WO2021087839A1 - Séquence polypeptidique spécifique d'une tumeur et application associée - Google Patents

Séquence polypeptidique spécifique d'une tumeur et application associée Download PDF

Info

Publication number
WO2021087839A1
WO2021087839A1 PCT/CN2019/116164 CN2019116164W WO2021087839A1 WO 2021087839 A1 WO2021087839 A1 WO 2021087839A1 CN 2019116164 W CN2019116164 W CN 2019116164W WO 2021087839 A1 WO2021087839 A1 WO 2021087839A1
Authority
WO
WIPO (PCT)
Prior art keywords
polypeptide
seq
tumor
peptide
cells
Prior art date
Application number
PCT/CN2019/116164
Other languages
English (en)
Chinese (zh)
Inventor
邱思
李波
李佑平
张乐
Original Assignee
武汉华大吉诺因生物科技有限公司
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 武汉华大吉诺因生物科技有限公司 filed Critical 武汉华大吉诺因生物科技有限公司
Priority to CN201980102087.4A priority Critical patent/CN114651002A/zh
Priority to PCT/CN2019/116164 priority patent/WO2021087839A1/fr
Priority to TW109105388A priority patent/TWI748349B/zh
Publication of WO2021087839A1 publication Critical patent/WO2021087839A1/fr

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/10—Peptides having 12 to 20 amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/10—Cells modified by introduction of foreign genetic material

