Polypeptide for specificity detection of tubercle bacillus infection contamination and reagent kit thereof
A Mycobacterium tuberculosis, specific technology, applied in the field of immunology, can solve the problems of high false negative, insufficient peptide stimulation intensity, easy to miss tuberculosis patients, etc., and achieve the effect of reducing the false positive rate
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Embodiment 1
[0024] A total of 58 healthy volunteers were selected, and all of them were negative in the traditional tuberculin skin test. The lymphocytes in the blood of each healthy volunteer were extracted by conventional methods, and their lymphocytes were divided into two parts, which were tested by ELISPOT for tuberculosis.
[0025] The specific steps were carried out according to the method listed in the literature Selected Pool of Peptides from ESAT-6 and CFP-10Proteins for Detection of Mycobacterium tuberculosis Infection (PubMed15297485). The stimulating polypeptide library used in the first part completely adopts the polypeptide library listed in this document, which contains the polypeptide CFP-10 51-70 (Seq ID No.1). The second part uses the same polypeptide library, but replaces CFP-10 51-70 with the polypeptide DKW51-70 of the present invention (Seq ID No.2).
[0026] No healthy volunteers should have a positive reaction, and any positive reaction is a false positive. Resu...
Embodiment 2
[0028] Select 23 patients who were clinically diagnosed as tuberculosis patients. The lymphocytes in the patient's blood were extracted by conventional methods, and their lymphocytes were divided into two parts for tuberculosis ELISPOT examination.
[0029]The specific steps were carried out according to the method listed in the literature Selected Pool of Peptides from ESAT-6 and CFP-10Proteins for Detection of Mycobacterium tuberculosis Infection (PubMed15297485). The stimulating polypeptide library used in the first part completely adopts the polypeptide library listed in this document, which contains the polypeptide CFP-10 51-70 (Seq ID No.1). The second part uses the same polypeptide library, but replaces CFP-10 51-70 with the polypeptide DKW51-70 of the present invention (Seq ID No.2).
[0030] Results In the two reagent groups, there were 20 positive reactions, and the diagnostic sensitivity was exactly the same, both being 87%. This shows that compared with the exist...
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