CA2154368C - Therapeutic applications of chimeric organogenesis - Google Patents

Abstract

A process for culturing and generating a chimeric cell culture, in particular chimeric epithelium, is disclosed. The chimeric epithelium oan be used to treat skin trauma such as burn victims. Autologous epithelial grafts have been used on burn patients although this requires that the patient's cells are cultured and expanded in vitro which generally takes four to five weeks.
The chimeric epithelium of the present invention is composed of cells that are both autologous and allogeneic to the host. Therefore, the allogeneic cells can be maintained in a cell bank and co--cultured with autologous host cells when needed.
This significantly reduces the time required (by up to 50 %) for autologous cell expansion and culture prior to grafting. Furthermore, it has been demonstrated that the allogeneic cells are passively eliminated from the graft without rejection of the total graft.

Description

THERAPEUTIC APPLICATIONS OF CHIMERIC ORGANOGENESIS
FIELD OF THE INVENTION
The present invention relates to the production of chimeric cell cultures. In particular, the invention relates to the production of chimeric epidermal cell cultures to be used in skin grafting.
BACKGROUND OF THE INVENTION
Uninjured tissues and organs of the body are com-posed of different cell types, and extracellular matrices that affect cell, tissue and organ functions. Noncongeni-tal injury to cells and tissues causes wounds and initiates common mechanisms of wound healing at all sites in the body (Robbins SL. et al, (Eds.) "Pathologic Basis of Disease", 2nd ed Philadelphia: WB Saunders, 1979:55-106). Fundament-al components of wound closure include restoration of stable ectoderm-derived tissue(epithelium or endothelium) and of uniform vascular supply in the adjacent mesoderm-derived tissue. For optimal closure, wounds caused by traumatic injury or elective surgery require rapid restor-ation of normal tissue anatomy in the absence of infection (Bucknall TE, et al. (Eds.) "Wound healing for surgeons", Philadelphia: Bailliere Tindall, 1984: 42-74).
In the last decade, technological achievements in the in vitro culture of human epithelial cells has attract-ed a remarkable interest for its therapeutic application.
The most striking practical application is undoubtedly the successful use of in vitro cultured epithelial sheets as autografts on patients with extensive tegumental losses (Green H. et al., 1979, Proc. Natl. Acad. Sci. USA, 76:
5665; Gallico G. et al., 1984, N. Eng. J. Med., 31:448).
It has been shown that a biopsy specimen of 1 to 2 cm2 can be expanded in surface area by a factor of 10,000 when cultured in vitro.
Early excision of full skin thickness burns followed by grafting of autologous meshed skin have de-creased the mortality rate of patients suffering from large burn wounds (Heimbach DM., M.D. 1987. Surg. Clin. North.
Am., 67: 93). However, burns covering more than 50% of the SUBSTITUTE SHEET

total body surface lead to very high mortality rates which are directly related to the limited availability of donor sites for epithelium split thickness meshed grafts.

In vitro reconstructed human epithelium has been successfully used since 1981 in the treatment of major burns (O'Connor et al, 1981, Lancet, January 10, 75). This process presents a high level of success for burned patients wounded over 50% of their body surface. However, the long time interval (3 to 5 weeks) required for cell growth and graftable sheets production, a period during which the patient may become progressively ill, is a major disadvantage of this technique. One of our interests is to provide quick and safe methods for skin trauma therapy.
This critical goal may be reached by the below described invention.

SUMMARY OF THE INVENTION

The present invention relates to a process for growing and generating chimeric epithelium in vitro for treating skin trauma. A novel aspect of the invention is the use of allogeneic cells in the production of graftable epidermal sheets. These skin grafts can be used to treat a variety of skin trauma, notably burn wounds but also including other conditions such as large congenital nevi, chronic ulceration, nonhealing wounds, and other types of traumatic skin loss that may require therapeutic skin replacement. Indeed for patients who are massively burned the availability of donor skin is the limiting factor for wound coverage and survival. It is predicted that using allogeneic cells would save considerable time (up to 50%) in the production of the chimeric epithelium in vitro since the allogeneic cells can be stored in a skin bank.

