IL105063A - Anti-tumor vaccine - Google Patents

Description

Anti-tumor vaccine, YEDA RESEARCH AND DEVELOPMENT COMPANY LIMITED »"V1 mjlOl npn»i> man V7> C:- 89245 ANTI-TUMOR VACCINES FIELD OF THE INVENTION The present invention is generally in the field of cancer therapy and concerns novel immunogens, anti-tumor vaccines for use in human and veterinary medicine comprising them, and process for the preparation of said immunogens.

The immunogens of the present invention are derived from tumor cells which were treated to increase their specific immunogenicity. The immunogen may be the cells, plasma membranes of such cells or tumor-specific immunogenic proteins obtained from these cells or membranes.

BACKGROUND OF THE INVENTION AND PRIOR ART As is well known and documented, cancer cells generally contain on their external surface specific neo-antigens which are foreign to the host body. Nevertheless, for reasons which are not entirely clear, the immune system fails to develop an effective immune reaction against the tumor cells. Attempts have been made to immunize *cancer patients with preparations that will stimulate their immune systems to develop a reaction against the neo-antigens with the hope that such an immune reaction will destroy the residing cancer.

U.S. Patent No. 4,931,275 discloses anti-tumor vaccines which contain as active ingredient tumor cells which have been treated to augment their immunogenic properties, their plasma membranes or specific membrane proteins obtained from these cells or membranes. The treatment which augments their immunogenicity in accordance with this patent consists of either exposure of the cells to cholesteryl hemisuccinate which rigidifies the lipid layer of the plasma membrane, the application of hydrostatic pressure up to about 1500 atm, or a combination of these two treatments.

Ramakrishna & Shinitzky {Cancer Immunol. Immunother., 1991, 33:1-8) showed that delayed type hypersensitivity (DTH) response to syngeneic tumors could be potentiated by cells treated with either hydrostatic pressure up to 1200 atm, crosslinking with adenosine 2',3'-dialdehyde, or with hydrostatic pressure followed by crosslinking.

It is an object of the present invention to provide a novel . immunogen capable of inducing an anti-tumor immune response. More specifically, it is an object of the present invention to provide such an immunogen which is derived from modified tumor cells, which may be such cells, membranes thereof or immunogenic proteins obtained from said cells or membranes.

It is another object of the present invention to provide a process for preparing said immunogen.

It is a further object of the present invention to provide a vaccine comprising said immunogen.

GENERAL DESCRIPTION OF THE INVENTION .

In accordance with the present inventioi it was found, that an immunogen having superior anti-tumor immunogenicity can be obtained from tumor cells treated by simultaneous exposure of a crosslinking agent being a 2',3'-nucleoside or nucleotide dialdehyde (hereinafter "said crosslinking agent"), and to hydrostatic pressure in the range of about 1200- 1400 atm.

By one of its aspects the present invention provides an immunogen derived from modified tumor cells and capable of inducing an anti-tumor immune response, wherein said modified tumor cells have been prepared by exposing tumor cells simultaneously to said crosslinking agent at a concentration and for a time sufficient to cause crosslinking of proteins in the cell's plasma membranes and to hydrostatic pressure within the range of about 1200-1400 atm.

The concentration of said crosslinking agent is preferably above about 20 mM.

The application and release of pressure is preferably gradual, e.g. over a period of 5-10 minutes.

Said crosslinking agent is preferably a 2',3'-dialdehyde of a natural nucleotide or nucleoside as non-naturally occurring, i.e. synthetic nucleosides or nucleotides are very often highly toxic.

The preferred crosslinking agents are represented by the following formula I: wherein R is H, or a mono-, di-or tri-phosphate group, and B is a nucleotide base selected from the group consisting of adenine, guanine, cytosine, thymine, uracil and inosine.

Examples of such a crosslinking agent are 2',3'-adenosine dialdehyde (Ad A) and 2',3' -adenosine monophosphate dialdehyde (AMPdA).

The compound of formula I may be prepared by reacting a nucleoside or a nucleotide of the following formula II: wherein R and B have the meanings given above for formula I, with an oxidizing agent, e.g. an alkali periodate.

The immunogen may consist of the whole modified tumor cells, membranes derived from such cells, as well as proteinaceous material obtained from such cells or membranes which substantially retains the capability of the modified tumor cells to induce the anti-tumor immune response.