Definitions

  • the present invention relates to the field of biomedicine, in particular to a tumor-specific polypeptide sequence and its application, and specifically to a set of isolated polypeptides, isolated nucleic acids, constructs, expression vectors, host cells, pharmaceutical compositions, antigen-presenting cells, and immunity Use of effector cells, tumor vaccines, and polypeptides in preparing drugs for preventing or treating tumors and methods for treating patient tumors.
  • Cancer as a disease in which gene mutations in cells cause cell proliferation to go out of control, has become a major threat to human health and a major cause of human death.
  • the incidence of malignant tumors in China in 2015 was approximately 3.929 million and the deaths were approximately 2.338 million.
  • the burden of cancer continues to rise.
  • the incidence of malignant tumors has maintained an annual increase of about 3.9%, and the mortality rate has maintained an annual increase of 2.5%.
  • the main high-incidence malignant tumors are lung cancer, gastric cancer, colorectal cancer, liver cancer, breast cancer and esophageal cancer in order. Therefore, finding effective and specific cancer treatment methods has great clinical value.
  • Immunotherapy By modulating the body’s immune system, immunotherapy enhances the tumor microenvironment’s anti-tumor immunity, so as to achieve the purpose of controlling and killing tumor cells. It has the advantages of high efficiency, strong specificity and good tolerance, and has broad applications in tumor treatment. prospect.
  • Immunotherapy mainly includes cytokine therapy, immune checkpoint monoclonal antibodies, adoptive cell reinfusion, and tumor immunotherapy vaccines.
  • tumor immunotherapy vaccines mainly include tumor cell vaccines, dendritic cell vaccines, protein & peptide vaccines, nucleic acid vaccines, genetic engineering vaccines and anti-idiotypic antibody vaccines. The main mechanism of these vaccines killing tumors is by causing patients to target The tumor's immune response allows T cells to recognize tumor cells and then kill tumor cells.
  • Tumor antigens targeted by tumor immunotherapy vaccines include tumor-associated antigens and neoantigens.
  • Tumor-associated antigens are derived from proteins that are highly expressed in tumor tissues but are low or not expressed in normal tissues; and tumor neoantigens are derived from variant proteins produced by mutations in the tumor genome. Because tumor neoantigens only exist in tumor cells and not in normal cells, neoantigens can bypass the central immune tolerance and cause a strong T cell immune response, which has the characteristics of good effect; at the same time, tumor-specific characteristics The tumor neoantigen has the advantages of good safety and low side effects. However, the tumor neoantigens targeted by suitable tumor immunotherapy vaccines need to be further improved.
  • an object of the present invention is to propose a tumor-specific polypeptide sequence and its application, specifically related to a set of isolated polypeptides, isolated nucleic acids, constructs, expression vectors, host cells, pharmaceutical compositions, antigen-presenting cells, Use of immune effector cells, tumor vaccines, and polypeptides in preparing drugs for preventing or treating tumors and methods for treating tumor patients.
  • tumor-associated antigens that are highly expressed in the patient’s tumor. This type of treatment may be due to the presence of tumor-associated antigens in some normal tissues. Expression, low immunogenicity, which makes the effect poor.
  • the patient’s tumor-specific mutations and the variant peptides that these mutations may produce can be obtained by analyzing the sequencing data of its genome and transcriptome, and then pass The machine learning algorithm predicts which variant peptides may be presented as antigens by MHC molecules, and then uses these predicted tumor neoantigens for patient treatment.
  • a sequencing-based personalized tumor neoantigen screening program although the genome and transcriptome sequencing of a certain patient can be used to screen out the tumor neoantigens that can treat a certain patient through sequencing data analysis and algorithm prediction, but the whole process
  • the cost is high, the time is long, and because the accuracy of the current antigen prediction algorithm is not high, the false positives of the selected antigens are high, and some of the predicted antigens cannot effectively cause the immune response in the patient's body, thus leading to the poor efficacy of the patient. 4.
  • Combining the above schemes that is, using the identified tumor-associated antigens and tumor neoantigen collections, combined with individualized tumor neoantigen screening programs.
  • the present invention has discovered the high-frequency mutation gene MUC3A (wild-type MUC3A gene encodes mucin 3A, which provides lubrication, cell signaling pathway and chemical barrier function), which is repeated in a variety of cancers.
  • the high frequency mutation gene causes the amino acid at position 326 to be changed from serine (S) to threonine (T).
  • S serine
  • T threonine
  • the mutant polypeptide can be specifically and highly expressed in tumor tissues.
  • the present invention verifies the high affinity of the mutant polypeptide with HLA-A11:01 typed molecules and the presentation in tumor cells through experiments.
  • mutant polypeptide was improved, and a large number of experiments were performed to screen out a mutant polypeptide that can be recognized by the same T cells as the original mutant polypeptide, but activates T cells and induces antigen-specific T cells to kill tumors.
  • the present invention provides the following technical solutions:
  • the present invention proposes a set of isolated polypeptides.
  • the polypeptide includes at least any one polypeptide in the first peptide group, and may optionally include at least any one polypeptide in the second peptide group;
  • the first peptide group includes a polypeptide having SEQ ID The polypeptides of the amino acid sequence shown in NO: 1 to SEQ ID NO: 5;
  • the second peptide group includes derivative peptides of the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5, and the derivative peptides include sequentially connected peptides.
