DRUG FOR PREVENTING AND/OR TREATING BRAIN TUMOR AND APPLICATION THEREOF

Abstract

A drug for preventing and/or treating a brain tumor and an application thereof. The drug comprises Plasmodium. The drug has significant preventive and/or therapeutic effects on a brain tumor, and is capable of inhibiting the growth of the brain tumor and prolonging the life span of a patient, and has no obvious side effects and has a high safety level. The drug expands treatment methods for brain tumors. Due to the specificity and sensitivity of brain tissues, chemotherapeutic drugs cannot easily cross the blood-brain barrier and exert anti-tumor effects. The drug mainly regulates the immunological functions and inflammation-related factors of the body to break through the blood-brain barrier by fully activating immunocompetence and inhibiting the growth of a brain tumor, thereby extending lifespan.

Claims

1. A drug for preventing and/or treating brain tumors, comprising Plasmodium.

2. The drug for preventing and/or treating brain tumors of claim 1, wherein the brain tumors comprise primary brain tumors or metastatic brain tumors.

3. The drug for preventing and/or treating brain tumors of claim 1, wherein the brain tumors comprise glioma, meningioma, pituitary adenoma or neurilemmoma, preferably glioma.

4. The drug for preventing and/or treating brain tumors of claim 1, wherein the Plasmodium comprises any one or a combination of at least two of Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, Plasmodium ovale or Plasmodium knowlesi, preferably Plasmodium vivax and Plasmodium falciparum.

5. The drug for preventing and/or treating brain tumors of claim 1, wherein the Plasmodium is cryopreserved and/or resuscitated Plasmodium or cryopreserve and/or resuscitated Plasmodium sporozoites.

6. The drug for preventing and/or treating brain tumors of claim 1, wherein a dosage form of the drug is any pharmaceutically acceptable dosage form.

7. The drug for preventing and/or treating brain tumors of claim 1, wherein the dosage form of the drug is injection.

8. The drug for preventing and/or treating brain tumors of claim 1, further comprising any one or a combination of at least two of pharmaceutically acceptable pharmaceutical excipients; preferably, the pharmaceutical excipient includes any one or a combination of at least two of a thickener, a diluent, a flavoring agent, an adhesive or a filler.

9. The drug for preventing and/or treating brain tumors of claim 1, wherein the drug is a drug carried on a pharmaceutical carrier; preferably, the pharmaceutical carrier comprises a liposome, a micelle, a dendrimer, a microsphere or a microcapsule.

10. A method for treating brain tumors, comprising: (a) administering to patients a therapeutically effective amount of the drug according to claim 1; and (b) maintaining Plasmodium infection to a chronic or subacute phase.

11. The method of claim 10, wherein step (b) is: maintaining the Plasmodium infection for 6 to 8 weeks.

12. The method of claim 10, wherein the brain tumors comprise primary brain tumors or metastatic brain tumors.

13. The method of claim 12, wherein the brain tumors comprise glioma, meningioma, pituitary adenoma or neurilemmoma, preferably glioma.

14. The method of claim 10, further comprising: (c) administering an antimalarial drug to terminate the Plasmodium infection; and wherein steps (a), (b) and (c) are carried out one or more times.

15. (canceled)

16. A method for preventing and/or treating brain tumors, comprising administering an effective amount of the drug according to claim 1 to subject in need thereof.

Description

BRIEF DESCRIPTION OF DRAWINGS

[0092] FIG. 1 shows results of the effect of Plasmodium infection on the glioma growth in tumor-bearing mice in subcutaneous inoculation model.

[0093] FIG. 2 shows results of the effect of Plasmodium infection on the survival time of tumor-bearing mice in subcutaneous inoculation model.

[0094] FIG. 3 shows results of the effect of Plasmodium infection on the weight of tumor-bearing mice in subcutaneous inoculation model.

[0095] FIG. 4 is the trend chart of the Plasmodium parasitemia of the Plasmodium treatment group in subcutaneous inoculation model.

[0096] FIG. 5 is the schematic diagram of pWPXLd-mcherry-F2A-Luciferase-Puro lentivirus vector.

[0097] FIG. 6 is the visual field view of positive rate detection of a GL261.mcherry-Luc cell line monoclonal.

[0098] FIG. 7 is the graph of the statistical result of Luciferase activity of GL261.mcherry-Luc cell line.

[0099] FIG. 8 shows results of the in vivo imaging of Plasmodium infection on the glioma growth of tumor-bearing mice in intracranial in situ inoculation model.

[0100] FIG. 9 shows results of the effect of Plasmodium infection on the glioma growth of tumor-bearing mice in intracranial in situ inoculation model.

[0101] FIG. 10 shows results of the effect of Plasmodium infection on the survival time of tumor-bearing mice in intracranial in situ inoculation model.

[0102] FIG. 11 shows results of the effect of Plasmodium infection on the weight of tumor-bearing mice in intracranial in situ inoculation model.

[0103] FIG. 12 is the trend chart of the Plasmodium parasitemia of the Plasmodium treatment group in intracranial in situ inoculation model.

