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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
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Genetic Polymorphism and Th1/Th2 Orientation

Authors: BOTTINI, NUNZIO; GLORIA, FULVIA; AMANTE, ADA; SACCUCCI, PATRIZIA; BOTTINI, EGIDIO;

Genetic Polymorphism and Th1/Th2 Orientation

Abstract

<i>Background:</i> It is likely that besides developmental and environmental factors, genetic factors also play an important role in Th1/Th2 orientation and susceptibility to related disorders. Thus, for each genetic factor involved one would expect an opposite pattern of susceptibility towards Th1- and Th2-associated diseases. <i>Methods:</i> We report a comparative analysis of the pattern of association of four genetic polymorphisms with bronchial asthma (Th2 disease) and Crohn’s disease (CD; Th1 disease). The study population included 291 Roman children with bronchial asthma and 72 adult Romans with CD, and haptoglobin, adenosine deaminase (ADA), acid phosphatase locus 1 (ACP1) and MN phenotypes were determined. <i>Results:</i> Compared with controls from the same population, the pattern of phenotype association observed in bronchial asthma is exactly opposite to that observed in CD. The analysis of pairwise gametic type distribution for ACP1, ADA and MN polymorphisms has shown that the pattern of differences between bronchial asthma and controls is opposite to that observed between CD and controls. <i>Conclusions:</i> The pattern of differences between bronchial asthma versus CD is compatible with the hypothesis that some of the genetic systems considered contribute to Th1/Th2 orientation.

Country
Italy
Keywords

Adult, Male, Adenosine Deaminase, Settore MED/01 - STATISTICA MEDICA, Carbonic Anhydrase, Cohort Studies, Genetic, Crohn Disease, Antigens, Neoplasm, Haplotype, Humans, Polymorphism, Antigens, Th2 Cell, Preschool, Carbonic Anhydrase IX, Child, Carbonic Anhydrases, Proto-Oncogene Protein, Polymorphism, Genetic, Haptoglobins, Infant, Newborn, Infant, Middle Aged, Newborn, Isoenzyme, Asthma, Isoenzymes, Th1 Cell, Haplotypes, Haptoglobin, Child, Preschool, Th2 Cells; Male; Th1 Cells; Protein Tyrosine Phosphatases; Isoenzymes; Middle Aged; Asthma; Infant; Female; Child, Preschool; Adenosine Deaminase; Humans; Polymorphism, Genetic; Antigens, Neoplasm; Cohort Studies; Proto-Oncogene Proteins; Haptoglobins; Child; Haplotypes; Infant, Newborn; Adult; Carbonic Anhydrases; Crohn Disease, Neoplasm, Female, Protein Tyrosine Phosphatase, Cohort Studie, Human

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
11
Average
Top 10%
Top 10%
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