  • the pro-peptide segment, the mid-peptide segment and the post-peptide segment, the mid-peptide segment has at least 80% homology with the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5, the pro-peptide segment The sum of the length of the latter peptide segment is 14-16 amino acids.
  • the polypeptide sequence proposed by the present invention is a tumor-specific antigen and its variants generated by tumor gene mutations, and will not be expressed and presented in normal tissues, thus overcoming the problem of low safety in treatment with tumor-related antigens.
  • the proposed peptide sequence is derived from genes with high frequency mutations in a variety of cancers, and can be presented by HLA molecules frequently occurring in the population. Therefore, it can be repeated in the tumors of patients with multiple cancers and can cover currently known tumors. Patients whose antigen sequence cannot be covered.
  • the isolated polypeptide described above may further include the following technical features:
  • the mid-peptide segment has at least 90% homology with the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5.
  • the mid-peptide segment is the same as the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5.
  • the derivative peptide has an amino acid sequence shown in SEQ ID NO: 6 to SEQ ID NO: 10.
  • polypeptide is selected from at least one of the following:
  • At least one polypeptide having the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5 At least one polypeptide having the amino acid sequence shown in SEQ ID NO: 6 to SEQ ID NO: 10.
  • the present invention provides an isolated nucleic acid.
  • the nucleic acid encodes the above-mentioned polypeptide or its complementary sequence.
  • the above-mentioned polypeptides can be presented as antigens on the surface of tumor cells by HLA molecules that have affinity with them, and have the ability to activate T cells and direct these T cells to kill tumors, so they can encode the nucleic acid sequences of the above-mentioned polypeptides or these codes.
  • the complementary sequence of the nucleic acid sequence of the above polypeptide can be used to prevent or treat tumors.
  • the present invention proposes a construct.
  • the construct comprises the nucleic acid according to the second aspect of the present invention and a control sequence, and the control sequence is operably linked to the nucleic acid.
  • the constructs proposed in the embodiments of the present invention can efficiently express the above-mentioned polypeptides in suitable host cells under suitable conditions, and thus can be effectively used for the treatment or prevention of tumors.
  • the control sequence can instruct the nucleic acid to express the above-mentioned polypeptide in the host, and there can be one or more of these control sequences.
  • These control sequences can be promoters, terminators, SD sequences, regulatory genes for regulating the expression of genes, etc., as required.
  • the present invention provides an expression vector.
  • the expression vector comprises the construct according to the third aspect of the present invention.
  • the expression vector provided by the present invention can efficiently express the above-mentioned polypeptide in a host under suitable conditions, and the expression vector can be effectively used for the treatment or prevention of tumors.
  • the present invention proposes a host cell.
  • the host cell carries the construct according to the third aspect of the present invention or the expression vector according to the fourth aspect of the present invention, and the host cell can be obtained by transfection or transformation of the aforementioned nucleic acid construct or expression vector of.
  • the host cell can efficiently express the above-mentioned polypeptide under suitable conditions, and the host cell can be effectively used for the treatment or prevention of tumors.
  • the present invention proposes the use of polypeptides in preparing drugs for preventing or treating tumors or preparing kits for diagnosing tumors. If the tumor expresses the above-mentioned mutant gene MUC3A, the high-frequency mutant gene causes the amino acid at position 326 to be changed from serine (S) to threonine (T), and expresses the HLA-A11:01 type that has affinity with the polypeptide.
  • HLA molecules, the above-mentioned polypeptides have the ability of HLA molecules typed by HLA-A11:01 with affinity to be presented on the surface of tumor cells as antigens, activating T cells and directing these T cells to kill tumors.
  • the proposed polypeptide can be used to prevent and control tumors.
  • the polypeptide proposed by the present invention is specifically expressed in tumor cells, it is used for the treatment or prevention of tumors and has good safety. It can also be used in the preparation of kits for diagnosing tumors.
  • the present invention proposes a pharmaceutical composition.
  • the pharmaceutical composition includes the aforementioned polypeptide and pharmaceutically usable excipients.
  • the pharmaceutical composition containing the aforementioned polypeptides and adjuvants can significantly stimulate the proliferation of tumor-specific T cells and the secretion of cytokines of these T cells, thereby killing tumor cells expressing corresponding mutant genes, and can be used for the treatment or prevention of tumors.
  • the pharmaceutical composition provided can also include some pharmaceutically usable adjuvants. These adjuvants act as non-specific immune enhancers.
  • Useful adjuvants include but are not limited to PD-1 inhibitors.
  • the present invention provides an antigen presenting cell.
  • the antigen-presenting cell can present the aforementioned polypeptide.
  • Antigen-presenting cells can be obtained by loading the polypeptide, transfecting or transforming the aforementioned nucleic acid construct or expression vector, or phagocytosing the aforementioned host cell.
  • the antigen-presenting cells presenting the aforementioned polypeptides significantly stimulate the proliferation of tumor-specific T cells and the secretion of cytokines of these T cells, thereby killing tumor cells expressing corresponding mutant genes, and can be used for the treatment or prevention of tumors.
  • These available antigen-presenting cells can be dendritic cells, macrophages, B cells and the like.
