The Repair Process of the Uterine Cervix Subjected to CO2 Laser Vaporization: A Pilot Study Volume 8 - Issue 2

Claudia Bianchi*, Serena Tarani, Noemi Auzzi, Giuseppe Cariti, Felice Petraglia and Annalisa Pieralli

• Department of Woman and Child Health, Section of Oncological Gynecology, Careggi University Hospital, Italy

Received: July 31, 2018;   Published: August 22, 2018

*Corresponding author: Claudia Bianchi, Largo Brambilla 3, 50134 Florence, Italy

DOI: 10.26717/BJSTR.2018.08.001622

Abstract PDF

Objective: Cervical intraepithelial neoplasia (CIN) frequently affects young women in childbearing age. Present literature does not provide scientific consensus on the real incidence of obstetric complications after the various conservative techniques performed. Most of all literature data are still lacking a pathophysiological basis to explain the different impact of various treatment techniques on the functional integrity of the uterine cervix. The gold standard conservative treatment is the excisional therapy. This study tried to analyze the evolution of tissue repair of cervix subjected to CO₂ laser conization for high grade CIN with the aim of identifying eventual differences between the repaired tissue and the original cervical one.

Study Design: The analysis was conducted on histological seriated samples of uterine cervix obtained at standardized times after conization treatments and then analyzed using histological examination and immunohistochemical staining.

Results: This study showed that the tissue concentration of TGF01 was significantly low in patients treated with CO₂ laser, confirming the reduced inflammatory reaction after laser treatment. Another very interesting result was the high ratio of type III and type I collagen: the prevalence of type III collagen suggested a regeneration of tissue without scarring after laser therapy.

Conclusion: Tissue repair process after CO₂ laser cervical treatment is able to compensate the loss of substance in damaged area and at the same time to limit the deposition of disorganized connective matrix, typical of scars, leading to a morphologic and functional restitutio ad integrum of the treated cervical tissue, which tends to be similar to the original one.

Tissue repair process after CO₂ laser cervical treatment is able to compensate the loss of substance in damaged area and at the same time to limit the deposition of disorganized connective matrix, typical of scars, leading to a restitutio ad integrum of the treated cervical tissue, which tends to be similar to the original one.

Patients with cervical intraepithelial disease are mostly in childbearing age. Preventive treatment of non-invasive lesions in young patients requires minimally invasive procedures with few adverse effects on female fertility and on future obstetric outcome [1-2]. The gold standard treatment for high grade cervical intraepithelial neoplasia (CIN II/III) is excisional therapy, such as LEEP (loop electrosurgical excision procedure), cold knife conization and CO2 laser conization [1]. Observational studies described excisional methods as at risk of dysfunctional repair ofthe cervix with a high risk of obstetric complications, such as preterm delivery caused by cervical incontinence. However, conclusions are often not unique. Recent meta-analysis showed only a modest increased obstetric risk in women undergoing CO₂ laser conization. This suggests an influence of the treatment technique on the regeneration and functionality of the treated cervical tissue [2-4]. Studies on repair process of different tissues treated with CO₂ laser showed that this procedure is associated with less bleeding and post-operative pain than other techniques, due to the hemostatic effect of the laser and to the reduced tissue edema [5].

Furthermore, histological analysis of tissue samples underlined a less capillary neoangiogenesis, a re-epithelialization of the wound and a reduced early deposition of collagen. These elements would be at the base of a reduced rate of scarring and of a better healing process with an organic and functional restitutio ad integrum [67]. To authors' knowledge, no studies on the repair process of the uterine cervix affected by high grade CIN and treated with CO₂ laser excision are present in literature [8]. The aim of this study is to describe the characteristics of the cervical tissue damage produced by CO₂ laser on women of childbearing age treated for pre-invasive cervical lesions and to follow the time evolution of reparative process.