Preferably, after the treatment in accordance with the invention, the modified tumor cells are exposed to high intensity radiation in order to destroy their genetic material. This is particularly important where the whole modified tumor cells are used for immunization and may not necessarily be - 5 - 105063/2 required where said immunogcn consists of membranes preparations or said proteinaceous substances.

By another aspect, the present invention provides a process for preparing an immunogen derived from modified tumor cells and capable of inducing an anti-tumor immune response, said process comprising the steps of: (a) providing tumor cells; (b) exposing said tumor cells simultaneously to the action of a 2', 3' nucleoside or nucleotide dialdehyde crosslinking agent at a concentration and for a time sufficient to cause crosslinking of proteins in the cells' plasma membranes, and to hydrostatic pressure of about 1200 to 1400 atmospheres; and (c) separating the tumor cells from the crosslinking agent.

If desired, tumor cells modified by the above-described process may be purified.

Where the desired immunogen consists of the whole modified tumor cells, the product of the above process may be used per se or after several purification treatments, e.g. consisting of centrifugation and removal of the supernatant.

Where the desired immunogen consists of membranes of the modified tumor cells, the modified tumor cells are subjected to further treatment in which the cells are disrupted, e.g. by exposure to a hypotonic medium or by sonication, and then the membrane fragments are collected e.g. by centrif gation in a sucrose gradient, as generally known per se.

Where the desired immunogen consists of said proteinaceous material, the whole modified cells or the plasma membranes are subjected to further treatment consisting for example of dissolving the membranes by the use of detergents, separating the proteinaceous material by one of various methods known per se, e.g: gel filtration, and then determining which of the separated proteinaceous material fragments possesses the desired immunogenicity.

Said immunogen may be used for the immunization of cancer patients against their tumor or may be used for the sensitization of immune cells in vitro. For immunization, said immunogen may be injected into a patient together with a pharmaceutically acceptable carrier or adjuvant in an amount sufficient to achieve anti-cancer immune response.

For in vitro sensitization, immune cells, i.e. leukocytes or lymphocytes, are withdrawn from the patient by means known per se and then cultured together with said immunogen until a population of such immune cells reactive against said immunogen is obtained. Said population · may then be reinjected into a cancer patient in order to treat his tumor.

By another of its aspects, the present invention thus provides a vaccine composition comprising said immunogen and a pharmaceutically acceptable carrier.

While the immunization of patients in accordance with the present invention can be performed by the use of an allogeneic immunogen, it is preferably performed by the use of an autologous immunogen, i.e. an immunogen derived from tumor cells of the same patient. The use of an autologous immunogen entails significant advantages in that the immune response which occurs is primarily directed against the neo-antigen of the tumor, while where an allogenic immunogen is used the resulting immune response will be against all the non-self antigens of such an immunogen. A further advantage of the use of an autologous immunogen is in that the neo-antigens associated with a specific tumor may differ from one patient to another. Where an autologous preparation is used, the immunization of a patient comprises the following steps: (a) withdrawing tumor growth from a patient by biopsy or surgery; (b) dissociating intact tumor cells by mechanical or enzymatic means; (c) dispersing said tumor cells in a medium; (d) exposing said tumor cells simultaneously to said crosslinking agent at a concentration and for a time sufficient to cause crosslinking of proteins in the cell's plasma membranes and to hydrostatic pressure within the range of about 1200-1400 atm; (e) removing the crosslinking agent and preparing a tumor- specific immunogen derived from the modified cells obtained; and (f) injecting said immunogen into the patient, whereby an anti- ■ tumor immune response in said patient is induced.

Where an allogeneic immunogen is being used, an immunogen derived from modified tumor cells obtained from a defined tumor cell line may be used.

The invention will now be illustrated with reference to some non-limiting examples.

