The genetics of asthma.

In this paper we have summarized the evidence for a genetic contribution to asthma as well as the recent advances in techniques for identifying the location and function of genes that cause complex diseases. We have also reviewed how these techniques have been applied to the study of asthma and allergy. It is likely that rapid additional advances will be made over the next several years. There are ongoing genome-wide searches to identify additional genes. An understanding of the genetic variation that predisposes people to asthma and the atopic diseases could open a variety of potential diagnostic and therapeutic avenues. Firstly, the identification of the specific mutations that alter the immune response could provide targets for gene therapy. However, in the short run this is unlikely because the risks and costs associated with gene therapy do not presently justify application to alleviate the relatively nonlethal manifestations of allergic diseases. The second potential avenue will be in the development of specific pharmacologic therapy. For example, if variants of the IL-4 gene with enhanced function or of the IFN-gamma gene that have deficient function are identified as causative factors, drug development could be directed toward specific modulators of their effects. However, it is possible that redundancy in the immune and inflammatory responses, coupled with the likelihood of multiple gene involvement, will make such targeting fruitless or dangerous. The third consequence of identifying genetic variants predisposing to asthma and allergy is the possibility of screening. This is perhaps the most likely beneficial outcome of the present search for atopy genes. Recent studies suggest that the clinical onset of atopic diseases can be modified by preventing exposure to cigarette smoke and highly allergenic proteins in the first few years of life (188). At present the power of such studies is limited by the inability to predict those at risk with any certainty. Genetic screening of children born to atopic parents will allow more precise identification of those carrying atopy genes, and this could allow a focused attempt at environmental modification. In the short run this will allow the design of much more powerful prospective studies of prophylaxis, and in the long run screening may prove an effective strategy for asthma prevention.

[1]  H. Scheffer,et al.  Allele sharing on chromosome 11q13 in sibs with asthma and atopy , 1993, The Lancet.

[2]  B. Johnson,et al.  HLA-DR2, [HLA-B7, SC31, DR2], and [HLA-B8, SC01, DR3] haplotypes distinguish subjects with asthma from those with rhinitis only in ragweed pollen allergy. , 1992, Journal of immunology.

[3]  N. Mendell,et al.  Genetic transmission of serum IgE Levels. , 1981, American journal of medical genetics.

[4]  G. Lathrop,et al.  Maternal inheritance of atopic IgE responsiveness on chromosome 11 q , 1992, The Lancet.

[5]  T. Nicolai,et al.  Familial aggregation of asthma in a South Bavarian population. , 1996, American journal of respiratory and critical care medicine.

[6]  S. Harrap,et al.  Linkage of high-affinity IgE receptor gene with bronchial hyperreactivity, even in absence of atopy , 1995, The Lancet.

[7]  M. Klinnert,et al.  Promoter polymorphisms in the chromosome 5 gene cluster in asthma and atopy , 1995, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[8]  G. Lathrop,et al.  Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13. , 1992, Journal of medical genetics.

[9]  M. Wjst,et al.  Genetic risk for asthma, allergic rhinitis, and atopic dermatitis. , 1992, Archives of disease in childhood.

[10]  W. Cookson,et al.  A new variant of the beta subunit of the high-affinity receptor for immunoglobulin E (Fc epsilon RI-beta E237G): associations with measures of atopy and bronchial hyper-responsiveness. , 1996, Human molecular genetics.

[11]  Y. Kawakami,et al.  Association between high serum total IgE levels and D11S97 on chromosome 11q13 in Japanese subjects. , 1995, Journal of medical genetics.

[12]  N. Morton,et al.  Allelic association of gene markers on chromosomes 5q and 11q with atopy and bronchial hyperresponsiveness. , 1996, American journal of respiratory and critical care medicine.

[13]  C. C. Johnson,et al.  Parental history of atopic disease and concentration of cord blood IgE , 1996 .

[14]  L. Caraballo,et al.  HLA-DR3 is associated with the IgE immune responsiveness to a recombinant allergen from Blomia tropicalis (BT). , 1996, Advances in experimental medicine and biology.

[15]  T. Beaty,et al.  Genetics of total serum IgE levels: A regressive model approach to segregation analysis , 1991, Genetic epidemiology.

[16]  J. Hoffmann,et al.  Intermediate α1‐antitrypsin deficiency in atopic allergy , 1981 .

[17]  S. Liggett,et al.  Mutations in the gene encoding for the beta 2-adrenergic receptor in normal and asthmatic subjects. , 1993, American journal of respiratory cell and molecular biology.

[18]  I. Hall,et al.  The glutamine 27 beta2-adrenoceptor polymorphism is associated with elevated IgE levels in asthmatic families. , 1997, The Journal of allergy and clinical immunology.

[19]  D. Postma,et al.  Susceptibility loci regulating total serum IgE levels, bronchial hyperresponsiveness, and clinical asthma map to chromosome 5q. , 1997, Chest.

[20]  M. Wjst,et al.  High serum IgE concentrations: association with HLA-DR and markers on chromosome 5q31 and chromosome 11q13. , 1997, The Journal of allergy and clinical immunology.

[21]  J. Faux,et al.  LINKAGE BETWEEN IMMUNOGLOBULIN E RESPONSES UNDERLYING ASTHMA AND RHINITIS AND CHROMOSOME 11q , 1989, The Lancet.

