Critical wounds are well known to develop in elderly people and in other conditions where inflammation, vascular, and nervous disease lead to chronical inefficiency in running up healing processes. Recent researches have been focusing on microenvironment, and specific technologies have contributed to design and produce new materials (the era of biomaterials and devices in wound healing).
- adipose-derived stem cells
- difficult wounds
- vascular supply
Wound healing is a highly structured physiological process involving cells and signal molecules; it is known to run throughout inflammation, cell proliferation, angiogenesis, collagen deposition, and re-epithelization . In the very first steps, natural immunity  plays an important role through aggregation of inflammasomes. The next step goes through inflammatory cell types, and messages from the first to this step together with monocyte responsivity are able to determine whether inflammation will prolong to a sort of a steady, chronically established state, which freezes the whole process transforming it into a chronic inflammation [2–6].
Monocyte/macrophage sequestration together with their lack of switch to type 2 [3, 4, 6] impairs angiogenesis and cell activities resulting in a delayed re-epithelialization, reduced call for fibroblasts and diminishing collagen deposition, as well as a decreased cell proliferation.
The aim of this chapter is to report our experience on how to modify impaired wound healing, starting from our experimental studies and concluding with our recent clinical experiences.
Following our studies  and those by Mirza et al. [4, 5], we started to focus on the role of accumulation and insufficiency of macrophages in wound healing. Macrophage dysfunction has been shown to produce prolonged inflammatory responses in critical wounds, in diabetes through local secretion of proinflammatory cytokines, such as IL-1β, TNF-α, MMP-9, and IL-6, in particular, lack of switch to a second macrophage phenotype secreting proregenerative factors, such as IL-10, IGF-1, and TGF-β .
The result is an important interruption of healing with persistence of inflammation, whether hyperglycemia through cascade of ROS is its cause or not.
This produces critical wounds. Obviously, single biological steps can be analyzed in experimental studies, whereas in clinical practice this single factor must often be added to other associated diseases, such as reduction of blood supply due to vascular obstruction. In the latter case, translation from experimental to clinical work must also take into account adding proangiogenetic factors even to provide a complete care.
Our clinical experience deals with persistence of inflammation through both monocyte and vascular insufficiency.
2.1. Our experimental studies on wound healing
In this section, we report our experimental evidences leading to the results about the above-mentioned inflammasome inhibition . Plastic surgeons together with pharmacologists of the University of Messina have been working on wound healing for more than 15 years developing some models on rodents.
For these experiments adult male mice have been chosen, caged alone, and maintained under a controlled environment (12-hour light cycles day/night and 23°C room temperature, food, and water ad libitum) following Helsinki’s declaration and European and Italian laws and Guidelines for Animal Laboratory Experiments.
Animals aging 8 weeks and weighing 20–25 g were used.
2.2. Model of incisional wound healing
The animals (mice) underwent general anesthesia with sodium thiopental (80 mg/kg intraperitoneal injection) were scrubbed with iodine povidone on their back – their back skin shaved and rinsed with physiological serum. Two longitudinal parallel 4 cm incisions were performed and sutured with alternate stitches placed 1 cm from one another.
Sacrifices were conducted on Days 7 and 14, respectively, and wounds were divided into three segments of 80 mm large and 120 mm long. Caudal and cranial strips were used for molecular studies, whereas the central one was used for histology and immunohistochemistry.
2.3. Model of dorsal skin flap
The animals (mice) underwent general anesthesia with sodium thiopental (80 mg/kg intraperitoneal injection) were scrubbed with iodine povidone on their back – their back skin shaved and rinsed with physiological serum. Double H flap consists of two opposite flaps: the former pedicled from the cranial side and the latter from the caudal one, both to be incised and elevated on the dorsal skin. The central horizontal wound together with the two distal parts of the flaps acts as critical ischemia-risk area. The flaps were sutured back with separate stitches in Nylon 4/0. The animals were divided into three groups and sacrifices were performed on Days 3, 6, and 12, respectively. As for incisional wounds, three flap segments were taken and processed the cranial and distal one for molecular essays, the central one for histology and immunocytochemistry
2.4. Model of burn injury
Under the same anesthesia and dorsum preparation described above, the dorsum of mice was immersed in an 80°C bath for 10 seconds to produce a scald burn. Fluid resuscitation was achieved through a subcutaneous 1 mL saline injection, treated with different agents (last used EPO Z in comparison with EPO alpha), divided into three groups, and sacrificed on Days 3, 6, and 12, respectively. Burned skin has been divided into two flaps that have been, respectively, used for molecular essays and histology.