BRIEF DESCRIPTION OF THE DRAWINGS In the following, reference will at times be made to the accompanying drawings in which: Fig. 1 is a graphic representation of an experiment in which the survivability of mice challenged with tumor cells after immunization with one of the following preparations was tested: EL4 leukemia cells treated with various levels of hydrostatic pressure in the presence of 40 mM AdA (filled squares); EL4 leukemia cells treated with increasing levels of hydrostatic pressure and then with 40 mM AdA (empty squares); B16 melanoma cells treated by various levels of hydrostatic pressure in the presence of 40 mM AdA (filled circles); and B16 melanoma cells treated with hydrostatic pressure and then with 40 mM AdA; - Fig. 2 shows the survivability of mice challenged with tumor cells following immunization with one of the following preparations: EL4 leukemia cells treated for 10 min with hydrostatic pressure of 1350 atm in the presence of various concentrations of AdA (filled squares); B16 melanoma cells treated in the same manner (filled circles); B16 melanoma cells treated in the same manner with AMPdA (empty circles); Fig. 3 shows a three-dimensional overlay of antigen expression on B16-BL6 melanoma cell plasma membrane surface as analyzed on. FACScan by indirect immunofluorescence: A & B -negative controls (A - - autofJuorescence; B -cells reacted only with secondary antibody); C - unmodified cells; D & X -cells exposed to 20mM AdA; E & Z -cells exposed to hydrostatic pressure of 1,200 atm for 15 minutes; F & Y -cells exposed simultaneously to both 20 mM AdA and 1,200 atm pressure; Fig. 4 shows the effect (as per cent of positive cells counted by FACScan instrument out of 10,000 events) of graded levels of hydrostatic pressure (applied for 15 minutes) combined with a constant dose of AdA 20 mM on antigen expression in B16-BL6 melanoma cells: filled bars - class I antigen, gray bars - B16 antigen; and Fig. 5 shows the effect (per cent positive as determined on FACScan out of 10,000 events) of varying concentrations of AdA combined with a constant level of hydrostatic pressure (1200 atm, 15 minutes) on antigen expression in B16-B16 melanoma cells: black bars -MHC class I antigen, gray bars B16 antigen.

EXAMPLE 1: Materials and Tumor Cells' Modification Methods* ' Cells: Cells from an EL4 tumor, which is a chemically induced T- leukemia (Gorrer, 1961. In: Harris RJG, ed., Biological Approach to Cancer Chemotherapy. Academic Press, New York) were maintained in ascites form in the peritoneal cavity of 6-8-week old C57B1/6J female mice. About 105 cells were inoculated i.p. and 10 days later the cells (approximately 5x10s cells per animal) were harvested.

Cells of ARadLV 136, which is a radiation-induced leukemogenic variant of ARadLV, were maintained in vitro as described previously (Haran-Ghera et al. , 1977, J. Immunol. 118:600).

BL6 melanoma cells which are a very invasive variant of the B16 cell line (Hart 1979, Am. J. Patholog. 97:587). The B16-BL6 tumor was serially passaged in syngeneic C57B1 mice by s.c. inoculation of 2 -5 x 106 cells.

Adenosine 2 ',3' -dialdehyde (AdA): AdA, which is a biologically compatible chemical crosslinker, was synthesized by a modification of the procedure previously described (Hansske et al., 1914, Bioorg. Chem. 3:367): Adenosine (Sigma Chemical Co., St. Louis, Mo) and sodium metaperiodate (Fluka Chemie AG, Buchs. FRG) were mixed in 100 ml aqueous solution to a final concentration of 10 mM of each of these substances, stirred in the dark and cooled with ice water for 1 h, and then concentrated to 5 ml in vacuum at 30°C. The resulting concentrate was then incubated for 12 h at 4°C and the crystalline product which was obtained was separated and found to be homogeneous in thin-layer chromatography (silica gel G plate, 0.2 mm thickness, Merck Darmstadt; running solvent; acetonitrile/water, 4:1 v/v, RF 0.80). The crystals were filtered, washed three times with cold water and dried over silica gel in vacuum (12 mm Hg; 1.6 kPa).

The yield of the above preparation procedure was found to be approximately 90%. The obtained product had a melting point of 110°C and melting was accompanied by decomposition, this being in agreement with previous reports (Hansske et al, 1974, supra).

Modification of tumor cells: After harvesting, the cells were washed twice with PBS (pH 7.4) and then subjected to one of the following modification treatments. The viability of the modified tumor cells was assessed by trypan blue dye exclusion.

Modification I: crosslinking of proteins on tumor cell surface - About 108 cells/ml were inoculated into a 50 ml tube (Falcon, Becton Dickinson Labware, N.J.) holding a PBS solution containing 0.5% AdA and were incubated in this solution for 1 h at room temperature with occasional mixing. Unbound AdA was removed by three cycles of centrifugation at 1500 rpm for 5 min, followed by gentle resuspending of the pellet in PBS (in the final resuspension PBS was added to obtain a desired cell concentration).