DETAILED DESCRIPTION

[0104] The technical solutions of the present application are further described below through the detailed description. It is to be understood by those skilled in the art that examples described herein are merely used for a better understanding of the present application and are not to be construed as specific limitations of the present application.

Example 1

[0105] This example provides a method of cryopreservation and resuscitation of Plasmodium blood, and the specific operations are as follows.

[0106] After the blood infected with Plasmodium was stored in the warehouse, the Plasmodium blood was quickly packed separately as required, and the packaged Plasmodium blood was labeled and cryopreserved in liquid nitrogen.

[0107] (I) Cryopreservation of Plasmodium

[0108] (1) Preparation of Experimental Materials:

[0109] Plasmodium: the peripheral blood of a malaria patient without other legal blood-borne infectious diseases, or Plasmodium blood cultured in the laboratory;

[0110] reagents: sodium chloride injection, 10% NaCl solution, 3.5% NaCl solution, RPMI1640 culture medium, and 28% glycerol cryopreservation solution (by mixing 28 g of glycerol, 3 g of sorbitol and sodium chloride injection and filling the volume of the mixture to 100 mL);

[0111] consumables: cryopreservation tubes, 50 mL centrifuge tubes, 15 mL centrifuge tubes, 250 mL culture medium bottles, Pasteur pipettes, printed labels, and registration forms;

[0112] instruments: pipettors, pipettes, sterilization scissors, and liquid nitrogen tank.

[0113] (2) Blood collection and microscopic examination: An appropriate amount of Plasmodium blood samples were taken to make thin blood smears for microscopic examination. The 30% and more of cryopreserved Plasmodium were in the early trophozoite phase. The report of microscopic examination was written.

[0114] (3) 20 mL Plasmodium blood per tube was centrifuged at 300×g for 10 minutes (the acceleration and deceleration speeds were set to 1), and the plasma was transferred to new 50 mL centrifuge tubes.

[0115] (4) The buffy coat in the upper layer at the bottom of the centrifuge tubes was sucked off, 1640 culture medium with twice the volume of Plasmodium blood was added, and the resulting mixture was mixed well and centrifuged at 300×g for 5 minutes (the acceleration and deceleration speeds ware set to 1).

[0116] (5) Gently flick the bottom of the 50 mL centrifuge tubes. 28% glycerol cryopreserved solution whose volume was equal to that of Plasmodium blood was slowly added into the 50 mL centrifuge tubes, and the resulting mixture was pipetted evenly using a pipettor and incubated at room temperature for 5 minutes.

[0117] (6) The mixture of RBC and 28% glycerol cryopreservation solution was separately packed in cryopreservation tubes, 1.0 mL volume per tube, labeled with printed labels, put into cryopreservation boxes and directly put into liquid nitrogen for cryopreservation.

[0118] (7) Quality control of cryopreservation: An appropriated amount of the RBC-28% glycerol cryopreservation solution mixture before cryopreservation was added to an appropriated amount of 10% FBS-RPMI1640 culture medium, the resulting mixture was cultured in an incubator with CO.sub.2 at 37° C. for 72 hours, and the color of the culture medium was observed to confirm that there was no turbidity.

[0119] (II) Resuscitation of Plasmodium

[0120] (1) Preparation of reagents and consumables: a water bath cauldron (37° C.), 15 mL centrifuge tubes, 3.5% NaCl, sodium chloride injection, centrifuges, printed labels, and forms.

[0121] (2) The cryopreserved Plasmodium blood (1.0 mL per tube) was quickly shaken in a 37° C. water bath cauldron and quickly thawed to keep the activity of Plasmodium.

[0122] (3) The Plasmodium blood was added to 15 mL centrifuge tubes, the equal volume of 3.5% NaCl was slowly added along the tube wall, the resulting mixture was gently pipetted, mixed well, allowed to stand at room temperature for 5 minutes and centrifuged at 300×g for 5 minutes, and the supernatant was discarded.

[0123] (4) 0.9% NaCL solution whose volume was 5 times that of Plasmodium blood was added along the tube wall, gently pipetted, mixed well and centrifuged at 300×g for 5 minutes, and the supernatant was discarded.

[0124] (5) Normal saline was added until the hematocrit was 50% and mixed well, the red blood cell density was counted and recorded, and the resulting mixture was temporarily stored at 4° C. for clinical inoculation.

[0125] (6) Quality control of resuscitation: After inoculation, the remaining blood samples were smeared to form blood smears, and the Plasmodium parasitemia and the Plasmodium status before injection were observed by microscopic examination and recorded.

Example 2

[0126] This example provides a method of cryopreservation, resuscitation and inoculation of Plasmodium sporozoites, and the specific operations are as follows.

[0127] (I) Blood feeding of Anopheles and acquisition of sporozoites;

[0128] (1) Preparation of Anopheles: More than 300 Anopheles were fasted for 24 hours in advance.

[0129] (2) Collection of Plasmodium blood: The Plasmodium density and gametophyte of the volunteers with malaria were detected, and 2 mL of peripheral blood of the volunteers was collected intravenously, immediately put into a thermos cup and transported to the mosquito room within 2 hours.

