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Mechanisms of Long-Term Persistence of Mycoplasmas in Children with Asthma
Luisa G Gorina1, Natalya A Krylova2, Irina V Rakovskaya1
1Gamaleya National Research Center of Epidemiology and Microbiology, 123098 Moscow, Russia.
Abstract:
Improving the management of children with asthma associated with mycoplasma infection is important. Aim: To study the duration of the persistence of antigens, and DNA in a free state, in the structures of circulating immune complexes (CICs) and living cells of Mycoplasma pneumoniae (Mpn) and Mycoplasma hominis (Mh) in children with asthma. In total, 205 children with asthma from 1 to 14 years were observed. The reaction of aggregate-hemagglutination (AHAA), the direct immunofluorescence reaction (DIF), the reaction of the polymerase chain reaction (PCR), and the culture method were used. In addition, 47 children were re-examined 1.5 months after the treatment of mycoplasma infection with azithromycin. The number of samples positive for antigens and DNA in the free state and in the structures of CICs significantly decreased. Then, 50 blood serum samples containing Mh antigens, and 50 samples containing Mpn antigens were analyzed by culture method. Mh was isolated in 21 (65.5%) of 32 samples containing DNA. Mpn was isolated from antigen-positive samples in nine cases. The presented data indicate the long-term persistence of antigens, and DNA of mycoplasma cells in the free state, in the structure of CICs, as well as in the form of "microcolonies". A high level of CICs can be used to predict the course of the disease and the response to therapy.
Insights
Mycoplasma pneumoniae and Mycoplasma hominis DNA and antigens persist long-term in children with asthma. Circulating immune complexes (CICs) indicate disease severity and treatment response.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Immunology
Background:
- Mycoplasma infections are linked to childhood asthma, complicating disease management.
- Understanding the persistence of Mycoplasma in asthmatic children is crucial for effective treatment strategies.
Purpose of the Study:
- To investigate the duration of Mycoplasma pneumoniae (Mpn) and Mycoplasma hominis (Mh) persistence in children with asthma.
- To analyze the presence of Mpn and Mh antigens and DNA in free states, circulating immune complexes (CICs), and cells.
Main Methods:
- Observed 205 children (1-14 years) with asthma.
- Utilized aggregate-hemagglutination (AHAA), direct immunofluorescence (DIF), polymerase chain reaction (PCR), and culture methods.
- Re-examined 47 children after azithromycin treatment for Mycoplasma infection.
Main Results:
- Mycoplasma antigens and DNA were found to persist long-term in free states, CICs, and as "microcolonies".
- Post-treatment, samples showed a significant decrease in free-state and CIC-associated antigens and DNA.
- Culture confirmed Mh in 65.5% of DNA-positive samples and Mpn in 9 antigen-positive samples.
Conclusions:
- Mycoplasma infection contributes to long-term antigen and DNA persistence in asthmatic children.
- High levels of CICs can predict disease progression and therapeutic outcomes in pediatric asthma.
- Targeting Mycoplasma persistence may improve asthma management in children.
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