Sociedad Americana de Hirudoterapia

Hirunipin-2

Specific hirunipin variant (Kumar 2025) active against multi-drug-resistant Acinetobacter baumannii — biofilm eradication, antibiotic synergy, anti-inflammatory in macrophages.

Preclínico / mecanísticoLast updated: 2026-05-27 · Reviewed by ASH Editorial Board
Molecular weight of Hirunipin-2 compared with other characterized leech-derived compoundsHementerin80 kDaHementin80 kDaHementin-Like Protein (HLP-1)80 kDaLeech Collagenase70 kDaHaemadipsa yanyuanensis Progr…70 kDaLeech Apyrase67 kDaCalin65 kDaHyaluronidase60 kDaAntithrombin III binding prot…58 kDaCollagenolytic Fibrinolysin55 kDaLeech Thrombospondin-Like Pro…50 kDaHirunipin-23.2 kDa
Molecular weight (kilodaltons) of Hirunipin-2 (highlighted) alongside other characterized leech salivary compounds. Smaller proteins/peptides generally diffuse and act faster.

Mechanistic Evidence Box

Preclinical / mechanistic
Page type
Compound profile
Evidence type
Specific hirunipin variant (Kumar 2025) active against multi-drug-resistant Acinetobacter baumannii — biofilm eradication, antibiotic synergy, anti-inflammatory in macrophages.
Evidence level
In vitro
Drug vs leech
Purified natural compound
Safety domains
Antibiotic stewardship

Clinical translation limit

Hirunipin-2's in vitro antimicrobial and antibiofilm activity does NOT establish clinical efficacy. No FDA-approved hirunipin derivative exists; in vitro 'comparable to melittin' framing is a research benchmark, not a clinical milestone.

Molecular Profile

Category
Antimicrobial
Evidence tier
Preclinical
Molecular weight
3,200 Da
Source species
Hirudo medicinalis (secretory cells)
Discovered
2025 · Kumar SD et al.
Hirunipin-2 molecular structure

Biological Targets

  • multi-drug-resistant Acinetobacter baumannii (MDRAB)
  • bacterial membrane permeability
  • biofilm matrix

Key Citations

  1. Kumar SD et al. (2025), Adv Sci (Weinh) · PMID 39792785

External Resources

    Related Antimicrobial Compounds

    Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.