Abstract

The objective : using double-site enzyme immunoassay (ELISA) to evaluate the specificity of the antigens of digestive and chemically modified cell walls (CW) of M. tuberculosis. Subjects and methods . Hyperimmune sera of mice were obtained against modified CW antigens; immunoglobulins of different subclasses were isolated from them. With their help, 152 Bactec cultures with mycobacterial and non-mycobacterial growth from patients with lung diseases were tested by ELISA. Results . When CW was treated with proteinase K (prK), the protein content decreased by 10 times, and upon hydrolysis of NaOH, by more than 30 times. In immunoblotting, there was a narrowing of the spectrum of recognized antigens by the sera of hyperimmune mice (compared with whole CW), which indicated a decrease in their immunogenicity. Modification of WC of M. tuberculosis disavows 54 kDa antigen, causing a strong IgG1 subclass response. Diagnostic efficacy in ELISA with Bactec cultures increases with the use of immunoglobulins obtained against antigens treated with proteinase K – 79.14% (Pr.A) and 86.68% (Pr.G), when compared with immunoglobulins against the original drug – 70.69% (Pr.A) and 69.11% (Pr.G). Specificity increases significantly when using IgG1 antibodies after immunization with CW treated with prK (71.92% versus 25.93% in the initial preparation). Thus, new antigens of M. tuberculosis were identified, new antibody preparations for diagnosis in microbiological cultures were created against them.

Highlights

  • Hyperimmune sera of mice were obtained against modified cell walls (CW) antigens; immunoglobulins of different subclasses were isolated from them

  • When CW was treated with proteinase K, the protein content decreased by 10 times, and upon hydrolysis of NaOH, by more than 30 times

  • There was a narrowing of the spectrum of recognized antigens by the sera of hyperimmune mice, which indicated a decrease in their immunogenicity

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Summary

Subjects and methods

Hyperimmune sera of mice were obtained against modified CW antigens; immunoglobulins of different subclasses were isolated from them.

Results
Материалы и методы
Результаты исследования
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