  • the present invention proposes an immune effector cell.
  • the immune effector cell can recognize the aforementioned polypeptide or the antigen-presenting cell described in the eighth aspect of the present invention.
  • the immune effector cells can be induced by the aforementioned polypeptides or the aforementioned antigen-presenting cells.
  • the immune effector cells can specifically kill tumor cells expressing the corresponding mutant genes, and are used for the treatment or prevention of tumors.
  • These available immune effector cells can be T cells, effector T cells, NK cells and the like.
  • the present invention proposes a tumor vaccine.
  • the tumor vaccine comprises the aforementioned nucleic acid, or the aforementioned nucleic acid construct, or the aforementioned expression vector, or the aforementioned host cell, or the aforementioned antigen presentation Cells, or immune effector cells as described above.
  • the present invention provides a method for treating patients with tumors, the method comprising administering to the patients an effective amount of a pharmaceutical composition or an effective amount of a tumor vaccine, the pharmaceutical composition being the seventh aspect of the present invention
  • the tumor vaccine is the tumor vaccine according to the tenth aspect of the present invention.
  • the "effective amount" of the pharmaceutical composition means that as long as it can achieve the purpose of inhibiting tumor growth or interfering with tumor proliferation.
  • Effective amount of tumor vaccine refers to the introduction of these tumor vaccines into the patient's body, which can overcome the immunosuppressive state caused by the tumor and activate the patient's own immune system, so as to achieve the purpose of controlling or eliminating the tumor.
  • Fig. 1 is a diagram of the results of the mass spectrometry identification of mutant polypeptides provided by an embodiment of the present invention.
  • Figure 2 is a flow cytometric verification result diagram of the affinity of a polypeptide to T2 according to an embodiment of the present invention.
  • Fig. 3 is a diagram of the detection results of polypeptides and in vitro immunogenic ELISPOTs according to an embodiment of the present invention.
  • Figure 4 is a diagram showing the results of the polypeptide vaccine provided according to an embodiment of the present invention in controlling tumor growth in mice.
  • Figure 5 is a diagram showing the results of the polypeptide DC vaccine provided according to an embodiment of the present invention in controlling tumor growth in mice.
  • Figure 6 is a diagram showing the results of the DC-CTL vaccine provided in accordance with an embodiment of the present invention in controlling tumor growth in mice.
  • first peptide group or “second peptide group” respectively refer to polypeptides containing different amino acid sequences.
  • derived peptide is used to indicate a polypeptide sequence derived from a polypeptide having the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5. These derived sequences are from N-terminus to C-terminus, including the connected propeptide segments in turn , The mid-peptide segment and the post-peptide segment, wherein the mid-peptide segment has at least 80% homology with the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5, preferably at least 90% homology, The sum of the length of the front and back peptides is 14-16 amino acids. There are no special restrictions on the specific types of amino acids in the pre- and post-peptide segments.
  • these derived peptides may be long peptide sequences with a total length of 23mer-25mer obtained by extending the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5 to both sides.
  • these derived peptides may be polypeptides having the amino acid sequence shown in SEQ ID NO: 6 to SEQ ID NO: 10.
  • the isolated polypeptide provided by the present invention is selected from at least one of the following groups: 1) A polypeptide having the amino acid sequence shown in SEQ ID NO: 1-SEQ ID NO: 5; (2) ) At least any polypeptide having the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 5, and at least any polypeptide having the amino acid sequence shown in SEQ ID NO: 6 to SEQ ID NO: 10.
  • polypeptides of the amino acid sequence shown in SEQ ID NO: 1 to SEQ ID NO: 10 are shown in Table 1 below.
  • These peptide sequences are derived from tumor-specific antigens produced by tumor gene mutations, and will not be expressed and presented in normal tissues. Therefore, they have higher specificity and cause immune responses with higher specificity. They are safe for treatment. The side effect is small, and its structure is simple, and it is easy to artificially synthesize. At the same time, these peptide sequences have the characteristics of affinity with HLA molecules, the ability to stimulate T cell expansion and secretion of cytokines, and the ability to induce antigen-specific T cells to kill target cells, without changing the relationship between them and T cells. Specificity and better tumor control effect.
  • the derivative peptide sequence is a polypeptide sequence formed by the polypeptide sequence extending to a length of 23 amino acids on both sides.
  • the derivative peptide sequence is as SEQ ID NO: 6 ⁇ SEQ ID NO: 10.
  • polypeptide sequences and derived peptide sequences are studied.
  • sequence shown in SEQ ID NO: 3 can be called a mutant polypeptide
  • sequence shown in SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 4, and SEQ ID NO: 5 can be called a variant.
  • Peptides are studied.
  • Example 2 Mass spectrometry experiments verify that polypeptides are presented by HLA molecules on the surface of tumor cells
  • the polypeptide sequence and derived peptide coding gene obtained in Example 1 are transfected into tumor cells by lentivirus, and then the polypeptide-MHC complex on the cell surface is enriched by the combined method of co-immunoprecipitation and mass spectrometry. Whether the MHC molecules on the cell surface presented the mutant polypeptide was identified.
  • the specific method is as follows:
  • pan-MHC-I A/B/C antibody (clone number: w6/32) to bind protein A molecule sepharose CL-4B beads on the surface for 1 hour at 4°C, use NanoDrop to detect the residual antibody content in the supernatant, Antibody binding rate >90% is considered qualified, prepare pan-MHC-I A/B/C combined sepharose, 4°C for use.
