The Cathelicidin Anti-Microbial Peptide LL-37 is Involved in Re-Epithelialization of Human Skin Wounds and is Lacking in Chronic Ulcer Epithelium
Open accessAbstract
The human cathelicidin anti-microbial protein, hCAP18 is a component of the innate immune system and has broad anti-microbial activity conferred by its C-terminal fragment LL-37. hCAP18 is constitutively produced in leukocytes and is induced in barrier organs upon inflammation and infection. We demonstrate here a novel role for this peptide in re-epithelialization of skin wounds. We show that high levels of hCAP18 are produced in skin in vivo upon wounding. The highest hCAP18 levels are attained at 48 h post-injury, declining to pre-injury levels upon wound closure. hCAP18 is detected in the inflammatory infiltrate and in the epithelium migrating over the wound bed. In chronic ulcers, however, hCAP18 levels are low and immunoreactivity for hCAP18/LL-37 is absent in ulcer edge epithelium. Using a noninflammatory ex vivo wound healing model, composed of organ-cultured human skin, we show that hCAP18 is strongly expressed in healing skin epithelium, and that treatment with antibodies raised and affinity purified against LL-37, inhibits re-epithelialization in a concentration-dependent manner. Immunoreactivity for the proliferation marker Ki67 is absent in the epithelium of such inhibited wounds, suggesting that LL-37 may play a part in epithelial cell proliferation. Thus, we suggest that, in addition to being an anti-microbial peptide, LL-37 also plays a part in wound closure and that its reduction in chronic wounds impairs re-epithelialization and may contribute to their failure to heal.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Abnormal or dysfunctional AMP production has been associated with susceptibility to microbial infections and several other cutaneous diseases, including nonhealing wounds.
“Abnormal or dysfunctional AMP production has been associated with susceptibility to microbial infections and several other cutaneous diseases, including nonhealing wounds.29”
From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [29]
Wound fluids and skin wounds show elevated levels of cathelicidin expression in keratinocytes and other immune cells, reaching a maximum at 48 h.
“Wound fluids and skin wounds show elevated levels of cathelicidin expression in keratinocytes and other immune cells, reaching a maximum at 48 h.29”
From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [29]
Using a noninflammatory ex vivo wound healing model comprising organ-cultured human skin, hCAP18 is strongly expressed in healing skin epithelium and treatment with affinity-purified antibodies raised against LL-37 inhibits reepithelialization in a concentration-dependent manner.
“Using a noninflammatory ex vivo wound healing model comprising organ-cultured human skin, it has been shown that hCAP18 is strongly expressed in healing skin epithelium and that treatment with affinity-purified antibodies raised against LL-37 inhibits reepithelialization in a concentration-dependent manner.29”
From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [29]
Cathelicidin is low in venous leg ulcers and absent at the margin of other nonhealing wounds.
“Cathelicidin is low in venous leg ulcers and absent at the margin of other nonhealing wounds.29”
From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [29]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works
Solid phase peptide synthesis utilizing 9‐fluorenylmethoxycarbonyl amino acids
Fields, G., & NOBLE, R. L. (1990) · International journal of peptide & protein research · doi:10.1111/j.1399-3011.1990.tb00939.x · Cited by 2,490 · see citing works
A peptide antibiotic from human skin
Harder, J., Bartels, J., Christophers, E., & Schröder, J. ‐. (1997) · Nature · doi:10.1038/43088 · Cited by 1,365 · see citing works
Yang, D., Chen, Q., Schmidt, A. P., Anderson, G. M., Wang, J., Wooters, J., Oppenheim, J. J., & Chertov, O. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.7.1069 · Cited by 1,238 · see citing works
Innate antimicrobial peptide protects the skin from invasive bacterial infection
Nizet, V., Ohtake, T., Lauth, X., Trowbridge, J., Rudisill, J., Dorschner, R. A., Pestonjamasp, V., Piraino, J., Huttner, K., & Gallo, R. L. (2001) · Nature · doi:10.1038/35106587 · Cited by 1,198 · see citing works
Human β-Defensin-1 Is a Salt-Sensitive Antibiotic in Lung That Is Inactivated in Cystic Fibrosis
Goldman, M. J., Anderson, G. M., Stolzenberg, E. D., Kari, U. P., ZASLOFF, M. A., & Wilson, J. M. (1997) · Cell · doi:10.1016/s0092-8674(00)81895-4 · Cited by 1,077 · see citing works
Defensins: Antimicrobial and Cytotoxic Peptides of Mammalian Cells
Lehrer, R. I., Lichtenstein, A. K., & Ganz, T. (1993) · Annual Review of Immunology · doi:10.1146/annurev.iy.11.040193.000541 · Cited by 1,000 · see citing works
Analysis of the acute and chronic wound environments: the role of proteases and their inhibitors
Trengove, N. J., Stacey, M. C., Macauley, S., Bennett, N., Gibson, J., Burslem, F., Murphy, G., & Schultz, G. (1999) · Wound Repair and Regeneration · doi:10.1046/j.1524-475x.1999.00442.x · Cited by 908 · see citing works
