An antibody against dengue virus or ns1 protein thereof and application thereof

Abstract

The application discloses an antibody against dengue virus or NS1 protein thereof and application thereof, and relates to the field of antibodies.The antibody against dengue virus or NS1 protein thereof provided by the application comprises a heavy chain complementarity determining region and a light chain complementarity determining region, provides an important raw material source for detection of dengue virus or NS1 protein thereof, and has good affinity or activity.

Description

[0001] Cross-reference to related applications

[0002] This invention claims priority to Chinese Patent Application No. 202311094281.7, filed on August 28, 2023, entitled "An antibody against dengue virus or its NS1 protein and its application", the entire contents of which are incorporated herein by reference. Technical Field

[0003] This invention relates to the field of antibody technology, and more specifically, to an antibody against dengue virus or its NS1 protein and its application. Background Technology

[0004] Dengue fever (DF) is an acute mosquito-borne infectious disease caused by four serotypes of the virus (DENV-1, DENV-2, DENV-3, and DENV-4), primarily transmitted by Aedes aegypti and Aedes albopictus mosquitoes. DF is the most widespread, most prevalent, and most harmful vector-borne viral disease, prevalent in more than 100 countries and regions in tropical and subtropical Africa, the Americas, Southeast Asia, and the western Pacific region worldwide.

[0005] Clinically, dengue fever (DF) is a severe, flu-like illness. It is characterized by sudden onset, high fever, severe headache, retro-orbital pain, muscle and joint pain, and may be accompanied by rash, swollen lymph nodes, and leukopenia. It can affect all population groups, but symptoms can vary depending on the patient's age. This type is generally called classic dengue fever. It spreads rapidly and can cause large-scale epidemics. During dengue epidemics, the incidence rate in susceptible populations is typically 40%-50%, but can reach as high as 80%-90%, although the mortality rate is very low. Dengue hemorrhagic fever is characterized by high fever, hemorrhage, hepatomegaly, and in severe cases, circulatory failure. It has a high mortality rate and is a more severe clinical type. When accompanied by shock syndrome, it is called dengue shock syndrome.

[0006] There is no specific treatment for dengue fever. Without appropriate treatment, the mortality rate of dengue hemorrhagic fever can exceed 20%, but with effective supportive care, the mortality rate can be less than 1%. Key diagnostic points for dengue fever include: 1) Epidemiological data: activity in the 15 days following onset, including travel to endemic areas and mosquito bite history; 2) Clinical features: sudden onset, fever, "three pains and three reds" (redness, pain, and redness), and skin examination; 3) Laboratory tests: decreased white blood cell and platelet counts; positive serum IgM; a fourfold increase in IgG during the convalescent phase compared to the acute phase; and isolation of the virus or specific antigens.

[0007] Currently, methods for detecting dengue virus include virus culture, serological testing, and immunoassay. Virus isolation is time-consuming and cannot achieve rapid diagnosis, while conventional serological diagnosis is subject to interference from widespread cross-reactivity. Immunoassay, with its advantages of speed, simplicity, lack of reliance on sophisticated equipment, and ability to perform on-site testing, has become a hot research topic in the rapid diagnosis of infectious diseases. The principle of immunoassay is based on antigen-antibody reaction. NS1 protein is a glycoprotein in the non-structural proteins of dengue virus, with extremely strong antigenicity and no ADE (antibody-dependent enhancement), so it is often used as a target in immunoassay.

[0008] Immunoassays require antibodies against dengue virus or its NS1 protein; therefore, there is a strong demand in the field for antibodies with good performance against dengue virus or its NS1 protein. Summary of the Invention

[0009] This application provides an antibody or antigen-binding fragment against dengue virus or its NS1 protein, providing an important source of raw materials for the detection of dengue virus or its NS1 protein, and exhibiting good activity or affinity.

[0010] To achieve the above objectives, according to one aspect of the present invention, an antibody or antigen-binding fragment thereof against dengue virus or its NS1 protein is provided, said antibody or antigen-binding fragment comprising three complementary determining regions having a heavy chain variable region having any one of the amino acid sequences SEQ ID NO: 17, 18, 19 and three complementary determining regions having a light chain variable region having any one of the amino acid sequences SEQ ID NO: 20, 21, 22.

[0011] To achieve the above objective, according to a second aspect of the present invention, an antibody or antigen-binding fragment thereof against dengue virus or its NS1 protein is provided, said antibody or antigen-binding fragment comprising the following complementarity-determining region:

[0012] HCDR1, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:1;

[0013] HCDR2, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:2 or 29;

[0014] HCDR3, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:3 or 30;

[0015] LCDR1, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:4;

[0016] LCDR2, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:5; and

[0017] LCDR3, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:6.

[0018] To achieve the above objectives, according to a third aspect of the present invention, an antibody against dengue virus or its NS1 protein or an antigen-binding fragment thereof is provided, comprising a heavy chain variable region and / or a light chain variable region, wherein the amino acid sequence of the heavy chain variable region is shown in any one of SEQ ID NO: 17, 18, 19; and the amino acid sequence of the light chain variable region is shown in any one of SEQ ID NO: 20, 21, 22.

[0019] To achieve the above objectives, according to a fourth aspect of the present invention, an antibody against dengue virus or its NS1 protein or an antigen-binding fragment thereof is provided, comprising a heavy chain and / or a light chain, wherein the amino acid sequence of the heavy chain is as shown in any one of SEQ ID NO: 23, 24, 25; and the amino acid sequence of the light chain is as shown in any one of SEQ ID NO: 26, 27, 28.

[0020] To achieve the above objectives, according to a fifth aspect of the present invention, an antibody conjugate is provided, the antibody conjugate comprising the antibody or its antigen-binding fragment described above.

[0021] To achieve the above objectives, according to a sixth aspect of the present invention, a reagent or kit is provided, the reagent or kit comprising the above-described antibody or its antigen-binding fragment or the above-described antibody conjugate.

[0022] To achieve the above objectives, according to a seventh aspect of the present invention, a method for detecting dengue virus or its NS1 protein is provided, comprising: a) contacting the antibody or its antigen-binding fragment, antibody-drug conjugate, or reagent or kit with dengue virus or its NS1 protein in a sample to be tested under conditions sufficient to induce an antibody / antigen binding reaction to form an immune complex; and b) detecting the presence of the immune complex, the presence of which indicates the presence of the antigen in the test sample.