  • the concentrated MHC-I restricted epitope peptide solution was analyzed by Q Exactive mass spectrometer (Thermo Fisher Scientific) connected to nanoflow HPLC (Thermo Fisher Scientific) online, and the ReproSil-Pur C18-AQ 1.9um filler was manually filled with a length of 15 cm, A separation column with an inner diameter of 75um was used for separation, and a linear gradient of 2-30% buffer B (80% ACN/0.5% acetic acid) was used to elute the peptides. The flow rate was set to 250 nl/min, and the elution time was 90 min.
  • the secondary mass spectrometer uses HCD for fragmentation, and data acquisition selects the "Top 20" method on which the data depends.
  • the acquisition resolution of MS spectrum is 70,000, 200m/z, and the target value is 3E6 ion; the top 10 ions in ion intensity are usually separated and accumulated with a maximum injection time of 120ms until the value of the automatic gain controller is displayed as 1E5.
  • the peptide matching option is set to "disable”, and the MS/MS resolution is set to 17,500 (200m/z).
  • MaxQuant version 1.3.10.15
  • human whole protein library Uniprot, 86,749 proteins
  • tumor-associated antigens tumor-associated antigens
  • tumor-specific mutant peptides and one that contains 247 common pollutants (keratin, cattle
  • Variable modification detection settings N-terminal acetylation and methionine oxidation.
  • the second peptide identification setting enable; specific enzyme digestion setting: unspecific; peptide identification FDR (false discovery rate) is set to 1%, protein identification FDR is not set; the sequence matching length limit is set to 8-15aa, and the maximum peptide quality is set to 1500Da, the maximum charge state is set to 3.
  • the initial allowable mass deviation of the lead ion is set to 6 ppm, and the maximum fragment mass deviation is set to 20 ppm.
  • the "match between runs” setting is enabled.
  • the output of the identification result is saved in the "peptide.txt” file, the peptides matching the anti-library and the contaminated library are removed, and the rest are the identification results of the MHC-I restricted epitope.
  • the experimental results showed that surface mutant polypeptides, modified polypeptides and various derived peptide sequences can be expressed and presented on HLA molecules on the cell surface.
  • mutant polypeptide SEQ ID NO: 3 the mutant polypeptide SEQ ID NO: 3 as an example, the mass spectrum of the polypeptide is shown in Figure 1. The results show that the above-mentioned polypeptide can be expressed and presented on the cell surface HLA molecules.
  • T2 cells are essential antigen polypeptide transporter-deficient cell strains in the endogenous antigen presentation pathway, and can be used to study the process of antigen presentation and the strength of the mutual recognition of MHC molecules.
  • a peptide that has been confirmed to have a strong affinity with T2 cells was used as a positive control, and T2 cells without added peptides were used as a background control, and the exogenous peptides were combined with the surface MHC of T2 cells.
  • the binding of class I molecules can increase the expression of MHC class I molecules on the surface. The more stable the combination of the two, the more MHC class I molecules can be detected.
  • the average fluorescence intensity is used as the detection index, and the fluorescence coefficient (FI) As a measure. Based on this, the affinity between the polypeptide and T2 cells is judged. The higher the FI value, the stronger the affinity between the polypeptide and T2 cells, which is conducive to the subsequent identification of specific CD8 + T cells.
  • the synthesized polypeptide was added to 2*10 5 T2 cells, and human ⁇ 2 microglobulin (final concentration, 3ug/ml) was added, and cultured in a 24-well plate, in an incubator (37°C, 5%). CO 2 ), incubate overnight.
  • T2 cells without added peptides were used as background control, and CMV peptide (its sequence is NLVPMVATV, which is a viral peptide, is a known peptide that has been confirmed to have a strong affinity with T2 cells) as a positive control, experiment setting 2 Replicate holes and take the average value.
  • Example 4 Polypeptide stimulates and expands CD8+ T cells in vitro
  • PBMC cells of the volunteers with positive polypeptide corresponding subtypes Take the PBMC cells of the volunteers with positive polypeptide corresponding subtypes, 2 ⁇ 10 7 PBMC cells, and separate the monocytes by the adherence method (sticking for 3 hours), and the CD8 magnetic beads method to separate CD8+ T cells.
  • the induced mature DC cells are polypeptide-specific mature DC cells.
  • the obtained polypeptide-specific mature DC cells were co-cultured with CD8 + T cells of volunteers, and IL-21 was added.
  • IL-2 and IL-7 were supplemented. After that, IL-2 and IL-7 were supplemented once on the 5th and 7th day, and the co-cultured cells were taken for counting on the 10th day, and the follow-up ELISPOTs and LDH detection were performed.
  • Example 5 ELISPOTs method verifies that polypeptide activates CD8+ T cell immune response
  • the ELISPOT method known as Enzyme-linked immunospot assay, can detect the cytokines secreted by a single cell.
  • the culture plate is coated with specific monoclonal antibodies, and then the cells to be tested and antigen stimuli are added for culture. Under the stimulation of the stimuli, T cells secrete corresponding cytokines, and the secreted cytokines are coated Captured by the antibody on the culture plate. After washing away the cells, the captured cytokines can be combined with the fluorescently labeled secondary antibody to form spots. That is, the coated antibody can be used to capture the cytokines secreted by the cells in culture and present them in the form of enzyme-linked spots to detect and verify the strength of the immune response of the polypeptide to activate CD8+ T cells.
  • ELISPOTs kit instructions combine the cultured cells in Experimental Example 4 with the experimental polypeptide (ie TTLPTTITR) and irrelevant polypeptides (referring to polypeptides that do not stimulate T cells to secrete IFN-gamma interferon, the specific sequence is LSYRNKPSI (The irrelevant polypeptides used in the following examples are also of this sequence) T2 cells were added to the ELISPOTs plate for culture, and the ELISPOTs detection was performed 20 hours later (see the kit instructions). The results of ELISPOTs are shown in Figure 3, and the results are summarized in Table 3 below:
