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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

An antimicrobial peptide of the cathelicidin family that provides innate immune defense by killing pathogens and modulating inflammation and wound healing.

Quick Stats
Studies 2230
Trials 95
Formula C205H340N60O53
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Utility 2
pubmed Feb 2, 2012

Msb2 shedding protects Candida albicans against antimicrobial peptides.

Szafranski-Schneider. Eva E; Swidergall. Marc M; Cottier. Fabien F; Tielker. Denis D; Román. El...

The fungus Candida albicans releases a large sugar‑coated piece of a protein called Msb2 that can bind and neutralize the human antimicrobial peptide LL‑37, stopping it from killing the fungus. This protection isn’t because the peptide is broken down, but because the Msb2 fragment blocks its activity. Fungi lacking Msb2 are much more vulnerable to LL‑37.

Utility 2
pubmed Jul 16, 2012

Effect of vitamin D supplementation on Mycobacterium tuberculosis-induced innate immune responses in a Canadian Dené First Nations cohort.

Larcombe. Linda L; Orr. Pamela P; Turner-Brannen. Emily E; Slivinski. Caroline R CR; Nickerson. Pete...

Taking vitamin D didn’t raise the blood levels of the antimicrobial peptide LL‑37 and didn’t change how immune cells make LL‑37, but it did shift other immune signals in ways that differed between Caucasian and Canadian First Nations people. This means vitamin D isn’t a reliable way to boost LL‑37 for most people, and its immune effects may vary by ethnicity.

Utility 2
pubmed Jan 14, 2013

Cathelicidin LL-37 bloodstream surveillance is down regulated during septic shock.

Barbeiro. Denise Frediani DF; Barbeiro. Hermes Vieira HV; Zampieri. Fernando Godinho FG; César...

The study shows that the immune peptide LL‑37, which normally helps protect the body from infection, actually falls to lower levels in the blood during septic shock, and this drop isn’t caused by low vitamin D.

Utility 2
pubmed Jul 3, 2012

Alveolar macrophage cathelicidin deficiency in severe sarcoidosis.

Barna. Barbara P BP; Culver. Daniel A DA; Kanchwala. Ali A; Singh. Ravinder J RJ; Huizar. Isham I; A...

The study found that people with severe sarcoidosis have lower levels of the immune‑boosting peptide LL‑37 in their lung cells, even though their active vitamin D3 levels are normal. This drop is linked to high inflammation signals (TNF‑α) that suppress a helper protein (SRC3) needed for LL‑37 production. In simpler terms, inflammation can block the body’s natural production of this antimicrobial peptide despite adequate vitamin D.

Utility 2
pubmed Feb 26, 2013

Real-time attack of LL-37 on single Bacillus subtilis cells.

Barns. Kenneth J KJ; Weisshaar. James C JC

The study shows that the human antimicrobial peptide LL‑37 kills Bacillus subtilis bacteria in a dose‑dependent way: low levels (2 µM) just slow bacterial growth, while higher levels (4 µM) quickly break the cell membrane and kill the bacteria irreversibly.

Utility 2
pubmed Jan 30, 2013

Effects of high-dose cholecalciferol on serum markers of inflammation and immunity in patients with early chronic kidney disease.

Alvarez. J A JA; Zughaier. S M SM; Law. J J; Hao. L L; Wasse. H H; Ziegler. T R TR; Tangpricha. V V

A year‑long study gave people with early kidney disease a high dose of vitamin D (50,000 IU weekly then every other week). After 12 weeks their blood level of the inflammation signal MCP‑1 went down, but the effect faded by the end of the year. Other immune markers, including the peptide LL‑37, didn’t change.

Utility 2
pubmed Aug 28, 2012

Defense peptides secreted by helminth pathogens: antimicrobial and/or immunomodulator molecules?

Cotton. Sophie S; Donnelly. Sheila S; Robinson. Mark W MW; Dalton. John P JP; Thivierge. Karine K

Scientists found that some worm parasites make tiny proteins that look a lot like the human immune peptide LL‑37. These worm‑derived peptides can kill microbes and also tweak the immune system, possibly explaining why worm infections sometimes reduce inflammation. The study is basic research and doesn’t give any dosage or supplement advice for everyday use.