[0023] To achieve the above objectives, according to an eighth aspect of the present invention, the use of the above-described antibody or its antigen-binding fragment, antibody-drug conjugate, reagent or kit in the preparation of a product for detecting dengue virus or its NS1 protein is provided.

[0024] To achieve the above objectives, the present invention also provides a nucleic acid, a vector, a cell, and a method for preparing the above-mentioned antibody or its antigen-binding fragment. Attached Figure Description

[0025] To more clearly illustrate the technical solutions of the embodiments of the present invention, the accompanying drawings used in the embodiments will be briefly introduced below. It should be understood that the following drawings only show some embodiments of the present invention and should not be regarded as a limitation on the scope. For those skilled in the art, other related drawings can be obtained based on these drawings without creative effort.

[0026] Figure 1 The results of reductive SDS-PAGE for Anti-DN 9H10 Rmb1 to Anti-DN 9H10 Rmb4 are shown. Detailed Implementation

[0027] In a first aspect, embodiments of the present invention provide an antibody or antigen-binding fragment against dengue virus or its NS1 protein, wherein the antibody or antigen-binding fragment comprises three complementary determinant regions having any one of the heavy chain variable regions of amino acid sequences SEQ ID NO:17, 18, 19 and three complementary determinant regions having any one of the light chain variable regions of amino acid sequences SEQ ID NO:20, 21, 22.

[0028] It should be noted that HCDR1, HCDR2, and HCDR3 are amino acid sequences identical to those of HCDR1, HCDR2, and HCDR3 in the same heavy chain variable region defined in the antibody or its antigen-binding fragment described in the first aspect, and LCDR1, LCDR2, and LCDR3 are amino acid sequences identical to those of LCDR1, LCDR2, and LCDR3 in the same light chain variable region defined in the antibody or its antigen-binding fragment described in the first aspect.

[0029] For example, HCDR1, HCDR2, and HCDR3 are amino acid sequences consistent with HCDR1, HCDR2, and HCDR3 of the heavy chain variable region shown in SEQ ID NO:17; LCDR1, LCDR2, and LCDR3 are amino acid sequences consistent with LCDR1, LCDR2, and LCDR3 of the light chain variable region shown in SEQ ID NO:20.

[0030] In this invention, the term "antibody" is used in the broadest sense, and may include full-length monoclonal antibodies, bispecific or multispecific antibodies, and chimeric antibodies, as long as they exhibit the desired biological activity.

[0031] In this invention, the terms "complementarity-determining region," "CDR," or "CDRs" refer to highly variable regions of the heavy and light chains of immunoglobulins, specifically regions containing one or more, or even all, of the major amino acid residues that contribute to the binding of an antibody or antigen-binding fragment to the antigen or epitope it recognizes. In specific embodiments of this invention, CDRs refer to highly variable regions of the heavy and light chains of the antibody.

[0032] In this invention, the heavy chain complementarity determination region is represented by HCDR, which includes HCDR1, HCDR2 and HCDR3; the light chain complementarity determination region is represented by LCDR, which includes LCDR1, LCDR2 and LCDR3.

[0033] Methods for defining CDRs are well-known in the art and include: Kabat definition, Chothia definition, IMGT definition, Contact definition, and AbM definition. As described herein, "Kabat definition" refers to the definition system described in Kabat et al., USDept. of Health and Human Services, "Sequence of Proteins of Immunological Interest" (1983). "Chothia definition" is found in Chothia et al., J Mol Biol 196:901-917 (1987). Other CDR definition methods may not strictly follow one of the above schemes but will still overlap with at least a portion of the CDR region defined by Kabat, although they may be shortened or lengthened based on predictions or experimental results of specific residues or residue groups. Exemplary defined CDRs are listed in Table 1 below; definitions vary slightly in different literature. Given the amino acid sequence of the variable region of an antibody, those skilled in the art can routinely determine which residues contain a specific CDR. It should be noted that CDRs defined by other methods, not limited to those in Table 1, are also within the scope of this disclosure.

[0034] Table 1: CDR Definition 1

[0035] HCDR1 <![CDATA[H31~H35 3 ]]> <![CDATA[H26~H35 3 ]]> <![CDATA[H26~H33..5 5 ]]> <![CDATA[H26~H32..34 4 ]]> HCDR2 H50~H65 H50~H58 H51~H57 H52~H56 HCDR3 H95~H102 H95~H102 H93~H102 H95~H102 LCDR1 L24~L34 L24~L34 L27~L32 L24~L34 LCDR2 L50~L56 L50~L56 L50~L51 L50~L56 LCDR3 L89~L97 L89~L97 L89~L97 L89~L97

[0036] 1The CDRs defined in Table 1 are numbered according to the Kabat numbering system (see below), with amino acid numbers on the heavy chain represented by "H + number" and amino acid numbers on the light chain represented by "L + number". Those skilled in the art can readily map this Kabat numbering system to any variable region sequence without relying on any experimental data outside the sequence itself. As used herein, "Kabat numbering" refers to the numbering system described by Kabat et al., USD ept. of Health and Human Services, "Sequence of Proteins of Immunological Interest" (1983).

[0037] 2 As used in Table 1, “AbM” with a lowercase “b” refers to the CDR defined by the “AbM” antibody modeling software of Oxford Molecular.

[0038] 3 If neither H35A nor H35B exists, then CDR-H1 ends at bit 35; if only H35A exists, then CDR-H1 ends at bit 35A; if both H35A and H35B exist, then CDR-H1 ends at bit 35B.

[0039] 4 If neither H35A nor H35B exists, then CDR-H1 ends at bit 32; if only H35A exists, then CDR-H1 ends at bit 33; if both H35A and H35B exist, then CDR-H1 ends at bit 34.

[0040] 5 If neither H35A nor H35B exists, then CDR-H1 ends at bit 33; if only H35A exists, then CDR-H1 ends at bit 34; if both H35A and H35B exist, then CDR-H1 ends at bit 35.

[0041] According to embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2 or LCDR3 is defined by any one or a combination of systems such as Kabat, Chothia, IMGT, AbM or Contact.

[0042] In some alternative embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are defined by the Kabat system.

[0043] In some optional embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are defined by the Chothia system.

[0044] In some alternative embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are defined by the IMGT system.

[0045] In some alternative embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are defined by the AbM system.