  • the second and third columns in Table 3 respectively represent the number of spots detected using experimental peptides as stimuli or irrelevant polypeptides as stimuli
  • the multiples in the fourth column represent the use of experimental peptides as stimuli and irrelevant peptides.
  • LDH lactate dehydrogenase
  • the cells cultured in Experimental Example 4 are co-cultured with T2 cells that have been loaded with experimental polypeptides or unrelated polypeptides or not loaded with polypeptides.
  • the maximum release hole, volume correction hole, medium control hole, spontaneous release hole, and different targets are set in the experiment.
  • the ratio (the ratio of the number of T cells to T2 cells) and other controls, each group set 3 replicate wells, 4h later, take out 50 ⁇ l of the co-cultured cell supernatant and add it to 50ul LDH substrate mixture to make the cell supernatant catalyze LDH substrate reaction, finally read the 490nm wavelength and 680nm reference wavelength, and calculate the killing activity of target cells to kill T2 based on the control well.
  • Table 4 The results are shown in Table 4 below. The larger the value shown in Table 4, the stronger the killing effect.
  • T cells specifically recognize and kill target cells that present experimental polypeptides
  • a mouse subcutaneous xenograft tumor model was constructed. This model is used to verify the tumor control effect of the polypeptide drug combination, antigen presenting cell, and vaccine proposed in the present invention.
  • each polypeptide is introduced by means of lentiviral transfection, and a recombinant lentivirus expressing the aforementioned mutant polypeptide or its modification is constructed and packaged.
  • the human lung cancer cell line HCC827 was purchased from ATCC (number: CRL-2868), and its HLA subtype is HLA-A*1101 positive.
  • the cells were cultured in DMEM medium containing 10% fetal bovine serum, 100 U/mL penicillin and streptomycin. Cultivate in a 37°C, 5% CO 2 incubator.
  • the packaged lentivirus was transfected into the HCC827 cell line, and Puromycin antibiotic (puromycin) was used to continuously screen the surviving HCC827 cell line, and finally the HCC827 cell line expressing the polypeptide was established.
  • the established human lung cancer cell line was cultured in DMEM medium containing 10% fetal bovine serum, 100U/mL penicillin and streptomycin. Cultivate in a 37°C, 5% CO 2 incubator. The tumor cells were collected, centrifuged at 3000 rpm, and the tumor cells were washed 3 times with sterile saline. Make proper dilution, take 40 microliters of cell suspension, add 10 microliters of 0.4% trypanol blue to stain and count under microscopy to make a tumor cell suspension with a concentration of 1*10 8 cells/ml, and select the NOD after immune reconstitution. SCID mice, each mouse is inoculated subcutaneously with 100 ml of tumor cell suspension.
  • mice with immune reconstitution for 4 weeks were treated with DC vaccine respectively, and the tumor volume was recorded every 3-4 days.
  • the HCC827 subcutaneous tumor model NOD/SCID mice with immune reconstitution for 4 weeks were randomly divided into 4 groups: adjuvant + wild-type peptide group (the wild-type peptide is TTLPTTISR), adjuvant + blank peptide group (that is, only containing adjuvant) , Adjuvant + mutant polypeptide group (the mutant polypeptide is TTLPTTITR), adjuvant + modified polypeptide group (which can be divided into four groups according to the different modified polypeptides used, and the modified polypeptides used are TILPTTITK, TSLPTTITK) , TTLPTTITK, TVLPTTITK), 6 in each group.
  • the adjuvant used is Freund's adjuvant.
  • the results show that compared to the adjuvant+wild-type polypeptide-loaded polypeptide vaccine group and the adjuvant+blank polypeptide group, the adjuvant+mutant polypeptide or adjuvant+modified polypeptide-loaded polypeptide vaccine group can significantly slow down the growth of mouse tumors.
  • PBMC peripheral blood mononuclear cells
  • RPMI 1640 medium 2-3*10 6 /ml
  • Adherent cells are DCs.
  • Aspirate Non-adherent cells are peripheral blood lymphocytes (PBL) for use.
  • Adopt GM-CSF 1000U/ml
  • IL-4 1000U/ml
  • IFN-gamma 100U/ml
  • CD40L 10ng/ml
  • the wild-type peptide combination and the mutant peptide combination were added to induce the adherent cells to become mature DC cells, and the mature DC were harvested and washed 3 times with physiological saline.
  • the DC loaded with the polypeptide was adjusted to (4.0 ⁇ 0.5)*10 7 /ml with physiological saline for subsequent experiments.
  • mice were randomly divided into 4 groups: DC-loaded wild-type polypeptide group (the wild-type polypeptide is TTLPTTISR), DC-loaded mutant polypeptide group (the mutant polypeptide is TTLPTTITR), DC-loaded modified polypeptide group (wherein according to the used
  • the denatured peptides obtained are different and can be divided into four groups.
  • the denatured peptides used are TILPTTITK, TSLPTTITK, TTLPTTITK, TVLPTTITK), blank peptide group (that is, no peptide group loaded), each with 6 mice.
  • mice were injected intracutaneously into the inner thighs near the groin, 0.1ml on each side, once a week.
  • the dose is (4.0 ⁇ 0.5)*10 6 cells/time, with a total of 2 injections.
  • the vital signs of the mice were observed, and the vertical and horizontal size of the tumor was measured with a vernier caliper every 3-4 days.
  • the changes in the weight of the mice were recorded. The results are shown in Figure 5.
  • PI cell proliferation index
  • the cells were resuspended with saline, resuspended volume of 0.2ml, via the tail vein transfusion, each tumor model mouse cells reinfusion of about l * l0 8 cells.
  • the changes in the weight of the mice were recorded. The results are shown in Figure 6.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biotechnology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Biophysics (AREA)
  • Veterinary Medicine (AREA)
  • Molecular Biology (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Toxicology (AREA)
  • Cell Biology (AREA)
  • Microbiology (AREA)
  • Immunology (AREA)
  • General Engineering & Computer Science (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)

