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Component

g216 nCyn d 1, Bermuda grass

g216 nCyn d 1, Bermuda grass Scientific Information

Type:

Component

Name; WHO/IUIS:

nCyn d 1, Bermuda grass

Allergen code:

g216

Molecular Weight:

32 - 34 kDa

Description

Bermuda grass is found in warm climates all over the world and its pollen contains at least 12 IgE-binding proteins (3, 4). Cyn d 1 is a major Bermuda grass allergen and is an expansin protein of 32 - 34 kDa.

Expansins are unusual proteins that mediate cell wall extension in plants. They are also known as Group 1 grass allergens, which are highly cross-reactive glycoproteins exclusively expressed in the pollen of many grasses (2).

Cyn d 1 is a member of this group and 95% of patients allergic to grass pollen are allergic to Group 1 grass allergens (5). The frequency of sensitization to Cyn d 1 in Bermuda grass-allergic individuals has been reported to be between 76% and 100% (6, 7).

Potential Cross Reactivity

Bermuda grass is expected to be highly cross-reactive with other species of the subfamily Chloridoideae e.g. Buffalo, Windmill and Grama grasses (12-15).

Single recombinant Group 1 grass allergen contains many of the IgE epitopes of group 1 isoallergens found in a number of different grass species (16). Thus Group 1 grass pollen allergens are highly homologous, but not all of the antigenic epitopes are cross-reactive (8).

Cyn d 1 is to some extent immunologically distinct from Phl p 1 from timothy grass and is therefore a suitable marker for sensitization to Bermuda grass.

Clinical Experience

Bermuda grass is an important source of seasonal aero-allergens in many areas of the world, especially in tropical and subtropical climates. Bermuda grass pollen is a potent inducer of asthma, allergic rhinitis and allergic conjunctivitis (8-10).

Specific IgE tests for Bermuda grass demonstrate that it is one of the most prevalent allergen among children with allergic rhinitis (11). Bermuda grass pollen is also significantly associated with sinusitis (8).

Clinical Unity

Cyn d 1 belongs to Group 1 grass pollen allergens which are the most frequently recognized grass pollen allergens. This allergen group is unique to the grass family and no cross-reactive allergens in pollen of other plants are known. Some diversity exists among members of the Group 1 grass pollen allergens of different subfamilies of grasses, making Cyn d 1 from Bermuda grass at least partly immuno-logically distinct from Phl p 1 from timothy grass. Thus, Cyn d 1 is specifically suited as a marker of Bermuda grass pollen sensitization (1, 2).

References
  1. Kazemi-Shirazi L, Niederberger V, Linhart B, Lidholm J, Kraft D, Valenta R. Recombinant marker allergens: diagnostic gatekeepers for the treatment of allergy. Int Arch Allergy Immunol 2002;127(4):259-68
  2. Andersson K, Lidholm J. Characteristics and immunobiology of grass pollen allergens. Int Arch Allergy Immunol 2003;130:87-107
  3. Everberg H, Thunberg R, Ahlberg M, Högbom E, Movérare R. Purification and characterization of the Bermuda grass pollen major allergen, Cyn d1, for component resolved diagnostics in ImmunoCAP. (Poster) 2nd Int Symp Molecular Allergol, Rome, Italy 2007;April 22-24
  4. Su SN, Lau GX, Tsai JJ, Yang SY, Shen HD, Han SH. Isolation and partial characterization of Bermuda grass pollen allergen, BG-60a. Clin Exp Allergy 1991;21(4):449-55
  5. Mohapatra SS, Lockey RF, Shirley S. Immunobiology of grass pollen allergens. Curr Allergy Asthma Rep 2005 Sep;5(5):381-7
  6. Kao SH, Su SN, Huang SW, Tsai JJ, Chow LP. Sub-proteome analysis of novel IgE-binding proteins from Bermuda grass pollen. Proteomics 2005 Sep;5(14):3805-13
  7. Smith PM, Avjioglu A, Ward LR, Simpson RJ, Knox RB, Singh MB. Isolation and characterization of group-I isoallergens from Bermuda grass pollen. Int Arch Allergy Immunol 1994;104(1):57-64
  8. Weber RW. Bermuda grass. Ann Allergy Asthma Immunol 2002;88(3):A-6
  9. Adler TR, Beall GN, Heiner DC, Sabharwal UK, Swanson K. Immunologic and clinical correlates of bronchial challenge responses to Bermuda grass pollen extracts. J Allergy Clin Immunol 1985;75(1 Pt 1):31-6
  10. Sompolinsky D, Samra Z, Zavaro A, Barishak Y. Allergen-specific immunoglobulin E antibodies in tears and serum of vernal conjunctivitis patients. Int Arch Allergy Appl Immunol 1984;75(4):317-21
  11. Esch RE, Klapper DG. Cross-reactive and unique Group I antigenic determinants defined by monoclonal antibodies. J Allergy Clin Immunol 1987;78:489-95
  12. Suphioglu C, Blaher B, Rolland JM, McCluskey J, Schappi G, Kenrick J, Singh MB, Knox RB. Molecular basis of IgE-recognition of Lol p 5, a major allergen of rye- grass pollen. Mol Immunol 1998; 35(5):293-305
  13. Niederberger V, Laffer S, Froschl R, Kraft D, Rumpold H, et al. IgE antibodies to recombinant pollen allergens (Phl p 1, Phl p 2, Phl p 5, and Bet v 2) account for a high percentage of grass pollen-specific IgE. J Allergy Clin Immunol 1998;101(2 Pt 1):258-64
  14. Smith PM, Xu H, Swoboda I, Singh MB. Identification of a Ca2+ binding protein as a new Bermuda grass pollen allergen Cyn d 7: IgE crossreactivity with oilseed rape pollen allergen Bra r 1. Int Arch Allergy Immunol 1997;114(3):265-71
  15. Suphioglu C, Ferreira F, Knox RB. Molecular cloning and immunological characterisation of Cyn d 7, a novel calcium-binding allergen from Bermuda grass pollen. FEBS Lett 1997;402(2-3):167-72
  16. Laffer S, Valenta R, Vrtala S, Susani M, van Ree R, Kraft D, Scheiner O, Duchene M. Complementary DNA cloning of the major allergen Phl p I from timothy grass (Phleum pratense); recombinant Phl p I inhibits IgE binding to group I allergens from eight different grass species. J Allergy Clin Immunol 1994;94(4):689-98