[0046] In some optional embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are defined by the Contact system.

[0047] In some alternative embodiments of the present invention, HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and LCDR3 are defined by a combination of Kabat, Chothia, IMGT, AbM, or Contact systems.

[0048] According to embodiments of the present invention, the Kabat numbering positions corresponding to the amino acid sequences of HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, or LCDR3 defined by the Kabat, Chothia, AbM, or IMGT systems are as follows:

[0049] HCDR1 H31~H35 H26~H35 H26~H33 H26~H32 HCDR2 H50~H65 H50~H58 H51~H57 H52~H56 HCDR3 H95~H102 H95~H102 H93~H102 H95~H102 LCDR1 L24~L34 L24~L34 L27~L32 L24~L34 LCDR2 L50~L56 L50~L56 L50~L51 L50~L56 LCDR3 L89~L97 L89~L97 L89~L97 L89~L97

[0050] Secondly, embodiments of the present invention provide an antibody or antigen-binding fragment against dengue virus or its NS1 protein, wherein the antibody or antigen-binding fragment includes the following complementarity-determining region:

[0051] HCDR1, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:1;

[0052] HCDR2, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:2 or 29;

[0053] HCDR3, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:3 or 30;

[0054] LCDR1, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:4;

[0055] LCDR2, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:5; and

[0056] LCDR3, which contains, or is composed of, the amino acid sequence shown in SEQ ID NO:6.

[0057] According to an embodiment of the present invention, the HCDRs and LCDRs are defined by the Kabat system.

[0058] In this invention, the "frame region" or "FR" region includes the heavy chain frame region and the light chain frame region, referring to the regions in the antibody heavy chain variable region and light chain variable region other than the CDR; wherein, the heavy chain frame region can be further subdivided into adjacent regions separated by the CDR, including the HFR1, HFR2, HFR3 and HFR4 frame regions; the light chain frame region can be further subdivided into adjacent regions separated by the CDR, including the LFR1, LFR2, LFR3 and LFR4 frame regions.

[0059] In this invention, the heavy chain variable region is obtained by connecting the following numbered CDRs and FRs in the following combination: HFR1-HCDR1-HFR2-HCDR2-HFR3-HCDR3-HFR4; the light chain variable region is obtained by connecting the following numbered CDRs and FRs in the following combination: LFR1-LCDR1-LFR2-LCDR2-LFR3-LCDR3-LFR4.

[0060] In an optional embodiment, the antibody or its antigen-binding fragment described in the first or second aspect further comprises at least one of HFR1, HFR2, HFR3, HFR4, LFR1, LFR2, LFR3, and LFR4;

[0061] The HFR1 includes / is such as SEQ ID NO:7 or an amino acid sequence having at least 80% identity with it;

[0062] The HFR2 includes / is such as SEQ ID NO:8 or an amino acid sequence having at least 80% identity with it;

[0063] The HFR3 includes / is, for example, SEQ ID NO:9 or an amino acid sequence having at least 80% identity with it;

[0064] The HFR4 includes / is, for example, SEQ ID NO:10 or an amino acid sequence having at least 80% identity with it;

[0065] The LFR1 includes / such as SEQ ID NO:11 or an amino acid sequence having at least 80% identity with it;

[0066] The LFR2 includes / is, for example, SEQ ID NO:12 or an amino acid sequence having at least 80% identity with it;

[0067] The LFR3 includes / is, for example, SEQ ID NO:13 or an amino acid sequence having at least 80% identity with it;

[0068] The LFR4 includes / such as SEQ ID NO:14 or an amino acid sequence having at least 80% identity with it.

[0069] It should be noted that, in other embodiments, the amino acid sequences of each frame region of the antibody against dengue virus or its NS1 protein or its antigen-binding fragment provided by the present invention may have at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity with the corresponding frame regions (SEQ ID NO: 7, 8, 9, 10, 11, 12, 13, or 14) mentioned above.

[0070] In an optional embodiment, the LFR2 includes / such as the amino acid sequence shown in SEQ ID NO:31 or 32.

[0071] Thirdly, embodiments of the present invention provide an antibody or antigen-binding fragment against dengue virus or its NS1 protein, comprising a heavy chain variable region and / or a light chain variable region, wherein the amino acid sequence of the heavy chain variable region is shown in any one of SEQ ID NO: 17, 18, 19, and the amino acid sequence of the light chain variable region is shown in any one of SEQ ID NO: 20, 21, 22.

[0072] In an optional implementation, the heavy chain variable region and the light chain variable region described in the first or third aspect above are selected from any combination of the following:

[0073] 1 SEQ ID NO:17 SEQ ID NO:20 2 SEQ ID NO:18 SEQ ID NO:21 3 SEQ ID NO:19 SEQ ID NO:20 4 SEQ ID NO:19 SEQ ID NO:22 .

[0074] In optional embodiments, the antibody or antigen-binding fragment thereof described in the first, second or third aspects above further includes a constant region.

[0075] In an optional implementation, the constant region includes a heavy chain constant region and / or a light chain constant region.

[0076] In an optional implementation, the heavy chain constant region is selected from any one of the heavy chain constant regions of IgG, IgA, IgM, IgE, and IgD, or a combination of multiple constant region segments.

[0077] In an optional embodiment, the heavy chain constant region includes CH1 of IgG, the hinge region of IgG, CH2 of IgM, CH3 of IgM, and / or CH4 of IgM.

[0078] In an optional implementation, the IgG is selected from IgG1, IgG2, IgG3 or IgG4.

[0079] In an optional implementation, the light chain constant region is selected from the κ-type or λ-type light chain constant region.

[0080] In an optional implementation, the species source of the constant region is cattle, horses, dairy cows, pigs, sheep, rats, mice, dogs, cats, rabbits, donkeys, deer, mink, chickens, ducks, geese, turkeys, fighting cocks, or humans.

[0081] In an optional implementation, the species source of the constant region is mice.

[0082] In an optional embodiment, the heavy chain constant region sequence (CH) is as shown in SEQ ID NO:15, and the light chain constant region sequence (CL) is as shown in SEQ ID NO:16.

[0083] It should be noted that, in other embodiments, the constant region sequence may have at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity with the aforementioned constant region (SEQ ID NO: 15 or 16).

[0084] In an optional embodiment, the antigen-binding fragment is selected from any one of the antibody's F(ab)2, F(ab')2, Fab', Fab, Fv, and scFv.