The study was conducted at the Laser Therapy Center of the Maternal and Child Department, Careggi University Hospital, Florence. The inclusion criteria were: CIN II/III [9]; age under 40 years; no previous cervical treatment; no chronic disease; no smoking. Patients had to accept to undergo cervical biopsy on the treated area at standardized times after conization. All patients signed informed consent to the study. The conization treatments were performed in an outpatient setting under local anesthesia using CO₂ laser model SmartXide 50HS (DEKA MELA SRL, Italy), connected to a colposcope ZEISS OPMI (Carl Zeiss,Oberkochen, Germany).The beam spot diameter ranged from 0.5 to 1 mm with an irradiance ranging from 2500 to 3500W/cm, guided by a micromanipulator. After delineating the area of abnormality with Lugol's iodine, local anesthesia was administered performing at the 3, 6, 9 and 12 o'clock site of the cervix injections of 3.6-5.4mL of 2% lidocaine mixed with epinephrine 1:100,000. The first step of procedure was to direct the laser beam perpendicularly to the cervical surface achieving an initial 0.5-1cm deep circular section and then to guide it obliquely by manipulating the on-going excised specimen using a small steel hook. To assure the complete clearance of the lesion, after the excision the crater base and the walls were vaporized with defocused laser beam.

With these settings, we ensured an emission with high peak power and high energy density to induce the phenomenon of photoablation with rapid destruction of the tissue and reduced propagation of thermal damage to surrounding tissue. At the end of the treatment, we executed a sample of tissue at 12 o’clock in the treated cervical area using punch biopsy forceps. Subsequent specimens were performed 2, 7 and 14 days after surgery at 3, 6 and 9 o'clock of the treated area, respectively, in order to take samples of tissue from areas not affected by previous biopsies. A further specimen was then collected at the first follow-up visit 3 months after treatment. All specimens were sent to the laboratory and prepared for histological evaluation with light microscopy. In order to describe the characteristics of the cervical tissue damage, standard histological analysis and immunohistochemical research of inflammatory markers, neoangiogenesis and tissue regeneration were conducted. Samples providing a good histological readability in terms of stratification of the tissue and representation of its various components were considered eligible to immunohistochemical analysis.

Immuno Histochemical Evaluation on Tissue Samples Focused on

a) IL-1β - Inflammatory cytokine (No. Catalogue: MAB 201,Clone: 8516. R & D Systems. Minneapolis, USA);

b) TGFK1 - Inflammatory cytokine with chemotactic action for fibroblasts and angiogenesis (No. Catalogue: MAB 240; Clone: 9016. R & D Systems. Minneapolis, USA);

c) Factor VIII Related - A marker for endothelial cells (No.Catalogue: CP 039. Bio Care Medical. Concord, USA); Type I collagen - a protein with a structural function (No. Catalogue: 2150-0030. Abd Sero tec. Kidlington, UK);

d) Type III collagen - A protein with a structural function(No. Catalogue: nbpi-67528. Novus Biologicals. Littleton, USA).

Tissue samples were collected and fixed in 4% buffered formalin; specimens were oriented, reduced and embedded in paraffin. Three microns thick sections were obtained by microtome. For each specimen, some sections were subjected to standard staining with hematoxylin-eosin for histological evaluation, while others were used for immunohistochemistry. Immunohistochemistry was prepared by immune enzymatic technique with indirect method with immune complexes using peroxidase as tracer, the Avidin-Biotin complex (ABC) as immune complex and the DAB (3,3'-diamino- benzidine) as chromogen. All sections were affixed on polarized glass slides, deparaffinizated in xylene and then rehydrated through a descending scale of alcohol until deionized water.

Slides were passed to the microwave in citrate solution for unmasking antigens, then black incubated in hydrogen peroxide for inhibition of the endogenous peroxidases. After this first phase, goat serum was used to eliminate any effect of non-specific binding (background) antibodies, before being incubated with the primary antibody. A similar passage was performed again with the normal serum, before proceeding to incubation with the secondary antibody. In the last phase of the procedure the immune complex (ABC) and subsequently the solution DAB was added. After adding chromogen, the sections were observed under a microscope and then fixed by soaking in deionized water at the onset of the color reaction. To complete the preparation, the sections were counterstained with hematoxylin, dehydrated, passed in xylol and finally covered with a coverslip mounted. The observation of samples was performed using an optical microscope Nikon Eclipse 80th (Nikon, Shinjuku, Japan).