[0130] (3) Blood feeding of Anopheles: Before blood feeding, the temperature of the mosquito room was adjusted to 26° C., the membrane feeding system was prepared, and the collected peripheral blood was added to the membrane feeding system for blood feeding for 30 minutes.

[0131] (4) Anopheles feeding: The non-full Anopheles were removed, the labels were written, the Anopheles were put in an incubator at 26° C., and the sugar water cotton containing 10% glucose and 0.05% PABA was put in the incubator.

[0132] (5) The temperature before and after the transportation of thermos cup, blood feeding time, the number of Anopheles and blood feeding situation of Anopheles were recorded.

[0133] (6) Oocyst examination: 7 to 10 days after blood feeding and infection, the oocyst examination was carried out, 10 Anopheles were dissected, and the ratio of positive Anopheles was calculated. The standard of oocyst infection degree was as follows: +: 1 to 10; ++: 11 to 100; +++: 101 and above; if the ratio of the oocyst infection degree “++” and above was less than 50%, 20 Anopheles were reexamined.

[0134] (7) Sporozoite examination: 14 to 16 days after blood feeding and infection, sporozoite examination was carried out, 20 Anopheles were dissected, and the total number of sporozoites and the average number of sporozoites each Anopheles were calculated.

[0135] (8) Sporozoite acquisition: After 14 to 20 days of blood feeding and infection, Anopheles were taken out, disinfected with 75% ethanol 3 times, 5 seconds each time, and then washed with insect saline 3 times, 5 seconds each time. The salivary glands were dissected and collected in the EP tubes containing 200 μL of AB+ human serum. The EP tubes were always placed on ice. In a case of direct inoculation, the dissected salivary glands were just directly put into normal saline.

[0136] (9) The salivary glands of Anopheles were obtained and repeatedly pipetted with an 18G needle syringe 30 to 40 times to crush the salivary glands and tissues and centrifuged at 1000 rpm at 4° C. for 5 minutes, and the supernatant containing sporozoites was collected. The complete salivary gland of Anopheles was dissected to avoid to collect tissue fragments, otherwise the crush of salivary glands and the purification of sporozoites were affected; sporozoites were better to be acquired separately according to different insect strains and labeled clearly to prevent cross-contamination between different insect strains in the process of sporozoite acquisition; the acquisition process of sporozoites was controlled to be carried out within 1 hour.

[0137] (II) Cryopreservation of Sporozoites

[0138] (1) A small amount of the preceding supernatant containing sporozoites was taken out, and the sporozoites were counted with a blood cell counting chamber.

[0139] (2) The preceding supernatant was centrifuged at 12000 rpm at 4° C. for 10 minutes, the supernatant was discarded, an appropriate amount of AB type human serum containing 1% triple antibiotics was added for resuspension and precipitation, and the sporozoite concentration was adjusted to 2.5×10.sup.8/mL.

[0140] (3) The sporozoites were separately packed into cryopreservation tubes, 200 μL per tube, labeled, put into alcohol at −80° C. for quick cryopreservation, and then 3 hours later, transferred to the liquid nitrogen tank.

[0141] (III) Direct Inoculation of Sporozoites

[0142] (1) A small amount of acquired sporozoite suspended in normal saline suspension was taken out through sterile operation, the sporozoites were counted with a blood cell counting chamber, and the sporozoite concentration was adjusted to the inoculation quantity.

[0143] (2) The sporozoites were inoculated by intravenous injection, then isolated and observed. A small number of samples before inoculation were reserved for sterility test and recorded. 3 days after inoculation, Plasmodium was examined by microscopy every day through blood smears.

[0144] (IV) Inoculation after Sporozoite Resuscitation

[0145] (1) The preserved sporozoites were taken out from the liquid nitrogen tank and thawed in a water bath cauldron at 37° C. for 1 to 2 minutes.

[0146] (2) The sporozoites were centrifuged at 12000 rpm at 4° C. for 10 minutes, the supernatant was discarded, and 10 volumes of normal saline were added for resuspension.

[0147] (3) The sporozoites were centrifuged at 12000 rpm at 4° C. for 10 minutes, the supernatant was discarded, and 200 μL of normal saline was added for resuspension.

[0148] (4) The sporozoites were inoculated by intravenous injection, then isolated and observed.

[0149] (5) A small number of samples before inoculation were reserved for sterility test and recorded.

[0150] (6) 3 days after inoculation, Plasmodium was examined by microscopy every day through blood smears.

Example 3

[0151] This example explores the therapeutic effect of Plasmodium infection on tumor-bearing mice in subcutaneous inoculation models of brain tumor.

[0152] (I) Experimental Materials and Reagents animal: C57BL/6 mice, female, 6 to 8 weeks old, from SHANGHAI SLAC LABORATORY ANIMAL CO. LTD.; Plasmodium: mouse Plasmodium yoelii (P. yoelii 17XNL, MRA-593, Py), freely offered by MALARIA RESEARCH AND REFERENCE REAGENT RESOURCE CENTER (MR4); microscope: Olympus microscope CX31; vernier caliper: electronic digital vernier caliper, No.: 678040, purchased from EXPLOIT TOOLS; Giemsa dye powder: purchased from SIGMA-ALDRICH COMPANY; pathological-grade slide: No.: 10127101P-G, purchased from JIANGSU CITOTEST LABWARE MANUFACTURING CO., LTD.; cedar: from SHANGHAI BIAOBEN MOULD FACTORY; PBS buffer: SH30256.01, purchased from HYCLONE COMPANY; and normal saline: purchased from CISEN PHARMACEUTICAL CO., LTD.