Abstract

La présente invention concerne une séquence polypeptidique spécifique d'une tumeur et une application associée. Le polypeptide comprend au moins n'importe quel polypeptide dans un premier groupe peptidique, et peut éventuellement comprendre au moins un polypeptide dans un second groupe peptidique. Le premier groupe de peptides comprend des polypeptides ayant les séquences présentées dans SEQ ID NO : 1 à SEQ ID NO : 5 ; le second groupe peptidique comprend des peptides dérivés ayant les séquences présentées dans SEQ ID NO : 1 à SEQ ID NO : 5. Les peptides dérivés comprennent des segments peptidiques avant, intermédiaire et arrière reliés en séquence. Le segment de peptide intermédiaire présente au moins 80 % d'homologie avec les séquences présentées dans SEQ ID NO : 1 à SEQ ID NO : 5, et la somme des longueurs des segments peptidiques avant et arrière est de 14-16 acides aminés. L'invention concerne également un acide nucléique isolé, une construction, un vecteur d'expression, une composition pharmaceutique, une cellule de présentation d'antigène, une cellule effectrice immunitaire, un vaccin antitumoral, et l'utilisation du polypeptide dans la préparation d'un médicament pour la prévention ou le traitement d'une tumeur et un procédé de traitement d'un patient atteint d'une tumeur.
PCT/CN2019/116164 2019-11-07 2019-11-07 Séquence polypeptidique spécifique d'une tumeur et application associée WO2021087839A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN201980102087.4A CN114651002A (zh) 2019-11-07 2019-11-07 肿瘤特异性多肽序列及其应用
PCT/CN2019/116164 WO2021087839A1 (fr) 2019-11-07 2019-11-07 Séquence polypeptidique spécifique d'une tumeur et application associée
TW109105388A TWI748349B (zh) 2019-11-07 2020-02-20 腫瘤特異性多肽序列及其應用

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2019/116164 WO2021087839A1 (fr) 2019-11-07 2019-11-07 Séquence polypeptidique spécifique d'une tumeur et application associée

Publications (1)

Publication Number Publication Date
WO2021087839A1 true WO2021087839A1 (fr) 2021-05-14

Family

ID=75849465

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/CN2019/116164 WO2021087839A1 (fr) 2019-11-07 2019-11-07 Séquence polypeptidique spécifique d'une tumeur et application associée

Country Status (3)

Country Link
CN (1) CN114651002A (fr)
TW (1) TWI748349B (fr)
WO (1) WO2021087839A1 (fr)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050226888A1 (en) * 2003-12-11 2005-10-13 Sidney Kimmel Cancer Center Methods for generating immunity to antigen
WO2007039109A1 (fr) * 2005-09-20 2007-04-12 Ralf Huss Inhibiteur tissulaire de metalloproteinases (timp) lie a des ancres glycosylphosphatidylinositol (gpi) pour traiter le cancer et des lesions cutanees
WO2007062844A1 (fr) * 2005-12-02 2007-06-07 Lmu Muenchen Couples chimiokines-mucines lies a des ancrages glycosylphosphatidylinositol (gpi) pour la regeneration tissulaire et utilises en tant qu'adjuvants destines a l'immunite tumorale
WO2014193999A2 (fr) * 2013-05-28 2014-12-04 Caris Science, Inc. Méthodes et compositions d'identification de biomarqueurs
CN107750278A (zh) * 2015-04-27 2018-03-02 癌症研究技术有限公司 治疗癌症的方法
CN110272874A (zh) * 2018-03-15 2019-09-24 北京卡替医疗技术有限公司 一种包含负载新抗原的b细胞疫苗的免疫细胞药物