Accordingly, the present invention provides a process for producing a chimeric cell culture suitable for transplanting onto a host, said process comprising culturing cells that are autologous to said host with cells that are not autologous to said host under conditions suitable to promote growth of the cells. Cells of the chimeric cell culture are the same cell type.

The present invention also provides a transplantable chimeric cell culture suitable for transplanting onto a host comprising a mixture of cells that are autologous to said host and cells that are not autologous to said host. In a preferred embodiment, both the cells are epidermal cells, in particular keratinocytes.
Chimeric cell cultures can also be produced by the process described above.

The present invention further provides a use of the chimeric cell culture described above as a skin graft.

The present invention yet also provided a method of transplanting skin comprising grafting onto a patient in need of such treatment the chimeric cell culture described above.

3a The present invention further provides a use of a chimeric cell culture described herein for the treatment of a patient in need of such treatment.

The present invention also provides a use of a chimeric cell culture described herein for the preparation of a medicament for the treatment of a patient in need of such treatment.

The present invention yet also provides a commercial package comprising the chimeric cell culture described herein and instructions for the preparation of a medicament for the treatment of a patient in need of such treatment.

The present invention still provides a commercial package comprising the chimeric cell culture described herein and instructions for the treatment of a patient in need of such treatment.

BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 represents a flow cytometry analysis of various cultures of keratinocytes. Panel (a) represents the percentage of H-2d positive cells in a pure Balb/c keratinocyte culture. Panel (b) represents the percentage of H-2k positive cells in a pure C3H/HeN keratinocyte culture. Panel (c) represents the percentage of H-2d positive and H-2k positive cells in a chimeric keratinocyte culture.

3b Figure 2 represents the histological analysis of (a) isograft, (b) allogeneic and (c) chimeric grafts on C3H/HeN mice, 14 days post grafting.

Figure 3 represents immunofluorescence staining of a chimeric graft and an isograft, 30 days, post grafting, on C3H/HeN. Panel (a) is an isograft stained with H-2k' Panel (b) is a chimeric graft stained with H-2K. Panel (c) is a chimeric graft stained with H-2d.

DETAILED DESCRIPTION OF A PREFEREED EMBODIMENT

The following is a description, by way of example, of one embodiment of the present invention wherein murine chimeric epidermal cell cultures are prepared and grafted onto murine hosts.

EPIDERMAL CELL PREPARATION AND CULTURE

Primary cultures of murine epidermal keratinocytes were established from neonatal Balb/c and C3H/HeN

mouse skin according to the method of Yuspa and Harris (Exp. Cell. Res 1974, 86: 95). Briefly, newborn mice were killed by cervical dislocation, then washed 3 times with 70% ethanol, cold proviodine, and 70% ethanol respectively.
Limbs and tail were amputated, a longitudinal incision was made from tail to snout, and the skin was removed with for-ceps. Epidermis was separated from dermis after flotation of the skin on 0.25%-20 gg/ml of trypsin-DNase solution in phosphate buffer saline (PBS) overnight at 4 C. The detached epidermal pieces were aseptically transferred to a medium containing serum to inhibit the action of residual enzyme and to release the epidermal cells mechanically.
Single-cell suspensions were washed twice and the pellets were resuspended in 5 ml of 10%FCS medium. The epidermal cell suspensions were applied onto Lympholyte-M gradients (Cedarlane Laboratories Limited, Canada) and spun at room temperature at 300 g for 30 min. The resulting pellet con-taining keratinous material and other debris was discarded.
The interface layer containing nucleated epidermal cells was collected, washed twice, and resuspended in Dulbecco-Vogt modification of Eagle's medium (DME) mixed with Ham's F-12 in 3:1 proportion (Flow Labs, Mississauga, Ontario, Canada). This medium was supplemented with 5 gg/ml of insulin, 10-10M cholera toxin (Schwarz/Mann, Cleveland, OH, U.S.A.), 24.3 gg/ml adenine, 5 gg/ml human transferrin, 2x10-9 M 3,3',5'-triiodo-L-thyronine (Sigma Chemicals), 0.4 JiM of hydrocortisone (Calbiochem, La Jolla, CA, U.S.A), 100 lU/ml penicillin G, 25 gg/ml gentamicin (Schering Canada Inc.), 10 ng/ml epidermal growth factor (EGF, Chiron Corp., Emeryville, CA., USA) and 10% of fetal calf serum (FCS, Flow Lab). Cell viability and a count of the epi-dermal cell suspension were ascertained by the trypan blue exclusion technique.
Cell culture Balb/c keratinocytes (BK) or C3H(CK) were grown individually in culture flasks, or mixed together at 50%BK-50%CK ratio. The seeding cell concentration was 105cells/
SUBSTITUTE SHEET