During three months, seven patients were recruited, aged 24-37 years, who met the inclusion criteria and accepted to undergo the study schedule. The indications for treatment were CIN II (six), and CIN III (one). Four patients were able to complete all 5 specimens according to the study protocol, two patients refused to continue the study. One patient was excluded because follow-up colposcopy showed a CIN I confirmed by biopsy and underwent laser ablation. Cyto-colposcopic monitoring at three months after treatment was negative in four subjects providing a cure rate of 80%. A total of 27 specimens were collected, 7 of which at t0 (time of treatment), 6 at t1 (48 hours after treatment), 5 at t2 (one week after treatment), 5 at t3 (two weeks postoperatively) and 4 at t4 (three months after treatment) (Table 1). All specimens were evaluated by light microscopy; immunohistochemistry analysis was performed, and 15 samples were processed: 4 at t0, 3 at t1, 3 at t2, 3 at t3 and 2 at t4 (Table 1). The histological evaluation was performed on a descriptive basis caring of the presence or absence of carbonized areas, vacuolar degeneration of superficial epithelium, grading of cell maturation and stratification, inflammatory infiltration, neoangiogenesis and new gland formation.

Table 1: Enrolled patients.

t₀- Specimens taken at the time of treatment

t₁ - Specimens taken 2 days after treatment

t₁- Specimens taken 7 days after treatment

t₃ - Specimens taken 14 days after treatment

t₄- Specimens taken during follow-up visit 3 months after treatment

X - Specimens analyzed in IHC

NP - Sampling not performed

The immunohistochemical evaluation took into consideration TGFβ1, Factor VIII Related (FVIIIR) and Collagen type I and III. All 15 samples analyzed both histologically and immunohistochemically displayed homogeneous aspects within each group (t0, t1, t2, t3, t4) for the considered markers (Table 1). At t0, the histological analysis showed only traces of carbonization on luminal side with adjacent area of vacuolar degeneration of cells, phenomena which are produced by laser-treatment. No structural alterations of the underlying tissue were found. At t0 the immunostaining was negative for TGFtel and FVIIIR. Only a weak positivity of type I and type III collagen was seen on remaining native basal membranes. At t1 the thermal damage became evident; the carbonized area was mostly substituted by homogeneous coagulated and poorly cellular tissue with peripherical inflammatory infiltration. The limit between the two layers resulted positive to FVIIIR immunostaining, while TGFtel was still absent. Type I collagen was completely absent while type III collagen resulted positive in the coagulated area linking denatured fibers.

At t2 a newly formed reparative tissue substituted the coagulated area; this tissue was characterized by a weak positivity to TGFtel and by neoangiogenesis, glandular genesis and epithelial regeneration. An intense positivity to type I collagen was evident at the intermediate layer of epithelium and to type III at the basal one. FVIIIR was only present in the stromal vessels. Reduced inflammatory infiltration was noticed. At t3 no angiogenesis and inflammatory infiltration were noticed; neoangiogenesis and gland regeneration were completed, the epithelia had an increased stratification and maturation, although large and nucleated cells still remained. Presence of collagen types I and III was similar to t2. Positivity to TGFtel and FVIIIR was no longer visible. At t4 the reparative stage was almost entirely completed even if small areas of high cellularity persisted. TGFtel and FVIIIR were negative. The analysis of type I collagen showed a fibrillar organization at the polarizer inspection, while type III collagen antibodies were widely bound to connective tissue, highlighting a fibrillar structure.

Comment

When a tissue damage is caused for therapeutic purposes, especially in anatomical regions in which the functional integrity is important, such as uterine cervix, the clinical interest is to shift the equilibrium of reparative process to the regeneration of a tissue with mechanical and functional characteristics similar to the original one. It is known that, in the prenatal period, the tissues are able to repair without scarring, therefore are able to regenerate [10]. Fetal wounds heal rapidly and without the scarring and inflammation that characterize adult wounds. The prenatal wound healing process is faster and more efficient than adult repair and produces new tissue rather than scar. However, the difference between fetal and adult repair isn't completely explained [10-12]. An important difference between embryonic and adult reparation process is highlighted by the concentration of TGFp and its isoforms: in embryo low levels of TGFpi and 2 and very high levels of TGFβ3 are present.