Sørensen, O. E., Follin, P., Johnsen, A. H., Calafat, J., Tjabringa, G. S., Hiemstra, P. S., & Borregaard, N. (2001) · Blood · doi:10.1182/blood.v97.12.3951 · Cited by 894 · see citing works
Self-citationFrohm, M., Agerberth, B., Ahangari, G., Ståhle‐Bäckdahl, M., Lidén, S., Wigzell, H., & Gudmundsson, G. H. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.24.15258 · Cited by 803 · see citing works
Self-citationAgerberth, B., Charo, J., Werr, J., Olsson, B., Idali, F., Lindbom, L., Kiessling, R., Jörnvall, H., Wigzell, H., & Gudmundsson, G. H. (2000) · Blood · doi:10.1182/blood.v96.9.3086 · Cited by 758 · see citing works
Bals, R., Wang, X., ZASLOFF, M. A., & Wilson, J. M. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.16.9541 · Cited by 745 · see citing works
Antimicrobial peptides in mammalian and insect host defence
Lehrer, R. I., & Ganz, T. (1999) · Current Opinion in Immunology · doi:10.1016/s0952-7915(99)80005-3 · Cited by 723 · see citing works
Conformation-dependent Antibacterial Activity of the Naturally Occurring Human Peptide LL-37
Johansson, J., Gudmundsson, G. H., Rottenberg, M. E., Berndt, K. D., & Agerberth, B. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.6.3718 · Cited by 662 · see citing works
Gudmundsson, G. H., Agerberth, B., Odeberg, J., Bergman, T., Olsson, B., & Salcedo, R. (1996) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1996.0325z.x · Cited by 579 · see citing works
Dorschner, R. A., Pestonjamasp, V. K., Tamakuwala, S., Ohtake, T., Rudisill, J., Nizet, V., Agerberth, B., Gudmundsson, G. H., & Gallo, R. L. (2001) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2001.01340.x · Cited by 567 · see citing works
Agerberth, B., Gunne, H., Odeberg, J., Kogner, P., Boman, H. G., & Gudmundsson, G. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.1.195 · Cited by 502 · see citing works
Growth factors and wound healing: Part II. Role in normal and chronic wound healing
Bennett, N. T., & Schultz, G. S. (1993) · The American Journal of Surgery · doi:10.1016/s0002-9610(05)80589-6 · Cited by 455 · see citing works
Islam, D., Bandholtz, L., Nilsson, J., Wigzell, H., Christensson, B., Agerberth, B., & Gudmundsson, G. H. (2001) · Nature Medicine · doi:10.1038/84627 · Cited by 429 · see citing works
Delayed wound repair and impaired angiogenesis in mice lacking syndecan-4
Echtermeyer, F. G., Streit, M., Wilcox‐Adelman, S. A., Saoncella, S., Denhez, F., Detmar, M. J., & Goetinck, P. F. (2001) · Journal of Clinical Investigation · doi:10.1172/jci10559 · Cited by 427 · see citing works
PR39, a peptide regulator of angiogenesis
Li, J., Post, M. J., Volk, R., Gao, Y., Li, M., Métais, C., Sato, K., Tsai, J. C., Aird, W. C., ROSENBERG, R. D., et al. (2000) · Nature Medicine · doi:10.1038/71527 · Cited by 387 · see citing works
Sørensen, O. E., Arnljots, K., Cowland, J. B., Bainton, D. F., & Borregaard, N. (1997) · Blood · doi:10.1182/blood.v90.7.2796 · Cited by 364 · see citing works
Self-citationGallo, R. L., Ono, M., Povsic, T. J., Page, C., Eriksson, E. K., Klagsbrun, M., & Bernfield, M. R. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.23.11035 · Cited by 361 · see citing works
Nilsson, M. F., Sandstedt, B., Sørensen, O. E., Weber, G., Borregaard, N., & Ståhle‐Bäckdahl, M. (1999) · Infection and Immunity · doi:10.1128/iai.67.5.2561-2566.1999 · Cited by 351 · see citing works
Self-citationhCAP‐18, a cathelin/pro‐bactenecin‐like protein of human neutrophil specific granules
Cowland, J. B., Johnsen, A. H., & Borregaard, N. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00634-l · Cited by 347 · see citing works
Self-citationAntimicrobial Peptides as Mediators of Epithelial Host Defense
Huttner, K. M., & Bevins, C. L. (1999) · Pediatric Research · doi:10.1203/00006450-199906000-00001 · Cited by 280 · see citing works
Inhibition of cell proliferation by chronic wound fluid
BUCALO, B. D., Eaglstein, W. H., & Falanga, V. (1993) · Wound Repair and Regeneration · doi:10.1046/j.1524-475x.1993.10308.x · Cited by 262 · see citing works
Nagaoka, I., Hirota, S., Niyonsaba, F., Hirata, M., Adachi, Y., Tamura, H., & Heumann, D. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.6.3329 · Cited by 258 · see citing works
Herrick, S. E., Sloan, P., McGurk, M., Freak, L., McCollum, C. N., & Ferguson, M. W. J. (1992) · PubMed Central · Cited by 246 · see citing works
Malm, J., Sørensen, O. E., Persson, T., Frohm‐Nilsson, M., Johansson, B., Bjartell, A. S., Lilja, H. G., Ståhle‐Bäckdahl, M., Borregaard, N., & Egesten, A. (2000) · Infection and Immunity · doi:10.1128/iai.68.7.4297-4302.2000 · Cited by 223 · see citing works
Self-citationBiochemical and Antibacterial Analysis of Human Wound and Blister Fluid
Frohm, M., Gunne, H., Bergman, A., Agerberth, B., Bergman, T., Boman, A., Lidén, S., Jörnvall, H., & Boman, H. G. (1996) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1996.0086n.x · Cited by 212 · see citing works
An ELISA for hCAP-18, the cathelicidin present in human neutrophils and plasma
Sørensen, O. E., Cowland, J. B., Askaa, J., & Borregaard, N. (1997) · Journal of Immunological Methods · doi:10.1016/s0022-1759(97)00084-7 · Cited by 209 · see citing works
Self-citationPrimary structures of MCP-1 and MCP-2, natural peptide antibiotics of rabbit lung macrophages.