WO 94/17179 2 15' 4368 PCT/CA93/00546 cm2. All cultures were allowed to attach for 24 h in a humidified atmosphere with 5% C02 at 37 C and then trans-ferred to 31 C, and epidermal growth factor (EGF) was added to the medium. The medium was changed every 2 days. For 5 the first 48 hours of culture, the Mg2+ concentration in the medium was adjusted to 2 mM; then it was increased to 5 mM (Molloy C.J. and Laskin J.D., 1988, Differentiation, 37:86).
Immunofluorescence staining of chimeric cultured cell suspensions Confluent cultures were treated with 0.01%-0.05%
Trypsin-EDTA solution to make cell suspensions. Cells were then treated with an anti-H-2k monoclonal antibody (speci-fic for C3H/HeN cells) for 45 min at 4 C . After two washes with PBS containing 1% bovine serum albumin (BSA) and 0.1% sodium azide (Az), cells were exposed to a goat anti-mouse IgM-IgG-fluorescein (FITC) conjugate (1/300 dilution) for 45 min in the dark at 4 C. Cells were washed arid then treated with an anti-H-2d monoclonal antibody (specific for Balb/c cells) coupled to phycoerytrin (PE) for 45 minutes at 4 C in the dark. After this incubation, cells were washed 3 times with PBS-1%BSA-0.1%Az. Each pellet was then resuspended in 1 ml of 1% paraformaldehyde solution and analyzed by flow cytometry (Becton Dickinson, Montreal, Qc., Canada). As controls, pure Balb/c and C3H/HeN confluent keratinocyte cultures were enzymatically resuspended then stained separately with an anti-H-2d-PE
labelled and H-2k plus IgM-IgG-F1TC monoclonal antibodies respectively.
Chimeric sheet preparation Epidermal sheets were prepared when the primary cultures of keratinocytes had reached confluence. Cultures were washed twice with sterile PBS; then 5 ml of dispase (Sigma) at 2.5 mg/ml were added to each flask and incubated at 37 C for 20 to 30 minutes, to release these sheets from the flask's surface. Sheets were washed twice and trans-ferred to a vaseline gauze (Ethicon Ltd, Johnson and ~ 6 Johnson, Peterborough Ont., Canada) basal side up and then fixed with Ligaclips (Sherwood Medical Industries Ltd, Markham, Ont., Canada). These sheets were left immersed in the appropriate medium until grafting.
Transplantation Procedures The recipient mice used in the transplantation experiments were Balb/c and C3H/HeN mice. Each strain received transplants of epidermal sheets that were (a) iso-logous, (b) allogeneic or (c) chimeric to the mouse receiving the transplant. For example, Balb/c mice were transplanted with epidermal sheets derived from (a) Balb/c mice (isologous transplant or isograft), (b) C3H/HeN mice (allogeneic graft) or (c) both Balb/c and C3H/HeN mice (chimeric graft).
Inbred strains of mice, such as Balb/c and C3H/HeN mice, represent a homogeneous population wherein all members of one strain have the identical genetic make up. Therefore, it can be appreciated that an isograft can be considered as an experimental equivalent to an autograft since, in both situations, both the recipient and the transplant are of the same genetic make up. For the pur-poses of the present experiments, isografts were used in-stead of autografts, since the mice from which the epidermal sheets are prepared are sacrificed when the epidermal cells are isolated.
Recipient mice were anaesthetized with an intra-muscular injection of ketamine xylazine at 0.05 ml/lOg weight. Mouse dorsum was prepared for grafting by shaving and washing the area with proviodine and 70% ethanol. Full thickness skin was excised down to the muscle. A Fusenig transplantation chamber (Fusenig N.E. et al. 1980. In :
"Tissue Culture in Medical Research", Vol. 2, Richard R.G.
and Rayan K. (Eds), Oxford, Pergamon. pp 87) was installed and a homogeneous or chimeric sheet was deposited over the muscle. The vaseline gauze was then gently detached. The top of the transplantation chamber was installed and fixed by four cutaneous stitches (silk 4-0 from Ethicon Ltd., Peterborough, Ont.) for five days and then removed.
Fourteen and thirty days after grafting, biopsies were taken for histology and immunohistochemical analysis.
Histological studies Fourteen days post grafting, biopsies were harv-ested from the isograft and the allogeneic and chimeric grafts, fixed in Bouin's solution and embedded in paraffin.
Then 4-5 m sections were stained with hematoxylin phloxine and saffron, and observed under an optic microscope (Nikon Optiphot; Japan) For indirect immunofluorescence, intact' biopsies were harvested 30 days postgrafting from the isograft and the chimeric implants, embedded in OCT compound (Miles, Elkhart, IN.), frozen in liquid nitrogen, and stored at -70 C until needed. Four m cryostat sections were pre-pared from each biopsy and stained with anti-H-2d or anti-H-2k monoclonal antibodies for 45 minutes at room tempera-ture in a 95% humidified chamber, rinsed extensively with PBS-BSA-Az, and then overlaid with F1TC-conjugated goat anti-mouse IgM-IgG for 45 minutes as above in the dark.