Modification II: application of hydrostatic pressure - This modification was performed in a similar manner as previously described (Richert et al, 1986, Cancer Immunol. Immunother. 22:119). Cells were dispersed in PBS at a concentration of 10s cells/ml in a capped Eppendorf plastic tube (1.5 ml, Netheler and Hinz GmbH, Hamburg, FRG) and filled to the brim. A 0.5 in. (1.27 cm) 18G needle, was inserted through the cap and served as a vent for pressure equalization. Both the needle and the tube were filled with PBS and the cap was pressed down without entrapping any air bubbles (Removal of all air bubbles is important as these may cause cell disruption upon release of pressure). The tubes were then placed inside a pressure bomb of 40 ml capacity (Aminco, American Instruments Co., Md.), filled with PBS and sealed.

Pressure was gradually applied to reach a level of about 1200 atm within 7-8 min and this pressure was maintained for about 15 min. Thereafter, the bomb was unlocked and allowed to decompress gradually to ambient pressure in about 8-10 min. The cells were then transferred into a 50 ml tube in 10 ml PBS and centrifuged at 1500 rpm for 5 min. The pellet was then gently resuspended in PBS to the desired concentration.

Modification III: hydrostatic pressure and crosslinking in sequence - Cells were pressurized and then immediately crosslinked by the two modification procedures outlined above.

Modification IV: hydrostatic pressure and crosslinking simultaneously - In this modification, which is the one performed in accordance with the invention cells were pressurized and crosslinked at the same time by the two modification treatments described above.

EXAMPLE 2 The viability of C57B1 mice challenged with 105 viable untreated tumor cells following pretreatment with various immunogenic preparations was tested. Survival after challenge was scored at day 30.

The pretreatment consisted of two vaccinations, one three weeks and the other one week prior to the challenge, with an immunogenic preparation which consisted of cells subjected to one of the following modification treatments: exposure to AdA, application of hydrostatic pressure or a combination of the two, by the modification procedures described above in Example 1. The cells used for vaccination were of the same kind as the cells used to challenge the mice.

The cells used in this experiment were either EL-4 of BL6.

Test No. 1: Four groups of mice were used, each pretreated with one of the following preparations: EL-4 leukemia cells treated for 10 minutes by various levels of hydrostatic pressure, in the presence of 40 mM AdA; EL-4 leukemia cells treated for 10 minutes by various levels of hydrostatic pressure and then by 40 mM AdA; B16 melanoma cells treated as Group 1; B16 melanoma cells treated as Group 2.

The results are shown in Fig. 1 (each point represents an average of 10 animals): Group 1 -filled squares; Group 2 -empty squares; Group 3 -filled circles; Group 4 -empty circles.

The results demonstrate that the maximal survivability was obtained after vaccination with an immunogenic preparation exposed to a hydrostatic pressure of 1200-1400 and surprisingly far inferior results were obtained after exposure to hydrostatic pressure of 1500 atm. Furthermore, these results show that the simultaneous exposure to both hydrostatic pressure and AdA leads to a higher survivability of the mice than these two treatments in sequence.

Test No. 2: Several groups of C57B1 mice (10 mice in each group) were pretreated by one of the following preparations: Treatment 1 EL-4 leukemia cells treated for 10 minutes by hydrostatic pressure of 1350 atm in the presence Sf various increasing concentrations of AdA; Treatment 2: B16 melanoma cells treated as in Treatment 1.

Treatment 3: B16 melanoma cells treated for 10 min. by hydrostatic pressure of 1350 atm in the presence of various concentrations of AMPdA.

The results of the experiments are shown in Fig. 2 (each point represents an average of 10 animals): Treatment 1 -filled squares; Treatment 2 -filled circles; Treatment 3 -empty circles.

As can be clearly seen the maximal survival rate was obtained with an AdA or AMPdA concentration of above 30 mM.

Test No. 3: Five groups of C57B1 mice (6 mice in each group) were immunized subcutaneously and then challenged with B16-BL6 cells. The preparation used for immunization consisted of plasma membranes isolated by discontinuous sucrose gradient centrifugation (Maeda et al, 1983, Biochim. Biosphys. Acta 731:115) from untreated or treated cells. Details of the immunizing preparations is given in Table 1.

The following parameters were tested for each group of animals: survival rate; mean tumor diameter, measured using standard callipers in three orthogonal directions and presented by the mean value; metastatic nodules in lungs, scored after removal of the lungs, and fixations with Bouin's fixative and then washing with 70 ethanol. The results of this experiment are also shown in the following Table 1.