Selsted, M. E., Brown, D. M., DeLange, R. J., & Lehrer, R. I. (1983) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)43888-9 · Cited by 205 · see citing works
Antibiotic peptides from higher eukaryotes: biology and applications
Ganz, T., & Lehrer, R. I. (1999) · Molecular Medicine Today · doi:10.1016/s1357-4310(99)01490-2 · Cited by 197 · see citing works
Schmidtchen, A., Frick, I.-M., & Björck, L. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02251.x · Cited by 160 · see citing works
Primary structure of a new cysteine proteinase inhibitor from pig leucocytes
Ritonja, A., Kopitar, M., Jerala, R., & Türk, V. (1989) · FEBS Letters · doi:10.1016/0014-5793(89)81093-2 · Cited by 148 · see citing works
Inoue, M., Kratz, G., Hægerstrand, A., & Ståhle‐Bäckdahl, M. (1995) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12605917 · Cited by 137 · see citing works
Self-citationGrowth Factors and Chronic Wounds: The Need to Understand the Microenvironment
Falanga, V. (1992) · The Journal of Dermatology · doi:10.1111/j.1346-8138.1992.tb03756.x · Cited by 126 · see citing works
Structural, functional analysis and localization of the human CAP18 gene
Larrick, J. W., Lee, J., Ma, S.-W., Li, X., Francke, U., Wright, S. C., & Balint, R. F. (1996) · FEBS Letters · doi:10.1016/s0014-5793(96)01199-4 · Cited by 76 · see citing works
Effect of chronic wound fluid on fibroblasts
Phillips, T. J., Al-Amoudi, H. O., Leverkus, M., & Park, H.-Y. (1998) · Journal of Wound Care · doi:10.12968/jowc.1998.7.10.527 · Cited by 69 · see citing works
Expression of 92-kDa Type IV Collagenase mRNA by Eosinophils Associated with Basal Cell Carcinoma
Ståhle‐Bäckdahl, M., Sudbeck, B. D., Eisen, A. Z., Welgus, H. G., & Parks, W. C. (1992) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12616171 · Cited by 66 · see citing works
Self-citationKratz, G., Lake, M., & Gidlund, M. (1994) · Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery · doi:10.3109/02844319409071187 · Cited by 58 · see citing works
Self-citationAnalysis of extracellular matrix synthesis during wound healing of retinal pigment epithelial cells
Kamei, M., Kawasaki, A., & Tano, Y. (1998) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19980901)42:5 · Cited by 22 · see citing works
Self-citationPhillips, T. J., Palko, M. J., & Bhawan, J. (1994) · Journal of the American Academy of Dermatology · doi:10.1016/s0190-9622(94)70009-5 · Cited by 16 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide
Lande, R., Gregorio, J., Facchinetti, V., Chatterjee, B., Wang, Y.-H., Homey, B., Cao, W., Wang, Y.-H., Su, B., Nestle, F. O., et al. (2007) · Nature · doi:10.1038/nature06116 · Cited by 1,910 · see citing works
Cutting Edge: 1,25-Dihydroxyvitamin D3 Is a Direct Inducer of Antimicrobial Peptide Gene Expression
Wang, T. T., Nestel, F. P., Bourdeau, V., Nagai, Y., Wang, Q., Liao, J. L., Tavera-Mendoza, L. E., Lin, R., Hanrahan, J. W., Mader, S., et al. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.5.2909 · Cited by 1,640 · see citing works
Epithelialization in Wound Healing: A Comprehensive Review
Pastar, I., Stojadinović, O., Yin, N. C., Ramirez, H. A., Nusbaum, A. G., Sawaya, A. P., Patel, S. B., Khalid, L., Isseroff, R. R., & Tomic‐Canic, M. (2014) · Advances in Wound Care · doi:10.1089/wound.2013.0473 · Cited by 1,549 · see citing works
Antimicrobial host defence peptides: functions and clinical potential
Mookherjee, N., Anderson, M. A., Haagsman, H. P., & Davidson, D. J. (2020) · Nature Reviews Drug Discovery · doi:10.1038/s41573-019-0058-8 · Cited by 1,502 · see citing works
AMPed up immunity: how antimicrobial peptides have multiple roles in immune defense
Lai, Y., & Gallo, R. L. (2009) · Trends in Immunology · doi:10.1016/j.it.2008.12.003 · Cited by 1,275 · 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
Falanga, V., Isseroff, R. R., Soulika, A. M., Romanelli, M., Margolis, D. J., Kapp, S., Granick, M. S., & Harding, K. G. (2022) · Nature Reviews Disease Primers · doi:10.1038/s41572-022-00377-3 · Cited by 1,102 · 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
The immunology of host defence peptides: beyond antimicrobial activity
