, S. Y., Zhao, J. J., Wang, C. F., Yan, L., Xu, G. T., et al. (2017) · Virulence · doi:10.1080/21505594.2017.1346756 · Cited by 49 · see citing works

The Role of Dectin-2 for Host Defense Against Disseminated Candidiasis

Ifrim, D. C., Quintin, J., Courjol, F., Verschueren, I., van Krieken, J. H., Köentgen, F., Fradin, C., Gow, N. A. R., Joosten, L. A. B., van der Meer, J. W. M., et al. (2016) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2015.0040 · Cited by 59 · see citing works

Dectin-2-dependent adaptive immunity governs intestinal clearance of systemic Candida albicansPreprint

Dambuza, I. M., Salazar, F., Harvey, J. A., Phillips-Brookes, A., Kaplan, D. H., & Brown, G. D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.28.702262

Dectin-1 is required for host defense against Pneumocystis carinii but not against Candida albicans

Saijo, S., Fujikado, N., Furuta, T., Chung, S.-H., Kotaki, H., Seki, K., Sudo, K., Akira, S., Adachi, Y., Ohno, N., et al. (2006) · Nature Immunology · doi:10.1038/ni1425 · Cited by 612 · see citing works

Dectin-1 is required for β-glucan recognition and control of fungal infection

Taylor, P. R., Tsoni, S. V., Willment, J. A., Dennehy, K. M., Rosas, M., Findon, H., Haynes, K., Steele, C. H., Botto, M., Gordon, S., et al. (2006) · Nature Immunology · doi:10.1038/ni1408 · Cited by 1,155 · see citing works