Table 1 Effect of modification in the immunogenicity of B16-BL6 melanoma membranes * All modifications on B16-BL6 melanoma consisted of simultaneous treatment of tumor cells with 40 mM AdA and 1350 atm hydrostatic pressure.

These results demonstrate that immunization with an immunizing preparation consisting of plasma membrane's isolated from B16- BL6 cells treated by pressure and AdA in accordance with the invention (Treatments 4 and 5) brought a very high survival rate, the mean tumor diameter was minimal and no metastatic nodules in the lungs were observed.

These results prove the unexpected high potency of the vaccination treatment of the invention.

EXAMPLE 3 The presence of MHC class I antigens (H-2kb) and the tumor- specific retroviral antigen on B16-BL6 melanoma cells, derived from s.c. tumors either directly after obtaining single cell suspensions or passaging the cells in culture 6-8 times over a period of 3-4 weeks, was analyzed by flow cytometry.

About 106 modified or unmodified B16-BL6 tumor cells were incubated at a first step with unlabelled primary antibodies: 30μ1 (25 μg) of anti-class I monoclonal antibody (clone 28-8-6, obtained from Dr. D. Sachs, National Cancer Institute, U.S.A.) or ΙΟμΙ (8 g) of monoclonal antibody against a retroviral antigen on the surface of B16 cells (MM2.9B6, Leong et al. 1988, Cancer Res. 48:4954) in a final volume of 50 μΐ containing 1% FCS (fetal calf serum) and 0.01% of sodium azide and incubated for 45 minutes at 4°C. Cells were washed twice in HBS (hepes buffered saline) and the pellet was resuspended in a solution of a labeled secondary antibody: 50 μΐ of a solution containing 40 μg of the F(ab')2 fragment of FITC-GAMIG (fluorescein isothiocyanate labeled goat anti-mouse IgG) in HBS with 1% FCS and 0.1% sodium azide and incubated for an additional 45 minutes at 4°C in the dark. Thereafter cells were washed as before and fixed in 1% freshly prepared paraformaldelyde for 20 minutes. Fixed cells were washed thrice in HBS, resuspended in 0.5 ml HBS and passed through ΙΟΟμ nylon mesh prior to flow cytrometric analysis. Samples were stored for no more than 24 hours in the dark at 4°C as samples stored for longer period gave rise to high autofluorescence.

Non-reacted B16-BL6 cells and B16-BL6 cells which reacted directly with FITC-GAMIG, and 2% BSA (bovine serum albumin) served as negative controls. Modified as well as unmodified cells were labeled and analyzed on either FACS 440 (Becton-Dickinson, Mountainview, CA) or on the FACScan instrument (Becton-Dickinson). Populations which were determined as positive on dual parameter (forward and orthogonal light scatter) analysis were gated and data was acquired on live gates. Histrograms were generated using either consort 40 software on FACS 440 or consort 30 with LYSYS software available with FACScan. Appropriate controls were introduced in order to apply logic threshold values. Amelanotic cells which appeared in the population were gated out in the present analysis by light scatter gating. Approximately 10,000 events were tested in each sample.

Exposure to AdA or to hydrostatic pressure was carried out in a similar manner to that described in Example 1.

As can be seen in Fig. 3, maximum expression of both class I and melanoma-specific antigen was noted with B16-BL6 cells which were modified by 1,200 atmospheres of hydrostatic pressure and simultaneous crosslinking with 20mM AdA.

In another set of experiments B16-BL6 cells were exposed to hydrostatic pressure in the range of 600-1,200 atm and to a constant concentration of AdA of 20mM and the results are shown in Fig. 4. In a further experiment B16-BL6 cells were exposed to a constant level of 1,200 atm of hydrostatic pressure while incubation with AdA at concentrations from 0.002mM to 20mM, and the results are shown in Fig. 5. As can be seen in these Figures, maximum fluorescent intensity for both class I and B16-BL6 tumor antigen was observed with the combination of a high level of pressure (1,200 atm) and the highest in the series^of concentrations of AdA, 20mM.

EXAMPLE 4 Immunogenicity of autologous tumor cells modified by a simultaneous pressure-crosslinking procedure was tested in five cancer patients, using the Delayed Type Hypersensitivity (DTH) test.

