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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 2
2022 pubmed 11 citations

<i>In vitro</i> Screening of Herbal Medicinal Products for Their Supportive Curing Potential in the Context of SARS-CoV-2.

Tran. Hoai Thi Thu HTT; Peterburs. Philipp P; Seibel. Jan J; Abramov-Sommariva. D D; Lamy. Evelyn E

Key Findings

  • Imupret and Bronchipret thyme‑ivy reduced spike‑ACE2 binding in vitro
  • Bronchipret thyme‑primula increased LL‑37 release from lung cells when exposed to spike protein
  • Sinupret, Tonsipret and Bronchipret thyme‑ivy raised IFN‑γ production in immune cells

Practical Outcomes

  • These herbs might help stimulate innate immunity, but there’s no human data on effective doses or safety for this purpose. Biohackers could experiment with standard commercial doses as a supplemental immune boost, while watching for any side effects, and should not rely on them as a cure for COVID‑19.

Summary

In lab tests, a few herbal mixes used for colds (Imupret, Bronchipret thyme‑ivy, and Bronchipret thyme‑primula) showed the ability to block the virus‑spike protein from binding to the ACE2 receptor and to boost natural antimicrobial peptides like LL‑37 and immune signals such as IFN‑γ. These effects were seen only in cell cultures, not in people, so they are early clues rather than proven treatments.

Abstract

COVID-19 herbal medicinal products may have the potential for symptom relief in nonsevere or moderate disease cases. In this <i>in vitro</i> study we screened the five herbal medicinal products Sinupret extract (SINx), Bronchipret thyme-ivy (BRO-TE), Bronchipret thyme-primula (BRO TP), Imupret (IMU), and Tonsipret (TOP) with regard to their potential to (i) interfere with the binding of the human angiotensin-converting enzyme 2 (ACE2) receptor with the SARS-CoV-2 spike S1 protein, (ii) modulate the release of the human defensin HBD1 and cathelicidin LL-37 from human A549 lung cells upon spike S1 protein stimulation, and (iii) modulate the release of IFN-<i>&#x3b3;</i> from activated human peripheral blood mononuclear cells (PBMC). The effect of the extracts on the interaction of spike S1 protein and the human ACE2 receptor was measured by ELISA. The effects on the intracellular IFN-<i>&#x3b3;</i> expression in stimulated human PBMC were measured by flow cytometry. Regulation of HBD1 and LL-37 expression and secretion was assessed in 25&#x2009;d long-term cultured human lung A549 epithelial cells by RT-PCR and ELISA. IMU and BRO-TE concentration-dependently inhibited the interaction between spike S1 protein and the ACE2 receptor. SINx, TOP, and BRO-TE significantly upregulated the intracellular expression of anti-viral IFN-<i>&#x3b3;</i> from stimulated PBMC. Cotreatment of A549 cells with IMU or BRO TP together with SARS-CoV-2 spike protein significantly upregulated mRNA expression (IMU) and release of HBD1 (IMU and BRO TP) and LL-37 (BRO TP). The <i>in vitro</i> screening results provide first evidence for an immune-activating potential of some of the tested herbal medicinal extracts in the context of SARS-CoV-2. Whether these could be supportive in symptom relief or curing from SARS-CoV-2 infection needs deeper understanding of the observations.

Study Information

Provider

pubmed

Year

2022

Date

2022-09-06T00:00:00.000Z

DOI

10.1155/2022/8038195

Citations

11

References

56