Utility 2
pubmed Jun 14, 2013

Using electrospun poly(ethylene-oxide) nanofibers for improved retention and efficacy of bacteriolytic antibiotics.

Gatti. John W JW; Smithgall. Marie C MC; Paranjape. Shruti M SM; Rolfes. Ronda J RJ; Paranjape. Maka...

Scientists showed that the antimicrobial peptide LL‑37 can be mixed into ultra‑thin fibers made from a polymer (PEO) using a process called electrospinning, and it still works to kill bacteria. The fibers slowly release the peptide, creating a small antibacterial zone in lab tests.

Utility 2
pubmed Dec 10, 2012

IQ-motif peptides as novel anti-microbial agents.

McLean. Denise T F DT; Lundy. Fionnuala T FT; Timson. David J DJ

Researchers tested short pieces of proteins called IQ‑motif peptides and found some of them can kill common bacteria and a fungus as well as the well‑known antimicrobial peptide LL‑37, while causing little damage to human cells. This shows they could be useful starting points for new antimicrobial agents, but they’re still early‑stage lab findings.

Utility 2
pubmed Apr 29, 2013

Cigarette smoke extract induces differential expression levels of beta-defensin peptides in human alveolar epithelial cells.

Pierson. Tony T; Learmonth-Pierson. Sarah S; Pinto. Daniel D; van Hoek. Monique L ML

Researchers exposed lung cells to cigarette smoke extract and measured antimicrobial peptide genes. They saw that three beta-defensin genes (hBD3, hBD5, hBD9) went up, while LL‑37 and several others stayed the same. This shows smoking changes some, but not all, of these immune‑related peptides in lung cells.

Utility 2
pubmed Jul 15, 2013

Cathelicidin antimicrobial peptide inhibits fibroblast migration via P2X7 receptor signaling.

Kumagai. Shohei S; Matsui. Kazuki K; Kawaguchi. Haruyo H; Yamashita. Tomomi T; Mohri. Tomomi T; Fuji...

The study found that the natural peptide LL-37 can slow down the movement of heart fibroblast cells, which are key players in forming scar tissue (fibrosis) after heart inflammation. It does this by activating a specific receptor (P2X7) and downstream signaling pathways. While this suggests LL-37 might help prevent heart scarring, the work was done in mouse hearts and cell cultures, not in people.

Utility 2
pubmed Dec 1, 2011

Antimicrobial peptides in nasal secretion and mucosa with respect to Staphylococcus aureus colonization in chronic rhinosinusitis with nasal polyps.

Thienhaus. Maike Luisa ML; Wohlers. Janet J; Podschun. Rainer R; Hedderich. Jürgen J; Ambrosch....

The study shows that the antimicrobial peptide LL‑37 normally spikes in the nose when Staph aureus is present, but this boost is missing in people with chronic sinus inflammation and nasal polyps, suggesting a weakened local defense. The other peptide hBD‑3 didn’t change, and nasal cells can still make LL‑37 when directly exposed to the bacteria.

Utility 2
pubmed May 31, 2013

Gingival crevicular fluid levels of human beta-defensin-2 and cathelicidin in smoker and non-smoker patients: a cross-sectional study.

Ertugrul. A S AS; Sahin. H H; Dikilitas. A A; Alpaslan. N Z NZ; Bozoğlan. A A; Tekin. Y Y

The study measured two natural antimicrobial proteins, LL‑37 and hBD‑2, in the gum fluid of people with gum disease. It found that smokers have higher levels of these proteins than non‑smokers, especially in severe gum disease, while people with mild gum inflammation have the lowest levels.

Utility 2
pubmed Apr 1, 2012

MxA expression induced by α-defensin in healthy human periodontal tissue.

Mahanonda. Rangsini R; Sa-Ard-Iam. Noppadol N; Rerkyen. Pimprapa P; Thitithanyanont. Arunee A; Subba...