Following further rinsing with PBS-BSA-Az, sections were mounted in 30% glycerol-2% glycine-PBS solution, overlaid with a coverslip, examined using a fluorescence microscope (Nikon Optiphot), and photographed with Kodak Tmax*400 ASA
film.
Results The inventors have developed a new epithelial culture method to produce chimeric graftable sheets.com-posed of two different keratinocyte types, using a murine model. These graftable sheets should have use in treating and accelerating burn therapy as well as treating other dermatological trauma.
The chimeric cultures, comprising a 50:50 mixture of Balb/c and C3H/HeN keratinocytes were co-cultured until confluence. The confluent cultures were either (i) stained to assess the percentage of each cell type on these graft-able chimeric sheets, using specific anti-H-2d (for Balb/c) * Trade-mark and/or anti-H-2k (for C3H/HeN) monoclonal antibodies, or (ii) epithelia were obtained from confluent cultures by dispase treatment and grafted onto recipient Balb/c or C3H/HeN male mice 6 to 8 weeks old. Figure 1 shows that the chimeric culture contains approximately the same pro-portions of each cell type after 3 days of culture when assessed with both anti-H-2d and anti-H-2k monoclonal anti-bodies used in combination, or with each antibody used individually. As shown in panel (c), the percentage of Balb/c keratinocytes in the chimeric culture was 40% while the percentage of C3H/HeN keratinocytes was 42%. This immunostaining shows no growth inhibition of the Balb/c keratinocyte (BK) proliferation when co-cultured with the C3H/HeN keratinocytes (CK) and vice versa. Furthermore, the epithelial sheets ready for grafting were composed of the two cell types essentially at the same ratio as at the beginning of the culture seeding. The negative control represents staining with the second antibody, Anti-Mouse-IgG-FITC, only.
Chimeric sheets were grafted and left on the recipient dorsum. Fourteen days postgrafting, biopsies were taken from the isograft and the allogeneic and chim-eric grafts for histological analysis. The hematoxylin and phloxine staining (Figure 2) showed a well structured epi-dermis with the presence of stratum corneum, stratum spino-sum and stratum germinativum. No monocyte infiltration was observed in the chimeric graft or the isograft. However, the cultured epithelium allografts showed disorganized epithelial cells and an important monocyte and polymorpho-nuclear cell infiltration which is a sign of the implant rejection. The chimeric graft and the isograft were not rejected.
In order to determine the origin of the keratin-ocytes which constitute the epidermis after a chimeric sheet grafting, biopsies from the autologous and the chimeric implant were taken at the 30th day post grafting, embedded on OCT and frozen in liquid nitrogen. Thin WO 94/17179 2 15'4368 PCT/CA93/00546 sections were prepared from each biopsy and stained with an anti-H-2d or anti-H-2k monoclonal antibody. As shown in Figure 3, chimeric sheets previously grafted on Balb/c recipient mice showed that the epidermis contains only Balb/c (BK) cells as in the isograft. No C3H/HeN (CK) cells remained in the transplant. The CK cells were passively eliminated from the transplant without the usual rejection of the whole implant. The same results were obtained after the transplantation of chimeric sheets on C3H/HeN recipient mice.
The inventors have also shown that similar re-sults have been obtained when the chimeric culture consists of as little as 25% of isologous cells, with 75% allogeneic cells. Therefore, this invention for generating chimeric epidermis using isologous and allogeneic epidermal cell suspensions shows high quality results for skin replace-ment.
It is predicted that using this technology for human treatment could significantly cut down the delay in time required to obtain graftable sheets by approximately 50%. Indeed, in the presence of the feeder layer of 3T3 fibroblasts, freshly isolated keratinocytes grow in colonies through many cycles of cell division (Rheinwald J.G. and Green H., 1975, Cell, 6: 331). The size of colonies increases with time until they fuse and give rise to continuous multilayered sheets of keratinocytes in approximately 10 days. At this time, proliferation stops (Tenchini et al. 1992, Burns, 18: lls). In parallel, allogeneic keratinocytes stored in a cell bank, beforehand tested for virus infection and other diseases, may be thawed and plated onto culture flasks until confluence.
Cell suspensions can be made separately from both the autologous and allogeneic cultures. The two cell types can then be mixed together at an appropriate ratio and then plated in new flasks and incubated for graftable sheet production. At this stage, the epithelial sheets produced will be used for skin trauma therapy such as in burns.