Molecular essays are consisted in cytoplasmic protein dosage (Bio-Rad Protein Assay (Bio-Rad Lab, Richmond, CA, USA), spectrophotometry, using albumin as a standard); Western blot for GFs and cell cycle molecules; histology measured the presence of inflammatory infiltrates, necrosis, and repair in standard hematoxylin (eosin, trichromic, and immunohistochemistry were used to visualize and quantify alpha-smooth positive cells such as a response to VEGF in both neoangiogenesis and neovasculogenesis).
Statistical analysis was conducted with parametric essays for repeated measures (ANOVA) and bonferroni test was used to evaluate intergroup positivity, with a
Our experimental studies have pointed out some important features of antioxidant molecules in impaired wound healing (diabetic mice), as well as the role of some cytokine-related molecules and endogenous products belonging to natural immunity cascade  in normal and impaired wound healing [9–13].
2.5. Another important contribution to the study of neoangiogenesis and biomaterials prefabrication
Our group also developed a collaboration with the group from Padriciano, International Center for Genetic Engineering and Biology, United Nations, to study a model of prefabricated flap in the groin of adult rats creating an artero-venus loop that was included into a dermal regenerative template; this new regeneration chamber was then injected with different viral vectors (AAV 156) encoding for the production of VEGF. Results were remarkable, demonstrating enhancement of neoangiogenesis and neovasculogenesis and the utility of this novel model of regeneration chamber that could act as a bioreactor and stimulate healing and even repair poor vascularized tissues [14, 15].
3. Clinical experiences
Chronic wounds are produced either by an interruption in healing processes, as an effect of lack of positive (vascular supply and neurotrophism) or of an excess of inhibitory factors (metallo proteinases in ECM, some cytokines), or by a lack of switch in inflammatory cell phenotypes, such as in diabetes.
As a final effect, wound bed does not progress beyond detersion, typically presenting itself as necrosis or debris. They are especially present in lower limbs, often as a result of complex mix of the above-mentioned factors.
Vascular and diabetic ulcers are the most common chronic wounds affecting nearly 2–5% of the general population and have received an important impact in terms of morbidity, absence from work, and social costs.
Traditional wound dressings do not restore vascular supply, which is a
An important role is played by vascular surgery and endovascular techniques, which act restoring the lost vascular supply or producing bypasses to revascularize the area.
At present, some novel suggestions come from regenerative surgery.
3.1. Lipograft in chronic wounds
The target is endothelial insufficiency, as documented in diabetes and vascular obstructive diseases.
A well-established clinical experience with lipografting has been obtained in the early years of this century, especially in scar treatment after important fibrotic status, such as in postburn scars and in postradiation mastectomy scars [17, 18].
Since 2001, Zuk et al. documented that lipoaspirate from adipose tissue represents a source of adipose tissue-derived stem cells, which are adult mesenchymal stem cells .
Starting from the first regenerative approach with lipografting on fibrotic tissues, its role has been expanded to chronic wounds, applying as a rationale, and has the potential to induce angiogenesis and regeneration. The potential of ADSCs to differentiate into adipocytes, osteoblasts, chondrocytes, cardiomiocytes, and endothelial cells, in vitro and in vivo, was shown by several authors. In particular, ADSCs are able to express endothelial markers when cultured in the presence of VEGF.
Application of ADSCs or ADSC-derived molecules could be an innovative therapeutic approach in the treatment of chronic wounds and other conditions; it has been proposed in association with platelet-rich plasma  or under particular conditions .
The surgical procedure was performed under local anesthesia together with midazolam medication (see below). The periumbilical area and the hip were the preferred donor site because of the good quantity and quality of dermal fat graft.