Hancock, R. E. W., Haney, E. F., & Gill, E. E. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.29 · Cited by 947 · see citing works
Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea
Yamasaki, K., Nardo, A. D., Bardan, A., Murakami, M., Ohtake, T., Coda, A. B., Dorschner, R. A., Bonnart, C., Descargues, P., Hovnanian, A., et al. (2007) · Nature Medicine · doi:10.1038/nm1616 · Cited by 852 · see citing works
The Roles of Antimicrobial Peptides in Innate Host Defense
Diamond, G., Beckloff, N., Weinberg, A., & Kisich, K. O. (2009) · Current Pharmaceutical Design · doi:10.2174/138161209788682325 · Cited by 643 · see citing works
Innate immunity in the lung: how epithelial cells fight against respiratory pathogens
Bals, R., & Hiemstra, P. S. (2004) · European Respiratory Journal · doi:10.1183/09031936.03.00098803 · Cited by 589 · see citing works
Yang, D., Biragyn, A., Hoover, D. M., Lubkowski, J., & Oppenheim, J. J. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104603 · Cited by 572 · see citing works
Mookherjee, N., Brown, K. L., Bowdish, D. M. E., Doria, S., Falsafi, R., Hokamp, K., Roche, F. M., Mu, R., Doho, G., Pistolic, J., et al. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.4.2455 · Cited by 562 · see citing works
A comprehensive summary of LL-37, the factotum human cathelicidin peptide
Vandamme, D., Landuyt, B., Luyten, W. H. M. L., & Schoofs, L. (2012) · Cellular Immunology · doi:10.1016/j.cellimm.2012.11.009 · Cited by 565 · see citing works
Niyonsaba, F., Ushio, H., Nakano, N., Ng, W., Sayama, K., Hashimoto, K., Nagaoka, I., Okumura, K., & Ogawa, H. (2006) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700599 · Cited by 544 · see citing works
The Immune Functions of Keratinocytes in Skin Wound Healing
Piipponen, M., Li, D., & Xu, N. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21228790 · Cited by 521 · see citing works
Alarmins: awaiting a clinical response
Chan, J. K.-K., Roth, J., Oppenheim, J. J., Tracey, K. J., Vogl, T., Feldmann, M., Horwood, N. J., & Nanchahal, J. (2012) · Journal of Clinical Investigation · doi:10.1172/jci62423 · Cited by 507 · see citing works
Antimicrobial Peptides: A New Hope in Biomedical and Pharmaceutical Fields
Moretta, A., Scieuzo, C., Petrone, A. M., Salvia, R., Manniello, M. D., Franco, A., Lucchetti, D., Vassallo, A., Vogel, H., Sgambato, A., et al. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.668632 · Cited by 499 · see citing works
Host defense peptides: front-line immunomodulators
Mansour, S., Pena, O. M., & Hancock, R. E. W. (2014) · Trends in Immunology · doi:10.1016/j.it.2014.07.004 · Cited by 493 · see citing works
Antimicrobial peptides as therapeutic agents: opportunities and challenges
Mahlapuu, M., Björn, C., & Ekblom, J. (2020) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2020.1796576 · Cited by 490 · see citing works
Antimicrobial Peptides and Their Therapeutic Potential for Bacterial Skin Infections and Wounds
Pfalzgraff, A., Brandenburg, K., & Weindl, G. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00281 · Cited by 488 · see citing works
Mookherjee, N., & Hancock, R. E. W. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-6475-6 · Cited by 465 · see citing works
Wound healing in the 21st century
Schreml, S., Szeimies, R., Prantl, L., Landthaler, M., & Babilas, P. (2010) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2009.10.048 · Cited by 424 · see citing works
Schwalfenberg, G. (2010) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201000174 · Cited by 416 · see citing works
Antimicrobial peptides and wound healing: biological and therapeutic considerations
Mangoni, M. L., McDermott, A. M., & ZASLOFF, M. A. (2016) · Experimental Dermatology · doi:10.1111/exd.12929 · Cited by 416 · see citing works
The Role of Cathelicidins in the Innate Host Defenses of Mammals
Zanetti, M. (2005) · Current Issues in Molecular Biology · doi:10.21775/cimb.007.179 · Cited by 413 · see citing works
Antimicrobial Peptides: Old Molecules with New Ideas
Nakatsuji, T., & Gallo, R. L. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.387 · Cited by 397 · see citing works