[0153] (II) Experimental Steps

[0154] (1) An animal model was established in the following specific method.

[0155] (1.1) Cell revival: The mouse glioma cell line GL261 was revived and incubated in an incubator with 5% CO.sub.2 at the constant temperature of 37° C.

[0156] (1.2) Cell amplification culture: Cells were passaged every 2 to 3 days, and when the cells grew to 80% of the bottom of the petri dish, the cells were digested with 0.25% trypsin-EDTA digestion solution, passaged at a dilution of 1:3.

[0157] (1.3) Mouse shaving: C57BL/6 mice were shaved clean from the right scapula to the right back.

[0158] (1.4) Preparation of single cell suspension: The cells in the logarithmic growth phase were digested with 0.25% trypsin-EDTA digestive solution, washed with PBS 3 times and then resuspended with serum-free 1640 medium, with the cell concentration of 5×10.sup.6.

[0159] (1.5) Subcutaneous inoculation of tumor cells in mice: C57BL/6 mice were subcutaneously inoculated in the right scapular region. Each mouse was injected with 0.1 mL volume of cell suspension with an inoculation dosage of 5×10.sup.5 GL261 cells/mouse. The day of inoculation was recorded as Day 0 of tumor inoculation.

[0160] (IV) Experimental grouping: Mice were randomly divided into two groups according to the weight of the mice: a glioma control group (GL261) and a P. yoelii treatment group (GL261+Py), 10 mice per group.

[0161] (2) Tumor-bearing mice were inoculated with Plasmodium in the following specific method.

[0162] (2.1) Plasmodium revival: Murine Plasmodium blood (1.0 mL/vial) cryopreserved in a liquid nitrogen tank was quickly shaken in a 37° C. water bath cauldron, mixed well and thawed to keep the activity of Plasmodium.

[0163] (2.2) Plasmodium inoculation: After the Plasmodium blood was mixed well, the Plasmodium blood was inoculated intraperitoneally into C57BL/6 mice with 0.2 mL/mouse, and two mice were inoculated each time as breeding mice.

[0164] (2.3) Preparation of thin smear film and microscopic examination: About 1 to 1.5 μL of blood was collected from tails of mice and smeared on slides to prepare a long tongue-shaped thin smear film with a length of 2.5 cm, and the prepared smear was blow-dried with a blower. The smear film was infiltrated with methanol for 1 minute, stained with 1× Giemsa stain solution for 30 minutes, rinsed with tap water and blow-dried. The Plasmodium infection rate was observed by a 100× oil immersion objective lens. Changes of the Plasmodium parasitemia were observed.

[0165] (2.4) Preparation of a Plasmodium solution: When the parasitemia reached 3% to 10%, the red blood cells (of one breeding mouse infected with Plasmodium and one Naïve mouse not inoculated with Plasmodium) were counted. 5 μL of blood was taken from tails and resuspended in 995 μL of PBS, the red blood cells were counted, and the number of red blood cells infected with Plasmodium per mL was calculated. An EP tube was moistened with 0.2 mL of 3.8% sodium citrate anticoagulant, the blood was taken from eyeballs, the required concentration and total amount of Plasmodium to be inoculated were calculated, and the Plasmodium was prepared into a concentration of 2.5×10.sup.6/mL with PBS.

[0166] (2.5) Inoculation of tumor-bearing mice: 1 day after the tumor was subcutaneously inoculated, each mouse was inoculated with 0.2 mL of red blood cell solution, each mouse in the P. yoelii treatment group was inoculated with the red blood cell solution containing 5×10.sup.5 Plasmodium parasites, and each mouse in the control group was inoculated with the same volume of red blood cell solution containing no Plasmodium.

[0167] (3) Detection index

[0168] (3.1) Tumor volume measurement: The tumor volume was measured every 3 days by the formula for calculating the volume of an ellipsoid (unit: cubic mm): (D×d×d)/2, where D denotes the long diameter of tumor, and d denotes the short diameter of the tumor. The size of the tumor was represented by a mean tumor volume±standard error of the mean (SEM), and the tumor growth curve was drawn. The statistical analysis between groups was performed by two-way analysis of variance (ANOVA), where “*” represents p≤0.05, and “**” represents p≤0.01, indicating that differences between groups were statistically significant.

[0169] (3.2) Survival statistics of mice: The survival was evaluated by the median survival time and the percentage of prolonged survival time. The survival rate was estimated by the Kaplan-Meier method, and the survival curve was drawn, and the median survival time was calculated, where “*” represents p≤0.05, and “**” represents p≤0.01, indicating that differences between groups were statistically significant.

