Combined reagent and system for evaluating chronic lymphocytic leukemia prognosis

A lymphocyte and leukemia technology, applied in the field of medical technology detection, can solve the problems of time-consuming and difficult to use, and achieve the effect of covering a wide range, facilitating result judgment and rapid detection.

Active Publication Date: 2019-05-14
GUANGZHOU KINGMED DIAGNOSTICS CENT
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0007] Based on this, it is necessary to provide a combined reagent and system for evaluating the prognosis of chronic lymphocytic leukemia in view of the cumbersome, time-consuming, and difficu

Method used

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  • Combined reagent and system for evaluating chronic lymphocytic leukemia prognosis
  • Combined reagent and system for evaluating chronic lymphocytic leukemia prognosis
  • Combined reagent and system for evaluating chronic lymphocytic leukemia prognosis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0061] A combined reagent for evaluating the prognosis of chronic lymphocytic leukemia, the monoclonal antibodies in each group are respectively labeled with the following fluorescent labels FITC, PE, ECD, PE-Cy TM 5. PE-CY7, as follows:

[0062] Antibody combination 1: CD5, IgG1, CD3, CD19, CD45;

[0063] Antibody combination 2: CD5, ZAP70, CD3, CD19, CD45;

[0064] Antibody combination 3: CD38, CD49d, CD19, CD5, CD45.

[0065] The fluorescent labels and dosages of relevant monoclonal antibodies in the above combinations are shown in the table below.

[0066] Table 2. The dosage of each monoclonal antibody

[0067] fluorescent label

[0068] Note: The concentration gradient of the commercially available antibodies was verified to determine the optimal dosage, so the above-mentioned monoclonal antibodies were loaded into flow tubes numbered 1, 2, and 3, respectively.

Embodiment 2

[0070] A system for evaluating the prognosis of chronic lymphocytic leukemia, including: a detection module, a data acquisition module and a data analysis module.

[0071] The detection module performs flow cytometry detection on the cells to be tested;

[0072] The data acquisition module acquires the flow cytometry detection result data of the cells to be tested stained with the combined reagent described in Example 1;

[0073] The data analysis module analyzes the above acquired data, and evaluates the prognosis of chronic lymphocytic leukemia according to predetermined criteria.

[0074] The specific workflow of using the above system is as follows:

[0075] 1. Prepare reagents.

[0076] The combination reagents described in Example 1 were prepared.

[0077] 2. Prepare a single cell suspension.

[0078] The sample source of the cells to be tested can be bone marrow, peripheral blood, pleural effusion, ascites, etc., and the concentration is adjusted to 1×10 according t...

Embodiment 3

[0102] The system for evaluating the prognosis of chronic lymphocytic leukemia in Example 2 was used to evaluate the prognosis of chronic lymphocytic leukemia, and 166 daily samples were randomly selected for detection. The positive rate of IGHV gene mutation detection was 81.2%, and the coincidence rate between the results of this method and the results of IGHV reached 85.3 %, proving that the above system can comprehensively and rapidly evaluate the prognosis of chronic lymphocytic leukemia through multi-parameter flow cytometry analysis.

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Abstract

The invention relates to a combined reagent and a system for evaluating chronic lymphocytic leukemia prognosis, and belongs to the field of medical technology detection. The combined reagent comprisesat least one of the following antibody combinations: an antibody combination 1 including CD5, IgG1, CD3, CD 19 and CD45 antibodies, an antibody combination 2 including CD5, ZAP70, CD3, CD19 and CD45antibodies, and an antibody combination 3 including CD38, CD49d, CD19, CD5 and CD45 antibodies. In the above antibody combinations which aim at CLL (Chronic Lymphocytic Leukemia), the expression of ZAP70, CD38 and CD49d has a great value on an aspect of prognosis evaluation, ZAP70 is accurate, bus since an intracellular dyeing and gating technology restricts clinical application, and the combinedreagent solves the problem to a maximum degree. In addition, two indexes are increased, markers are combined, and chronic lymphocytic leukemia prognosis can be more comprehensively evaluated.

Description

technical field [0001] The invention relates to the field of medical technology detection, in particular to a combined reagent and system for evaluating the prognosis of chronic lymphocytic leukemia. Background technique [0002] Chronic lymphocytic leukemia (CLL) is a malignant tumor that originates in hematopoietic tissue. Tumor cells accumulate in the blood, bone marrow, and lymphoid tissues. More than 95% of CLL is the clonal proliferation of B cells (i.e. B-CLL), and less than 5% of the cases are T cell phenotype (i.e. T-CLL). See a doctor for lymph node enlargement or unexplained increase in the absolute value of lymphocytes. Patients have non-specific manifestations such as mild fatigue and easy fatigue. Once it enters the advanced stage, in addition to generalized lymph nodes and splenomegaly, symptoms of weight loss, repeated infections, bleeding and anemia may appear. Due to the older age of the susceptible population, patients often suffer from exacerbation of ...

Claims

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Application Information

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IPC IPC(8): G01N33/574
Inventor 潘建华张静文郑倩李明敏郭鸣琪
Owner GUANGZHOU KINGMED DIAGNOSTICS CENT
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