Vitamin D Signaling, Infectious Diseases, and Regulation of Innate Immunity
White, J. H. (2008) · Infection and Immunity · doi:10.1128/iai.00353-08 · Cited by 381 · see citing works
Izadpanah, A., & Gallo, R. L. (2005) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2004.08.026 · Cited by 381 · see citing works
Thapa, R. K., Diep, D. B., & Tønnesen, H. H. (2019) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.12.025 · Cited by 378 · see citing works
Impact of LL-37 on anti-infective immunity
Bowdish, D. M. E., Davidson, D. J., Lau, Y. E., Lee, K. C. L., Scott, M. G., & Hancock, R. E. W. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.0704380 · Cited by 374 · see citing works
Biology and Biomarkers for Wound Healing
Lindley, L. E., Stojadinović, O., Pastar, I., & Tomic‐Canic, M. (2016) · Plastic & Reconstructive Surgery · doi:10.1097/prs.0000000000002682 · Cited by 365 · see citing works
Tokumaru, S., Sayama, K., Shirakata, Y., Komatsuzawa, H., Ouhara, K., Hanakawa, Y., Yahata, Y., Dai, X., Tohyama, M., Nagai, H., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.7.4662 · Cited by 357 · see citing works
Cytokinocytes: the diverse contribution of keratinocytes to immune responses in skin
Jiang, Y., Tsoi, L. C., Billi, A. C., Ward, N. L., Harms, P. W., Zeng, C., Maverakis, E. M., Kahlenberg, J. M., & Gudjonsson, J. E. (2020) · JCI Insight · doi:10.1172/jci.insight.142067 · Cited by 350 · see citing works
Salivary Defense Proteins: Their Network and Role in Innate and Acquired Oral Immunity
Fábián, T., Hermann, P., Beck, A., Fejérdy, P., & Fábián, G. (2012) · International Journal of Molecular Sciences · doi:10.3390/ijms13044295 · Cited by 349 · see citing works
In vitro and In vivo Wound Healing-Promoting Activities of Human Cathelicidin LL-37
Carretero, M., Escamez, M. J., García, M., Duarte, B., Holguín, A., Retamosa, L., Jorcano, J. L., Río, M. D., & Larcher, F. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5701043 · Cited by 345 · see citing works
Rosenfeld, Y., & Shai, Y. (2006) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2006.05.017 · Cited by 322 · see citing works
Postsecretory Processing Generates Multiple Cathelicidins for Enhanced Topical Antimicrobial Defense
Murakami, M., López‐García, B., Braff, M. H., Dorschner, R. A., & Gallo, R. L. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.5.3070 · Cited by 309 · see citing works
Antimicrobial Peptides: An Introduction
Haney, E. F., Mansour, S., & Hancock, R. E. W. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-6737-7_1 · Cited by 303 · see citing works
Parisien, A., Allain, B., Zhang, J., Mandeville, R., & Lan, C. Q. (2007) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2007.03498.x · Cited by 300 · see citing works
Alcayaga‐Miranda, F., Cuenca, J., & Khoury, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00339 · Cited by 297 · see citing works
'MHC-I-opathy'—unified concept for spondyloarthritis and Behçet disease
McGonagle, D., Aydın, S. Z., Gül, A., Mahr, A., & Di̇reskeneli̇, H. (2015) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2015.147 · Cited by 295 · see citing works
Coffelt, S. B., Marini, F. C., Watson, K., Zwezdaryk, K. J., Dembinski, J. L., LaMarca, H. L., Tomchuck, S. L., zu Bentrup, K. H., Danka, E. S., Henkle, S. L., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900244106 · Cited by 292 · see citing works
The Innate Immune System in Acute and Chronic Wounds
MacLeod, A. S., & Mansbridge, J. N. (2016) · Advances in Wound Care · doi:10.1089/wound.2014.0608 · Cited by 289 · see citing works
“Using a noninflammatory ex vivo wound healing model comprising organ-cultured human skin, it has been shown that hCAP18 is strongly expressed in healing skin epithelium and that treatment with affinity-purified antibodies raised against LL-37 inhibits reepithelialization in a concentration-dependent manner.(29) Induct…”
BackgroundInfluentialAntimicrobial Peptide Resistance Mechanisms of Human Bacterial Pathogens
Nizet, V. (2006) · Current Issues in Molecular Biology · doi:10.21775/cimb.008.011 · Cited by 289 · see citing works