[0085] The antigen-binding fragments of the aforementioned antibodies typically possess the same binding specificity as the source antibody. Those skilled in the art will readily understand, based on the description of this invention, that the antigen-binding fragments of the aforementioned antibodies can be obtained, for example, by enzymatic digestion (including pepsin or papain) and / or by chemical reduction of disulfide bonds. Based on the complete antibody structure disclosed in this invention, those skilled in the art can readily obtain the aforementioned antigen-binding fragments.

[0086] The antigen-binding fragments of the aforementioned antibodies can also be obtained by recombinant genetic techniques known to those skilled in the art or by synthesizing, for example, automated peptide synthesizers sold by Applied BioSystems.

[0087] Fourthly, the present invention provides an antibody against dengue virus or its NS1 protein or an antigen-binding fragment thereof, comprising a heavy chain and / or a light chain, wherein the amino acid sequence of the heavy chain is as shown in any one of SEQ ID NO:23, 24, 25, and the amino acid sequence of the light chain is as shown in any one of SEQ ID NO:26, 27, 28.

[0088] In an optional embodiment, the antibody or its antigen-binding fragment described in the first, second, third, or fourth aspect above includes any combination of the heavy chain and light chain:

[0089] 1 SEQ ID NO:23 SEQ ID NO:26 2 SEQ ID NO:24 SEQ ID NO:27 3 SEQ ID NO:25 SEQ ID NO:26 4 SEQ ID NO:25 SEQ ID NO:28 .

[0090] Fifthly, the present invention provides an antibody conjugate comprising the antibody or its antigen-binding fragment described above.

[0091] In an optional embodiment, the antibody conjugate further includes biotin or a biotin derivative conjugated to the antibody or its antigen-binding fragment.

[0092] In an optional embodiment, the antibody conjugate further includes a marker conjugated to the antibody or its antigen-binding fragment.

[0093] In an optional implementation, the aforementioned marker refers to a type of substance that has properties such as luminescence, color development, and radioactivity that can be directly observed by the naked eye or detected or probed by instruments. Through these properties, qualitative or quantitative detection of the corresponding target can be achieved.

[0094] In optional embodiments, the markers include, but are not limited to, fluorescent dyes, enzymes, radioisotopes, chemiluminescent reagents, and nanoparticle markers.

[0095] In practical use, those skilled in the art can select appropriate markers according to the detection conditions or actual needs. Regardless of the marker used, it falls within the protection scope of this invention.

[0096] In optional embodiments, the fluorescent dyes include, but are not limited to, fluorescein dyes and their derivatives (e.g., including but not limited to fluorescein isothiocyanate (FITC), hydroxyfluorescein (FAM), tetrachlorofluorescein (TET), etc., or their analogues), rhodamine dyes and their derivatives (e.g., including but not limited to red rhodamine (RBITC), tetramethylrhodamine (TAMRA), rhodamine B (TRITC), etc., or their analogues), and Cy series dyes and their derivatives (e.g., including but not limited to Cy2, Cy3, Cy3B, Cy3.5, C...). y5, Cy5.5, Cy3 and other similar substances), Alexa series dyes and their derivatives (including but not limited to Alexa Fluor 350, 405, 430, 488, 532, 546, 555, 568, 594, 610, 33, 647, 680, 700, 750 and other similar substances) and protein dyes and their derivatives (including but not limited to phycoerythrin (PE), phycocyanin (PC), allophycocyanin (APC), polydiophytoxanthin-chlorophyll protein (preCP) and other similar substances).

[0097] In optional embodiments, the enzymes include, but are not limited to, horseradish peroxidase, alkaline phosphatase, β-galactosidase, glucose oxidase, carbonic anhydrase, acetylcholinesterase, and glucose-6-phosphate dehydrogenase.

[0098] In optional embodiments, the radioactive isotopes include, but are not limited to, 212Bi, 131I, 111In, 90Y, 186Re, 211At, 125I, 188Re, 153Sm, 213Bi, 32P, 94mTc, 99mTc, 203Pb, 67Ga, 68Ga, 43Sc, 47Sc, 110mIn, 97Ru, 62Cu, 64Cu, 67Cu, 68Cu, 86Y, 88Y, 121Sn, 161Tb, 166Ho, 105Rh, 177Lu, 172Lu, and 18F.

[0099] In optional embodiments, the chemiluminescent reagents include, but are not limited to, luminol and its derivatives, luciferin, fluorescein and its derivatives, ruthenium bipyridine and its derivatives, acridine ester and its derivatives, dioxane and its derivatives, rofenine and its derivatives, and peroxazone and its derivatives.

[0100] In optional embodiments, the nanoparticle-based markers include, but are not limited to, nanoparticles, colloids, organic nanoparticles, magnetic nanoparticles, quantum dot nanoparticles, and rare earth complex nanoparticles.

[0101] In optional embodiments, the colloid includes, but is not limited to, colloidal metals, dispersed dyes, dye-labeled microspheres, and latexes.

[0102] In optional embodiments, the colloidal metal includes, but is not limited to, colloidal gold, colloidal silver, and colloidal selenium.

[0103] In an optional embodiment, the colloidal metal is colloidal gold.

[0104] In an optional embodiment, the antibody conjugate further includes a solid-phase carrier conjugated to the antibody or its antigen-binding fragment.

[0105] In optional embodiments, the solid support includes, but is not limited to, magnetic microspheres, plastic microspheres, plastic microparticles, microporous plates, glass, capillaries, nylon, and nitrocellulose membranes.

[0106] In a sixth aspect, the present invention provides a reagent or kit comprising the antibody or antigen-binding fragment thereof described above or the antibody-conjugate described above.

[0107] As previously mentioned, the antibodies or antigen-binding fragments thereof in some embodiments or examples of the present invention can effectively bind to dengue virus or its NS1 protein. Therefore, reagents or kits containing the antibodies or antigen-binding fragments thereof against dengue virus or its NS1 protein can effectively perform qualitative or quantitative detection of dengue virus or its NS1 protein. The reagents or kits provided by the present invention can be used, for example, for detections involving the specific binding properties of dengue virus or its NS1 protein and its antibodies, such as immunoblotting and immunoprecipitation. As previously mentioned, the antibodies or antigen-binding fragments thereof in some embodiments or examples of the present invention have higher binding activity or affinity to dengue virus or its NS1 protein; therefore, reagents or kits containing the antibodies or antigen-binding fragments thereof have higher detection sensitivity or specificity.