[0170] (3.3) Statistics of the Plasmodium parasitemia: The Plasmodium parasitemia was evaluated by a percentage of red blood cells infected with Plasmodium in mice, where the calculation formula was (number of red blood cells infected with Plasmodium/total number of red blood cells)×100%. Specific operations are as follows: blood was taken from tail veins and smeared on the slides, fixed with methanol, and stained with Giemsa stain solution. The number of red blood cells infected with Plasmodium and the total number of red blood cells were observed under the microscope. The total number of red blood cells was about 1000. The Plasmodium parasitemia was calculated and represented by a mean parasitemia±standard error of the mean (SEM). The cycle curve of Plasmodium infection was drawn, and whether the chemotherapeutic agent had an effect on Plasmodium infection was observed.

[0171] (3.4) Mice weight: The mice were weighed every 3 days, and the weight growth was represented by the mean weight±standard error of the mean (SEM). The effect of the Plasmodium infection on the weight of tumor-bearing mice was observed.

[0172] (4) Experimental results

[0173] (4.1) The tumor growth curve is shown in FIG. 1. Compared with the uninfected control group, in the Plasmodium treatment group, the Plasmodium infection significantly inhibited the growth of glioma GL261 (p=0.0244, *).

[0174] (4.2) The survival curve of tumor-bearing mice is shown in FIG. 2. Compared with the uninfected control group, in the Plasmodium treatment group, the Plasmodium infection significantly prolonged the survival time of tumor-bearing mice (p=0.0479, *), and the median survival time was prolonged from 35.5 days to 41.5 days.

[0175] (4.3) The weight change of tumor-bearing mice is shown in FIG. 3, and the change of Plasmodium infection rate is shown in FIG. 4. With the increase of Plasmodium infection, the weight of tumor-bearing mice gradually decreased, the weight was the lowest when the parasitemia was the highest, and then with the gradual decrease of Plasmodium infection, the weight of mice gradually increased.

Example 4

[0176] In this example, the GL261/mcherry-luc cell line was constructed for exploring the therapeutic effect of Plasmodium infection on tumor-bearing mice in intracranial in situ inoculation models of brain tumor in Example 5.

[0177] (I) Experimental Materials and Reagents

[0178] cells: GL261, mouse glioma cell line; HEK293T cell line for lentivirus packaging; plasmid: pWPXLd-mcherry-F2A-Luciferase-Puro; transfection reagent: PEI, purchased from POLYSCIENCES COMPANY; Bright-Glo™ luciferase detection system: from PROMEGA COMPANY; Countstar FL automatic cell fluorescence analyzer: purchased from SHANGHAI COUNTSTAR INC.; endotoxin-free plasmid DNA mass extraction kit: N1051, purchased from GUANGZHOU DONGSHENG BIOTECH CO., LTD.; puromycin: purchased from INVIVOGEN COMPANY; DMEM basic medium: 11995065, purchased from GIBCO; FBS fetal bovine serum: 04-001-1ACS, purchased from BIOLOGICAL INDUSTRIES; Opti-MEM®I Reduced Serum Medium: No. 31985-070, purchased from THERMOFISHER INC.

[0179] (II) Experimental Steps

[0180] (1) Lentiviral vector plasmid

[0181] (1.1) A pWPXLd-mcherry-F2A-Luciferase-Puro plasmid was constructed, as shown in FIG. 5.

[0182] (1.2) Plasmid extraction: Plasmid extraction was carried out with reference to the instruction manual of the endotoxin-free plasmid DNA mass extraction kit N1051.

[0183] (2) Lentiviral packaging

[0184] (2.1) HEK-293T cell culture: The cells were in an exponential growth state.

[0185] (2.2) Cell digestion: The cells were digested with trypsin one day before transfection, centrifuged, resuspended in a fresh complete culture medium, passaged to a 10 cm culture dish and cultured in an incubator with 5% CO.sub.2 at 37° C. to make the adherence fusion degree of cells reach 80% and above.

[0186] (2.3) The fresh complete culture medium was replaced 2 hours before transfection.

[0187] (2.4) The PEI, each plasmid and Opti-MEM I Reduced Serum Medium needed for transfection were placed at room temperature for equilibrium.

[0188] (2.5) Preparation of the mixed solution of plasmids: Three plasmids and Opti-MEM I Reduced Serum Medium were added according to the following dosage, then pipetted evenly and left at room temperature for 10 minutes.

TABLE-US-00001 Plasmid/reagent Mass/volume Target plasmid pWPXLd 21 μg psPAX2 14 μg pMD2.G 7 μg Opti-MEM 1 mL

[0189] (2.6) Then 120 μL of PEI transfection reagent and 1 mL of Opti-MEM I Reduced Serum Medium were taken respectively, mixed well and left at room temperature for 10 minutes.

[0190] (2.7) Finally, the above solutions were gently mixed and left at room temperature for 10 minutes to form the mixed solution for transfection.

[0191] (2.8) The mixed solution was added to the cell surface dropwise and mixed well.

[0192] (2.9) 6 hours after transfection, the medium was replaced.

[0193] (2.10) 48 and 72 hours after transfection, the supernatant was collected.

[0194] (2.11) The collected virus supernatant was centrifuged at 3000 rpm for 30 minutes.