Vitamin D and the skin: Focus on a complex relationship: A review
Mostafa, W. Z., & Hegazy, R. A. (2014) · Journal of Advanced Research · doi:10.1016/j.jare.2014.01.011 · Cited by 283 · see citing works
The impact of the pH value on skin integrity and cutaneous wound healing
Schreml, S., Szeimies, R., Karrer, S., Heinlin, J., Landthaler, M., & Babilas, P. (2010) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/j.1468-3083.2009.03413.x · Cited by 279 · see citing works
Antimicrobial peptides: natural effectors of the innate immune system
Radek, K. A., & Gallo, R. L. (2007) · Seminars in Immunopathology · doi:10.1007/s00281-007-0064-5 · Cited by 276 · see citing works
Braff, M. H., Hawkins, M. A., Nardo, A. D., López‐García, B., Howell, M. D., Wong, C., Lin, K. H., Streib, J. E., Dorschner, R. A., Leung, D. Y. M., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.7.4271 · Cited by 275 · see citing works
Froicu, M., & Cantorna, M. T. (2007) · BMC Immunology · doi:10.1186/1471-2172-8-5 · Cited by 274 · see citing works
Wound healing activity of the human antimicrobial peptide LL37
Ramos, R. R., Silva, J. P., Rodrigues, A. C., Costa, R., Guardão, L., Schmitt, F. C., Soares, R. A., Vilanova, M., Domingues, L., & Gama, M. (2011) · Peptides · doi:10.1016/j.peptides.2011.06.005 · Cited by 273 · see citing works
Immunomodulatory Properties of Defensins and Cathelicidins
Bowdish, D. M. E., Davidson, D. J., & Hancock, R. E. W. (2006) · Current topics in microbiology and immunology · doi:10.1007/3-540-29916-5_2 · Cited by 268 · see citing works
Cutaneous Defense Mechanisms by Antimicrobial Peptides
Braff, M. H., Bardan, A., Nizet, V., & Gallo, R. L. (2005) · Journal of Investigative Dermatology · doi:10.1111/j.0022-202x.2004.23587.x · Cited by 265 · see citing works
Human defensins and LL-37 in mucosal immunity
Doss, M., White, M. R., Tecle, T., & Hartshorn, K. L. (2009) · Journal of Leukocyte Biology · doi:10.1189/jlb.0609382 · Cited by 257 · see citing works
Antimicrobial peptides important in innate immunity
Cederlund, A., Gudmundsson, G. H., & Agerberth, B. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08302.x · Cited by 254 · see citing works
Human endogenous antibiotic LL-37 stimulates airway epithelial cell proliferation and wound closure
Shaykhiev, R., Beißwenger, C., Kändler, K., Senske, J., Püchner, A., Damm, T., Behr, J., & Bals, R. (2005) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00286.2004 · Cited by 254 · see citing works
Vitamin D Induces the Antimicrobial Protein hCAP18 in Human Skin
Weber, G., Heilborn, J. D., Chamorro, C. I., Hammarsjö, A., Törmä, H., & Ståhle, M. (2005) · Journal of Investigative Dermatology · doi:10.1111/j.0022-202x.2005.23687.x · Cited by 251 · see citing works
Self-citationGordon, Y. J., Huang, L. C. L., Romanowski, E. G., Yates, K. A., Proske, R. J., & McDermott, A. M. (2005) · Current Eye Research · doi:10.1080/02713680590934111 · Cited by 251 · see citing works
Antimicrobial skin peptides and proteins
Schröder, J. ‐., & Harder, J. (2006) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-5364-0 · Cited by 252 · see citing works
Anti-Fungal Activity of Cathelicidins and their Potential Role in Candida albicans Skin Infection
López‐García, B., Lee, P. H. A., Yamasaki, K., & Gallo, R. L. (2005) · Journal of Investigative Dermatology · doi:10.1111/j.0022-202x.2005.23713.x · Cited by 250 · see citing works
Duplantier, A. J., & van Hoek, M. L. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00143 · Cited by 247 · see citing works
Host defense peptides and their antimicrobial-immunomodulatory duality
Steinstraesser, L., Kraneburg, U. M., Jacobsen, F., & Al‐Benna, S. (2010) · Immunobiology · doi:10.1016/j.imbio.2010.07.003 · Cited by 245 · see citing works
Tjabringa, G. S., Ninaber, D. K., Drijfhout, J. W., Rabe, K. F., & Hiemstra, P. S. (2006) · International Archives of Allergy and Immunology · doi:10.1159/000092305 · Cited by 246 · see citing works
Song, D. W., Kim, S. H., Kim, H. H., Lee, K. H., Ki, C. S., & Park, Y. H. (2016) · Acta Biomaterialia · doi:10.1016/j.actbio.2016.05.008 · Cited by 238 · see citing works