[22]  J. Lieberman,et al.  A role for intermediate, heterozygous alpha 1-antitrypsin deficiency in obstructive lung disease. , 1990, Chest.

[23]  T. Arinami,et al.  Evidence for linkage between asthma/atopy in childhood and chromosome 5q31-q33 in a Japanese population. , 1997, American journal of respiratory and critical care medicine.

[24]  D. Meyers,et al.  Evidence for linkage of total serum IgE and bronchial hyperresponsiveness to chromosome 5q: a major regulatory locus important in asthma , 1995, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[25]  T. Bouchard,et al.  Atopic disease and immunoglobulin E in twins reared apart and together. , 1991, American journal of human genetics.

[26]  T. Shirakawa,et al.  Association between atopic asthma and a coding variant of Fc epsilon RI beta in a Japanese population. , 1996, Human molecular genetics.

[27]  I. Hall,et al.  Association of Glu 27 β2-adrenoceptor polymorphism with lower airway reactivity in asthmatic subjects , 1995, The Lancet.

[28]  D. Postma,et al.  Evidence for a locus regulating total serum IgE levels mapping to chromosome 5. , 1994, Genomics.

[29]  E. P. Sarafino,et al.  Genetic factors in the presence, severity, and triggers of asthma. , 1995, Archives of disease in childhood.

[30]  R. Townley,et al.  Association of MS Pi phenotype with airway hyperresponsiveness. , 1990, Chest.

[31]  J. Hyde,et al.  Protease inhibitor variants in children and young adults with chronic asthma. , 1979, Annals of allergy.

[32]  D. Marsh,et al.  Molecular genetics of human immune responsiveness to allergens. , 1989, Ciba Foundation symposium.

[33]  W. Cookson,et al.  Tumour necrosis factor haplotypes and asthma. , 1997, Human molecular genetics.

[34]  M. Hill,et al.  Detection of a recessive major gene for high IgE levels acting independently of specific response to allergens , 1995, Genetic epidemiology.

[35]  M. Blettner,et al.  Analysis of familial aggregation of atopic eczema and other atopic diseases by ODDS RATIO regression models. , 1996, The Journal of investigative dermatology.

[36]  N. Morton,et al.  Genetic analysis of atopy and asthma as quantitative traits and ordered polychotomies , 1994, Annals of human genetics.

[37]  N. M. Kjellman,et al.  ATOPIC DISEASE IN SEVEN‐YEAR‐OLD CHILDREN Incidence in Relation to Family History , 1977, Acta paediatrica Scandinavica.

[38]  D. Duffy,et al.  Evidence for linkage of chromosome 12q15-q24.1 markers to high total serum IgE concentrations in children of the German Multicenter Allergy Study. , 1997, Genomics.

[39]  R Kucherlapati,et al.  Linkage of asthma and total serum IgE concentration to markers on chromosome 12q: evidence from Afro-Caribbean and Caucasian populations. , 1996, Genomics.

[40]  W. Morgan,et al.  Evidence for Mendelian inheritance of serum IgE levels in Hispanic and non-Hispanic white families. , 1994, American journal of human genetics.

[41]  R. Erickson,et al.  Association between genetic polymorphisms of the beta2-adrenoceptor and response to albuterol in children with and without a history of wheezing. , 1997, The Journal of clinical investigation.

[42]  J. D. Neely,et al.  Linkage analysis of IL4 and other chromosome 5q31.1 markers and total serum immunoglobulin E concentrations. , 1994, Science.

[43]  R. Matran,et al.  Evidence of a strong, positive association between atopy and the HLA class II alleles DR4 and DR7 , 1996, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[44]  T. Chatila,et al.  The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor. , 1997, The New England journal of medicine.

[45]  G. Lathrop,et al.  A genome-wide search for quantitative trait loci underlying asthma , 1996, Nature.

[46]  W. Cookson,et al.  Investigation of an interleukin-4 promoter polymorphism for associations with asthma and atopy. , 1996, Journal of medical genetics.

[47]  T. Shirakawa,et al.  Association between atopy and variants of the β subunit of the high–affinity immunoglobulin E receptor , 1994, Nature Genetics.

[48]  D. Duffy,et al.  Genetics of asthma and hay fever in Australian twins. , 1990, The American review of respiratory disease.

[49]  J. Kallenbach,et al.  Alpha-1-protease inhibitor in bronchial asthma: phenotypes and biochemical characteristics. , 1992, The American review of respiratory disease.

[50]  J. Mathews,et al.  Twin concordance for a binary trait: III. A bivariate analysis of hay fever and asthma , 1990, Genetic epidemiology.

[51]  R. Katz,et al.  Alpha-1 antitrypsin levels and prevalence of Pi variant phenotypes in asthmatic children. , 1976, The Journal of allergy and clinical immunology.

[52]  S. Green,et al.  Genetic polymorphisms of the beta 2-adrenergic receptor in nocturnal and nonnocturnal asthma. Evidence that Gly16 correlates with the nocturnal phenotype. , 1995, The Journal of clinical investigation.

[53]  T. Takeshita,et al.  Linkage between severe atopy and chromosome 11q13 in Japanese families , 1994, Clinical genetics.