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109790224A (zh) * 2016-09-30 2019-05-21 武汉华大吉诺因生物科技有限公司 Cacna1h衍生的肿瘤抗原多肽及其应用
WO2019126186A1 (fr) * 2017-12-18 2019-06-27 Neon Therapeutics, Inc. Néo-antigènes et leurs utilisations

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050226888A1 (en) * 2003-12-11 2005-10-13 Sidney Kimmel Cancer Center Methods for generating immunity to antigen
WO2007039109A1 (fr) * 2005-09-20 2007-04-12 Ralf Huss Inhibiteur tissulaire de metalloproteinases (timp) lie a des ancres glycosylphosphatidylinositol (gpi) pour traiter le cancer et des lesions cutanees
WO2007062844A1 (fr) * 2005-12-02 2007-06-07 Lmu Muenchen Couples chimiokines-mucines lies a des ancrages glycosylphosphatidylinositol (gpi) pour la regeneration tissulaire et utilises en tant qu'adjuvants destines a l'immunite tumorale
WO2014193999A2 (fr) * 2013-05-28 2014-12-04 Caris Science, Inc. Méthodes et compositions d'identification de biomarqueurs
CN107750278A (zh) * 2015-04-27 2018-03-02 癌症研究技术有限公司 治疗癌症的方法
CN110272874A (zh) * 2018-03-15 2019-09-24 北京卡替医疗技术有限公司 一种包含负载新抗原的b细胞疫苗的免疫细胞药物

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
BHATIA RAKESH; GAUTAM SHAILENDRA K.; CANNON ANDREW; THOMPSON CHRISTOPHER; HALL BRADLEY R.; AITHAL ABHIJIT; BANERJEE KASTURI; JAIN : "Cancer-associated mucins: role in immune modulation and metastasis", CANCER METASTASIS., KLUWER ACADEMIC PUBLISHERS, DORDRECHT., NL, vol. 38, no. 1, 8 January 2019 (2019-01-08), NL, pages 223 - 236, XP036833426, ISSN: 0167-7659, DOI: 10.1007/s10555-018-09775-0 *
LIANG ZHAODUAN, QIN LILI, CHEN LEI, LI WENHUI, CHEN CHAO, HUANG YALING, ZHANG LE, LIU SONGMING, QIU SI, GE YUPING, PENG WENTING, L: "The common neoantigens in colorectal cancer are predicted and validated to be presented or immunogenic", BIORXIV, 3 July 2019 (2019-07-03), XP055810590, Retrieved from the Internet <URL:https://www.biorxiv.org/content/10.1101/682617v2.full.pdf> DOI: 10.1101/682617 *

Also Published As

Publication number Publication date
TW202118772A (zh) 2021-05-16
TWI748349B (zh) 2021-12-01
CN114651002A (zh) 2022-06-21

Similar Documents

Publication Publication Date Title
WO2021087840A1 (fr) Polypeptide d&#39;immunothérapie antitumorale et son utilisation
CN110214144B (zh) 多肽及其应用
CN116970058B (zh) 针对tp53基因r249s突变的肿瘤新抗原多肽及其应用
CN109923121B (zh) 多肽及其应用
CN109803978B (zh) 多肽及其应用
CN112142837A (zh) 新抗原肽组合物及其在肿瘤免疫治疗药物中的应用
TWI750594B (zh) 腫瘤特異性多肽序列及其應用
CN110167956B (zh) 多肽及其应用
TWI748349B (zh) 腫瘤特異性多肽序列及其應用
US11548925B2 (en) CACNA1H-derived tumor antigen polypeptide and use thereof
TWI838465B (zh) 腫瘤免疫治療多肽及其應用
WO2018045510A1 (fr) Polypeptide et son application
US11612643B2 (en) Col14A1-derived tumor antigen polypeptide and use thereof
CN109952308B (zh) 多肽及其应用
CN110072876B (zh) 多肽及其应用
WO2023226261A1 (fr) Vaccin associé à ido1 et son utilisation
CN114702569B (zh) Pd-l1相关疫苗及其应用
WO2018094570A1 (fr) Polypeptide et son application
CN116948004B (zh) 针对ctnnb1基因h36p突变的肿瘤新抗原多肽及其应用
CN117586353A (zh) 肝癌相关多肽、复合物、药物组合物及用途
CN116350758A (zh) 肿瘤共享新抗原表位肽或其编码核酸在制备药物中的应用

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19951634

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19951634

Country of ref document: EP

Kind code of ref document: A1