The −308G/A polymorphism of TNF-α influences immunological parameters in old subjects affected by infectious diseases

• Published in: International journal of immunogenetics 2005-02, Vol.32 (1), p.13-18
• Main Authors: Cipriano, C., Caruso, C., Lio, D., Giacconi, R., Malavolta, M., Muti, E., Gasparini, N., Franceschi, C., Mocchegiani, E.
• Format: Article
• Language: English
• Subjects: Adult; Aged; Bronchitis, Chronic - genetics; Bronchitis, Chronic - immunology; Bronchitis, Chronic - microbiology; Bronchopneumonia - genetics; Bronchopneumonia - immunology; Bronchopneumonia - microbiology; Communicable Diseases - genetics; Communicable Diseases - immunology; Female; Gene Frequency; Genotype; Humans; Interleukin-6 - genetics; Interleukin-6 - metabolism; Killer Cells, Natural - immunology; Male; Metallothionein - metabolism; Middle Aged; Polymorphism, Genetic; Tumor Necrosis Factor-alpha - genetics; Zinc - metabolism
• ISSN: 1744-3121; 1744-313X
• DOI: 10.1111/j.1744-313X.2005.00490.x

Summary Abnormal increments of pro‐inflammatory cytokines (IL‐6 and TNF‐α) characterize the outbreak of infectious diseases, which are the major cause of death in the elderly. A counterbalance to the inflammation is exerted by IL‐10 with an inhibitory role on TNF‐α production. As is well known, some cytokine gene polymorphisms influence the cytokine production, playing a role as susceptibility or resistance factors against immune‐mediated and infectious disease. Genetic variations in the −308A/G locus for TNF‐α seems to affect the clinical outcome of some infectious diseases. In fact, the −308A allele is associated with severe septic shock and death. On this basis, we have screened healthy old subjects, nonagenarians and old patients affected by the acute phase of chronic obstructive bronchitis and bronchopneumonia of bacteria origin for the −308G/A locus (PCR–RFLP). Subjects are grouped in A+ (AG, AA genotypes) and A– (GG genotype) and data on IL‐6, TNF‐α, IL‐10, NK cell cytotoxicity, zinc and metallothioneins (MTs) gene expression (RT–PCR) were stratified according to different TNF‐α genotypes. The frequency of the A allele was increased in infected patients in comparison with healthy old controls. No differences existed between A+ and A– young adult, old and nonagenarian controls in tested parameters. Conversely, A+‐infected patients displayed elevated IL‐6, TNF‐α and MTmRNA, low IL‐10 coupled with impaired NK cell cytotoxicity and lower zinc ion than A– patients. However, the data reported are gender independent. Therefore, the −308A polymorphism at the locus of TNF‐α may be one of the susceptibility factor for infectious diseases in old persons, particularly considering its association to the increased release of pro‐inflammatory cytokines and to the reduction of zinc release and MTs synthesis involved in the control of the inflammatory response. These data strongly suggest that the genetic screening of the −308G/A polymorphism may be a valid tool for identification of subjects needing a more appropriate therapy when affected by acute and/or recurrent infectious diseases.