How does the healing process of a wound occur?

Approximately 24 hours later, the haemostasis phase is followed by a dilation of the blood capillaries, allowing the influx of various inflammatory cells, such as neutrophils, monocytes, and lymphocytes, towards the wound. It is the chemoattractants, growth factors, and cytokines, released by the platelets, that promote this migration of inflammatory cells to reach the damaged tissue. At this stage, the wound exhibits all the characteristic signs of inflammation: redness and heat due to vasodilation, pain due to pressure on sensitive nerve endings, and swelling due to plasma exudation.

Neutrophils are the first inflammatory cells to arrive, peaking after 24 hours. They phagocytose bacteria and eliminate cellular debris, enabling wound decontamination. Polymorphonuclear leukocytes, on the other hand, release reactive oxygen species (ROS) that potentiate this destruction process.

Macrophages assist in initiating the proliferation phase. These cells also fulfil various functions, including promoting the inflammatory healing process through the release of cytokines, the removal of cellular debris, and the attraction of blast cells to the wound area. All processes occur simultaneously but in a synchronised manner. The duration of the inflammatory phase typically lasts between three and six days.

Once the wound is stabilised, it switches to reconstruction mode. This proliferation phase does not occur at a specific time, but continues constantly in the background. Immediately after the inflammatory phase begins to organise within a network of collagen and elastin, produced by the fibroblasts, a granulation tissue with new capillary formation (neovascularisation or angiogenesis) that will deliver in situ the oxygen, nutrients and cells necessary for tissue repair. Around days 5 to 7, the platelet-derived growth factor attracts the fibroblasts and, along with the transforming growth factor (TGF), enhances the division and multiplication of fibroblasts.

They infiltrate the wound site, proliferate and differentiate into myofibroblasts to begin producing new collagen, hyaluronic acid, and fibronectin. These components form the core of the wound that will serve as a scaffold. Subsequently, re-epithelialisation begins to occur with the migration of cells from the periphery of the wound and adjacent edges.

Initially, only a thin superficial layer of epithelial cells is deposited, but a thicker and more durable layer of cells will fill the wound over time. Subsequently, neovascularisation occurs both through angiogenesis, forming new blood vessels from existing ones, and through vasculogenesis, which is the formation of new vessels from endothelial progenitor cells (EPCs). Once the collagen fibres are deposited on the fibrin structure, the wound begins to mature. It also begins to contract and is facilitated by the continuous deposition of fibroblasts and myofibroblasts. At this stage, the skin appears red and raised.

At this stage, macrophages continue to play a crucial role by producing growth factors or cytokines capable of promoting fibroblastic proliferation and collagen synthesis. At this point, the scar is a young fibrosis containing numerous fibroblasts and a loose fibrillar framework on the periphery of the substance loss.

The fleshy bud is composed of fibroblasts, an inflammatory infiltrate (monocytes, lymphocytes, polymorphonuclear cells), fibrin on the surface, and neo-vessels within an oedematous fibrillar framework. The contraction of the wound to bring its edges closer together is closely linked to the formation of granulation tissue and the transformation of certain fibroblasts into myofibroblasts capable of contracting and transmitting their contractile activity to the surrounding tissue through interaction between the proteins of the cytoskeleton and the extracellular matrix. This phase, very active from the 7th day, can last up to 3 weeks.

Following tissue repair, the wound contracts and is gradually covered by a new epithelium (epithelialisation). The epidermal cells (keratinocytes) multiply and begin to cover the granulation tissue, starting from the edges of the wound. In order to migrate properly, these keratinocytes require a healthy, moist and level granulation tissue. Following the formation of this initial cellular layer, the epithelium is thickened by cell division and soon becomes more resilient. The wound is closed.

Maturation is the healing stage when a scar softens, flattens, and fades. During this final phase, which begins around the third week, the wound reaches maximum strength as it matures. Depending on the severity of the wound, the remodelling may take a year or more to be fully completed.

During this stage, the contraction of the wound has reached its peak. The maximum tensile strength of the incision wound occurs after approximately 11 to 14 weeks. The resulting scar will never have 100% of the initial strength of the wound and only about 80% of its tensile strength.

The granulation tissue recedes, giving way to fibrous connective tissue. The thickening collagen fibres increase resistance to tensile forces. The number of capillaries, as well as blood flow, decrease. Excess water and vessels then disappear, and the scar tightens. However, scars are always less resilient and less elastic than normal skin, partly due to a certain deficit in elastin. This phase can last from several months to 2 years.