Compared to the standard culture methods, the chimeric sheets could be used for grafting on the first passage of cultured autologous keratinocytes rather than waiting for the second or, in many cases, the third passage. This method should allow significant reduction in the skin wound treatment duration.
While the above description relates to chimeric skin grafts it is predicted that this chimeric technology could also be used for preparing chimeric vascular organs, chimeric ligaments as well as other chimeric organs.

Claims (15)

CLAIMS:

1. A process for producing a chimeric cell culture suitable for transplanting onto a host, said process comprising culturing epithelial cells that are autologous to said host with epithelial cells that are non-autologous to said host under conditions suitable to promote growth of the cells, wherein both said autologous and non-autologous cells are the same cell type.

2. The process according to claim 1, wherein said cells are epidermal cells.

3. The process according to claim 2, wherein said epidermal cells are keratinocytes.

4. The process according to claim 3, wherein the chimeric cell culture is suitable for skin grafts.

5. The process according to any one of claims 1 to 4, wherein said non-autologous cells are allogeneic or xenogeneic to said host.

6. A chimeric cell culture suitable for transplanting onto a host comprising a mixture of epithelial cells that are autologous to said host with epithelial cells that are non-autologous to said host, wherein both said autologous and non-autologous cells are the same cell type.

7. The cell culture according to claim 6, wherein said cells are epidermal cells.

8. The cell culture according to claim 7, wherein said epidermal cells are keratinocytes.

9. The cell culture according to claim 8, wherein said cell culture is suitable for skin grafts.

10. The cell culture according to any one of claims 6 to 9, wherein said non-autologous cells are allogeneic or xenogeneic to said host.

11. Use of the chimeric cell culture according to any one of claims 6 to 10 as a skin graft.

12. The use of claim 11 for the treatment of a burn patient.

13. The use of claim 11 for the preparation of a medicament for the treatment of a burn patient.

14. Commercial package comprising the chimeric cell culture defined in any one of claims 6 to 10 and instructions for the preparation of a skin graft for the treatment of a burn patient.

15. Commercial package comprising the chimeric cell culture defined in any one of claims 6 to 10 and instructions for its use as a skin graft for the treatment of a burn patient.