Potential role of propolis in wound healing: Biological properties and therapeutic activities
Oryan, A., Alemzadeh, E., & Moshiri, A. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.12.069 · Cited by 238 · see citing works
Multifunctional antimicrobial peptides: therapeutic targets in several human diseases
Zaiou, M. (2007) · Journal of Molecular Medicine · doi:10.1007/s00109-006-0143-4 · Cited by 236 · see citing works
Aberg, K. M., Radek, K. A., Choi, E., Kim, D.-K., Demerjian, M., Hupe, M., Kerbleski, J. F., Gallo, R. L., Ganz, T., Mauro, T. M., et al. (2007) · Journal of Clinical Investigation · doi:10.1172/jci31726 · Cited by 234 · see citing works
Bowdish, D. M. E., Davidson, D. J., Speert, D. P., & Hancock, R. E. W. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.6.3758 · Cited by 233 · see citing works
MicroRNA-132 enhances transition from inflammation to proliferation during wound healing
Li, D., Wang, A., Liu, X., Meisgen, F., Grünler, J., Botusan, I. R., Narayanan, S., Erikci, E., Li, X., Blomqvist, L., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci79052 · Cited by 231 · see citing works
The cutaneous innate immune response in patients with atopic dermatitis
Kuo, I., Yoshida, T., Benedetto, A. D., & Beck, L. A. (2013) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2012.12.1563 · Cited by 232 · see citing works
Kurosaka, K., Chen, Q., Yarovinsky, F., Oppenheim, J. J., & Yang, D. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.10.6257 · Cited by 222 · see citing works
Co-Regulation and Interdependence of the Mammalian Epidermal Permeability and Antimicrobial Barriers
Aberg, K. M., Man, M., Gallo, R. L., Ganz, T., Crumrine, D. A., Brown, B. E., Choi, E., Kim, D.-K., Schröder, J. M., Feingold, K. R., et al. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5701099 · Cited by 221 · see citing works
Dean, S. N., Bishop, B., & van Hoek, M. L. (2011) · BMC Microbiology · doi:10.1186/1471-2180-11-114 · Cited by 220 · see citing works
Auvynet, C., & Rosenstein, Y. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07360.x · Cited by 213 · see citing works
Innate and Adaptive Immune Responses in Wound Epithelialization
Strbo, N., Yin, N., & Stojadinovic, O. (2014) · Advances in Wound Care · doi:10.1089/wound.2012.0435 · Cited by 200 · see citing works
Strömstedt, A. A., Pasupuleti, M., Schmidtchen, A., & Malmsten, M. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00477-08 · Cited by 201 · see citing works
Vitamin D as an inducer of cathelicidin antimicrobial peptide expression: Past, present and future
White, J. H. (2010) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2010.03.034 · Cited by 199 · see citing works
Antimicrobial peptides and self-DNA in autoimmune skin inflammation
Gilliet, M. F., & Lande, R. (2008) · Current Opinion in Immunology · doi:10.1016/j.coi.2008.06.008 · Cited by 197 · see citing works
Zhang, L., Sen, G. L., Ward, N. L., Johnston, A., Chun, K., Chen, Y., Adase, C. A., Sanford, J. A., Gao, N. J., Chensee, M., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.06.021 · Cited by 196 · see citing works
Therapeutic Potential of Host Defense Peptides in Antibiotic-resistant Infections
Afacan, N. J., Yeung, A. T. Y., Pena, O. M., & Hancock, R. E. W. (2012) · Current Pharmaceutical Design · doi:10.2174/138161212799277617 · Cited by 192 · see citing works
Grönberg, A., Mahlapuu, M., Ståhle, M., Whately‐Smith, C., & Rollman, O. (2014) · Wound Repair and Regeneration · doi:10.1111/wrr.12211 · Cited by 191 · see citing works
Antimicrobial proteins and peptides: anti-infective molecules of mammalian leukocytes
Levy, O. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.0604320 · Cited by 190 · see citing works
Innate Immunity and Angiogenesis
Frantz, S., Vincent, K. A., Féron, O., & Kelly, R. A. (2005) · Circulation Research · doi:10.1161/01.res.0000153188.68898.ac · Cited by 185 · see citing works
Function and therapeutic potential of host defence peptides
McPhee, J. B., & Hancock, R. E. W. (2005) · Journal of Peptide Science · doi:10.1002/psc.704 · Cited by 184 · see citing works
Antimicrobial peptides in human skin disease.