The study shows that healthy gum tissue naturally has more of an antiviral protein called MxA, and this boost comes from a natural peptide called α‑defensin, not from the peptide LL‑37. In lab tests, only α‑defensin made gum cells produce MxA and helped protect them from flu virus, while LL‑37 had no effect.

Utility 2
pubmed Jul 18, 2012

Functional epistatic interaction between rs6046G>A in F7 and rs5355C>T in SELE modifies systolic blood pressure levels.

El Shamieh. Said S; Ndiaye. Ndeye Coumba NC; Stathopoulou. Maria G MG; Murray. Helena A HA; Masson....

The study found that two common genetic variants, one in the F7 gene and another in the SELE gene, each lower blood pressure and together have a bigger effect. The F7 variant also raises levels of a protein called NAMPT, which in turn is linked to higher expression of the antimicrobial peptide LL‑37. Higher LL‑37 levels were modestly associated with higher systolic blood pressure, explaining about 4% of its variation. These results suggest a genetic‑inflammation link to blood pressure but don’t give a clear way to change it.

Utility 2
pubmed Jan 31, 2012

Peptides in oral diseases.

Lucchese. Alberta A; Guida. Agostino A; Petruzzi. Massimo M; Capone. Giovanni G; Laino. Luigi L; Ser...

This paper reviews how natural antimicrobial proteins like LL‑37 might help fight gum disease, cavities, and other mouth problems caused by microbes, but it doesn’t give a clear recipe for using them. It points out that LL‑37 can kill bacteria and viruses and also calm inflammation, making it an interesting candidate for future mouth‑care products.

Utility 2
pubmed Dec 10, 2012

A novel role of a lipid species, sphingosine-1-phosphate, in epithelial innate immunity.

Park. Kyungho K; Elias. Peter M PM; Shin. Kyoung-Oh KO; Lee. Yong-Moon YM; Hupe. Melanie M; Borkowsk...

The study shows that a skin lipid called sphingosine‑1‑phosphate (S1P) triggers skin cells to make more of the natural antibiotic peptide LL‑37 when they’re under stress, and this extra LL‑37 helps kill Staph bacteria on the skin.

Utility 2
pubmed Oct 4, 2012

A bacterial pathogen co-opts host plasmin to resist killing by cathelicidin antimicrobial peptides.

Hollands. Andrew A; Gonzalez. David D; Leire. Emma E; Donald. Cortny C; Gallo. Richard L RL; Sanders...

The study shows that a common bacteria (Group A Strep) can hijack a human enzyme called plasmin to chop up the natural antimicrobial peptide LL‑37, helping the bug avoid being killed. When the bacteria can’t use plasmin, they’re more vulnerable to LL‑37, and blocking plasmin in mice makes infections less severe.

Utility 2
pubmed Sep 28, 2012

Rhinovirus infection induces degradation of antimicrobial peptides and secondary bacterial infection in chronic obstructive pulmonary disease.

Mallia. Patrick P; Footitt. Joseph J; Sotero. Rosa R; Jepson. Annette A; Contoli. Marco M; Trujillo-...

In people with COPD, catching a common cold virus often leads to a follow‑up bacterial lung infection. The virus triggers a rise in an enzyme called neutrophil elastase, which breaks down natural antimicrobial proteins (like SLPI and elafin) that normally keep bacteria in check. When these defenses are weakened, bacteria grow, worsening symptoms. The study suggests that blocking elastase or boosting innate immunity could help prevent these secondary infections.

Utility 2
pubmed Aug 2, 2012

Antimicrobial peptides and nitric oxide production by neutrophils from periodontitis subjects.

Mariano. F S FS; Campanelli. A P AP; Nociti. F H FH; Mattos-Graner. R O RO; Gonçalves. R B RB

The study shows that people with gum disease have immune cells that make more of the antimicrobial peptide LL‑37 but less nitric oxide, which together might affect how the disease progresses. It doesn’t test any treatments, just compares healthy and diseased individuals.