[0108] In a seventh aspect, the present invention provides a method for detecting dengue virus or its NS1 protein, comprising: a) contacting the antibody or its antigen-binding fragment, antibody-conjugate, reagent or kit with dengue virus or its NS1 protein in a sample to be tested under conditions sufficient to induce an antibody / antigen binding reaction to form an immune complex; and b) detecting the presence of the immune complex, the presence of the complex indicating the presence of the antigen in the test sample.

[0109] In an optional embodiment, the immune complex further includes a second antibody that binds to the antibody or its antigen-binding fragment.

[0110] In an optional embodiment, the immune complex further includes a second antibody that binds to dengue virus or its NS1 protein.

[0111] Eighthly, the present invention provides the use of the above-described anti-dengue virus or its NS1 protein antibody or its antigen-binding fragment, antibody conjugate or the above-described reagent or kit in the preparation of products for detecting dengue virus or its NS1 protein.

[0112] In a ninth aspect, the present invention provides a nucleic acid molecule encoding the above-mentioned antibody or its antigen-binding fragment.

[0113] In a tenth aspect, the present invention provides a carrier containing the above-mentioned nucleic acid molecules.

[0114] In the eleventh aspect, the present invention provides cells containing the above-described carrier.

[0115] In a twelfth aspect, the present invention provides a method for preparing an antibody against dengue virus or its NS1 protein or an antigen-binding fragment thereof, comprising: culturing cells as described above.

[0116] Based on the amino acid sequence of the anti-dengue virus or its NS1 protein antibody or its antigen-binding fragment disclosed in this invention, those skilled in the art will readily conceive of using genetic engineering or other techniques (chemical synthesis, recombinant expression) to prepare the anti-dengue virus or its NS1 protein antibody or its antigen-binding fragment. For example, the antibody or its antigen-binding fragment can be isolated and purified from the culture product of recombinant cells capable of recombinantly expressing the antibody or its antigen-binding fragment as described in any of the preceding claims. This is easily achievable by those skilled in the art. Therefore, regardless of the technique used to prepare the anti-dengue virus or its NS1 protein antibody or its antigen-binding fragment of this invention, it falls within the protection scope of this invention.

[0117] To make the objectives, technical solutions, and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below. Where specific conditions are not specified in the embodiments, conventional conditions or conditions recommended by the manufacturer shall apply. Reagents or instruments whose manufacturers are not specified are all conventional products that can be purchased commercially.

[0118] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure pertains. While any methods and materials similar to or equivalent to those described herein may be used in the practice or testing of formulations or unit doses herein, some methods and materials are described hereby. Unless otherwise stated, the techniques employed or considered herein are standard methods. Materials, methods, and examples are illustrative and not limiting in nature.

[0119] Unless otherwise specified, the practice of this invention will employ conventional techniques of cell biology, molecular biology (including recombinant technologies), microbiology, biochemistry, and immunology, which are within the capabilities of those skilled in the art. This technique is well explained in the literature, such as *Molecular Cloning: A Laboratory Manual*, 2nd edition (Sambrook et al., 1989); *Oligonucleotide Synthesis* (edited by M.J. Gait, 1984); *Animal Cell Culture* (edited by R.R. Freshney, 1987); *Methods in Enzymology* (Academic Press, Inc.); *Handbook of Experimental Immunology* (edited by D.M. Weir and C.C. Blackwell); *Gene Transfer Vectors for Mammalian Cells* (edited by J.M. Miller and M.P. Calos, 1987); *Current Protocols in Molecular Biology* (edited by F.M. Mausubel et al., 1987); and *PCR: The Polymerase Chain Reaction*. The references cited in the references are: "Reaction" (Mullis et al., ed., 1994); and "Current Protocols in Immunology" (JEColigan et al., ed., 1991), each of which is explicitly incorporated herein by reference.

[0120] The features and performance of the present invention will be further described in detail below with reference to embodiments.

[0121] Example 1: Preparation of Anti-DN 9H10 Monoclonal Antibody

[0122] In this embodiment, restriction endonucleases and Prime Star DNA polymerase were purchased from Takara. The MagExtractor RNA extraction kit was purchased from TOYOBO. BD SMART TMThe RACE cDNA Amplification Kit was purchased from Takara. The pMD-18T vector was purchased from Takara. The plasmid extraction kit was purchased from Tiangen Biotech. Primer synthesis and gene sequencing were performed by Invitrogen. The hybridoma cell line secreting the Anti-DN 9H10 monoclonal antibody was a hybridoma cell line prepared in our laboratory and was revived for later use.

[0123] (1) Antibody gene preparation

[0124] mRNA was extracted from hybridoma cell lines secreting Anti-DN 9H10 monoclonal antibody, and DNA products were obtained by RT-PCR. The product was then inserted into the pMD-18T vector after an A-addition reaction with rTaq DNA polymerase. The vector was then transformed into DH5α competent cells. After bacterial growth, four clones of the Heavy Chain and Light Chain genes were collected and sent to a gene sequencing company for sequencing.

[0125] (2) Sequence analysis of the variable region gene of Anti-DN 9H10 antibody

[0126] The gene sequences obtained from the sequencing were analyzed in the Kabat antibody database and VNTI11.5 software was used to confirm that the genes amplified by both heavy and light chain primer pairs were correct. Among the gene fragments amplified by the Light Chain primer pair, the VL gene sequence was 324 bp, with a 57 bp leader peptide sequence preceding it; among the gene fragments amplified by the Heavy Chain primer pair, the VH gene sequence was 351 bp, belonging to the VH1 gene family, with a 57 bp leader peptide sequence preceding it.

[0127] (3) Construction of recombinant antibody expression plasmid

[0128] pcDNA TM 3.4 The vector is a constructed recombinant antibody eukaryotic expression vector. This expression vector has been introduced with multiple cloning restriction sites such as HindIII, BamHI, and EcoRI, and is named pcDNA3.4A expression vector, hereinafter referred to as 3.4A expression vector. Based on the sequencing results of the variable region gene of the antibody in pMD-18T, VL and VH gene-specific primers of this antibody were designed, with HindIII and EcoRI restriction sites and protective bases at both ends, respectively. The 0.70kb Light Chain gene fragment and the 1.42kb Heavy Chain gene fragment were amplified by PCR.