Tumor cells were isolated from each of five cancer patients and were subjected to a hydrostatic pressure of 1200 atm for 15 min. in the presence of 20 mM AdA in accordance with "Modification IV" in Example 1. The cells were then irradiated by a dose of 10,000 rads after which they lost their proliferation potential while remaining immunogenic. 106 modified and irradiated autologous tumor cells (i.e. cells derived from patient's own tumor) were then injected intra dermally (I.D.). An immune reaction elicited by the injected cells was evidenced in the patients by a swollen red area which appeared in the skin at the inoculation site.

The degree of the patients' skin reaction was determined by the diameter of the erythema (redness) and induration (swelling) (according to the method of Skornick et al, Cancer Immunol. Immunother., 11, 93, 1981; a copy of this reference is attached hereto and marked "C"). The skin reaction was expressed by a score, "+", "++" or "+++" where "-" indicated no reaction and "+++" indicated the maximal reaction. A standard maximal reaction was such obtained by injection with tuberculin (a lipoprotein of Mycobacterium tuberculosis) to people having a history of tuberculosis infection or previous vaccination.

The DTH reaction was monitored 24, 36, 48 and 72 hours after the inoculation of the cells. The peak of the reaction was normally observed 24-48 hours after inoculation.

The results were compared with control results obtained following injection by the same procedure of autologous irradiated but unmodified cells. These control cells were injected to the patient on the same days at an adjacent site.

The skin reaction was rated as described above by measuring the diameter of the erythema and the degree of induration at different periods of time after the injections and the results obtained with the five cancer patients is presented in the following Table 2: Table 2 The results show that while non-treated cells cause a minimal DTH reaction (- or ±), the injection of the modified cells resulted in a very strong immune reaction in all patients (++ to +++). The maximal reaction appeared 36-48 hours after the injection of the cells in line with the expected progress of the DTH reaction.

Claims (9)

CLAIMS:

1. An immunogen derived from modified tumor cells and capable of inducing an anti-tumor immune response, wherein said modified rumor cells are prepared by exposing tumor cells simultaneously to the action of a crosslinking agent being a 2',3 '-nucleoside or nucleotide dialdehyde at a concentration and for a time sufficient to cause crosslinking of proteins in the cell's plasma membranes, and to hydrostatic pressure of about 1200- 1400 atm.

2. An immunogen according to Claim 1, wherein said modified tumor cells were prepared by exposing tumor cells simultaneously to said hydrostatic pressure and to a crosslinking agent represented by the following formula I: wherein R is H or a mono-, di-or tri-phosphate group, B is a nucleotide base selected from the group consisting of adenine, guanine, cytosine, thymine, uracil and inosine.

3. An immunogen according to Claim 2, wherein said crosslinking agent is 2',3'-adenosine dialdehyde or 2',3'-adenosine monophosphate dialdehyde.

4. An immunogen according to any one of the preceding claims, wherein said crosslinking agent is at a concentration of above about 20mM.

5. An immunogen according to any one of the preceding claims, and being a member of the group consisting of whole modified tumor cells, plasma membranes obtained therefrom, and proteinaceous material obtained from said cells or membranes which substantially retains the capability of said cells to induce an anti-tumor immune response.

6. A process for preparing an immunogen derived from modified tumor cells and being capable of inducing an anti-tumor immune response, comprising the steps of: (a) providing tumor cells; (b) exposing tumor cells simultaneously to the action of a crosslinking agent being a 2',3'-nucleoside or nucleotide dialdehyde at a concentration and for a time sufficient to cause crosslinking of proteins in the cell's plasma membranes, and to hydrostatic pressure of about 1200-1400 atm; and (c) separating the tumor cells and said crosslinking agent and if desired purifying the modified cells obtained.

7. A process according to Claim 6, wherein said crosslinking agent has a concentration of above about 20mM.

8. A process according to Claims 6 or 7, wherein the modified cells are disrupted and then the membrane fragments are collected.

9. A method of sensitizing immune cells to attack tumor cells comprising withdrawing immune cells from a patient and culturing said immune cells with a tumor immunogen derived from modified tumor cells and capable of inducing an anti-tumor immune response, wherein said modified tumor cells were prepared by exposing tumor cells to a crosslinking agent being a 2',3'-nucleoside or nucleotide dialdehyde at a concentration and for a time sufficient to cause crosslinking of proteins in the cell's plasma membranes for a time sufficient to obtain a culture of said immune cells reactive against said immunogen.