[0195] (2.12) The centrifuged virus solution was filtered with a 0.45 μm filter, and the filtrate was stored at −80° C. for later use.

[0196] (III) Construction of GL261-Luc-Mcherry Cell Line

[0197] (3.1) The GL261 cell line was resuscitated and passaged to make the cells in the logarithmic growth phase.

[0198] (3.2) The GL261 cells were cultured in a T25 cell culture flask and digested into the single cell suspension with 0.25% trypsin-EDTA.

[0199] (3.3) The cells were counted, 5×10.sup.5 cells were put into the 6-well plate, and the culture medium was added until the final volume was 1.8 mL.

[0200] (3.4) 2 μL of Polybrene was added to each well of the 6-well plate and shaken well.

[0201] (3.5) 600 μL of pWPXLd-mCherry-F2A-Luciferase virus supernatant was added to each well of the 6-well plate, shaken well and cultured in the incubator at 37° C.

[0202] (3.6) 24 hours after transfection, the transfection solution was discarded and replaced with normal culture medium to continue the culture.

[0203] (3.7) 48 hours after transfection, the transfection solution was discarded and replaced with the selection medium with 2 μg/mL puromycin to continue the culture.

[0204] (3.8) The expression of mCherry in transfected cells was observed.

[0205] (IV) Monoclonal screening of GL261/mcherry-luciferase

[0206] (4.1) 72 hours after transfection, GL261/mCherry-Luc cells were digested and counted.

[0207] (4.2) An appropriate amount of cell suspension was diluted, the puromycin concentration was 2 μg/mL, and 50 to 100 cells were added in the 10-cm cell culture dish, shaken well and cultured at 37° C.

[0208] (4.3) The single positive cell was labeled under the microscope on the next day, and the medium was changed every two and a half days.

[0209] (4.4) 18 days after the screening, clones that had normal morphology and expressed mCherry were observed under the microscope and then selected into a 6-well plate for amplification culture.

[0210] (V) Identification of GL261/Mcherry-Luciferase Monoclonal Cell Line

[0211] (5.1) Positive rate calculated by using Count Star counter: The cell sample was pipetted sufficiently and mixed well, 20 μL of the cells was taken out and added to the counting chamber and allowed to stand for 10 to 30 seconds, and the parameters were set to let the counter automatically count the cells.

[0212] (5.2) The Bright-Glo™ buffer was added to the Bright-Glo substrate, reversed, mixed well until all substrate was completely dissolved, and left at room temperature until the substrate was equilibrated to room temperature.

[0213] (5.3) The cells were counted, the cell concentration was adjusted to 1×10.sup.6 cells/mL, 100 μL of cells was added to each well of the 96-well plate, namely 1×10.sup.5 cells, and then 100 μL of the mixed Bright-Glo detection reagent was added to each well.

[0214] (5.4) The cells were incubated at room temperature for 2 minutes until the cell lysis was complete.

[0215] (5.5) The chemiluminescence detection was carried out using the multifunctional microplate reader.

[0216] (6) Experimental results

[0217] (6.1) The visual field view of positive rate detection of the GL261.mcherry-Luc cell line monoclone is shown in FIG. 6: the calculated positive rate of monoclone reached 96.49%, so the cell line could be considered as a monoclonal cell line.

[0218] (6.2) The graph of the statistical result of Luciferase activity of GL261.mcherry-Luc cell line is shown in FIG. 7 (con is the control group in the figure): the luciferase activity of GL261/mcherry-luciferase-C1 monoclone was very strong, so the cell line could be used for in vivo imaging experiment in mice.

Example 5

[0219] This example explores the therapeutic effect of Plasmodium infection on tumor-bearing mice in intracranial in situ inoculation models of a brain tumor.

[0220] (I) Experimental Materials and Reagents

[0221] animal: C57BL/6 mice, female, 6 to 8 weeks old, from SHANGHAI SLAC LABORATORY ANIMAL CO. LTD.; tumor cell: GL261/mcherry-Luciferase, self-constructed, see Example 4; Plasmodium: mouse Plasmodium yoelii (P. yoelii 17XNL, MRA-593, Py), freely offered by MALARIA RESEARCH AND REFERENCE REAGENT RESOURCE CENTER (MR4); luciferase substrate: D-Luciferin, Potassium Salt D-fluorescein potassium salt, purchased from Shanghai Yisheng Biotechnology Co., Ltd.; Giemsa dye powder: purchased from SIGMA-ALDRICH COMPANY; DMEM basic medium: 11995065, purchased from GIBCO; FBS fetal bovine serum: 04-001-1ACS, purchased from BIOLOGICAL INDUSTRIES; Avertin (anesthetic, self-prepared), alcohol, iodine tincture, hydrogen peroxide, normal saline, silicone oil, gentamicin sulfate injection, and erythromycin ointment.