[0129] The Heavy Chain and Light Chain gene fragments were digested with HindIII / EcoRI, and the 3.4A vector was also digested with HindIII / EcoRI. After purification and recovery of the fragments and vector, the Heavy Chain gene and Light Chain gene were ligated into the 3.4A expression vector to obtain recombinant expression plasmids of Heavy Chain and Light Chain, respectively.

[0130] 2. Recombinant antibody production

[0131] HEK293 cells were revived early and passaged to a 200ml volume to achieve a cell density of 3–5 × 10⁻⁶ cells / mL. 6 Cell density reached the required antibody concentration and cell viability >95%; cells were washed by centrifugation, reconstituted with culture medium, and the cell density was adjusted to 2.9 × 10⁻⁶ cells / ml. 6 Cells were washed at a concentration of cells / ml and reconstituted with culture medium, which served as a cell dilution buffer. Plasmid DNA and transfection reagent dilution buffers were prepared separately using culture medium. The transfection reagent dilution buffer was added to the plasmid DNA dilution buffer, mixed well, and incubated at room temperature for 15 min. This mixture was then slowly added to the cell dilution buffer over 1 min, mixed well, and samples were taken for cell counting. Cell viability after transfection was recorded and observed. The cells were then incubated at 35°C with a rotation speed of 120 rpm and a CO2 concentration of 8%. After 13 days, the samples were centrifuged and collected. The supernatant was purified using a protein A affinity chromatography column. 6 μg of the purified antibody was subjected to reducing SDS-PAGE, as shown in the figure. The reducing SDS-PAGE showed two bands: one with a Mr of 50 kDa (heavy chain) and the other with a Mr of 28 kDa (light chain).

[0132] The resulting antibody was named Anti-DN 9H10Rmb1. Mutations were performed on Anti-DN 9H10Rmb1 to obtain a mutant antibody. The heavy chain (H) and light chain (L) sequences of the above antibody are shown in the table below:

[0133] Table 2 Antibody Sequences

[0134] Anti-DN 9H10Rmb1 SEQ ID NO:23 SEQ ID NO:26 Anti-DN 9H10Rmb2 SEQ ID NO:24 SEQ ID NO:27 Anti-DN 9H10Rmb3 SEQ ID NO:25 SEQ ID NO:26 Anti-DN 9H10Rmb4 SEQ ID NO:25 SEQ ID NO:28

[0135] Example 2: Antibody Performance Detection

[0136] 1. Activity identification

[0137] Coating buffer (mainly NaHCO3) was used to dilute goat anti-mouse IgG 1ug / ml and coated in microplates at 100µL per well, overnight at 4°C. The next day, the plates were washed twice with washing buffer (mainly Na2HPO4 + NaCl) and patted dry. Blocking buffer (20% BSA + 80% PBS) was added at 120µL per well, and the plates were incubated at 37°C for 1 hour, then patted dry. Diluted purified antibody was added at 100µL per well, and the plates were incubated at 37°C for 60 minutes. The liquid in the plates was discarded, and the plates were patted dry. 20% mouse negative blood was added for blocking at 120µL per well, and the plates were incubated at 37°C for 1 hour. Diluted dengue NS1 antibody was added. Original (from Phytobio), 100 μL / well, 37℃, 40 min; wash 5 times with washing buffer, pat dry; add HRP-labeled anti-dengue NS1 antibody (from Phytobio, which is compatible with the purified antibody), 100 μL / well, 37℃, 30 min; wash 5 times with washing buffer, pat dry; add chromogenic solution A (50 μL / well), add chromogenic solution B (50 μL / well), 10 min; add stop solution, 50 μL / well; read OD value at 450 nm (reference 630 nm) on the microplate reader.

[0138] Notes: Solution A (main components: citric acid + sodium acetate + acetanilide + urea peroxide); Solution B (main components: citric acid + EDTA·2Na + TMB + concentrated HCl); Stop solution (EDTA·2Na + concentrated H2SO4)

[0139] Table 3 Activity Data

[0140] Comparison 0.811 0.492 0.201 0.115 0.017 0.003 Anti-DN 9H10Rmb1 1.287 0.699 0.278 0.193 0.087 0.097 Anti-DN 9H10Rmb2 1.439 0.859 0.417 0.216 0.163 0.094 Anti-DN 9H10Rmb3 1.314 0.845 0.442 0.247 0.171 0.097 Anti-DN 9H10Rmb4 1.907 1.333 0.705 0.365 0.234 0.093

[0141] 2. Application of antibodies in colloidal gold detection

[0142] 2.1 Preparation of Colloidal Gold Test Strips

[0143] 2.1.1 Preparation of nitrocellulose membrane

[0144] Preparation of nitrocellulose membrane: Dilute the anti-dengue NS1 protein antibody Anti-DN (purchased from Feipeng Biotechnology) to 1-5 mg / mL with coating buffer, adjust the machine, and draw the T line (detection line), close to the gold-labeled pad. Dilute the goat anti-mouse IgG antibody to 1-5 mg / mL with coating buffer, adjust the machine, and draw the C line (control line), close to the absorbent pad. The two lines should be 5-8 mm apart and uniform. Dry at 37℃ and package for later use.

[0145] 2.1.2 Preparation of colloidal gold and gold-labeled monoclonal antibodies

[0146] Dilute 1% chloroauric acid to 0.01% with double-distilled deionized water, bring to a boil on an electric stove, add 2 mL of 1% trisodium citrate per 100 mL of 0.01% chloroauric acid, and continue boiling until the liquid turns bright red. Stop heating, cool to room temperature, and replenish any lost water. The prepared colloidal gold should be pure, clear, and free of precipitates and floating matter.

[0147] Adjust the pH of the colloidal gold to 8.2 using 0.1M potassium carbonate. Add the aforementioned antibodies Anti-DN 9H10Rmb1 to Anti-DN 9H10Rmb4 and mainstream commercial raw materials, respectively. Mix with a magnetic stirrer for 30 min. Add BSA to a final concentration of 1% while stirring, and let stand for 1 hour. Centrifuge at 13000 rpm and 4℃ for 30 min, discard the supernatant, and wash the precipitate twice with labeled washing buffer. Resuspend the precipitate with one-tenth of the initial colloidal gold volume of labeled washing buffer. Store the prepared colloidal gold-labeled antibodies Anti-DN 9H10Rmb1 to Anti-DN 9H10Rmb4 at 4℃ for later use.

