Author/Authors :
Dhaouadi, Tarak Laboratory of Research in Immunology of Renal Transplantation and Immunopathology - Charles Nicolle Hospital - Tunis El Manar University, Tunis, Tunisia , Sfar, Imen Laboratory of Research in Immunology of Renal Transplantation and Immunopathology - Charles Nicolle Hospital - Tunis El Manar University, Tunis, Tunisia , Skhiri, Hajer Aounallah National Institute of Public Health, Tunis, Tunisi , Ayed, Saloua Jendoubi Laboratory of Research in Immunology of Renal Transplantation and Immunopathology - Charles Nicolle Hospital - Tunis El Manar University, Tunis, Tunisia , Bouacha, Hend Pneumonology Department - Charles Nicolle Hospital, Tunis, Tunisia , Ben Abdallah, Taieb Laboratory of Research in Immunology of Renal Transplantation and Immunopathology - Charles Nicolle Hospital - Tunis El Manar University, Tunis, Tunisia , Gorgi, Yousr Laboratory of Research in Immunology of Renal Transplantation and Immunopathology - Charles Nicolle Hospital - Tunis El Manar University, Tunis, Tunisia
Abstract :
Chemokines and their receptors play an important role in the late inflammatory stage
of asthma. In this study, we aimed to investigate polymorphisms of MCP-1 (CCL2), CCR2 and
CCR5 which can affect qualitatively and/or quantitatively their production and thus influence
both susceptibility and severity of asthma and its clinical and biological features.
MCP-1 (A/G -2518), CCR2 (+/64I), CCR5 (G/A -59029) and CCR5 (032)
polymorphisms were evaluated by PCR in 107 Tunisian patients with asthma and 169 healthy
controls.
No significant association was found between the four investigated polymorphisms
and asthma. Nevertheless the haplotype MCP1*AG/CCR2*+/+ was significantly l
ess frequent in patients (20.5%) compared to controls (32.5%) (p=0.03; OR=0.54; 95% CI:
0.29-0.98). Whereas no difference was observed in CCR2/CCR5 haplotypes between
patients and controls. Analysis of polymorphisms with clinical and biological features showed
that the concomitant presence of MCP-1*G/CCR2*64I alleles was less frequent in
severe forms (4.34%) compared to moderate disease (12%) but the difference was not
significant (p=0.27). No association was observed between the four polymorphisms and the
presence of atopic rhinitis or atopic conjunctivitis and an elevated rate of serum IgE over 200
IU/ml.
Additional effects of MCP-1 and its receptor CCR2 polymorphisms seem to be involved in
disease susceptibility to asthma in Tunisian patients; nevertheless they could be protective
against its severe forms.
Keywords :
Asthma , Atopy , Chemokines , MCP-1 , Polymorphism