TB-500
TB-500 is a commercial research name associated with thymosin beta-4–related material. The peer-reviewed literature is overwhelmingly about thymosin beta-4 (Tβ4), an endogenous 43-amino-acid actin-binding peptide. Because commercial TB-500 identity and formulation can vary, WILGO does not treat every Tβ4 paper as proof about every material sold under the TB-500 name.
What kind of evidence exists?
This page deliberately distinguishes native thymosin β4 evidence from the looser commercial label TB-500.
The naming problem is scientifically important.
Many websites collapse “TB-500” and “thymosin beta-4” into a single term. That is too loose for a research index. WILGO therefore labels the underlying literature as Tβ4 evidence and keeps the commercial-name inference explicit.
Selected studies.
Selected sources are grouped by study type so model limitations remain visible.
Thymosin beta4 accelerates wound healing
In a full-thickness rodent wound model, Tβ4 increased re-epithelialization, wound contraction, collagen deposition, and angiogenesis; it also stimulated keratinocyte migration in vitro. This is foundational preclinical wound-healing evidence for native Tβ4.
The actin binding site on thymosin beta4 promotes angiogenesis
Using endothelial migration and vessel-sprouting assays, the study identified the actin-binding motif of Tβ4 as essential to its angiogenic activity.
Thymosin beta4 enhances endothelial cell differentiation and angiogenesis
Exogenous Tβ4 increased endothelial tube formation and vascular sprouting in experimental systems, supporting autocrine/paracrine roles in vessel formation.
Thymosin β4 has a major role in dermal burn wound healing that involves actin cytoskeletal remodelling via heat-shock protein 70
Cell and dermal-burn experiments linked Tβ4 with HSP70-related actin remodeling, wound closure, and vascularization. The work remains preclinical.
The regenerative peptide thymosin β4 accelerates the rate of dermal healing in preclinical animal models and in patients
This translational review describes animal wound models and two phase 2 clinical trials involving stasis and pressure ulcers, reporting faster healing among wounds that healed.
Thymosin β4 and the vasculature: multiple roles in development, repair and protection against disease
The review covers vasculogenesis, angiogenesis, arteriogenesis, endothelial-mesenchymal transition, extracellular-matrix remodeling, and remaining uncertainty about molecular mechanisms.
Primary sources.
Direct PubMed links are used wherever possible.