With the patient in supine position, the donor area was infiltrated with 250 cc of saline solution (NaCl 0.9%), 0.5 cc adrenalin 1/1000, 10 cc of lidocain 2%, and 10 cc ropivacain 7.5%; the incision to introduce the cannula was made with a no. 11 scalpel (Figure 1).
Adipose tissue was harvested through the same incision by a blunt 2 mm cannula connected to a Luer-Lock syringe of 10 cc, a small amount of aspirate (about 10 cc) was sufficient.
The full syringe was placed into a sterile cup and washed with NaCl 0.9% to remove the anesthetic solution.
The authors used Coleman’s technique and centrifuged the fat (3000 rpm for 3 minutes) to separate cellular blood components with infiltration solution, adipocytes with vascular stromal tissue and oil derived from the breakdown of fat cells.
The adipose-stromal fraction was transferred from a 10 cc syringe to a 1 mL Luer-Lock syringe to allow a precise control of the amount of injected fat (Figure 1).
The adipose tissue fraction was then implanted with gentle care; small “pearls” of adipose tissue were placed at the dermal-hypodermal junction in the ulcer’s edges and into the wound bed. Many radiating passages were made through the same incision, to place fat in different directions.
The access incisions in the donor areas were sutured with Nylon 5/0.
The treated area after surgical procedure was covered with non-adherent gauze, whereas an elastic adhesive bandage was applied to the fat donor site to prevent hematomas and seromas.
A second grafting session was performed, if needed, 3 months later.
3.2. Mononuclear cells in chronic wounds
Cell therapy is an innovative and promising approach for regeneration of damaged tissues. In particular, new scientific evidence shows that the total mononuclears from peripheral blood are cells with high angiogenic and vasculogenic capacity and, in general, in tissue regeneration processes.
Patients with CLI, who suffer from rest pain, nonhealing ischemic ulcers, or necrosis (Fontaine 3–4), rarely respond to standard therapy as drug therapy (e.g., prostaglandin and anticoagulant, etc.) and surgical revascularization.
The autologous transplantation of peripheral blood mononuclear cells (PBMNCs) can produce tissue regeneration and improve physiological healing process through their paracrine action, consisting in production of cytokines, especially VEGF and bFGF.
The monocells have three principal roles:
– progenitors of multipotent cells,
– angiogenesis and vasculogenesis, and
The PBMNCs isolated from peripheral blood have the same differentiating and regenerating capacities as the bone marrow mononuclear cells (BMMNCs), but their isolation is simpler and minimally invasive.
Monocytes and macrophages are capable of producing a large variety of growth factors, metalloproteinases, chemokines, and vasoactive substances such as nitric oxide; all can facilitate angiogenesis and arteriogenesis [30–34].
During chronic inflammation, macrophages/monocells are polarized in the antimicrobial form (M1), or in the regenerative form (M2). The implantation of concentrated PBMNCs in this condition can address M1 to M2 promoting the regenerative form.
In the theater, under sedation and local anesthesia of the patient, 120 mL of peripheral venous blood was drawn and added to 12 mL of ACD-A (anticoagulant by apheresis). This was then processed by the WB Pall Celeris system to obtain 12 mL of concentrated PBMNCs (Figure 4).
The concentrated PBMNCs were transferred to a 1 mL Luer-Lock syringe to allow a precise control during injection (Figure 4).
After an appropriate surgical cleansing of the wound bed, the concentrate was implanted into the perilesional area in a single-stage procedure with multiple local subcutaneous perilesional and intralesional injections and intramuscular injections.
The suspension was placed along the relevant damaged vascular axis too, at intervals of 1–2 cm and at a mean depth of 1.5–2 cm, using a 21G needle (Figure 4).
After the A-PBMNCs implant, the wound was always covered with hyaluronic acid monolayer.
This treatment was repeated three times, once a month for three months (Figure 5).
One month after the first treatment, the size of the ulcers of all patients were significantly reduced. At the end of the third session, ulcers seemed totally healed, the skin overlying the wound appeared perfectly normal, and the skin complexion was ruddy (Figure 5).
Because of their early capability to stimulate vascular ingrowth, monocell implant can be used in one step only to prepare wound bed to receive an autologous skin graft (Figure 6).