[0148] 2.1.3 Preparation of gold-labeled pads

[0149] The gold-labeled pads were immersed in blocking solution for 30 minutes and then dried at 37°C. The prepared gold-labeled antibodies were then evenly spread on the gold-labeled pads, with 20 square centimeters per milliliter of solution. The pads were then freeze-dried, encapsulated, and stored at 4°C for later use.

[0150] 2.1.4 Assembly of test strips

[0151] The absorbent pad (purchased from Millipore), nitrocellulose membrane, gold label pad, and sample pad were placed on a non-absorbent support sheet and cut into 3mm wide strips. Ten strips were packaged together, a desiccant was added, and the packages were vacuum sealed to obtain the test strip.

[0152] 2.2 Application of Antibodies in Colloidal Gold Detection

[0153] The assembled test strips were used to detect whether the tested material contained dengue virus NS1 protein, thereby determining the effectiveness of antibodies Anti-DN 9H10Rmb1 to Anti-DN 9H10Rmb4 in detecting dengue virus NS1 protein.

[0154] A double-antibody sandwich assay is used to detect the presence of dengue virus NS1 protein in the test material. During detection, the dengue virus NS1 protein first binds to a colloidal gold-labeled antibody to form a dengue virus NS1 protein-colloidal gold-labeled antibody complex. Due to capillary action, this complex migrates forward along the nitrocellulose membrane. Upon reaching the test line, it binds to the anti-dengue virus NS1 protein antibody Anti-DN prepared in step 3.1.1 of the above embodiment, forming an Anti-DN-dengue virus NS1 protein-colloidal gold-labeled antibody complex, which accumulates on the test line, forming a red precipitate line. The dengue virus NS1 protein-colloidal gold-labeled antibody complex that does not bind to the anti-dengue virus NS1 protein antibody on the test line passes through the test line and is captured by goat anti-mouse IgG antibody, accumulating on the control line and forming a red precipitate line. A positive result is indicated when both the test line and the control line show red precipitate lines. If the sample does not contain dengue virus NS1 protein, when the colloidal gold-labeled antibody that does not bind to dengue virus NS1 protein reaches the test line, it will not form a complex of Anti-DN-dengue virus NS1 protein-colloidal gold-labeled antibody. The colloidal gold-labeled antibody complex that does not bind to dengue virus NS1 protein passes through the test line and only accumulates on the quality control line to form a red precipitation line. At this time, it is judged as a negative result.

[0155] Note: The color development of gold standard is composed of C followed by a number. The smaller the number after C, the stronger the color development and the higher the activity; the higher the number after C, the weaker the color development and the lower the activity; a "+" after the number indicates slightly stronger (0.5C), a "-" after the number indicates slightly weaker (0.5C), and "B" represents negative.

[0156] Note: DF I / DF II / DF III: Positive control serum; Clinical serum: Negative control serum

[0157] Table 4 Performance Evaluation Data

[0158] mainstream raw materials in the market C5+ C4 C5 C6+ B Anti-DN 9H10Rmb1 C4+ C4 C5 C5+ B Anti-DN 9H10Rmb2 C4+ C4+ C4 C5+ B Anti-DN 9H10Rmb3 C4+ C4 C4 C5+ B Anti-DN 9H10Rmb4 C4+ C4+ C4+ C5+ B

[0159] 3. Stability assessment

[0160] The above-mentioned antibodies were placed at 4℃ (refrigerator), -80℃ (refrigerator), and 37℃ (incubator) for 21 days. Samples were taken at 7, 14, and 21 days for observation of their state, and the activity of the 21-day sample was tested. The results showed that no significant changes in protein state were observed under the three testing conditions after 21 days, and the activity did not decrease with increasing testing temperature, indicating that the above-mentioned antibodies were stable. Table 5 below shows the OD results of enzyme immunoassay for antibody Anti-DN 9H10Rmb4 after 21 days of testing.

[0161] Table 5 Stability Data

[0162] 4℃, 21-day sample 1.366 0.746 0.055 -80℃, 21-day sample 1.357 0.772 0.054 37℃, 21-day sample 1.349 0.711 0.059

[0163] The above description is merely a preferred embodiment of the present invention and is not intended to limit the invention. Various modifications and variations can be made to the present invention by those skilled in the art. Any modifications, equivalent substitutions, improvements, etc., made within the spirit and principles of the present invention should be included within the scope of protection of the present invention.

[0164] The partial amino acid sequences involved in this application are shown in Table 6:

[0165]

[0166]

[0167]

Claims

1. An antibody against dengue virus NS1 protein or an antigen-binding fragment thereof, characterized in that, The complementarity-determining regions of the antibody or its antigen-binding fragment are: three complementarity-determining regions of the heavy chain variable region as shown in any of SEQ ID NO:17, 18, 19, and three complementarity-determining regions of the light chain variable region as shown in SEQ ID NO:20; the complementarity-determining regions of the variable region are defined by any one of the Kabat, Chothia, IMGT, AbM, or Contact systems.

2. An antibody against dengue virus NS1 protein or its antigen-binding fragment, characterized in that, The antibody or its antigen-binding fragment includes the following complementarity-determining region: HCDR1, whose amino acid sequence is shown in SEQ ID NO:1; HCDR2, whose amino acid sequence is shown in SEQ ID NO:2 or 29; HCDR3, the amino acid sequence of which is shown in SEQ ID NO:3; LCDR1, whose amino acid sequence is shown in SEQ ID NO:4; LCDR2, whose amino acid sequence is shown in SEQ ID NO:5; and LCDR3, whose amino acid sequence is shown in SEQ ID NO:6; or HCDR1, whose amino acid sequence is shown in SEQ ID NO:1; HCDR2, whose amino acid sequence is shown in SEQ ID NO:29; HCDR3, whose amino acid sequence is shown in SEQ ID NO:30; LCDR1, whose amino acid sequence is shown in SEQ ID NO:4; LCDR2, whose amino acid sequence is shown in SEQ ID NO:5; and LCDR3, whose amino acid sequence is shown in SEQ ID NO:

6.

3. The antibody or its antigen-binding fragment according to claim 1 or 2, characterized in that, The antibody or its antigen-binding fragment also has HFR1, HFR2, HFR3, HFR4, LFR1, LFR2, LFR3 and LFR4.