TGFβ3 stimulates fibroblast migration and directs their orientation as to allow the correct position of connective matrix deposited by fibroblasts, ensuring a regeneration of tissue similar to the original one. Conversely, in adult damaged tissue, the degranulation of platelets, monocytes and macrophages releases large amounts of TGFβl and 2, while the liberation of TGFβ3 by keratinocytes and fibroblasts is poor. In the presence of a tissue damage, the adult tissue responds with a high inflammatory response, promoted by pro-inflammatory cytokines, including TGFpi and 2. They lead to the deposition of granulation tissue, which fills the loss of substance, but prevents the proper migration of fibroblasts from the edges of damaged areas. The low concentration of TGFβ3 does not support the interweaving of proper collagen fibers, which are arranged predominantly in parallel with each other, without ensuring adequate mechanical strength. Trying to compensate the reduced tensile strength, fibroblasts accumulate fibers giving rise to a fibrous scar that becomes prominent in time [13].

Another important element in repair tissue is type III collagen. It's responsible for maintaining the structural integrity of the fabric and it's also considered able to adjust the diameter of collagen fibers during reparative phase and to modulate the transformation of fibroblasts into myofibroblasts, responsible for contraction of wounds. The important role of this element in tissue regeneration without scarring is supported by the observation of increased expression of type III collagen in fetal tissue repair, with high ratio of type III/I collagen. From these considerations, it's evident that the method to generate a tissue damage for therapeutic purposes should consider functional needs of the tissue itself. Treatment modalities should try to stimulate a regenerative process in the damaged tissue characterized by high growth and tissue differentiation, poor inflammatory response and poor angiogenesis, in order to reconstitute a tissue as similar as possible to the original one. According to some studies, even if conducted on tissues other than the uterine cervix, the laser would be capable of inducing a repair process that tends to have these characteristics [14-15].

The carbonized area which represents the loss of tissue induced by the laser on the margins of the treated area is as small as to be fulfilled in term of a few days (t0-t1). The low positive response to TGFβ1 in all samples suggests a reduced pattern of inflammatory cytokines, that would be desirable in the context of a tissue regeneration with poor scarring. The low release of TGFβ1 after the lesion induced by CO₂ laser, compared to other techniques, has been described in literature by Manolis et al. [16]. This trial showed that the tissue concentration of TGFβ1 was significantly lower in patients treated with CO₂ laser compared to traditional surgery, confirming the reduced inflammatory reaction after laser treatment. The FVIIIR was used as an indirect element for the evaluation of inflammatory stimulus.

In fact, in our study angiogenesis, marked by FVIIIR, is stimulated both by initial vascular damage and by inflammatory cytokines including the TGFp. In our samples, the FVIIIR presence is mainly evident 48 hours after treatment: it's localized diffusely throughout the tissue and decreases progressively to be localized exclusively in regenerated vessels at t3 and t4. This allows us to deduce that the poor neoangiogenic stimulus present in laser CO₂ damaged cervix is supported by TGFβ1. In regard to the search of type I and type III collagen, there is a trend similar to that proposed by other trials, with a progressive increase of their positivity in 7-10 days after treatment [6]. A very interesting result in our case, however, is the high ratio of type III and type I collagen observed at t4. Thus, the prevalence of type III collagen suggests a regeneration of tissue without scarring after laser therapy.

These initial data represent an interesting basis for the comprehension of the reparative process after CO₂ laser damage on the uterine cervix performed for therapeutic purposes. This is of utmost importance to understand how to tailor excisional therapy in order to prevent functional damage. On the basis of our results, in agreement with some studies conducted on tissues other than cervix, tissue repair after CO₂ laser seems to be more similar to tissue regeneration typical of prenatal period compared with other kinds of treatment. The immunohistochemical analysis on the collected samples showed a low concentration of TGFβ1, a pro- inflammatory cytokine which is responsible for a high inflammatory response leading to the deposition of granulation tissue and the developing of scar tissue. Another important characteristic was the high rate of collagen type III/I; type III collagen is responsible for maintaining the structural integrity of the tissue and is able to adjust the diameter of collagen fibers during reparative phase, promoting a regeneration of tissue without scarring. These features show that tissue repair process after CO₂ laser treatment is able to compensate the loss of substance in damaged area and at the same time to limit the deposition of disorganized connective matrix, typical of scars, leading to a restitutio ad integrum of the treated cervical tissue, which tends to be similar to the original one.

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