Yamasaki, K., & Gallo, R. L. (2008) · PubMed · doi:10.1684/ejd.2008.0304 · Cited by 179 · see citing works
Pinegin, B. V., Vorobjeva, N. V., & Pinegin, V. B. (2015) · Autoimmunity Reviews · doi:10.1016/j.autrev.2015.03.002 · Cited by 178 · see citing works
Reactive Oxygen Species, Apoptosis, Antimicrobial Peptides and Human Inflammatory Diseases
Oyinloye, B. E., Adenowo, A. F., & Kappo, A. P. (2015) · Pharmaceuticals · doi:10.3390/ph8020151 · Cited by 170 · see citing works
Barlow, P. G., Li, Y., Wilkinson, T. S., Bowdish, D. M. E., Lau, Y. E., Cosseau, C., Haslett, C., Simpson, A. J., Hancock, R. E. W., & Davidson, D. J. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.1005560 · Cited by 168 · see citing works
Host Defense Peptides in Wound Healing
Steinstraesser, L., Koehler, T., Jacobsen, F., Daigeler, A., Goertz, O., Langer, S., Kesting, M. R., Steinau, H. U., Eriksson, E. K., & Hirsch, T. (2008) · Molecular Medicine · doi:10.2119/2008-00002.steinstraesser · Cited by 166 · see citing works
Vitamin D and the skin: an ancient friend, revisited
Reichrath, J. (2007) · Experimental Dermatology · doi:10.1111/j.1600-0625.2007.00570.x · Cited by 166 · see citing works
Functionalization of electrospun polymeric wound dressings with antimicrobial peptides
Felgueiras, H. P., & de Amorim, M. T. P. (2017) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2017.05.001 · Cited by 165 · see citing works
Intracellular Receptor for Human Host Defense Peptide LL-37 in Monocytes
Mookherjee, N., Lippert, D. N. D., Hamill, P., Falsafi, R., Nijnik, A., Kindrachuk, J., Pistolic, J., Gardy, J. L., Miri, P., Naseer, M., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802586 · Cited by 162 · see citing works
Cathelicidins Modulate TLR-Activation and Inflammation
Scheenstra, M. R., van Harten, R. M., Veldhuizen, E. J. A., Haagsman, H. P., & Coorens, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01137 · Cited by 164 · see citing works
The host defence peptide LL-37/hCAP-18 is a growth factor for lung cancer cells
von Haussen, J., Koczulla, A. R., Shaykhiev, R., Herr, C., Pinkenburg, O., Reimer, D., Wiewrodt, R. G., Biesterfeld, S., Aigner, A. M., Czubayko, F., et al. (2007) · Lung Cancer · doi:10.1016/j.lungcan.2007.07.014 · Cited by 161 · see citing works
Antimicrobial Peptides: An Essential Component of the Skin Defensive Barrier
Braff, M. H., & Gallo, R. L. (2006) · Springer eBooks · doi:10.1007/3-540-29916-5_4 · Cited by 159 · see citing works
Tomasinsig, L., Pizzirani, C., Skerlavaj, B., Pellegatti, P., Gulinelli, S., Tossi, A., Virgilio, F. D., & Zanetti, M. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m802185200 · Cited by 158 · see citing works
Antimicrobial peptides: Clinical relevance and therapeutic implications
da Silva, F. P., & Machado, M. C. C. (2012) · Peptides · doi:10.1016/j.peptides.2012.05.014 · Cited by 155 · see citing works
Alalwani, S. M., Sierigk, J., Herr, C., Pinkenburg, O., Gallo, R. L., Vogelmeier, C. F., & Bals, R. (2010) · European Journal of Immunology · doi:10.1002/eji.200939275 · Cited by 151 · see citing works
Attenuation of the Transforming Growth Factor β-Signaling Pathway in Chronic Venous Ulcers
Pastar, I., Stojadinović, O., Krzyzanowska, A. K., Barrientos, S., Stuelten, C. H., Zimmerman, K. K., Blumenberg, M., Brem, H., & Tomic‐Canic, M. (2010) · Molecular Medicine · doi:10.2119/molmed.2009.00149 · Cited by 153 · see citing works
- Authors
- Heilborn, J. D., Nilsson, M. F., Sørensen, O., Ståhle-Bäckdahl, M., Kratz, G., Weber, G., & Borregaard, N.
- Affiliations
- Karolinska Institutet (SE)
- Rigshospitalet (DK)
- Venue
- Journal of Investigative Dermatology
- Publisher
- Elsevier BV
- Published
- 2003-03
- Volume
- 120
- Issue
- 3
- Pages
- 379-389
- ISSN
- 0022-202X (ISSN-L)
- OpenAlex
- W2072432297
- Cited by
- 572
- References
- 44
- Citations by year
- 2026: 16 · 2025: 13 · 2024: 15 · 2023: 22 · 2022: 19 · 2021: 28 · 2020: 17 · 2019: 15 · 2018: 21 · 2017: 28 · 2016: 28 · 2015: 25 · 2014: 25 · 2013: 33 · 2012: 39
- FWCI
- 24.02
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Investigative Dermatology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Life Sciences › Immunology and Microbiology › Microbiology › Antimicrobial Peptides and Activities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › S100 Proteins and Annexins
- Keywords
- LL-37, cathelicidin, hCAP18, re-epithelialization, skin wound healing, chronic wounds, chronic ulcers, epithelial cell proliferation, Ki-67, innate immunity, antimicrobial peptides, antibody inhibition
- MeSH terms
- Antibodies, Bacillus megaterium, Chronic Disease, Dose-Response Relationship, Drug, Epithelium, Humans, Immune Sera, Leg Ulcer, Organ Culture Techniques, Skin, Wound Healing, Wounds, Penetrating, Keratinocytes, Ki-67 Antigen, Antimicrobial Cationic Peptides, Cathelicidins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review