[0222] (II) Experimental Instruments

[0223] in vivo imager: IVIS Spectrum, purchased from PERKINELMER COMPANY; stereotaxic instrument: purchased from SHENZHEN RWD LIFE SCIENCE CO., LTD.; micro hand-held cranial drill: purchased from SHENZHEN RWD LIFE SCIENCE CO., LTD.; microsyringe: specification of 5 μL, purchased from HAMILTON; electronic digital vernier caliper: No.: 678040, purchased from EXPLOIT TOOLS; surgical instruments (surgical pads, timers, surgical blades, surgical handles, ophthalmic scissors, ophthalmic straight tweezers, ophthalmic curved tweezers, needle holders, sewing needles, cotton swabs, and sutures).

[0224] (III) Experimental Steps

[0225] (1) Establishment of animal model

[0226] (1.1) Cell revival: The mouse glioma cell line GL261/mcherry-luc was revived and incubated in a constant temperature incubator with 5% CO.sub.2 at 37° C.

[0227] (1.2) Cell amplification culture: Cells were passaged every 2 to 3 days, and when the cells grew to 80% of the bottom of the petri dish, the cells were digested with 0.25% trypsin-EDTA digestion solution, passaged at a dilution of 1:3.

[0228] (1.3) GL261/mcherry-luc cell preparation: The GL261/mcherry-luc cells in the exponential phase growth phase were washed with PBS, digested with trypsin, washed with PBS 3 times, counted, resuspended with RPIM 1640 medium, with the cell concentration of 2×10.sup.8/μL, and stored on ice.

[0229] (1.4) Surgical instruments were disinfected with 75% alcohol.

[0230] (1.5) Preparation of injection needles and microsyringes: The injection needle and the connecting hose were filled with silicone oil with a 1 mL syringe to check whether there were blockages and prevent air bubbles. The syringe was replaced with a microsyringe, the injection needle was installed, and an appropriate number of cells were sucked to check whether there was air leakage.

[0231] (1.6) Mouse anesthesia: Avertin anesthetic was administered intraperitoneally at a dose of 0.4 mL/20 g of body weight to anesthetize mice.

[0232] (1.7) Mouse shaving: The hair on the top of the head was shaved with a shaving knife, and the hair between eyes and ears was shaved clean.

[0233] (1.8) The mouse was fixed to the brain stereotaxic instrument, firstly, the mouse teeth were fixed (the incisors were put on the opening of the nose clip), the mouth was slightly opened with tweezers, the tongue was pulled out, then the back of the head was fixed (the ear rods were put in both ears mainly to fix the cheekbones), and finally, the nose clip was fixed tightly.

[0234] (1.9) The skin was disinfected with iodine tincture, the skin was cut with a scalpel along the midline, the incision was made approximately 10 mm from the back of the eyes to the ears, the connective tissue on the skull was scraped with the assistance of the scalpel, and the skull was wiped with cotton swabs dipped with hydrogen peroxide to make the anterior fontanel of the skull clearer.

[0235] (1.10) The tip of the injection needle was aimed at anterior fontanelle, with anterior fontanelle as the reference point, the transverse direction of the head of the mouse was taken as the X-axis, the longitudinal midline was taken as the Y-axis, the X-axis and Y-axis of the stereotaxic instrument were both set as 0 mm, the injection needle was moved, 1 mm ahead the X-axis was the drilling position, at 1.8 mm right to the midline of the Y-axis, the injection needle was lowered to aim at the surface of mouse skull, the Z-axis was set as 0 mm, the injection needle was raised, and the drilling position of the skull was marked with a pencil, with the hole diameter of about 2 mm.

[0236] (1.11) Injection of cells: The injection needle was set at the position of anterior fontanel, and the injection position (1.8 mm right, 1 mm ahead and 3.4 mm deep) was set using an XYZ digital display spectrometer, cells were injected with the injection volume of 1 μL for about 1 minute, the needle was retained for 5 minutes, and the needle was slowly withdrawn.

[0237] (1.12) Suture: After suture, erythromycin ointment was applied to the wound, and then 0.1 mL of gentamicin sulfate injection was injected intramuscularly.

[0238] (1.13) In vivo imaging: On Day 7 after tumor inoculation, the mouse was imaged in vivo, and the total luminous flux of the tumor site in the head of the mouse was calculated.

[0239] (1.14) Experimental grouping: By stratified random sampling, the mice were divided into two groups: control glioma group (GL261) and P. yoelii treatment group (GL261+Py).

[0240] (2) Tumor-bearing mice were inoculated with Plasmodium in the following specific method.

[0241] (2.1) Plasmodium revival: Murine Plasmodium blood (1.0 mL/vial) cryopreserved in the liquid nitrogen tank was quickly shaken in a 37° C. water bath cauldron, mixed well and thawed to keep the activity of Plasmodium.

[0242] (2.2) Plasmodium inoculation: After the Plasmodium blood was mixed well, the Plasmodium blood was inoculated intraperitoneally into C57BL/6 mice with 0.2 mL/mouse, and two mice were inoculated each time.

[0243] (2.3) Preparation of thin blood film and microscopic examination: About 1 to 1.5 μL of blood was collected from tails of mice and smeared on slides to prepare a 2.5-cm long tongue-shaped thin smear blood film, and the prepared smear was blow-dried with a blower. The blood film was infiltrated with methanol for 1 minute, stained with 1× Giemsa stain solution for 30 minutes, rinsed with tap water and blow-dried. The Plasmodium parasitemia was observed by a 100× oil immersion objective lens. Changes of the Plasmodium infection rate were observed.