4. The antibody according to claim 3, characterized in that, The HFR1 is an amino acid sequence with at least 80% identity to SEQ ID NO:7; the HFR2 is an amino acid sequence with at least 80% identity to SEQ ID NO:8; the HFR3 is an amino acid sequence with at least 80% identity to SEQ ID NO:9; the HFR4 is an amino group sequence with at least 80% identity to SEQ ID NO:10; the LFR1 is an amino acid sequence with at least 80% identity to SEQ ID NO:11; the LFR2 is an amino acid sequence with at least 80% identity to SEQ ID NO:12; the LFR3 is an amino group sequence with at least 80% identity to SEQ ID NO:13; and the LFR4 is an amino acid sequence with at least 80% identity to SEQ ID NO:

14.

5. The antibody or its antigen-binding fragment according to claim 4, characterized in that, The amino acid sequence of HFR1 is shown in SEQ ID NO:7; the amino acid sequence of HFR2 is shown in SEQ ID NO:8; the amino acid sequence of HFR3 is shown in SEQ ID NO:9; the amino acid sequence of HFR4 is shown in SEQ ID NO:10; the amino acid sequence of LFR1 is shown in SEQ ID NO:11; the amino acid sequence of LFR2 is shown in SEQ ID NO:12; the amino acid sequence of LFR3 is shown in SEQ ID NO:13; and the amino acid sequence of LFR4 is shown in SEQ ID NO:

14.

6. An antibody against dengue virus NS1 protein or an antigen-binding fragment thereof, comprising a heavy chain variable region and a light chain variable region, characterized in that, The amino acid sequence of the heavy chain variable region is shown in SEQ ID NO:17, and the amino acid sequence of the light chain variable region is shown in SEQ ID NO:20; The amino acid sequence of the heavy chain variable region is shown in SEQ ID NO:18, and the amino acid sequence of the light chain variable region is shown in SEQ ID NO:21; The amino acid sequence of the heavy chain variable region is shown in SEQ ID NO:19, and the amino acid sequence of the light chain variable region is shown in SEQ ID NO:20; or The amino acid sequence of the heavy chain variable region is shown in SEQ ID NO:19, and the amino acid sequence of the light chain variable region is shown in SEQ ID NO:

22.

7. The antibody or its antigen-binding fragment according to any one of claims 1, 2, 4, 5, and 6, characterized in that, The antibody or its antigen-binding fragment also includes a constant region.

8. The antibody or its antigen-binding fragment according to claim 7, characterized in that, The constant region includes the heavy chain constant region and / or the light chain constant region.

9. The antibody or its antigen-binding fragment according to claim 8, characterized in that, The heavy chain constant region is selected from any one of the heavy chain constant regions of IgG, IgA, IgM, IgE, and IgD, or a combination of multiple constant region segments.

10. The antibody or its antigen-binding fragment according to claim 8, characterized in that, The heavy chain constant region includes CH1 of IgG, the hinge region of IgG, CH2 of IgM, CH3 of IgM, and / or CH4 of IgM.

11. The antibody or its antigen-binding fragment according to claim 7, characterized in that, The species source of the constant region is cattle, horses, pigs, sheep, goats, rats, mice, dogs, cats, rabbits, donkeys, deer, mink, chickens, ducks, geese, or humans.

12. The antibody or its antigen-binding fragment according to claim 7, characterized in that, The species source of the constant region is mice.

13. The antibody or its antigen-binding fragment according to claim 8, characterized in that, The heavy chain constant region sequence is an amino acid sequence that has at least 80% identity with SEQ ID NO:15; the light chain constant region sequence is an amino acid sequence that has at least 80% identity with SEQ ID NO:

16.

14. The antibody or its antigen-binding fragment according to claim 8, characterized in that, The heavy chain constant region sequence is shown in SEQ ID NO:15, and the light chain constant region sequence is shown in SEQ ID NO:

16.

15. The antibody according to any one of claims 1, 2, 4, 5, and 6, characterized in that, The antigen-binding fragment is selected from any one of the antibody's F(ab')2, Fab', Fab, Fv, and scFv.

16. An antibody against dengue virus NS1 protein or an antigen-binding fragment thereof, comprising a heavy chain and a light chain, characterized in that, The amino acid sequence of the heavy chain is shown in SEQ ID NO:23, and the amino acid sequence of the light chain is shown in SEQ ID NO:

26. The amino acid sequence of the heavy chain is shown in SEQ ID NO:24, and the amino acid sequence of the light chain is shown in SEQ ID NO:

27. The amino acid sequence of the heavy chain is shown in SEQ ID NO:25, and the amino acid sequence of the light chain is shown in SEQ ID NO:26; or The amino acid sequence of the heavy chain is shown in SEQ ID NO:25, and the amino acid sequence of the light chain is shown in SEQ ID NO:

28.

17. An antibody conjugate, characterized in that, The antibody-drug conjugate comprises the antibody or antigen-binding fragment thereof as described in any one of claims 1 to 16 and biotin conjugated to the antibody or antigen-binding fragment thereof.

18. An antibody conjugate, characterized in that, The antibody-drug conjugate comprises the antibody or antigen-binding fragment thereof as described in any one of claims 1 to 16 and a label or solid-phase carrier conjugated to the antibody or antigen-binding fragment thereof.

19. The antibody conjugate according to claim 18, characterized in that, The markers are selected from fluorescent dyes, enzymes, radioactive isotopes, chemiluminescent reagents, and nanoparticle markers.

20. A reagent or kit, characterized in that, The reagent or kit comprises the antibody or antigen-binding fragment thereof as described in any one of claims 1 to 16 or the antibody-drug conjugate as described in any one of claims 17 to 19.

21. Use of the antibody or antigen-binding fragment thereof according to any one of claims 1 to 16, the antibody-drug conjugate according to any one of claims 17 to 19, or the reagent or kit according to claim 20 in the preparation of a product for detecting dengue NS1 protein.

22. A nucleic acid, characterized in that, It encodes the antibody or antigen-binding fragment thereof as described in any one of claims 1 to 16.

23. A carrier, characterized in that, It contains the nucleic acid as described in claim 22.

24. A cell characterized by, It contains the nucleic acid as described in claim 22 or the vector as described in claim 23.

25. A method for preparing the antibody according to any one of claims 1 to 16, characterized in that, It includes: Culture the cells as described in claim 24.

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