[0244] (2.4) Preparation of a Plasmodium solution: When the parasitemia reached 3% to 10%, firstly, the red blood cells were counted, 5 μL of blood was taken from tails and resuspended in 995 μL of PBS, and the red blood cells were counted. The number of red blood cells infected with Plasmodium per mL was calculated. The EP tubes were moistened with 0.2 mL of 3.8% sodium citrate anticoagulant, the blood was taken from eyeballs, the required concentration and total amount of Plasmodium to be inoculated were calculated, and the Plasmodium was prepared into the concentration of 2.5×10.sup.6/mL with PBS.

[0245] (2.5) Inoculation of tumor-bearing mice: 7 days after the tumor was subcutaneously inoculated, each mouse was inoculated with 0.2 mL of red blood cell solution, that is, each mouse was inoculated with 5×10.sup.5 Plasmodium parasites, and each mouse in the control group was inoculated with the same amount of red blood cell solution containing no Plasmodium.

[0246] (3) Detection indexes

[0247] (3.1) In vivo imaging of mice: In vivo imaging was carried out on mice every 7 days, and the total luminous flux of the brain was calculated to characterize the size of the brain tumor. The tumor size was represented by the mean tumor volume±the standard error of the mean (SEM), and the tumor growth curve was drawn. The statistical analysis between groups was performed through the two-way ANOVA, where “*” represents p≤0.05, and “**” represents p≤0.01, indicating that differences between groups were statistically significant.

[0248] (3.2) Survival statistics of mice: The survival was evaluated by a median survival time and a percentage of a prolonged survival time. The survival rate was estimated by the Kaplan-Meier method, the survival curve was drawn, and the median survival time was calculated, where “*” represents p≤0.05, and “**” represents p≤0.01, indicating that differences between groups were statistically significant.

[0249] (3.3) Statistics of the Plasmodium parasitemia: The Plasmodium parasitemia was evaluated by the percentage of red blood cells infected with Plasmodium in mice, where the calculation formula was (the number of red blood cells infected with Plasmodium/the total number of red blood cells)×100%. Specific operations were as follows: blood was taken from tail veins and smeared on a slide, fixed with methanol, and stained with Giemsa stain solution. The number of red blood cells infected with Plasmodium and the total number of red blood cells were observed under a microscope. The total number of red blood cells was about 1000. The Plasmodium parasitemia was calculated and represented by the mean infection rate±the standard error of the mean (SEM), the Plasmodium infection cycle curve was drawn, and whether the chemotherapeutic agent had an effect on Plasmodium infection was observed.

[0250] (3.4) Weight of mice: The mice were weighed every 3 days and the weight growth was represented by the mean weight±the standard error of the mean (SEM). The effects of the chemotherapeutic agent and Plasmodium infection on the weight of tumor-bearing mice were observed.

[0251] (4) Experimental results

[0252] (4.1) The in vivo imaging results of Plasmodium infection on the glioma growth in tumor-bearing mice are shown in FIG. 8, and the change of total tumor luminous flux with time is shown in FIG. 9. As can be seen from FIGS. 8 and 9, compared with the control group, in the Plasmodium treatment group, the growth of glioma GL261 intracranially inoculated in situ in mice was significantly inhibited (p=0.0003, **).

[0253] (4.2) The survival curve of tumor-bearing mice is shown in FIG. 10. Compared with the control group, in the Plasmodium treatment group, the Plasmodium infection significantly prolonged the survival time of tumor-bearing mice intracranially inoculated in situ, and the median survival time was prolonged from 40.5 days to 55.5 days (p=0.0479, *).

[0254] (4.3) The weight change of tumor-bearing mice is shown in FIG. 11, and the change of Plasmodium parasitemia is shown in FIG. 12. As can be seen from FIGS. 11 and 12, the body weight of the mice in the control group began to decrease gradually due to the increase of tumor load; with the increase of Plasmodium infection, the weight of tumor-bearing mice in the Plasmodium treatment group gradually decreased, the weight was the lowest when the infection rate was the highest, and then with the gradual decrease of Plasmodium infection, the weight of mice gradually increased.

[0255] The applicant has stated that although the drug for preventing and/or treating brain tumors and the use thereof in the present application are described through the preceding embodiments, the present application is not limited to the preceding embodiments, which means that implementation of the present application does not necessarily depend on the preceding embodiments. It should be apparent to those skilled in the art that any improvements made to the present application, equivalent replacements of raw materials of the product of the present application, additions of pharmaceutical excipient ingredients, selections of specific manners, etc., all fall within the protection scope and the disclosure scope of the present application.

[0256] Although the preferred embodiments of the present application have been described above in detail, the present application is not limited to details of the preceding embodiments, and various simple modifications can be made to the technical solutions of the present application without departing from the technical concept of the present application. These simple modifications are all within the protection scope of the present application.

[0257] In addition, it is to be noted that if not in collision, the specific technical features described in the preceding embodiments may be combined in any suitable manner. In order to avoid unnecessary repetition, the present application does not further specify any of various possible combination manners.